Ocular parasitic infections and geographical distribution
\r\n\tLiterature showed the presence of ACE2 receptors on the membrane of erythrocyte or red blood cell (RBC), indicating that erythrocyte (RBC) can be considered as a peripheral biomarker for SARS-C0V2 infection.
\r\n\r\n\tIncreased levels of glycolysis and fragmentation of RBC membrane proteins were observed in the SARS-C0V2 infected patients, demonstrating that not only RBC’s metabolism and proteome but its membrane lipidome could be influenced by SARS-C0V2 infection changing the homeostasis of the infected erythrocyte. This altered RBC may result in the clot and thrombus formation; the major signs of critically ill Covid-19 patients.
\r\n\r\n\tThis book is going to be a succinct source of knowledge not only for the specialists, researchers, academics and the students in this area but for the general public who are concern about the present situation and are interested in knowing about simple non-invasive measures for identifying viral and bacterial infections through their red blood cells.
",isbn:"978-1-83969-121-8",printIsbn:"978-1-83969-120-1",pdfIsbn:"978-1-83969-122-5",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,hash:"fa5f4b6ef59e28b6e7c1a739c57c5d2f",bookSignature:"Prof. Kaneez Fatima Shad",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/10494.jpg",keywords:"Spike Protein, Hemoglobin, Proteins for Oxygen Transport, Altered Protein Structures, RBC ACE Receptors, RBC ACE-2 Receptors, Carboxypeptidase, Mas Receptor, Metabolomics, Gas Transport, Glucose-6-Phosphate, Phosphoglycerate",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"October 15th 2020",dateEndSecondStepPublish:"November 30th 2020",dateEndThirdStepPublish:"January 29th 2021",dateEndFourthStepPublish:"April 19th 2021",dateEndFifthStepPublish:"June 18th 2021",remainingDaysToSecondStep:"2 months",secondStepPassed:!0,currentStepOfPublishingProcess:3,editedByType:null,kuFlag:!1,biosketch:"Dr. Shad is a governing body member and mentor of Women in World Neuroscience (WWN), a division of the International Brain Research Organization (IBRO). 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During this period, she was also engaged in doing research by getting local and international grants (total of over 3.3 million USD) and translating them into products such as a rapid diagnostic test for stroke and other vascular disorders. She published over 60 articles in refereed journals, edited 8 books, and wrote 7 book chapters, presented at 97 international conferences, mentored 34 postgraduate students. 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The common protozoal parasites primarily infecting the ocular tissue(s) are Acanthamoeba species and Toxoplasma gondii [2–7]. In addition, case studies of eye diseases caused by Leishmania, Trypanosoma cruzi, Entamoeba histolytica, Hartmannella, Plasmodium falciparum, Microsporidia and Giardia lamblia have been rarely reported [1, 8, 9]. Among the helminths, ocular infections are caused primarily by nematode parasites (Onchocerca volvulus, Loa loa, Toxocara canis and Toxocara cati) [1, 8, 10–12]. In addition, case studies of ocular infections caused by other nematodes (Angiostrongylus cantonensis, Dirofilaria repens, Trichinella spiralis, Thelazia callipaeda, Baylisascaris procyonis, Wuchereria bancrofti and B. malayi), cestodes (T.solium cysticercus, Echinococcus granulosus, and Multiceps multiceps larvae) and trematodes (Fasciola hepatica and Schistosoma species) have been reported from different geographical areas [1, 8, 13–15]. The ectoparasites infecting the eye include larvae of flies [16] (Oestrus ovis, Rhinoestrus purpureus, Dermatobia hominis, Chrysomia bezziana, Lucilia spp., Cuterebra, Hypoderma, Cochliomyia, Wohlfahrtia, Gastrophilus), Phthirus pubis, hard and soft ticks (belonging to class Arachnida) [1, 17]. Ocular pentastomiasis caused by the larval stage of Pentastomida, the crustacean-related parasites, is reported to cause permanent loss of vision due to the retinal detachment or lens subluxation [18]. Further, with the advent of HIV/AIDS (human immunodeficiency virus/acquired immune deficiency syndrome), few ocular infections have also been reported in HIV-infected patients [19, 20].
Ocular parasitic infections have been widely reported from different geographical areas (Table 1), mainly depending on the endemicity of the parasite(s). The prevalence depends primarily on the geographical distribution of the parasite, socioeconomic environment and immune status of the patient. The common modes of infection are direct contact (blepharoconjunctivitis caused by Leishmania, Acanthamoeba keratitis, microsporidial infections, infestation caused by lice and mites) [21–23], through blood stream (Toxoplasma chorioretinitis, retinal involvement in malaria, uveitis caused by Toxocara) [1, 23, 24], congenital transmission (Toxoplasmosis) and zoonotic transmission (primarily infectious diseases of animals that can naturally be transmitted to humans) [25]. In addition, few of the helminths that may lead to ocular infection are transmitted by vectors (onchocerciasis, dirofilariasis and thelaziasis), consumption of contaminated food (sparganosis, trichinellosis) and indirectly from the environment (fascioliasis, ascariasis and echinococcosis).
Adult and/or larval stages of the parasites may reside in human ocular tissues externally or in the ocular globe. The clinical symptoms and signs vary, depending on the etiological agent and the ocular tissue/part involved. However, local defense mechanisms and host immune responses play role in establishing the infection. The pathology in the eye can occur due to direct damage by the infecting pathogen, indirectly by toxic products, immune mediated or ectopic localization by ectoparasites. The clinical diagnosis usually mimics other pathologies due to numerous etiologies both infectious and non-infectious, which can cause conjunctivitis, keratitis, uveitis and endopthalmitis [26]. Thus, a high index of clinician suspicion is required for infective parasite etiology in patients having inflammation in the eye. In addition, eye can be involved in various systemic disorders and thorough ocular examination along with history of travel to the endemic area, risk factors and other associated medical illness that help in establishing the preliminary diagnosis. However, confirmatory diagnosis is usually achieved by direct demonstration of parasite in clinical samples and/or pathological changes observed by either slit lamp or biopsy examination [1, 8, 27, 28]. The antigen and antibody detection in ocular fluids and/or serum usually substantiates the clinical diagnosis in few parasitic infections (Toxoplasmosis, malaria, leishmaniasis, ocular gnathostomiasis, cysticercosis, toxocariasis, echinococcosis) [1, 10, 29, 30]. Molecular techniques including detection of parasite DNA by polymerase chain reaction (PCR) have added new dimensions in the diagnosis and species identification [31–36]. The treatment of choice is mostly surgical excision, while in few infections, medical treatment is usually advised either in conjunction with surgical procedure (onchocerciasis, dirofilariasis [37], cysticercosis [38], echinococcosis [39], myiasis, infections due to ticks and mites) or for inoperable patients. Although surgical excision is usually reserved for worms that are large, it is also recommended for space-occupying lesions of the orbit. Drug resistance is posing problem for the effective medical treatment, thus necessitating the discovery of new antiparasitic drugs [32]. Prevention and control measures differ in various infections and usually include proper health education and awareness of various risk factors. The various experimental animal models for few of the ocular infections have been successfully established to study the pathogenic mechanisms, drug efficacy and local immune responses [40, 41].
Although issues mainly are the timely diagnosis and treatment, yet many challenges need to be considered/addressed.
Diagrammatic representation of human eye depicting significant ocular parasitic infections is shown in Figure 1.
Human eye anatomy depicting significant ocular parasitic infections.
The eye balls along with extraocular muscles, nerves, blood vessels and fat are situated in the bony cavities known as orbits. The periosteal covering of the bony orbit fuses with orbital septum and duramater. Abscess due to infectious agent can localize in the space beneath the periostium. The paranasal sinuses are separated from it by the floor, medial wall and roof of the orbit and may act as the source of orbital infection. Lamina papyracea are the thinnest bony walls, which separate orbit from ethmoidal sinuses. Thus, any breach in it causes the ingress of sinus microbiota to orbital tissue leading to infection. Orbital cellulitis can also be caused by direct extension of the infection from the ethmoidal sinuses to the orbital cavity. The lateral wall of the sphenoidal sinus constitutes the medial wall of the optic canal and infection of the former can percolate to the latter causing optic nerve damage and visual loss. There are various apertures present in the orbital cavity, which provides the route of communication with the adjacent structures. The superior and inferior orbital fissures, the lacrimal fossa, nasolacrimal duct and the optic canal constitute such important apertures [1, 42–46].
The ophthalmic artery and its branches constitute main arterial supply of orbit. The majority of the venous drainage occurs through superior ophthalmic vein, which drains into cavernous sinus that is located just posterior to the orbital apex. Veins from the facial region and many anterior ophthalmic veins anastomose and drain into cavernous sinus through superior orbital vein. Thus, cavernous sinus is prone to infection from facial region and also from the orbital region through the superior ophthalmic vein leading to a serious complication.
The eyelids impart two protective anatomical barriers, i.e., orbital septum and conjunctiva. Former divides the orbit from the eyelid into preseptal and postseptal spaces and provides a physical barrier to infectious agents and latter one is reflected back on itself, which provides protection by hindering the free movement of the material posteriorly from the anterior surface of the globe.
Lacrimal system consists of lacrimal gland, accessory gland and excretory system. Tears are secreted by lacrimal gland, which flows over the cornea and finally drain into nasal cavity by nasolacrimal duct through lacrimal sac. Any obstruction to the nasolacrimal duct can lead to regurgitation of the accumulated fluid onto the ocular surface leading to increased chances of infection.
The basic structure of eye ball or globe consists of three concentric layers. The outermost covering is composed of sclera and cornea. The middle covering is composed of uveal tract, consisting of choroid, ciliary body and iris. The inner most covering is retina. The sclera is almost avascular except for the presence of superficial small blood vessels. The choroid is a highly vascular structure and provides nutrition and oxygenation to the retina beneath it. Due to these qualities, choroid serves as a fertile area for the proliferation of various pathogens, which spread by hematogenous route.
Anterior segment of the eye in front of the vitreous humor comprises anterior one-third of the eye and is further divided into anterior chamber and posterior chamber. Anterior chamber is the space between posterior surface of cornea and the iris, whereas posterior chamber is the space between iris and the front of vitreous. The aqueous humor is produced by non-pigmented ciliary epithelium in the posterior chamber and drains through the pupillary aperture into the anterior chamber. Cornea is composed of well-organized collagen fibrils, which is avascular in nature. Lens is also an avascular crystalline structure, which continues to grow throughout life. Thus, aqueous humor fills these spaces and provides nutrition to the surrounding structures.
It is a gel-like substance present in front of retina and posterior to the lens in the posterior segment of the eye. It is optically clear and is composed of collagen framework interspersed with hyaluronic acid. During intraocular inflammation, it becomes hazy and may cause impairment of vision.
Retina constitutes the innermost covering of the eye ball and captures the light energy with the help of rods and cones. The outer half of the retina is supplied by central retinal artery, whereas inner half receives its blood supply from the choroid.
The optic nerve is formed by axons of the inner cell layer that exits the globe. It is covered by all the three meningeal coverings, which are direct extensions of the brain coverings. Thus, it is vulnerable to infections originating from both within cranial vault and within orbits.
The surface of the eye is well protected by both mechanical and immunological defense mechanisms. To breach the defense mechanism, some form of trauma is essential. The eyelids provide mechanical protection to the surface of eyeball. The eyelashes protect against airborne particles and trauma by initiating blink reflex. The cornea is also sensitive to tactile sensation and helps in the initiation of blink reflex, which is provided by dense sensory nerve endings. The lids direct the tears, particulate debris, allergens and microbes to the lacrimal excretory system by its sweeping action over the anterior surface of the eyeball. Bell’s phenomenon also provides protection to cornea as globe is turned upwards and slightly outwards during eyelid closure to avoid corneal exposure [47]. Meibomian glands secrete lipids, which provide stability to the tear film. The epithelial surface of the cornea and conjunctiva provides anatomical barrier to the pathogens. This function is further strengthened by the impermeability provided by the basement and cellular junctional complexes of the cornea. Indigenous flora of the eye also provides protection by creating a competition for colonization by the pathogens.
Immune defense mechanisms are provided by the vascular supply of the eye. Any breach in the anatomical defense system initiates the ocular inflammatory response, which helps in vasodilation and exudation of immunologically active substances and cells [1, 8, 48–52].
There are three layers of the tear film: oil, aqueous and mucous. Majority of the tear film is composed of aqueous layer and pH of the tear film helps in neutralization of toxic substances. Flow of tears help in mechanical flushing of the foreign particles and allergens into the lacrimal excretory system. Mucosal layer helps in entrapment of pathogens. Tear film contains various immunological active substances such as lactoferrin, lysozyme, β-lysin, ceruloplasmin, complement and immunoglobulins.
The conjunctival associated lymphoid tissue lies beneath the conjunctiva. It consists of both B and T lymphocytes. B and T cell precursors mature when exposed to foreign particles or allergens, then migrate to regional lymph nodes for further development, and thereafter return to the conjunctiva through blood stream to produce specific immunoglobulins and cellular defense responses.
Although the cornea is avascular, it is provided by limited defense mechanisms in the form of Langerhans cells (dendritic cells) and immunoglobulins. The surface of the cornea is covered by mucous glycoprotein, which helps in cross-linkage of the IgA and protects the anterior surface of the cornea. Immune defense mechanisms are activated whenever injury occurs, leading to recruitment of the polymorphonuclear cells, lymphocytes and fibroblasts.
Langerhans cells are situated along the peripheral margin of the cornea and conjunctiva. These cells possess receptors, which help in phagocytosis and processing of certain antigens for presentation. Langerhans cells stimulate B and T cells to elicit a strong cellular immune response. During inflammation Langerhans cells migrate toward the cornea, causing increased release of inflammatory substances.
Polymorphonuclear leukocytes are the hallmark of acute inflammation and are associated with oxygen-dependent pathways for the generation of free radicals that help in killing of the invading pathogens. Another immune defense mechanism operated by the production of defensins is antimicrobial proteins active against wide range of pathogens.
Ocular surface is constantly exposed to environment and foreign bodies, thus there are greater chances of infection. However, robust innate immune system at ocular surface protects the eye from infection. There are several peptides of defensins and cathelicidin families that are present in tear film and secreted by corneal and conjunctival cells. These are not only antimicrobial in nature but also help in the recruitment of immune cells and thus provide a link to adaptive immunity. The important defensins present in human eye are hBD-1 (human beta defensins), hBD-2, hBD-3, CAP37 (Cathelicidin-related antimicrobial peptide), LL37 (type of cathelicidin) and HNP-1, 2, 3 (human neutrophil defensins) [53].
Toxoplasmosis is caused by obligatory intracellular protozoan parasite known as Toxoplasma gondii. The mode of infection is either by the ingestion of oocysts shed in feces of the cats or other Felidae (definitive host) or by the consumption of tissue cyst present in the raw or uncooked meat. Life cycle of Toxoplasma includes three stages that are oocysts, tachyzoites and bradyzoites. It completes its life cycle in two phases, one as an intestinal phase in its homologous host, such as cats and another as an extraintestinal phase in its heterologous host, such as mouse, man and other animals. When cats feed on mouse brain containing tissue cysts of T. gondii, a large number of oocysts are released in the infected cat’s feces. After 1–5 days, oocysts get matured and become infective to man and other animals. After ingestion, oocysts liberate sporozoites, which penetrate intestinal mucosa and reach to distant organs such as brain, eyes, liver, spleen, lymph nodes, heart, skeletal muscles and placenta by blood and lymphatic stream. Toxoplasma tissue cysts also occur in the skeletal muscles of the intermediate host such as sheep and pigs (Figure 2) [54]. In addition, developing fetus can acquire the infection transplacentally from the mother during pregnancy. Rarely, infection may also result from consumption of drinking water contaminated with oocysts. The ocular infection can be either congenital or acquired.
Life cycle of T. gondii (Diagrammatic representation).
Approximately, one-third of the world’s population is thought to be infected by T. gondii. It is common in hot and humid climates such as Central America, Asia and the Caribbean region (Table 1, Figure 3). In Europe, toxoplasmosis is common and the highest prevalence rates have been reported in France. Various risk factors such as geographical region, meat consumption, personal habits, animal reservoir and climatic conditions play a significant role in the transmission of infection. In recent years, due to indoor keeping of livestock and improvement in hygiene standards, the risk of acquiring infection has decreased tremendously in the developed nations. However, in the developing nations, risk has increased due to population growth, urbanization trends and increase in meat consumption. Drinking water, seawater and seafood contaminated with oocysts when consumed may account for many unreported cases. Therefore, exact prevalence would be much higher than reported in the literature [55–58].
World map showing geographical areas endemic for ocular protozoal infections.
Ocular toxoplasmosis usually manifests in immunocompromised T. gondii-infected individuals and in neonates who acquire infection transplacentally [4]. The main target organs in congenital toxoplasmosis are the brain, eyes and placenta. T. gondii disseminates through the blood stream, lodges at particular site(s) and develops into tissue cysts. The dendritic cells and macrophages act as “Trojan horses” to guide the parasite through blood-brain barrier to reach at its target site in brain [59]. Inside the host cell, it protects itself from the toxic host molecules by hiding inside the parasitophorous vacuole (structure produced by apicomplexan parasites that allows the parasite to develop inside host cell and protects from phagolysosomes). There are three main clonal lineages of T. gondii. Type I strains being the highest virulent, whereas types II and III are moderately virulent. However, at present more than 130 “atypical” genotypes are known, but their exact role in pathogenesis is not well established. Host genetic factors such as polymorphism in Toll-like receptors (TLR) (TLR2, 5 and 9) are also known to play a role in the susceptibility to and severity of ocular toxoplasmosis [60, 61].
Congenital ocular toxoplasmosis usually involves both the eyes, whereas acquired ocular toxoplasmosis is usually unilateral [62, 63]. Chorioretinitis is caused by necrotizing inflammation due to the rupture of an older cyst. Intense form of choriretinitis may occur in newborns and patients infected with HIV. In addition, congenital toxoplasmosis patients may present with wide range of ocular symptoms such as strabismus, nystagmus and blindness. Acute, acquired infection may result in photophobia, scotoma and loss of central vision. Ptosis may occur due to oculomotor nerve involvement.
Diagnosis of ocular toxoplasmosis in children with congenital infection is established by recognizing distinctive clinical findings such as focal necrotizing retinitis, vitritis, anterior uveitis and cataract [64] However, in cases with atypical presentation or having severe fulminant disease, diagnosis is usually established by analyzing the intraocular fluid for the presence of specific antibodies or the presence of parasite DNA by molecular techniques such as PCR or real-time PCR [65, 66]. PCR is performed by targeting the Toxoplasma B1 gene or other multiple repeat sequences [67–69]. Though, in general, PCR with amniotic fluid is known to have significantly high sensitivity (64%) and specificity (100%) for the diagnosis of toxoplasmosis [70], sensitivity of only 53 and 83% has been documented for the diagnosis of ocular toxoplasmosis [71]. PCR can be performed on either aqueous humor or vitreous fluid, but aqueous humor can be collected more easily. However, the DNA burden in aqueous humor is low, and in rare instances a confirmation would necessitate vitreous sampling [72].
Antibody detection in serum samples is widely used for establishing the diagnosis of toxoplasmosis [73–76], while its role is limited in establishing the diagnosis of the ocular toxoplasmosis. A rising titer of specific IgG over a period of 3 weeks helps in establishing the diagnosis [77]. The detection of specific antibodies in intraocular fluids by the enzyme-linked immunosorbent assay (ELISA) is the most commonly used test for the diagnosis of toxoplasmosis. The Goldmann-Witmer coefficient (GWC) calculation is a common method to estimate the local versus systemic Toxoplasma-specific IgG. This index helps in measuring the intraocular levels of specific antibodies against Toxoplasma. It is expressed as the level of Toxoplasma-specific IgG relative to the level of total IgG in the aqueous humor as a fraction of the level of Toxoplasma-specific IgG relative to the level of the total IgG in the serum. A value of 2 or above is considered as an evidence of intraocular infection. Toxoplasma specific IgG antibodies are produced in response to the actively multiplying tachyzoites at local site of infection [72, 78] The presence of T. gondii-specific IgM is the hallmark of a recently acquired systemic or, possibly, ocular infection. However, high rate of false-positive results due to the persistence of antibodies, decreases its utility as a diagnostic marker for recent ocular toxoplasmosis. In patients with reactivated ocular toxoplasmosis, it is not useful as T. gondii-specific IgM antibodies are either absent or present in very low quantity [79]. Saliva samples have also been tested for the detection of specific antibodies for the diagnosis of toxoplasma encephalitis in immunocompromised individuals, but it may play a limited role in ocular toxoplasmosis [74].
An algorithm for the laboratory confirmation of clinically suspected cases of ocular toxoplasmosis has been reported [72]. Reactivated form of ocular toxoplasmosis is considered in patients with typical lesions of toxoplasmic retinochoroiditis, specific IgG seropositive, specific IgM seronegative and responding to anti-Toxoplasma treatment. However, if patients are specific IgM seropositive, then additional laboratory tests are required. If doubt persists about diagnosis, paired serum and aqueous samples are required to be tested in parallel. The clinical diagnosis along with laboratory evidence is documented in 60-85% of cases and thus, laboratory evidence is lacking in 15-40% of clinically suspected patients. Analysis of aqueous humor is useful in patients presenting with atypical ocular lesions or not responding to specific treatment [72].
In immunocompetent individuals, toxoplasma retinochoroiditis usually resolves within 2–3 months [80]. Classic therapy or triple therapy with a combination of pyrimethamine, sulfadiazine and systemic corticosteroids is recommended for lesions involving or near to fovea, an area critical for vision. Classic therapy is usually associated with significant side effects, therefore other drugs such as trimethoprim-sulfamethoxazole, clindamycin, atovaquone and azithromycin are being evaluated for the treatment of ocular toxoplasmosis [81].
Trimethoprim-sulfamethoxazole (Bactrim) appears to be a safe and effective substitute for sulfadiazine, pyrimethamine and folinic acid for the treatment of ocular toxoplasmosis.
Progressive and recurring necrotizing retinitis, with vision-threatening complications such as retinal detachment, choroidal neovascularization and glaucoma, may occur at any time during the clinical course if the infection is not treated on time. Congenital toxoplasmosis can lead to cataract. The aim of the treatment is to arrest parasite multiplication during the active period of retinochoroiditis and to minimize damage to the retina and optic disc [64].
Animal model(s) can be used to study various aspects of ocular toxoplasmosis [40].
Acanthamoeba keratitis (AK) is caused by Acanthamoeba spp., a free-living protest parasite [82]. The word “acanth” in Greek means “spikes” and has been added as a prefix to “amoeba” to denote the spine-like structures present on its surface. The parasite is present ubiquitously in the environment and exists in two forms, trophozoite and cyst forms. In humans, it can enter through eye, nasal passage or ulcerated broken skin (Figure 4). Infection of the eye can cause blinding keratitis and life-threatening granulomatous encephalitis. Various risk factors contributing to the development of AK are (1) wearing of contact lenses for long time, (2) poor personal hygiene, (3) cleaning of lenses with contaminated water and (4) formation of biofilm on contact lenses [82].
Life cycle of Acanthamoeba (Diagrammatic representation).
Acanthamoeba keratitis is common among the contact lens users, and its geographic distribution is depicted in Table 1 and Figure 3. However, in India the infection is reported even in non-contact lens users [7]. The incidence of Acanthamoeba keratitis in developed nations varies from 1 to 33 cases per million contact lens wearers. In developing nations where contact lens users are limited, the other suggested risk factors are trauma, exposure to contaminated water, use of traditional eye medicine, low socioeconomic background, splashing contaminated water into the eye following dust fall and corneal injury with mud [7, 22, 83]. The pathogenesis of Acanthamoeba involves following sequential events, i.e., breach in the epithelial barrier, invasion of stroma by amoeba, depletion of keratocytes, induction of inflammatory response, photophobia and finally necrosis of stroma leading to blindness [82].
\n\t\t\t\tOcular protozoal infections\n\t\t\t | \n\t\t\t\n\t\t\t\tGeographical distribution\n\t\t\t | \n\t\t
Toxoplasmosis | \n\t\t\tWorldwide particularly in Central America, Asia, Caribbean region, Europe particularly in France | \n\t\t
Acanthamoeba keratitis | \n\t\t\tWorldwide significantly in Chicago, San Francisco, Boston, Philadelphia, Sweden, Portland, New Zealand, United Kingdom, India, Africa | \n\t\t
Chagas disease | \n\t\t\tCentral and South America | \n\t\t
Malaria | \n\t\t\tAfrica, Central & South America, Middle East and Asia | \n\t\t
Leishmaniasis | \n\t\t\tAfrica, Mediterranean region, Middle East, Central and South America, parts of Asia | \n\t\t
Microsporidiosis | \n\t\t\tWorldwide | \n\t\t
Giardiasis | \n\t\t\tSoutheast Asia, South Africa, Europe and USA | \n\t\t
\n\t\t\t\tOcular nematode infections\n\t\t\t | \n\t\t\t\n\t\t |
Onchocerciasis | \n\t\t\tAfrica, South America, Arabian peninsula | \n\t\t
Loiasis | \n\t\t\tCentral and West Africa | \n\t\t
Dirofilariasis | \n\t\t\tAsia, Africa and Europe | \n\t\t
Gnathostomiasis | \n\t\t\tSouth East Asia particularly Thailand, China, Japan and India, Central and South America particularly in Mexico, Guatemala, Peru and Ecuador | \n\t\t
Thelaziasis | \n\t\t\tAsia Pacific region - China, India, Thailand, Indonesia, Japan and Korea | \n\t\t
Toxocariasis | \n\t\t\tWorldwide particularly in Asia, Japan, Korea, Ireland, Alabama | \n\t\t
\n\t\t\t\tOcular cestode infections\n\t\t\t | \n\t\t\t\n\t\t |
Cysticercosis | \n\t\t\tIndian subcontinent, Central and South America, Africa and Far East | \n\t\t
Echinococcosis | \n\t\t\tSouth America, Middle East, Mediterranean countries, India and Australia | \n\t\t
\n\t\t\t\tOcular trematode infections\n\t\t\t | \n\t\t\t\n\t\t |
Fascioliasis | \n\t\t\tFrance, Spain, Italy, Austria, Belgium, United Kingdom, Algeria, Tunisia, Iran, Uzbekistan, Korea, China, Argentina, Chile, Peru, Brazil, Guatemala | \n\t\t
Schistosomiasis | \n\t\t\tSub-Saharan Africa, China, South Asia | \n\t\t
Philopthalmosis | \n\t\t\tEurope (Yugoslavia), Israel, Asia (Thailand, India, Sri Lanka, Japan) and America (i.e., Mexico, and the United States) | \n\t\t
\n\t\t\t\tClinostomum lacramalitis | \n\t\t\tThailand | \n\t\t
Fascioliasis | \n\t\t\tIran | \n\t\t
\n\t\t\t\tAlaria mesocercariasis \n\t\t\t | \n\t\t\tSan Francisco, California | \n\t\t
\n\t\t\t\tOcular infections by ectoparasites\n\t\t\t | \n\t\t\t\n\t\t |
Myiasis | \n\t\t\tWorldwide with greater abundance in poor socioeconomic regions of tropical and subtropical countries, Mediterranean basin and Middle East | \n\t\t
Phthiriasis palpebrum | \n\t\t\tCase reports from Tunisia, Taiwan, India, Pakistan, China, Korea, Lebanon, Israel, Brazil, Turkey, United Kingdom, Belgium, Italy, Cyprus, United States of America (USA) | \n\t\t
Tick infestation | \n\t\t\tCase reports from Ireland, Turkey and USA | \n\t\t
Ocular parasitic infections and geographical distribution
The diagnosis of AK is difficult as it is usually confused with symptoms of bacterial, fungal or viral keratitis. However, history of contact lens use together with a history of excruciating pain is a strong indication toward the diagnosis of AK. For establishing the clinical diagnosis with high sensitivity, in vivo confocal microscopy can be used, which is a non-invasive procedure. The Acanthamoeba cysts appear as hyper-reflective, spherical structures that are well defined because of their double wall. However, trophozoites are difficult to distinguish from leukocytes and keratocyte nuclei [84, 85]. Laboratory confirmation is established by direct demonstration of parasite by immunofluorescence microscopy or by isolating the parasite in culture. Although culture remains the gold standard, it is tedious and time consuming. Multiplex real-time PCR assays (multiplex assays targets more than one region and simultaneously can detect two or more target regions) have also been developed for the detection of different pathogenic free-living amoeba and/or different genotypes of Acanthamoeba. Although molecular techniques have high sensitivity and specificity, these are only available at apex laboratories and also require a well-established molecular laboratory [86]. Newer techniques such as Matrix-Assisted Laser Desorption Ionization Time-Of-Flight (MALDI-TOF) and 1H-NMR spectroscopy [87] are also being tested for the rapid identification of Acanthamoeba in the clinical specimens [88].
Chances of recovery are good if the pathogen is restricted to cornea epithelium but can lead to vision loss, if it invades stroma leading to necrosis and intense inflammation. Medical treatment, if started early, can lead to a significant improvement within 2–3 weeks [89].
Preventive measures include thorough and adequate disinfection of contact lenses. It is recommended to remove contact lenses before any activity involving contact with water, including showering, using a hot tub, or swimming. Hands should be washed with soap and water and dried before handling contact lenses. Contact lenses should not be rinsed with tap water and should be cleaned and stored as per manufacturer’s guidelines. It is suggested that the increased awareness about the other predisposing factors (corneal injury, fall of foreign body in eye) among the general public may enable early and frequent recognition and proper management of AK in patients other than contact lens wearers [7].
Chagas disease or American trypanosomiasis is caused by Trypanosoma cruzi [90]. It is a chronic systemic disease, included in the WHO’s list of most neglected tropical diseases. Approximately, 8 million people are known to be affected in Latin America (Table 1, Figure 3) [8]. The life cycle of the parasite is passed in two stages involving trypomastigotes and amastigotes forms as depicted briefly in Figure 5. T. cruzi passes its life cycle in two hosts: one in man or the reservoir host and other in the transmitting insect. The infection is transmitted by the blood-sucking triatomine bugs when infective metacyclic trypomastigotes in bug’s feces are released onto the skin of humans. These infective trypomastigotes enter the human host when bite wound is either scratched or rubbed, or through permissive mucosal or conjunctival surfaces. Parasites circulate in the human body affecting various tissues and organs. If the initial bite of the triatomine bug is near the orbit, it may lead to severe palpebral and periorbital edema (Romana’s sign) [91]. It causes a painless edema and constitutional symptoms of fever, malaise and anorexia are common. Ocular involvement (posterior uveitis) in congenital Chagas disease is recently reported. Although ocular fundus examination has been unobtrusive, small parafoveolar retinal pigment epithelium defects have been reported in 7.6% of chagasic patients [92].
Life cycle of Trypanosoma cruzi (Diagrammatic representation).
The diagnosis of acute Chagas disease is established by the direct demonstration of trypomastigotes in the blood/buffy coat preparation. Parasites can also be isolated by direct culturing of blood on NNN medium (Novy, MacNeal, Nicolle’s medium). It may take 7 to 10 days for culture to become positive. Diagnosis may also be established by xenodiagnosis. During acute phase, the role of serology is limited in the diagnosis as antibodies take time to develop and false positive results have also been known to be associated with serological tests due to cross-reaction of antibodies to non-pathogenic Trypanosoma rangeli [8, 91]. Furthermore, detailed examination by the ophthalmologist may aid in establishing the diagnosis. However, accumulation of retinal pigment epithelium defects have been shown in patients with intraocular involvement of intermediate and chronic Chagas disease in Paraguay/South America, but overall fundus examination has shown to be unobtrusive [92, 93].
Acute cases of Chagas disease are treated by nifurtimox and benznidazole. Benznidazole is given as 5–7.5 mg/kg per day orally in two divided doses for 60 days. Nifurtimox is given as 8–10 mg/kg per day orally in three or four divided doses for 90 days [91, 94].
Within few weeks, symptoms of acute Chagas disease such as Romana’s sign fade away, but infection persists. The average life-time risk of developing complications of chronic phase is around 30%. It may take more than 20 years to develop chronic complications. However, trypanocidal therapy did not significantly reduce cardiac clinical deterioration through 5 years of follow-up as documented by randomized trial of benznidazole for chronic Chagas’ cardiomyopathy [95, 96].
Leishmaniasis is caused by protozoan parasite that belongs to genus Leishmania. Humans get infection by the bite of phlebotomine sand flies. There are different clinical forms of leishmaniasis, such as visceral leishmaniasis (VL), cutaneous, diffuse cutaneous and mucocutaneous caused by different species of Leishmania. Worldwide, approximately 1.3 million new cases occur every year with a mortality of 20,000 to 30,000 persons per annum [97]. While taking the blood meal, infected sandfly injects promastigotes into humans. Further in the human body, the promastigotes are transformed into amastigote forms, and these are engulfed by tissue macrophages. Amastigote forms replicate inside the cells and further spread either systemically or through cutaneous route, depending on the species of the parasite (Figure 6). Ocular involvement due to leishmaniasis has been reported from various countries such as India, Sudan, Italy, Norway, Turkey and Iran (Table 1, Figure 3) [98–103]. Anterior uveitis is the most common ocular manifestation in VL, which can occur during the course of infection and can further progress to glaucoma [104, 105]. Focal retinal whitening, cotton wool spots, hemorrhages and increased vessel tortuosity have also been reported on fundus examination [106–110]. In severe cases, flame-shaped lesions also appear, which denote hemorrhage from the anterior capillaries of the nerve fiber layer. These findings have also been correlated with anemia and thrombocytopenia as these hemorrhages usually get resolved with treatment, leading to improvement in anemia/thrombocytopenia. Optic neuropathy has been reported due to mucosal leishmaniasis. Eyelid involvement has been documented in cutaneous and mucocutaneous leishmaniasis [111, 112]. Severe involvement can progress to ptosis and ectropion secondary to cutaneous leishmaniasis leading to keratopathy and altered vision [112]. However, eyelid is rarely involved by leishmaniasis and is reported in approximately only 2.5% of cases with cutaneous leishmaniasis [113]. The most common aspect of eyelid leishmaniasis is chalazion-like lesions, but other forms such as ulcerous, phagedenic, cancer-like forms and unilateral chronic granulomatous blepharitis may be observed. Chronic dacryocystitis has been reported in patients suffering from mucocutaneous leishmaniasis, which can effect formation of tear film, leading to dryness of eyes [114]. Endo-ocular lesions have been observed in patients having disseminated cutaneous leishmaniasis. A report from Brazil documented the presence of Leishmania in the aqueous humor along with iridiocyclitis [115]. Although ocular manifestations are not very common, it is suggested that a person with ocular manifestation from endemic country should undergo fundus examination for early diagnosis [116].
Life cycle of Leishmania (Diagrammatic representation).
Diagnosis of leishmaniasis can be achieved by the direct demonstration of parasites in the tissue smears and/or biopsy samples, culture technique(s), antigen and/or antibody detection and molecular technique(s). However, each technique has its own merits and demerits. Amastigotes can be easily identified in the cutaneous and mucocutaneous lesions but are not easily identified in cases with ocular disease [103, 117, 118]. Molecular techniques such as PCR/real-time PCR can identify the genome of parasite with greater sensitivity (100%) and specificity (100%) [119, 120]. The treatment of leishmaniasis depends on several factors such as clinical form of the disease. The antileishmanial drugs include pentavalent antimony, sodium stibogluconate, liposomal Amphotericin B, miltefosine and paromomycin [118, 121].
Ocular lesions do not heal without treatment and could lead to vision loss if conjunctiva is involved due to severe ulceration. Healing occurs without visual impairment if treatment is initiated early during the course of infection and vigorous treatment is required to prevent blindness [121, 122].
Malaria is caused by the parasites of Genus Plasmodium and is transmitted by the bite of female anopheles mosquitoes. The malarial parasite passes its life cycle in humans and mosquitoes. Inside human host, Plasmodium undergoes exoerythrocytic and erythrocytic schizogony as shown briefly in Figure 7. Malarial parasite multiplies by asexual method (schizogony) while residing inside liver cell and the red blood cells. After the parasites have undergone erythrocytic schizogony for a certain period, some of the merozoites give rise to gametocytes, which are taken up by mosquitoes during their blood meal. The gametocytes further develop into sporozoites that are infective to man. Sporozoites when introduced into humans are not directly infective for red blood cells, but undergo development initially in hepatic cells (exoerythrocytic schizogony) and later on invade red blood cells to complete erythrocytic schizogony. As per World Malaria Report 2014 [123], an estimated 3.3 billion people are at risk of developing malaria (Table 1, Figure 3). Complications of severe malaria due to P. falciparum mainly occur due to the sequestration of malarial parasite in the microvasculature leading to occlusion and hypoxia. Most of the ocular manifestations occurring in malaria are a result of the same mechanism. Sequestration is further amplified by auto agglutination and resetting [124, 125].
Life cycle of Plasmodium (Diagrammatic representation).
Wide range of ocular symptoms has been reported in patients suffering from malaria. Uncomplicated malaria is usually not associated with significant ocular findings but rarely may be associated with edema and hyperemia of the eyelids, chemosis of conjunctiva, conjunctival hemorrhage and anterior uveitis [126]. On the other hand, severe ocular manifestations may occur in cerebral malaria due to P. falciparum leading to visual field defects, cortical blindness, optic neuritis, papilledema and optic atrophy [127]. Ocular motor disturbances have also been reported. Occasionally, infarcts in brainstem may cause changes in pupillary reaction and disorders of eye movements. Patients with cerebellar syndromes may present as nystagmus [128, 129]. Characteristics features such as retinal whitening consisting of irregular patchy areas may be localized or diffused in all segments of retina [130]. Blood vessel changes manifest as discoloration (white or orange) occurring mainly in the peripheral fundus, whereas white-centered retinal hemorrhages may manifest as malaria retinopathy. Discoloration of retinal vessels occurs due to the absence of hemoglobin in parasitized erythrocytes, sequestered within retinal vasculature and thus cannot reflect normal red color. Retinal changes in cerebral malaria are considered as poor prognostic markers [131]. The prevalence of any retinopathy, papilledema, hemorrhages, vessel changes, macular whitening and peripheral whitening has been reported in 61, 15, 46, 32, 46 and 44%, respectively, among children with cerebral malaria in Malawi [132].
Diagnosis of malaria is established by light microscopy or by rapid antigen detection kits. Light microscopic examination of Giemsa-stained peripheral blood smear is considered as gold standard for the diagnosis of malaria with a threshold of about 50–100 parasites/µL [133]. However, in addition, ocular examination may provide clue to the diagnosis as specific retinal changes can be seen directly [129, 134, 135].
Treatment depends on the species of Plasmodium causing infection. Artemisinin combination therapy is recommended for malaria due to P. falciparum. Artemisinin combination therapy includes short-acting artemisinin derivative and long-acting antimalarial (sulphadoxine-pyrimethamine, lumefantrine). Chloroquine along with primaquine is recommended for malaria due to P. vivax. Ocular toxicity [136] is very well documented with chloroquine therapy. This includes corneal changes (cornea verticillata) and corneal deposits. Toxic maculopathy and scotoma has also been reported. Quinine overdose has also been known to cause decreased vision, retinal and macular degeneration, mild scotomas and color vision defects [136].
If not treated, malarial retinopathy is associated with serious consequences as reports indicate that the severity of retinopathy is related to prolonged death and coma. After antimalarial treatment and resolution of coma in severe malaria, malarial retinopathy resolves after some time [132, 137].
Microsporidiosis is the term used to denote the infection caused by microsporidia belonging to phylum Microspora [23]. Microsporidia were once thought to be protists but are now known to be fungi. Although it is classified as a protozoal disease in ICD-10, their phylogenetic placement has been resolved to be within the fungi [138]. Microsporidiosis is considered as an opportunistic infection in AIDS/HIV-infected individuals and is prevalent worldwide (Table 1) [1]. Microsporidia are small, unicellular, spore forming, obligate intracellular pathogens. Important genera responsible for ocular manifestations are Encephalitozoon and Nosema. Another species, Septata, has also been reported to cause keratoconjunctivitis [139]. The prevalence of microsporidiosis ranges from 2 to 50% among severely immunocompromised, HIV-infected patients found in North America, western Europe and Australia. The prevalence data for microsporidiosis is limited among non-HIV-infected persons [9].
The life cycle of parasite involves three stages (Figure 8):
The resistant spore (infective form)
The spore injects the infective sporoplasm into the host cell. Inside the host cell, sporoplasm undergoes multiplication either in the cell cytoplasm or inside parasitophorous vacuole. Microsporidia develop to mature spores by sporogony that are released by disruption of cell membrane. The free mature spores are the infective forms.
Life cycle of Microsporidia (Diagrammatic representation).
Ocular manifestations caused by Microsporidia are mainly limited to conjunctiva and cornea. Corneal involvement may lead to punctate epithelial keratitis, hyphema, necrotizing keratitis and corneal ulcer. Symptoms include foreign body sensation, photophobia and decrease in visual acuity [23].
Diagnosis is established by direct demonstration of the spores by microscopy or electron microscopy of the corneal scrapping or biopsy specimens. Isolation of the parasites in culture has also been attempted [140]. There are no reports on use of serological tests to detect antibodies in serum or tears in ocular microsporidiosis [9]. Lesions usually heal after 1–2 weeks as it is self-limiting. Treatment of microsporidial keratoconjunctivitis with polyhexamethylene biguanide does not offer any significant advantage but treatment with topical fumagillin showed significant improvement [141–143].
Giardiasis is caused by Giardia duodenalis (syn. G. lamblia or G. intestinalis) [144]. The infection is transmitted by ingestion of contaminated water/food or directly by feco-oral route. The parasite exists in trophozoite and cyst forms as shown in Figure 9. In the trophozoite stage the parasite multiplies in the intestine of man by binary fission. When conditions become unfavorable in the small intestine, encystment occurs and cysts are released along with feces. After ingestion, within 30 minutes, cyst hatches out trophozoites that further multiply in the small intestine. It is found both in developing and developed nations (Table 1, Figure 3). Although it mainly causes diarrhea and malabsorption, in one-third of the patients, it can also result in long-term extra intestinal manifestations [145].
Life cycle of Giardia lamblia (Diagrammatic representation).
Barraquer was the first to report the ocular manifestation (iridiocyclitis, choroiditis and retinal hemorrhages) in patients who were suffering from diarrhea due to G. duodenalis. Retinal changes in the form of ”salt and pepper” degeneration have been reported in children suffering from giardiasis. Corsi et al. [146] reported salt and pepper retinal changes in 19.9% of the patients with giardiasis. This occurs due to the damage of the retinal cells and subsequent release of pigment granules in retina giving an appearance of blackish dots on a background of light yellow pink retina. The exact mechanism(s) by which giardiasis leads to ocular manifestations is still unknown, although possibility of direct invasion by the parasite is excluded (137). Further studies are desired to exactly pinpoint the mechanism by which retinal manifestations follow the occurrence of intestinal giardiasis. Alterations in the retinal pigment layer are most common but do not cause functional changes in retina, and these lesions do not progress or regress with time [146].
The diagnosis is established by direct demonstration of the parasite in the fecal samples by microscopy. Concentration techniques of the samples yield higher sensitivity. Nitroimidazole group of drugs are highly effective against G. duodenalis. Most commonly used drugs are metronidazole for 5–7 days or ornidazole/tinidazole in single dose [147]. Treatment of intestinal infection is recommended if present, but no specific treatment is required for ocular manifestations related to retina [146].
Onchocerciasis, also known as “river blindness”, is caused by Onchocerca volvulus, the filarial nematode. It is transmitted from person-to-person by the repeated bites of infected blackflies (Simulium species). These blackflies are mostly found near the flowing rivers and streams and transmit the infection to the people residing in nearby remote villages [148]. The life cycle of the parasite passes between black flies and humans as shown in Figure 10. While taking a blood meal, stage 3 larvae present in infected blackfly are transmitted onto human skin and penetrate into bite wound. In subcutaneous tissue, these larvae develop into adult filariae. Adult worm produces hundreds of thousands of embryonic larvae (microfilariae) that may persist for 3-5 years in the human host. These embryonic larvae migrate to the skin, eyes and other organs. The microfilariae are ingested by the female blackfly when it bites infected humans and develop further in the blackfly. During subsequent bites, it transmits infection to new human host [148, 149].
Life cycle of Onchocerca volvulus (Diagrammatic representation).
Onchocerciasis mainly occurs in tropical countries and majority of the cases (99%) have been reported from sub-Saharan Africa. It is also found in some countries of the Middle East and Latin America such as Brazil, Guatemala, Mexico and Venezuela (Table 1, Figure 11). Approximately, 25 million people are known to be affected by onchocerciasis worldwide, and it is known to cause visual impairment and blindness in approximately 800,000 and 300,000 people, respectively [148, 150]. The inflammatory response initiated against dying microfilariae causes gradual and progressive loss of vision due to sclerosal keratitis [149, 151]. Apart from causing keratitis, clinical features may also manifest as iridiocyclitis, chorioretinitis and optic atrophy. Autoimmune mechanisms have also been postulated to cause inflammation in the posterior eye. Accumulation of retinal and retinoic acids, strong eosinophilic response and immune reaction against Wolbachia antigens [152] released by dying microfilariae also contributes to the ocular pathogenesis [153].
World map showing geographical areas endemic for ocular nematode and cestode infections.
The filarial parasites of major medical importance in humans contain the symbiotic bacterium Wolbachia, and reports have revealed that targeting of these bacteria with antibiotics results in a reduction in worm viability, development, embryogenesis and survival. Wolbachia is present as an intracellular bacteria symbiont in all the developmental stages of Onchocerca volvulus. Clearance of the endosymbionts by antibiotic treatment causes inhibition of worm development. Wolbachia contributes directly to the metabolic activity of the nematode. Various biochemical pathways such as heme, nucleotide and enzyme co-factor biosynthesis are intact in Wolbachia but absent or incomplete in nematode [154].
Diagnosis is difficult to establish in light infections. Skin snips can be subjected to microscopy for visualizing the larvae, but it yields very low sensitivity. Infections of the eye can be diagnosed with direct demonstration of the parasite by slit-lamp examination or by demonstrating the parasite in sclerocorneal punch biopsy. Newer techniques such as skin-snip PCR can establish the diagnosis if larvae are not visualized [155]. Antibodies can be detected by ELISA or EIA, but these tests cannot distinguish between past and current infections [156, 157]. Skin-snip PCR has 84–91% sensitivity and 100% specificity [149]. The sensitivity and specificity of serum antibody detection has been reported to be 78–99% and 95–100%, respectively [149]. A promising antigen detection by dipstick assay was recently developed, but its specificity was found to be low in high endemic areas due to cross reaction with urine filarial antigen [158, 159]. Xenodiagnosis (exposing possible infected tissue to a vector and then examining the vector for the presence of microorganism) has also provided clue in some cases.
If the infection is not treated on time, it can progress toward blindness [160]. Drug of choice for the treatment is ivermectin, given 150 to 200 µg /kg body weight, every 6 months to prevent the skin damage and blindness. Treatment with ivermectin has been shown to decrease visual field loss and severity of keratitis. Ivermectin only kills the larvae but not the adult worms. Doxycycline can be used to kill the adult worm. The mechanism of action is that it kills the Wolbachia bacteria residing in the worm, on which the adult worm depends for its survival. Treatment with a 6-week course of doxycycline has been shown to kill more than 60% of adult female worms and to sterilize 80–90% of females 20 months after treatment. Thus, treatment with ivermectin is advised one week prior to treatment with doxycycline to provide relief to patient [148, 161].
The best method to get the protection from insect bite is the use of insect repellent. Community-directed treatment with ivermectin (CDTI) along with vector control measures is the main approach to control onchocerciasis. Ivermectin kills microfilariae and also prevents adult worms from producing more microfilariae for few months following treatment, so reduces transmission [148].
Loiasis is caused by Loa loa, the African eyeworm. It is transmitted by the bite of tabanid flies, belonging to the genus Chrysops. It affects approximately 3 million people, residing in certain rain forests of Central and West Africa (Table 1, Figure 11) [162, 163]. The tabanid flies most commonly bite during day time and are more common during rainy season. The smoke of wood fires and movement of people attract them. These flies are more commonly found near rubber plantations and are attracted by the well-lit homes. The larvae are passed from flies to humans when humans are bitten by these flies [162]. The larvae develop into adults in the human host over one year and migrate through cutaneous and subcutaneous tissue (Figure 12). Migration of the adult worm is painless, but it is associated with mild tingling sensation. It may involve the nasal area, bulbar conjunctiva and eyelids [164].
Life cycle of Loa loa (Diagrammatic representation).
Ocular manifestations may occur due to the presence of both microfilariae and adult worms. The adult worms may survive up to 15 years and have been found in the conjunctiva, vitreous, eyelid and anterior chamber. Calabar swellings [165] may occur as a result of localized angioedema due to intense atopic reaction. Retinal hemorrhages may occur due to aneurysmal dilatation of the retinal vessels due to the invasion of the retinal and choroid vessels by the microfilariae present in blood stream. Perivascular inflammation can also be present, and ocular examination under slit lamp examination is useful in establishing the diagnosis.
The diagnosis is usually confirmed by the direct demonstration of the microfilariae in the blood by visualizing Giemsa-stained slides under the microscope. However, many of the individuals having visible worm in the eye may test as amicrofilaraemic [166]. Blood should be drawn during the midday as this time coincides with the periodicity of the microfilariae in the blood. The microfilariae can also be demonstrated in unstained blood smear. Adult worm extraction establishes the diagnosis in patients having conjunctival involvement [167]. Antibody detection [168] may aid in establishing the diagnosis, but its presence cannot differentiate between recent and past infection. Eosinophilia and high IgE also indicate active infection [169].
Eye worm if not treated causes very little damage to eye as it lasts less than one week (often just hours). Surgical removal relieves eye symptoms, in addition medical treatment is required for treating loiasis [170]. Therapy involves manual removal of adult worms and administration of diethylcarbamazine (DEC), which kills both adult worms and microfilariae.
Dirofilariasis is caused by nematodes belonging to the genus Dirofilaria. The various species of Dirofilaria that are natural parasites of domestic and wild animals are D. immitis, D. repens, D. tenuis and D. ursi [37]. It is prevalent worldwide and is an important zoonotic infection. It is being reported in increasing numbers from Mediterranean countries such as Italy and have also been reported from France, Greece, Spain, Croatia, India, Serbia, Denmark, Russia and Tunisia (Table 1, Figure 11). The parasite passes its life cycle in canids as definitive host as shown in Figure 13. Mosquitoes act as intermediate host and vector for the transmission of infection from animals to human host. Mosquitoes take up microfilariae along with blood meal from the infected host, develop inside the mosquitoes and are subsequently transmitted to other hosts while taking a fresh blood meal. Larvae migrate from the subcutaneous tissue to the right side of the heart and/or to other parts of the body where maturation takes place. Depending on the site of lodgment, it can cause pulmonary, cardiovascular, subcutaneous or ocular infection [28].
Life cycle of Dirofilaria repens (Diagrammatic representation).
There are several cases that document ocular involvement due to dirofilariasis [37, 171–173]. Ocular symptoms depend on the site of infection. Eyelid involvement [174] leads to edema, pain, pruritus and congestion of conjunctiva, whereas intraocular [175] involvement leads to foreign body sensation, diplopia, photophobia and floaters.
Diagnosis can be established by the direct demonstration and identification of the adult worm. Intraocular presence of the parasite can be confirmed by ophthalmoscopy. Serological techniques are not useful in establishing the diagnosis due to the cross reaction with other parasitic helminths, particularly Toxocara canis. Recombinant proteins proved to exhibit 100% sensitivity and 90% specificity by ELISA for the diagnosis of pulmonary dirofilariasis [176].
Without treatment, worm remains in eye causing symptoms due to its presence [177]. Surgical excision is the treatment of choice; however use of diethylcarbamazine (DEC) has also been reported with some success [37, 178].
Gnathostomiasis is a food-borne zoonotic parasitic infection, caused by ingestion of raw or undercooked freshwater fish, pork, chicken, frog and snake [179, 180] contaminated with the third-stage larvae of Gnathostoma species. The life cycle of the parasite passes in pigs, cats and wild animals as definitive host, whereas small crustaceans act as first intermediate host and fish, frog or snake act as second intermediate host as depicted in Figure 14. In the infected person, larvae migrate through viscera and reach internal organs and subcutaneous tissues. Depending on the location of lodgment, it can cause cutaneous, visceral, ocular or cerebral gnathostomiasis. Majority of the cases have been reported from East Asia (Thailand, China, Japan and India) and Central and South America (Mexico, Guatemala, Peru and Ecuador) (Table 1, Figure 11). However, sporadic cases have been reported worldwide [181]. Gnathostoma spinigerum is the most common species causing infection in humans.
Life cycle of Gnathostoma (Diagrammatic representation).
Ocular manifestations occur due to the migration of the parasite and its metabolites, leading to inflammatory response. Conjunctiva and corneal infection may lead to congestion of the conjunctiva and corneal ulceration, respectively. Intraocular involvement may lead to glaucoma, uveitis, retinitis and vitreous hemorrhage [182, 183]. In severe cases, retinal detachment has also been reported due to the fibrinous scarring along the migratory path.
Diagnosis is difficult to establish and high index of suspicion is required. Patients may present with marked eosinophilia [184] and elevated IgE levels [185]. ELISA for specific antibody detection and histopathological examination of the biopsy samples may assist in establishing the diagnosis [186–188]. ELISA for antibody detection reported to have low sensitivity, ranging from 59 to 87%, with a specificity of 79–96% [189, 190]. If parasite is not removed, it leads to persistence of visual disturbances such as floaters. Surgical treatment is curative and only modality available [191].
Thelaziasis is caused by nematode Thelazia callipaeda, transmitted to humans by drosophilid flies [192]. It is also known as oriental eyeworm due to its geographical distribution in Asia Pacific region (China, India, Thailand, Indonesia, Japan and Korea) and Russia [12, 193] (Table 1, Figure 11). The life cycle passes in dogs and other canids, cattle and horses as definitive host and flies act as intermediate host as shown in Figure 15. First-stage larvae are present in the lacrimal secretions of infected humans/animals. The arthropod vectors while feeding on infected lacrimal secretions ingest these larvae, which further develop into infective third-stage larvae. The vector transmits accidentally third-stage larvae when it feeds on lacrimal secretion of other persons/animals. Within 5–6 weeks, these larvae further develop into adult form in the eye of an infected person. These parasites mainly cause infection of the anterior segment of the eye, but intraocular infections involving vitreous and retina have also been reported. It is a disease associated with poor personal hygiene.
Life cycle of Thelazia (Diagrammatic representation).
Without treatment, worm remains in eye causing symptoms due to its presence [194]. Treatment is surgical removal of worms along with the topical application of thiabendazole. Preventive measures include use of bed nets at night, maintenance of personal hygiene and keeping surroundings clean to control the vector population responsible for the transmission of infection [8].
Toxocariasis is caused by Toxocara species. Toxocara canis and T. cati are the most common species causing toxocariasis in humans worldwide, particularly in Asia, Japan, Korea, Ireland and Alabama [195–199] (Table 1, Figure 11). The life cycle of Toxocara involves dogs (T. canis)/cats (T. cati) as definitive host (dog/cat). Infection is transmitted by consumption of eggs of Toxocara parasites, passed in the feces of definitive host (dog/cat) as shown in Figure 16. After the ingestion of eggs, larvae hatch out from the eggs in the small intestine and penetrate mucosa to migrate to different organs such as liver, lung and trachea, leading to visceral larva migrans (VLM). Sometimes, target larvae may migrate to eyes causing ocular larva migrans (OLM) [200, 201]. Host immune response is weaker in ocular larva migrans than visceral larva migrans. Various ocular clinical manifestations such as keratitis, hypopyon, iritis, uveitis, posterior pole granuloma, vitreous abscess and retinal detachment, strabismus, vision loss are attributed due to vitritis, cystoid macular edema and tractional retinal detachment [11, 202–204]. Based on clinical and physical examination, ocular toxocariasis is classified as chronic endophthalmitis, posterior granuloma and peripheral granuloma [205]. Approximately 25–50% of ocular toxocariasis patients present as posterior pole granuloma, due to lodging of the parasite in small perifoveal end-arteries, and approximately in 50% of ocular toxocariasis patients peripheral granuloma is present. Acute lesion appears as hazy, white mass in the peripheral fundus that may mimic the appearance of snowbank seen in patients with pars planitis.
Life cycle of Toxocara (Diagrammatic representation).
High index of suspicion is required for establishing the diagnosis of OLM during ocular examination [205]. Marked eosinophilia along with positive serology by ELISA [206] helps in confirming the diagnosis [207]. Detection of specific antibodies in the vitreous fluid also helps in differentiating it from retinoblastoma [208]. ELISA based on the excretory-secretory antigens of T. canis reported to have a sensitivity of 78% [209]. ELISA developed by Seoul National University, using crude antigen of Toxocara larvae, showed a sensitivity of 92.2% and specificity of 86.6% [210]. PCR available in research laboratories [211] may help in the diagnosis of ocular toxocariasis. Nucleotide homology of 97–99% has been reported between Vietnamese Toxocara canis and other Toxocara geographical strains by comparing the nucleotide sequence of internal transcribed spacer 2 (ITS2) of ribosomal DNA of T. canis [212]. Although PCR has been shown to be the best diagnostic modality in animal models of ocular toxocariasis, molecular techniques are not available in hospitals of resource limiting countries [213]. Vision loss, eye inflammation or damage to the retina occurs if not treated. Prognosis is good with medical and surgical treatment [200].
Albendazole and mebendazole are the drugs of choices for the treatment of VLM [214, 215]. However, there is a limited role of antiparasitic drugs in the treatment of OLM. Photocoagulation along with steroids has been recommended for the treatment of OLM.
Cysticercosis is caused by the larval cysts of the tapeworm Taenia solium. Humans acquire cysticercosis infection by the consumption of food contaminated with the Taenia solium eggs, passed in feces of the infected humans, harboring the adult worms in their intestine as depicted in Figure 17 [216]. Autoinfection has also been reported in persons suffering from taeniasis that may result in cysticercosis. Eating of raw or uncooked pork results in adult worm infection, the taeniasis. It is considered as one of the important neglected parasitic infections (NPIs), prevalent in Asia, Africa and Latin America where poor sanitation conditions prevail (Figure 11) [217]. These larval cyst may lodge into different organs/tissues (brain, muscles, eyes or other tissues) [218], resulting in varying clinical symptoms.
Life cycle of Taenia solium (Diagrammatic representation).
Ocular involvement is well documented and several case reports have documented the orbital, intraocular, subretinal and optic nerve involvement due to cysticercosis [219, 220]. Free-floating cyst can be found in vitreous or anterior chamber of the eye. Cranial nerve or intraocular muscles lesions may result in gaze palsies [221–223].
Diagnosis is usually established by ophthalmoscopic examination along with imaging evidence of ultrasonography, CT scan or MRI scan. Although serology is easy to perform, it is usually negative in isolated ocular cysticercosis patient [224]. Molecular techniques such as conventional PCR, real-time PCR [218] and loop-mediated isothermal amplification (LAMP) [225] can be utilized for establishing the diagnosis of ocular cysticercosis and for genotyping [30, 226]. However, it requires a sophisticated molecular laboratory setup, which is not available widely in developing nations.
Without treatment, symptoms related to visual disturbances persist. Symptoms resolve with surgical and medical treatment [227]. Albendazole along with steroids are the main drugs used in the treatment. Steroid treatment decreases the inflammatory response associated with the antihelminthic therapy around the lesions. Surgical removal of large cysts is recommended where there is an impairment of the vision [224].
Echinococcosis/hydatidosis is caused by infection of the larval stages of the Echinococcus spp [228], and ocular manifestations occur approximately in 1% of the cases suffering from hydatid disease [229]. Echinococcosis is mainly found in Asia, Africa, Latin America, Russia, Australia and the Mediterranean regions (Figure 11) [230]. It is acquired by the consumption of contaminated food and water with fecal matter containing eggs of Echinococcus parasites. The life cycle includes development of adult worms in small bowel of definitive hosts such as dogs and other canids. Eggs are passed in feces and contaminate environment as shown in Figure 18.
Life cycle of Echinococcus (Diagrammatic representation).
The symptoms and signs depend on the location of the cyst in the target organ. Most common ocular finding is the development of proptosis due to the presence of intraorbital space occupying lesion. This may further lead to exposure to keratitis and ulceration of the cornea. Other complications due to the local invasion of the expanding cyst may lead to erosion of orbital wall, optic atrophy and optic neuritis. Subretinal hydatid cyst has been reported. In severe cases, blindness may also occur [231].
The diagnosis depends on the clinical findings suggestive of hydatid cyst on ocular examination and confirmed by radiological techniques such as ultrasonography, CT scan and/or MRI [232, 233]. “Double wall” sign is a characteristic of orbital hydatid cyst seen by ultrasonography [232]. Serology may also aid in diagnosis. However, in majority of the commercially and in-house serological assays, hydatid fluid is the main antigenic component and sensitivity of IgG-ELISA reported in various studies varies from 64.8 to 100%, while specificity varies from 87.5 to 100%. Purified and recombinant antigens are also being tried for developing ELISA with high sensitivity and specificity [234]. Fine needle aspiration cytology can also be performed for establishing the diagnosis [235].
Symptoms persist if not treated [236]. Surgical removal of the cyst is the treatment of choice. Medical therapy includes administration of albendazole or mebendazole to prevent the recurrences due to the contents of the cyst leaking into the surgical sites [237]. If the cyst is accidently ruptured, in situ irrigation with hypertonic saline should be performed. However, it causes local inflammatory reaction that may lead to atrophy of optic nerve [238].
Fascioliasis is a food-borne parasitic infection caused by trematodes that mainly affect liver. It is acquired by eating metacercaria of Fasciola hepatica encysted on leaves that are eaten raw. Two important species are Fasciola hepatica and F. gigantica. The life cycle includes release of eggs from adult flukes that further develop into miracidia, sporocysts, rediae, cercariae and metacercariae as shown in Figure 19. The parasite passes its life cycle in two different hosts: sheep, goat, cattle and man act as definitive host and snails of the genus Lymnaea act as intermediate host. The eggs are passed out in the feces of definitive hosts that mature in water. Ciliated miracidium develops inside each egg in 2–3 weeks. Miracidium after getting released from egg finds its way to its suitable intermediate host. Inside the lymph spaces of the molluscan host, the miracidium passes through stages of sporocyst, two generations of rediae and finally to the stage of cercariae. The mature cercariae escape from the snail into the water and encyst (metacercariae) in blades of grass or water-cress, which is ingested by herbivorous animals and occasionally by man. On entering the digestive tract, the metacercariae excyst in the duodenum and migrate through intestinal wall into peritoneal cavity. It further traverses through liver capsule, parenchyma and ultimately settle in the biliary passages, where it mature into adults. The eggs are liberated in the feces through bile, completing the life cycle.
Life cycle of Fasciola (Diagrammatic representation).
Opthalmofascioliasis is the term used for those cases in which eye infection is directly caused by migrant ectopic fasciolid fluke. All other patients with ocular manifestations due to fasciolids located in liver or other organs should be classified as fascioliasis with ocular implications. Although ocular involvement in fascioliasis is rare, cases have been reported from France, Spain, Italy, Austria, Belgium, United Kingdom, Algeria, Tunisia, Iran, Uzbekistan, Korea, China, Argentina, Chile, Peru, Brazil and Guatemala (Figure 20) [239]. Symptoms and signs usually relate to the affected eye and may cause conjunctival hyperaemia, corneal oedema, dilated episcleral vessels, paralysis of extraocular muscles, decrease in perception of light, deep anterior chamber with flare, uveitis and so on. Diagnosis is established directly by visualization of leaf-shaped like organism in the eye or by studying the morphological features of the surgically removed worm. Eosinophilia, positive serology by ELISA or presence of eggs in stools may aid in diagnosis. Severe complications may occur if not treated. Early surgical intervention is associated with rapid response and reasonable final visual acuity [14]. Thus, ophthalmological manifestations have been known to be cured with surgical treatment without any antiparasitic treatment [14]. However, triclabendazole is the drug of choice if medical treatment is required.
World map showing geographical areas endemic for ocular trematode infections.
Schistosomiasis, or bilharziasis, is caused by trematode flatworm of the genus Schistosoma. Freshwater snails release the larval forms in the water, which penetrate the skin of human host while swimming, bathing, fishing and even domestic chores such as laundry and herding livestock. In the human body, the larvae mature into adult schistosomes, which reside in the blood vessels. Eggs released by females are passed out of the body in the urine or feces. It is prevalent in sub-Saharan Africa, China and South Asia (Figure 20) [8].
Ocular involvement is not the usual site that is involved in schistosomiasis, but cases have been reported where Schistosoma ova or even the adult worm can reach the systemic circulation and can lodge itself at ectopic sites such as eyes. Although schistosomiasis is very common, ocular cases are rare. It can cause uveitis or subretinal granuloma [240]. Diagnosis is established by direct demonstration of eggs/cercariae in the eye. Detection of eggs in the urine and feces may aid in establishing the diagnosis. Symptoms persist if not treated. Praziquantel is the drug of choice for all forms of schistosomiasis [8].
The cases of acute nodular conjunctivitis and anterior chamber granuloma formation have been documented, which are caused by endemic water-borne trematode infection. The identification of the remnants of parasites aspirated from such cases revealed that these parasites belong to the genus Philophthalmus that are known to parasitize birds [25, 241]. Humans acquire infection accidently while bathing or playing in contaminated water. Conjunctival nodules heal spontaneously, and anterior chamber nodules can be treated with topical/oral corticosteroids. Surgical removal is recommended in cases having large nodules. First human case of Clinostomum lacramalitis was reported in Thailand [242]. Human cases of intraocular infection with mesocercariae of Alaria americana and other Alaria mesocercariae have been reported in patients who had ingested undercooked contaminated frogs legs [243].
Myiasis is an infection caused by larvae of flies. It is common in tropical and subtropical areas. It is known as ophthalmomyiasis when ocular structures are involved. Ophthalmomyiasis is categorized into three clinical categories (ophthalmomyiasis externa, ophthalmomyiasis interna and orbital myiasis), depending on the location of larvae in the eyes. Several genera have been reported to cause myiasis such as Dermatobia, Gasterophilus, Oestra, Cordylobia, Chrysomyia, Wohlfahrtia, Cochliomyia and Hypoderma [1]. Significantly, larvae causing ophthalmomyiasis belong to the genus Hypoderma [16]. Three cases of external ophthalmomyiasis, two due to Oestrus ovis and one due to Cochliomyia hominivorax were reported earlier from North India [17]. Oestra ovis also known as sheep nasal botfly is responsible for causing ophthalmomyiasis externa in shepherding areas [244–247]. It mainly involves eyelids, conjunctiva, lacrimal sac and nasolacrimal ducts. Most common clinical feature is the foreign body sensation and may be associated with conjunctivitis and keratitis.
Diagnosis is established by the identification of the maggots. Treatment usually involves the surgical removal of the maggots. Medical treatment involves just one oral dose (150 to 200 µg/kg of body weight) of ivermectin [16]. However, the use of ivermectin for the treatment of myiasis is an off-label treatment in many countries and should be used for selected cases. The side effects such as dermal eruptions, fever, dizziness, migraines and muscular pains are common. Antibiotics and steroids may also be required to prevent the inflammation and superadded bacterial infection. Opthalmomyiasis interna [248] is caused by the invasion of the ocular structures leading to uveitis, lens dislocation and retinal detachment. Diagnosis is established by visualizing the migratory tracks along subretina by the ophthalmoscopy. Symptoms persist if not treated. Serious complications may also occur such as lens dislocation and retinal detachment due to invasion of tissue [1]. Steroid therapy is advocated if there is severe inflammation, and surgical removal is performed in severe cases. Orbital myiasis is seen in patients who are not able to maintain good personal hygiene [16]. Treatment is directed at removal of maggots and control of secondary infection. Preventive measures include maintenance of good sanitation conditions and proper disposal of waste material to control the flies in surrounding areas.
Important genera of the lice causing human infestation belong to Pediculus and Phthirus. Geographical areas where Phthiriasis palpebrarum is commonly found have been depicted in Table 1 and Figure 21. Eggs or nits laid down by lice glue themselves to body hairs or clothing fibers. Nymphs emerge from eggs and feed on the host, causing pruritis. Eyebrows and eyelashes are most commonly, involved. Excoriation marks along with small erythematous papules aid in diagnosis. Nits can be found at the base of eyelashes, substantiating the clinical diagnosis. Symptoms persist if not treated. Eyelid disease is treated by petrolatum and non-eyelid involvement may be treated with lindane, permethrin, pyrethrin or malathion [1].
World map showing geographical areas endemic for ocular ectoparasites. Phthiriasis palpebrarum; Tick infestation.
Ticks belonging to the class Arachnida are important vectors for the transmission of several infections to humans [1]. Geographical regions where ticks’ infestation has been reported are depicted in Table 1 and Figure 21. Ticks complete their life cycle in three different stages, i.e. larva, nymph and adult, and all the life cycle stages require blood meals. Ticks have been reported to attach to ocular structures that may appear as meibomian gland mass. Symptoms persist if not treated. Treatment includes removal of ticks, and tick bite granuloma may resolve after several weeks.
Ocular parasitic infections are of medical importance worldwide because of significant morbidity rates, and if not diagnosed and treated on time could lead to vision loss. High index of clinical suspicion is required to establish the diagnosis for further confirmation by laboratory techniques followed by specific treatment. Direct demonstration of the parasite is possible in few ocular parasitic infections, while in few, specific clinical features such as changes in retina on direct ocular examination may point toward specific diagnosis. Serology has limited role in the diagnosis as most of the ocular parasitic infections are localized in the eye. Utility of different diagnostic techniques in various parasitic ocular infections has been summarized in Table 2. Although reports reveal that the serology for antibody detection and/or molecular techniques for parasite DNA detection, when applied directly on the ocular tissues, aqueous or vitreous humor usually confirm the diagnosis, these techniques have its own merits and demerits. IgG immunoblot technique has been applied for the diagnosis of ocular toxoplasmosis with some success, and it is suggested that local antibody production is presumed to have occurred, if immunoreactive bands are detected in the aqueous humor but not in the serum [249]. Future reports in this direction may throw further light on its utility. Moreover, application of Western blotting technique may be possible only in limited diagnostic centers.
Report on “Diagnostic Approach to Ocular Toxoplasmosis” revealed in conclusion that the clinical diagnosis of ocular toxoplasmosis may be supported by laboratory tests in 60–85% of cases, depending on the time of sampling. Analysis of the aqueous humor is particularly helpful in patients with atypical lesions or in individuals who are irresponsive to specific therapy. Even so, a laboratory confirmation of the clinical diagnosis is not achieved in 15–40% of cases [72].
In general, it can be concluded that the clinical awareness and multiple approaches/techniques for the confirmatory diagnosis of clinically suspected ocular parasitic infections may yield higher sensitivity and diagnostic efficacy, as suggested earlier [250].
Treatment depends on the causative agent and may involve surgical removal and/or medical treatment with antiparasitic drugs (Table 2). In few infections, steroids are also prescribed to prevent the damage from the inflammatory response associated with the dying parasites. Preventive strategies depend on the type of parasitic infection and mainly include control of vector population for vector borne parasitic infections, maintenance of good personal hygiene and providing awareness to people about ocular parasitic infections through information, education and communication (IEC).
The need of increased awareness and clinical suspicion of OPI for prompt and specific diagnosis followed by application of sensitive and specific diagnostic technique(s) for confirmation and effective treatment are the main challenges.
The future research priorities need to be directed to study exact host-pathogen mechanisms, local immune responses and to establish more sensitive and specific diagnostic techniques. The molecular techniques can provide rapid diagnosis of multiple ocular parasitic infections and species identification for specific therapy. Multiplex PCR assay, if developed, can add new dimensions in the diagnosis. Efforts to develop animal models are desired that may further help to study the exact host-pathogen mechanisms, local immune responses and in developing new treatment strategies.
\n\t\t\t\tOcular protozoal infections\n\t\t\t | \n\t\t\t\n\t\t\t\tDiagnosis\n\t\t\t | \n\t\t\t\n\t\t\t\tTreatment\n\t\t\t | \n\t\t
Toxoplasmosis | \n\t\t\tSerology – IgM, IgG, IgA Molecular: PCR, Real-time PCR | \n\t\t\ta. Pyrimethamine and sulfadiazine plus corticosteroids b. Trimethoprim/sulfamethoxazole plus oral prednisolone c. Intravitreal clindamycin (1-1.5mg) injection and dexamethasone d. Surgery reserved for severe complicated cases | \n\t\t
Acanthamoeba keratitis | \n\t\t\tMicroscopy, culture on non-nutrient plates (coated with bacteria)/ in flasks (PBS+Bacteria), PCR, Real-time PCR | \n\t\t\ta. Biguanides – PHMB (0.02%) b. Chlorhexidine 0.02% in combination with aromatic diamidines such as 0.1% propamidine isethionate, 0.15% dibromopropamidine, hexamidine 0.1% and neomycin (Topical antimicrobials should be administered every hourly for first several days and there after frequency reduced to every 3 hours with a minimum duration of therapy of 3-4 weeks c. Surgical treatment includes keratoplasty or its variation known as DALK (Deep Anterior Lamellar Keratoplasty) | \n\t\t
Chagas disease | \n\t\t\tBlood smear, Buffy coat, culture, xenodiagnoses and PCR | \n\t\t\ta. Benznidazole 5-10 mg/kg daily in 2-3 divided doses for 60 days b. Nifurtimox 15 mg/kg daily in 3 divided doses for 60-90 days | \n\t\t
Malaria | \n\t\t\tThin and thick blood film for microscopy, antigen detection, PCR | \n\t\t\ta. Plasmodium vivax – Chloroquine + primaquine b. P. falciparum – Artemisinin combination therapy (Artemisinin + sulfadoxine-pyrimethamine or artemisinin + lumefantrine) as per WHO guidelines \n\t\t\t | \n\t\t
Leishmaniasis | \n\t\t\tMicroscopy of tissue smears, culture on NNN media, PCR | \n\t\t\tPentavalent antimonial compounds, liposomal amphotericin B, miltefosine (dose is weight dependent), paromomycin, azoles such as ketoconazole, itraconazole and fluconazole | \n\t\t
Microsporidiosis | \n\t\t\tMicroscopy, Immunofluorescence assay, PCR | \n\t\t\tTopical fumagillin bicylohexylammonium (Fumidil B) 3 mg/mL in saline (fumagillin 70 µg/mL) eye drops: two drops every 2 hours for 4 days, then two drops four times daily (investigational use only in United States) plus albendazole 400 mg orally twice daily for management of systemic infection. | \n\t\t
Giardiasis | \n\t\t\tConfirming by intestinal infection | \n\t\t\tMetronidazole, tinidazole, and nitazoxanide. Others include paromomycin, quinacrine, and furazolidone | \n\t\t
Ocular nematode infections | \n\t\t\t\n\t\t\t | \n\t\t |
Onchocerciasis | \n\t\t\tSlit-lamp examination, Biopsy of skin to identify larvae, skin nodules examination for identification of adult worms, PCR, antibody detection | \n\t\t\ta. Ivermectin: given every 6 months for the life span of the adult worm or as long as infected person has evidence of skin or eye infection b. New treatment: Doxycycline, before starting treatment infection with Loa loa has to be ruled out c. Removal of adult worms | \n\t\t
Loiasis | \n\t\t\t\n\t\t\t | a. Surgical removal of the worm under the skin or across the eye b. Diethylcarbamazine (DEC) is the drug of choice c. Albendazole is given to patients not responding to DEC | \n\t\t
Dirofilariasis | \n\t\t\t\n\t\t\t | a. Surgical removal of the worm b. DEC is given for medical treatment | \n\t\t
Gnathostomiasis | \n\t\t\tIdentification of the removed worm Serology to detect antibodies | \n\t\t\ta. Surgical removal of worm | \n\t\t
Thelaziasis | \n\t\t\tb. Identification of worm removed from conjunctival sac c. Eggs and larvae may be seen by microscopy of tears and other eye secretions | \n\t\t\tRemoval of worm | \n\t\t
Toxocariasis | \n\t\t\tHistological demonstration of toxocara larva Serology by ELISA | \n\t\t\td. Topical and systemic corticosteroids are useful in managing intraocular inflammation e. Role of anthelmintic therapy in ocular toxocariasis remains unclear f. Recommended drugs for systemic toxocariasis are: g. Albendazole 400mg given twice daily for 7-14 days h. Diethylcarbamazine - given at 3-4 mg/kg/day for 21 days | \n\t\t
Ocular cestode infections | \n\t\t\t\n\t\t\t | \n\t\t |
Cysticercosis | \n\t\t\tImaging with MRI, CT scan and USG Serology | \n\t\t\ta. Antiparasitic drugs – Albendazole 15mg/kg/day for 4 weeks, Praziquantel b. Corticosteroids in tapering dose over a period of 1 month c. Surgery | \n\t\t
Echinococcosis | \n\t\t\tImaging | \n\t\t\ta. Surgical removal b. Albendazole is given as an anti-infective prophylaxis | \n\t\t
Ocular trematode infections | \n\t\t\t\n\t\t\t | \n\t\t |
Fascioliasis | \n\t\t\tDetection of adult worm in the eye Other features such as eosinophilia, stool examination and serology may help | \n\t\t\ta. Surgical removal of worm b. Triclabendazole 10mg/kg body weight as a single dose | \n\t\t
Schistosomiasis | \n\t\t\tStool and urine examination for detection of parasitic eggs or detection of eggs or cercariae in eye Serology | \n\t\t\tPraziquantel 40-60mg/kg per day in two to three divided doses for one day | \n\t\t
Philopthalmosis | \n\t\t\tIdentification of the remnants of parasites aspirated from such cases | \n\t\t\ta. Conjunctival nodules heal spontaneously and anterior chamber nodules can be treated with topical/ oral corticosteroids. b. Surgical removal is recommended in cases having large nodules | \n\t\t
Ocular infections by ectoparasites | \n\t\t\t\n\t\t\t | \n\t\t |
Myiasis | \n\t\t\ta. Identification of the maggots b. Visualizing the migratory tracks along sub retina | \n\t\t\ta. Surgical removal of the maggots b. Ivermectin 150-200 µg/kg of body weight in single dose c. Steroid therapy | \n\t\t
Phthiriasis palpebrum | \n\t\t\ta. Excoriation marks along with small erythematous papules b. Nits can be found at the base of eyelashes | \n\t\t\ta. Eyelid disease is treated by petrolatum b. Non-eyelid involvement may be treated with lindane, permethrin, pyrethin or malathion | \n\t\t
Tick infestation | \n\t\t\tBiomicroscopy may reveal ticks | \n\t\t\tRemoval of ticks | \n\t\t
Diagnosis and treatment of various ocular parasitic infections
Pump intake is the part of a pump that draws fluid from the reservoir called the sump as a result of pressure difference generated by the impeller. In most cases, pumped fluid enters the intake in a swirling motion due to geometric features of the sump [1]. Inappropriate sump design such as abrupt changes in sump boundaries, narrow clearance under the pump inlet and asymmetric orientation of the approach channel to the sump will lead to the formation of swirls and vortices [2]. Strong vortices may cause damages to the pump impeller by channelling air to the impeller surface and initiate adverse effects such as cavitation and vibration [3]. On the other hand, excessive swirls in the intake flow can impose imbalance loading to the impeller and even bring resistance to the impeller rotation by introducing swirl rotation in the opposite direction [4]. Due to site condition and operational restrictions, optimal sump design may not be achieved, and therefore local flow correction devices are used as remedial measures.
\nThese devices which are commonly known as anti-vortex device (AVD) come in different shapes and sizes, depending on its application. The conceptual design of AVD is outlined in ANSI/HI 9.8-2018 [5] standard which is a guideline to assist engineers and designers in optimal intake sump design. Among the AVD types employed in real applications are floor splitter [6], floor cone [7] and corner fillet [8]. These AVD types serve the purpose of eliminating submerged vortices formed at the sump floor. Floor splitters are the most widely used AVD type due to its effectiveness in eliminating vortices and reducing vorticity in the pump intake flow. There are two versions of floor splitter, namely the prism and the plate types. The use of plate type floor splitter is favourable in many applications due to its fabrication friendly-feature and economic design [9]. However, there are a limited number of articles in the literature which discuss the features of floor splitter plate in detail. In this chapter, the characteristics of swirl angle reduction of a floor splitter plate installed in pump sump are studied.
\nThe study was carried out by both experimental and numerical approaches. A single intake pump sump model, as shown in \nFigure 1\n, was utilized for the study in which the sample of a floor splitter was installed beneath an intake suction pipe in the sump model. The layout of the sump model test section and the dimensions of the floor splitter installed is illustrated in \nFigure 2(a)\n and \n(b)\n, respectively.
\nThe experimental rig.
Main dimensions of the sump model and splitter.
The main objective of the study is to evaluate the swirling motion in the intake pipe and associated with submerged vortex without and with the installation of floor splitter plate. Initially, the experiment was conducted without the installation of floor splitter plate to capture the initial conditions of the setup. The measurement of the intensity of swirl in the intake pipe was performed according to the procedure described in ANSI/HI 9.8-2018 standard for pump sump model test. The parameter used to quantify the measurement data is the swirl angle θ which is defined in the following equation:
\nwhere d is the inner diameter of the intake pipe, n is the revolution count of the measurement instrument called the swirl metre and a is the average axial velocity at the location of the swirl metre. The swirl metre consists of a shaft with four straight blades used to capture the swirling motion in the intake pipe, and the revolution count of the swirl metre blade is measured using a tachometer. \nFigure 3\n shows typical swirl metre installation according to ANSI/HI 9.8-2018 standard. Basically, θ is the convention for describing the ratio between the axial velocity and the tangential velocity of the intake flow which characterizes the intensity of the swirling motion in the fluid. The acceptance criteria according to ANSI/HI 9.8-2018 is that the swirl angle must be lower than 5° to prevent excessive swirl in the intake flow.
\nSwirl metre installation according to ANSI/HI 9.8-2018 standard.
In order to generate the submerged vortex, the clearance under the pipe was set to 0.3 times the diameter of the inlet D and two types of flow conditioners were installed: a sloped floor with an inclination angle of 30° and a sloped wall with the same inclination angle. These flow conditioners were installed at a distance of about 5D from the centre of the intake pipe as shown in \nFigure 4(a)\n and \n(b)\n, respectively. The measurement was conducted in a range of pump submergence levels which are normalized by the minimum inlet submergence Smin\n, a threshold value before the occurrence of a surface vortex. Smin\n is calculated by the following equation:
\nFalse floor and false wall arrangements.
\nFrin\n is the Froude number at the pipe inlet and is given by:
\nwhere νin\n is the flow velocity at the inlet and g is the gravitational acceleration. The range of the dimensionless parameter S/Smin\n was set between 0.8 and 1.2.
\nThe numerical approach part of the study is set for the simulation of the flow in a full-scale pump sump. As the construction cost for a full-scale pump sump cannot be afforded, a computational fluid dynamics (CFD) simulation was employed as a replacement. The numerical model was validated with experimental data and incorporated with a combined flow conditioner that consists of inclined floor and inclined wall as the ones used in the experiment and built at a scale of 9:1. The flow rate of the pump was set to 2170 l/s, and the pump submergence took the value of Smin\n which is, after the calculation by using Eq. (2), equals to 2678 mm. The mesh structure and the dimensions of the full-scale pump sump are illustrated in \nFigures 5\n and \n6\n, respectively, while the values of the model dimensions are listed in \nTable 1\n.
\nNumerical model of the full-scale pump sump; (a) the computational domain, (b) model without floor splitter plate, (c) model with floor splitter plate.
Dimensions of the full-scale model.
Parameter | \nDimension (mm) | \n
---|---|
Inlet diameter D\n | \n1275 | \n
Pipe diameter d\n | \n850 | \n
Right side distance W1 | \n1190 | \n
Left side distance W2 | \n1360 | \n
Water entrance width W3 | \n1275 | \n
Intake pipe height H1 | \n9350 | \n
Sump height H2 | \n4250 | \n
Water entrance height H3 | \n2975 | \n
Floor length L1 | \n6375 | \n
Water entrance distance from sloped floor L2 | \n8417 | \n
Clearance C\n | \n382.5 | \n
Dimension values of the full-scale model shown in \nFigure 6\n.
\n\nFigures 7\n and \n8\n show the distribution of swirl angle values at different submergence ratios in the case of false floor and false wall flow conditioner, respectively. Generally, the installation of floor splitter plate has shown reduction in the swirl angle values. The parameter that can be used to characterize the reduction effect of the floor splitter plate is the swirl angle reduction factor Rθ\n which is defined as follows:
\nSwirl angle values at different submergence ratios for the false floor case.
Swirl angle values at different submergence ratios for the false wall case.
In this experiment, the average value of Rθ\n for the false floor case is 1.53, while in the false wall case, the average value of Rθ\n is 1.62. In \nFigure 7\n, the swirl angle values show a decreasing trend with increasing submergence ratio for S/Smin\n greater than 1 when installed with floor splitter plate. This is due to the fact that for S/Smin\n greater than 1, there was only a submerged vortex present in the sump. As the function of floor splitter plate is to eliminate submerged vortices, this result proved that the installation of floor splitter plate has served the purpose. When S/Smin\n is decreased below 1, the swirl angle values increase with decreasing submergence ratio. The inception of free surface vortex at S/Smin\n below 1 has caused bigger fluctuation in swirl angle as can be seen in the larger uncertainties within this region. The higher swirl angle values are contributed by the increase in approach flow velocity at lower water levels. The floor splitter vortex has shown limited swirl angle reduction effect if the submergence ratio is decreased below 1.
\nIn \nFigure 8\n, the swirl angle values show a sinusoidal trend with increasing submergence ratio for S/Smin\n greater than 1 when installed with floor splitter plate. The trend is contributed by the inception of free surface vortex at S/Smin\n greater than 1. Although the theory behind the minimum inlet submergence Smin\n is that there should be no free surface vortex formed in the sump if the submergence S is greater than Smin\n, this deviation from the theory was contributed by the use of false wall in which the flow has been prerotated at the beginning of the sump. The prerotation has therefore caused the flow to develop a free surface vortex earlier than expected. In the experiment, this situation occurred at S/Smin\n = 1.15. As the swirl angle decreases when S/Smin\n decreases below 1.15, the reduction effect of the floor splitter plate can be observed in the decreasing trend of the swirl angle values. Similar to the case of false floor, the swirl angle increases as the submergence ratio decreases due to the increasing approach flow velocity at low water levels.
\nDespite the swirl angle reduction effect of floor splitter plate, the fulfilment of the requirement of swirl angle reduction below 5° has not been achieved for most of the cases. In the case of false floor, there is no submergence ratio value at which the swirl angle has been reduced below 5°; however, for the false wall case, the reduction of swirl angle values below 5° can be seen between S/Smin\n = 1.00 and S/Smin\n = 1.05, i.e. the requirement for all submergence ratios when installed with floor splitter plate. This result shows that there is a limiting factor that prevented the swirl angle reduction below 5° and that factor lies on the design of the floor splitter as suggested by Kang et al. [9].
\nThe first part of the discussion on the result of simulation of flow in full-scale pump sump model is about the vortex elimination by the installation of floor splitter plate. The evaluation is based on the vorticity in the y-axis ωy\n due to its influence on the swirling motion of the flow. The value of ωy\n is normalized by the ratio of velocity in the suction pipe and the pipe inner diameter νd/d. \nFigure 9\n shows the cross section along x-y plane in which the evaluation of the result in the streamwise direction takes place and its corresponding results which are shown in \nFigure 10\n.
\nEvaluation area in x-y plane of the pump sump model (z = 1600 mm).
Contour plot of ωy/(νd/d) at the location of vortex in x-y plane; (a) without floor splitter plate, (b) with floor splitter plate. Dashed circular lines denote pipe diameter.
From \nFigure 10\n, it can be observed that the core of the vortex, indicated by the high-intensity region extending from the floor towards inside of the pump, has been eliminated with the installation of floor splitter plate. The vorticity in the pipe has also been reduced which can be seen from the contour colors. The velocity vectors, which appear to point diagonally to the left indicating a strong swirling flow in the pipe, have been straightened in a direction vertically upward towards the direction of suction when installed with floor splitter plate.
\nWhen observing the cross section in the spanwise direction (in the plane illustrated in \nFigure 11\n), similar results are presented. Basically the flow that enters the pump is divided into two regions, namely the right side and the left side flow, due to the geometry of the sump. The flow entrance velocity from the right and the left side of the inlet are nearly the same because of the nearly symmetrical positioning of the pump. The flow entered the pump in a spiral manner without the installation of floor splitter which resulted in vortex formation near to the left side of the pump. When installed with floor splitter plate, the flow is reorganized, and therefore the spiral motion of the flow has been reduced and hence the vortex eliminated. This situation is reflected by the discontinued vortex core shown in \nFigure 12\n with the installation of floor splitter plate.
\nEvaluation area in y-z plane of the pump sump model (x = 15,860 mm).
Contour plot of ωy/(νd/d) at the location of vortex in y-z plane; (a) without floor splitter plate, (b) with floor splitter plate.
As the main function of floor splitter plate is to eliminate vortices formed at the sump floor, an evaluation about the vorticity in the plane at the sump floor is necessary. This location is shown in \nFigure 13\n. The vortex core is indicated by the spiralling streamline under the pump inlet which can be seen in \nFigure 14\n in the case without floor splitter plate. As the floor splitter plate was installed, the path of the spiral streamline was interrupted by the plate, and therefore the formation of vortex was prevented. Due to the suction by the pump, a small vortex attached to the side of the floor splitter plate was formed which is inherited from the flow without floor splitter plate as shown in \nFigure 14(b)\n. However, this vortex constitutes a much smaller vortex core diameter (estimated to be less than 0.1D based on the scale at the x-axis of the graph) and relatively weak compared to the large vortex (estimated to be about 0.2D) which can be seen in \nFigure 14(a)\n, and therefore it can be considered as nondestructive to the pump impeller.
\nEvaluation area in z-x plane of the pump sump model (y = 10 mm).
Contour plot of ωy/(νd/d) at the floor of the sump in z-x plane; (a) without floor splitter plate, (b) with floor splitter plate.
The next part of the evaluation is about the swirl angle reduction characteristics of floor splitter plate installation. For this purpose, an evaluation plane was selected at the position comparable to the installation of swirl metre in the experimental model. The location of the plane is shown in \nFigure 15\n, and its corresponding results are displayed in in \nFigure 16\n. The flow at the swirl metre location was rotational with relatively high velocity components as indicated by the velocity vectors. The two visible vorticity regions show the divided inflow field in the pipe as explained in the previous paragraph which is considerably high in reference to the value of νd/d as shown in \nFigure 16\n. With the installation of floor splitter, the magnitude of both vorticity regions is significantly reduced and the resulting velocity vectors are also smaller in size compared to the case without floor splitter. This indicates that the spiral flow has been dissolved by the floor splitter plate into a relatively straight flow and the outcome is consistent with the experimental result presented in the previous subsection.
\nEvaluation area at the position of swirl metre in z-x plane of the pump sump model (y = 4250 mm).
Contour plot of ωy/(νd/d) at the swirl metre position in z-x plane; (a) without floor splitter plate, (b) with floor splitter plate.
To get a better understanding about the result, a 3D streamline visualization of the intake flow in the sump is illustrated for every case as comparison in \nFigure 18\n. It can be seen that the intake flow was spiral before the installation of floor splitter plate and as the floor splitter was installed, the spiral motion of the flow was dissolved and went into a relatively straight path. Quantitative values can also be extracted from the result to obtain the associated swirl angle values. The approach for the calculation of swirl angle from the simulation results is based on the principle of Eq. (1) itself where by definition the swirl angle is the angle between the velocity components of the intake flow in the axial and tangential direction. From Eq. (1), the term πdn represents the tangential velocity component, while the term v represents the axial velocity component; both are at the location of the swirl metre used in the experiment. \nFigure 17\n shows the velocity triangle diagram which shows the relationship between swirl angle and both of the velocity components in a schematic representation.
\nSwirl angle definition using velocity triangle diagram as shown in Kang et al. [9].
3D streamline plot showing the intake flow in the sump with the seeding of the flow starts at the floor of the sump; (a) without floor splitter plate, (b) with floor splitter plate.
Based on this approach in Eq. (1), the velocity components in the axial and tangential direction were derived from the simulation results. As the result was given in vorticity values, the tangential velocity component must be derived from the angular velocity which equals to half of the vorticity [10]. The vorticity of the flow at the position of the swirl metre is calculated by the integration of the vorticity in the plane and divided by the cross section to obtain the vorticity value per unit area. After getting the value of angular velocity, the following correlation is used to calculate the tangential velocity:
\nThe method to derive the value of axial velocity component from the results was based on the same principle in which the integral value of axial velocity component in the plane was extracted and divided by cross-sectional area of the pipe at the swirl metre location to get the velocity per unit area. The reason of performing integration to find the velocity values is that the swirling motion of the intake flow in the pipe constitutes a solid body rotation and the swirl angle value describes the rotation body as a whole [1], and this is where the integration of the velocity across the cross-sectional area becomes the most practical way of calculating the swirl angle in the simulation. After obtaining both velocity values, the swirl angle was then calculated using the velocity triangle diagram as shown in \nFigure 17\n.
\nBy following the described procedure, the swirl angle value for the case without floor splitter plate installation is 7.58°, while for the case with floor splitter plate, the swirl angle value is 4.09°. Although these values are based on average velocities as the simulation was conducted in a steady-state simulation and therefore are much smaller than the actual swirl angle values, it can be considered as adequate because they are used for comparison purpose and not for the determination of absolute values. Once again, the results are in agreement with the experimental data. This study complements a previous experimental investigation in which the effects of floor splitter heights have been analysed [11].
\nA study on the application of vortex control principle at pump intake was carried out by using an anti-vortex device type called the floor splitter plate. The device was installed in a pump sump model to eliminate vortices formed at the intake and reduce the swirling motion in the intake pipe as a method to improve pump efficiency in actual applications. Evaluation of the effect was conducted based on experimental and numerical approaches. The experimental part comprised swirl angle measurement which was performed according to ANSI/HI 9.8-2018 standard. To complement the results obtained in the experiment, a numerical simulation of the flow in a full-scale pump sump was conducted. The results showed that the installation of floor splitter plate has successfully eliminated the vortex formed at the sump floor and reduced the swirl angle in the intake flow. However, the reduction effect was not sufficient to achieve the criteria set in the ANSI/HI 9.8-2018 standard which requires the swirl angle to be less than 5°, and therefore optimization of the floor splitter plate design is needed. The simulation of flow in a full-scale pump sump produced similar findings with the experimental results. From the contour and streamline plot, it was found that the immersion of the floor splitter plate has disrupted the vortical flow under the pump inlet and provided a flow straightening effect to eliminate destructive vortices and reduce swirl angle in the pump intake.
\nThe research has been funded by the Ministry of Energy, Science, Technology, Environment and Climate Change (MESTECC), Malaysia, under Science Fund grant No. SF1326 and carried out in collaboration with the Department of Irrigation and Drainage (DID), Malaysia.
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