Open access peer-reviewed chapter
Abstract
In common with other invertebrates, molluscs are known to have internal immune response against foreign particles and organisms. The innate immunity of molluscs reflects the inherent non-specific response that provides the first line of defense. Anatomic barriers, phagocytic cells, and physiological components are the main elements of the innate immune response in molluscs. It is composed of both cellular and humoral elements. The cellular components are the circulating hemocytes. Small invaders are eliminated by the phagocytic hemocytes, while large invaders are eliminated by encapsulation. The ingested foreign particles are then hemolyzed by the action of certain toxic enzymes that catalyze oxidative burst reactions capable of killing pathogens and foreign invaders. Humoral components of molluscan immunity involve nitric oxide, lysozyme activity, lectins, and the phenyloxidase system. The current chapter sheds light on the elements of the molluscan innate immune system and presents a case study of the immune response of Lymnaea stagnalis mollusc against Chaetogaster limnaei parasite. The effect of the parasite on some humoral immune response parameters such as nitric oxide, phenol oxidase, and lysozyme production was investigated. In conclusion, the snail Lymnaea stagnalis exerts humoral immune response against Chaetogaster limnaei parasite. However, this response is insufficient to eliminate the parasite.
Keywords
- Chaetogaster limnaei
- humoral immune response
- Lymnaea stagnalis
- molluscs
1. Introduction
1.1 Lymnaea stagnalis in the animal kingdom
Molluscs are invertebrates that form one of the largest groups in the animal kingdom, with more than 100,000 known species. A wide range of molluscs including families of Pulmonata, Gastropoda, Planorbidae, and Lymnaeidae are intermediate hosts of trematodes.
Gastropods or snails are asymmetrical molluscs with a well-developed foot and radula. The visceral mass is spirally coiled. They occur in seas, freshwater, and terrestrial environments. The class Gastropoda is divided into three subclasses: Prosobranchia, Opisthobranchia, and Pulmonata. The snail
Plate 1.
A
1.2 Major parasitic infections associated with Lymnaea stagnalis
Plate 2.
(a) A cercaria of
Plate 3.
(a) A cercaria of
In addition, some annelids are found associated with the mantle area of
Plate 4.
In common with other invertebrates, molluscs are known to have internal immune response against foreign particles and organisms. The innate immunity of molluscs reflects the inherent non-specific response that provides the first line of defense. Anatomic barriers, phagocytic cells, and physiological components are the main elements of the innate immune response. It is composed of both cellular and humoral elements. The cellular components are the circulating phagocytic hemocytes. Small invaders are eliminated by phagocytic hemocytes, while large invaders are eliminated by encapsulation. The ingested foreign particles are then hemolyzed by the action of certain toxic enzymes that catalyze oxidative burst reactions capable of killing pathogens and foreign invaders. Humoral components of molluscan immunity involve nitric oxide, lysozyme activity, lectins, and the phenyloxidase system [7, 8].
2. Innate response of molluscs
2.1 Anatomic barriers
Shells of molluscs act as physical barriers that prevent some pathogens from penetrating into the host’s body. Mollusc shells are composed of organominerals with different structures and compositions depending on the species. Most of these shells are composed of an aragonite nacreous and a calcite prismatic layer [9]. The layers of the skin are tightly packed and the acidic environment in these layers is not suitable for the growth of most micro-organisms. The mucous membrane that lines the tissues and tracts contains normal micro-flora that competes with pathogenic micro-organisms for essential nutrients and attachment sites on these layers. The mucosal barrier may also act as a trap for antigens that are then inactivated by phage encapsulation by hemocytes. In addition, the movement of the outer cells expels the trapped pathogens to the outside environment. The flushing action of secretions helps to prevent infection of certain pathogens [10].
2.2 Key cells in innate immunity
There are immune cells in molluscs equivalent to the white blood cells in higher animals that play a role in the non-specific immune response. These cells are called hemocytes. Most of these cells are capable of engulfing extracellular particles by phagocytosis, endocytosis, and encapsulation. Others can produce substances that play a role in the killing process of pathogens. Circulating hemocytes proliferate and differentiate after exposure to pathogens or foreign particles. It was noticed that circulating hemoblasts are present at various phases of mitosis [11, 12].
The role of these phagocytic cells in the hemolymph of gastropods is considered to be the first line of defense system against invading or established organisms and particles. These hemocytes are circulating within the hemolymph as well as residing in the connective tissues. There are also cells lining the hemolymph spaces and are able to trap micro-organisms. Other cells are the fixed phagocytic reticulum cells that are fixed in the tissues by fibrils [13, 14].
A lot of studies have been done to determine the types and numbers of hemocytes in molluscs. This is considered to be a debating question because these hemocytes are morphologically and functionally heterogeneous. In addition to phagocytosis, these cells participate in digestion, excretion, healing of wounds, shell repair, transport, and encapsulation [14]. Classification of mollusc’s hemocytes depends mainly on morphological criteria like cell size, nucleus to cytoplasm ratio, shape of nucleus, and the presence of granules in the cytoplasm using light microscopy. Studies have revealed the presence of two distinct types of hemocytes. These are the granulocytes and the agranulocytes. Acidophilic and basophilic granulocytes and slightly granular cells were also observed [15, 16]. The agranulocytes are relatively small cells and are also called hyalinocytes, they are less than 8 μm in size; while the granulocytes are larger spreading cells with pseudopodia and a polymorphic nucleus. The majority of cells in the hemolymph of molluscs are large spreading cells. Interestingly, there are intermediate stages between the round and the spreading cells in terms of morphology. Some scientists have suggested that the small and round cells are young cells and the larger spreading cells are old cells that are more capable of phagocytosis [17]. On the other hand, the small round cells in
Plate 5.
Hemocytes of
Plate 6.
Phase-contrast micrograph of L. stagnalis hemocyte. R is a round cell and the others are spreading hemocytes.
Tripp and Kent [18] have reported that 90% in vitro invading bacteria can be removed by hemocytes from molluscs within 24 h and 99% can be removed within 72 h. The glycolytic pathway in the cells was suggested to supply the hemocytes with the energy that is needed for phagocytosis, this was first proved by the work of Cheng [19] that has shown that hemocytes of the hard clam,
2.3 Physiological elements of innate immunity in molluscs
In addition to the phagocytic hemocytes that are involved in the innate immunity, there are soluble physiological elements that play a role in defending the host from invading foreign substances and pathogens. Cellular and soluble elements coordinate in a sophisticated network of interactions to mount effective innate immune responses capable of eliminating foreign antigens. These soluble physiological elements include: nitric oxide, lysozyme activity, lectins, and the phenyloxidase system [7, 8].
2.3.1 Complement system
The complement system is considered to be an important element of the innate immune system that also triggers the adaptive immunity in higher animals in the animal kingdom. Similar hemolytic complement-like activity was also reported against parasites and other pathogens in molluscs [20, 21].
Complement components are proteins and glycoproteins that are mainly synthesized in the liver. Other cells such as the tissue macrophages and the blood monocytes are involved in the complement production. These proteins are circulating in the blood in an inactive form. Once activated upon exposure to an antigen, they enter an enzymatic biochemical cascade that helps in the elimination of antigens by lysis of cells, opsonization, binding to specific complement receptors on cells of the immune system, and/or immune clearance of immune complexes [22, 23, 24].
There are three different pathways by which the complement cascade is activated, namely the classical pathway, the alternative pathway, and the mannan-binding lectin pathway. The classical pathway is antibody-dependent, so it is more related to the adaptive immunity. It is initiated by antigen-antibody binding to form immune complexes or when an antibody binds to an antigen on the surface of a pathogen. Activation of complement component 1, often simply called C1 (a protein of the immune system) then occurs when it binds to such antibodies of type IgM and some classes of type IgG. On the other hand, the alternative and the mannan-binding lectin pathways are more related to the innate immunity because they are antibody-independent. The former is initiated by complement component 3 (C3 complement), activation upon exposure of foreign substances on the cell wall of pathogens like bacteria, while mannan-binding lectin pathway is activated when a lectin binds to a mannose residue on the cell wall of pathogens such as
2.3.2 Nitric oxide production
Many evidences have proven the presence of immunological factors in molluscs capable of working against infectious elements. Nitric oxide (NO) is a gaseous intercellular signaling molecule that has several functions in the cardiovascular, reproductive, nervous, and immune systems. Post infection by a pathogen, high levels of NO is synthesized in the immunocytes of the host in order to eliminate the pathogen or induce inflammation. Recently, NO has been reported to be involved in the immune response of several mollusc species such as scallop, clam, mussel, oyster, and snail. In addition to killing the invasive pathogens, high concentrations of NO can prove fatal to normal host cells as a result of strong cytotoxicity produced during the immune response. Modifying the NO concentration is crucial in order to maintain immune homeostasis and other physiological processes. Also, neuroregulation of NO is of utmost importance so as to prevent prolonged immune response [28].
Nitric oxide synthase was reported to play an important role in the phagocytic activity of hemocytes of molluscs such as
2.3.3 Tyrosinase production
Tyrosinase is also considered to be a defense line system in the primary immune response of molluscs, it is involved in tanning and melanin formation. It is considered to be a non-self-recognition system because this enzymatic reaction can be triggered by minuscule amounts of molecules such as lipopolysaccharide, peptidoglycan and beta-1,3-glucans from micro-organisms. In
2.3.4 Lysosymes production
Lysozymes are enzymes that hydrolyze the 1,4-beta links between N-acetylmuramic acid and N-acetylglucosamine, they are known to destroy the cell walls of certain bacteria. They can be found in tears, saliva, egg whites, some plant tissues, and Sweat. Lysozymes have been recognized as a classic mollusc immune effector in innate immune system. It is a bacteriolytic enzyme produced from a range of organisms such as bacteria and bacteriophages to fungi, plants, and animals. They are characterized by their ability to bacterial peptidoglycan between two amino sugars, N-acetylmuramic acid and N-acetylglucosamine, which results in bacterial cell lysis and also has bactericidal and digestive abilities. In addition to this, they perform numerous other functions such as for growth stimulation, digestion, antiviral, anti-inflammatory, and are even associated with tumors. They are classified into six types based on their structural, catalytic and immunological characteristics. These are chicken-type (c-type), goose-type (g-type), plant, bacteria, T4 phage, and invertebrate type (i-type) lysozymes. The c-, g-, and i-type have been recorded in molluscs. They are the secreting type, which consist of signal peptide and 8, 6, and 14 cysteine residues, respectively. All three exhibit antibacterial and digestive ability and i-type has antifungi activity [35]. It was reported that the concentration of lysozymes in the hemolymph of molluscs changes as an immune response. Hemocytes of
2.3.5 Lectin production
Lectins binding phenomenon have been known since the turn of the nineteenth century, and have been widely used in the field of histochemistry for research and clinical purposes to detect specific carbohydrate structures and derivatives like glycolipids and glycoproteins in cells and tissues at the level of electron and light microscopy. They are also used for purification and isolation of carbohydrates and other specific cells like lymphocytes and bone marrow. In addition, lectins are very important tools in analyzing membrane structures of cells, glycosylation pathways, differentiation, cell division, growth and developmental changes, and mapping neuronal connections [37].
Lectin production is considered as an innate immune parameter against infection. These are non-enzymatic and non-immunoglobulin carbohydrate-binding proteins present in plants, bacteria, fungi, and animals which preferentially bind reversibly to specific carbohydrate structures, either free in solution or on cell surfaces. They are often classified based on saccharide-specificity. This specificity is usually defined by the monosaccharides or oligosaccharides that are best at inhibiting the agglutination or precipitation reactions caused by lectins. Lectins in the same category (e.g., galactose-specific lectins) show considerably different sugar-binding preferences. Interestingly, an increasing number of lectins which never show high affinity to simple saccharides have been found. Lectins can be detected by binding to fluorescent markers such as enzymes, biotin, and FITC and 125Iodine [38, 39, 40, 41].
Immune factors that consist of a fibrinogen domain (FBG) are now emerging as important components of the innate immune response of invertebrates. In recent times, some arthropod and mollusc model systems have contributed to the study of the functional role of fibrinogen-related proteins (FREPs) in invertebrate defense mechanism. FREPs have been identified in mussels, scallops, oysters, and gastropods. The FREPs of gastropod molluscs are interesting due to their unique structure, capacity for somatic diversification and their function in the immune system.
Gastropods and Digenean trematodes have shared a parasitic relationship for nearly 200 million years. These trematodes rely heavily on molluscs, mainly on gastropods to complete their larval development. They have developed mechanisms to evade and suppress specific snail immune processes so as to reproduce within the snail host. However, not every nematode can infect the snail species equally; this suggests that snails have developed mechanisms to fight trematode infections. A component of the snail immune response is BgFREPs; they are soluble lectin-like factors. Agglutinins have been discovered in gastropods such as
2.3.6 Phenoloxidase activity
Phenoloxidase (PO) is an enzyme that oxidizes phenols to produce melanin which plays an important role in egg production in gastropods, sclerotization of a new postmolt exoskeleton, and immunity of invertebrates. PO occurs as inactive precursors known as prophenoloxidses (proPO). They are activated by a proteolytic cascade system. Studies to investigate PO activity in
3. Immune response of the snail Lymnaea stagnalis against parasites: study
The current chapter sheds light on some parameters that are associated with the immune response that is resulting from the interaction between the pond snail
3.1 Material and methods
3.1.1 Collection of snails and parasites
A total of 150
3.1.2 Bleeding of the snails
Stroking the end of a dissecting pin over the foot of the snail would cause the snail’s body to shrink back into the shell. This would expel any excess water outside the shell. Then, a dissecting needle was used to remove a portion of the shell just between the first and the second ring of the shell. Then, the gray membrane was punctured by a dissecting needle. Once punctured, the hemolymph is released and can be collected by using an Eppendorf micropipette set at 100 μl. This hemolymph was then collected in sterile Eppendorf tubes and kept on an ice tray in order to avoid aggregation of the cells.
3.1.3 Staining the hemocytes with Giemsa’s stain
Thin smears of the hemolymph were made on microscopic slides and were let to dry for 20 min. 70% ethanol was used to fix the cells. The smears were then washed with distilled water and were stained with Giemsa’s stain diluted in phosphate-buffered saline (PBS) containing sodium chloride, sodium phosphate, potassium chloride, and potassium phosphate at pH 7.3. The purpose of PBS is to maintain the constant pH and osmolarity of the hemocytes. The slides were washed, dried, and examined under light microscope at different powers.
3.1.4 Lysozyme standard curve
2 g of purified agar were added to 200 ml of phosphate-buffered saline (PBS) that has a pH value of 6.2. To this was added 0.15 g of
Lysozyme standard solutions were prepared by dissolving 25 mg of frozen-lysozyme in 5 mls of PBS at pH 6.2 to give a concentration of 5 mg/ml. Then, 12 serial two-fold dilutions were produced by removing 2.5 ml from the 5 mg/ml solution and add it to a tube containing 2.5 ml of PBS, this process was repeated until 12 serial dilutions were produced. These known concentrations of the lysozyme were dispensed into the wells that were produced in the agar plates, approximately 30 μl in a well. These plates were then incubated over night at 27°C. Areas of hydrolysis were observed around each well. The diameter of each zone was measured using a ruler and a lysozyme standard curve was plotted with the x-axis representing the lysozyme concentration and the y-axis representing the diameter (squared).
3.1.5 Lysozyme assay
4 agar plates were prepared as mentioned above, each containing 12 wells. 37 snails were bled and each hemolymph from each snail was placed into one of the wells. So, 37 wells in 4 agar plates were occupied. The plates were then incubated at 27°C overnight. The diameters of the hydrolysis zones were measured. The same assay was then repeated for 12 mucous samples and 12 parasite product samples.
3.1.6 Nitric oxide standard curve
A sodium nitrite standard solution was prepared. 100 μl of this solution was then placed in 2 wells at the top of a 96 wells enzymatic plate (ELISA plate) in duplicate. 50 μl of the culture medium was dispensed along the remaining 7 wells in duplicate. Then, serial two-fold dilutions of the standard solution were made going down the plate except for the last set of wells that were used as controls, they only contained culture medium without the standard solution. The culture medium is supplemented with 10% fetal calf serum.
Then, 50 μl of Griess reagent was added to all the wells. Once prepared, the tube should be inverted for 10 min and kept in the refrigerator. After addition of Griess reagent, the absorbance of the solutions in the wells should be read within 30 min using a plate reader with an absorbance filter of 570 nm. A nitric oxide standard curve was then plotted with the x-axis representing the nitrite concentration and the y-axis representing the absorbance.
3.1.7 Nitric oxide assay
Circular glass cover slips were placed in 15 wells of the 24-well tissue/cell culture plates using a pair of fine forceps. Ethanol was used to sterilize the cover slips. Poly-L-lysine solution was used to cover the cover slips in the wells, 100 μl in each well. This solution increases the hemocytes attachment to the cover slips. An incubation period of 1 h at 37°C was allowed in order for the poly-L-lysine to fix on the cover slips. After then, the excess poly-L-lysine solution was removed from the wells by Pasteur pipette and the wells were washed with sterile distilled water. Freshly collected hemolymph was then added to the wells, 50 μl in each well. The plate was then put in the refrigerator for 1 h to allow the hemocytes to attach themselves to the cover slips. The excess hemolymph was then removed by Pasteur pipette and the wells were washed by sterile distilled water.
The culture medium was then added to all the wells, 200 μl to each well. The plate was then incubated at 27°C for 1 h to enhance the growth of the hemocytes that can be observed under the light microscope. Approximately 10 live
3.1.8 Phenol oxidase standard curve
Different concentrations of L-DOPA and fixed concentration of the tyrosinase enzyme were used to measure the initial rate of dopachrome formation at 475 nm wavelength. 5 × 10−3 mol dm−3 L-DOPA solution was used to prepare different solutions.
The 5 × 10−3 mol dm−3 DOPA solution was prepared by dissolving 0.0493 g of DOPA powder that has a molecular weight of 197.19 in 50 ml of the phosphate buffer saline. Then, 3 ml of each solution (tubes 1–8) were placed in plastic cuvette tubes and 0.1 ml of the tyrosinase solution was added. The enzyme solution was made by dissolving 10 mg of the enzyme (power) in 1 ml of the PBS. The tubes were quickly inverted once the enzyme was added and the absorbance was measured at 475 nm using a spectrophotometer. A graph was plotted with the x-axis representing the concentration of the L-DOPA solution and the y-axis representing the absorbance. From that graph, the most suitable concentration of the L-DOPA substrate to be used in the next step was determined. This concentration was shown to be the 0.1. Different concentrations of the enzyme were then used with the fixed concentration of the L-DOPA substrate that was determined in the previous step. 10 mg of the enzyme powder was dissolved in 1 ml of the phosphate buffer saline and serial dilutions of that stock solution were made. First, 0.2 ml of that stock solution was added into 1.8 ml of PBS to make a dilution of 1/10. Then, 0.2 ml of that solution was added again into 1.8 PBS to make a dilution of 1/100. Another 0.2 ml of the last solution was added into 1.8 of PBS to make 1/1000 dilution and so on until nine serial dilutions were made. Then, 1 ml of each enzyme dilution was added into 1 ml of the 0.1 concentration of the L-DOPA substrate solution. The tubes were then inverted quickly and the absorbance was read at 475 nm. A standard tyrosinase (phenol oxidase) curve was plotted and was used to determine the concentration of the enzyme in the samples.
3.1.9 Phenol oxidase assay
Monolayers of hemocytes were prepared as mentioned previously. Approximately 10 parasites were placed in to 3 wells (triplicate), another 10 dead parasites were added in to another 3 wells. Parasite products were placed in to 3 wells. 3 wells containing the monolayer and the medium and another 3 wells containing only the medium were used as the controls. The plate was then incubated for 1 h at 27°C. This previous procedure was repeated using incubation periods of 3 h, 6 h, and overnight. Then, 200 μl of the substrate solution (L-DOPA), 0.1 concentration of the 5 × 10−3 mol dm−3 solution was added to all the wells. The absorbance was then read at 475 nm wavelength using the ELIZA plate reader.
3.2 Results
All the 150 snails collected were found to be infected with the parasite
3.2.1 Lysozyme assay
A standard curve of this experiment was first created (Figure 1). According to the equation of the standard curve, Y = 1.0158 X + 1.7312, the lysozyme concentration in the 37 hemolymph samples can be estimated. Figure 2 shows the lysozyme concentration for the 37 hemolymph samples. Then, the lysozyme concentrations of the 12 mucous samples were estimated using the standard curve (Figure 3).
Figure 1.
Lysozyme standard curve.
Figure 2.
Lysozyme concentrations of 37 hemolymph samples.
Figure 3.
Lysozyme concentrations of 12 mucous samples.
3.2.2 Nitric oxide assay
A standard curve was first plotted for the nitric oxide assay (Figure 4). Using the equation of the standard curve, y = 0.0014x + 0.0504, the x values that represent the nitrite concentration in the different samples were estimated. Figure 5 shows the production of nitric oxide in response to live parasites, dead parasites, and parasite products.
Figure 4.
Nitric oxide standard curve.
Figure 5.
Production of nitric oxide in response to live parasites, dead parasites, and parasite products. LP + M + M = live parasite, monolayer, and medium; DP + M + M = dead parasite, monolayer, and medium; PP + M + M = parasite product, monolayer, and medium; M + M = monolayer and medium; M = culture medium.
3.2.3 Phenol oxidase assay
The absorbance of different concentrations of L-DOPA substrate is shown in Figure 6 and the absorbance of different enzyme concentrations with fixed substrate concentration is shown in Figure 7. According to the equation of the standard curve, Y = 6.5223X + 0.0677, the x values that represent the phenol oxidase concentration in the different samples were estimated. Figure 8 illustrates the previous results graphically.
Figure 6.
Absorbance of different concentrations of the L-DOPA substrate.
Figure 7.
Phenol oxidase standard curve: absorbance of different enzyme concentration.
Figure 8.
Phenol oxidase production in response to live, dead parasites, and parasite products over a period of 24 h. LP + M + M = live parasite, monolayer, and medium; DP + M + M = dead parasite, monolayer, and medium; PP + M + M = parasite product, monolayer, and medium; M + M = monolayer and medium; M = culture medium.
4. Conclusion and discussion
The current work was conducted to shed light on some parameters that are associated with the immune response that is resulting from the interaction between the pond snail
Lysozyme assay was carried out for hemolymph, mucous, and parasite products. Care was taken when mucous was collected in order not to contaminate mucous with hemolymph. The lysozyme standard curve was plotted on linear and logarithmic scale and the equation of that curve was used to estimate the lysozyme concentration in the unknown samples. In case of parasite product, zones of hydrolysis were not formed on the agar plates. This indicates that the parasite products did not contain any lysozymes. On the other hand, zones of hydrolysis were observed in the case of hemolymph and mucous samples. Accordingly, hemolymph and mucous of
It can be noticed from Figure 2 that there is a considerable fluctuation in the lysozyme concentration among the 37 hemolymph samples. This is due to variations in response to the presence of the bacteria in the agar. This may be due to the fact that some samples contain more hemolymph than hemocytes.
Figure 3 shows the lysozyme concentration in 12 mucous samples. As noticed, there is a little variation in the lysozyme concentrations among the 12 samples, indicating that different mucous samples contain different amounts of lysosomal enzymes. This is maybe due to differences in ages and sizes of the snails. Accordingly, it seems that the mucous represents the first defense line that prevents the establishment of the parasite in the snail’s body.
Nitric oxide production results in response to live, dead parasites, and parasite products (Figure 5) do show considerable increase in nitric oxide production due to these inoculations. Figures 5 and 6 are the same except for the control results (medium) that are shown in Figure 5 and not in Figure 6 in order for the reader to view the difference graphically. Figure 5 shows that the culture medium does contain some nitric oxide, so, this value should be subtracted from the results of the samples to ensure that the resulting values are representing nitric oxide production from the hemocytes upon inoculation and not from the culture medium as shown in Figure 5. Figures 5 and 6 have shown that there is some nitric oxide produced in the case of cultured hemocytes monolayer and that the concentration of nitric oxide has increased upon inoculation of live, dead parasites, and parasite products. As shown in Figure 5, the optimum period of time for production of nitric oxide is 6 h postexposure to live parasites, followed by dead parasite, and then parasite products. In other words, live parasites induce more nitric oxide production than did dead parasites and parasite products. This indicates that viable parasites may produce antigens that are more efficient in initiating the production of nitric oxide. These antigens are less, in terms of efficiency or amount, in the case of dead parasites and parasite products. Another possibility is that some of the measured nitric oxide may be originated from the live parasite it’s self.
It is noticed from Figure 5 that the trend of the graphs in the case of different inoculations (live, dead parasites, and parasite products) is almost the same. After 1 and 3 h, there was little nitric oxide production, and then the concentration increased drastically after 6 h. The concentration of the nitric oxide decreased drastically after 24 h. This drop of nitric oxide concentration after 6 h may be due to the possibility that the hemocytes were viable and were able to produce high amounts of nitric oxide after 6 h. Then, the cells began to lose their viability and they were unable to produce the same amounts of that material. In addition, since different culture plates were used for different time intervals, the concentration of the hemocytes in the 6-h plates may be much more than the concentration in the overnight plate. Accordingly, more nitric oxide was measured in the 6-h plate than in the overnight plate. Moreover, this result may represent what is happening naturally in the snails’ body. The concentration of nitric oxide at 6 h may be sufficient to get rid of the infection. After then, the concentration drops away because it already reaches the optimum and there is no need for more amounts. Another possibility is that some contaminants like detritus may be present in high amounts in the 6 h wells.
Results of the phenol oxidase assay are shown in Figure 8. The control results (medium and monolayer and medium by its self) were shown in the same figure and were not subtracted in order for the reader to view the difference graphically. It is noticed that the results of the controls, medium and monolayer, and medium alone are showing trace levels of phenol oxidase production (0.0040 mg/ml for the medium and 0.005 mg/ml for the medium and monolayer). It is also noticed that the production rate is steady throughout the experimental period. This indicates that there was no contamination with any other material that may induce sudden increase in the phenol oxidase production. It is shown in Figure 8 that the optimum period of time for production of phenol oxidase is 6 h postexposure to the live parasites, followed by the dead parasites, and then the parasite products. In other words, live parasites induce more enzyme production than do dead parasites and parasite products. This indicates that viable parasites may produce antigens that are more efficient in initiating the production of phenol oxidase. These antigens are less in the case of dead parasites and parasite products or are not that efficient in stimulating the production of the enzyme. In the case of live parasites, there was little increase in the phenol oxidase production until 3 h. Then the production rate increased drastically to reach its maximum at 6 h postinoculation. After then, it decreased throughout the experimental period. This peak may be due to some contaminants that stimulate the hemocytes to produce more phenol oxidase in the 6 h wells. Also, the hemocytes maybe more viable and were able to produce high amounts of phenol oxidase at 6 h. Then, the cells began to loose their viability and they were unable to produce the same amounts of that enzyme at 24 h. In addition, since different culture plates were used for different time intervals, the concentration of the hemocytes in the 6-h plates may be much more than the concentration in the other plates. Accordingly, more phenol oxidase was measured in the 6-h plate than in the other plates. Another possibility is that this happens naturally in the snails’ body. The concentration of phenol oxidase at 6 h may be sufficient and enough to get rid of the infection. After then, the concentration drops away because it already reaches the optimum and there is no need for more amounts.
It is shown in Figure 8 that the phenol oxidase production in the case of the dead parasites increases until it reaches its maximum at 24 h. However, the amount produced is much more less than in the case of live parasites. This indicates the antigenic nature of the materials produced by the dead parasites is much less than those produced by the live organisms. The maximum amount produced did not drop away, this may be due to the possibility that this amount is still not sufficient to get rid of the dead parasites and more amounts are needed to be produced. If these samples are kept more than 24 h, a decrease in phenol oxidase production maybe observed.
The production of phenol oxidase in the case of parasite products has almost the same trend as in the case of dead parasites until 6 h postinoculation. After then, the enzyme production decreased. So, there is a slight peak for phenol oxidase production in the case of parasite products, as can be noticed in Figure 8. This peak maybe due to the same possibilities discussed earlier. So, phenol oxidase production results in response to live, dead parasites, and parasite products (Figure 8) do show a noticeable increase in enzyme production due to these inoculations.
In a similar study, in the first experiment, snails were randomly assigned into six different treatment groups. There was no difference in their sizes. The first group was not exposed to any immune elicitor, the second group was injected with 100 μl of snail saline, the third and fourth groups were injected with lyophilized
5. Conclusion
In conclusion, lysozymes, nitric oxide, and phenol oxidase play an important role in the non-specific immune response against invading parasites and foreign particle in
Acknowledgments
The authors would like to extend their gratitude and appreciation to the management of the Kuwait Institute for Scientific Research for their continuous technical and financial support of scientific research.
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