Open access peer-reviewed chapter

Ixodes ventalloi Gil Collado, 1936: A Vector Role to be Explored

Written By

Ana Sofia Santos and Maria Margarida Santos-Silva

Submitted: 16 July 2018 Reviewed: 20 September 2018 Published: 05 November 2018

DOI: 10.5772/intechopen.81615

From the Edited Volume

Vectors and Vector-Borne Zoonotic Diseases

Edited by Sara Savić

Chapter metrics overview

1,333 Chapter Downloads

View Full Metrics


Ixodes Latreille, 1795 is the largest and broadest distributed genus of the family Ixodidae Murray, 1877. Its members are present in all zoogeographic regions, remote islands, and territories close to the poles. Plus, 63 species out of the 244 described have been recorded to feed on humans. Some are mega vectors, as those belonging to Ixodes ricinus-I. persulcatus complex, but others are so poorly studied that their vector role is difficult to access. This is the case of Ixodes ventalloi Gil Collado, 1936. This species is recorded in Northern Africa and Western Europe, mostly in Mediterranean basin countries, occurring along with other moisture-demanding ticks, as Haemaphysalis spp., I. frontalis, and I. ricinus. In fact, I. ventalloi not only shares vertebrate hosts (including humans) with the latter but may as well play a role in the enzootic cycle of some Ixodes-borne agents. This chapter updates information regarding this poorly studied tick, revising the available systematic, ecological, and microbiological data, discussing the potential public health relevance.


  • Ixodes ventalloi
  • taxonomy
  • distribution
  • vertebrate hosts
  • tick-borne agents

1. Introduction

Ticks are a highly specialized group of obligate, bloodsucking, nonpermanent ectoparasitic arthropods of terrestrial vertebrates with a worldwide distribution. They present a hematophagic behavior in all active phases and parasitize mammals, birds, reptiles, amphibians, and occasionally man. Unique among Acari, ticks have a large body size being considered large mites with specialized mouthparts (hypostome) and specialized sensory structures on legs (tarsus I, Haller’s organ) [1, 2]. These arthropods are among the most important vectors of human and animal disease. They are associated to the transmission of a great variety of pathogenic agents, including viruses, bacteria, and protozoa [3]. These pathogens are usually acquired by immatures, larvae, or nymphs, when ticks feed on infected hosts being maintained through their life and transmitted to naïve animals during the next blood meals, as nymphs and adults (horizontal transmission). Depending on the pathogen, ticks can also pass infection to the offspring (vertical transmission) or even to other ticks by feeding close to them (co-feeding). Ticks may also injure hosts without the involvement of infectious agents, just by the effects of salivary secretions, causing from a simple irritation to allergic reactions, toxicosis, and paralysis [4].

Among the family Ixodidae Murray 1877, the genus Ixodes Latreille 1795 is the largest, the broadest distributed, and one of the most important taxon regarding tick-borne diseases. It comprises a total number of 244 species of which 63 have been recorded to feed on humans [5]. Its members are present in all zoogeographic regions, remote islands, and territories close to the poles. In Europe and North Africa, the genus Ixodes is represented by 25 species [5]. Within this genus, several ticks may be considered mega vectors as those that belong to the Ixodes ricinus-I. persulcatus complex, but others are so poorly studied that their vector role is difficult to access. This is the case of Ixodes ventalloi Gil Collado, 1936. This is a species that is infrequently targeted in field trials and laboratory collections are scarce. In Portugal, an expansion of its distribution was observed, most likely as a collateral result of concerted efforts to increase knowledge on the subject [6, 7, 8, 9, 10, 11, 12]. The recent interest of other specialists has also generated updated descriptions of the morphological features relevant for diagnosis and the first molecular characterization of I. ventalloi populations with the analysis of its phylogenetic position in the group Ixodes [13, 14]. Regardless of this, information on the vector role of I. ventalloi remains challenging to access and poorly understood. This chapter intends to update information on I. ventalloi in order to call attention to this insufficiently studied tick, revising the available systematic, ecological, and microbiological data, discussing the potential public health relevance.


2. One species three names: a question of synonymy

I. ventalloi was first described by Gil Collado based on the morphological characters of a female tick parasitizing an Athene noctua captured in Barcellona [15]. The identification of this small-sized Ixodes, among other features, was based on the presence of particularly large and curved auriculae (Figure 1), differentiating it from the other European species, as the author wrote “Las aurículas de la base del capítulo, muy típicas y de forma de “asta de touro” (…) la distinguen netamente de las espécies europeas (…)” [15]. In the following years of its description, I. ventalloi was misclassified and as a consequence, confusion arose regarding the morphological features and the ecology of this tick. I. ventalloi was either incorrectly ascribed as a new species, I. thompsoni, or confounded with I. festai and used for the redescription of the latter species mistaking both entities, as detailed by Gilot and Perez [16]. I. festai, originally described by Rondelli in 1926 based on the analysis of a female specimen found parasitizing a Libyan Alectoris barbara, is a bird-associated tick contrasting with the more permissive nature of I. ventalloi, as revised bellow in this chapter. Several works mention I. thompsoni and I. festai sensu Arthur as a synonym of I. ventalloi, but the definitive validation of this species was only achieved with the studies of Gilot, Morel and Perez [16, 17, 18].

Figure 1.

Morphological features of Ixodes ventalloi: (A) Size comparison of questing I. ventalloi female (F Iv), male (M Iv), and nymph (N Iv) with a questing Ixodes ricinus nymph (N Ir), dorsal view, scale bar 2 mm; (B) ventral view of a questing I. ventalloi female, scale bar 2 mm; (C) scanning electron microscopy detail of the recurved auriculae (au), the hallmark feature first pointed by Gill Collado [15] for differentiation from the other European Ixodes, scale bar 200 μm.

Detailed descriptions of relevant morphological features have been subsequently updated, in some cases supported by illustrations and microscope images to better assist acarologists in I. ventalloi identification [14, 19, 20, 21]. Moreover, the application of mitochondrial DNA analysis using molecular targets, such as 12S rRNA, 16S rRNA, cytochrome c oxidase subunit 1 (cox1), has proven useful to complement the traditional morphological identification [12, 13, 14]. It also enabled the study of the population genetic structure. The molecular characterization of 92 I. ventalloi adults collected in cats from Lipari Island (Southern Italy) revealed the presence of a great genetic variability with the identification of eight haplotypes for 16S rRNA and 16 haplotypes for cox1, clustering in two sister clades—genogroup A, comprising 71% of the samples and genogroup B [13]. Interestingly, 16S rRNA sequences closest to those belonging to genogroup A were also documented in Spain and Portugal [1214]. In the latter study, 12S and 16S rRNA genes have been targeted in 48 questing I. ventalloi (nymphs and adults), resulting in the identification of six haplotypes (IvH1-H6) but with a low degree of nucleotide variation placing them all in Latrofa’s genogroup A [12]. Figure 2 represents the phylogenetic distance, based on 16S rRNA sequences, of the I. ventalloi specimens collected in Italy, Spain, and Portugal, comparing to those related (>91% homology) Ixodes species. These results highlight the need for further genetic characterization of I. ventalloi population, increasing both the molecular coverage and the number of studied specimens from other geographical origins.

Figure 2.

Phylogenetic trees based on 16S rRNA sequences obtained from Ixodes ventalloi collected in Italy, Spain and Portugal, comparing to sequences of other related (>91% homology) Ixodes species available in GenBank. Phylogenetic relationships were assessed computing the maximum likelihood method on MEGA7 [22]. Best fitting substitution models were determined using MEGA7 model selection method. Phylogenetic tree was constructed using General time reversible model, modulated by using a discrete Gamma distribution (+G) and based on the analysis of 1000 replicates. All positions with less than 75% site coverage were eliminated. That is, fewer than 25% alignment gaps, missing data, and ambiguous bases were allowed at any position. There were a total of 247 positions in the final dataset. Accession numbers are followed by species name, and in some case the origin of sequences and haplotypes designation. Branch lengths represent the number of substitutions per site inferred according to the scale-bar.

The I. ventalloi sequences obtained in the aforementioned studies were deposited in GenBank under the accession numbers: KU178964-KU178979 for cox1; KU178956-KU178963, KY231931, MF370642-43, MF621228, MF621233, MG210719-20 for 16S rDNA; MF370631-32, MF621221, MF621226, MG210717-18 for 12S rDNA.


3. The permissive “rabbit-tick”

The geographical distribution of I. ventalloi includes areas of western Mediterranean Europe (Portugal, Spain, Southern France, Central and Southern Italy, and Cyprus) and Northern Africa (Marroco and Tunisia) [14, 21]. This tick species was also documented in Great Britain (Channel Islands, Lundy Island, and Isles of Scilly) and in southwest Germany, probably as the result of introductions, but the establishment of I. ventalloi populations was only confirmed in the Britain islands [23, 24]. In Portugal, I. ventalloi was first identified in 1985, and since then, it has been described across the country mainly in littoral mainland areas and along with other moisture-demanding ticks, such as Haemaphysalis spp., Ixodes frontalis, I. ricinus [6, 7, 8, 10, 11, 12, 25].

I. ventalloi is regarded as a three-host, endophilic, and monotropic tick. All development stages are commonly found parasitizing Oryctolagus cuniculus and associated to lagomorph’s environment; thus, it is popularly designated as the “rabbit-tick” [716, 17, 18, 23, 25, 26, 27, 28, 29, 30]. However, the list of vertebrate hosts parasitized by I. ventalloi is much more broader, including several species of rodents and other small mammals, medium-size carnivores, and occasionally ground-dwelling birds and birds of prey [6, 7, 8, 9, 10, 11, 13, 15, 16, 23, 26, 27, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43]. Table 1 resumes the host species that have been documented with I. ventalloi ticks. Close to 40 species are so far listed revealing the permissive feeding behavior of this tick, which is not restricted to wild animals. In fact, I. ventalloi were found feeding on humans and companion animals, mostly cats and sporadically dogs, as shown in Table 1. Regarding cats, the first record of this tick-host association date back to the description of I. thompsoni (synonym of I. ventalloi) from the material collected in Lundy Island by Thompson [16]. Since then, I. ventalloi has been recurrently found feeding on cats in almost all areas where it occurs and in some cases described as the predominant tick species found on this host [8, 10, 11, 13, 27, 32, 36, 37]. Cat parasitism by I. ventalloi might be explained by the host free-roaming and hunting habits that place them in close contact with the ground and low vegetation when ambushing small animals. Although I. ventalloi is regarded as having a limited potential for dispersal, it can be found actively seeking for hosts at the ground level. This was proven by us in previous studies, when dragging vegetation and grassy ground resulted in the collection of 175 questing I. ventalloi, including nymphs, males and females [8, 9, 10, 11, 12]. The same result was recently obtained by Torina et al. [45] that have collected 1425 questing I. ventalloi, including all tick stages, by dragging vegetation in Palermo’s areas during a 2-year study.

Host order and speciesTick stage/sexCountry (or region)References
Asio flammeusF, M, NPortugal[9]
Asio otusFGreat Britain[16]a, [27]
Athene noctuaFSpain,[15]
Tyto albaNPortugal[11]
Alectoris chukarNDCyprus[31]
Alectoris rufaF(+)France, Italy[16]b, [32]
Phasianus colchicusF(+)France, Italy, North Africa[16]c, [32]
Pica picaFFrance[16]b
Turdus merulaNGreat Britain, Portugal[23, 33]
Turdus pilarisFFrance[16]b
Rallus aquaticusNDItaly[32]
Lepus europaeusF(+)Cyprus, other European regions[16]e, [31]
Oryctolagus cuniculusF, M, N, LFrance, Great Britain, Portugal, Spain, Morocco, North Africa[7], [16]d[17, 18], [26]i, [23, 27, 28, 29, 30]
Apodemus sylvaticusImMorocco[26]i
Eliomys quercinusF, N, LMorocco, Portugal[7], [26]i
Gerbillus campestrisImMorocco[26]i
Hystrix cristataNDItaly[34]
Lemniscomys barbarusImMorocco[26]i
Mus spretusF, N, LMorocco, Portugal[7], [26]i
Rattus rattusImMorocco[26]i
Rattus norvegicusNPortugal[11]
Sciurus vulgarisFNorthern Africa[16]f
Crocidura russulaNPortugal[7]
Erinaceus europaeusF, M, NPortugal, Spain and North Africa[6], [16]f, [35]
Canis familiarisFPortugal[11]
Felis catusF, M, NFrance, Great Britain, Italy, Portugal, North Africa[8, 10, 11, 13], [16]h, [27, 32, 36], [37]
Genetta genettaF, MSpain, other European regions[16]g, [38]
Herpestes ichneumonF, MSpain[38, 39]
Lynx pardinusF, MSpain[38, 39]
Martes foinaFFrance[16]b
Meles melesFFrance[16]b
Mustela nivalisF, M, N, LPortugal[7, 11]
Mustela n. numidicaImMorocco[26]i
Vulpes vulpesF, M, ImCyprus, Morocco Portugal, Spain[6], [26]i, [31, 38, 39, 40]
Homo sapiensF(+)France, Italy, Portugal[16]b, [41, 42, 43, 44]
Agama impalearisImMorocco[26]i
Chalcides polylepisImMorocco[26]i
Eumeces algeriensisImMorocco[26]i
Psammodromus algirusImMorocco[26]i

Table 1.

List of vertebrate species found with Ixodes ventalloi ticks.

Thompson collection.

Gilot collection.

Gilot and Morel collection.

Gilot, Morel, Institute Pasteur and Clifford collections.

Institute Pasteur collection.

Morel collection.

Neumann collection.

Gilot, Morel and Thompson collections.

Bailly-Choumara et al. [26] list of the Moroccan host is used with reservations since it was published prior to the differentiation of I. ventalloi from I. festai. In any case, the authors were aware about the synonymy of I. ventalloi and I. festai sensu Arthur. Moreover, I. festai is also listed but placed apart from I. ventalloi.

ND—No detail is provided regarding sex/stage of the collected tick(s); Im—Immature(s) stage(s) not detailed; F—Female(s); F(+)—Female(s) and possible other specimens as information regarding sex/stage is not detailed in all references; M—Male(s); N—Nymph(s); L—Larva(e).

a–hIn Gilot and Perez [16], the country or geographical regions was deduced based on the authors’ descriptions of the origin of I. ventalloi specimens.

The particular association of cats to I. ventalloi may contribute to bring this tick to domestic environments and to promote human exposure. In fact, I. ventalloi has long been listed as a human-biting tick [16, 41]. In Portugal, the authors recorded the first case of human parasitism by this species in 2014, on behalf of the Surveillance Network for Vectors and Vector-borne Diseases (REVIVE), and keep documenting it every year since then [44, 46]. Although I. ventalloi represents a small percentage (less than 1%) of the species found feeding on humans, it is under the scope for potential infections by human pathogens [44, 46]. The increasing number of agents associated to this species in recent years brought back the question regarding the I. ventalloi public health relevance.


4. A vector’s potential neglected or negligible?

During several years, information regarding I. ventalloi pathobiome was almost absent. The first association of this tick to a potential tick-borne agent was reported in 1984 by Chastel et al. [47]. In this study, strains of the coltivirus Eyach (EYAV), a virus belonging to Colorado tick fever group, were isolated from both I. ventalloi and I. ricinus ticks that were found parasitizing a wild rabbit in Northwestern France. Eyach virus was previously described in I. ricinus from West Germany, subsequently found on several wild mammals and indirectly linked to patients with neurological disorders, as tick-borne encephalitis, polyradiculoneuritis, and meningopolyneuritis, on a base of serology [48]. In 2004, we have also reported I. ventalloi infection by Anaplasma phagocytophilum, a species with variant strains implicated in human and domestic animal cases of granulocytic anaplasmosis [8]. The growing interest on I. ventalloi observed in the last 10 years has resulted in an increasing number of papers and the detection of diverse microorganisms associated to this tick species. Table 2 resumes the microbial agents that have been found in I. ventalloi, providing information on ticks stage, sex, and molecular identification (haplotypes), when available. Overall, 13 agents have already been associated to I. ventalloi, and infected ticks were found feeding on wild animals, as well as on domestic cats and on a human, pointing for a potential role as vector that might have both medical and veterinary implications.

MicroorganismTicks originTicks haplotypes§Reference
Coltivirus EyachOryctolagus cuniculusND[47]
Anaplasma marginaleVegetationND[49]
A. phagocytophilumVegetation, Felis catusND[8, 10]
VegetationIvH1, IvH3, IvH5[12]
Ehrlichia canisFelis catusND[36]
Ca Neoehrlichia sp.VegetationND[12]
Rickettsia helveticaAsio flammeusND[9]
Lynx pardinus, Vulpes vulpesND[38]
Felis catus, Rallus aquaticusND[32]
Felis catus*ND[36]
Homo sapiensHaplotype 1[13, 37]
R. monacensisOryctolagus cuniculusND[29]
Lynx pardinus, Vulpes vulpes, Genetta genettaND[38]
Felis catus*ND[32, 36]
Coxiella burnetiiAlectoris chukar, Lepus europaeusND[31]
VegetationIvH2, IvH3, IvH5, IvH6[12]
Bartonella clarridgeiaeFelis catusND[36]
Borrelia valaisianaFelis catus, Rallus aquaticus, Phasianus colchicus¥ND[32]
B. spielmaniiFelis catus, Phasianus colchicus¥ND[32]
Leishmania infantumFelis catusND[36]
Theileria annulataVegetationND[49]

Table 2.

List of microorganisms and parasites found in Ixodes ventalloi.

One tick co-infected with Rickettsia helvetica and R. monacensis [36].

One female tick coinfected with Bartonella clarridgeiae and Leishmania infantum.

One tick co-infected with Borrelia valaisiana and B. spielmanii.

All these haplotypes have been identified as belonging to genogroup A and were submitted to Genbank under the accession numbers: Haplotype 1, KU178956 (16S rDNA) and KU178964 (cox1); IvH1, MF370631 (12S rDNA) and MF370642 (16S rDNA); IvH2, MF621226 (12S rDNA) and MF621233 (16S rDNA); IvH3, MG210717 (12S rDNA) and MG210719 (16S rDNA); IvH5, MF621221 (12S rDNA) and MF621228 (16S rDNA); IvH6, MF370632 (12S rDNA) and MF370643 (16S rDNA), as previously described [12, 13].

Another justification for the presence of agent’s nucleic acids in parasitizing ticks can also be the presence of host-infected blood in arthropods´ midgut rather than a true vector potential. However, it is worthy of note that some of the I. ventalloi positives were indeed unfed ticks, as detailed. The first record dates back to 2004 when the authors were investigating A. phagocytophilum in I. ricinus and their sympatric ticks in Setubal District, Portugal [8]. The screened sites were mainly suburban wooded areas in some cases used for grazing and with evidence of wild animals presence, as rabbits. Out of the 93 I. ventalloi collected, A. phagocytophilum was recorded in a questing nymph and also in a male found attached to a free-roaming cat. The sequences obtained from both ticks were found to be a new A. phagocytophilum variant based on groEL and msp2 gene analysis [8]. This finding was subsequently reinforced by the detection of the same A. phagocytophilum variant also in an I. ventalloi female feeding on a cat from another district of mainland, Santarém District [10]. More recently, a retrospective study using the DNA material stored from Setúbal district ticks also resulted in the detection of questing I. ventalloi specimens of Anaplasma marginale (four nymphs and one male) and Theileria annulata (one female) [49]. New data that link more agents to questing I. ventalloi were submitted for publication in the beginning of 2018 [12]. That study was undertaken in Parque Florestal de Monsanto (PFM), a recreational area located in the urban perimeter of Lisbon city. This is a highly used park for petting and several outdoor activities. Overall, eight tick species were found questing in PFM with a preponderance of I. ventalloi. A preliminary 1-year screening to define the best season for collection, established that the period of activity for this species extended from November to June, with a peak in spring (Figure 3) [50]. Interesting, both of these findings (abundance and seasonality) were reinforced in Torina et al. comprehensive study [45]. In our case, the diversity of PFM ticks and the particular abundance of I. ventalloi were attributed to the park’s wild population, composed of over 100 species of small mammals and birds [51].

Figure 3.

The distribution of immature and adult tick species collected in PFM during 1-year period (2011–2012) [50].

Regarding tick-borne agents, questing I. ventalloi in PFM were found harboring A. phagocytophilum (two males, one female, and two nymphs), Coxiella burnetii (five males, three females, and one nymph), and a potentially new agent close related to Candidatus (Ca.) Neoehrlichia mikurensis (one female and one male). Interestingly, two A. phagocytophilum variants were detected [12]. The more representative was a new variant of A. phagocytophilum previously detected in both Setúbal and Santarém districts (and here found on four ticks) [8, 10]. This reinforces previous data sustaining a divergent variant of A. phagocytophilum, not clustering in none of the four ecotypes defined by Jahfari et al. [52], with the closest sequence sharing only 95% homology and belonging to ecotype IV that is composed of sequences of the agent derived from birds. Another A. phagocytophilum variant was obtained from a single I. ventalloi, clustering the ecotype I that is composed by agent’s sequences associated to human and domestic animal cases of granulocytic anaplasmosis [52]. It was also worth of mention that positive ticks were found questing in different occasions showing the existence of active cycles for these agents in PFM [12]. The molecular identification of nine positive ticks confirmed that all belonged to Latrofa’s genotype A, based on 16S rDNA analysis. The obtained haplotypes and the GenBank accession numbers are presented in Table 2.

In all the aforementioned Portuguese areas, infected I. ventalloi were found questing along with other moisture-demanding ticks, as the mega-vector I. ricinus. Both tick species are considered sympatric sharing geographical distribution, vertebrate hosts, and possible their agents [11]. The presence of alternate ticks (generally endophilic ticks) has been associated to the existence of secondary maintenance cycles for some Ixodes-borne agents [53]. If I. ventalloi has such a role and thus contributes indirectly to the occurrence of I. ricinus-borne diseases is yet to be investigated.


5. Conclusion

I. ventalloi has been relegated to the sidelines for years due to its endophilic nature, apparent host specificity, and unknown vector importance. Accumulated evidence is, however, revealing a different reality for this small Ixodes. As revised here, I. ventalloi presents a permissive feeding behaviors that might promote exposure to several blood-borne pathogens and the list of agents found in this species keeps growing. Of note is the fact that I. ventalloi is broadly found feeding on cats and can also parasitize men. Moreover, it is sympatric to the mega-vector I. ricinus and might contribute to the maintenance of its agents. Altogether these suggest a vector role for I. ventalloi, either directly or by sympatry with other ticks species, with potential public health implications and deserving further investigation.



This work was supported by the FCT project PTDC/SAU-PAR/28947/2017. The authors thank Miguel Flores for the library assistance.


Conflict of interest

The authors do not disclose any conflict of interest.


  1. 1. Balashov YS. Bloodsucking ticks (Ixodoidea): Vectors of diseases of man and animals. Vol. 8. Miscellaneous Publications of the Entomological Society of America. Baltimore: Entomological Society of America; 1968. pp. 1-376
  2. 2. Krantz GW. A Manual of Acarology. 2nd ed. Corvallis: Oregon State University Book Stores; 1978
  3. 3. Sonenshine DE, Roe RM. Overview ticks, people, and animals. In: Sonenshine DE, Roe RM, editors. Biology of Ticks. 2nd ed. Vol. 1. New York: Oxford University Press; 2014. pp. 3-16
  4. 4. Estrada-Peña A, Mans BJ. Tick-induced paralysis and toxicoses. In: Sonenshine DE, Roe EM, editors. Biology of Ticks. 2nd ed. Vol. 2. New York: Oxford University Press; 2014. pp. 313-332
  5. 5. Guglielmone AA, Robbins RG, Apanaskevich DA, Petney TN, Estrada-Peña A, Horak IG. Ticks feeding on humans. In: Guglielmone AA, Robbins RG, Apanaskevich DA, Petney TN, Estrada-Peña A, Horak IG, editors. Hard Ticks of the World: (Acari: Ixodida: Ixodidae). Netherlands: Springer Science+Business Media Dordrecht; 2014. pp. 715-716. DOI: 10.1007/978-94-007-7497-1
  6. 6. Dias JATS. Um novo Ixodídeo (Acarina, Ixodoidea) para a fauna de Portugal. Ixodes ventalloi Gil Collado, 1936. Actas do II Congresso Ibérico de Entomologia. Boletim da Sociedade Portuguesa de Entomologia. 1985;4(Supl I):149-158
  7. 7. Dias JATS, Santos-Reis M. A carraça Ixodes ventalloi Gil Collado, 1936 como principal ectoparasita de uma população de doninhas (Mustela nivalis Linnaeus, 1766) em Portugal. Garcia de Orta: Série de Zoologia. 1989;14:35-50
  8. 8. Santos AS, Santos-Silva MM, Almeida VC, Bacellar F, Dumler JS. Detection of Anaplasma phagocytophilum DNA in Ixodes ticks (Acari: Ixodidae) from Madeira Island and Setúbal District, mainland Portugal. Emerging Infectious Diseases. 2004;10(9):1643-1648
  9. 9. Santos-Silva MM, Sousa R, Santos AS, Melo P, Encarnação V, Bacellar F. Ticks parasitizing wild birds in Portugal: detection of Rickettsia aeschlimannii, R. helvetica and R. massiliae. Experimental and Applied Acarology. 2006;39:331-338. DOI: 10.1007/s10493-006-9008-3
  10. 10. Santos AS, Santos-Silva MM, Sousa R, Bacellar F, Dumler JS. PCR-based survey of Anaplasma phagocytophilum in Portuguese ticks (Acari: Ixodidae). Vector Borne and Zoonotic Diseases. 2009 Feb;9(1):33-40. DOI: 10.1089/vbz.2008.0051
  11. 11. Santos-Silva MM, Beati L, Santos AS, De Sousa R, Núncio MS, Melo P, et al. The hard-tick fauna of mainland Portugal (Acari: Ixodidae): An update on geographical distribution and known associations with hosts pathogens. Experimental and Applied Acarology. 2011;55(1):85-121. DOI: 10.1007/s10493-011-9440-x
  12. 12. Santos AS, de Bruin A, Veloso AR, Marques C, Pereira da Fonseca I, de Sousa I, et al. Detection of Anaplasma phagocytophilum, Candidatus Neoehrlichia sp., Coxiella burnetii, and Rickettsia spp. in questing ticks from a recreational park, Portugal. Tick and Tick-Borne Diseases. 2018;9(6):1555-1564. DOI: 10.1016/j.ttbdis.2018.07.010
  13. 13. Latrofa MS, Giannelli A, Persichetti MF, Pennisi MG, Solano-Gallego L, Brianti E, et al. Ixodes ventalloi: Morphological and molecular support for species integrity. Parasitology Research. 2017;116(1):251-258. DOI: 10.1007/s00436-016-5286-9
  14. 14. Estrada-Peña A, Venzal JM, Nava S. Redescription, molecular features, and neotype deposition of Rhipicephalus pusillus Gil Collado and Ixodes ventalloi Gil Collado (Acari, Ixodidae). Zootaxa. 2018;4442(2):262-276. DOI: 10.11646/zootaxa.4442.2.4
  15. 15. Gil Collado J. Acaros Ixodoideos de Cataluña y Baleares. Treballs del Museu de Ciencies Naturals de Barcelona, Serie Entomologica. 1936;11(2):1-8
  16. 16. Gilot B, Perez C. Individualisation et caractérisation de deux Ixodes actuelement confondus: I. festai Rondelli, 1926, I. ventalloi Gil Collado, 1936 (Acarina, Ixodoidea). Revue Suisse de Zoologie. 1978;85(1):143-149
  17. 17. Morel PC, Perez C. Morphologie des stages preimaginales des ixodoidea s. str. d’Europe occidentale. V – Les larves des Ixodes s. str. Acarologia. 1977;19(3):395-402
  18. 18. Morel PC, Perez C. Morphologie des stages preimaginales des ixodoidea s. str. dÉurope occidentale. V – Les nymphs des Ixodes s. str. Acarologia. 1977;19(4):579-586
  19. 19. Gil Collado J, Guillen Llera J, Zapateiro Ramos LM. Clave para la Identificacion de los Ixodoidea Españoles (Adultos). Revista Ibérica de Parasitologia. 1979;39:107-118
  20. 20. Gil Collado J, Sanchez-Covisa A, Rodrigues Rodriguez JÁ. Detalles ultraestructurales de Ixodes ventalloi, Gil Collado 1936 (Acarina: Metastigmata). Proceedings of the VI Congreso Nacional de Parasitología y I Congresso Ibérico de Parasitología, Cáceres: In; 1989
  21. 21. Pérez-Eid C. Ixodes (Ixodes) ventalloi Gil Collado, 1936. In: Pérez-Eid C, editor. Les tiques. Identification, biologie importance médicale et vétérinaire. Monographies de microbiologie. Paris: TEC & DOC Lavoisier; 2007. pp. 124-127
  22. 22. Kumar S, Stecher G, Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Molecular Biology and Evolution. 2016;33:1870-1874. DOI: 10.1093/molbev/msw054
  23. 23. Jameson LJ, Medlock JM. Tick surveillance in Great Britain. Vector Borne and Zoonotic Diseases. 2011;11(4):403-412. DOI: 10.1089/vbz.2010.0079
  24. 24. Petney TN, Pfäffle MP, Skuballa JD. An annotated checklist of the ticks (Acari: Ixodida) of Germany. Systematic and Applied Acarology. 2012;17(2):115-170
  25. 25. Petney TN, Otranto D, Dantas-Torres F, Pfäffle MP. Ixodes ventalloi Gil Collado, 1936. In: Estrada-Peña A, Mihalca AD, Petney, editors. Ticks of Europe and North Africa. A Guide to Species Identification. Switzerland: Springer International Publishing; 2017. pp. 183-187. DOI: 10.1007/978-3-319-63760-0
  26. 26. Bailly-Choumara H, Morel PC, Rageau J. Sommaire des donnes actuelles sur les tiques du Maroc (Acari, Ixodoidea). Le Bulletin de l'Institut Scientifique. 1976;1:101-117
  27. 27. Martin KP. Provisional Atlas of the Ticks (Ixodoidea) of the British Isles. Biological Recods Center, Institute of Terrestrial Ecology Monks Wood Experimental Station, Dorchester, Great Britain: Henry Ling Ltd at the Dorset Press; 1988. p. 62
  28. 28. Marquez FJ, Guiguen C. Distribution sur l’hote des ixodoides parasites d’Oryctolagus cuniculus (L.) et facteurs qui l’affectent. Acarologia. 1992;23:141-148
  29. 29. Márquez FJ. Spotted fever group Rickettsia in ticks from southeastern Spain natural parks. Experimental and Applied Acarology. 2008;45(3-4):185-194. DOI: 10.1007/s10493-008-9181-7
  30. 30. González J, Valcárcel F, Pérez-Sánchez JL, Tercero-Jaime JM, Olmeda AS. Seasonal dynamics of ixodid ticks on wild rabbits Oryctolagus cuniculus (Leporidae) from Central Spain. Experimental and Applied Acarology. 2016;70(3):369-380. DOI: 10.1007/s10493-016-0069-7
  31. 31. Psaroulaki A, Chochlakis D, Angelakis E, Ioannou I, Tselentis Y. Coxiella burnetii in wildlife and ticks in an endemic area. Transactions of the Royal Society of Tropical Medicine and Hygiene. 2014;108(10):625-631. DOI: 10.1093/trstmh/tru134
  32. 32. Tomassone L, Grego E, Auricchio D, Iori A, Giannini F, Rambozzi L. Lyme borreliosis spirochetes and spotted fever group rickettsiae in ixodid ticks from Pianosa Island, Tuscany Archipelago, Italy. Vector Borne and Zoonotic Diseases. 2013;13(2):84-91. DOI: 10.1089/vbz.2012.1046
  33. 33. Norte AC, da Silva LP, Tenreiro PJ, Felgueiras MS, Araújo PM, Lopes PB, et al. Patterns of tick infestation and their Borrelia burgdorferi s.l. infection in wild birds in Portugal. Ticks and Tick-borne Diseases. 2015;6(6):743-750. DOI: 10.1016/j.ttbdis.2015.06.010
  34. 34. Mori E, Sforzi A, Menchetti M, Mazza G, Lovari S, Pisanu B. Ectoparasite load in the crested porcupine Hystrix cristata Linnaeus, 1758 in Central Italy. Parasitology Research. 2015;114(6):2223-2229. DOI: 10.1007/s00436-015-4413-3
  35. 35. Domínguez G. Ectoparásitos de los mamíferos silvestres del norte de Burgos (España). Galemys. 2003;15(1):47-60
  36. 36. Pennisi MG, Persichetti MF, Serrano L, Altet L, Reale S, Gulotta L, et al. Ticks and associated pathogens collected from cats in Sicily and Calabria (Italy). Parasites & Vectors. 2015;8:512. DOI: 10.1186/s13071-015-1128-3
  37. 37. Otranto D, Dantas-Torres F, Napoli E, Solari Basano F, Deuster K, Pollmeier M, et al. Season-long control of flea and tick infestations in a population of cats in the Aeolian archipelago using a collar containing 10% imidacloprid and 4.5% flumethrin. Veterinary Parasitology. 2017;248:80-83. DOI: 10.1016/j.vetpar.2017.10.023
  38. 38. Márquez FJ, Millán J. Rickettsiae in ticks from wild and domestic carnivores of Doñana National Park (Spain) and surrounding area. Clinical Microbiology and Infection. 2009;15(Suppl 2):224-226. DOI: 10.1111/j.1469-0691.2008.02147.x
  39. 39. Millán J, Ruiz-Fons F, Márquez FJ, Viota M, López-Bao JV, Paz Martín-Mateo M. Ectoparasites of the endangered Iberian lynx Lynx pardinus and sympatric wild and domestic carnivores in Spain. Medical and Veterinary Entomology. 2007;21(3):248-254
  40. 40. Martínez-Carrasco C, Ruiz de Ybáñez MR, Sagarminaga JL, Garijo MM, Moreno F, Acosta I, et al. Parasites of the red fox (Vulpes vulpes Linnaeus, 1758) in Murcia, southeast Spain. Revue de Médecine Vétérinaire. 2007;158(7):331-335
  41. 41. Gilot B, Marjolet M. Contribution à l’étude du parasitisme humain par les tiques (Ixodidae et Argasidae), plus particulièrement dans le sud-est de la France. Médecine et Maladies Infectieuses. 1982;12(6):340-351
  42. 42. Sanogo YO, Parola P, Shpynov S, Camicas JL, Brouqui P, Caruso G, et al. Genetic diversity of bacterial agents detected in ticks removed from asymptomatic patients in northeastern Italy. Annals of the New York Academy of Sciences. 2003;990:182-190
  43. 43. Otranto D, Dantas-Torres F, Giannelli A, Latrofa MS, Cascio A, Cazzin S, et al. Ticks infesting humans in Italy and associated pathogens. Parasites & Vectors. 2014;7:328
  44. 44. Santos-Silva MM, Lopes de Carvalho I, Santos AS, Núncio S, Sousa R, Equipa REVIVE. Estudo dos ixodídeos removidos de humanos no âmbito do programa REVIVE, 2011-2015. Boletim Epidemiológico Observações. 2017;18(2):10-13
  45. 45. Torina A, Blanda V, Blanda M, Auteri M, La Russa F, Scimeca S, et al. A geographical information system based approach for integrated strategies of tick surveillance and control in the peri-urban natural reserve of Monte Pellegrino (Palermo, Southern Italy). International Journal of Environmental Research and Public Health. 2018;15:404. DOI: 10.3390/ijerph15030404
  46. 46. Santos AS, Santos-Silva M, Lopes de Carvalho I, Milhano N, Chaínho L, Luz T, et al. REVIVE, a surveillance program on vectors and vector-borne pathogens in Portugal—Four years experience on ticks. In: Abstract Book the 2nd Conference on Neglected Vectors and Vector-borne Diseases; 31 March-2 April 2015; Izmir, Turquia. pp. 39-40
  47. 47. Chastel C, Main AJ, Couatarmanac'h A, Le Lay G, Knudson DL, Quillien MC, et al. Isolation of Eyach vírus (Reoviridae, Colorado tick fever group) from Ixodes ricinus and I. ventalloi ticks in France. Archives of Virology. 1984;82(3-4):161-171
  48. 48. Attoui H, Mohd Jaafar F, de Micco P, de Lamballerie X. Coltiviruses and seadornaviruses in North America, Europe, and Asia. Emerging Infectious Diseases. 2005;11(11):1673-1679
  49. 49. Antunes S, Ferrolho J, Domingues N, Santos AS, Santos-Silva MM, Domingos A. Anaplasma marginale and Theileria annulata in questing ticks from Portugal. Experimental and Applied Acarology. 2016;70(1):79-88. DOI: 10.1007/s10493-016-0057-y
  50. 50. Veloso AR. Pesquisa de Coxiella burnetii em ixodídeos capturados em parques urbanos de Lisboa [thesis]. Lisboa: Faculdade de Medicina Veterinária, Universidade Técnica de Lisboa; 2013
  51. 51. Biodiversidade: Biodiversidade na Cidade de Lisboa: Uma estatégia para 2020 [Internet]. 2015. Available from: [Accessed: May 29, 2018]
  52. 52. Jahfari S, Coipan EC, Fonville M, van Leeuwen AD, Hengeveld P, Heylen D, et al. Circulation of four Anaplasma phagocytophilum ecotypes in Europe. Parasites & Vectors. 2014;7:365
  53. 53. Bown KJ, Begon M, Bennett M, Woldehiwet Z, Ogden NH. Seasonal dynamics of Anaplasma phagocytophila in a rodent-tick (Ixodes trianguliceps) system, United Kingdom. Emerging Infectious Disease. 2003;9:63-70

Written By

Ana Sofia Santos and Maria Margarida Santos-Silva

Submitted: 16 July 2018 Reviewed: 20 September 2018 Published: 05 November 2018