- Open Access
Drosophilidae feeding on animals and the inherent mystery of their parasitism
© Maca and Otranto; licensee BioMed Central Ltd. 2014
- Received: 13 August 2014
- Accepted: 2 November 2014
- Published: 18 November 2014
Insect evolution, from a free to a parasitic lifestyle, took eons under the pressure of a plethora of ecological and environmental drivers in different habitats, resulting in varying degrees of interactions with their hosts. Most Drosophilidae are known to be adapted to feeding on substrates rich in bacteria, yeasts and other microfungi. Some of them, mainly those in the Steganinae subfamily, display a singular behaviour, feeding on animal tissues or secretions. This behaviour may represent an evolving tendency towards parasitism. Indeed, while the predatory attitude is typical for the larval stages of a great proportion of flies within this subfamily, adult males of the genera Amiota, Apsiphortica and Phortica display a clearly zoophilic attitude, feeding on the lachrymal secretions of living mammals (also referred as to lachryphagy). Ultimately, some of these lachryphagous species act as vectors and intermediate hosts for the spirurid nematode Thelazia callipaeda, which parasitizes the eyes of domestic and wild carnivores and also humans. Here we review the scientific information available and provide an opinion on the roots of their evolution towards the parasitic behaviour. The distribution of T. callipaeda and its host affiliation is also discussed and future trends in the study of the ecology of Steganinae are outlined.
- Phortica variegata
- Thelazia callipaeda
Initial stages of parasitism in insects
Insects and arachnids of medical and veterinary concern (e.g., mosquitoes, sand flies, stable flies, black flies, and ticks) have been studied extensively over the centuries, primarily because of the effect of their parasitic feeding habits on many species of domestic and wild animals, and humans. Indeed, these arthropods affect the health, welfare and production of animals through the transmission of disease-causing pathogens or just through biting them, therefore causing blood loss, allergic reactions, and/or nuisance and disturbance . Evolution of arthropods, from a free to a parasitic lifestyle, took eons under the pressure of a wide range of ecological and environmental drivers, resulting in varying degrees of interactions with their hosts, e.g. from virtually necrophagous larvae, occasionally also causing facultative myiasis, to obligate parasitism. However, scientific information on the insect taxa that evolved only partial parasitic interactions with their hosts, is scant ,, and it puts them in a group of organisms of an as yet undefined parasitic status. For example, most Drosophilidae are known to be adapted to feeding on substrates rich in bacteria, yeasts and other fungi (e.g., decaying or fermenting fruit) . However, some of them display a different feeding behaviour as they may feed on animal tissues or secretions (hereinafter referred as to “zoophagy”), therefore being of medical and veterinary importance. This particular behaviour may represent an evolving step towards parasitism. Indeed, there is still paucity of information on the natural history of these drosophilids, and great part of knowledge available to date derives from incidental findings from studies from the 19th century . The still limited entomological data on these insects is partly due to the difficulties in breeding these species under laboratory conditions . Here we review the scientific information available and provide an opinion about the main drivers, which might have affected some drosophilid genera of the subfamily Steganinae towards parasitic behaviour.
Zoophagy in Drosophilidae
Drosophila melanogaster (Diptera, Drosophilidae), the “vinegar fly” , is the quintessential member of this large family of insects, having had an enormous impact on various fields of science over the last century. Indeed, studies using this insect as a laboratory model have enabled great achievements in the field of developmental sciences (e.g. genetics, heredity, evolution, biochemistry, molecular biology, and cell biology)  as well as in applied disciplines such as neuroscience , the study of intellectual disability , metabolic disorders (e.g., obesity)  and oncology . The reasons for the success of these tiny flies in science are related to their tolerance to environmental conditions, ease of rearing, short reproduction times, large numbers of offspring and the occurrence of several types of hereditary variations within a small genome size (i.e., four pairs of chromosomes). With the exception of this iconic species, as many as ca. 4,200 known species are included in the Drosophilidae family ,, displaying wide variations in morphology, behaviour, biology and ecology .
Two subfamilies are ranked in this family, namely the Drosophilinae, which at present includes 3,182 described species, and the less well-represented Steganinae, with 1,008 species . Morphological characteristics of these subfamilies have been described in ,. In Drosophilinae, zoophagous and/or commensal behaviour is restricted to larvae of a few scattered clades, classified at present as parts of the genera Drosophila (mainly simulivora group species), Zygothrica (1 species), Scaptomyza (subgenus Titanochaeta) and Lissocephala (1 species); altogether ca. 20 species . Most other Drosophilinae are generally micromycetophagous (Sacharomycetales are clearly preferred substrates), although mycetophagy, saprophagy and phytophagy are typical for some genera or species groups .
Additional file 1: Phortica variegata flying around human eyes. Description: This video shows the typical questing fly of Phortica variegata during a summer day in Basilicata region (southern Italy), an area highly endemic for Thelazia callipaeda. These insects are attracted by animal perspiration and ocular secretions. (M4V 4 MB)
Peculiar behaviour of lachryphagous Steganinae
Lachryphagy has been identified for many species of Amiota and Phortica - subcosmopolitan, moderately common and moderately species-rich genera, each comprising about 130 described species . However lachryphagy is unknown in the Allophortica (subgenus of Phortica) comprising five described species. Flies belonging to the genera Amiota and Phortica are distributed mostly across temperate to tropical forests and lacking in arid biotopes such as those of central Asia. Conversely, the third lachryphagous genus, Apsiphortica, includes only six rare species in Africa and Southeast Asia. Finally, there are also single observations of lachryphagy in the genera Gitona, Paraleucophenga and Apenthecia (S. Prigent, personal communication), but confirmatory studies are needed. Although the subdivision of Steganinae has not been clearly resolved, it appears that lachryphagous genera do not represent a monophyletic group ,. On the other hand, the genus Phortica, of which adult flies display a marked lachryphagy, was recently separated from Amiota and its monophyly was confirmed by cladistic analyses -. Studies of the feeding habits of Phortica variegata confirmed previous observations, showing that whilst females prevailed on the fruit bait (male:female ratio 1:3.8), lachryphagous behaviour is exclusively by males . Similar observations, although on smaller scale, exist in a number of other species of relevant genera. This behaviour is opposite to that of blood-feeding insects showing sex-related preferences (e.g., mosquitoes, ceratopogonids, sand flies, black flies and tabanids), where only adult females are haematophagous , with the remarkable exception of the hematophagous males of the genus Calyptra (Lepidoptera).
Males of P. variegata hover around animals and humans, possibly resting close to their eyes, imbibing tears (i.e., lachryphagy) and, occasionally, also sucking their perspiration. When trying to access their eyes, this behaviour ultimately causes a nuisance to animals . Such behaviour of males is a remarkable characteristic of the abovementioned lachryphagous Steganinae (Figure 3), similarly to the members of the family Cryptochetidae (genus Cryptochetum), representing a sister-group of Drosophilidae . Importantly, in other lachryphagous Diptera (some Muscidae, Fanniidae, Chloropidae and Paraleucopidae) females are prevalent, while the restriction of the lachryphagous behaviour to males is a rule in various Lepidoptera (except the moths Arcyophora and Lobocraspis, where both sexes are involved) .
Drosophilidae, and some other lachryphagous Diptera, can only feed on tears and perspiration, Paraleucopis mexicana can also intake blood from fresh wounds and some Chloropidae (e.g., Liohippelates spp.) cause direct injury except lachryphagy: they developed morphological adaptations of their mouthparts to reopen wounds of their hosts . This is not the only pathway to parasitism: facultative bloodsucking moths of the genus Calyptra evolved from the fruit-piercing ancestors ,, various necrophagous flies may cause myiasis. However, lachryphagous insects feed on living animals, which makes the boundary between lachryphagy and true parasitism not obvious, and thus we tentatively consider lachryphagous behaviour as parasitical in the broad sense.
The role of some Steganinae as vectors of helminths
Some of the lachryphagous Steganinae are known as vectors and intermediate hosts for the spirurid Thelazia callipaeda (Spirurida, Thelaziidae), which parasitizes the eyes of domestic and wild carnivores and some lagomorphs (see below) . While feeding on animal tears, male flies have contact with the first larval stages of T. callipaeda and act as their intermediate hosts. In comparison to the relative species richness of lachryphagous Steganinae, strikingly few species have been confirmed as vectors of T. callipaeda larvae. This spirurid, known for a long time as the “oriental eyeworm” because of its occurrence in Far Eastern Countries , has become established in Europe . Indeed, following the first description in dogs, cats and foxes in Italy , the infection has been increasingly reported in France, Switzerland, Spain, and Portugal  and recently in countries of the Balkans .
Human cases (in Europe still sparse) occur predominantly in children and elderly people and are associated with poor, rural communities and contexts of low health and socio-economic standards, where heavily infected dogs and cats live in close contact with humans -. High parasitic burdens cause various symptoms in humans such as conjunctivitis, lachrymation, corneal ulcers, rarely perforation of the cornea and even blindness . In China, 84 cases of human thelaziasis were reported by the end of the 1970s and 700 additional cases between 1980 and 2006, which illustrates a rapid increase in its prevalence, although an increase in its reporting may play a role . The host range of this nematode is wide as it parasitizes the eyes of dogs, cats, beech martens, foxes, wolves, rabbits, hares and humans . Racoon dog (Nyctereutes procyonoides), a host species known from the Russian Far East , gained its importance as an invasive species in Europe. For a long time it was suspected that, like Thelazia species parasitizing cattle or horses (e.g., Thelazia gulosa, Thelazia lacrimalis, Thelazia rhodesi, Thelazia skrjabini), T. callipaeda has been transmitted by calyptrate flies (predominantly females) of the families Muscidae and Fanniidae to receptive animals due to their ability to suck perspiration, conjunctival liquid and exudates of their hosts. However, laboratory and field studies indicated that Musca domestica is not a vector of T. callipaeda under experimental or natural conditions . The role of Amiota nagatai Okada, Phortica magna (Okada) and P. okadai (Máca) as vectors of T. callipaeda was first suggested in Japan ,. In an independent study, the life cycle of T. callipaeda was investigated under experimental conditions in easternmost Russia ; the suspected vector P. variegata has never been confirmed later on in this area. The vectorial role of P. variegata (Fallén) was conclusively demonstrated under field and experimental conditions in Europe , and that of P. okadai (Máca) in China . In addition, P. kappa (Máca, 1977) was found to harbour T. callipaeda second stage larvae . Thus, the range of vectors of T. callipaeda is apparently limited (see above), although probably wider than the few ascertained species.
Those Phortica species, known to be associated with thelaziosis, belong to the subgenus Phortica s. str., which is widely occurring in the Palaearctic and Oriental Regions. According to the phylogenetic data on Phortica it can be argued that the coevolution of T. callipaeda with Phortica spp. did not begin earlier than 13.1-19.5 million years ago, when Phortica s. str. diverged from other clades of the genus (the time given with 95% probability) . Lachryphagy, which apparently occurs more widely amongst the Steganinae, must have emerged prior to that event, or/and polyphyletically. Furthermore, the present vicariant distribution of T. callipaeda is likely due to parasitizing almost or completely vicariant European (P. variegata) and East Asian species (P. magna, P. kappa, P. okadai) of Phortica s. str. and this should be preceded by its preglacial and/or interglacial continuous Eurasian distribution. This discontinuous distribution resulted in the occurrence of a single haplotype of T. callipaeda, thus far, in Europe in spite of testing specimens of various European countries and as many as eight host species (e.g., dogs, cats, beech martens, foxes, wolves, rabbits, hares and humans), in contrast to the eight haplotypes found in different Far Eastern countries . The low genetic variability of T. callipaeda in Europe seems to be in accordance with only P. variegata as a confirmed vector, whilst at least four species of Steganinae have been suggested to act as vectors of the eight haplotypes of this nematode found in Asian countries. This finding ultimately supports a tight affiliation of T. callipaeda with the ecology of the intermediate hosts.
Distribution and host affiliation of Thelazia callipaeda
The distribution of P. variegata, the (main) European vector of T. callipaeda, is not known in sufficient detail for some countries . Based on the ranges of temperature (i.e., 20-25°C) and relative humidity (50-75%) optimal for Phortica flies, as well as on the natural niche of this insect, a desktop implementation of the Genetic Algorithm for Rule-Set Prediction anticipated that large areas of Europe were likely to represent suitable habitats for P. variegata, therefore suggesting a potential expansion of thelaziosis . Less than 10 years after this predictive niche model was published, T. callipaeda has been found in many areas of Europe predicted by the model -. Geographically, the prevalence of thelaziasis in different regions varies considerably in animals and humans, with most cases being recorded from the temperate to subtropical zones of the Old World, albeit in Europe only eight cases have been recorded in humans to date . Case reports of human thelaziosis are much more frequent in Japan (southern part, mostly on Kyushyu island) with about 100 cases ,, South Korea (n = 24 cases) , China (about 800 cases), especially the Shandong, Hebei, Anhui and Jiansu provinces where about half of all known human cases (n = about 450) were reported . The low prevalence of human thelaziosis in the Russian Far East (n = 2) may show that this region, like northern Japan, lies close to the limits of the occurrence of T. callipaeda, although fox farming boosted its prevalence in animals ,.
Interestingly, the majority of the Phortica s. str. species occur in the tropics of the Oriental Region, notwithstanding that data from India is sparse, most likely due to sparse use of appropriate collection methods (i.e., canopy traps). Indeed, sixty-three species of Phortica s. str. are known to be exclusively Oriental, six species are common to the Palaearctic and Oriental Regions, eight are exclusively Palaearctic and four are offshoots to other zoogeographical regions . On the contrary, records of T. callipaeda from the Oriental region are sparse, with the exception of densely populated southern China, where up to 50 cases of human thelaziosis are known , including one case in Taiwan . Cases of human thelaziosis from other countries of the Oriental Region come from India and Bangladesh (n = 10), Indonesia (n = 1), and Thailand (n = 5) ,,. The sporadic occurrence of T. callipaeda is well illustrated in Thailand by H. Bänziger, who anecdotally mentioned capturing 172 individuals of at least 31 species of lachryphagous drosophilids (including a few females) sucking on his eyes; in spite of that, he never mentioned any disorder of his eyes . However, his collections were made in forest habitats where no or few potential hosts of T. callipaeda were present (Banziger, pers. comm.). As yet we do not even know the name of any of the Oriental species of Steganinae transmitting T. callipaeda. It should be investigated whether the Oriental species show lesser susceptibility to this nematode, or if environmental conditions of tropical humid biota represent a barrier to the perpetuation of this infection.
The host range of Phortica spp. is simplest in Europe, where virtually only P. variegata and P. semivirgo (and P. erinacea in the extreme southeast) are potential vectors of T. callipaeda, although just the first-mentioned species is a confirmed vector.
Vertical microdistribution (stratification) of the genera Phortica and Amiota is of epidemiological importance, considering that adult flies dwell predominantly in the tree canopies . However, they fly much lower when patrolling along forest tracks and clearings, repeatedly approaching to contact objects of interest from various angles before landing on his eyes. According to H. Bänziger (personal communication) contacts with human eyes last for 35–163 seconds. Both tree canopy animals, such as beech martens, and terrestrial ones (e.g., foxes, wolves) may be contacted by these flies and infected with T. callipaeda larvae, whereas this may not be the case of subterranean/nocturnal European badgers . Indeed, tree canopies are not the exclusive niches, at least for Phortica spp.; their captures in caves may indicate their facultative overwintering there ,,.
Male lachryphagy: cherchez la femme?
Undoubtedly, various aspects of the natural history of Steganinae need to be elucidated, mostly in relation to the extent of zoophagous behavior in various genera. Refined data on this taxon of drosophilids could prove useful to the biological control of phytophagous pests from the order Homoptera, as an alternative to chemical treatment. The rare experiments carried out in this field have been referenced ,. From a parasitological perspective, the reasons for the lachryphagy of adult insects remain yet to be elucidated, although the need for protein is most likely the main driver for this. Similarly, the possible role of sodium ions in this process also requires study.
Elucidation of the biology of lachryphagous drosophilids, including mating behavior, might also be addressed by rearing experiments (Figure 6). Indeed, although the rearing of P. variegata has been described, the results do not guarantee continual rearing . Therefore, further protocols should be prepared or implemented in order to improve the rearing of Steganinae. Indeed, providing a larger space for rearing may facilitate the mating behaviour. In addition, since males are apparently protandric, and it is difficult to keep them alive whilst obtaining females, experiments with simultaneous rearing under different temperatures and light exposure may enable the study of seasonal rhythms and perhaps to align them. Although Phortica larvae have been found in fermenting tree sap , they may be virtually zoophagous as observed in P. xyleboriphaga; fruit or other Drosophila breeding media do not seem suitable in supporting their development under laboratory conditions. Zoophagy in this genus is also suggested for P. (Sinophthalmus) picta (Coquillett) that lays either single eggs or numerous eggs for rapid propagation . This egg-laying pattern might indicate parasitism and/or an adaptation for predation on gregarious prey. The possibility of larval zoophagy should be assessed by rearing Phortica (and allies) larvae together with those of other drosophilids (e.g. D. melanogaster). A better understanding of vector biology may assist not only in controlling the transmission of T. callipaeda, but also in discovering the origin of the predatory behaviour in this group of insects, thus leading to understanding the main drivers of their parasitism. Knowledge of the species composition of the vectors of T. callipaeda in Asia, mainly in its subtropical/tropical part, is still meagre. This should also be improved by implementing nematode detection in these flies as well as attempting experimental infections of various species of lacryphagous Steganinae.
Both authors equally conceived this review article and equally contributed to writing it. Both read and approved the final version of the manuscript.
We greatly appreciate personal information communicated by Hans Bänziger (Chiang Mai, Thailand), Stéphane R. Prigent (Paris, France) and Hiró Takaoka (Oita, Japan). Thanks to Klavs Nielsen (Kobenhavn, Denmark), and R.P. Lia (The University of Bari, Italy) for some of the photographs used in the review. Bronwyn Campbell (The University of Bari, Italy) is acknowledged for her useful comments on the manuscript.
- Russell RC, Otranto D, Wall RL: Encyclopedia of Medical & Veterinary Entomology. 2013, CAB International, Wallingford UKGoogle Scholar
- Bänziger H, Boongird S, Sukumalanand P, Bänziger S: Bees (Hymenoptera: Apidae) that drink human tears. J Kansas Entomol Soc. 2009, 82: 135-150. 10.2317/JKES0811.17.1.View ArticleGoogle Scholar
- Ashburner M, Golic KG, Hawley RS: Drosophila. A Laboratory Handbook. 2005, Cold Spring Harbor Lab Press, New YorkGoogle Scholar
- Okada T: Systematic Study of the Early Stages of Drosophilidae. 1968, Bunka Zugeisha Co, TokioGoogle Scholar
- Michan L, Sortibran AC, Rodriguez-Arnaiz R, Ayala FJ: Global Drosophila Research: a bibliometric analysis. Dros Inf Serv. 2010, 93: 232-243.Google Scholar
- Martin CA, Krantz DE:Drosophila melanogaster as a genetic model system to study neurotransmitter transporters. Neurochem Int. 2014, 73: 71-88. 10.1016/j.neuint.2014.03.015.PubMed CentralView ArticlePubMedGoogle Scholar
- van der Voet M, Nijhof B, Oortveld MA, Schenck A: Drosophila models of early onset cognitive disorders and their clinical applications.Neurosci Biobehav Rev, in press,Google Scholar
- Smith WW, Thomas J, Liu J, Li T, Moran TH. From fat fruit fly to human obesity.Physiol Behav, in press,Google Scholar
- Ntziachristos P, Lim JS, Sage J, Aifantis I: From fly wings to targeted cancer therapies: a centennial for notch signalling. Cancer Cell. 2014, 25: 318-334. 10.1016/j.ccr.2014.02.018.PubMed CentralView ArticlePubMedGoogle Scholar
- Bächli G: TaxoDros. The database on Taxonomy of Drosophilidae. 2014Google Scholar
- Brake I, Bächli G: Drosophilidae (Diptera). World catalogue of insects. Apollo Books, Stenstrup; 2008.View ArticleGoogle Scholar
- Ashburner M: Entomophagous and other bizarre Drosophilidae. The Genetics and Biology of Drosophila Vol. 3a. Edited by: Ashburner M, Carson HL, Thompson JN, Ashburner M, Carson HL, Thompson JN. 1981, Academic Press, London, 395-429.Google Scholar
- Grimaldi DA: A phylogenetic, revised classification of the genera in the Drosophilidae (Diptera). Bull Am Mus Natural History (New York). 1990, 197: 1-139.Google Scholar
- Yassin A: Phylogenetic classification of the Drosophilidae Rondani (Diptera): the role of morphology in the postgenomic era. Syst Entomol. 2013, 38: 349-364. 10.1111/j.1365-3113.2012.00665.x.View ArticleGoogle Scholar
- Baer W: Ueber Stegana curvipennis Fall. Naturwiss Z für Forst und Landwirtsch (Stuttgart). 1914, 12: 379-Google Scholar
- Máca J: Octomilkovití (Diptera: Drosophilidae Jizerských hor a Frýdlantska. Drosophilidae (Diptera) of the Jizerské hory Mts and Frýdlant region (northern Bohemia, Czech Republic). Sborník Severočeského Muzea, Přírodní Vědy Acta Musei Bohemiae Borealis, Scientiae Naturales. 2009, 27: 173-184.Google Scholar
- Schiner JR: Catalogus Systematicus Dipterorum Europae. 1864, Societas zoologico-botanica, VindobonaView ArticleGoogle Scholar
- Máca J: Revision of Palearctic species of Amiota subg. Phortica (Diptera, Drosophilidae). Acta Ent Bohemoslov. 1977, 74: 114-130.Google Scholar
- Kozlov DP: Perviy sluchai obnaruzhenia Thelazia callipaeda Railliet et Henry, 1910 u cheloveka na teritorii SSSR. [First discovery of Thelazia callipaeda Railliet et Henry, 1910 in a human on the teritory of USSR]. Akademia Nauk SSSR Trudy gelmintologicheskoi laboratorii (Moskva). 1963, 13: 75-77.Google Scholar
- Otranto D, Stevens JR, Testini G, Cantacessi C, Máca J: Molecular characterization and phylogenesis of Steganinae (Diptera, Drosophilidae) inferred by the mitochondrial cytochrome c oxidase subunit 1. Med Vet Entomol. 2008, 22: 37-47. 10.1111/j.1365-2915.2008.00714.x.View ArticlePubMedGoogle Scholar
- Chen HW, Toda MJ: A revision of the Asian and European species in the subgenus Amiota Loew (Diptera, Drosophilidae) and the establishment of species-groups based on phylogenetic analysis. J Nat Hist. 2001, 35: 1517-1563. 10.1080/002229301317067665.View ArticleGoogle Scholar
- Máca J: Taxonomic notes to the genera previously classified in the genus Amiota Loew (Diptera: Drosophilidae, Steganinae). Acta Universitatis Carolinae, Biol. 2003, 47: 247-274.Google Scholar
- Cao HL, Wang XL, Gao JJ, Prigent SR, Watabe H, Zhang YP, Chen HW: Phylogeny of the African and Asian Phortica (Drosophilidae) deduced from nuclear and mitochondrial DNA sequences. Mol Phylogenet Evol. 2011, 61: 677-685. 10.1016/j.ympev.2011.08.002.View ArticlePubMedGoogle Scholar
- Otranto D, Brianti E, Cantacessi C, Lia RP, Máca J: The zoophilic fruitfly Phortica variegata: morphology, ecology and biological niche. Med Vet Entomol. 2006, 20: 358-364. 10.1111/j.1365-2915.2006.00643.x.View ArticlePubMedGoogle Scholar
- Yuval B: Mating systems of blood-feeding flies. Ann Rev Entomol. 2006, 51: 413-440. 10.1146/annurev.ento.51.110104.151058.View ArticleGoogle Scholar
- Bächli G, Vilela CR, Andersson Escher SA, Saura A: The Drosophilidae (Diptera) of Fennoscandia and Denmark. Fauna Entomologica Scandinavica, Volume 39. 2004, Brill, LeidenGoogle Scholar
- Okada T: Systematic Study of Drosophilidae and Allied Families of Japan. 1956, Gihodo Co, TokyoGoogle Scholar
- Smith RL: The trouble with bobos, Paraleucopis mexicana Steyskal, at Kino bay, Sonora, Mexico (Diptera, Chamaemyiidae). Proc Ent Soc Washington. 1981, 83: 406-412.Google Scholar
- Bänziger H: Skin-piercing blood-sucking moths III: Feeding act and piercing mechanism of Calyptra eustrigata (Hmps.) (Lep., Noctuidae). Mitt Schweiz Ent Ges. 1980, 53: 127-142.Google Scholar
- Zaspel JM, Zahiri R, Hoy MA, Janzen D, Weller SJ, Wahlberg N: A molecular phylogenetic analysis of the vampire moths and their fruit-piercing relatives (Lepidoptera: Erebidae: Calpinae). Mol Phylogenet Evol. 2012, 65: 786-791. 10.1016/j.ympev.2012.06.029.View ArticlePubMedGoogle Scholar
- Otranto D, Dantas-Torres F, Mallia E, DiGeronimo PM, Brianti E, Testini G, Traversa D, Lia RP:Thelazia callipaeda (Spirurida, Thelaziidae) in wild animals: Report of new host species and ecological implications. Vet Parasitol. 2009, 166: 262-267. 10.1016/j.vetpar.2009.08.027.View ArticlePubMedGoogle Scholar
- Anderson RC: Nematode Parasites of Vertebrates. Their Development and Transmission. 2000, CABI Publishing, Wallingford, UKView ArticleGoogle Scholar
- Otranto D, Dantas-Torres F, Brianti E, Traversa D, Petrić D, Genchi C, Capelli G: Vector-borne helminths of dogs and humans in Europe. Parasit Vectors. 2013, 6: 16-10.1186/1756-3305-6-16.PubMed CentralView ArticlePubMedGoogle Scholar
- Rossi L, Bertaglia P: Presence of Thelazia callipaeda Railliet and Henry, 1910, in Piedmont, Italy. Parassitologia. 1989, 31: 167-172.PubMedGoogle Scholar
- Otranto D, Ferroglio E, Lia RP, Traversa D, Rossi L: Current status and epidemiological observation of Thelazia callipaeda (Spirurida, Thelaziidae) in dogs, cats and foxes in Italy: a “coincidence” or a parasitic disease of the Old Continent?. Vet Parasitol. 2003, 116: 315-325. 10.1016/j.vetpar.2003.07.022.View ArticlePubMedGoogle Scholar
- Hodzic A, Latrofa MS, Annoscia G, Alic A, Beck R, Lia RP, Dantas-Torres F, Otranto D: The spread of zoonotic Thelazia callipaeda in the Balkan area. Parasit Vectors. 2014, 7: 328-10.1186/1756-3305-7-352.View ArticleGoogle Scholar
- Shen JL, Gasser RB, Chu DY, Wang ZX, Yuan XS, Cantacessi C, Otranto D: Human thelaziosis - a neglected parasitic disease of the eye. J Parasitol. 2006, 92: 872-875. 10.1645/GE-823R.1.View ArticlePubMedGoogle Scholar
- Otranto D, Dutto M: Human thelaziasis, Europe. Emerg Infect Dis. 2008, 14: 647-649. 10.3201/eid1404.071205.PubMed CentralView ArticlePubMedGoogle Scholar
- Fuentes I, Montes I, Saugar JM, Gárate T, Otranto D: Thelaziosis, a zoonotic infection, Spain, 2012. Emerg Infect Dis. 2012, 18: 2073-2075. 10.3201/eid1812.120472.PubMed CentralView ArticlePubMedGoogle Scholar
- Otranto D, Eberhard ML: Zoonotic helminths affecting the human eye. Parasit Vectors. 2011, 23: 41-10.1186/1756-3305-4-41.View ArticleGoogle Scholar
- Kozlov DP: Izuchenie biologii Thelazia callipaeda Railliet et Henry, 1910 [Study of the biology of Thelazia callipaeda Railliet et Henry, 1910]. Akademia Nauk SSSR Trudy gelmintologicheskoi laboratorii (Moskva). 1963, 13: 330-346.Google Scholar
- Otranto D, Lia RP, Testini G, Milillo P, Shen JL, Wang ZX:Musca domestica is not a vector of Thelazia callipaeda in experimental or natural conditions. Med Vet Entomol. 2005, 19: 135-139. 10.1111/j.0269-283X.2005.00554.x.View ArticlePubMedGoogle Scholar
- Nagata Y: [The discovery of eye-worm, Thelazia callipaeda, VIII]. Jap J Vet Sci. 1959, 21: 103-10.1292/jvms1939.21.103.View ArticleGoogle Scholar
- Nagata Y: [The discovery of eye-worm, Thelazia callipaeda, IX-X]. Jap J Vet Sci. 1960, 22: 475-Google Scholar
- Kozlov DP: Raschifrovka tsikla razvitia nematody Thelazia callipaeda – parazita glaza cheloveka i plotoiadnykh mlekopitaiushikh [The life cycle of nematode Thelazia callipaeda parasitic in the eye of the man and carnivores]. Dokl Akad Nauk SSSR. 1962, 142: 732-733.Google Scholar
- Otranto D, Lia RP, Cantacessi C, Testini G, Troccoli A, Shen JL, Wang ZX: Nematode biology and larval development of Thelazia callipaeda (Spirurida, Thelaziidae) in the drosophilid intermediate host in Europe and China. Parasitology. 2005, 131: 847-855. 10.1017/S0031182005008395.View ArticlePubMedGoogle Scholar
- Otranto D, Cantacessi C, Testini G, Lia RP:Phortica variegata is an intermediate host of Thelazia callipaeda under natural conditions: evidence for pathogen transmission by a male arthropod vector. Int J Parasitol. 2006, 36: 1167-1173. 10.1016/j.ijpara.2006.06.006.View ArticlePubMedGoogle Scholar
- Wang ZX, Hu Y, Wang KC, Wang HY, Jiang BL, Zhao P, Wang ZC, Ding W, Wang F, Xia XF: Longitudinal investigation and experimental studies on thelaziasis and the intermediate host of Thelazia callipaeda in Guanhua county of Hubei province. Chin J Epidemiol. 2003, 24: 588-590.Google Scholar
- Aoki C, Otsuka Y, Takaoka H, Hayashi T: [Natural infections of three Amiota species with larvae of Thelazia in Oita]. Med Entomol Zool. 2003, 54: 52-Google Scholar
- Otranto D, Testini G, De Luca F, Hu M, Shamsi S, Gasser RB: Analysis of genetic variability within Thelazia callipaeda (Nematoda: Thelazioidea) from Europe and Asia by sequencing and mutation scanning of the mitochondrial cytochrome c oxidase subunit 1 gene. Mol Cell Probes. 2005, 19: 306-313. 10.1016/j.mcp.2005.05.001.View ArticlePubMedGoogle Scholar
- Malacrida F, Hegglin D, Bacciarini L, Otranto D, Nägeli F, Nägeli C, Bernasconi C, Scheu U, Balli A, Marenco M, Togni L, Deplazes P, Schnyder M: Emergence of canine ocular thelaziosis caused by Thelazia callipaeda in southern Switzerland. Vet Parasitol. 2008, 157: 321-327. 10.1016/j.vetpar.2008.07.029.View ArticlePubMedGoogle Scholar
- Miró G, Montoya A, Hernández L, Dado D, Vázquez MV, Benito M, Villagrasa M, Brianti E, Otranto D:Thelazia callipaeda: infection in dogs: a new parasite for Spain. Parasit Vectors. 2011, 4: 148-10.1186/1756-3305-4-148.PubMed CentralView ArticlePubMedGoogle Scholar
- Vieira L, Rodrigues FT, Costa A, Diz-Lopes D, Machado J, Coutinho T, Tuna J, Latrofa MS, Cardoso L, Otranto D: First report of canine ocular thelaziosis by Thelazia callipaeda in Portugal. Parasit Vectors. 2012, 21: 124-10.1186/1756-3305-5-124.View ArticleGoogle Scholar
- Kamakura K, Kamakura S, Tamura S, Shiomi C, Nobukiyo A, Furukawa T: Incidence of parasitosis associated with Oriental eye worm (Thelazia callipaeda) in dogs and cats in Hiroshima Prefecture. The Hiroshima J Vet Med. 1998, 13: 63-68.Google Scholar
- Koyama Y, Ohira A, Kono T, Yoneyama T, Shiwaku K: Five cases of thelaziasis. Br J Ophthalmol. 2000, 84: 441-10.1136/bjo.84.4.439c.View ArticlePubMedGoogle Scholar
- Miroshnichenko VA, Desiaterik MP, Novik AP, Gorbach TV, Papernova HI: Sluchai teliaziosa glaz u rebionka v vozraste 3 let. [Case of the eye thelaziosis in the 3years old child]. Vestn Oftalmol. 1988, 104: 64-PubMedGoogle Scholar
- Chen HW, Máca J: Ten new species of the genus Phortica from the Afrotropical and Oriental regions (Diptera: Drosophilidae). Zootaxa. 2012, 3478: 493-509.Google Scholar
- Cheung WK, Lu HJ, Liang CH, Peng ML, Lee HH: Conjunctivitis caused by Thelazia callipaeda infestation in a woman. J Formos Med Assoc (Taipei). 1998, 97: 425-427.Google Scholar
- Akhanda AH, Akonjee AR, Hossain MM, Rahman MA, Mishu FA, Hasan MF, Akhanda TH: Thelazia callipaeda infestation in Bangladesh: a case report. Mymensingh Med J. 2013, 22 (3): 581-584.PubMedGoogle Scholar
- Handique AK, Khan AM, Tamuli A: Ocular thelaziasis in a 7-month-old infant. Indian J Med Microbiol. 2014, 32: 84-86. 10.4103/0255-0857.124333.View ArticlePubMedGoogle Scholar
- Toda MJ: Vertical microdistribution of Drosophilidae (Diptera) within various forests in Hokkaido III. The Tomakomai Experiment Forest, Hokkaido University. Res Bull Coll Exp Forests, Faculty of Agric Hokkaido University. 1987, 44: 611-632.Google Scholar
- Beschovsky VL: Representatives of Diptera – Brachycera in the caves of Bulgaria. Académie Bulgare des Sci Bulletin de l’Institut de Zool et Musée. 1972, 35: 23-29.Google Scholar
- Bächli G, Weber D: Taufliegen oder Kleine Fruchtfliegen (Insecta, Diptera, Drosophilidae) aus Höhlen des Grossherzogtums Luxemburg. Ferrantia. 2013, 69: 349-353.Google Scholar
- Rauen HM: Biochemisches Taschenbuch. 2. Teil. 1964, Springer, BerlinView ArticleGoogle Scholar
- Alonso-Pimentel H, Tolbert LP, Heed WB: Ultrastructural examination of the insemination reaction in Drosophila. Cell Tissue Res. 1994, 275: 467-479. 10.1007/BF00318816.View ArticlePubMedGoogle Scholar
- Otranto D, Stevens JR, Cantacessi C, Gasser RB: Parasite transmission by insects: a female affair?. Trends Parasitol. 2008, 24: 116-120. 10.1016/j.pt.2007.12.005.View ArticlePubMedGoogle Scholar
- Arzone A:Acletoxenus formosus (Loew) (Diptera Drosophilidae) predatore di Trialeurodes vaporariorum (Westwood). Boll Zool agr bachic, Ser II, Milano. 1998, 30: 55-59.Google Scholar
- Otranto D, Cantacessi C, Lia RP, Grunwald Kadow IC, Purayil SK, Dantas-Torres F, Máca J: First laboratory culture of Phortica variegata (Diptera, Steganinae), a vector of Thelazia callipaeda. J Vector Ecol. 2012, 37: 458-461. 10.1111/j.1948-7134.2012.00251.x.View ArticlePubMedGoogle Scholar
- Wheeler MR: The Drosophilidae of the Nearctic Region exclusive of the genus Drosophila. Univ Tex Publ (Austin). 1952, 5204: 162-218.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.