Abstract
The first case of feline ocular Thelazia callipaeda infection and two new canine imported infections in West Germany are here described. The three animals had a history of recent travel to/from other countries. The young adult cat imported from Spain presented an intermittent unilateral ocular discharge. During in-depth ophthalmic examination, a single alive nematode was removed from the conjunctival compartment of the affected eye. Referring to the canine cases, an adult female dog originated from Kenya presented epiphora and mucous whitish-grey discharge of the right eye. During flushing of the nasolacrimal duct two small, thin and long nematodes were removed. Furthermore, a male Borzoi racing dog with regular visit to racing tracks in different countries presented ocular mucous discharge. At ophthalmologic examination, two transparent-whitish vital nematodes were removed. All nematode specimens of the three cases were morphologically identified as adult T. callipaeda parasites. The animals were treated orally with milbemycin oxime (2.0 mg/kg; cat) or milbemycin oxime/praziquantel (0.5 mg/kg and 5.0 mg/kg; dogs) twice with 1-week interval resulting in complete resolution of symptoms. The repeated introduction of patent T. callipaeda-infected animals, especially from southern and eastern endemic countries, will ease the establishment of ophthalmic thelaziosis in Northern Europe. The male fruit fly, Phortica variegata, an intermediate host of T. callipaeda, is endemic within European countries. Considering the clinical and zoonotic relevance of ophthalmic thelaziosis, enhanced disease awareness of European medical and veterinarian doctors and in-depth eye examination for proper detection of T. callipaeda are crucial for appropriate anthelmintic treatments and to limit spreading of the infection.
Avoid common mistakes on your manuscript.
Introduction
Thelazia spp. (Spirurida, Thelaziidae) parasites are ophthalmic vector-borne nematodes commonly found in Southern European countries, North America and Asia. In Europe, eye worms have been reported in cattle (T. rhodesii, T. skrjabini, T. gulosa), horses (T. lacrymalis) and carnivores (T. callipaeda), such as dogs, cats, foxes and wolves. Recently, various reports brought to light T. callipaeda infections of dogs but also of cats, rabbits and humans, mainly from poor socio-economic settings in different Asian countries (Otranto and Traversa 2005; do Vale et al. 2019) but also in several European regions. Consequently, this vector-borne helminthiasis is currently considered as an emergent disease (Colella et al. 2016a, 2020).
Transmission of T. callipaeda occurs via males of Phortica variegata (Drosophilidae, Steganinae) flies. These non-biting dipteran insects (Otranto et al. 2004) uptake first stage larvae (L1) present in the conjunctival fluid. Within 4 weeks, L1 develops into infective L3 in the insect intermediate host and can be transmitted to final hosts during male fly feeding on conjunctival fluids of other permissive hosts (Otranto et al. 2004). Prepatency lasts from 2 to 6 weeks. Adult eye worms can persist in the conjunctival sac and under the third eyelid of infected hosts for more than 1 year (Motta et al. 2014).
Larvae and adult parasites both are involved in the pathogenesis of ocular thelaziosis (Maia et al. 2016). Clinical signs range from asymptomatic/subclinical to moderate or severe ocular disorders, such as epiphora, blepharitis, photophobia, conjunctivitis, keratitis, corneal opacity or ulcers (Otranto and Traversa 2005). Feline infections are less common than canine ones. Thus, feline thelaziosis seems more sporadic, most probably due to intensive cleaning habits of cats, resulting in less availability of L1 to the vectors (Motta et al. 2014) or even in the mechanical removal of adult eye worms.
Parasites within the conjunctival or nasolacrimal duct cause epiphora, ocular discharge, mild to severe conjunctivitis, follicular hypertrophy of the conjunctiva, foreign body sensation, pruritus, conjunctival hyperaemia, swelling, hypersensitivity to light and keratitis (Hermosilla et al. 2004).
Human thelaziosis has been described not only in adults but also in children, including a 6-month-old child (Otranto et al. 2013). Consistently, also in Germany, the first case of human thelaziosis was reported (Dolff et al. 2020). The patient lived in an urban area of Germany and had a history of several flies being detected in the conjunctival sac after cycling tours in Eastern Europe in summer 2018, constituting most probably an imported case. She presented foreign body sensation, epiphora and redness of the left eye, which already lasted for 2 months before discovering a transparent filamentous structure in the left eye. At ophthalmologic examination, four T. callipaeda parasites were extracted, and another nematode was removed the next day under local anaesthesia (Dolff et al. 2020).
Here, we report the first case of feline ocular thelaziosis and new canine imported cases in Germany, bringing awareness not only to veterinary but also to medical doctors to this emergent and neglected zoonosis.
Cases presentation
Feline case
A cat of approximately 1 year of age was adopted from the streets in Southern Spain and thereafter imported to West Germany (Freinsheim, Rhineland-Palatinate), in spring 2015. A few weeks later, during a routine visit at the small animal clinics for a regular health check-up, the cat presented an intermittent unilateral ocular discharge. The cat had shown slight epiphora in the previous days. At physical examination, only epiphora was observed. However, due to the origin of the cat (Spain), an exhaustive in-depth eye examination was performed, and a single vital nematode was collected from the conjunctival compartment of the affected eye and conserved in 70% alcohol for subsequent morphological identification. No nematodes/larvae were observed in the other eye. An adult female T. callipaeda parasite (Fig. 1) was morphologically identified by typical morphological characteristics: a yellowish-white nematode of 1.1 cm length with a serrated cuticle, crown-shaped buccal capsule (Fig. 1A, (a)) and vulvar flap (Fig. 1A, (b)) located anterior to the oesophageal-intestinal junction (Fig. 1A, (c)). Moreover, in the uterus in the posterior end of the parasite (Fig. 1B), oocytes (Fig. 1B, (d)) were present. The cat was treated twice with milbemycin oxime (2.0 mg/kg, per os, Interceptor®) with 7-day interval. One month later, no further parasites were observed at ocular control examination.
Canine case no. 1
At the beginning of 2019, a mixed-Dobermann female spayed dog born in 2008 presented epiphora and mucous whitish-grey discharge in the right eye, which had started several months before clinical submission. The dog showed these ocular signs since being rescued from an animal shelter in Germany (Wiesbaden, Hesse), but it was originally from Kenya. Previous treatments with gentamicin eye drops (TID), followed by ofloxacin eye ointment (TID) were discontinued due to a lack of efficacy. Bacteriological investigations as well as a fluorescein test had shown negative results. At current clinical presentation (Wiesbaden), ophthalmological examination revealed slightly hyperaemic conjunctiva in both eyes, diffuse follicles in the lower conjunctival fornix and a reduced tear film break-up time of 4–5 s. In the right eye, mucous discharge in the nasal corner of the eye was observed and after nasolacrimal flushing, small, thin, long nematodes appeared from the lower lacrimal punctum. A total of two parasites were collected and stored in 70% alcohol for further morphological identification. As treatment, milbemycin oxime and praziquantel (0.5 mg/kg and 5 mg/kg, respectively; per os; Milbemax™) were administrated twice, with 7-day interval. The parasites were identified as T. callipaeda by morphological and morphometric features, as previously detailed. At the beginning of March 2019, at control ophthalmologic examination, neither clinical signs nor parasites were observed.
Canine case no. 2
In January 2020, a 4-year-old, unspayed male Borzoi racing dog from Wiesbaden (Hesse) presented mucous ocular discharge for more than 1 week and was treated with gentamicin eye ointment (TID), without further clinical improvement. The dog was in close contact with several dogs from different countries at various racing tracks, in the Netherlands and Austria. At ophthalmologic examination, the left eye showed no pathological alterations, but the right eye showed a mucopurulent discharge, hyperaemic conjunctiva and follicles. Two transparent-whitish vital nematodes were removed from behind the nictitating membrane and preserved in 70% alcohol for further identification. After careful removal, minor conjunctival haemorrhage on the bulbar side of the nictitating membrane was observed. Nasolacrimal flashing revealed no further nematodes. The parasites were identified as T. callipaeda specimen by morphological/morphometric characteristics, as described above. Four days later, the dog showed no alterations of the left eye at control examination, and the right eye presented only mild congestion of the bulbar side of the nictitating membrane. Gentamicin eye ointment (TID) was continued for six more days. For treatment of ophthalmic T. callipaeda infection, milbemycin/praziquantel (0.5 mg/kg and 5 mg/kg, respectively; per os; Milbemax™) was administrated twice, with 7-day interval.
Discussion
Ocular thelaziosis is spreading in Europe (do Vale et al. 2019; Marino et al. 2020), and the number of reports on T. callipaeda infections has increased throughout the continent (do Vale et al. 2019), not only in domestic and wild animals but also in humans (e.g. Dolff et al. 2020). Reported clinical cases resulted not only from imported but also autochthonous infections, thereby emphasizing the medical importance of this zoonotic disease.
Animal movements between regions, countries and continents bring the risk of relocating pathogens with zoonotic potential that these animals might harbour (Fooks and Johnson 2015). Domestic pet displacements (e.g. import/export, adoption/rescue and travel) from countries that might be endemic for ocular thelaziosis (Magnis et al. 2010; Graham-Brown et al. 2017) are very common in Germany. Dogs and cats from endemic areas, such as Italy, Portugal, France, Greece and Spain, among others, can pose an increased risk of ocular thelaziosis establishment across Europe. Additionally, German owners regularly travel with their pets to neighbouring European countries and other endemic geographic areas. Furthermore, the existence of a sylvatic life cycle for T. callipaeda with infections of a large number of wildlife species (i.e. foxes, wolves, beech martens, wild cats, hares and rabbits), could play an important role as natural reservoirs of this eye worm species (Otranto et al. 2013). This constitutes another risk for translocation and emergence of ocular thelaziosis mainly based on migration of T. callipaeda-infected wild carnivores which might also spread the disease into previously non-endemic areas of Europe (Otranto et al. 2013). All together, these aspects can explain the geographical expansion of ocular thelaziosis over the last years (Hodžić et al. 2019), which represents a warning signal also for human populations (Otranto et al. 2013).
The male fruit fly P. variegata is the obligate intermediate host of T. callipaeda, and it is considered as endemic in Europe, including the north of the Alps. Establishment of this particular intermediate host in new geographic areas occurs especially in regions with decaying fruits and fruit plantations, such as strawberry fields and orchards comprising apple and plum trees (Magnis et al. 2010; do Vale et al. 2019) contributing to an increase of ocular thelaziosis episodes. Interestingly, in contrast to a high degree of genetic variability among isolates from Asia (Otranto et al. 2005b), no genetic variation was recorded between individual nematodes collected from different host species (i.e. dogs, cats and foxes) and locations of Europe (i.e. Italy, Germany and the Netherlands). These findings suggest a strict link of T. callipaeda to P. variegata and a rather low degree of specificity for definitive hosts (Otranto et al. 2013). Ocular thelaziosis was considered in the past as a seasonal disease closely associated with the presence, density and activity of P. variegata, which presents high biological activities at temperature ranges of 20–25 °C and at a relative humidity of 50–75% (Otranto et al. 2006a). However, if T. callipaeda-infected P. variegata males have the ability to overwinter, as already experimentally demonstrated (Otranto et al. 2005a), it may prove to be an important feature to the establishment in cooler northern latitudes and thus autochthonous transmission of T. callipaeda. Moreover, the seasonality and crepuscular activities of P. variegata males overlap the activity of potentially infected wild species hosts (Otranto et al. 2013), thereby contributing to sylvatic life cycle maintenance.
Canine thelaziosis has been sporadically reported in Germany (Hermosilla et al. 2004; Magnis et al. 2010; Hammerich et al. 2020), but, so far, no case of feline thelaziosis had been reported. On the contrary, neighbouring countries, such as France (Dorchies et al. 2007), Switzerland (Motta et al. 2014) and, more recently, Austria (Hodžić et al. 2019) reported both imported and autochthonous feline ocular thelaziosis. In line with other European reports (Rodrigues et al. 2012), the current feline case was diagnosed in summer, i.e. at times of maximum activity of the vector (Otranto et al. 2006b). However, the fact that the cat originated from Spain, where thelaziosis is endemic (Marino et al. 2020), implies that this case might rather be considered as imported than autochthonous infection. Current canine cases were both diagnosed in January (2019 and 2020), which may either rely on the developmental period of the parasite to reach adult stage (Hodžić et al. 2019), on the capability of adult T. callipaeda to survive more than 1 year in the conjunctival fornix of the hosts (Motta et al. 2014) or on the absence of seasonality of P. variegata in endemic areas (Maia et al. 2016; do Vale et al. 2019), confirming the distribution of the parasite would be expected to coincide with that of suitable vectors (Otranto et al. 2005b; Dorchies et al. 2007). Referring to previous canine cases in Germany, one was considered an imported case based on a long stay in Italy (Hermosilla et al. 2004), whilst another case seemed autochthonous (Magnis et al. 2010). In the three cases reported here, all animals had regular outdoor access thereby being at risk of infection by potential contact to T. callipaeda-infected fruit flies (Rodrigues et al. 2012). Also, pets that coexist with other animals (e.g. sheep, rabbits, cattle, poultry) could be at higher risk of ocular thelaziosis, due to attraction of P. variegata to places with large number of hosts (Maia et al. 2016).
Besides T. callipaeda, other nematode parasites have been described to cause canine [e.g. Onchocerca spp., Angiostrongylus vasorum and Dirofilaria repens (Hermosilla et al. 2005a, b; Colella et al. 2016b)], feline [e. g. Onchocerca lupi (Labelle et al. 2011) and Gurltia paralysans (Udiz-Rodríguez et al. 2018)] and human (O. lupi and D. repens) ocular infections. Hence, in case of conjunctivitis, besides viral or bacterial aetiology, differential diagnosis should include parasitic agents as well (Magnis et al. 2010).
Probably due to the low number of parasites per eye, cats generally show minor to no clinical signs (Motta et al. 2014; Maia et al. 2016), which are easily disregarded by owners and veterinarians (Motta et al. 2014). Intensive cleaning of eye discharges and the small body index of cats were considered as important factors of low feline thelaziosis prevalence (Motta et al. 2014). In addition, reliable in-depth ophthalmic examinations might be less common in cats than in dogs, due to an anticipated increased difficulty, most likely resulting in an underestimation of feline Thelazia infections (Motta et al. 2014).
T. callipaeda treatments not only clear infections but also avoid the spread of the parasite in previously non-endemic areas (Motta et al. 2012) which is also of major importance regarding the zoonotic potential of the parasite. Treatment of ocular thelaziosis is based on both, mechanical removal of parasites from affected eyes and topical, systemic or spot-on administration of antiparasitic drugs (Rodrigues et al. 2012; Hodžić et al. 2019). Of note, several anthelmintic drugs are ineffective against T. callipaeda (i.e. benzimidazoles, quinolines, benzoles, depsipeptides, pyrimidines). Thus, macrocyclic lactones are regarded currently as the drugs of choice to treat T. callipaeda infections (Ferroglio et al. 2008; Motta et al. 2012, 2014). High therapeutic efficacies in naturally T. callipaeda-infected dogs and cats were reported for different formulations, such as oral (milbemycin oxime/praziquantel) and spot-on (milbemycin oxime/afoxolaner, moxidectin/imidacloprid) application (Motta et al. 2012; Lebon et al. 2019; Otranto et al. 2016, 2019). Two consecutive (7-day interval) milbemycin oxime/praziquantel treatments showed an efficacy of 90.9% and 73.3% in dogs and cats, respectively (Motta et al. 2012), whereas in another study, this drug showed an efficacy of 92.79% in dogs at day 14 after first administration and of 100% at days 28 and 35 (Otranto et al. 2016). Following the second treatment with milbemycin oxime 1 week after the first administration, an accurate concentration of the product in the conjunctiva justifies the higher efficacy against the parasite (Ferroglio et al. 2008). However, a lower efficacy was observed when the treatment was administered without food (Motta et al. 2012). A single treatment by spot-on formulation containing moxidectin 1.0% (+ imidacloprid 10%) resulted in 100% efficacy in naturally infected cats 28 days after treatment (Otranto et al. 2019). In line, an efficacy of 100% was reported in dogs treated with a single spot-on application of 2.5% moxidectin and 10% imidacloprid (Otranto et al. 2016).
Prophylaxis of ocular thelaziosis can be achieved by monthly administration of macrocyclic lactones (Ferroglio et al. 2008; Motta et al. 2012; Otranto et al. 2016, 2019; Lebon et al. 2019) resulting in prevalence reduction and therefore limited human infection risk in endemic areas (Otranto et al. 2013). Moreover, an in-depth eye inspection, even in the absence of ocular manifestations, should be included in routine clinical examinations of dogs and cats throughout the year (Maia et al. 2016). This recommendation not only refers to endemic areas but to all European countries where ocular thelaziosis was ever reported. Actually, if established deworming protocols (e.g. see ESCCAP.org) would be followed in a similar fashion as recommended for dirofilariosis and other helminth control, animals living in T. callipaeda endemic areas would benefit of an early elimination of larval stages, thus potentially abrogating host-parasite transmission chain (Motta et al. 2012, 2014). In this context, it seems necessary to keep in mind that older animals are at higher risk of infection due to the decrease in deworming frequency (deworming is usually associated with vaccinations and other veterinary actions, more frequent during the first years of animals’ life). Moreover, owners tend to consider anthelmintic treatments less necessary in older animals, resulting in a high number of adult pets remaining untreated (Motta et al. 2014).
Considering the fast spread of ocular thelaziosis within European countries and the zoonotic relevance of this parasitosis, increased awareness of medical and veterinarian surgeons seems important to limit the risk of further infections, especially in Germany where awareness is low even though a human case was recently reported (Dolff et al. 2020).
References
Colella V, Kirkova Z, Fok É, Mihalca AD, Tasić-Otašević S, Hodžić A, Dantas-Torres F, Otranto D (2016a) Increase in eyeworm infections in Eastern Europe. Emerg Infect Dis 22:1513–1515
Colella V, Lia RP, Premont J, Gilmore P, Cervone M, Latrofa MS, D’Anna N, Williams D, Otranto D (2016b) Angiostrongylus vasorum in the eye: new case reports and a review of the literature. Parasit Vectors 9:161–161. https://doi.org/10.1186/s13071-016-1440-6
Colella V, Nguyen VL, Tan DY, Lu N, Fang F, Zhijuan Y, Wang J, Liu X, Chen X, Dong J, Nurcahyo W, Hadi UK, Venturina V, Tong KBY, Tsai YL, Taweethavonsawat P, Tiwananthagorn S, le TQ, Bui KL, Watanabe M, Rani PAMA, Annoscia G, Beugnet F, Otranto D, Halos L (2020) Zoonotic vectorborne pathogens and ectoparasites of dogs and cats in Asia. Emerg Infect Dis 26:1221–1233. https://doi.org/10.3201/eid2606.191832
do Vale B, Lopes AP, da Conceição Fontes M et al (2019) Thelaziosis due to Thelazia callipaeda in Europe in the 21st century—a review. Vet Parasitol 275:108957
Dolff S, Kehrmann J, Eisermann P, Dalbah S, Tappe D, Rating P (2020) Case report: Thelazia callipaeda eye infection: the first human case in Germany. Am J Trop Med Hyg 102:350–351. https://doi.org/10.4269/ajtmh.19-0483
Dorchies P, Chaudieu G, Siméon LA, Cazalot G, Cantacessi C, Otranto D (2007) First reports of autochthonous eyeworm infection by Thelazia callipaeda (Spirurida, Thelaziidae) in dogs and cat from France. Vet Parasitol 149:294–297. https://doi.org/10.1016/j.vetpar.2007.08.005
Ferroglio E, Rossi L, Tomio E, Schenker R, Bianciardi P (2008) Therapeutic and prophylactic efficacy of milbemycin oxime (interceptor) against Thelazia callipaeda in naturally exposed dogs. Vet Parasitol 154:351–353. https://doi.org/10.1016/j.vetpar.2008.03.011
Fooks A, Johnson N (2015) Jet set pets: examining the zoonosis risk in animal import and travel across the European Union. Vet Med (Auckl) 6:17–25. https://doi.org/10.2147/vmrr.s62059
Graham-Brown J, Gilmore P, Colella V, Moss L, Dixon C, Andrews M, Arbeid P, Barber J, Timofte D, McGarry J, Otranto D, Williams D (2017) Three cases of imported eyeworm infection in dogs: a new threat for the United Kingdom. Vet Rec 181:346
Hammerich H, Dickomeit M, Glatz J (2020) Thelaziose-induzierte Konjunktivitis bei einem Hund in Deutschland. Prakt Tierarzt 101:138–147. https://doi.org/10.2376/0032-681X-1942
Hermosilla C, Herrmann B, Bauer C (2004) First case of Thelazia callipaeda infection in a dog in Germany. Vet Rec 154:568–569. https://doi.org/10.1136/vr.154.18.568
Hermosilla C, Hetzel U, Bausch M, Grubl J, Bauer C (2005a) First autochthonous case of canine ocular onchocercosis in Germany. Vet Rec 156:450–452. https://doi.org/10.1136/vr.156.14.450
Hermosilla C, Pantchev N, Dyachenko V, et al (2005b) Erste autochthone okuläre Dirofilaria repens - Infektion beim Hund in Deutschland. In: Preoceedings of the DVG Meeting "Parasitologie und parasitäre Krankenheiten. Postdam, p 59
Hodžić A, Payer A, Duscher GG (2019) The first autochthonous case of feline ocular thelaziosis in Austria. Parasitol Res 118:1321–1324. https://doi.org/10.1007/s00436-019-06275-0
Labelle AL, Daniels JB, Dix M, Labelle P (2011) Onchocerca lupi causing ocular disease in two cats. Vet Ophthalmol 14:105–110. https://doi.org/10.1111/j.1463-5224.2011.00911.x
Lebon W, Guillot J, Álvarez M-J, Antonio Bazaga J, Cortes-Dubly ML, Dumont P, Eberhardt M, Gómez H, Pennant O, Siméon N, Beugnet F, Halos L (2019) Prevention of canine ocular thelaziosis (Thelazia callipaeda) with a combination of milbemycin oxime and afoxolaner (Nexgard Spectra®) in endemic areas in France and Spain. Parasite 26:1. https://doi.org/10.1051/parasite/2019001
Magnis J, Naucke TJ, Mathis A, Deplazes P, Schnyder M (2010) Local transmission of the eye worm Thelazia callipaeda in southern Germany. Parasitol Res 106:715–717. https://doi.org/10.1007/s00436-009-1678-4
Maia C, Catarino AL, Almeida B, Ramos C, Campino L, Cardoso L (2016) Emergence of Thelazia callipaeda infection in dogs and cats from East-Central Portugal. Transbound Emerg Dis 63:416–421. https://doi.org/10.1111/tbed.12284
Marino V, Gálvez R, Montoya A, Mascuñán C, Hernández M, Barrera JP, Domínguez I, Zenker C, Checa R, Sarquis J, Miró G (2020) Spain as a dispersion model for Thelazia callipaeda eyeworm in dogs in Europe. Prev Vet Med 175:104883. https://doi.org/10.1016/j.prevetmed.2020.104883
Motta B, Schnyder M, Basano FS et al (2012) Therapeutic efficacy of milbemycin oxime/praziquantel oral formulation (Milbemax) against Thelazia callipaeda in naturally infested dogs and cats. Parasit Vectors 5:85. https://doi.org/10.1186/1756-3305-5-85
Motta B, Nägeli F, Nägeli C, Solari-Basano F, Schiessl B, Deplazes P, Schnyder M (2014) Epidemiology of the eye worm Thelazia callipaeda in cats from southern Switzerland. Vet Parasitol 203:287–293. https://doi.org/10.1016/j.vetpar.2014.04.009
Otranto D, Traversa D (2005) Thelazia eyeworm: an original endo- and ecto-parasitic nematode. Trends Parasitol 21:1–4. https://doi.org/10.1016/j.pt.2004.10.008
Otranto D, Lia RP, Buono V et al (2004) Biology of Thelazia callipaeda (spirurida, thelaziidae) eyeworms in naturally infected definitive hosts. Parasitology 129:627–633. https://doi.org/10.1017/S0031182004006018
Otranto D, Lia RP, Cantacessi C et al (2005a) Nematode biology and larval development of Thelazia callipaeda (Spirurida, Thelaziidae) in the drosophilid intermediate host in Europe and China. Parasitology 131:847–855. https://doi.org/10.1017/S0031182005008395
Otranto D, Testini G, De Luca F et al (2005b) 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 19:306–313. https://doi.org/10.1016/j.mcp.2005.05.001
Otranto D, Brianti E, Cantacessi C et al (2006a) The zoophilic fruitfly Phortica variegata: morphology, ecology and biological niche. Med Vet Entomol 20:358–364. https://doi.org/10.1111/j.1365-2915.2006.00643.x
Otranto D, Cantacessi C, Testini G, Lia RP (2006b) Phortica variegata as an intermediate host of Thelazia callipaeda under natural conditions: evidence for pathogen transmission by a male arthropod vector. Int J Parasitol 36:1167–1173. https://doi.org/10.1016/j.ijpara.2006.06.006
Otranto D, Dantas-Torres F, Brianti E, Traversa D, Petrić D, Genchi C, Capelli G (2013) Vector-borne helminths of dogs and humans in Europe. Parasit Vectors 6:16
Otranto D, Colella V, Crescenzo G, Solari Basano F, Nazzari R, Capelli G, Petry G, Schaper R, Pollmeier M, Mallia E, Dantas-Torres F, Lia RP (2016) Efficacy of moxidectin 2.5% and imidacloprid 10% in the treatment of ocular thelaziosis by Thelazia callipaeda in naturally infected dogs. Vet Parasitol 227:118–121. https://doi.org/10.1016/j.vetpar.2016.07.035
Otranto D, Solari Basano F, Pombi M, Capelli G, Nazzari R, Falsone L, Petry G, Pollmeier MG, Lia RP (2019) Effectiveness of the spot-on combination of moxidectin and imidacloprid (Advocate®) in the treatment of ocular thelaziosis by Thelazia callipaeda in naturally infected cats. Parasit Vectors 12:25. https://doi.org/10.1186/s13071-018-3262-1
Rodrigues FT, Cardoso L, Coutinho T, Otranto D, Diz-Lopes D (2012) Ocular thelaziosis due to Thelazia callipaeda in a cat from northeastern Portugal. J Feline Med Surg 14:952–954. https://doi.org/10.1177/1098612X12459645
Udiz-Rodríguez R, Garcia-Livia K, Valladares-Salmerón M, Dorta-Almenar MN, Martín-Carrillo N, Martin-Alonso A, Izquierdo-Rodriguez E, Feliu C, Valladares B, Foronda P (2018) First ocular report of Gurltia paralysans (Wolffhügel, 1933) in cat. Vet Parasitol 255:74–77. https://doi.org/10.1016/j.vetpar.2018.03.027
Funding
Open Access funding provided by Projekt DEAL.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Additional information
Section Editor: Elizabeth Marie Warburton
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
L. M. R., S., Spoerel, S., Wiesner, L. et al. Ophthalmic Thelazia callipaeda infections: first feline and new canine imported cases in Germany. Parasitol Res 119, 3099–3104 (2020). https://doi.org/10.1007/s00436-020-06785-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00436-020-06785-2