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Volume 30, Number 3—March 2024
Dispatch

Emergence of Thelaziosis Caused by Thelazia callipaeda in Dogs and Cats, United States

Author affiliations: Cornell University, Ithaca, New York, USA (R.R.S. Manoj, H. White, R. Young, M. Lejeune); Warwick Valley Veterinary Hospital, Warwick, New York, USA (C.E. Brown); Countryside Animal Hospital, Staatsburg, New York, USA (R. Wilcox); University of Bari Aldo Moro, Bari, Italy (D. Otranto); City University of Hong Kong, Hong Kong, China (D. Otranto)

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Abstract

We report 2 autochthonous feline thelaziosis cases caused by the eyeworm Thelazia callipaeda and discuss the spread among dogs in the northeastern United States. Phylogenetic analysis suggests the parasite was introduced from Europe. Adopting a One Health approach is needed to limit further spread of T. callipaeda eyeworms in North America.

Figure 1

Locations of thelaziosis cases caused by Thelazia callipaeda eyeworm in dogs (circles) and cats (squares), New York, New Jersey, and Connecticut, USA. Star indicates the dog case reported in New York in 2020. Inset map indicates the area where T. callipaeda infections were reported (box). The dog case reported from Nevada was not included in the map because the travel history for that animal was unknown.

Figure 1. Locations of thelaziosis cases caused by Thelazia callipaedaeyeworm in dogs (circles) and cats (squares), New York, New Jersey, and Connecticut, USA. Star indicates the dog case reported in...

Thelazia callipaeda eyeworm was considered an exotic parasite in North America until an autochthonous case was reported in a dog from New York, USA, in 2020 (1). T. callipaeda eyeworm has been reported in countries in East Asia and the Soviet Union, later expanding its geographic range into Europe (2,3). This zoonotic parasite primarily infects the orbital cavity of its host causing thelaziosis (3). The zoophilic secretophagous male fly, Phortica variegata, is a T. callipaeda vector; flies ingest first-stage T. callipaeda larvae from the lacrimal secretions of an infected host and redeposit them as infective third-stage larvae, which eventually complete their life cycle by developing into adult worms (4). P. variegata flies have been found in Orange and Monroe Counties in New York (5,6), which has likely promoted the emergence of T. callipaeda eyeworm in North America (4). Since the T. callipaeda infection in a dog reported in New York in 2020, a total of 11 canine cases (6 in New York, 3 in New Jersey, 1 each in Connecticut and Nevada) and 2 feline cases (both from New York) (Figure 1) have been confirmed morphologically at the Cornell Animal Health Diagnostic Center (AHDC) in Ithaca, New York, USA. We describe 2 feline thelaziosis cases and discuss new canine cases in northeastern United States (New York/New Jersey border) during February 2021–December 2022 and One Health approaches to limit spread of this emerging disease in the United States.

The Study

Case 1 was in a 16-year-old neutered male, domestic shorthair cat from Greenwood Lake, Orange County, New York, that had been regularly cared for at the Warwick Valley Veterinary Hospital in New York, since October 2019. The animal had a recurrent history of flea infestation, which was managed with selamectin. The cat received routine rabies vaccinations at the clinic and was regularly dewormed with a combination of emodepside (3 mg/kg) and praziquantel (12 mg/kg) applied topically to the skin by the owner. Since June 2021, the animal has been treated for progressive chronic kidney disease. During a visit in April 2022, the cat had crusty lesions on its swollen right eye. Initial treatment with an ophthalmic ointment containing tobramycin resolved the eye infection. In August 2022, the cat manifested squinting, epiphora, and mucus accumulation in the right eye, which did not improve after tobramycin treatment. Detailed examination of the right eye revealed a constricted pupil and an elevated nictitating membrane with 4 thread-like worms, which were recovered mechanically at the clinic by flushing with saline solution. Of the 4 worms collected, 1 intact worm was received at AHDC for identification. The cat did not travel outside of New York. The animal was prescribed an ophthalmic ointment containing neomycin and polymyxin B and a dewormer (combination of emodepside [3 mg/kg] and praziquantel [12 mg/kg]) applied topically to the skin. No relapse was observed after treatment.

Figure 2

Adult parasites (red arrow) in the bulbar conjunctiva of the left eye of a 2.5-year-old spayed female domestic shorthair cat (case 2) examined in October 2022.

Figure 2. Adult parasites (red arrow) in the bulbar conjunctiva of the left eye of a 2.5-year-old spayed female domestic shorthair cat (case 2) examined in October 2022.

Case 2 was in a 2.5-year-old spayed female, domestic shorthair cat from a multicat household in Clinton Corners, Dutchess County, New York (adopted in Columbia County, New York). The cat did not travel outside of New York and was examined in October 2022 at a pet hospital during a routine rabies vaccination appointment. Ophthalmic examination revealed multiple white thread-like worms on the bulbar conjunctiva of both eyes (Figure 2). The cat had no clinical signs and was prescribed a dewormer (combination of emodepside [3 mg/kg] and praziquantel [12 mg/kg]) applied topically to the skin. Follow-up after 2 weeks revealed the presence of 8 worms, which were manually removed under local anesthesia. Two intact worms were sent to AHDC for identification. The cat was prescribed a combination of imidacloprid (10 mg/kg) and moxidectin (1 mg/kg) applied topically to the skin. Complete recovery was noted during a follow-up visit in November 2022.

At AHDC, we identified 1 male worm from case 1 and 2 female worms from case 2 morphologically as T. callipaeda eyeworm, primarily on the basis of transverse cuticular striations. The female worms were 11 and 14 mm long, and the male worm was 8.1 mm long; all 3 had a wide, moderately deep buccal cavity. The number of transverse cuticular striations at the cephalic, midbody, and caudal regions ranged 150–400/mm/region in both male and female worms. In the male worm, the long spicule was ≈2 mm long and the short spicule was 0.1 mm long. The vulval opening in the female worms was anterior to the esophageal/intestinal junction (Appendix Figure 1).

We performed PCR on 1 female worm sample from feline case 2 and 1 sample from a dog case targeting 12S rRNA, 18S rRNA, and cytochrome oxidase c subunit 1 (cox1) using previously described protocols (79). The amplified PCR products for both worm samples were 421 bp for 12S rRNA, 891 bp for 18S rRNA, and 612 bp for cox1. We Sanger sequenced the PCR products, edited and aligned the sequences by using BioEdit (https://bioedit.software.informer.com), and compared them with available GenBank sequences by using BLAST analysis (https://blast.ncbi.nlm.nih.gov). We observed 100% sequence identity with corresponding genes available for T. callipaeda in GenBank. We deposited the sequences from this study in GenBank under accession nos. OR545549, OR545261, and OR982681. Phylogenetic analysis of the cox1 sequences revealed clustering as a monophyletic clade with T. callipaeda haplotype 1 from Europe (10,11) (Appendix Figure 2). This study and the previous report on a dog (1) reconfirm the possibility that this parasite was introduced from Europe and subsequently spread in the United States.

Conclusions

The presence of T. callipaeda eyeworm in 2 cats and 11 dogs with no travel history outside of the United States suggests that this parasite is emerging in North America. Indeed, a previous study documented the presence of P. variegata flies in 2 counties in New York and indicated this fly species is a competent vector for T. callipaeda eyeworm, further suggesting an emerging threat by this eyeworm in the northeastern region of the United States (6). In addition, a wide variety of wildlife in New York, including coyotes, red foxes, gray foxes, black bears, raccoons, minks, least weasels, striped skunks, cottontail rabbits, and snowshoe hares, might act as potential hosts for T. callipaeda eyeworm (6); no human cases have been reported from this geographic area. A canine thelaziosis case was also found in the western United States (Nevada), although the travel history is unknown for that dog. Adopting proper diagnosis and surveillance measures is critical to limit the spread of this zoonotic parasite. Studies on control and treatment approaches for dogs suggest mechanical removal of adult and larval T. callipaeda nematodes coupled with the administration of diverse deworming drugs is effective (12). Because vector control using fly repellents is ineffective (3), control of T. callipaeda infections mainly rely on diagnosis and timely anthelmintic treatment. The presence of the natural vector, P. variegata flies (4,6), and the potential involvement of the sylvatic cycle promote the spread of this exotic parasite. Most cases in this study were diagnosed in late summer and autumn, which correlates with peak fly activity. Therefore, prophylactic anthelmintic administration coinciding with fly seasons would be an effective control strategy. Furthermore, as indicated in previous reports (1,4), adoption of a holistic One Health approach will be effective in further limiting the spread of T. callipaeda eyeworm in North America.

Dr. Manoj is a postdoctoral associate and Merck parasitology resident at the National Center for Veterinary Parasitology at the Animal Health Diagnostic Center, Cornell University, New York. Her research interests include vectorborne zoonotic diseases, particularly filarioids and their endosymbiont Wolbachia.

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Acknowledgment

We thank Nicholas A. Hollingshead for his assistance in preparing the map and Antech Diagnostics for sharing information about Thelazia infection cases.

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References

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Cite This Article

DOI: 10.3201/eid3003.230700

Original Publication Date: February 13, 2024

Table of Contents – Volume 30, Number 3—March 2024

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Manigandan Lejeune, Department of Population Medicine and Diagnostic Sciences, Cornell University College of Veterinary Medicine, Ithaca, NY 14853, USA

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Page created: January 31, 2024
Page updated: February 22, 2024
Page reviewed: February 22, 2024
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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