Role of Zoo-Housed Animals in the Ecology of Ticks and Tick-Borne Pathogens-A Review

. 2021 Feb 16 ; 10 (2) : . [epub] 20210216

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid33669161

Grantová podpora
QK1920258 Národní Agentura pro Zemědělský Výzkum
20205013 Česká Zemědělská Univerzita v Praze

Ticks are ubiquitous ectoparasites, feeding on representatives of all classes of terrestrial vertebrates and transmitting numerous pathogens of high human and veterinary medical importance. Exotic animals kept in zoological gardens, ranches, wildlife parks or farms may play an important role in the ecology of ticks and tick-borne pathogens (TBPs), as they may serve as hosts for local tick species. Moreover, they can develop diseases of varying severity after being infected by TBPs, and theoretically, can thus serve as reservoirs, thereby further propagating TBPs in local ecosystems. The definite role of these animals in the tick-host-pathogen network remains poorly investigated. This review provides a summary of the information currently available regarding ticks and TBPs in connection to captive local and exotic wildlife, with an emphasis on zoo-housed species.

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Sonenshine D.E., Roe R.M., editors. Biology of Ticks Volume 1. 2nd ed. Oxford University Press; Oxford, UK: 2014. pp. 4–8.

Krasnov B.R., Mouillot D., Shenbrot G.I., Khokhlova I.S., Vinarski M.V., Korallo-Vinarskaya N.P., Poulin R. Similarity in Ectoparasite Faunas of Palaearctic Rodents as a Function of Host Phylogenetic, Geographic or Environmental Distances: Which Matters the Most? Int. J. Parasitol. 2010;40:807–817. doi: 10.1016/j.ijpara.2009.12.002. PubMed DOI

McCoy K.D., Léger E., Dietrich M. Host Specialization in Ticks and Transmission of Tick-Borne Diseases: A Review. Front. Cell. Infect. Microbiol. 2013;3 doi: 10.3389/fcimb.2013.00057. PubMed DOI PMC

Jia N., Wang J., Shi W., Du L., Sun Y., Zhan W., Jiang J.-F., Wang Q., Zhang B., Ji P., et al. Large-Scale Comparative Analyses of Tick Genomes Elucidate Their Genetic Diversity and Vector Capacities. Cell. 2020;182:1328–1340.e13. doi: 10.1016/j.cell.2020.07.023. PubMed DOI

Hansford K.M., Fonville M., Gillingham E.L., Coipan E.C., Pietzsch M.E., Krawczyk A.I., Vaux A.G.C., Cull B., Sprong H., Medlock J.M. Ticks and Borrelia in Urban and Peri-Urban Green Space Habitats in a City in Southern England. Ticks Tick-Borne Dis. 2017;8:353–361. doi: 10.1016/j.ttbdis.2016.12.009. PubMed DOI

Lindquist L. Recent and Historical Trends in the Epidemiology of Japanese Encephalitis and Its Implication for Risk Assessment in Travellers. J. Travel Med. 2018;25:tay006. doi: 10.1093/jtm/tay006. PubMed DOI

Lydecker H.W., Hochuli D.F., Banks P.B. Peri-Urban Black Rats Host a Rich Assembly of Ticks and Healthier Rats Have More Ticks. Ticks Tick-Borne Dis. 2019;10:749–753. doi: 10.1016/j.ttbdis.2019.03.007. PubMed DOI

Sormunen J.J., Kulha N., Klemola T., Mäkelä S., Vesilahti E.-M., Vesterinen E.J. Enhanced Threat of Tick-Borne Infections within Cities? Assessing Public Health Risks Due to Ticks in Urban Green Spaces in Helsinki, Finland. Zoonoses Public Health. 2020;67:823–839. doi: 10.1111/zph.12767. PubMed DOI PMC

Cicuttin G.L., De Salvo M.N., Venzal J.M., Nava S. Borrelia Spp. in Ticks and Birds from a Protected Urban Area in Buenos Aires City, Argentina. Ticks Tick-Borne Dis. 2019;10:101282. doi: 10.1016/j.ttbdis.2019.101282. PubMed DOI

Heylen D., Lasters R., Adriaensen F., Fonville M., Sprong H., Matthysen E. Ticks and Tick-Borne Diseases in the City: Role of Landscape Connectivity and Green Space Characteristics in a Metropolitan Area. Sci. Total Environ. 2019;670:941–949. doi: 10.1016/j.scitotenv.2019.03.235. PubMed DOI

Klemola T., Sormunen J.J., Mojzer J., Mäkelä S., Vesterinen E.J. High Tick Abundance and Diversity of Tick-Borne Pathogens in a Finnish City. Urban Ecosyst. 2019;22:817–826. doi: 10.1007/s11252-019-00854-w. DOI

Estrada-Peña A., de la Fuente J. The Ecology of Ticks and Epidemiology of Tick-Borne Viral Diseases. Antivir. Res. 2014;108:104–128. doi: 10.1016/j.antiviral.2014.05.016. PubMed DOI

Millán J., Proboste T., Fernández de Mera I.G., Chirife A.D., de la Fuente J., Altet L. Molecular Detection of Vector-Borne Pathogens in Wild and Domestic Carnivores and Their Ticks at the Human–Wildlife Interface. Ticks Tick-Borne Dis. 2016;7:284–290. doi: 10.1016/j.ttbdis.2015.11.003. PubMed DOI

Swei A., Couper L.I., Coffey L.L., Kapan D., Bennett S. Patterns, Drivers, and Challenges of Vector-Borne Disease Emergence. Vector-Borne Zoonotic Dis. 2019;20:159–170. doi: 10.1089/vbz.2018.2432. PubMed DOI PMC

Kazimírová M., Hamšíková Z., Kocianová E., Marini G., Mojšová M., Mahríková L., Berthová L., Slovák M., Rosá R. Relative Density of Host-Seeking Ticks in Different Habitat Types of South-Western Slovakia. Exp. Appl. Acarol. 2016;69:205–224. doi: 10.1007/s10493-016-0025-6. PubMed DOI

Diuk-Wasser M.A., VanAcker M.C., Fernandez M.P. Impact of Land Use Changes and Habitat Fragmentation on the Eco-Epidemiology of Tick-Borne Diseases. J. Med. Entomol. 2020 doi: 10.1093/jme/tjaa209. PubMed DOI

Froeschke G., van der Mescht L., McGeoch M., Matthee S. Life History Strategy Influences Parasite Responses to Habitat Fragmentation. Int. J. Parasitol. 2013;43:1109–1118. doi: 10.1016/j.ijpara.2013.07.003. PubMed DOI

Adler P.H., Tuten H.C., Nelder M.P. Arthropods of Medicoveterinary Importance in Zoos. Annu. Rev. Entomol. 2011;56:123–142. doi: 10.1146/annurev-ento-120709-144741. PubMed DOI

Stoebel K., Schoenberg A., Streich W.J. The Seroepidemiology of Lyme Borreliosis in Zoo Animals in Germany. Epidemiol. Infect. 2003;131:975–983. doi: 10.1017/S0950268803008896. PubMed DOI PMC

Širmarová J., Tichá L., Golovchenko M., Salát J., Grubhoffer L., Rudenko N., Nowotny N., Růžek D. Seroprevalence of Borrelia Burgdorferi Sensu Lato and Tick-Borne Encephalitis Virus in Zoo Animal Species in the Czech Republic. Ticks Tick-Borne Dis. 2014;5:523–527. doi: 10.1016/j.ttbdis.2014.03.008. PubMed DOI

Gonzalez I.H.L., Labruna M.B., Chagas C.R.F., Salgado P.A.B., Monticelli C., Morais L.H., de Moraes A.A., Antunes T.C., Ramos P.L., Martins T.F. Ticks Infesting Captive and Free-Roaming Wild Animal Species at the São Paulo Zoo, São Paulo, Brazil. Rev. Bras. Parasitol. Veterinária. 2017;26:496–499. doi: 10.1590/s1984-29612017036. PubMed DOI

Ticha L., Golovchenko M., Oliver J.H., Grubhoffer L., Rudenko N. Sensitivity of Lyme Borreliosis Spirochetes to Serum Complement of Regular Zoo Animals: Potential Reservoir Competence of Some Exotic Vertebrates. Vector-Borne Zoonotic Dis. 2016;16:13–19. doi: 10.1089/vbz.2015.1847. PubMed DOI

Barlough J.E., Madigan J.E., Turoff D.R., Clover J.R., Shelly S.M., Dumler J.S. An Ehrlichia Strain from a Llama (Lama Glama) and Llama-Associated Ticks (Ixodes Pacificus) J. Clin. Microbiol. 1997;35:1005–1007. doi: 10.1128/JCM.35.4.1005-1007.1997. PubMed DOI PMC

Mathieu A., Pastor A.R., Berkvens C.N., Gara-Boivin C., Hébert M., Léveillé A.N., Barta J.R., Smith D.A. Babesia Odocoilei as a Cause of Mortality in Captive Cervids in Canada. Can. Vet. J. 2018;59:52–58. PubMed PMC

Nelder M.P., Reeves W.K., Adler P.H., Wozniak A., Wills W. Ectoparasites and Associated Pathogens of Free-Roaming and Captive Animals in Zoos of South Carolina. Vector-Borne Zoonotic Dis. 2009;9:469–477. doi: 10.1089/vbz.2008.0008. PubMed DOI

Sim R.R., Joyner P.H., Padilla L.R., Anikis P., Aitken-Palmer C. Clinical Disease Associated with Anaplasma Phagocytophilum Infection in Captive Przewalski’s Horses (Equus Ferus Przewalskii) J. Zoo Wildl. Med. 2017;48:497–505. doi: 10.1638/2016-0247R.1. PubMed DOI

Harvey J.W., Simpson C.F., Gaskin J.M., Sameck J.H. Ehrlichiosis in Wolves, Dogs, and Wolf-Dog Crosses. J. Am. Vet. Med. Assoc. 1979;175:901–905. PubMed

Williams C.V., Steenhouse J.L.V., Bradley J.M., Hancock S.I., Hegarty B.C., Breitschwerdt E.B. Naturally Occurring Ehrlichia Chaffeensis Infection in Two Prosimian Primate Species: Ring-Tailed Lemurs (Lemur Catta) and Ruffed Lemurs (Varecia Variegata)-Volume 8, Number 12—December 2002-Emerging Infectious Diseases Journal-CDC. Emerg. Infect. Dis. 2002;8:12. doi: 10.3201/eid0812.020085. PubMed DOI PMC

Nascimento K.K.G.D., Veríssimo S.M.M., Raia V.D.A., Guimarães R.C.S., Seade G.C.C., Azevedo A.C.P., Matos S.P., Oliveira J.M.D., Bezerra I.A., Martins T.F., et al. Tick Fauna of Wild Animals Received and Attended at the Santarém Zoological Park, Western Pará State, Brazil. Ciênc. Rural. 2017;47 doi: 10.1590/0103-8478cr20170159. DOI

Souza S.F., Medeiros L.S., Oliveira R.S., Deschk M., Carvalho Y.K., Ribeiro V.M.F., Souza A.P., Lavina M.S. Primeiro registro de Amblyomma geayi (Acari: Ixodidae) em preguiça (Bradypus variegatus) no estado do Acre, Amazônia Ocidental: Relato de caso. Arq. Bras. Med. Veterinária E Zootec. 2016;68:953–957. doi: 10.1590/1678-4162-8624. DOI

Leschnik M., Kirtz G., Virányi Z., Wille-Piazzai W., Duscher G. Acute Granulocytic Anaplasmosis in A Captive Timber Wolf (Canis Lupus Occidentalis) J. Zoo Wildl. Med. 2012;43:645–648. doi: 10.1638/2011-0224R.1. PubMed DOI

Novacco M., Hofmann-Lehmann R., Grimm F., Meli M.L., Stirn M. Fatal Acute Babesiosis Associated with Babesia Venatorum Infection (Babesia Sp. EU1) in a Captive Reindeer Calf in Switzerland. Vet. Parasitol. Reg. Stud. Rep. 2019;18:100336. doi: 10.1016/j.vprsr.2019.100336. PubMed DOI

Romano J.S., Grund L., Obiegala A., Nymo I.H., Ancin-Murguzur F.J., Li H., Krol N., Pfeffer M., Tryland M. A Multi-Pathogen Screening of Captive Reindeer (Rangifer tarandus) in Germany Based on Serological and Molecular Assays. Front. Vet. Sci. 2019;6:461. doi: 10.3389/fvets.2019.00461. PubMed DOI PMC

Wiegmann L., Silaghi C., Obiegala A., Karnath C., Langer S., Ternes K., Kämmerling J., Osmann C., Pfeffer M. Occurrence of Babesia Species in Captive Reindeer (Rangifer tarandus) in Germany. Vet. Parasitol. 2015;211:16–22. doi: 10.1016/j.vetpar.2015.04.026. PubMed DOI

Braks M.A.H., van Wieren S.E., Takken W., Sprong H. Ecology and Prevention of Lyme Borreliosis. Wageningen Academic Publishers; Wageningen, The Netherlands: 2016. pp. 31–35.

Larson S.R., Lee X., Paskewitz S.M. Prevalence of Tick-Borne Pathogens in Two Species of Peromyscus Mice Common in Northern Wisconsin. J. Med. Entomol. 2018;55:1002–1010. doi: 10.1093/jme/tjy027. PubMed DOI

Cull B., Vaux A.G.C., Ottowell L.J., Gillingham E.L., Medlock J.M. Tick Infestation of Small Mammals in an English Woodland. J. Vector Ecol. 2017;42:74–83. doi: 10.1111/jvec.12241. PubMed DOI

Mendoza-Roldan J., Ribeiro S.R., Castilho-Onofrio V., Grazziotin F.G., Rocha B., Ferreto-Fiorillo B., Pereira J.S., Benelli G., Otranto D., Barros-Battesti D.M. Mites and Ticks of Reptiles and Amphibians in Brazil. Acta Trop. 2020;208:105515. doi: 10.1016/j.actatropica.2020.105515. PubMed DOI

Wilhelmsson P., Jaenson T.G.T., Olsen B., Waldenström J., Lindgren P.-E. Migratory Birds as Disseminators of Ticks and the Tick-Borne Pathogens Borrelia Bacteria and Tick-Borne Encephalitis (TBE) Virus: A Seasonal Study at Ottenby Bird Observatory in South-Eastern Sweden. Parasit. Vectors. 2020;13:607. doi: 10.1186/s13071-020-04493-5. PubMed DOI PMC

Hamer S.A., Goldberg T.L., Kitron U.D., Brawn J.D., Anderson T.K., Loss S.R., Walker E.D., Hamer G.L. Wild Birds and Urban Ecology of Ticks and Tick-Borne Pathogens, Chicago, Illinois, USA, 2005–2010. Emerg. Infect. Dis. 2012;18:1589–1595. doi: 10.3201/eid1810.120511. PubMed DOI PMC

Dimanopoulou A.P., Starras A.G., Diakou A., Lefkaditis M., Giadinis N.D. Prevalence of Tick Species in Sheep and Goat Flocks in Areas of Southern Greece. J. Hell. Vet. Med. Soc. 2018;68:205. doi: 10.12681/jhvms.15606. DOI

Mysterud A., Hatlegjerde I.L., Sorensen O.J. Attachment Site Selection of Life Stages of Ixodes Ricinus Ticks on a Main Large Host in Europe, the Red Deer (Cervus elaphus) Parasit. Vectors. 2014;7:510. doi: 10.1186/s13071-014-0510-x. PubMed DOI PMC

Voordouw M.J. Co-Feeding Transmission in Lyme Disease Pathogens. Parasitology. 2015;142:290–302. doi: 10.1017/S0031182014001486. PubMed DOI PMC

Ferreri L., Bajardi P., Giacobini M. Non-Systemic Transmission of Tick-Borne Diseases: A Network Approach. Commun. Nonlinear Sci. Numer. Simul. 2016;39:149–155. doi: 10.1016/j.cnsns.2016.02.034. DOI

Balashov Y.S. Significance of Ixodid Tick (Parasitiformes, Ixodidae) Population Structure for Maintenance of Natural Foci of Infection. Biol. Bull. 2010;37:677–683. doi: 10.1134/S1062359010070022. DOI

Jaenson T.G.T., Petersson E.H., Jaenson D.G.E., Kindberg J., Pettersson J.H.-O., Hjertqvist M., Medlock J.M., Bengtsson H. The Importance of Wildlife in the Ecology and Epidemiology of the TBE Virus in Sweden: Incidence of Human TBE Correlates with Abundance of Deer and Hares. Parasit. Vectors. 2018;11:477. doi: 10.1186/s13071-018-3057-4. PubMed DOI PMC

Dzięgiel B., Adaszek Ł., Kalinowski M., Winiarczyk S. Equine Granulocytic Anaplasmosis. Res. Vet. Sci. 2013;95:316–320. doi: 10.1016/j.rvsc.2013.05.010. PubMed DOI

Bournez L., Umhang G., Moinet M., Boucher J.-M., Demerson J.-M., Caillot C., Legras L., Devillers E., Hansmann Y., Velay A., et al. Disappearance of TBEV Circulation among Rodents in a Natural Focus in Alsace, Eastern France. Pathogens. 2020;9:930. doi: 10.3390/pathogens9110930. PubMed DOI PMC

Stanek G. Pandora’s Box: Pathogens in Ixodes ricinus ticks in Central Europe. Wien. Klin. Wochenschr. 2009;121:673–683. doi: 10.1007/s00508-009-1281-9. PubMed DOI

Eisen L. Vector Competence Studies with Hard Ticks and Borrelia Burgdorferi Sensu Lato Spirochetes: A Review. Ticks Tick-Borne Dis. 2020;11:101359. doi: 10.1016/j.ttbdis.2019.101359. PubMed DOI PMC

Václavík T., Balážová A., Baláž V., Tkadlec E., Schichor M., Zechmeisterová K., Ondruš J., Široký P. Landscape Epidemiology of Neglected Tick-Borne Pathogens in Central Europe. Transbound. Emerg. Dis. 2020:1–12. doi: 10.1111/tbed.13845. PubMed DOI

Nelder M.P., Russell C.B., Sheehan N.J., Sander B., Moore S., Li Y., Johnson S., Patel S.N., Sider D. Human Pathogens Associated with the Blacklegged Tick Ixodes Scapularis: A Systematic Review. Parasit. Vectors. 2016;9:265. doi: 10.1186/s13071-016-1529-y. PubMed DOI PMC

Zieman E.A., Lawson T., Nielsen C.K., Jiménez F.A. Within-Season Changes in Cytauxzoon Felis Parasitemia in Bobcats. J. Parasitol. 2020;106:308–311. doi: 10.1645/19-173. PubMed DOI

Guillemi E.C., Orozco M.M., Argibay H.D., Farber M.D. Evidence of Ehrlichia Chaffeensis in Argentina through Molecular Detection in Marsh Deer (Blastocerus dichotomus) Int. J. Parasitol. Parasites Wildl. 2019;8:45–49. doi: 10.1016/j.ijppaw.2018.12.004. PubMed DOI PMC

Allan B.F., Goessling L.S., Storch G.A., Thach R.E. Blood Meal Analysis to Identify Reservoir Hosts for Amblyomma Americanum Ticks. Emerg. Infect. Dis. 2010;16:433–440. doi: 10.3201/eid1603.090911. PubMed DOI PMC

Mixson T.R., Campbell S.R., Gill J.S., Ginsberg H.S., Reichard M.V., Schulze T.L., Dasch G.A. Prevalence of Ehrlichia, Borrelia, and Rickettsial Agents in Amblyomma Americanum (Acari: Ixodidae) Collected from Nine States. J. Med. Entomol. 2006;43:1261–1268. doi: 10.1603/0022-2585(2006)43[1261:POEBAR]2.0.CO;2. PubMed DOI

Fritzen C.M., Huang J., Westby K., Freye J.D., Dunlap B., Yabsley M.J., Schardein M., Dunn J.R., Jones T.F., Moncayo A.C. Infection Prevalences of Common Tick-Borne Pathogens in Adult Lone Star Ticks (Amblyomma americanum) and American Dog Ticks (Dermacentor variabilis) in Kentucky. Am. J. Trop. Med. Hyg. 2011;85:718–723. doi: 10.4269/ajtmh.2011.10-0583. PubMed DOI PMC

Latrofa M.S., Dantas-Torres F., Giannelli A., Otranto D. Molecular Detection of Tick-Borne Pathogens in Rhipicephalus Sanguineus Group Ticks. Ticks Tick-Borne Dis. 2014;5:943–946. doi: 10.1016/j.ttbdis.2014.07.014. PubMed DOI

Dantas-Torres F., Otranto D. Further Thoughts on the Taxonomy and Vector Role of Rhipicephalus Sanguineus Group Ticks. Vet. Parasitol. 2015;208:9–13. doi: 10.1016/j.vetpar.2014.12.014. PubMed DOI

Soares R.L., da Silva A.O., Coelho M.L., Echeverria J.T., de Souza M.L., Babo-Terra V.J., Pasquatti T.N., Ramos R.A.N., Ramos C.A.D.N., Soares R.L., et al. Molecular Detection of Cercopithifilaria Bainae and Other Tick-Borne Pathogens in Rhipicephalus Sanguineus s.l. Isolated from Dogs in Midwest Brazil. Rev. Bras. Parasitol. Veterinária. 2020;29 doi: 10.1590/s1984-29612019109. PubMed DOI

Ogrzewalska M., Uezu A., Labruna M.B. Ticks (Acari: Ixodidae) Infesting Wild Birds in the Eastern Amazon, Northern Brazil, with Notes on Rickettsial Infection in Ticks. Parasitol. Res. 2010;106:809–816. doi: 10.1007/s00436-010-1733-1. PubMed DOI

Ogrzewalska M., Literak I., Cardenas-Callirgos J.M., Capek M., Labruna M.B. Rickettsia Bellii in Ticks Amblyomma Varium Koch, 1844, from Birds in Peru. Ticks Tick-Borne Dis. 2012;3:254–256. doi: 10.1016/j.ttbdis.2012.05.003. PubMed DOI

Lugarini C., Martins T.F., Ogrzewalska M., de Vasconcelos N.C.T., Ellis V.A., de Oliveira J.B., Pinter A., Labruna M.B., Silva J.C.R. Rickettsial Agents in Avian Ixodid Ticks in Northeast Brazil. Ticks Tick-Borne Dis. 2015;6:364–375. doi: 10.1016/j.ttbdis.2015.02.011. PubMed DOI

Labruna M.B., Whitworth T., Bouyer D.H., McBride J., Camargo L.M.A., Camargo E.P., Popov V., Walker D.H. Rickettsia Bellii and Rickettsia Amblyommii in Amblyomma Ticks from the State of Rondônia, Western Amazon, Brazil. J. Med. Entomol. 2004;41:1073–1081. doi: 10.1603/0022-2585-41.6.1073. PubMed DOI

Ogrzewalska M., Pacheco R.C., Uezu A., Richtzenhain L.J., Ferreira F., Labruna M.B. Rickettsial Infection in Amblyomma Nodosum Ticks (Acari: Ixodidae) from Brazil. Ann. Trop. Med. Parasitol. 2009;103:413–425. doi: 10.1179/136485909X451744. PubMed DOI

Miranda J., Portillo A., Oteo J.A., Mattar S. Rickettsia Sp. Strain Colombianensi (Rickettsiales: Rickettsiaceae): A New Proposed Rickettsia Detected in Amblyomma Dissimile (Acari: Ixodidae) From Iguanas and Free-Living Larvae Ticks From Vegetation. J. Med. Entomol. 2012;49:960–965. doi: 10.1603/ME11195. PubMed DOI

de Sousa K.C.M., Herrera H.M., Rocha F.L., Costa F.B., Martins T.F., Labruna M.B., Machado R.Z., André M.R. Rickettsia Spp. among Wild Mammals and Their Respective Ectoparasites in Pantanal Wetland, Brazil. Ticks Tick-Borne Dis. 2018;9:10–17. doi: 10.1016/j.ttbdis.2017.10.015. PubMed DOI

Luz H.R., Faccini J.L.H., McIntosh D. Molecular Analyses Reveal an Abundant Diversity of Ticks and Rickettsial Agents Associated with Wild Birds in Two Regions of Primary Brazilian Atlantic Rainforest. Ticks Tick-Borne Dis. 2017;8:657–665. doi: 10.1016/j.ttbdis.2017.04.012. PubMed DOI

Monje L.D., Nava S., Eberhardt A.T., Correa A.I., Guglielmone A.A., Beldomenico P.M. Molecular Detection of the Human Pathogenic Rickettsia Sp. Strain Atlantic Rainforest in Amblyomma Dubitatum Ticks from Argentina. Vector-Borne Zoonotic Dis. 2015;15:167–169. doi: 10.1089/vbz.2014.1741. PubMed DOI

Harris S.E., Munshi-South J. Signatures of Positive Selection and Local Adaptation to Urbanization in White-Footed Mice (Peromyscus leucopus) Mol. Ecol. 2017;26:6336–6350. doi: 10.1111/mec.14369. PubMed DOI PMC

Michelitsch A., Wernike K., Klaus C., Dobler G., Beer M. Exploring the Reservoir Hosts of Tick-Borne Encephalitis Virus. Viruses. 2019;11:669. doi: 10.3390/v11070669. PubMed DOI PMC

Klaus C., Hoffmann B., Beer M., Müller W., Stark B., Bader W., Stiasny K., Heinz F.X., Süss J. Seroprevalence of Tick-Borne Encephalitis (TBE) in Naturally Exposed Monkeys (Macaca sylvanus) and Sheep and Prevalence of TBE Virus in Ticks in a TBE Endemic Area in Germany. Ticks Tick-Borne Dis. 2010;1:141–144. doi: 10.1016/j.ttbdis.2010.06.001. PubMed DOI

Krause P.J., Fish D., Narasimhan S., Barbour A.G. Borrelia Miyamotoi Infection in Nature and in Humans. Clin. Microbiol. Infect. 2015;21:631–639. doi: 10.1016/j.cmi.2015.02.006. PubMed DOI PMC

Yoshii K. Epidemiology and Pathological Mechanisms of Tick-Borne Encephalitis. J. Vet. Med. Sci. 2019;81:343–347. doi: 10.1292/jvms.18-0373. PubMed DOI PMC

Paulsen K.M., Stuen S., das Neves C.G., Suhel F., Gurung D., Soleng A., Stiasny K., Vikse R., Andreassen Å.K., Granquist E.G. Tick-Borne Encephalitis Virus in Cows and Unpasteurized Cow Milk from Norway. Zoonoses Public Health. 2019;66:216–222. doi: 10.1111/zph.12554. PubMed DOI

Achazi K., Růžek D., Donoso-Mantke O., Schlegel M., Ali H.S., Wenk M., Schmidt-Chanasit J., Ohlmeyer L., Rühe F., Vor T., et al. Rodents as Sentinels for the Prevalence of Tick-Borne Encephalitis Virus. Vector Borne Zoonotic Dis. Larchmt. N. 2011;11:641–647. doi: 10.1089/vbz.2010.0236. PubMed DOI PMC

Duscher G.G., Leschnik M., Fuehrer H.-P., Joachim A. Wildlife Reservoirs for Vector-Borne Canine, Feline and Zoonotic Infections in Austria. Int. J. Parasitol. Parasites Wildl. 2015;4:88–96. doi: 10.1016/j.ijppaw.2014.12.001. PubMed DOI PMC

Süss J., Gelpi E., Klaus C., Bagon A., Liebler-Tenorio E.M., Budka H., Stark B., Müller W., Hotzel H. Tickborne Encephalitis in Naturally Exposed Monkey (Macaca sylvanus) Emerg. Infect. Dis. 2007;13:905–907. doi: 10.3201/eid1306.061173. PubMed DOI PMC

Kenyon R.H., Rippy M.K., McKee K.T., Zack P.M., Peters C.J. Infection of Macaca Radiata with Viruses of the Tick-Borne Encephalitis Group. Microb. Pathog. 1992;13:399–409. doi: 10.1016/0882-4010(92)90083-Z. PubMed DOI

Rumyantsev A.A., Chanock R.M., Murphy B.R., Pletnev A.G. Comparison of Live and Inactivated Tick-Borne Encephalitis Virus Vaccines for Safety, Immunogenicity and Efficacy in Rhesus Monkeys. Vaccine. 2006;24:133–143. doi: 10.1016/j.vaccine.2005.07.067. PubMed DOI

Cadavid D. The Mammalian Host Response to Borrelia Infection. Wien. Klin. Wochenschr. 2006;118:653–658. doi: 10.1007/s00508-006-0692-0. PubMed DOI

Gherman C.M., Sándor A.D., Kalmár Z., Marinov M., Mihalca A.D. First Report of Borrelia Burgdorferi Sensu Lato in Two Threatened Carnivores: The Marbled Polecat, Vormela Peregusna and the European Mink, Mustela Lutreola (Mammalia: Mustelidae) BMC Vet. Res. 2012;8:137. doi: 10.1186/1746-6148-8-137. PubMed DOI PMC

Honig V., Carolan H.E., Vavruskova Z., Massire C., Mosel M.R., Crowder C.D., Rounds M.A., Ecker D.J., Ruzek D., Grubhoffer L., et al. Broad-Range Survey of Vector-Borne Pathogens and Tick Host Identification of Ixodes Ricinus from Southern Czech Republic. FEMS Microbiol. Ecol. 2017;93 doi: 10.1093/femsec/fix129. PubMed DOI PMC

Grubhoffer L., Golovchenko M., Vancova M., Zacharovova-Slavickova K., Rudenko N., Oliver J.H. Lyme Borreliosis: Insights into Tick- / Host-Borrelia Relations. Folia Parasitol. (Praha) 2005;52:279–294. doi: 10.14411/fp.2005.039. PubMed DOI

Petrulionienė A., Radzišauskienė D., Ambrozaitis A., Čaplinskas S., Paulauskas A., Venalis A. Epidemiology of Lyme Disease in a Highly Endemic European Zone. Medicina (Mex.) 2020;56:115. doi: 10.3390/medicina56030115. PubMed DOI PMC

Nau R., Christen H.-J., Eiffert H. Lyme Disease—Current State of Knowledge. Dtsch. Arztebl. Int. 2009;106:72–82. doi: 10.3238/arztebl.2009.0525. PubMed DOI PMC

Štefančíková A., Štěpánová G., Derdáková M., Pet’ko B., Kysel’ová J., Cigánek J., Strojný L., Čisláková L., Trávniček M. Serological Evidence for Borrelia Burgdorferi Infection Associated with Clinical Signs in Dairy Cattle in Slovakia. Vet. Res. Commun. 2002;26:601–611. doi: 10.1023/A:1020912618950. PubMed DOI

Balmelli T., Piffaretti J.-C. Association between Different Clinical Manifestations of Lyme Disease and Different Species of Borrelia Burgdorferi Sensu Lato. Res. Microbiol. 1995;146:329–340. doi: 10.1016/0923-2508(96)81056-4. PubMed DOI

Coipan E.C., Jahfari S., Fonville M., Oei G.A., Spanjaard L., Takumi K., Hovius J.W.R., Sprong H. Imbalanced Presence of Borrelia Burgdorferi s.l. Multilocus Sequence Types in Clinical Manifestations of Lyme Borreliosis. Infect. Genet. Evol. J. Mol. Epidemiol. Evol. Genet. Infect. Dis. 2016;42:66–76. doi: 10.1016/j.meegid.2016.04.019. PubMed DOI

Zhong X., Nouri M., Råberg L. Colonization and Pathology of Borrelia Afzelii in Its Natural Hosts. Ticks Tick-Borne Dis. 2019;10:822–827. doi: 10.1016/j.ttbdis.2019.03.017. PubMed DOI

Divers T.J., Gardner R.B., Madigan J.E., Witonsky S.G., Bertone J.J., Swinebroad E.L., Schutzer S.E., Johnson A.L. Borrelia Burgdorferi Infection and Lyme Disease in North American Horses: A Consensus Statement. J. Vet. Intern. Med. 2018;32:617–632. doi: 10.1111/jvim.15042. PubMed DOI PMC

Bhide M., Yilmaz Z., Golcu E., Torun S., Mikula I. Seroprevalence of Anti-Borrelia Burgdorferi Antibodies in Dogs and Horses in Turkey. Ann. Agric. Environ. Med. 2008;15:85–90. PubMed

Appel M.J.G., Allan S., Jacobson R.H., Lauderdale T.L., Chang Y.F., Shin S.J., Thomford J.W., Todhunter R.J., Summers B.A. Experimental Lyme Disease in Dogs Produces Arthritis and Persistent Infection. J. Infect. Dis. 1993;167:651–654. doi: 10.1093/infdis/167.3.651. PubMed DOI

Borys M.A., Kass P.H., Mohr F.C., Sykes J.E. Differences in Clinicopathologic Variables between Borrelia C6 Antigen Seroreactive and Borrelia C6 Seronegative Glomerulopathy in Dogs. J. Vet. Intern. Med. 2019;33:2096–2104. doi: 10.1111/jvim.15586. PubMed DOI PMC

Belperron A.A., Bockenstedt L.K. Natural Antibody Affects Survival of the Spirochete Borrelia Burgdorferi within Feeding Ticks. Infect. Immun. 2001;69:6456–6462. doi: 10.1128/IAI.69.10.6456-6462.2001. PubMed DOI PMC

Bhide M.R., Travnicek M., Levkutova M., Curlik J., Revajova V., Levkut M. Sensitivity of Borrelia Genospecies to Serum Complement from Different Animals and Human: A Host–Pathogen Relationship. FEMS Immunol. Med. Microbiol. 2005;43:165–172. doi: 10.1016/j.femsim.2004.07.012. PubMed DOI

Bos J.H., Klip F.C., Sprong H., Broens E.M., Kik M.J.L. Clinical Outbreak of Babesiosis Caused by Babesia Capreoli in Captive Reindeer (Rangifer tarandus Tarandus) in the Netherlands. Ticks Tick-Borne Dis. 2017;8:799–801. doi: 10.1016/j.ttbdis.2017.06.006. PubMed DOI

Milnes E.L., Thornton G.L., Delnatte P., Léveillé A.N., Barta J.R., Smith D.A., Nemeth N.M. Molecular Detection of Babesia Odocoilei in Wild, Farmed, and Zoo Cervids in Ontario, Canada. J. Wildl. Dis. 2019;55:335–342. doi: 10.7589/2018-06-147. PubMed DOI

Schoelkopf L., Hutchinson C.E., Bendele K.G., Goff W.L., Willette M., Rasmussen J.M., Holman P.J. New Ruminant Hosts and Wider Geographic Range Identified For Babesia Odocoilei (Emerson and Wright 1970) J. Wildl. Dis. 2005;41:683–690. doi: 10.7589/0090-3558-41.4.683. PubMed DOI

Hildebrandt A., Gray J.S., Hunfeld K.-P. Human Babesiosis in Europe: What Clinicians Need to Know. Infection. 2013;41:1057–1072. doi: 10.1007/s15010-013-0526-8. PubMed DOI

Holman P.J., Craig T.M., Crider D.L.D., Petrini K.R., Rhyan J., Wagner G.G. Culture Isolation and Partial Characterization of a Babesia Sp. from a North American Elk (Cervus elaphus) J. Wildl. Dis. 1994;30:460–465. doi: 10.7589/0090-3558-30.3.460. PubMed DOI

Schnittger L., Rodriguez A.E., Florin-Christensen M., Morrison D.A. Babesia: A World Emerging. Infect. Genet. Evol. 2012;12:1788–1809. doi: 10.1016/j.meegid.2012.07.004. PubMed DOI

Kik M., Nijhof A.M., Balk J.A., Jongejan F. Babesia Sp. EU1 Infection in a Forest Reindeer, the Netherlands. Emerg. Infect. Dis. 2011;17:936–938. doi: 10.3201/eid1705.101834. PubMed DOI PMC

Langton C., Gray J., Waters P., Holman P. Naturally Acquired Babesiosis in a Reindeer (Rangifer tarandus Tarandus) Herd in Great Britain. Parasitol. Res. 2003;89:194–198. doi: 10.1007/s00436-002-0737-x. PubMed DOI

Pattullo K.M., Wobeser G., Lockerbie B.P., Burgess H.J. Babesia Odocoilei Infection in a Saskatchewan Elk (Cervus elaphus canadensis) Herd. J. Vet. Diagn. Invest. 2013;25:535–540. doi: 10.1177/1040638713491746. PubMed DOI

Petrini K.R., Holman P.J., Rhyan J.C., Jenkins S.J., Wagner G.G. Fatal Babesiosis in an American Woodland Caribou (Rangifer tarandus caribou) J. Zoo Wildl. Med. 1995;26:298–305.

Gallatin L.L., Irizarry-Rovira A.R., Renninger M.L., Holman P.J., Wagner G.G., Sojka J.E., Christian J.A. Babesia Odocoilei Infection in Elk. J. Am. Vet. Med. Assoc. 2003;223:1027–1032. doi: 10.2460/javma.2003.223.1027. PubMed DOI

Bartlett S.L., Abou-Madi N., Messick J.B., Birkenheuer A., Kollias G.V. Diagnosis and Treatment of Babesia Odocoilei in Captive Reindeer (Rangifer tarandus Tarandus) and Recognition of Three Novel Host Species. J. Zoo Wildl. Med. 2009;40:152–159. doi: 10.1638/2008-0011.1. PubMed DOI

André M.R., Adania C.H., Teixeira R.H.F., Allegretti S.M., Machado R.Z. Molecular and Serological Detection of Babesia Spp. in Neotropical and Exotic Carnivores in Brazilian Zoos. J. Zoo Wildl. Med. 2011;42:139–143. doi: 10.1638/2010-0074.1. PubMed DOI

André M.R., Baccarim Denardi N.C., Marques de Sousa K.C., Gonçalves L.R., Henrique P.C., Grosse Rossi Ontivero C.R., Lima Gonzalez I.H., Cabral Nery C.V., Fernandes Chagas C.R., Monticelli C., et al. Arthropod-Borne Pathogens Circulating in Free-Roaming Domestic Cats in a Zoo Environment in Brazil. Ticks Tick-Borne Dis. 2014;5:545–551. doi: 10.1016/j.ttbdis.2014.03.011. PubMed DOI

Phair K.A., Carpenter J.W., Smee N., Myers C.B., Pohlman L.M. Severe Anemia Caused by Babesiosis in a Maned Wolf (Chrysocyon brachyurus) J. Zoo Wildl. Med. 2012;43:162–167. doi: 10.1638/2010-0210.1. PubMed DOI

Wasserkrug Naor A., Lindemann D.M., Schreeg M.E., Marr H.S., Birkenheuer A.J., Carpenter J.W., Ryseff J.K. Clinical, Morphological, and Molecular Characterization of an Undetermined Babesia Species in a Maned Wolf (Chrysocyon brachyurus) Ticks Tick-Borne Dis. 2019;10:124–126. doi: 10.1016/j.ttbdis.2018.09.005. PubMed DOI

Mans B.J., Pienaar R., Latif A.A. A Review of Theileria Diagnostics and Epidemiology. Int. J. Parasitol. Parasites Wildl. 2015;4:104–118. doi: 10.1016/j.ijppaw.2014.12.006. PubMed DOI PMC

André M.R., Adania C.H., Machado R.Z., Allegretti S.M., Felippe P.A.N., Silva K.F., Nakaghi A.C.H., Dagnone A.S. Molecular Detection of Cytauxzoon Spp. in Asymptomatic Brazilian Wild Captive Felids. J. Wildl. Dis. 2009;45:234–237. doi: 10.7589/0090-3558-45.1.234. PubMed DOI

Peixoto P.V., Soares C.O., Scofield A., Santiago C.D., França T.N., Barros S.S. Fatal Cytauxzoonosis in Captive-Reared Lions in Brazil. Vet. Parasitol. 2007;145:383–387. doi: 10.1016/j.vetpar.2006.12.023. PubMed DOI

Sivakumar T., Hayashida K., Sugimoto C., Yokoyama N. Evolution and Genetic Diversity of Theileria. Infect. Genet. Evol. 2014;27:250–263. doi: 10.1016/j.meegid.2014.07.013. PubMed DOI

Yam J., Gestier S., Bryant B., Campbell-Ward M., Bogema D., Jenkins C. The Identification of Theileria Bicornis in Captive Rhinoceros in Australia. Int. J. Parasitol. Parasites Wildl. 2018;7:85–89. doi: 10.1016/j.ijppaw.2017.12.003. PubMed DOI PMC

Osman S.A., Al-Gaabary M.H. Clinical, Haematological and Therapeutic Studies on Tropical Theileriosis in Water Buffaloes (Bubalus Bubalis) in Egypt. Vet. Parasitol. 2007;146:337–340. doi: 10.1016/j.vetpar.2007.03.012. PubMed DOI

Oakes V.J., Yabsley M.J., Schwartz D., LeRoith T., Bissett C., Broaddus C., Schlater J.L., Todd S.M., Boes K.M., Brookhart M., et al. Theileria Orientalis Ikeda Genotype in Cattle, Virginia, USA. Emerg. Infect. Dis. 2019;25:1653–1659. doi: 10.3201/eid2509.190088. PubMed DOI PMC

Garner B.C., Holman P., Berent L.M. Theileriosis in a Reindeer (Rangifer tarandus Tarandus) Associated with a Potentially Novel Theileria Sp. Vet. Clin. Pathol. 2012;41:497–501. doi: 10.1111/j.1939-165x.2012.00475.x. PubMed DOI

de Souza Gonçalves T., de Nazaré Leite Barros F., Inoue L.S., de Farias D.M., dos Santos Lima J., Nobre A.V., Azenha Aidar E.S., Ferreira Diniz R.R., Gering A.P., Scofield A. Natural Theileria Equi Infection in Captive Tapirus Terrestris (Perissodactyla: Tapiridae) in the Brazilian Amazon. Ticks Tick-Borne Dis. 2020;11:101452. doi: 10.1016/j.ttbdis.2020.101452. PubMed DOI

Filoni C., Catão-Dias J.L., Cattori V., Willi B., Meli M.L., Corrêa S.H.R., Marques M.C., Adania C.H., Silva J.C.R., Marvulo M.F.V., et al. Surveillance Using Serological and Molecular Methods for the Detection of Infectious Agents in Captive Brazilian Neotropic and Exotic Felids. J. Vet. Diagn. Invest. 2011 doi: 10.1177/1040638711407684. PubMed DOI

Garner M.M., Lung N.P., Citino S., Greiner E.C., Harvey J.W., Homer B.L. Fatal Cytauxzoonosis in a Captive-Reared White Tiger (Panthera Tigris) Vet. Pathol. 1996;33:82–86. doi: 10.1177/030098589603300111. PubMed DOI

Clarke L.L., Rissi D.R. Neuropathology of Natural Cytauxzoon Felis Infection in Domestic Cats. Vet. Pathol. 2015;52:1167–1171. doi: 10.1177/0300985814564986. PubMed DOI

Aschenbroich S.A., Rech R.R., Sousa R.S., Carmichael K.P., Sakamoto K. Pathology in Practice. Cytauxzoon Felis Infection. J. Am. Vet. Med. Assoc. 2012;240:159–161. doi: 10.2460/javma.240.2.159. PubMed DOI

Lu M., Li F., Liao Y., Shen J.-J., Xu J.-M., Chen Y.-Z., Li J.-H., Holmes E.C., Zhang Y.-Z. Epidemiology and Diversity of Rickettsiales Bacteria in Humans and Animals in Jiangsu and Jiangxi Provinces, China. Sci. Rep. 2019;9:13176. doi: 10.1038/s41598-019-49059-3. PubMed DOI PMC

Yabsley M.J., Norton T.M., Powell M.R., Davidson W.R. Molecular and Serologic Evidence of Tick-Borne Ehrlichiae in Three Species of Lemurs from St. Catherines Island, Georgia, USA. J. Zoo Wildl. Med. 2004;35:503–509. doi: 10.1638/03-116. PubMed DOI

Yu X.-J., Walker D.H. The Order Rickettsiales. In: Dworkin M., Falkow S., Rosenberg E., Schleifer K.-H., Stackebrandt E., editors. The Prokaryotes. Springer New York; New York, NY, USA: 2006. pp. 493–528.

Seo M.-G., Kwon O.-D., Kwak D. Anaplasma Bovis Infection in a Horse: First Clinical Report and Molecular Analysis. Vet. Microbiol. 2019;233:47–51. doi: 10.1016/j.vetmic.2019.04.024. PubMed DOI

Torina A., Naranjo V., Pennisi M.G., Patania T., Vitale F., Laricchiuta P., Alongi A., Scimeca S., Kocan K.M., Fuente J. De La Serologic And Molecular Characterization of Tick-Borne Pathogens In Lions (Panthera leo) from the Fasano Safari Park, Italy. J. Zoo Wildl. Med. 2007;38:591–593. doi: 10.1638/2007-0043R1.1. PubMed DOI

André M.R., Adania C.H., Machado R.Z., Allegretti S.M., Felippe P.A.N., Silva K.F., Nakaghi A.C.H. Molecular and Serologic Detection of Ehrlichia Spp. in Endangered Brazilian Wild Captive Felids. J. Wildl. Dis. 2010;46:1017–1023. doi: 10.7589/0090-3558-46.3.1017. PubMed DOI

André M.R., Dumler J.S., Scorpio D.G., Teixeira R.H.F., Allegretti S.M., Machado R.Z. Molecular Detection of Tick-Borne Bacterial Agents in Brazilian and Exotic Captive Carnivores. Ticks Tick-Borne Dis. 2012;3:247–253. doi: 10.1016/j.ttbdis.2012.04.002. PubMed DOI

Zhang Y., Li T., Cui Y., Wang J., Lv Y., Wang R., Jian F., Zhang L., Wang J., Yang G., et al. The First Report of Anaplasma Phagocytophilum and a Novel Theileria Spp. Co-Infection in a South African Giraffe. Parasitol. Int. 2016;65:347–351. doi: 10.1016/j.parint.2016.04.006. PubMed DOI

Matsuno K., Nonoue N., Noda A., Kasajima N., Noguchi K., Takano A., Shimoda H., Orba Y., Muramatsu M., Sakoda Y., et al. Fatal Tickborne Phlebovirus Infection in Captive Cheetahs, Japan. Emerg. Infect. Dis. 2018;24:1726–1729. doi: 10.3201/eid2409.171667. PubMed DOI PMC

Benelli G. Pathogens Manipulating Tick Behavior—Through a Glass, Darkly. Pathogens. 2020;9:664. doi: 10.3390/pathogens9080664. PubMed DOI PMC

Inci A., Yildirim A., Duzlu O., Doganay M., Aksoy S. Tick-Borne Diseases in Turkey: A Review Based on One Health Perspective. PLoS Negl. Trop. Dis. 2016;10:e0005021. doi: 10.1371/journal.pntd.0005021. PubMed DOI PMC

Otranto D., Brianti E., Dantas-Torres F., Miró G., Latrofa M.S., Mutafchiev Y., Bain O. Species Diversity of Dermal Microfilariae of the Genus Cercopithifilaria Infesting Dogs in the Mediterranean Region. Parasitology. 2013;140:99–108. doi: 10.1017/S0031182012001357. PubMed DOI

Otranto D., Varcasia A., Solinas C., Scala A., Brianti E., Dantas-Torres F., Annoscia G., Martin C., Mutafchiev Y., Bain O. Redescription of Cercopithifilaria Bainae Almeida & Vicente, 1984 (Spirurida, Onchocercidae) from a Dog in Sardinia, Italy. Parasit. Vectors. 2013;6:132. doi: 10.1186/1756-3305-6-132. PubMed DOI PMC

Tahir D., Davoust B., Parola P. Vector-Borne Nematode Diseases in Pets and Humans in the Mediterranean Basin: An Update. Vet. World. 2019;12:1630–1643. doi: 10.14202/vetworld.2019.1630-1643. PubMed DOI PMC

Szatmari V., van Leeuwen M.W., Piek C.J., Venco L. False Positive Antigen Test for Dirofilaria Immitis after Heat Treatment of the Blood Sample in a Microfilaremic Dog Infected with Acanthocheilonema Dracunculoides. Parasit. Vectors. 2020;13:501. doi: 10.1186/s13071-020-04376-9. PubMed DOI PMC

Uni S., Bain O., Fujita H., Matsubayashi M., Fukuda M., Takaoka H. Infective Larvae of Cercopithifilaria Spp. (Nematoda: Onchocercidae) from Hard Ticks (Ixodidae) Recovered from the Japanese Serow (Bovidae) Parasite. 2013;20:1. doi: 10.1051/parasite/2012001. PubMed DOI PMC

Zhang X., Norris D.E., Rasgon J.L. Distribution and Molecular Characterization of Wolbachia Endosymbionts and Filarial Nematodes in Maryland Populations of the Lone Star Tick (Amblyomma americanum) FEMS Microbiol. Ecol. 2011;77:50–56. doi: 10.1111/j.1574-6941.2011.01089.x. PubMed DOI PMC

Tokarz R., Tagliafierro T., Sameroff S., Cucura D.M., Oleynik A., Che X., Jain K., Lipkin W.I. Microbiome Analysis of Ixodes Scapularis Ticks from New York and Connecticut. Ticks Tick-Borne Dis. 2019;10:894–900. doi: 10.1016/j.ttbdis.2019.04.011. PubMed DOI

Namrata P., Miller J.M., Shilpa M., Reddy P.R., Bandoski C., Rossi M.J., Sapi E. Filarial Nematode Infection in Ixodes Scapularis Ticks Collected from Southern Connecticut. Vet. Sci. 2014;1:5–15. doi: 10.3390/vetsci1010005. DOI

Olmeda-García A.S., Rodríguez-Rodríguez J.A. Stage-Specific Development of a Filarial Nematode (Dipetalonema dracunculoides) in Vector Ticks. J. Helminthol. 1994;68:231–235. doi: 10.1017/S0022149X00014395. PubMed DOI

Brianti E., Otranto D., Dantas-Torres F., Weigl S., Latrofa M.S., Gaglio G., Napoli E., Brucato G., Cauquil L., Giannetto S., et al. Rhipicephalus Sanguineus (Ixodida, Ixodidae) as Intermediate Host of a Canine Neglected Filarial Species with Dermal Microfilariae. Vet. Parasitol. 2012;183:330–337. doi: 10.1016/j.vetpar.2011.07.031. PubMed DOI

Parker J., White K. Lyme Borreliosis in Cattle and Horses-a Review of the Literature. Cornell Vet. 1992;82:253–274. PubMed

Gusset M., Dick G. The Global Reach of Zoos and Aquariums in Visitor Numbers and Conservation Expenditures. Zoo Biol. 2011;30:566–569. doi: 10.1002/zoo.20369. PubMed DOI

Little S.E., Barrett A.W., Nagamori Y., Herrin B.H., Normile D., Heaney K., Armstrong R. Ticks from Cats in the United States: Patterns of Infestation and Infection with Pathogens. Vet. Parasitol. 2018;257:15–20. doi: 10.1016/j.vetpar.2018.05.002. PubMed DOI

Panait L.C., Stock G., Globokar M., Balzer J., Groth B., Mihalca A.D., Pantchev N. First Report of Cytauxzoon Sp. Infection in Germany: Organism Description and Molecular Confirmation in a Domestic Cat. Parasitol. Res. 2020;119:3005–3011. doi: 10.1007/s00436-020-06811-3. PubMed DOI PMC

Penzhorn B.L., Oosthuizen M.C. Babesia Species of Domestic Cats: Molecular Characterization Has Opened Pandora’s Box. Front. Vet. Sci. 2020;7:134. doi: 10.3389/fvets.2020.00134. PubMed DOI PMC

Ma J., Hine P.M., Clough E.R., Fish D., Coughlin R.T., Beltz G.A., Shew M.G. Safety, Efficacy, and Immunogenicity of a Recombinant Osp Subunit Canine Lyme Disease Vaccine. Vaccine. 1996;14:1366–1374. doi: 10.1016/S0264-410X(96)00045-X. PubMed DOI

Guarino C., Asbie S., Rohde J., Glaser A., Wagner B. Vaccination of Horses with Lyme Vaccines for Dogs Induces Short-Lasting Antibody Responses. Vaccine. 2017;35:4140–4147. doi: 10.1016/j.vaccine.2017.06.052. PubMed DOI

Torina A., Moreno-Cid J.A., Blanda V., Fernández de Mera I.G., de la Lastra J.M.P., Scimeca S., Blanda M., Scariano M.E., Briganò S., Disclafani R., et al. Control of Tick Infestations and Pathogen Prevalence in Cattle and Sheep Farms Vaccinated with the Recombinant Subolesin-Major Surface Protein 1a Chimeric Antigen. Parasit. Vectors. 2014;7:10. doi: 10.1186/1756-3305-7-10. PubMed DOI PMC

Černý J., Lynn G., Hrnková J., Golovchenko M., Rudenko N., Grubhoffer L. Management Options for Ixodes Ricinus-Associated Pathogens: A Review of Prevention Strategies. Int. J. Environ. Res. Public. Health. 2020;17:1830. doi: 10.3390/ijerph17061830. PubMed DOI PMC

Hokynar K., Sormunen J.J., Vesterinen E.J., Partio E.K., Lilley T., Timonen V., Panelius J., Ranki A., Puolakkainen M. Chlamydia-Like Organisms (CLOs) in Finnish Ixodes Ricinus Ticks and Human Skin. Microorganisms. 2016;4:28. doi: 10.3390/microorganisms4030028. PubMed DOI PMC

Croxatto A., Rieille N., Kernif T., Bitam I., Aeby S., Péter O., Greub G. Presence of Chlamydiales DNA in Ticks and Fleas Suggests That Ticks Are Carriers of Chlamydiae. Ticks Tick-Borne Dis. 2014;5:359–365. doi: 10.1016/j.ttbdis.2013.11.009. PubMed DOI

Pilloux L., Aeby S., Gaümann R., Burri C., Beuret C., Greub G. The High Prevalence and Diversity of Chlamydiales DNA within Ixodes Ricinus Ticks Suggest a Role for Ticks as Reservoirs and Vectors of Chlamydia-Related Bacteria. Appl. Environ. Microbiol. 2015;81:8177–8182. doi: 10.1128/AEM.02183-15. PubMed DOI PMC

Burnard D., Weaver H., Gillett A., Loader J., Flanagan C., Polkinghorne A. Novel Chlamydiales Genotypes Identified in Ticks from Australian Wildlife. Parasit. Vectors. 2017;10:46. doi: 10.1186/s13071-017-1994-y. PubMed DOI PMC

Cheong H.C., Lee C.Y.Q., Cheok Y.Y., Tan G.M.Y., Looi C.Y., Wong W.F. Chlamydiaceae: Diseases in Primary Hosts and Zoonosis. Microorganisms. 2019;7:146. doi: 10.3390/microorganisms7050146. PubMed DOI PMC

Fritschi J., Marti H., Seth-Smith H.M.B., Aeby S., Greub G., Meli M.L., Hofmann-Lehmann R., Mühldorfer K., Stokar-Regenscheit N., Wiederkehr D., et al. Prevalence and Phylogeny of Chlamydiae and Hemotropic Mycoplasma Species in Captive and Free-Living Bats. BMC Microbiol. 2020;20:182. doi: 10.1186/s12866-020-01872-x. PubMed DOI PMC

Osman K.M., Ali H.A., ElJakee J.A., Galal H.M. Prevalence of Chlamydophila Psittaci Infections in the Eyes of Cattle, Buffaloes, Sheep and Goats in Contact with a Human Population. Transbound. Emerg. Dis. 2013;60:245–251. doi: 10.1111/j.1865-1682.2012.01337.x. PubMed DOI

Greco G., Corrente M., Buonavoglia D., Campanile G., Di Palo R., Martella V., Bellacicco A.L., D’Abramo M., Buonavoglia C. Epizootic Abortion Related to Infections by Chlamydophila Abortus and Chlamydophila Pecorum in Water Buffalo (Bubalus bubalis) Theriogenology. 2008;69:1061–1069. doi: 10.1016/j.theriogenology.2008.01.018. PubMed DOI

Wu S.-M., Huang S.-Y., Xu M.-J., Zhou D.-H., Song H.-Q., Zhu X.-Q. Chlamydia Felis Exposure in Companion Dogs and Cats in Lanzhou, China: A Public Health Concern. BMC Vet. Res. 2013;9:104. doi: 10.1186/1746-6148-9-104. PubMed DOI PMC

Schautteet K., Vanrompay D. Chlamydiaceae Infections in Pig. Vet. Res. 2011;42:29. doi: 10.1186/1297-9716-42-29. PubMed DOI PMC

Petersen J.M., Mead P.S., Schriefer M.E. Francisella Tularensis: An Arthropod-Borne Pathogen. Vet. Res. 2009;40:7. doi: 10.1051/vetres:2008045. PubMed DOI PMC

Zellner B., Huntley J.F. Ticks and Tularemia: Do We Know What We Don’t Know? Front. Cell. Infect. Microbiol. 2019;9:146. doi: 10.3389/fcimb.2019.00146. PubMed DOI PMC

Beckwith C.S. Tularemia as a Cause of Fever in a Squirrel Monkey. J. Am. Vet. Med. Assoc. 2006;229:269–273. doi: 10.2460/javma.229.2.269. PubMed DOI

Calle P.P., Bowerman D.L., Pape W.J. Nonhuman Primate Tularemia (Francisella tularensis) Epizootic in a Zoological Park. J. Zoo Wildl. Med. 1993;24:459–468.

Kuehn A., Schulze C., Kutzer P., Probst C., Hlinak A., Ochs A., Grunow R. Tularaemia Seroprevalence of Captured and Wild Animals in Germany: The Fox (Vulpes vulpes) as a Biological Indicator. Epidemiol. Infect. 2013;141:833–840. doi: 10.1017/S0950268812001008. PubMed DOI PMC

Preiksaitis J.K., Crawshaw G.J., Nayar G.S., Stiver H.G. Human Tularemia at an Urban Zoo. Can. Med. Assoc. J. 1979;121:1097–1099. PubMed PMC

Wechtaisong W., Bonnet S.I., Lien Y.-Y., Chuang S.-T., Tsai Y.-L. Transmission of Bartonella Henselae within Rhipicephalus Sanguineus: Data on the Potential Vector Role of the Tick. PLoS Negl. Trop. Dis. 2020;14:e0008664. doi: 10.1371/journal.pntd.0008664. PubMed DOI PMC

Asyikha R., Sulaiman N., Mohd-Taib F.S. Detection of Bartonella Sp. in Ticks and Their Small Mammal Hosts in Mangrove Forests of Peninsular Malaysia. Trop. Biomed. 2020;37:919–931. PubMed

Levytska V.A., Mushinsky A.B., Zubrikova D., Blanarova L., Dlugosz E., Vichova B., Slivinska K.A., Gajewski Z., Gizinski S., Liu S., et al. Detection of Pathogens in Ixodid Ticks Collected from Animals and Vegetation in Five Regions of Ukraine. Ticks Tick-Borne Dis. 2021;12:101586. doi: 10.1016/j.ttbdis.2020.101586. PubMed DOI

Ghafar A., Cabezas-Cruz A., Galon C., Obregon D., Gasser R.B., Moutailler S., Jabbar A. Bovine Ticks Harbour a Diverse Array of Microorganisms in Pakistan. Parasit. Vectors. 2020;13:1. doi: 10.1186/s13071-019-3862-4. PubMed DOI PMC

Breitschwerdt E.B., Maggi R.G., Chomel B.B., Lappin M.R. Bartonellosis: An Emerging Infectious Disease of Zoonotic Importance to Animals and Human Beings. J. Vet. Emerg. Crit. Care. 2010;20:8–30. doi: 10.1111/j.1476-4431.2009.00496.x. PubMed DOI

Ebani V.V., Guardone L., Marra F., Altomonte I., Nardoni S., Mancianti F. Arthropod-Borne Pathogens in Stray Cats from Northern Italy: A Serological and Molecular Survey. Animals. 2020;10:2334. doi: 10.3390/ani10122334. PubMed DOI PMC

Selmi R., Ben Said M., Ben Yahia H., Abdelaali H., Boulouis H.-J., Messadi L. First Report on Bartonella Henselae in Dromedary Camels (Camelus dromedarius) Infect. Genet. Evol. 2020;85:104496. doi: 10.1016/j.meegid.2020.104496. PubMed DOI

Hao L., Yuan D., Guo L., Hou W., Mo X., Yin J., Yang A., Li R. Molecular Detection of Bartonella in Ixodid Ticks Collected from Yaks and Plateau Pikas (Ochotona curzoniae) in Shiqu County, China. BMC Vet. Res. 2020;16:235. doi: 10.1186/s12917-020-02452-x. PubMed DOI PMC

Boularias G., Azzag N., Gandoin C., Bouillin C., Chomel B., Haddad N., Boulouis H.J. Bartonella Bovis and Bartonella Chomelii Infection in Dairy Cattle and Their Ectoparasites in Algeria. Comp. Immunol. Microbiol. Infect. Dis. 2020;70:101450. doi: 10.1016/j.cimid.2020.101450. PubMed DOI

Chochlakis D., Cutler S., Giadini N.D., Psaroulaki A. Bartonella Vinsonii Subsp. Arupensis Infection in Animals of Veterinary Importance, Ticks and Biopsy Samples. New Microbes New Infect. 2020;34:100652. doi: 10.1016/j.nmni.2020.100652. PubMed DOI PMC

Grech-Angelini S., Stachurski F., Vayssier-Taussat M., Devillers E., Casabianca F., Lancelot R., Uilenberg G., Moutailler S. Tick-Borne Pathogens in Ticks (Acari: Ixodidae) Collected from Various Domestic and Wild Hosts in Corsica (France), a Mediterranean Island Environment. Transbound. Emerg. Dis. 2020;67:745–757. doi: 10.1111/tbed.13393. PubMed DOI

Ben-Harari R.R. Tick Transmission of Toxoplasmosis. Expert Rev. Anti Infect. Ther. 2019;17:911–917. doi: 10.1080/14787210.2019.1682550. PubMed DOI

Sroka J., Chmielewska-Badora J., Dutkiewicz J. Ixodes Ricinus as a Potential Vector of Toxoplasma Gondii. Ann. Agric. Environ. Med. AAEM. 2003;10:121–123. PubMed

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