期刊论文详细信息
Particle and Fibre Toxicology
Canine vector-borne infections in Mauritius
Peter John Irwin2  Ian Duncan Robertson2  Jean Alain Ean Ignace1  Gary Kwok Cheong Lee2 
[1] Sir Seewoosagur Ramgoolam Animal Hospital, Mauritius Society for Animal Welfare, Rose Hill, Mauritius;Vector and Water-Borne Pathogen Research Group, School of Veterinary and Life Sciences, Murdoch University, Murdoch 6150, WA, Australia
关键词: Canine vector-borne diseases;    Amblyomma variegatum;    Rhipicephalus sanguineus;    Hepatozoon canis;    Dirofilaria immitis;    Anaplasma;    Ehrlichia;    Mauritius;   
Others  :  1146229
DOI  :  10.1186/s13071-015-0790-9
 received in 2014-11-23, accepted in 2015-03-10,  发布年份 2015
PDF
【 摘 要 】

Background

Canine vector-borne diseases have a worldwide distribution, but to the best of our knowledge, no research has been carried out to evaluate their presence on the Indian Ocean island of Mauritius. An investigation into canine vector-borne infections was conducted in dogs (n = 78) resident at an animal shelter in Port Louis, Mauritius using a combination of traditional microscopy and serological methods.

Methods

Ticks were manually collected from the stray dog population for identification as well as for quantifying tick burdens. Blood was also collected from each dog via either the jugular vein or the cephalic vein, and was stored in EDTA tubes. The stored blood was then used to measure PCV values, make blood smears for the identification of parasites, and used for serological testing of vector-borne disease.

Results

A total of 178 ticks were collected from 52 dogs and identified as Rhipicephalus sanguineus (175/178) or Amblyomma variegatum (3/178). Twenty-six (33%; 95% CI 23, 45) dogs were seropositive for Ehrlichia spp., and 12 (15%; 95% CI 8, 25) for Anaplasma spp., Dirofilaria antigen was detected in 14 (18%; 95% CI 10, 28), and nine (12%; 95% CI 5, 21) dogs had Hepatozoon canis gamonts observed in blood films during microscopic examination. Eleven (14%; 95% CI 7, 24) dogs were co-infected with two pathogens. Borrelia burgdorferi antibodies were not detected in any dogs.

Conclusions

Infection with these pathogens had no significant effect on the packed cell volume (PCV), but high tick burdens were significantly associated with the presence of a tick-borne pathogen. This is the first study of its kind on the dog population in Mauritius and demonstrates the presence of previously undocumented canine vector-borne infections on the island. The relatively high proportion of infected dogs within the study should alert clinicians to the presence of canine vector-borne diseases on the island of Mauritius.

【 授权许可】

   
2015 Lee et al.; licensee BioMed Central.

【 预 览 】
附件列表
Files Size Format View
20150403101225828.pdf 844KB PDF download
Figure 2. 31KB Image download
Figure 1. 78KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Barré N, Morel PC. Tiques (Acariens, Ixodoidea) des Mascareignes (Océan Indien) et maladies transmises. Rev Elev Med Vet Pays Trop. 1983; 36(4):371-8.
  • [2]Taylor MA, Jackson V, Zimmer I, Huntley S, Tomlinson A, Grant A: Qualitative Veterinary Risk Assessment: Introduction of Exotic Diseases (other than Rabies) in the UK. Appendix 5: Disease Distribution Tables [http://archive.defra.gov.uk/foodfarm/farmanimal/diseases/atoz/rabies/documents/appendix5.pdf]
  • [3]Rojas A, Rojas D, Montenegro V, Gutierrez R, Yasur-Landau D, Baneth G. Vector-borne pathogens in dogs from Costa Rica: first molecular description of Babesia vogeli and Hepatozoon canis infections with a high prevalence of monocytic ehrlichiosis and the manifestations of co-infection. Vet Parasitol. 2014; 199:121-8.
  • [4]Walker AR, Bouattour A, Camicas JL, Estrada-Pena A, Horak IG, Latif AA et al.. Ticks of domestic animals in Africa: a guide to identification of species. Bioscience Reports, Edinburgh; 2013.
  • [5]Walker JB, Keirans JE, Horak IG. The genus rhipicephalus (acari, ixodidae): a guide to the brown ticks of the world. Cambridge University Press, Cambridge; 2000.
  • [6]Allison RW, Meinkoth JH. Hematology without the numbers: in-clinic blood film evaluation. Vet Clin Small Anim. 2007; 37:245-66.
  • [7]Fourie JJ, Stanneck D, Luus HG, Beugnet F, Wijnveld M, Jongejan F. Transmission of Ehrlichia canis by Rhipicephalus sanguineus ticks feeding on dogs and on artificial membranes. Vet Parasitol. 2013; 197:595-603.
  • [8]Dantas- Torres F. The brown dog tick, Rhipicephalus sanguineus (Latreille 1806) (Acari: Ixodidae): from taxonomy to control. Vet Parasitol. 2008; 25:173-85.
  • [9]Waner T, Harrus S. Canine monocytic ehrlichiosis- from pathology to clinical manifestations. Isr J Vet Med. 2013; 68:12-8.
  • [10]Latrofa MS, Dantas-Torres F, Giannelli A, Otranto D. Molecular detection of tick-borne pathogens in Rhipicephalus sanguineus group ticks. Ticks Tick Borne Dis. 2014; 5:943-6.
  • [11]Brianti E, Otranto D, Dantas-Torres F, Weigl S, Latrofa MS, Gaglio G et al.. Rhipicephalus sanguineus (Ixodida, Ixodidae) as intermediate host of a canine neglected filarial species with dermal microfilariae. Vet Parasitol. 2012; 183:330-7.
  • [12]Barré N, Camus E, Borel G, Aprelon R. Sites de fixation de la tique Amblyomma variegatum sur ses hôtes en Guadeloupe (Antilles françaises). Rev Elev Med Vet Pays Trop. 1991; 44(4):453-8.
  • [13]Ogo NI, Fernandez de Mera IG, Galindo RC, Okubanjo OO, Inuwa HM, Agbede RIS et al.. Molecular identification of tick-borne pathogens in Nigerian ticks. Vet Parasitol. 2012; 187:572-7.
  • [14]Walker JB, Olwage A. The tick vectors of Cowdria ruminantium (Ixodida, Ixodidae, genus Amblyomma) and their distribution. Onderstepoort J Vet. 1987; 54(3):353-79.
  • [15]Stachurski F, Tortosa P, Rahajarison P, Jacquet S, Yssouf A, Huber K. New data regarding distribution of cattle ticks in the south-western Indian Ocean islands. Vet Res. 2013; 44(1):79-87. BioMed Central Full Text
  • [16]Mylonakis ME, Xenoulis PG, Theodorou K, Siarkou VI, Steiner JM, Harrus S et al.. Serum canine pancreatic lipase immunoreactivity in experimentally induced and naturally occurring canine monocytic ehrlichiosis (Ehrlichia canis). Vet Microbiol. 2014; 169:198-202.
  • [17]Wright CL, Gaff HD, Hynes WL. Prevalence of Ehrlichia chaffeensis and Ehrlichia ewingii in Amblyomma americanum and Dermacentor variabilis collected from southeastern Virginia, 2011–2012. Ticks Tick Borne Dis. 2014; 5(6):978-82.
  • [18]Ndip LM, Ndip RN, Esemu SN, Dickmu VL, Fokam EB, Walker DH et al.. Ehrlichial infection in Cameroonian canines by Ehrlichia canis and Ehrlichia ewingii. Vet Microbiol. 2005; 111(1–2):59-66.
  • [19]Oliveira LS, Oliveira KA, Mourao LC, Pescatore AM, Almeida MR, Conceicao LG et al.. First report of Ehrlichia ewingii detected by molecular investigation in dogs from Brazil. Clin Microbiol Infect. 2009; 15:55-6.
  • [20]Little S. Ehrlichiosis and anaplasmosis in dogs and cats. Vet Clin North Am Small Anim Pract. 2010; 40:1121-40.
  • [21]Stillman BA, Monn M, Liu J, Thatcher B, Foster P, Andrews B et al.. Performance of a commercially available in-clinic ELISA for detection of antibodies against Anaplasma phagocytophilum, Anaplasma platys, Borrelia burgdorferi, Ehrlichia canis, and Ehrlichia ewingii and Dirofilaria immitis antigen in dogs. J Am Vet Med Assoc. 2014; 245(1):80-6.
  • [22]Krupka I, Straubinger RK. Lyme borreliosis in dogs and cats: background, diagnosis, treatment and prevention of infections with Borrelia burgdorferi sensu stricto. Vet Clin North Am Small Anim Pract. 2010; 40:1103-19.
  • [23]Irwin PJ, Jefferies R. Arthropod-transmitted diseases of companion animals in Southeast Asia. Trends Parasitol. 2004; 20(1):27-34.
  • [24]Yabsley MJ, McKibben J, Macpherson CN, Cattan PF, Cherry NA, Hegarty BC et al.. Prevalence of Ehrlichia canis, Anaplasma platys, Babesia canis vogeli, Hepatozoon canis, Bartonella vinsonii berkhoffii, and Rickettsia spp. in dogs from Grenada. Vet Parasitol. 2008; 151:279-85.
  • [25]Rawlings CA, Dawe DL, McCall JW, Keith JC, Prestwood AK. Four types of occult Dirofilaria immitis infection in dogs. J Am Vet Med Assoc. 1982; 180(11):1323-6.
  • [26]Vieira AL, Vieira MJ, Oliveira JM, Simoes AR, Diez-Banos P, Gestal J. Prevalence of canine heartworm (Dirofilaria immitis) diseases in dogs of central Portugal. Parasite. 2014; 21(5):1-7.
  • [27]McCall J, Genchi C, Kramer L, Guerrero J, Dzimianski M, Supakorndej P et al.. Heartworm and Wolbachia: therapeutic implication. Vet Parasitol. 2008; 158:204-14.
  • [28]Megat Abd Rani PA, Irwin PJ, Gatne M, Coleman GT, McInnes LM, Traub RJ. A survey of canine filarial diseases of veterinary and public health significance in India. Parasit Vectors. 2010; 3:30. BioMed Central Full Text
  • [29]Gaunt S, Beall M, Stillman B, Lorentzen L, Diniz PPVP, Chadrashekar R et al.. Experimental infection and co-infection of dogs with Anaplasma platys and Ehrlichia canis: Hematologic, serologic and molecular findings. Parasit Vectors. 2010; 3:33. BioMed Central Full Text
  • [30]Laisser ELK, Kipanyula MJ, Msalya G, Mdegela RH, Karimuribo ED, Mwilawa AJ, Mwega ED, Kusiluka L, Chenyambuga SW. Tick burden and prevalence of Theileria parva infection in Tarime zebu cattle in the lake zone of Tanzania. Trop Anim Health Prod, in press.
  • [31]Hersh MH, LaDeau SL, Previtali MA, Ostfeld RS. When is a parasite not a parasite? Effects of larval tick burdens on white-footed mouse survival. Ecology. 2014; 95(5):1360-9.
  文献评价指标  
  下载次数:18次 浏览次数:3次