Antibody response to Phlebotomus perniciosus saliva in cats naturally exposed to phlebotomine sand flies is positively associated with Leishmania infection
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
SFRH/BD/116516/2016
Fundação para a Ciência e a Tecnologia
IF/01302/2015
Fundação para a Ciência e a Tecnologia
PubMed
30909940
PubMed Central
PMC6434892
DOI
10.1186/s13071-019-3376-0
PII: 10.1186/s13071-019-3376-0
Knihovny.cz E-zdroje
- Klíčová slova
- Antibodies, Cat, Leishmania infantum, Phlebotomus perniciosus, Portugal, Saliva,
- MeSH
- imunoglobulin G imunologie MeSH
- kočky MeSH
- Leishmania infantum imunologie MeSH
- leishmanióza viscerální veterinární MeSH
- nemoci koček imunologie parazitologie MeSH
- Phlebotomus imunologie MeSH
- rizikové faktory MeSH
- sliny imunologie MeSH
- tvorba protilátek MeSH
- zvířata MeSH
- Check Tag
- kočky MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- imunoglobulin G MeSH
BACKGROUND: Zoonotic leishmaniosis, caused by the protozoan Leishmania infantum, is a public and animal health problem in Asia, Central and South America, the Middle East and the Mediterranean Basin. Several phlebotomine sand fly species from the subgenus Larroussius are vectors of L. infantum. Data from dogs living in endemic areas of leishmaniosis advocate the use of antibody response to phlebotomine sand fly saliva as an epidemiological biomarker for monitoring vector exposure. The aim of this study was to analyse the exposure of cats to phlebotomine sand flies using detection of IgG antibodies to Phlebotomus perniciosus saliva. The association between phlebotomine sand fly exposure and the presence of Leishmania infection was also investigated. RESULTS: IgG antibodies to P. perniciosus saliva were detected in 167 (47.7%) out of 350 cats; higher antibody levels were present in sera collected during the period of phlebotomine sand fly seasonal activity (OR = 19.44, 95% CI: 9.84-38.41). Cats of 12-35 months had higher antibody levels than younger ones (OR = 3.56, 95% CI: 1.39-9.16); this difference was also significant with older cats (for 36-95 months-old, OR = 9.43, 95% CI: 3.62-24.48; for older than 95 months, OR = 9.68, 95% CI: 3.92-23.91). Leishmania spp. DNA was detected in the blood of 24 (6.9%) cats, while antibodies to L. infantum were detected in three (0.9%). Only one cat was positive to Leishmania by both techniques. Cats presenting IgG antibodies to P. perniciosus had a significantly higher risk of being positive for Leishmania infection. CONCLUSIONS: To our knowledge, this is the first study demonstrating anti-sand fly saliva antibodies in cats. The evaluation of the contact of this animal species with the vector is important to the development of prophylactic measures directed to cats, with the aim of reducing the prevalence of infection in an endemic area. Therefore, studies evaluating whether the use of imidacloprid/flumethrin collars reduces the frequency of P. perniciosus bites in cats are needed. It is also important to evaluate if there is a correlation between the number of phlebotomine sand fly bites and IgG antibody levels.
Animal and Veterinary Research Centre University of Trás os Montes and Alto Douro Vila Real Portugal
Clínica Veterinária Porto Seguro Olhão Portugal
Department of Parasitology Faculty of Science Charles University Prague Czech Republic
Global Health and Tropical Medicine Lisboa Portugal
Hospital Veterinário da Arrábida Azeitão Portugal
Hospital Veterinário de Berna Lisboa Portugal
Hospital Veterinário do Algarve Faro Portugal
Zobrazit více v PubMed
Pennisi M-G, Cardoso L, Baneth G, Bourdeau P, Koutinas A, Miró G, et al. LeishVet update and recommendations on feline leishmaniosis. Parasit Vectors. 2015;8:302. doi: 10.1186/s13071-015-0909-z. PubMed DOI PMC
Maia C, Campino L. Can domestic cats be considered reservoir hosts of zoonotic leishmaniasis? Trends Parasitol. 2011;27:341–344. doi: 10.1016/j.pt.2011.03.008. PubMed DOI
Maia C, Dantas-Torres F, Campino L. Parasite biology: the reservoir hosts. In: Bruschi F, Gradoni L, editors. The leishmaniases: old neglected tropical diseases. Basel: Springer; 2018. pp. 79–106.
Lestinova T, Rohousova I, Sima M, de Oliveira CI, Volf P. Insights into the sand fly saliva: blood-feeding and immune interactions between sand flies, hosts, and Leishmania. PLoS Negl Trop Dis. 2017;11:e0005600. doi: 10.1371/journal.pntd.0005600. PubMed DOI PMC
Teixeira C, Gomes R, Collin N, Reynoso D, Jochim R, Oliveira F, et al. Discovery of markers of exposure specific to bites of Lutzomyia longipalpis, the vector of Leishmania infantum chagasi in Latin America. PLoS Negl Trop Dis. 2010;4:e638. doi: 10.1371/journal.pntd.0000638. PubMed DOI PMC
Vlkova M, Rohousova I, Drahota J, Stanneck D, Kruedewagen EM, Mencke N, et al. Canine antibody response to Phlebotomus perniciosus bites negatively correlates with the risk of Leishmania infantum transmission. PLoS Negl Trop Dis. 2011;5:e1344. doi: 10.1371/journal.pntd.0001344. PubMed DOI PMC
Kostalova T, Lestinova T, Sumova P, Vlkova M, Rohousova I, Berriatua E, et al. Canine antibodies against salivary recombinant proteins of Phlebotomus perniciosus: a longitudinal study in an endemic focus of canine leishmaniasis. PLoS Negl Trop Dis. 2015;9:e0003855. doi: 10.1371/journal.pntd.0003855. PubMed DOI PMC
Kostalova T, Lestinova T, Maia C, Sumova P, Vlkova M, Willen L, et al. The recombinant protein rSP03B is a valid antigen for screening dog exposure to Phlebotomus perniciosus across foci of canine leishmaniasis. Med Vet Entomol. 2017;31:88–93. doi: 10.1111/mve.12192. PubMed DOI
Solcà MS, Andrade BB, Abbehusen MMC, Teixeira CR, Khouri R, Valenzuela JG, et al. Circulating biomarkers of immune activation, oxidative stress and inflammation characterize severe canine visceral leishmaniasis. Sci Rep. 2016;6:32619. doi: 10.1038/srep32619. PubMed DOI PMC
Quinnell RJ, Soremekun S, Bates PA, Rogers ME, Garcez LM, Courtenay O. Antibody response to sand fly saliva is a marker of transmission intensity but not disease progression in dogs naturally infected with Leishmania infantum. Parasit Vectors. 2018;11:7. doi: 10.1186/s13071-017-2587-5. PubMed DOI PMC
Velez R, Spitzova T, Domenech E, Willen L, Cairó J, Volf P, et al. Seasonal dynamics of canine antibody response to Phlebotomus perniciosus saliva in an endemic area of Leishmania infantum. Parasit Vectors. 2018;11:545. doi: 10.1186/s13071-018-3123-y. PubMed DOI PMC
Hostomska J, Rohousova I, Volfova V, Stanneck D, Mencke N, Volf P. Kinetics of canine antibody response to saliva of the sand fly Lutzomyia longipalpis. Vector Borne Zoonotic Dis. 2008;8:443–450. doi: 10.1089/vbz.2007.0214. PubMed DOI
Alten B, Maia C, Afonso MO, Campino L, Jiménez M, González E, et al. Seasonal dynamics of phlebotomine sand fly species proven vectors of Mediterranean leishmaniasis caused by Leishmania infantum. PLoS Negl Trop Dis. 2016;10:e0004458. doi: 10.1371/journal.pntd.0004458. PubMed DOI PMC
Cortes S, Vaz Y, Neves R, Maia C, Cardoso L, Campino L. Risk factors for canine leishmaniasis in an endemic Mediterranean region. Vet Parasitol. 2012;189:189–196. doi: 10.1016/j.vetpar.2012.04.028. PubMed DOI
Alvar J, Vélez ID, Bern C, Herrero M, Desjeux P, Cano J, et al. Leishmaniasis worldwide and global estimates of its incidence. PLoS One. 2012;7:e35671. doi: 10.1371/journal.pone.0035671. PubMed DOI PMC
Maia C, Sousa C, Ramos C, Cristóvão JM, Faísca P, Campino L. First case of feline leishmaniosis caused by Leishmania infantum genotype E in a cat with a concurrent nasal squamous cell carcinoma. JFMS Open Rep. 2015;1:2055116915593969. PubMed PMC
Vilhena H, Martinez-Díaz VL, Cardoso L, Vieira L, Altet L, Francino O, et al. Feline vector-borne pathogens in the north and centre of Portugal. Parasit Vectors. 2013;6:99. doi: 10.1186/1756-3305-6-99. PubMed DOI PMC
Maia C, Gomes J, Cristóvão J, Nunes M, Martins A, Rebêlo E, et al. Feline Leishmania infection in a canine leishmaniasis endemic region, Portugal. Vet Parasitol. 2010;174:336–340. doi: 10.1016/j.vetpar.2010.08.030. PubMed DOI
Maia C, Ramos C, Coimbra M, Bastos F, Martins A, Pinto P, et al. Bacterial and protozoal agents of feline vector-borne diseases in domestic and stray cats from southern Portugal. Parasit Vectors. 2014;7:115. doi: 10.1186/1756-3305-7-115. PubMed DOI PMC
Maia C, Nunes M, Campino L. Importance of cats in zoonotic leishmaniasis in Portugal. Vector-Borne Zoonotic Dis. 2008;8:555–560. doi: 10.1089/vbz.2007.0247. PubMed DOI
Maia C, Dionísio L, Afonso MO, Neto L, Cristóvão JM, Campino L. Leishmania infection and host-blood feeding preferences of phlebotomine sandflies and canine leishmaniasis in an endemic European area, the Algarve Region in Portugal. Mem Inst Oswaldo Cruz. 2013;108:481–487. doi: 10.1590/S0074-0276108042013014. PubMed DOI PMC
Branco S, Alves-Pires C, Maia C, Cortes S, Cristovão JMS, Gonçalves L, et al. Entomological and ecological studies in a new potential zoonotic leishmaniasis focus in Torres Novas municipality, Central Region, Portugal. Acta Trop. 2013;125:339–348. doi: 10.1016/j.actatropica.2012.12.008. PubMed DOI
Volf P, Volfova V. Establishment and maintenance of sand fly colonies. J Vector Ecol. 2011;36:S1–S9. doi: 10.1111/j.1948-7134.2011.00106.x. PubMed DOI
Maia C, Nunes M, Cristóvão J, Campino L. Experimental canine leishmaniasis: clinical, parasitological and serological follow-up. Acta Trop. 2010;116:193–199. doi: 10.1016/j.actatropica.2010.08.001. PubMed DOI
Cruz I, Cañavate C, Rubio JM, Morales MA, Chicharro C, Laguna F, et al. A nested polymerase chain reaction (Ln-PCR) for diagnosing and monitoring Leishmania infantum infection in patients co-infected with human immunodeficiency virus. Trans R Soc Trop Med Hyg. 2002;96(Suppl. 1):S185–S189. doi: 10.1016/S0035-9203(02)90074-X. PubMed DOI
Pereira M. Identificação e densidade das espécies flebotomínicas no concelho de Coimbra: vectores de leishmanioses. Coimbra: Faculdade de Ciências da Universidade de Coimbra; 2008.
Cristóvão J. Monitorização do risco de exposição à leishmaniose zoonótica. Lisbon: Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa; 2015.
Brodskyn CI, Kamhawi S. Biomarkers for zoonotic visceral leishmaniasis in Latin America. Front Cell Infect Microbiol. 2018;8:245. doi: 10.3389/fcimb.2018.00245. PubMed DOI PMC
Pereira A, Martins Â, Brancal H, Vilhena H, Silva P, Pimenta P, et al. Parasitic zoonoses associated with dogs and cats: a survey of Portuguese pet owners’ awareness and deworming practices. Parasit Vectors. 2016;9:245. doi: 10.1186/s13071-016-1533-2. PubMed DOI PMC
Jager KJ, Zoccali C, MacLeod A, Dekker FW. Confounding: what it is and how to deal with it. Kidney Int. 2008;73:256–260. doi: 10.1038/sj.ki.5002650. PubMed DOI
Maia C, Ramos C, Coimbra M, Cardoso L, Campino L. Prevalence of Dirofilaria immitis antigen and antibodies to Leishmania infantum in cats from southern Portugal. Parasitol Int. 2015;64:154–156. doi: 10.1016/j.parint.2014.11.006. PubMed DOI
Chatzis MK, Leontides L, Athanasiou LV, Papadopoulos E, Kasabalis D, Mylonakis M, et al. Evaluation of indirect immunofluorescence antibody test and enzyme-linked immunosorbent assay for the diagnosis of infection by Leishmania infantum in clinically normal and sick cats. Exp Parasitol. 2014;147:54–59. doi: 10.1016/j.exppara.2014.10.004. PubMed DOI PMC
Leishmania spp. in equids and their potential vectors in endemic areas of canine leishmaniasis