ABSTRACT
Leptospirosis is a zoonosis transmitted by contact with infected urine or water contaminated with the agent. Searches for Leptospira spp. in reptiles are scarce although most species have contact with aquatic environments. We evaluated the presence of anti-Leptospira spp. antibodies in Podocnemis expansa housed at the Amazonian Zoobotanical Garden, in Belém, Pará state, Brazil. We analyzed 74 serum samples through the microscopic agglutination test using 31 live antigens from different Leptospira spp. serogroups. Thirty samples (40.5%) were positive against Leptospira spp., with titrations between 100 and 3,200 for one or more serogroups. The Hebdomadis serogroup was the most prevalent, with 26 (87%) out of the 30 positive samples, followed by Djasiman, with two (7%) and Celledoni and Bataviae with one (3%) sample each. The detection of anti-Leptospira spp. agglutinins in P. expansa suggests that the aquatic environment is a transmission route for this pathogen among chelonians.
KEYWORDS:
chelonians; microscopic agglutination test; Hebdomadis; Djasiman; Celledoni; Bataviae
RESUMO
A leptospirose é uma zoonose transmitida pelo contato com urina infectada ou água contaminada com o agente. Estudos de Leptospira spp. em répteis são escassos, apesar da maioria das espécies terem contato com ambientes aquáticos. Avaliamos a presença de anticorpos anti-Leptospira spp. em Podocnemis expansa mantidas no Jardim Zoobotânico da Amazônia, em Belém, Pará, Brasil. Analisamos 74 amostras de soro por meio do teste de aglutinação microscópica usando 31 antígenos vivos de diferentes sorogrupos de Leptospira spp. Trinta amostras (40,5%) foram reagentes contra Leptospira spp., com titulações entre 100 e 3.200 para um ou mais sorogrupos. O sorogrupo Hebdomadis foi o mais prevalente, com 26 (87%) das 30 amostras positivas, seguido por Djasiman, com duas (7%) e Celledoni e Bataviae com uma (3%) amostra cada. A detecção de aglutininas anti-Leptospira spp. em P. expansa sugere que o ambiente aquático é uma via de transmissão para esse patógeno entre quelônios.
PALAVRAS-CHAVE:
quelônios; teste de aglutinação microscópica; Hebdomadis; Djasiman; Celledoni; Bataviae
Bacteria of the genus Leptospira cause leptospirosis, an anthropozoonosis of great public health concern (Mahajan and Daljeet 2008Mahajan, S.; Chhabra, Daljeet. 2008. Leptospirosis: a re-emerging disease. Veterinary World, 1: 182-185.). This pathogen affects humans and domestic and wild animals via direct or indirect contact with urine of infected animals or contaminated water (Cubas and Baptistotte 2014Cubas, P.H.; Baptistotte, C. 2014. Chelonia (Tartaruga, Cágado, Jabuti). In: Cubas, S.C.; Silva, J.C.R.; Catão-Dias, J.L. (Ed.). Tratado de Animais Selvagens. v.2. Roca, São Paulo, p.86-119.). Studies on Leptospira spp. infection in chelonians are limited and little is known about the relevance of these animals as reservoirs of the pathogen and their risk to public health (Andrews et al. 1965Andrews, R.D.; Reilly, J.R.; Ferris, D.; Hanson, L.E. 1965. Leptospiral agglutinins in sera from Southern Illinois Herpetofauna. Bulletin of the Wildlife Disease Association, 1: 55-59.; Glosser et al. 1974Glosser, J.W.; Sulzer, C.R.; Eberhardt, M.; Winkler, W.G. 1974. Cultural and serologic evidence of Leptospira interrogans serotype Tarassovi infection in turtles. Journal of Wildlife Diseases, 10: 429-435.; Lindtner-Knific et al. 2013Lindtner-Knific, R.; Vergles-Rataj, A.; Vlahović, K.; Zrimšek, P.; Dovč, A. 2013. Prevalence of antibodies against Leptospira sp. in snakes, lizards and turtles in Slovenia. Acta Veterinaria Scandinavica, 55: 65 (http://doi.org/10.1186/1751-0147-55-65).
http://doi.org/10.1186/1751-0147-55-65...
; Oliveira et al. 2016Oliveira, J.P.; Kawanami, A.E.; Silva, A.S.L.; Chung, D.G.; Werther, K. 2016. Detection of Leptospira spp. in wild Phrynops geoffroanus (Geoffroy’s side-necked turtle) in urban environment. Acta Tropica, 164: 165-168.; Fornazari et al. 2018Fornazari, F.; Langoni, H.; Marson, P.M.; Nóbrega, D.B.; Texeira, C.R. 2018. Leptospira reservoirs among wildlife in Brazil: Beyond rodents. Acta Tropica, 178: 205-212.). In Brazil, there are a few studies conducted in zoos that provide information on the sanitary status of chelonians regarding leptospirosis (Esteves et al. 2005Esteves, F.M.; Guerra-Neto, G.; Girio, R.J.S.; Silva-Vergara, M.L.; Carvalho, A.C.F.B. 2005. Detecção de anticorpos para Leptospira spp. em animais e funcionários do zoológico municipal de Uberaba, MG. Arquivos do Instituto Biológico, 72: 283-288.; Brasil et al. 2013Brasil, W.L.; Parentoni, R.N.; Farias, R.C.; Nery, T.F.L.; Vasconcellos, A.S.; Azevedo, S.S. 2013. Anticorpos anti-Leptospira spp. em animais mantidos em cativeiro na Paraíba. Semina: Ciências Agrárias, 34: 2945-2950.; Rocha et al. 2019Rocha, K.S.; Baia, I.W.M.; Monteiro, L.H.; Miranda, J.M.S.; Monteiro, T.R.M.; Silva, A.F.; Reis, T.A.; Ferreira, M.F.S.; Mesquita, E.Y.E.; Moraes, C.C.G. 2019. Identification of antibodies to Leptospira spp. in the spot-legged turtle (Rhinoclemmys punctularia) maintained in captivity. Semina: Ciências Agrárias , 40: 3763-3768.). In the Brazilian Amazon region, one turtle species, Rhynoclemmys punctularia, was found to test positive for anti-Leptospira spp. agglutinins, also in captive individuals (Rocha et al. 2019).
Serological studies using the microscopic agglutination test are used to evaluate the exposure of animals to pathogens and their susceptibility to infection with different Leptospira spp. isolates, and have already been used to test for exposure to Leptospira in chelonians (Glosser et al. 1974Glosser, J.W.; Sulzer, C.R.; Eberhardt, M.; Winkler, W.G. 1974. Cultural and serologic evidence of Leptospira interrogans serotype Tarassovi infection in turtles. Journal of Wildlife Diseases, 10: 429-435.; Lindtner-Knific et al. 2013Lindtner-Knific, R.; Vergles-Rataj, A.; Vlahović, K.; Zrimšek, P.; Dovč, A. 2013. Prevalence of antibodies against Leptospira sp. in snakes, lizards and turtles in Slovenia. Acta Veterinaria Scandinavica, 55: 65 (http://doi.org/10.1186/1751-0147-55-65).
http://doi.org/10.1186/1751-0147-55-65...
). In this study, we aimed at detecting the presence of anti-Leptospira spp. antibodies in South American river turtles, Podocnemis expansa (Schweigger, 1812) (Podocnemididae) housed in captivity in a public aquarium in the northern Brazilian city of Belém.
The study was authorized by the Brazilian federal environmental authority Sistema de Autorização e Informação em Biodiversidade - SISBIO license no. 59785-1. Turtles were sampled at Zoobotanical Park Amazonia (Bosque Rodrigues Alves - Jardim Zoobotânico da Amazônia), located in an urban neighborhood of the city of Belém, in the northern Brazilian state of Pará.
The studied specimens inhabit artificial lakes alongside other chelonian species (Rhinoclemmys punctularia and Podocnemis unifilis). Individuals of both sexes and different age groups originate from apprehensions of illegally traded wild animals or from reproduction in captivity in the park itself. Water in the lakes is replaced only when the compartments are completely drained for cleaning. On one such occasion, in August 2015, 74 P. expansa (23 males, 48 females and three juveniles of undetermined sex) were captured manually for blood sampling. About 1-2 mL of blood were collected by venipuncture into the caudal vertebrae or occipital sinus using 3-mL syringes and tubes without anticoagulant. The injection site was cleaned with 2% chlorhexidine prior to injection. The samples were transported to the Zoonosis and Public Health Laboratory of the Institute of Veterinary Medicine of Universidade Federal do Pará (IMV−UFPA), where they were centrifuged to separate coagulated blood from serum. The serum was placed in 1.5 ml Eppendorf® tubes, identified and stored at -20 ° C until analysis.
The samples were analyzed by the microscopic agglutination test (MAT), following Faine et al. (1999Faine, S.; Adler, B.; Bolin, C.; Perolat, P. 1999. Leptospira and Leptospirosis. 2nd ed. Medisci, Melbourne, 353p.), with Leptospira antigens. Leptospira strains were maintained in Ellinghausen-McCullough-Johnson-Harris broth at 29 °C in the laboratory. The group of Leptospira antigens used comprised 31 serovars, with four variants of the Hardjo serovar and the strain NUP-1 isolated from canine urine (Canicola serogroup), for a total of 19 serogroups (Australis, Autumnalis, Ballum, Bataviae, Canicola, Celedoni, Cynopteri, Djasiman, Grippotyphosa, Hebdomadis, Icterohaemorrhagiae, Javanica, Pamana, Pomona, Pyrogenes, Sejroe, Shermani, Andamana, and Seramanga). Serum samples presenting 50% or more of agglutination compared to the control were considered as positives.
Of the 74 serum samples analyzed, 40.5% (30/74) were positive for Leptospira spp., with titrations between 100 to 3.200 for one or more serogroups, while no samples showed coagglutination with two or more serogroups (Table 1). Two samples were positive for the Djasiman serogroup, with titrations between 100 and 200, and only one sample was positive for the Celledoni and Bataviae serogroups, with titrations of 400 and 100, respectively.
Distribution of agglutination reactions to detect anti-Leptospira spp. antibodies by the microscopic agglutination test (MAT) based on titrations of the most prevalent detected serogroups in the serum of 30 samples from captive South American river turtles (Podocnemis expansa).
Although little is known about how Leptospira spp. infection in turtles, or their role as possible reservoirs of bacteria in the epidemiological transmission cycle, some studies have already shown a high prevalence in the detection of anti-Leptospira spp. in chelonians in North America, such as Terrapene carolina carolina with 91% (29/32) of reactive animals (Andrews et al. 1965Andrews, R.D.; Reilly, J.R.; Ferris, D.; Hanson, L.E. 1965. Leptospiral agglutinins in sera from Southern Illinois Herpetofauna. Bulletin of the Wildlife Disease Association, 1: 55-59.), 96% (42/46) of Sternotherus odoratus and Pseudemys scripta elegans (Glosser et al. 1974Glosser, J.W.; Sulzer, C.R.; Eberhardt, M.; Winkler, W.G. 1974. Cultural and serologic evidence of Leptospira interrogans serotype Tarassovi infection in turtles. Journal of Wildlife Diseases, 10: 429-435.), and 93.5% (29/31) of Emydoidea blandingii in an urban area (Grimm et al. 2015Grimm, K.; Mitchell, M.A.; Thompson, D.; Maddox, C. 2015. Seroprevalence of Leptospira spp. in Blanding’s Turtles (Emydoidea blandingii) from DuPage County, Illinois USA. Journal of Herpetological Medicine and Surgery, 25: 28-32.). In Europe, 13.8% (09/65) of Testudo graeca, Testudo hermanni, Emys orbicularis, and the exotic Trachemys scripta elegans from Slovenia were positive for anti-Leptospira spp. antibodies (Lindtner-Knific et al. 2013Lindtner-Knific, R.; Vergles-Rataj, A.; Vlahović, K.; Zrimšek, P.; Dovč, A. 2013. Prevalence of antibodies against Leptospira sp. in snakes, lizards and turtles in Slovenia. Acta Veterinaria Scandinavica, 55: 65 (http://doi.org/10.1186/1751-0147-55-65).
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), as were 87.5% (14/16) of introduced Trachemys scripta in urban lagoons in Italy (Dezzutto et al. 2017Dezzutto, D.; Barbero, R.; Canale, G.; Acutis, P.L.; Biolatti, C.; Dogliero, A.; et al. 2017. Detection of Leptospira spp. in water turtle (Trachemys scripta) living in ponds of urban parks. Veterinary Sciences, 4: 1-5.).
In Brazil, reported prevalence of Leptospira spp. in chelonians was 27.5% (11/40) for Trachemys dorbigny and Phrynops hilarii from two urban lakes in Pelotas, in the southern state of Rio Grande do Sul (Silva et al. 2009Silva, E.F.; Seyffert, N.; Cerqueira, G.M. 2009. Serum antileptospiral agglutinins in freshwater turtles from Southern Brazil. Brazilian Journal of Microbiology, 40: 227-230.) and 45.5% (30/66) for Phrynops geoffroanus from urban streams in Jaboticabal, in the southeastern state of São Paulo (Oliveira et al. 2016Oliveira, J.P.; Kawanami, A.E.; Silva, A.S.L.; Chung, D.G.; Werther, K. 2016. Detection of Leptospira spp. in wild Phrynops geoffroanus (Geoffroy’s side-necked turtle) in urban environment. Acta Tropica, 164: 165-168.). In the municipal zoo of Ribeirão Preto, São Paulo, 52 chelonians of four species were tested for reaction to anti-Leptospira spp. antibodies, among which 59.1% (26/44) Trachemys scripta elegans, 50% (01/02) Phrynops geoffroanus, 50% (02/02) Podocnemis unifilis, and 75% (03/04) P. expansa tested positive (Silva et al. 2010Silva, C.S.; Gírio, R.J.S.; Guerra-Neto, G.; Brich, M.; Santana, L.A.S.; Amâncio, F.H.B.; Mariani, J.R.; Wessort, P.M.F. 2010. Anticorpos anti-Leptospira spp. em animais selvagens do zoológico municipal de Ribeirão Preto, Estado de São Paulo, Brasil. Brazilian Journal of Veterinary Research and Animal Science, 47: 237-242.).
Rhinoclemmys punctularia turtles kept in the same tanks as the P. expansa in our study showed a prevalence of 54.8% (17/31) of animals reactive to Leptospira spp. (Rocha et al. 2019Rocha, K.S.; Baia, I.W.M.; Monteiro, L.H.; Miranda, J.M.S.; Monteiro, T.R.M.; Silva, A.F.; Reis, T.A.; Ferreira, M.F.S.; Mesquita, E.Y.E.; Moraes, C.C.G. 2019. Identification of antibodies to Leptospira spp. in the spot-legged turtle (Rhinoclemmys punctularia) maintained in captivity. Semina: Ciências Agrárias , 40: 3763-3768.), a high frequency similar to that found in P. expansa. Although the animals were kept in the same environment, and blood collection was performed on the same day, only antigen-antibody reactions for the Celledoni serogroup occurred in both species. This suggests that the diversity of infecting strains and the pathophysiology of Leptospira spp. is variable among reptile species. The presence of anti-Leptospira spp. antibodies in aquatic turtles has been related to prolonged exposure to Leptospira present in water (Andrews et al. 1965Andrews, R.D.; Reilly, J.R.; Ferris, D.; Hanson, L.E. 1965. Leptospiral agglutinins in sera from Southern Illinois Herpetofauna. Bulletin of the Wildlife Disease Association, 1: 55-59.), contact with captive infected individuals (Grimm et al. 2015Grimm, K.; Mitchell, M.A.; Thompson, D.; Maddox, C. 2015. Seroprevalence of Leptospira spp. in Blanding’s Turtles (Emydoidea blandingii) from DuPage County, Illinois USA. Journal of Herpetological Medicine and Surgery, 25: 28-32.), to the presence of rodents in turtle farms (Lindtner-Knific et al. 2013Lindtner-Knific, R.; Vergles-Rataj, A.; Vlahović, K.; Zrimšek, P.; Dovč, A. 2013. Prevalence of antibodies against Leptospira sp. in snakes, lizards and turtles in Slovenia. Acta Veterinaria Scandinavica, 55: 65 (http://doi.org/10.1186/1751-0147-55-65).
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) or carnivorous habits, such as ingestion of small vertebrates that may have been exposed to bacteria (Glosser et al. 1974Glosser, J.W.; Sulzer, C.R.; Eberhardt, M.; Winkler, W.G. 1974. Cultural and serologic evidence of Leptospira interrogans serotype Tarassovi infection in turtles. Journal of Wildlife Diseases, 10: 429-435.).
Only four serogroups were detected in P. expansa in our study, yet the presence of different serogroups in a single species indicates that they circulate in the habitat and that the host species plays a role in the life cycle of the agent (Oliveira et al. 2013Oliveira, V.S.; Arsky, M.L.N.S.; Caldas, E.P. 2013. Reservatórios animais de leptospirose: uma revisão bibliográfica. Revista Saúde (Santa Maria), 39: 9-20.). Although the source of infection of the turtles is unknown, the aquatic environment was the likely transmission route, since the tanks in which turtles are kept are not cleaned regularly, which may result in the persistence of bacteria in the water and explain the high titration rate of antibodies (Andrews et al. 1965Andrews, R.D.; Reilly, J.R.; Ferris, D.; Hanson, L.E. 1965. Leptospiral agglutinins in sera from Southern Illinois Herpetofauna. Bulletin of the Wildlife Disease Association, 1: 55-59.).
The detected serogroups were initially isolated from humans (Kmety and Dikken 1993Kmety, E.; Dikken, H. 1993. Classification of the Species Leptospira interrogans and History of its Serovars. University Press, Groningen, 104p.), and later in domestic and wild animals (Rossetti et al. 2005Rossetti, C.A.; Liem, M.; Samartino, L.E.; Hartskeerl, R.A. 2005. Buenos Aires, a new Leptospira serovar of serogroup Djasiman, isolated from an aborted dog fetus in Argentina. Veterinary Microbiology, 107: 241-248.; Betance et al. 2017Betance, L.; Peda, A.; Conan, A.; Ribeiro, J. 2017. Seroprevalence of leptospirosis in the feral cat population of St. Kitts. Journal of Animal Research and Technology, 59: 38-42.; Rajeev et al. 2017Rajeev, S.; Conan, A.; Pratt, N.; Beierschmitt, A.; Palmour, R. 2017. High Leptospira seroprevalence in captive and wild-caught vervet monkeys (Chlorocebus sabeus) on the Caribbean island of Saint Kitts. Journal of Veterinary Diagnostic Investigation, 29: 930-934.; Fornazari et al. 2018Fornazari, F.; Langoni, H.; Marson, P.M.; Nóbrega, D.B.; Texeira, C.R. 2018. Leptospira reservoirs among wildlife in Brazil: Beyond rodents. Acta Tropica, 178: 205-212.), indicating that these serovars are not species-specific, making studies of their epidemiology more complicated, as transmission networks can be very complex. Little is known about infectious serotypes, their respective wild reservoirs, and their correlation between urban animals and wildlife (Grimm et al. 2015Grimm, K.; Mitchell, M.A.; Thompson, D.; Maddox, C. 2015. Seroprevalence of Leptospira spp. in Blanding’s Turtles (Emydoidea blandingii) from DuPage County, Illinois USA. Journal of Herpetological Medicine and Surgery, 25: 28-32.). The extent of the Amazon region, and the complexity of its habitats and biodiversity, can lead to regionally differentiated epidemiological cycles, so that turtles are possibly exposed to different serovars throughout their extensive distribution range (Ferrara et al. 2017Ferrara, C.R.; Fagundes, C.K.; Morcatty, T.Q.; Vogt, R.C. 2017. Tartaruga-da-Amazônia, Podocnemis expansa (Schweigger 1812). In: Ferrara, C.R.; Fagundes, C.K.; Morcatty, T.Q.; Vogt, R.C. (Eds.). Quelônios Amazônicos: Guia de identificação e distribuição. WCS, Manaus, p.130- 137. ).
We provide the first record of the presence of antibodies in P. expansa to the Hebdomadis, Djasiman, Celledoni and Bataviae serogroups. Our findings demonstrate that P. expansa in captive conditions were exposed to different Leptospira spp. serogroups, and that it is important to isolate environmental Leptospira and to test wild animals kept in captivity in the Amazon region for exposure to Leptospira.
ACKNOWLEDGMENTS
The authors acknowledge CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior) for the granting of the scholarship and Jardim Zoobotânico da Amazônia for the support in the capture of turtles and collection of biological samples.
REFERENCES
- Andrews, R.D.; Reilly, J.R.; Ferris, D.; Hanson, L.E. 1965. Leptospiral agglutinins in sera from Southern Illinois Herpetofauna. Bulletin of the Wildlife Disease Association, 1: 55-59.
- Betance, L.; Peda, A.; Conan, A.; Ribeiro, J. 2017. Seroprevalence of leptospirosis in the feral cat population of St. Kitts. Journal of Animal Research and Technology, 59: 38-42.
- Brasil, W.L.; Parentoni, R.N.; Farias, R.C.; Nery, T.F.L.; Vasconcellos, A.S.; Azevedo, S.S. 2013. Anticorpos anti-Leptospira spp. em animais mantidos em cativeiro na Paraíba. Semina: Ciências Agrárias, 34: 2945-2950.
- Cubas, P.H.; Baptistotte, C. 2014. Chelonia (Tartaruga, Cágado, Jabuti). In: Cubas, S.C.; Silva, J.C.R.; Catão-Dias, J.L. (Ed.). Tratado de Animais Selvagens v.2. Roca, São Paulo, p.86-119.
- Dezzutto, D.; Barbero, R.; Canale, G.; Acutis, P.L.; Biolatti, C.; Dogliero, A.; et al 2017. Detection of Leptospira spp. in water turtle (Trachemys scripta) living in ponds of urban parks. Veterinary Sciences, 4: 1-5.
- Esteves, F.M.; Guerra-Neto, G.; Girio, R.J.S.; Silva-Vergara, M.L.; Carvalho, A.C.F.B. 2005. Detecção de anticorpos para Leptospira spp. em animais e funcionários do zoológico municipal de Uberaba, MG. Arquivos do Instituto Biológico, 72: 283-288.
- Faine, S.; Adler, B.; Bolin, C.; Perolat, P. 1999. Leptospira and Leptospirosis 2nd ed. Medisci, Melbourne, 353p.
- Ferrara, C.R.; Fagundes, C.K.; Morcatty, T.Q.; Vogt, R.C. 2017. Tartaruga-da-Amazônia, Podocnemis expansa (Schweigger 1812). In: Ferrara, C.R.; Fagundes, C.K.; Morcatty, T.Q.; Vogt, R.C. (Eds.). Quelônios Amazônicos: Guia de identificação e distribuição WCS, Manaus, p.130- 137.
- Fornazari, F.; Langoni, H.; Marson, P.M.; Nóbrega, D.B.; Texeira, C.R. 2018. Leptospira reservoirs among wildlife in Brazil: Beyond rodents. Acta Tropica, 178: 205-212.
- Glosser, J.W.; Sulzer, C.R.; Eberhardt, M.; Winkler, W.G. 1974. Cultural and serologic evidence of Leptospira interrogans serotype Tarassovi infection in turtles. Journal of Wildlife Diseases, 10: 429-435.
- Grimm, K.; Mitchell, M.A.; Thompson, D.; Maddox, C. 2015. Seroprevalence of Leptospira spp. in Blanding’s Turtles (Emydoidea blandingii) from DuPage County, Illinois USA. Journal of Herpetological Medicine and Surgery, 25: 28-32.
- Kmety, E.; Dikken, H. 1993. Classification of the Species Leptospira interrogans and History of its Serovars University Press, Groningen, 104p.
- Lindtner-Knific, R.; Vergles-Rataj, A.; Vlahović, K.; Zrimšek, P.; Dovč, A. 2013. Prevalence of antibodies against Leptospira sp. in snakes, lizards and turtles in Slovenia. Acta Veterinaria Scandinavica, 55: 65 (http://doi.org/10.1186/1751-0147-55-65).
» http://doi.org/10.1186/1751-0147-55-65 - Mahajan, S.; Chhabra, Daljeet. 2008. Leptospirosis: a re-emerging disease. Veterinary World, 1: 182-185.
- Oliveira, J.P.; Kawanami, A.E.; Silva, A.S.L.; Chung, D.G.; Werther, K. 2016. Detection of Leptospira spp. in wild Phrynops geoffroanus (Geoffroy’s side-necked turtle) in urban environment. Acta Tropica, 164: 165-168.
- Oliveira, V.S.; Arsky, M.L.N.S.; Caldas, E.P. 2013. Reservatórios animais de leptospirose: uma revisão bibliográfica. Revista Saúde (Santa Maria), 39: 9-20.
- Rajeev, S.; Conan, A.; Pratt, N.; Beierschmitt, A.; Palmour, R. 2017. High Leptospira seroprevalence in captive and wild-caught vervet monkeys (Chlorocebus sabeus) on the Caribbean island of Saint Kitts. Journal of Veterinary Diagnostic Investigation, 29: 930-934.
- Rocha, K.S.; Baia, I.W.M.; Monteiro, L.H.; Miranda, J.M.S.; Monteiro, T.R.M.; Silva, A.F.; Reis, T.A.; Ferreira, M.F.S.; Mesquita, E.Y.E.; Moraes, C.C.G. 2019. Identification of antibodies to Leptospira spp. in the spot-legged turtle (Rhinoclemmys punctularia) maintained in captivity. Semina: Ciências Agrárias , 40: 3763-3768.
- Rossetti, C.A.; Liem, M.; Samartino, L.E.; Hartskeerl, R.A. 2005. Buenos Aires, a new Leptospira serovar of serogroup Djasiman, isolated from an aborted dog fetus in Argentina. Veterinary Microbiology, 107: 241-248.
- Silva, C.S.; Gírio, R.J.S.; Guerra-Neto, G.; Brich, M.; Santana, L.A.S.; Amâncio, F.H.B.; Mariani, J.R.; Wessort, P.M.F. 2010. Anticorpos anti-Leptospira spp. em animais selvagens do zoológico municipal de Ribeirão Preto, Estado de São Paulo, Brasil. Brazilian Journal of Veterinary Research and Animal Science, 47: 237-242.
- Silva, E.F.; Seyffert, N.; Cerqueira, G.M. 2009. Serum antileptospiral agglutinins in freshwater turtles from Southern Brazil. Brazilian Journal of Microbiology, 40: 227-230.
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CITE AS:
Souza Rocha, K.; et al. 2020. Detection of anti-Leptospira spp. agglutinins in captive South American river turtles, Podocnemis expansa. Acta Amazonica (Epub Ahead of Print).
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Publication Dates
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Publication in this collection
18 May 2020 -
Date of issue
Apr-Jun 2020
History
-
Received
10 May 2019 -
Accepted
31 Dec 2019