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Arquivo Brasileiro de Medicina Veterinária e Zootecnia

versão impressa ISSN 0102-0935versão On-line ISSN 1678-4162

Arq. Bras. Med. Vet. Zootec. vol.61 no.3 Belo Horizonte jun. 2009

https://doi.org/10.1590/S0102-09352009000300033 

COMUNICAÇÃO COMMUNICATION

 

Serum survey for antibodies to coronavirus, herpesvirus, calicivirus, and parvovirus in domestics cats from Rio Grande do Sul, Brazil

 

Inquérito sorológico para anticorpos contra coronavírus, herpesvírus, calicivírus e parvovírus em gatos domésticos do Rio Grande do Sul, Brasil

 

 

J.M. Johann, C.F. Caetano; R. Hass; T.N. Guim; G. Fischer; G.D. Vargas; T. Vidor, S.O. Hübner*

Faculdade de Veterinária - UFPel Campus Universitário 96010-900 - Pelotas, RS

 

 


Keywords: cat, virusis, antibodies, immunity


RESUMO

A ocorrência da infecção por coronavírus felino (FCoV), herpesvírus felino tipo 1 (FHV-1), calicivírus felino (FCV) e parvovírus felino (FPV) foi investigada mediante a detecção de anticorpos no soro de 97 gatos domésticos de Pelotas, RS, pelo teste de soro-neutralização. Entre os animais estudados, 51 não eram vacinados, 11 haviam sido vacinados contra FHV-1, FCV e FPV com pelo menos uma dose, e 35 tinham histórico de vacinação desconhecido. Foram detectados anticorpos para o FCoV em 75,2% (73/97) dos gatos. Anticorpos contra o FHV-1 estavam presentes em 38,1% (37/97): 73% (8/11) dos gatos vacinados, 39,2% (20/51) dos não vacinados e 25,7% (9/35) dos gatos com histórico de vacinação desconhecido. Anticorpos para o FCV estavam presentes em 56,7% (55/97): 81,8% (9/11) dos gatos vacinados, 52,9% (27/51) dos não vacinados, e 54,3% (19/35) dos gatos com histórico de vacinação desconhecido. Para o FPV, havia anticorpos em 69,1% (67/97): 100% (11/11) dos vacinados, 66,6% (34/51) dos não vacinados e 62,8% (22/35) dos gatos com histórico de vacinação desconhecido. Os resultados sugerem alta exposição ao FCoV, FHV-1, FCV e FPV na população de gatos na área estudada.

Palavras-chave: gato, viroses, anticorpos, imunidade


 

 

In Brazil, data regarding the occurrence of feline infections by Feline coronavirus (FCoV), Feline herpesvirus (FHV-1), Feline calicivirus (FCV), and Feline parvovirus (FPV) are scarce (Weiblen et al., 1988; Oliveira et al., 2003; Ruthner et al., 2005), and to this moment there are no scientific reports made in the region of Pelotas, RS, Southern Brazil. FCoV is associated to the development of mild enteritis (Vennema et al., 1998; Hartmann, 2005) or, when FCoV mutants are originated, it can lead to the development of a feline infectious peritonitis (FIP), a progressive systemic disease with a wide spectrum of clinical signs and high mortality rate (Hartmann, 2005). FHV-1 and FCV are agents causing mainly upper respiratory tract diseases, but cats can be infected by these agents without showing clinical signs and become persistent carriers (Maggs et al., 1999; Radford et al., 2007). FPV is highly contagious, inducing an acute disease characterized by leukopenia, fever, depression, dehydration, diarrhea, and vomiting (McKnight et al., 2007).

The present study investigated the presence of antibodies against FCoV, FHV-1, FCV, and FPV in the serum samples of 97 domestic cats from Pelotas, Rio Grande do Sul, Southern Brazil. The antibody frequency was analyzed regarding information about age, gender, and habitat that would allow contact with other animals. Serum samples were collected from animals that would be submitted to elective surgeries at the Veterinary Hospital at the Universidade Federal de Pelotas, RS and in five private clinics from the region, from August 2005 to October 2006. Blood samples were collected by cephalic or jugular vein puncturing and sent to the virology and immunology laboratory of UFPel where they were centrifuged for serum separation. The sera were submitted to serum neutralization test (SN) according to Hohdatsu et al. (1999), with a few modifications. Serum serial dilutions from 1:4 to 1:256 were incubated with 100 TCID50 of the virus to which the presence of neutralizing antibodies was investigated. The viruses were supplied by the virology laboratory at the Universidade Federal de Santa Maria and Institute Desidério Finamor. The serum and virus mixture was incubated at 37ºC for 1h and then a suspension with approximately 30,000 CRFK cells containing 20% of bovine fetal serum was added to each well. The plates were incubated at 37ºC in atmosphere with 5% CO2 for three to seven days. The readings were made when the 100 TCID50 was observed in the control cells.

Samples were obtained from cats aging from two-month old to 17-year old. From 97 cats analyzed, 33 (34%) were male, 64 (66%) female, and 81 (83.5%) mixed breed. Regarding age, 28 animals (28.8%) were less than one-year old, 41 (42.2%) from one to five-year old; nine (9.3%) were older than five-year old, and 19 cats (19.6%) were of unknown age. Forty-five cats (46.4%) were housed of which 15 (33.3%) had limited access to the streets (they lived in apartments); 17 (17.5%) lived in the streets, and 35 (36.1%) had no information about habitat. There was previous vaccination history against FHV-1, FCV and FPV, with at least one dose, for 11 cats (11.3%).

The SN results indicated that the majority of the cats were exposed to multiple agents (71.1%), and only 15.5% of the samples were negative for all the viruses. Antibodies against FCoV were detected in 75.2% (73/97) of the cats. Such antibodies represent natural exposure to the virus, as in Brazil there is no vaccine against FCoV commercially available. This high level is comparable to the ones described in cats that live in places of relative high population density (Addie and Jarret, 2003) and it can be explained by the fact that most of the cats has frequent access to the streets and, therefore, probable contact with other cats. A large proportion of cats infected by FCoV can intermittently shed the virus in the feces and by this way the virus is kept in the environment allowing infection of susceptible animals (Foley et al., 1997). For FHV-1, there were antibodies in 38.1% (37/97) of the animals: 73% (8/11) of the vaccinated, 39.2% (20/51) of the unvaccinated, and 25.7% (9/35) of the cats with unknown vaccination history. Antibodies against FCV were present in 56.7% (55/97) of the animals: 81.8% (9/11) of the vaccinated cats, 52.9% (27/51) of the unvaccinated, and 54.3% (19/35) of the cats with unknown vaccination history. The levels found for FHV-1 and FCV are similar to the ones reported in other countries (Lappin et al., 2002) and it can be explained by the existence of carriers; FCV carriers continuously discharge the virus while FHV carriers discharge it intermittently and the virus is latent most of the time (Maggs et al., 1999). For FPV, there were antibodies in 69.1% (67/97) of the animals: 100% (11/11) of the vaccinated, 66.6% (34/51) of the unvaccinated, and 62.8% (22/35) of the cats with unknown vaccination history. FPV is usually shed in the feces for a short period of time after infection, but it remains viable in the environment for several months (Scott, 1980). Then, infection in most of the animals may have happened due to environmental exposure.

There was a higher frequency of seropositivity for all the viruses analyzed among adult animals (older than one-year) comparing to young animals (Table 1). This fact may be a result of behavior differences; usually adult animals have higher migratory activity which allows more contact with other animals. Similarly, there was a tendency to a higher number of seropositives among animals that live in places which allows free contact with other animals. There was no difference in seropositivity between males and females.

The results suggest high FCoV, FHV-1, FCV, and FPV exposure in the population of cats in the studied area. This indicates the need for further studies in order to evaluate the impact of the infections caused by these viruses in the cat population, as well as to propose and evaluate preventive measures.

 

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Recebido em 17 de outubro de 2008
Aceito em 19 de março de 2009

 

 

* Autor para correspondência (correspoonding autor)
E-mail: sohubner@yahoo.com.br

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