1979
DOI: 10.1007/bf01348032
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Virus isolation and serum antibody responses after infection of cats with transmissible gastroenteritis virus

Abstract: Transmissible gastroenteritis virus was administered orally to cats. No clinical disease resulted but infectious virus was isolated from faeces for up to 22 days after infection and serum antibody was detected by neutralisation and immunofluorescence tests.

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Cited by 30 publications
(22 citation statements)
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“…Finally, cats can also be infected with heterologous coronaviruses from other species. Cats which were infected experimentally with TGEV shed the virus in their feces and mounted homologous and heterologous humoral immune responses (Reynolds and Garwes, 1979 ). Conversely, pigs infected orally with virulent FIPV demonstrated clinical signs, histologic lesions, and coronaviral antigen localization typical of TGEV infection (Woods, et al, 1981 ).…”
Section: Feline Coronavirusesmentioning
confidence: 99%
“…Finally, cats can also be infected with heterologous coronaviruses from other species. Cats which were infected experimentally with TGEV shed the virus in their feces and mounted homologous and heterologous humoral immune responses (Reynolds and Garwes, 1979 ). Conversely, pigs infected orally with virulent FIPV demonstrated clinical signs, histologic lesions, and coronaviral antigen localization typical of TGEV infection (Woods, et al, 1981 ).…”
Section: Feline Coronavirusesmentioning
confidence: 99%
“…This has been reinforced by observations that two-way cross-species infections with coronaviruses can occur naturally and experimentally among dogs, cats, and pigs (Reynolds and Gawes 1979;Woods et al 1981). Mice are not likely to be natural hosts for other coronaviruses.…”
Section: E Host Rangementioning
confidence: 97%
“…The traditional detection methods including virus isolation, virus immunodiagnostic assays, and PCR tests have shortcomings such as precise instruments requirement, demand of elaborate result analysis, high cost, and long detection time, which prevent these methods from being widely used (Reynolds and Garwes 1979 ;Rodak et al 2005 ;Denac et al 1997 ;Paton et al 1997 ). TGEV can be detected by using loop-mediated isothermal amplifi cation with the detection limit of about 10 pg RNA which is ten times more sensitive than that of PCR and having no cross-reaction with other viruses and found that the most conserved fragment of 187 bp was found in the nucleocapsid protein gene which showed highly homology among different TGEV strains/isolates (more than 97 %) and low homology among other similar viruses (less than 52.5 %).…”
Section: Other Animal Virusesmentioning
confidence: 99%