Warianty tytułu
Języki publikacji
Abstrakty
The aim of the study was to develop and optimise a single PCR and duplex PCR for the detection and differentiation of avian adenovirus serotypes 1 and 5 in poultry. The methods were based on sequence of hexon gene of the serotypes. The PCR and duplex PCR DNA products were 227 pb and 178 bp for serotypes 1 and 5, respectively, and were highly specific. The duplex-PCR method was found to be a highly specific, sensitive, and efficient rapid tool for the detection of serotypes 1 and 5 of adenoviruses, which could be detected in one reaction mixture. During this study, 30 of the isolates obtained from internal organs of healthy birds contained both serotypes of the adenovirus. In the case of six isolates, both serotypes were detected in one bird.
Wydawca
Rocznik
Tom
Numer
Opis fizyczny
p.451-455,fig.,ref.
Twórcy
autor
- Department of Poultry Viral Diseases, National Veterinary Research Institute, 24-100 Pulawy, Poland
autor
autor
Bibliografia
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- 4. Geanesh K., Suryanarayana V.V., Raghavan R.: Detection of fowl adenovirus associated with hydropericardium hepatitis syndrome by polymerase chain reaction. Vet Res Commun 2002, 26, 73-80.
- 5. Hess M.: Detection and differentiation of avian adenoviruses: a review. Avian Pathol 2000, 29, 195-206.
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- 13. Payet V., Arnauld C., Picault C.J.P., Jestin A., Langlois P.: Transcriptional organization of the avian adenovirus CELO. J Virol 1998, 72, 9278-9285.
- 14. Okuda Y., Ono M., Shibata I., Sato S., Akashi H.: Comparison of the polymerase chain reaction restriction fragment length polymorphism pattern of the fiber gene and pathogenicity of serotype-1 fowl adenovirus isolates from gizzard erosions and from feces of clinically healthy chickens in Japan. J Vet Diagn Invest 2006, 18, 162-167.
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- 16. Romanowa N., Corredor J.C., Nagy E.: Detection and quantification of fowl adenovirus genome by a real-time PCR assay. J Virol Methods 2009, 159, 58-63.
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Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
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