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Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR

We have developed a polymerase chain reaction (PCR) assay to facilitate detection of the major disease-associated serotypes of fowl adenovirus (FAdV) including serotypes 1, 2, 4, 8a and 8b; primers were designed based on serotype-specific sequences of the hexon gene. We tested field isolates from ch...

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Autores principales: MASE, Masaji, HIRAMATSU, Kanae, NISHIJIMA, Noriko, ISEKI, Hiroshi, WATANABE, Satoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870399/
https://www.ncbi.nlm.nih.gov/pubmed/33311002
http://dx.doi.org/10.1292/jvms.20-0400
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author MASE, Masaji
HIRAMATSU, Kanae
NISHIJIMA, Noriko
ISEKI, Hiroshi
WATANABE, Satoko
author_facet MASE, Masaji
HIRAMATSU, Kanae
NISHIJIMA, Noriko
ISEKI, Hiroshi
WATANABE, Satoko
author_sort MASE, Masaji
collection PubMed
description We have developed a polymerase chain reaction (PCR) assay to facilitate detection of the major disease-associated serotypes of fowl adenovirus (FAdV) including serotypes 1, 2, 4, 8a and 8b; primers were designed based on serotype-specific sequences of the hexon gene. We tested field isolates from chickens diagnosed with inclusion body hepatitis, gizzard erosion and hydropericardium syndrome together with reference FAdV strains characterized in Japan. We found that the primers were serotype specific; appropriate amplification of serotype-specific hexon genes was confirmed by sequence analysis of the PCR products. This PCR assay will be useful for detection of FAdV and for differentiation between disease-associated serotypes.
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spelling pubmed-78703992021-02-11 Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR MASE, Masaji HIRAMATSU, Kanae NISHIJIMA, Noriko ISEKI, Hiroshi WATANABE, Satoko J Vet Med Sci Avian Pathology We have developed a polymerase chain reaction (PCR) assay to facilitate detection of the major disease-associated serotypes of fowl adenovirus (FAdV) including serotypes 1, 2, 4, 8a and 8b; primers were designed based on serotype-specific sequences of the hexon gene. We tested field isolates from chickens diagnosed with inclusion body hepatitis, gizzard erosion and hydropericardium syndrome together with reference FAdV strains characterized in Japan. We found that the primers were serotype specific; appropriate amplification of serotype-specific hexon genes was confirmed by sequence analysis of the PCR products. This PCR assay will be useful for detection of FAdV and for differentiation between disease-associated serotypes. The Japanese Society of Veterinary Science 2020-12-14 2021-01 /pmc/articles/PMC7870399/ /pubmed/33311002 http://dx.doi.org/10.1292/jvms.20-0400 Text en ©2021 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Avian Pathology
MASE, Masaji
HIRAMATSU, Kanae
NISHIJIMA, Noriko
ISEKI, Hiroshi
WATANABE, Satoko
Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title_full Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title_fullStr Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title_full_unstemmed Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title_short Identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by PCR
title_sort identification of specific serotypes of fowl adenoviruses isolated from diseased chickens by pcr
topic Avian Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870399/
https://www.ncbi.nlm.nih.gov/pubmed/33311002
http://dx.doi.org/10.1292/jvms.20-0400
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