Development of a PCR-based dot blot assay for the detection of fowl adenovirus

ABSTRACT: Group-I Fowl adenovirus (FAdV) is still widespread in China's chicken farms, leading to huge economic losses. The traditional PCR method, which can detect all serotypes at the same time, is not sensitive enough to obtain accurate results, especially in some samples containing only a l...

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Autores principales: Lidan Hou, Qi Su, Yawen Zhang, Dan Liu, Yaqing Mao, Peng Zhao
Formato: article
Lenguaje:EN
Publicado: Elsevier 2022
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PCR
Acceso en línea:https://doaj.org/article/efe1acc515c3439b900914e2b61a6153
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spelling oai:doaj.org-article:efe1acc515c3439b900914e2b61a61532021-11-24T04:23:09ZDevelopment of a PCR-based dot blot assay for the detection of fowl adenovirus0032-579110.1016/j.psj.2021.101540https://doaj.org/article/efe1acc515c3439b900914e2b61a61532022-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0032579121005629https://doaj.org/toc/0032-5791ABSTRACT: Group-I Fowl adenovirus (FAdV) is still widespread in China's chicken farms, leading to huge economic losses. The traditional PCR method, which can detect all serotypes at the same time, is not sensitive enough to obtain accurate results, especially in some samples containing only a low titer of virus, such as contaminated live vaccine. In order to solve this problem, this study developed a dot blot assay based on the above PCR method. A total of 6 probes targeting the conserved region of FAdV were designed and systematically optimized through sensitivity, accuracy, and stability analyses. Results showed that it is not only suitable for 12 serotypes, but also effectively improve the sensitivity, which increased more than 100 times in comparison with PCR assay. Moreover, this sensitivity was increased 100 times when detecting contaminated live vaccine samples, showing the great prospect of this method in daily monitoring.Lidan HouQi SuYawen ZhangDan LiuYaqing MaoPeng ZhaoElsevierarticledot blotfowl adenovirusdetectionPCRserotypesAnimal cultureSF1-1100ENPoultry Science, Vol 101, Iss 1, Pp 101540- (2022)
institution DOAJ
collection DOAJ
language EN
topic dot blot
fowl adenovirus
detection
PCR
serotypes
Animal culture
SF1-1100
spellingShingle dot blot
fowl adenovirus
detection
PCR
serotypes
Animal culture
SF1-1100
Lidan Hou
Qi Su
Yawen Zhang
Dan Liu
Yaqing Mao
Peng Zhao
Development of a PCR-based dot blot assay for the detection of fowl adenovirus
description ABSTRACT: Group-I Fowl adenovirus (FAdV) is still widespread in China's chicken farms, leading to huge economic losses. The traditional PCR method, which can detect all serotypes at the same time, is not sensitive enough to obtain accurate results, especially in some samples containing only a low titer of virus, such as contaminated live vaccine. In order to solve this problem, this study developed a dot blot assay based on the above PCR method. A total of 6 probes targeting the conserved region of FAdV were designed and systematically optimized through sensitivity, accuracy, and stability analyses. Results showed that it is not only suitable for 12 serotypes, but also effectively improve the sensitivity, which increased more than 100 times in comparison with PCR assay. Moreover, this sensitivity was increased 100 times when detecting contaminated live vaccine samples, showing the great prospect of this method in daily monitoring.
format article
author Lidan Hou
Qi Su
Yawen Zhang
Dan Liu
Yaqing Mao
Peng Zhao
author_facet Lidan Hou
Qi Su
Yawen Zhang
Dan Liu
Yaqing Mao
Peng Zhao
author_sort Lidan Hou
title Development of a PCR-based dot blot assay for the detection of fowl adenovirus
title_short Development of a PCR-based dot blot assay for the detection of fowl adenovirus
title_full Development of a PCR-based dot blot assay for the detection of fowl adenovirus
title_fullStr Development of a PCR-based dot blot assay for the detection of fowl adenovirus
title_full_unstemmed Development of a PCR-based dot blot assay for the detection of fowl adenovirus
title_sort development of a pcr-based dot blot assay for the detection of fowl adenovirus
publisher Elsevier
publishDate 2022
url https://doaj.org/article/efe1acc515c3439b900914e2b61a6153
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AT danliu developmentofapcrbaseddotblotassayforthedetectionoffowladenovirus
AT yaqingmao developmentofapcrbaseddotblotassayforthedetectionoffowladenovirus
AT pengzhao developmentofapcrbaseddotblotassayforthedetectionoffowladenovirus
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