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建立一种用于同时检测鹅星状病毒 1 型和 2 型的双重实时逆转录聚合酶链反应检测方法。

Development of a duplex real-time reverse transcription-polymerase chain reaction assay for the simultaneous detection of goose astrovirus genotypes 1 and 2.

机构信息

Jiangsu Agri-Animal Husbandry Vocational College, Jiangsu Key Laboratory for High-Tech Research and Development of Veterinary Biopharmaceuticals, Taizhou 225300, PR China.

College of Food Science and Engineering, Jiangsu Ocean University, Lianyungang 222005, PR China.

出版信息

J Virol Methods. 2022 Dec;310:114612. doi: 10.1016/j.jviromet.2022.114612. Epub 2022 Sep 6.

DOI:10.1016/j.jviromet.2022.114612
PMID:36084767
Abstract

Goose astrovirus (GAstV) is a highly infectious pathogen that causes gout in goslings (<15 old) with typical symptoms of white urate disposition on the surface of the visceral organs and articular cavity, and a high mortality rate up to 50 %. To establish a real-time reverse transcription-polymerase chain reaction (rRT-PCR) assay for the rapid detection of the two GastV genotypes(GAstV-1 and GAstV-2), two pairs of primers and a pair of matching TaqMan probes were designed based on conserved regions of the ORF1b gene. The established duplex rRT-PCR assay showed no cross-reactivity with 10 other common waterfowl pathogens. The minimum detection limit was 10 copies/reaction for both GAstV-1 and GAstV-2. To validate the assay, 36 cloacal swabs from experimentally infected goslings and 33 field clinical samples were tested. The assay results of the experimentally infected goslings matched the infection scheme. The positive rates of GAstV-1 and GAstV-2 in the field clinical samples were 36.36 % and 54.55 %, respectively, and the co-infection rate of the two viruses was 21.21 % based on the duplex rRT-PCR assay. In conclusion, the established assay represents a specific, sensitive, and convenient tool for detecting GAstV-1, GAstV-2, and their co-infections, and for conducting epidemiological surveys.

摘要

鹅星状病毒(GAstV)是一种高度传染性病原体,可引起 15 日龄以下雏鹅痛风,其特征为内脏器官和关节腔内有白色尿酸盐沉着,死亡率高达 50%。为建立一种快速检测两种 GAstV 基因型(GAstV-1 和 GAstV-2)的实时逆转录聚合酶链反应(rRT-PCR)检测方法,根据 ORF1b 基因保守区设计了两对引物和一对 TaqMan 探针。建立的双重 rRT-PCR 检测方法与其他 10 种常见水禽病原体无交叉反应。GAstV-1 和 GAstV-2 的最低检测限均为 10 拷贝/反应。为验证该检测方法,对 36 份人工感染雏鹅的泄殖腔拭子和 33 份临床样本进行了检测。人工感染雏鹅的检测结果与感染方案相吻合。临床样本中 GAstV-1 和 GAstV-2 的阳性率分别为 36.36%和 54.55%,根据双重 rRT-PCR 检测,两种病毒的混合感染率为 21.21%。总之,该方法具有特异性强、灵敏度高、操作简便等优点,可用于 GAstV-1、GAstV-2 及其混合感染的检测和流行病学调查。

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