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评估饲料原料作为禽流感病毒在饲料厂和家禽养殖场之间潜在载体的情况。

Evaluation of Feedstuffs as a Potential Carrier of Avian Influenza Virus between Feed Mills and Poultry Farms.

作者信息

Azeem Shahan, Sato Yuko, Guo Baoqing, Wolc Anna, Kim Hanjun, Hoang Hai, Bhandari Mahesh, Mayo Kathleen, Yuan Jian, Yoon Jihun, Gauger Phillip C, Yoon Kyoung-Jin

机构信息

Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA 50011, USA.

Institute of Microbiology, Faculty of Veterinary Science, University of Veterinary and Animal Sciences, Lahore 54000, Pakistan.

出版信息

Pathogens. 2022 Jul 2;11(7):755. doi: 10.3390/pathogens11070755.

Abstract

The present study was conducted to assess the potential vector role of feedstuffs for the area spreading of avian influenza virus (AIV). Firstly, feed samples were collected from commercial poultry facilities that experienced highly pathogenic avian influenza (H5N2) in 2014−2015 for AIV testing by a real-time RT−PCR specific for the viral matrix gene. Secondly, feed materials obtained from an AIV-negative farm were spiked with various concentrations of a low pathogenic AIV H5N2. Virus-spiked cell culture media were prepared in the same manner and used for comparison. The spiked feed and media samples were tested by a multiplex real-time RT−PCR ran in a quantitative manner, either immediately or after incubation at −20, 4, 22, and 37 °C for 24, 48, and 72 h. Some of the feedstuffs collected from the poultry facilities or feed mills were positive for AIV RNA but negative by the virus isolation (VI) test, while all the formaldehyde-treated feedstuffs were PCR-negative. In the spiked feeds, the AIV titer was 1−3 logs lower than that in the corresponding media, even when tested immediately after spiking, suggesting that feed might have a negative impact on the virus or PCR detection. The half-life of AIV RNA was shorter at a higher temperature. A significant decay in the viral RNA over time was noted at 37 °C (p < 0.05), suggesting that feedstuffs should be maintained in the cold chain when testing is desired. Furthermore, the thermal degradation of AIV suggests that the heat treatment of feeds could be an alternative to chemical treatment when contamination is suspected. Collectively, the study observations indicate that AIV survivability in feed is relatively low, thus rendering it a low risk.

摘要

本研究旨在评估饲料作为禽流感病毒(AIV)区域传播潜在载体的作用。首先,从2014 - 2015年经历过高致病性禽流感(H5N2)的商业家禽养殖场采集饲料样本,通过针对病毒基质基因的实时RT - PCR进行AIV检测。其次,从一个AIV阴性农场获取的饲料原料中添加不同浓度的低致病性AIV H5N2。以同样方式制备病毒添加的细胞培养基用于比较。对添加病毒的饲料和培养基样本立即进行检测,或者在−20、4、22和37 °C下孵育24、48和72小时后,通过定量多重实时RT - PCR进行检测。从家禽养殖场或饲料厂收集的一些饲料样本AIV RNA呈阳性,但病毒分离(VI)试验呈阴性,而所有经甲醛处理的饲料样本PCR检测均为阴性。在添加病毒的饲料中,即使在添加后立即检测,AIV滴度也比相应培养基中的滴度低1 - 3个对数,这表明饲料可能对病毒或PCR检测有负面影响。AIV RNA在较高温度下半衰期较短。在37 °C时,病毒RNA随时间有显著衰减(p < 0.05),这表明在需要检测时饲料应保存在冷链中。此外,AIV的热降解表明,当怀疑有污染时,饲料的热处理可能是化学处理的一种替代方法。总体而言,研究观察结果表明AIV在饲料中的生存能力相对较低,因此风险也较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8840/9321594/8ae0fc0f011d/pathogens-11-00755-g001.jpg

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