制定监测奶牛牛奶中 H5N1 流感病毒的方法。

Elyse Stachler, Andreas Gnirke, Kyle McMahon, Michael Gomez, Liam Stenson, Charelisse Guevara-Reyes, Hannah Knoll, Toni Hill, Sellers Hill, Katelyn S Messer, Jon Arizti-Sanz, Fatinah Albeez, Elizabeth Curtis, Pedram Samani, Natalia Wewior, David H O'Connor, William Vuyk, Sophia Khoury, Matthew K Schnizlein, Nicole C Rockey, Zachariah Broemmel, Michael Mina, Lawrence C Madoff, Shirlee Wohl, Lorraine O'Connor, Catherine M Brown, Al Ozonoff, Daniel J Park, Bronwyn L MacInnis, Pardis C Sabeti
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引用次数: 0

摘要

高致病性禽流感菌株 H5N1 在美国奶牛中引发了多州疫情,自发病以来已蔓延至 15 个州,感染了数百个牛群。我们迅速开发并优化了基于 PCR 的检测方法和测序协议,以支持 H5N1 分子监测。我们使用来自 20 个州的 214 份零售牛奶进行方法开发,发现数字 PCR 的 H5N1 浓度与 qPCR 周期阈值 (Ct) 值密切相关,dPCR 的灵敏度更高。我们还发现,杂交选择后的元基因组测序最适合浓度较高的样本,而扩增子测序最适合浓度较低的样本。通过建立这些方法,我们能够支持建立一个全州范围的监控计划,每月检测马萨诸塞州内所有养牛场的散装牛奶样本,至今这些样本仍为阴性。本文介绍的方法、工作流程和建议为其他旨在开展 H5N1 监控工作的人员提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishing methods to monitor H5N1 influenza virus in dairy cattle milk.

Highly Pathogenic Avian Influenza strain H5N1 has caused a multi-state outbreak among US dairy cattle, spreading across 15 states and infecting hundreds of herds since its onset. We rapidly developed and optimized PCR-based detection assays and sequencing protocols to support H5N1 molecular surveillance. Using 214 retail milk from 20 states for methods development, we found that H5N1 concentrations by digital PCR strongly correlated with qPCR cycle threshold (Ct) values, with dPCR exhibiting greater sensitivity. We also found that metagenomic sequencing after hybrid selection was best for higher concentration samples while amplicon sequencing performs best for lower concentrations. By establishing these methods, we were able to support the creation of a statewide surveillance program to test bulk milk samples monthly from all cattle dairy farms within Massachusetts, which remain negative to date. The methods, workflow, and recommendations described here provide a framework for others aiming to conduct H5N1 surveillance efforts.

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