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基因组序列中血凝素裂解位点预测禽流感病毒的致病性表型:经统计学验证的数据有助于快速申报和减少对检测的依赖。

Genome sequences of haemagglutinin cleavage site predict the pathogenicity phenotype of avian influenza virus: statistically validated data for facilitating rapid declarations and reducing reliance on testing.

机构信息

College of Veterinary Medicine, Konkuk University, Seoul, Republic of Korea.

WOAH/FAO International Reference Laboratory for Avian Influenza National Veterinary Services Laboratories, Animal and Plant Health Inspection Service, US Department of Agriculture, Ames, IA, USA.

出版信息

Avian Pathol. 2024 Aug;53(4):242-246. doi: 10.1080/03079457.2024.2317430. Epub 2024 Feb 23.

DOI:10.1080/03079457.2024.2317430
PMID:38345041
Abstract

Based on the pathogenicity in chickens, most H1-H16 avian influenza viruses (AIV) cause mild diseases, whereas some of the H5 and H7 AI viruses cause severe, systemic disease. The number of basic amino acids in the haemagglutinin (HA) cleavage site of AIV plays a critical role in pathogenicity. As we gain a greater understanding of the molecular mechanisms of pathogenicity, genome sequencing of the HA0 cleavage site has assumed a greater role in assessment of the potential pathogenicity of H5 and H7 viruses. We validated the use of HA cleavage site motif analysis by comparing molecular pathotyping data against experimental (intravenous pathogenicity index [IVPI] and lethality) data for determination of both low pathogenicity and high pathogenicity AI virus declaration with the goal of expediting pathotype confirmation and further reducing the reliance on testing. Our data provide statistical support to the continued use of molecular determination of pathotype for AI viruses based on the HA cleavage site sequence in the absence of an study determination. This approach not only expedites the declaration process of highly pathogenic AIV (HPAIV) but also reduces the need for experimental testing of H5 and H7 viruses.

摘要

基于在鸡中的致病性,大多数 H1-H16 禽流感病毒(AIV)引起轻度疾病,而一些 H5 和 H7 AI 病毒引起严重的全身性疾病。AIV 的血凝素(HA)裂解位点中的碱性氨基酸数量在致病性方面起着关键作用。随着我们对致病性的分子机制有了更深入的了解,HA0 裂解位点的基因组测序在评估 H5 和 H7 病毒的潜在致病性方面发挥了更大的作用。我们通过将分子病理分型数据与实验(静脉致病性指数 [IVPI] 和致死率)数据进行比较,验证了 HA 裂解位点模式分析的用途,以确定低致病性和高致病性 AI 病毒的声明,目的是加快病理分型的确认,并进一步减少对 测试的依赖。我们的数据为在没有研究确定的情况下,基于 HA 裂解位点序列,继续使用分子确定 AI 病毒的病理分型提供了统计支持。这种方法不仅加快了高致病性禽流感病毒(HPAIV)的声明过程,而且减少了对 H5 和 H7 病毒的实验 测试的需求。

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Genome sequences of haemagglutinin cleavage site predict the pathogenicity phenotype of avian influenza virus: statistically validated data for facilitating rapid declarations and reducing reliance on testing.基因组序列中血凝素裂解位点预测禽流感病毒的致病性表型:经统计学验证的数据有助于快速申报和减少对检测的依赖。
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