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用于甲型流感病毒(H5Nx)2.3.4.4b分支监测的新型数字PCR检测方法。

Novel (d)PCR assays for influenza A(H5Nx) viruses clade 2.3.4.4b surveillance.

作者信息

Buttinger Gerhard, Petrillo Mauro, Valastro Viviana, Marciano Sabrina, Crimaudo Marika, D'Amico Valeria, Leoni Gabriele, Seigneuric Renaud, Paracchini Valentina, Robouch Piotr, Lambrecht Bénédicte, Gawlik Bernd Manfred, Terregino Calogero, Veneri Carolina, La Rosa Giuseppina, Suffredini Elisabetta, Querci Maddalena, Panzarin Valentina, Marchini Antonio

机构信息

These authors contributed equally.

European Commission, Joint Research Centre (JRC), Geel, Belgium.

出版信息

Euro Surveill. 2025 Aug;30(33). doi: 10.2807/1560-7917.ES.2025.30.33.2500183.

Abstract

BACKGROUNDSince March 2024, cases of highly pathogenic avian influenza (HPAI) caused by A(H5N1) virus of clade 2.3.4.4b have been reported in dairy cattle in the United States, followed by spillover to avian and other mammalian species including humans. Although human-to-human transmission has not been reported, the virus's ability to infect mammals and potential of adaptation raise public health concerns, necessitating enhanced monitoring and preparedness.AIMWe aimed to develop digital RT-PCR assays to detect and quantify influenza A(H5N1) 2.3.4.4b viruses in biological and environmental samples.METHODSWe developed two digital RT-PCR assays targeting the matrix protein (JRC-MP) and haemagglutinin (JRC-HA) genes of A(H5N1) 2.3.4.4b viruses. After in silico assessment of inclusivity and exclusivity, we evaluated the assays' performance using RNAs from influenza A(H5N1) viruses isolated from infected animal specimens, in an inter-laboratory exercise with diverse target and non-target isolates, and on wastewater samples either negative or spiked with A(H5N1) 2.3.4.4b RNA.RESULTSThe JRC-MP assay detects influenza A viruses of different subtypes and origins, while the JRC-HA assay specifically detects HPAI A(H5Nx) 2.3.4.4b strains. The assays demonstrated high sensitivity, showing consistent results in the inter-laboratory exercise. They also detected target RNAs in wastewater samples with high accuracy, despite background components, supporting potential use in wastewater surveillance programmes.CONCLUSIONSAligned with One Health strategies for zoonotic avian influenza surveillance, we propose the combined use of these two assays for the rapid and sensitive detection of influenza A(H5Nx) 2.3.4.4b in biological and environmental samples to enhance monitoring and outbreak control measures.

摘要

背景

自2024年3月以来,美国已报告由2.3.4.4b分支的A(H5N1)病毒引起的高致病性禽流感(HPAI)病例,随后该病毒传播至禽类和包括人类在内的其他哺乳动物物种。尽管尚未报告人传人情况,但该病毒感染哺乳动物的能力及其适应潜力引发了公共卫生担忧,因此需要加强监测和防范。

目的

我们旨在开发数字逆转录聚合酶链反应(RT-PCR)检测方法,以检测和定量生物及环境样本中的甲型流感病毒A(H5N1) 2.3.4.4b。

方法

我们开发了两种针对A(H5N1) 2.3.4.4b病毒基质蛋白(JRC-MP)基因和血凝素(JRC-HA)基因的数字RT-PCR检测方法。在对包容性和排他性进行计算机模拟评估后,我们使用从感染动物标本中分离出的甲型流感病毒A(H5N1)的RNA,在一项涉及多种目标和非目标分离株的实验室间实验中,以及在未感染或添加了A(H5N1) 2.3.4.4b RNA的废水样本上,评估了这些检测方法的性能。

结果

JRC-MP检测方法可检测不同亚型和来源的甲型流感病毒,而JRC-HA检测方法可特异性检测高致病性禽流感A(H5Nx) 2.3.4.4b毒株。这些检测方法显示出高灵敏度,在实验室间实验中结果一致。尽管存在背景成分,它们仍能高精度地检测废水样本中的目标RNA,支持其在废水监测项目中的潜在应用。

结论

与用于人畜共患禽流感监测的“同一健康”策略相一致,我们建议联合使用这两种检测方法,以快速、灵敏地检测生物和环境样本中的甲型流感病毒A(H5Nx) 2.3.4.4b,从而加强监测和疫情控制措施。

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