新型(d)PCR检测甲型流感病毒(H5Nx)分支2.3.4.4b的监测方法。

IF 7.8 2区 医学 Q1 INFECTIOUS DISEASES
Gerhard Buttinger, Mauro Petrillo, Viviana Valastro, Sabrina Marciano, Marika Crimaudo, Valeria D'Amico, Gabriele Leoni, Renaud Seigneuric, Valentina Paracchini, Piotr Robouch, Bénédicte Lambrecht, Bernd Manfred Gawlik, Calogero Terregino, Carolina Veneri, Giuseppina La Rosa, Elisabetta Suffredini, Maddalena Querci, Valentina Panzarin, Antonio Marchini
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引用次数: 0

摘要

自2024年3月以来,美国报告了由A(H5N1)进化枝2.3.4.4b病毒引起的高致病性禽流感(HPAI)病例,随后蔓延到鸟类和包括人类在内的其他哺乳动物物种。虽然尚未报告人与人之间的传播,但该病毒感染哺乳动物的能力和适应的可能性引起了公共卫生关注,有必要加强监测和防范。AIMWe旨在开发数字RT-PCR检测和定量生物和环境样本中的甲型H5N1流感病毒2.3.4.4b。方法建立了A(H5N1) 2.3.4.4b病毒基质蛋白(JRC-MP)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评估后,我们使用从受感染动物标本中分离的甲型H5N1流感病毒的RNA,在不同的目标和非目标分离物的实验室间实验中,以及在A(H5N1) 2.3.4.4b RNA阴性或加标的废水样品中评估了检测方法的性能。结果JRC-MP法可检测不同亚型和来源的甲型流感病毒,而JRC-HA法可特异性检测HPAI A(H5Nx) 2.3.4.4b株。分析显示高灵敏度,显示一致的结果在实验室间演习。他们还在废水样本中高精度地检测到目标rna,尽管存在背景成分,这支持了废水监测计划的潜在用途。结论结合“One Health”人畜共患禽流感监测策略,建议联合应用这两种方法快速、灵敏地检测生物和环境样本中的甲型H5Nx 2.3.4.4b流感病毒,以加强监测和疫情控制措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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

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.

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来源期刊
Eurosurveillance
Eurosurveillance INFECTIOUS DISEASES-
CiteScore
32.70
自引率
2.10%
发文量
430
审稿时长
3-8 weeks
期刊介绍: Eurosurveillance is a European peer-reviewed journal focusing on the epidemiology, surveillance, prevention, and control of communicable diseases relevant to Europe.It is a weekly online journal, with 50 issues per year published on Thursdays. The journal includes short rapid communications, in-depth research articles, surveillance reports, reviews, and perspective papers. It excels in timely publication of authoritative papers on ongoing outbreaks or other public health events. Under special circumstances when current events need to be urgently communicated to readers for rapid public health action, e-alerts can be released outside of the regular publishing schedule. Additionally, topical compilations and special issues may be provided in PDF format.
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