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英国高效且信息量丰富的实验室检测技术,助力快速确认 H5N1(2.3.4.4 分支)高致病性禽流感疫情。

Efficient and Informative Laboratory Testing for Rapid Confirmation of H5N1 (Clade 2.3.4.4) High-Pathogenicity Avian Influenza Outbreaks in the United Kingdom.

机构信息

Virology Department, Animal and Plant Health Agency (APHA-Weybridge), Woodham Lane, Addlestone KT15 3NB, UK.

出版信息

Viruses. 2023 Jun 9;15(6):1344. doi: 10.3390/v15061344.

Abstract

During the early stages of the UK 2021-2022 H5N1 high-pathogenicity avian influenza virus (HPAIV) epizootic in commercial poultry, 12 infected premises (IPs) were confirmed by four real-time reverse-transcription-polymerase chain reaction (RRT)-PCRs, which identified the viral subtype and pathotype. An assessment was undertaken to evaluate whether a large sample throughput would challenge laboratory capacity during an exceptionally large epizootic; hence, assay performance across our test portfolio was investigated. Statistical analysis of RRT-PCR swab testing supported it to be focused on a three-test approach, featuring the matrix (M)-gene, H5 HPAIV-specific (H5-HP) and N1 RRT-PCRs, which was successfully assessed at 29 subsequent commercial IPs. The absence of nucleotide mismatches in the primer/probe binding regions for the M-gene and limited mismatches for the H5-HP RRT-PCR underlined their high sensitivity. Although less sensitive, the N1 RRT-PCR remained effective at flock level. The analyses also guided successful surveillance testing of apparently healthy commercial ducks from at-risk premises, with pools of five oropharyngeal swabs tested by the H5-HP RRT-PCR to exclude evidence of infection. Serological testing at anseriform H5N1 HPAIV outbreaks, together with quantitative comparisons of oropharyngeal and cloacal shedding, provided epidemiological information concerning the chronology of initial H5N1 HPAIV incursion and onward spread within an IP.

摘要

在英国 2021-2022 年高致病性 H5N1 禽流感病毒(HPAIV)在商业家禽中爆发的早期阶段,通过四次实时逆转录聚合酶链反应(RRT-PCR)确认了 12 个感染场(IP),该检测方法鉴定了病毒亚型和病原体类型。为评估在异常大的疫情爆发期间大量样本是否会对实验室能力构成挑战,对我们的测试组合的性能进行了评估。RRT-PCR 拭子检测的统计分析支持将其重点放在三测试方法上,该方法具有基质(M)基因、H5 HPAIV 特异性(H5-HP)和 N1 RRT-PCR,该方法在随后的 29 个商业 IP 中成功进行了评估。M 基因的引物/探针结合区域中不存在核苷酸错配,H5-HP RRT-PCR 的错配有限,这突出了它们的高灵敏度。尽管灵敏度较低,但 N1 RRT-PCR 在禽群水平上仍然有效。这些分析还指导了对来自高危场所的商业鸭进行了明显健康的监测性测试,通过 H5-HP RRT-PCR 对五个咽拭子的混合液进行了测试,以排除感染的证据。在发生 H5N1 HPAIV 疫情时进行血清学检测,并对咽拭子和泄殖腔拭子的定量比较,为初始 H5N1 HPAIV 入侵以及在 IP 内的传播提供了有关时间顺序的流行病学信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3091/10304448/93c876b94993/viruses-15-01344-g001.jpg

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