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在埃及共同传播的潜在人畜共患禽流感病毒H5N1和H9N2的进化轨迹及诊断挑战

Evolutionary trajectories and diagnostic challenges of potentially zoonotic avian influenza viruses H5N1 and H9N2 co-circulating in Egypt.

作者信息

Naguib Mahmoud M, Arafa Abdel-Satar A, El-Kady Magdy F, Selim Abdullah A, Gunalan Vithiagaran, Maurer-Stroh Sebastian, Goller Katja V, Hassan Mohamed K, Beer Martin, Abdelwhab E M, Harder Timm C

机构信息

Federal Research Institute for Animal Health, Friedrich-Loeffler-Institut, Suedufer 10, 17493 Greifswald-Insel Riems, Germany; National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Dokki, P.O. Box 246, Giza 12618, Egypt.

National Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Dokki, P.O. Box 246, Giza 12618, Egypt.

出版信息

Infect Genet Evol. 2015 Aug;34:278-91. doi: 10.1016/j.meegid.2015.06.004. Epub 2015 Jun 3.

Abstract

In Egypt, since 2006, descendants of the highly pathogenic avian influenza virus (HP AIV) H5N1 of clade 2.2 continue to cause sharp losses in poultry production and seriously threaten public health. Potentially zoonotic H9N2 viruses established an endemic status in poultry in Egypt as well and co-circulate with HP AIV H5N1 rising concerns of reassortments between H9N2 and H5N1 viruses along with an increase of mixed infections of poultry. Nucleotide sequences of whole genomes of 15 different isolates (H5N1: 7; H9N2: 8), and of the hemagglutinin (HA) and neuraminidase (NA) encoding segments of nine further clinical samples (H5N1: 2; H9N2: 7) from 2013 and 2014 were generated and analysed. The HA of H5N1 viruses clustered with clade 2.2.1 while the H9 HA formed three distinguishable subgroups within cluster B viruses. BEAST analysis revealed that H9N2 viruses are likely present in Egypt since 2009. Several previously undescribed substituting mutations putatively associated with host tropism and virulence modulation were detected in different proteins of the analysed H9N2 and H5N1 viruses. Reassortment between HP AIV H5N1 and H9N2 is anticipated in Egypt, and timely detection of such events is of public health concern. As a rapid tool for detection of such reassortants discriminative SYBR-Green reverse transcription real-time PCR assays (SG-RT-qPCR), targeting the internal genes of the Egyptian H5N1 and H9N2 viruses were developed for the rapid screening of viral RNAs from both virus isolates and clinical samples. However, in accordance to Sanger sequencing, no reassortants were found by SG-RT-qPCR. Nevertheless, the complex epidemiology of avian influenza in poultry in Egypt will require sustained close observation. Further development and continuing adaptation of rapid and cost-effective screening assays such as the SG-RT-qPCR protocol developed here are at the basis of efforts for improvement the currently critical situation.

摘要

在埃及,自2006年以来,2.2分支的高致病性禽流感病毒(HP AIV)H5N1的后代继续给家禽生产造成巨大损失,并严重威胁公众健康。具有潜在人畜共患病传播能力的H9N2病毒在埃及的家禽中也呈地方流行状态,并与HP AIV H5N1共同传播,这增加了人们对H9N2和H5N1病毒之间重配以及家禽混合感染增加的担忧。对15个不同分离株(H5N1:7个;H9N2:8个)的全基因组,以及另外9个2013年和2014年临床样本(H5N1:2个;H9N2:7个)的血凝素(HA)和神经氨酸酶(NA)编码片段的核苷酸序列进行了测定和分析。H5N1病毒的HA与2.2.1分支聚类,而H9 HA在B组病毒中形成了三个可区分的亚组。贝叶斯进化分析显示,H9N2病毒自2009年起可能已在埃及存在。在分析的H9N2和H5N1病毒的不同蛋白中检测到了几种先前未描述的、可能与宿主嗜性和毒力调节相关的替代突变。预计在埃及HP AIV H5N1和H9N2之间会发生重配,及时检测此类事件关乎公众健康。作为检测此类重配体的快速工具,开发了针对埃及H5N1和H9N2病毒内部基因的鉴别性SYBR-绿荧光逆转录实时PCR检测方法(SG-RT-qPCR),用于从病毒分离株和临床样本中快速筛选病毒RNA。然而,根据桑格测序法,SG-RT-qPCR未发现重配体。尽管如此,埃及家禽中禽流感复杂的流行病学情况仍需要持续密切观察。进一步开发并持续改进如本文所开发的SG-RT-qPCR方案这样快速且经济高效的筛选检测方法,是改善当前危急状况工作的基础。

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