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小反刍兽疫病毒基因谱系的比较进化分析

Comparative evolutionary analyses of peste des petits ruminants virus genetic lineages.

作者信息

Courcelle Maxime, Salami Habib, Tounkara Kadidia, Lo Modou Moustapha, Ba Aminata, Diop Mariame, Niang Mamadou, Sidibe Cheick Abou Kounta, Sery Amadou, Dakouo Marthin, Kaba Lanceï, Sidime Youssouf, Keyra Mohamed, Diallo Alpha Oumar Sily, El Mamy Ahmed Bezeid, El Arbi Ahmed Salem, Barry Yahya, Isselmou Ekaterina, Habiboullah Habiboullah, Doumbia Baba, Gueya Mohamed Baba, Awuni Joseph, Odoom Theophilus, Ababio Patrick Tetteh, TawiahYingar Daniel Nana Yaw, Coste Caroline, Guendouz Samia, Kwiatek Olivier, Libeau Geneviève, Bataille Arnaud

机构信息

ASTRE, University of Montpellier, CIRAD, INRAE, Montpellier F-34398, France.

CIRAD, UMR ASTRE, Montpellier F-34398, France.

出版信息

Virus Evol. 2024 Mar 6;10(1):veae012. doi: 10.1093/ve/veae012. eCollection 2024.

Abstract

Peste des petits ruminants virus (PPRV) causes a highly infectious disease affecting mainly goats and sheep in large parts of Africa, Asia, and the Middle East and has an important impact on the global economy and food security. Full genome sequencing of PPRV strains has proved to be critical to increasing our understanding of PPR epidemiology and to inform the ongoing global efforts for its eradication. However, the number of full PPRV genomes published is still limited and with a heavy bias towards recent samples and genetic Lineage IV (LIV), which is only one of the four existing PPRV lineages. Here, we generated genome sequences for twenty-five recent (2010-6) and seven historical (1972-99) PPRV samples, focusing mainly on Lineage II (LII) in West Africa. This provided the first opportunity to compare the evolutionary pressures and history between the globally dominant PPRV genetic LIV and LII, which is endemic in West Africa. Phylogenomic analysis showed that the relationship between PPRV LII strains was complex and supported the extensive transboundary circulation of the virus within West Africa. In contrast, LIV sequences were clearly separated per region, with strains from West and Central Africa branched as a sister clade to all other LIV sequences, suggesting that this lineage also has an African origin. Estimates of the time to the most recent common ancestor place the divergence of modern LII and LIV strains in the 1960s-80s, suggesting that this period was particularly important for the diversification and spread of PPRV globally. Phylogenetic relationships among historical samples from LI, LII, and LIII and with more recent samples point towards a high genetic diversity for all these lineages in Africa until the 1970s-80s and possible bottleneck events shaping PPRV's evolution during this period. Molecular evolution analyses show that strains belonging to LII and LIV have evolved under different selection pressures. Differences in codon usage and adaptative selection pressures were observed in all viral genes between the two lineages. Our results confirm that comparative genomic analyses can provide new insights into PPRV's evolutionary history and molecular epidemiology. However, PPRV genome sequencing efforts must be ramped up to increase the resolution of such studies for their use in the development of efficient PPR control and surveillance strategies.

摘要

小反刍兽疫病毒(PPRV)引发一种高度传染性疾病,主要影响非洲、亚洲和中东大部分地区的山羊和绵羊,对全球经济和粮食安全产生重大影响。PPRV毒株的全基因组测序已证明对于增进我们对PPR流行病学的理解以及为当前全球根除该病毒的努力提供信息至关重要。然而,已发表的完整PPRV基因组数量仍然有限,且严重偏向近期样本和遗传谱系IV(LIV),而LIV只是现有的四个PPRV谱系之一。在此,我们生成了25个近期(2010 - 2016年)和7个历史(1972 - 1999年)PPRV样本的基因组序列,主要聚焦于西非的谱系II(LII)。这首次提供了比较全球占主导地位的PPRV遗传谱系LIV和西非地方流行的LII之间的进化压力和历史的机会。系统基因组分析表明,PPRV LII毒株之间的关系复杂,并支持该病毒在西非境内广泛的跨界传播。相比之下,LIV序列按区域明显分开,来自西非和中非的毒株作为所有其他LIV序列的姐妹分支分出,表明该谱系也起源于非洲。对最近共同祖先时间的估计表明,现代LII和LIV毒株在20世纪60年代至80年代发生分化,这表明该时期对PPRV在全球的多样化和传播尤为重要。来自谱系I、II和III的历史样本与更近样本之间的系统发育关系表明,直到20世纪70年代至80年代,非洲所有这些谱系都具有高度的遗传多样性,并且在此期间可能存在塑造PPRV进化的瓶颈事件。分子进化分析表明,属于LII和LIV的毒株在不同的选择压力下进化。在两个谱系的所有病毒基因中都观察到密码子使用和适应性选择压力的差异。我们的结果证实,比较基因组分析可为PPRV的进化历史和分子流行病学提供新的见解。然而,必须加大PPRV基因组测序力度,以提高此类研究的分辨率,用于制定有效的PPR控制和监测策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf88/10930206/c91881db8bae/veae012f1.jpg

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