Loureiro Carmen Luisa, Bonetti Valeria, Jaspe Rossana C, Sulbaran Yoneira, Alcazar Wilmer, Hernández Carlos, Rodríguez Nardraka, Rangel Hector R, Zambrano Jose Luis, Pujol Flor H
Laboratorio de Virologia Molecular, Centro de Microbiología y Biología Celular (CMBC), Instituto Venezolano de Investigaciones Científicas (IVIC), Caracas 1020, Venezuela.
Instituto Nacional de Salud Agricola Integral (INSAI), Maracay 2101, Venezuela.
Microorganisms. 2024 Dec 6;12(12):2519. doi: 10.3390/microorganisms12122519.
Avian influenza subtype H5N1 has caused outbreaks worldwide since 1996, with the emergence of the Guandong lineage in China. The current clade 2.3.4.4b has evolved from this lineage, with increased virulence and mass mortality events in birds and mammals. The objective of this study was the analysis of 17 viral genomes of H5N1 avian influenza isolated in Venezuela during the 2022-2023 outbreak. The eight viral genomic segments were amplified using universal primers and sequenced via next-generation sequencing. The sequences were analyzed to confirm the H5 hemagglutinin clade, identify possible genetic reassortments, and perform a phylogenetic and docking analysis of the viral isolates. The viruses found in Venezuela belonged, as expected, to clade 2.3.4.4b and formed a monophyletic clade with North American influenza viruses, with no evidence of further reassortment. The introduction of the virus in South America is associated with bird migration through the Atlantic (Venezuela), Atlantic/Mississippi (Choco, Colombia), and Pacific migratory flyways, with the emergence of several viral lineages. Several mutations were found in all segments of the genome, although none of the key mutations was involved in mammalian adaptation. Moreover, in silico structural analysis suggests, as expected, that the viral hemagglutinin maintained a predilection for avian α2,3-linked sialic acid. The unprecedented pathogenic outbreak of avian influenza disease in South America was associated with the circulation of three different lineages, which maintain a lower affinity for the mammalian receptor.
自1996年以来,H5N1亚型禽流感已在全球范围内引发疫情,中国出现了广东谱系。当前的2.3.4.4b分支就是从该谱系进化而来,在鸟类和哺乳动物中其毒力增强且出现了大规模死亡事件。本研究的目的是分析2022 - 2023年委内瑞拉禽流感疫情期间分离出的17个H5N1病毒基因组。使用通用引物扩增八个病毒基因组片段,并通过下一代测序进行测序。对序列进行分析以确认H5血凝素分支、识别可能的基因重配,并对病毒分离株进行系统发育和对接分析。不出所料,在委内瑞拉发现的病毒属于2.3.4.4b分支,与北美流感病毒形成一个单系分支,没有进一步重配的证据。该病毒在南美洲的引入与鸟类通过大西洋(委内瑞拉)、大西洋/密西西比河(哥伦比亚乔科省)和太平洋迁徙路线的迁徙有关,出现了几个病毒谱系。在基因组的所有片段中都发现了一些突变,尽管没有关键突变参与哺乳动物适应性。此外,计算机模拟结构分析表明,正如预期的那样,病毒血凝素对禽类α2,3 - 连接的唾液酸仍有偏好。南美洲前所未有的禽流感疾病致病性疫情与三种不同谱系的传播有关,这些谱系对哺乳动物受体的亲和力较低。