Exotic and Emerging Avian Viral Diseases Research Unit, Southeast Poultry Research Laboratory, U.S. National Poultry Research Center, Agricultural Research Service, U.S. Department of Agriculture, Athens, Georgia, United States of America.
Department of Pathobiology & Veterinary Science, University of Connecticut, Storrs, Mansfield, Connecticut, United States of America.
PLoS One. 2019 Sep 12;14(9):e0222457. doi: 10.1371/journal.pone.0222457. eCollection 2019.
Highly pathogenic avian influenza (HPAI) virus subtype H7N3 has been circulating in poultry in Mexico since 2012 and vaccination has been used to control the disease. In this study, eight Mexican H7N3 HPAI viruses from 2015-2017 were isolated and fully sequenced. No evidence of reassortment was detected with other avian influenza (AI) viruses, but phylogenetic analyses show divergence of all eight gene segments into three genetic clusters by 2015, with 94.94 to 98.78 percent nucleotide homology of the HA genes when compared to the index virus from 2012. The HA protein of viruses from each cluster showed a different number of basic amino acids (n = 5-7) in the cleavage site, and six different patterns at the predicted N-glycosylation sites. Comparison of the sequences of the Mexican lineage H7N3 HPAI viruses and American ancestral wild bird AI viruses to characterize the virus evolutionary dynamics showed that the nucleotide substitution rates in PB2, PB1, PA, HA, NP, and NS genes greatly increased once the virus was introduced into poultry. The global nonsynonymous and synonymous ratios imply strong purifying selection driving the evolution of the virus. Forty-nine positively selected sites out of 171 nonsynonymous mutations were identified in the Mexican H7N3 HPAI viruses, including 7 amino acid changes observed in higher proportion in North American poultry origin AI viruses isolates than in wild bird-origin viruses. Continuous monitoring and molecular characterization of the H7N3 HPAI virus is important for better understanding of the virus evolutionary dynamics and further improving control measures including vaccination.
高致病性禽流感(HPAI)病毒 H7N3 亚型自 2012 年以来一直在墨西哥的家禽中传播,并且已被用于控制该疾病的疫苗接种。在这项研究中,从 2015 年至 2017 年分离并完全测序了 8 株来自墨西哥的 H7N3 HPAI 病毒。未发现与其他禽流感(AI)病毒发生重配的证据,但系统发育分析显示,到 2015 年,所有 8 个基因片段均分为三个遗传簇,与 2012 年的索引病毒相比,HA 基因的核苷酸同源性为 94.94 至 98.78%。每个簇的病毒的 HA 蛋白在裂解位点具有不同数量的碱性氨基酸(n = 5-7),并且在预测的 N-糖基化位点有六种不同的模式。比较墨西哥系 H7N3 HPAI 病毒和美洲祖野生鸟类 AI 病毒的序列以表征病毒进化动态表明,一旦病毒引入家禽,PB2,PB1,PA,HA,NP 和 NS 基因中的核苷酸取代率大大增加。全球非同义与同义比率表明,强烈的纯化选择驱动了病毒的进化。在墨西哥 H7N3 HPAI 病毒中,在 171 个非同义突变中有 49 个被鉴定为阳性选择位点,包括在北美的家禽起源 AI 病毒分离物中观察到的 7 个氨基酸变化比在野鸟起源病毒中观察到的比例更高。持续监测和分子特征分析 H7N3 HPAI 病毒对于更好地了解病毒进化动态以及进一步改进包括疫苗接种在内的控制措施非常重要。