Southeast Poultry Research Laboratory, United States National Poultry Research Center, Agricultural Research Service, United States Department of Agriculture, Athens, Georgia, USA.
Department of Veterinary Medicine, Faculty of Animal Science and Food Engineering, University of São Paulo (FZEA-USP), Pirassununga, São Paulo, Brazil.
J Virol. 2021 Aug 25;95(18):e0095521. doi: 10.1128/JVI.00955-21.
Highly pathogenic avian influenza (HPAI) viruses from the H5Nx Goose/Guangdong/96 lineage continue to cause outbreaks in domestic and wild bird populations. Two distinct genetic groups of H5N8 HPAI viruses, hemagglutinin (HA) clades 2.3.4.4A and 2.3.4.4B, caused intercontinental outbreaks in 2014 to 2015 and 2016 to 2017, respectively. Experimental infections using viruses from these outbreaks demonstrated a marked difference in virulence in mallards, with the H5N8 virus from 2014 causing mild clinical disease and the 2016 H5N8 virus causing high mortality. To assess which gene segments are associated with enhanced virulence of H5N8 HPAI viruses in mallards, we generated reassortant viruses with 2014 and 2016 viruses. For single-segment reassortants in the genetic backbone of the 2016 virus, pathogenesis experiments in mallards revealed that morbidity and mortality were reduced for all eight single-segment reassortants compared to the parental 2016 virus, with significant reductions in mortality observed with the polymerase basic protein 2 (PB2), nucleoprotein (NP), and matrix (M) reassortants. No differences in morbidity and mortality were observed with reassortants that either have the polymerase complex segments or the HA and neuraminidase (NA) segments of the 2016 virus in the genetic backbone of the 2014 virus. assays showed that the NP and polymerase acidic (PA) segments of the 2014 virus lowered polymerase activity when combined with the polymerase complex segments of the 2016 virus. Furthermore, the M segment of the 2016 H5N8 virus was linked to filamentous virion morphology. Phylogenetic analyses demonstrated that gene segments related to the more virulent 2016 H5N8 virus have persisted in the contemporary H5Nx HPAI gene pool until 2020. Outbreaks of H5Nx HPAI viruses from the goose/Guangdong/96 lineage continue to occur in many countries and have resulted in substantial impact on wild birds and poultry. Epidemiological evidence has shown that wild waterfowl play a major role in the spread of these viruses. While HPAI virus infection in gallinaceous species causes high mortality, a wide range of disease outcomes has been observed in waterfowl species. In this study, we examined which gene segments contribute to severe disease in mallards infected with H5N8 HPAI viruses. No virus gene was solely responsible for attenuating the high virulence of a 2016 H5N8 virus, but the PB2, NP, and M segments significantly reduced mortality. The findings herein advance our knowledge on the pathobiology of avian influenza viruses in waterfowl and have potential implications on the ecology and epidemiology of H5Nx HPAI in wild bird populations.
高致病性禽流感(HPAI)病毒 H5Nx 鹅/广东/96 谱系继续在国内和野生鸟类种群中引发疫情。两种不同的 H5N8 HPAI 病毒血凝素(HA)进化枝 2.3.4.4A 和 2.3.4.4B,分别于 2014 年至 2015 年和 2016 年至 2017 年引发了洲际疫情。使用来自这些疫情的病毒进行的实验感染表明,在绿头鸭中,病毒的毒力存在明显差异,2014 年的 H5N8 病毒引起轻度临床疾病,而 2016 年的 H5N8 病毒引起高死亡率。为了评估哪些基因片段与 H5N8 HPAI 病毒在绿头鸭中的增强毒力有关,我们使用 2014 年和 2016 年的病毒生成了重组病毒。在 2016 年病毒的遗传背景下进行的单片段重组实验中,在绿头鸭中的发病机制实验表明,与亲本 2016 病毒相比,所有 8 种单片段重组病毒的发病率和死亡率均降低,聚合酶碱性蛋白 2(PB2)、核蛋白(NP)和基质(M)重组病毒的死亡率显著降低。与 2014 年病毒的聚合酶复合物片段或血凝素(HA)和神经氨酸酶(NA)片段在 2016 年病毒的遗传背景中具有相同的发病率和死亡率的重组病毒没有差异。酶联免疫吸附测定显示,当与 2016 年病毒的聚合酶复合物片段结合时,2014 年病毒的 NP 和聚合酶酸性(PA)片段降低了聚合酶活性。此外,2016 H5N8 病毒的 M 片段与丝状病毒形态有关。系统发育分析表明,与更具毒力的 2016 H5N8 病毒相关的基因片段在 2020 年之前一直存在于当代 H5Nx HPAI 基因库中。来自鹅/广东/96 谱系的 H5Nx HPAI 病毒的疫情继续在许多国家发生,并对野生鸟类和家禽造成了重大影响。流行病学证据表明,野生水禽在这些病毒的传播中发挥了主要作用。虽然 HPAI 病毒感染家禽物种会导致高死亡率,但在水禽物种中观察到广泛的疾病结果。在这项研究中,我们研究了哪些基因片段导致感染 H5N8 HPAI 病毒的绿头鸭发生严重疾病。没有任何病毒基因单独负责减弱 2016 H5N8 病毒的高毒力,但 PB2、NP 和 M 片段显著降低了死亡率。本研究结果提高了我们对水禽中禽流感病毒的病理生物学的认识,并对野生鸟类中 H5Nx HPAI 的生态学和流行病学具有潜在意义。