Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa, USA.
Bioinformatics and Computational Biology Program, Iowa State University, Ames, Iowa, USA.
J Virol. 2024 Mar 19;98(3):e0170323. doi: 10.1128/jvi.01703-23. Epub 2024 Feb 14.
The increased detection of H3 C-IVA (1990.4.a) clade influenza A viruses (IAVs) in US swine in 2019 was associated with a reassortment event to acquire an H1N1pdm09 lineage nucleoprotein (pdmNP) gene, replacing a TRIG lineage NP (trigNP). We hypothesized that acquiring the pdmNP conferred a selective advantage over prior circulating H3 viruses with a trigNP. To investigate the role of NP reassortment in transmission, we identified two contemporary 1990.4.a representative strains (NC/19 and MN/18) with different evolutionary origins of the NP gene. A reverse genetics system was used to generate wild-type (wt) strains and swap the pdm and TRIG lineage NP genes, generating four viruses: wtNC/19-pdmNP, NC/19-trigNP, wtMN/18-trigNP, and MN/18-pdmNP. The pathogenicity and transmission of the four viruses were compared in pigs. All four viruses infected 10 primary pigs and transmitted to five indirect contact pigs per group. Pigs infected via contact with MN/18-pdmNP shed virus 2 days earlier than pigs infected with wtMN/18-trigNP. The inverse did not occur for wtNC/19-pdmNP and NC/19-trigNP. This suggests that pdmNP reassortment resulted in a combination of genes that improved transmission efficiency when paired with the 1990.4.a hemagglutinin (HA). This is likely a multigenic trait, as replacing the trigNP gene did not diminish the transmission of a wild-type IAV in swine. This study demonstrates how reassortment and evolutionary change of internal genes can result in more transmissible viruses that influence HA clade detection frequency. Thus, rapidly identifying novel reassortants paired with dominant hemagglutinin/neuraminidase may improve the prediction of strains to include in vaccines.IMPORTANCEInfluenza A viruses (IAVs) are composed of eight non-continuous gene segments that can reassort during coinfection of a host, creating new combinations. Some gene combinations may convey a selective advantage and be paired together preferentially. A reassortment event was detected in swine in the United States that involved the exchange of two lineages of nucleoprotein (NP) genes (trigNP to pdmNP) that became a predominant genotype detected in surveillance. Using a transmission study, we demonstrated that exchanging the trigNP for a pdmNP caused the virus to shed from the nose at higher levels and transmit to other pigs more rapidly. Replacing a pdmNP with a trigNP did not hinder transmission, suggesting that transmission efficiency depends on interactions between multiple genes. This demonstrates how reassortment alters IAV transmission and that reassortment events can provide an explanation for why genetically related viruses with different internal gene combinations experience rapid fluxes in detection frequency.
美国 2019 年猪群中 H3 C-IVA(1990.4.a)分支流感病毒(IAV)的检出率增加,与获得 H1N1pdm09 谱系核蛋白(pdmNP)基因的重配事件有关,取代了 TRIG 谱系 NP(trigNP)。我们假设获得 pdmNP 相对于具有 trigNP 的先前循环 H3 病毒具有选择性优势。为了研究 NP 重配在传播中的作用,我们鉴定了两个具有不同 NP 基因进化起源的当代 1990.4.a 代表株(NC/19 和 MN/18)。使用反向遗传学系统生成野生型(wt)株并交换 pdm 和 TRIG 谱系 NP 基因,生成四种病毒:wtNC/19-pdmNP、NC/19-trigNP、wtMN/18-trigNP 和 MN/18-pdmNP。比较了这四种病毒在猪中的致病性和传播性。四种病毒均感染了 10 头原发性猪,并将病毒传播给每组 5 头间接接触猪。与感染 wtMN/18-trigNP 的猪相比,感染 MN/18-pdmNP 的猪更早地开始从鼻子中排出病毒。对于 wtNC/19-pdmNP 和 NC/19-trigNP,情况并非如此。这表明 pdmNP 重配导致了一组基因的组合,当与 1990.4.a 血凝素(HA)结合时,提高了传播效率。这可能是一个多基因特征,因为用 trigNP 基因替换不会降低野生型 IAV 在猪中的传播能力。本研究表明,内部基因的重配和进化变化如何导致更具传染性的病毒,从而影响 HA 分支的检测频率。因此,快速识别与优势血凝素/神经氨酸酶配对的新型重组体可能会提高对包括疫苗在内的菌株的预测能力。
意义:流感 A 病毒(IAV)由八个非连续的基因片段组成,在宿主的共感染过程中可以重组,形成新的组合。一些基因组合可能具有选择性优势,并被优先组合在一起。在美国的猪群中检测到了一种重配事件,涉及核蛋白(NP)基因的两种谱系(trigNP 到 pdmNP)的交换,这种交换成为监测中检测到的主要基因型。使用传播研究,我们证明了交换 trigNP 为 pdmNP 会导致病毒从鼻子中以更高水平排出,并更快地传播给其他猪。用 trigNP 替换 pdmNP 不会阻碍传播,这表明传播效率取决于多个基因之间的相互作用。这表明重配如何改变 IAV 的传播,以及重配事件如何解释为什么具有不同内部基因组合的遗传相关病毒的检测频率会迅速变化。