Bendall Emily E, Zhu Yuwei, Fitzsimmons William J, Rolfes Melissa, Mellis Alexandra, Halasa Natasha, Martin Emily T, Grijalva Carlos G, Talbot H Keipp, Lauring Adam S
Department of Microbiology & Immunology, University of Michigan, Ann Arbor, MI, USA.
Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
bioRxiv. 2024 Aug 19:2024.08.15.608152. doi: 10.1101/2024.08.15.608152.
While influenza A virus (IAV) antigenic drift has been documented globally, in experimental animal infections, and in immunocompromised hosts, positive selection has generally not been detected in acute infections. This is likely due to challenges in distinguishing selected rare mutations from sequencing error, a reliance on cross-sectional sampling, and/or the lack of formal tests of selection for individual sites. Here, we sequenced IAV populations from 346 serial, daily nasal swabs from 143 individuals collected over three influenza seasons in a household cohort. Viruses were sequenced in duplicate, and intrahost single nucleotide variants (iSNV) were identified at a 0.5% frequency threshold. Within-host populations were subject to purifying selection with >75% mutations present at <2% frequency. Children (0-5 years) had marginally higher within-host evolutionary rates than adolescents (6-18 years) and adults (>18 years, 4.4×10 vs. 9.42×10 and 3.45×10, p <0.001). Forty-five iSNV had evidence of parallel evolution, but were not overrepresented in HA and NA. Several increased from minority to consensus level, with strong linkage among iSNV across segments. A Wright Fisher Approximate Bayesian Computational model identified positive selection at 23/256 loci (9%) in A(H3N2) specimens and 19/176 loci (11%) in A(H1N1)pdm09 specimens, and these were infrequently found in circulation. Overall, we found that within-host IAV populations were subject to purifying selection and genetic drift, with only subtle differences across seasons, subtypes, and age strata. Positive selection was rare and inconsistently detected.
虽然甲型流感病毒(IAV)的抗原漂移在全球范围内、实验动物感染以及免疫功能低下的宿主中都有记录,但在急性感染中一般未检测到正向选择。这可能是由于难以将选定的罕见突变与测序错误区分开来、依赖横断面采样,和/或缺乏对单个位点的选择进行正式测试。在这里,我们对来自一个家庭队列中143名个体在三个流感季节收集的346份连续每日鼻拭子中的IAV群体进行了测序。病毒进行了重复测序,并以0.5%的频率阈值鉴定宿主内单核苷酸变异(iSNV)。宿主内群体受到纯化选择,超过75%的突变以低于2%的频率出现。儿童(0 - 5岁)的宿主内进化速率略高于青少年(6 - 18岁)和成年人(>18岁,分别为4.4×10、9.42×10和3.45×10,p<0.001)。45个iSNV有平行进化的证据,但在血凝素(HA)和神经氨酸酶(NA)中没有过度代表。有几个从少数水平增加到一致水平,各片段间的iSNV之间有很强的连锁关系。一个Wright Fisher近似贝叶斯计算模型在A(H3N2)标本的23/256个位点(9%)和A(H1N1)pdm09标本的19/176个位点(11%)中鉴定出正向选择,并且这些在流行中很少见。总体而言,我们发现宿主内IAV群体受到纯化选择和遗传漂移的影响,不同季节、亚型和年龄层之间只有细微差异。正向选择很少见且检测结果不一致。