Laboratory of Populations, Rockefeller University, New York, New York, United States of America.
PLoS One. 2010 Jan 1;5(1):e8544. doi: 10.1371/journal.pone.0008544.
Long-term influenza evolution has been well studied, but the patterns of sequence diversity within seasons are less clear. H3N2 influenza genomes sampled from New York State over ten years indicated intraseasonal changes in evolutionary dynamics. Using the mean Hamming distance of a set of amino acid or nucleotide sequences as an indicator of its diversity, we found that influenza sequence diversity was significantly higher during the early epidemic period than later in the influenza season. Diversity was lowest during the peak of the epidemic, most likely due to the high prevalence of a single dominant amino acid sequence or very few dominant sequences during the peak epidemic period, corresponding with rapid expansion of the viral population. The frequency and duration of dominant sequences varied by influenza protein, but all proteins had an abundance of one distinct sequence during the peak epidemic period. In New York State from 1995 to 2005, high sequence diversity during the early epidemic suggested that seasonal antigenic drift could have occurred primarily in this period, followed by a clonal expansion of typically one clade during the peak of the epidemic, possibly indicating a shift to neutral drift or purifying selection.
长期以来,流感的进化一直受到广泛研究,但季节内序列多样性的模式仍不太清楚。对过去十年中在纽约州采集的 H3N2 流感基因组进行研究表明,季节性流感的进化动态会发生变化。我们使用一组氨基酸或核苷酸序列的平均汉明距离作为其多样性的指标,发现流感序列的多样性在流行早期显著高于流感季节后期。在流行高峰期多样性最低,这很可能是由于在流行高峰期存在单一主导氨基酸序列或非常少数的主导序列,这与病毒群体的快速扩张相对应。主导序列的频率和持续时间因流感蛋白而异,但在流行高峰期所有蛋白都有一个独特序列的大量存在。在 1995 年至 2005 年的纽约州,流行早期的高序列多样性表明,季节性抗原漂移可能主要发生在这一时期,随后在流行高峰期会出现一个典型的单系克隆扩张,这可能表明向中性漂移或纯化选择的转变。