FDA Center for Biologics Evaluation and Research, Silver Spring, MD, United States of America.
Movement Disorders Institute and Department of Neurology, Sheba Medical Center, Tel Hashomer; and Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
PLoS Pathog. 2018 Mar 19;14(3):e1006943. doi: 10.1371/journal.ppat.1006943. eCollection 2018 Mar.
Deep sequencing was used to determine complete nucleotide sequences of echovirus 11 (EV11) strains isolated from a chronically infected patient with CVID as well as from cases of acute enterovirus infection. Phylogenetic analysis showed that EV11 strains that circulated in Israel in 1980-90s could be divided into four clades. EV11 strains isolated from a chronically infected individual belonged to one of the four clades and over a period of 4 years accumulated mutations at a relatively constant rate. Extrapolation of mutations accumulation curve into the past suggested that the individual was infected with circulating EV11 in the first half of 1990s. Genomic regions coding for individual viral proteins did not appear to be under strong selective pressure except for protease 3C that was remarkably conserved. This may suggest its important role in maintaining persistent infection.
深度测序用于确定从一名慢性 CVID 患者和急性肠道病毒感染病例中分离出的肠道病毒 11 型(EV11)菌株的完整核苷酸序列。系统进化分析显示,1980-90 年代在以色列流行的 EV11 株可分为四个分支。从慢性感染个体中分离出的 EV11 株属于其中一个分支,并在 4 年内以相对恒定的速度积累突变。将突变积累曲线外推到过去表明,该个体在 1990 年代上半叶感染了流行的 EV11。编码单个病毒蛋白的基因组区域似乎没有受到强烈的选择压力,除了蛋白酶 3C 非常保守。这可能表明其在维持持续性感染方面的重要作用。