Kaczorowska Joanna, Timmerman Anne L, Deijs Martin, Kinsella Cormac M, Bakker Margreet, van der Hoek Lia
Department of Medical Microbiology and Infection Prevention, Laboratory of Experimental Virology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.
Amsterdam Institute for Infection and Immunity, Postbus 22660, Amsterdam 1100 DD, The Netherlands.
Virus Evol. 2023 Jan 5;9(1):vead001. doi: 10.1093/ve/vead001. eCollection 2023.
Human anelloviruses (AVs) are extremely genetically diverse, are widespread in the human population, and cause chronic infections. However, the evolutionary dynamics of AVs within single hosts is currently unknown, and it is unclear whether these changes have an implication on the long-term persistence of AVs in the host. Here, we assessed the evolutionary dynamics of six AV lineages during 30 years of chronic infection at single host resolution. The total number of substitutions and the number of variable sites increased over time. However, not all substitutions reached population fixation, showing that AV lineages form heterogeneous swarms within the host. Most substitutions occurred within a hypervariable region (HVR) located between nucleotide positions 800 and 1,300 of , which is known to be located within the spike domain. Different regions of the gene undergo either positive or negative selection pressure. Sites under strong diversifying selection pressure were detected in the HVR, while the majority of the sites under purifying selection were detected outside this region. The HVR may play the role of an immunological decoy that prevents antibodies from binding to more vulnerable parts of ORF1. Moreover, the frequent substitutions in this region may increase the chances of AV particles escaping immune recognition.
人环曲病毒(AVs)在基因上具有极高的多样性,在人群中广泛传播,并会引发慢性感染。然而,目前尚不清楚AVs在单一宿主内的进化动态,也不清楚这些变化是否对AVs在宿主体内的长期持续存在有影响。在此,我们以单一宿主分辨率评估了6个AV谱系在30年慢性感染期间的进化动态。随着时间的推移,替换总数和可变位点数量均有所增加。然而,并非所有替换都达到群体固定,这表明AV谱系在宿主体内形成了异质群体。大多数替换发生在位于基因核苷酸位置800至1300之间的高变区(HVR)内,已知该区域位于刺突结构域内。基因的不同区域受到正向或负向选择压力。在HVR中检测到处于强多样化选择压力下的位点,而在该区域之外检测到的大多数位点处于纯化选择之下。HVR可能起到免疫诱饵的作用,防止抗体结合到ORF1更易受攻击的部分。此外,该区域频繁的替换可能会增加AV颗粒逃避免疫识别的机会。