School of Life Sciences, Center for Evolution and Medicine, Arizona State University, Tempe.
Division of Biological Sciences, University of Montana, Missoula.
Genome Biol Evol. 2023 Apr 6;15(4). doi: 10.1093/gbe/evad059.
Human cytomegalovirus (HCMV) represents a major threat to human health, contributing to both birth defects in neonates as well as organ transplant failure and opportunistic infections in immunocompromised individuals. HCMV exhibits considerable interhost and intrahost diversity, which likely influences the pathogenicity of the virus. Therefore, understanding the relative contributions of various evolutionary forces in shaping patterns of variation is of critical importance both mechanistically and clinically. Herein, we present the individual components of an evolutionary baseline model for HCMV, with a particular focus on congenital infections for the sake of illustration-including mutation and recombination rates, the distribution of fitness effects, infection dynamics, and compartmentalization-and describe the current state of knowledge of each. By building this baseline model, researchers will be able to better describe the range of possible evolutionary scenarios contributing to observed variation as well as improve power and reduce false-positive rates when scanning for adaptive mutations in the HCMV genome.
人巨细胞病毒(HCMV)对人类健康构成重大威胁,可导致新生儿出生缺陷,以及免疫功能低下个体的器官移植失败和机会性感染。HCMV 具有相当大的宿主间和宿主内多样性,这可能影响病毒的致病性。因此,了解各种进化力量在塑造变异模式方面的相对贡献,无论是从机制上还是从临床上来看,都是至关重要的。本文介绍了 HCMV 进化基准模型的各个组成部分,特别关注先天性感染,以说明包括突变和重组率、适应度效应分布、感染动力学和分隔-并描述了每一个的现有知识状态。通过构建这个基准模型,研究人员将能够更好地描述导致观察到的变异的可能的进化场景范围,并在 HCMV 基因组中扫描适应性突变时提高能力和降低假阳性率。