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日本流行的人巨细胞病毒全基因组序列测定及UL148基因地理基因组结构的发现

Determination of whole genome sequence of human cytomegalovirus circulating in Japan and discovery of geographic genome structure in UL148 gene.

作者信息

Wada Yuji, Ishioka Ken, Suzutani Tatsuo

机构信息

Department of Microbiology, School of Medicine, Fukushima Medical University, Japan.

Department of Microbiology, School of Medicine, Fukushima Medical University, Japan.

出版信息

Virus Res. 2025 Mar;353:199540. doi: 10.1016/j.virusres.2025.199540. Epub 2025 Feb 4.

DOI:10.1016/j.virusres.2025.199540
PMID:39894371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11846927/
Abstract

Human cytomegalovirus (HCMV), a member of the Herpesviridae family, is prevalent worldwide. HCMV is generally asymptomatic but causes severe disease in immunocompromised patients or infants who are congenitally infected. Recent advances in sequencing technology have led to the rapid expansion of the HCMV genetic database, providing a comprehensive resource for studying viral genetics. Although genetic investigations have been vigorously performed in European countries, information on the whole-genome sequence of HCMV in the East Asian region remains limited. In this study, we determined whole-genome sequences of two clinical isolates of HCMV circulating in Japan. Partial genome sequences of 26 genes in UL/b' region were also identified using additional seven clinical isolates. Phylogenetic analysis of the UL148 gene revealed a characteristic genetic clade predominantly constructed from HCMV isolates from Japan and China, suggesting a geographic gene structure in the East Asian region. We consider that this research will contribute to expanding the genetic database of HCMV and unveiling novel genetic characteristics of HCMV in Asia.

摘要

人巨细胞病毒(HCMV)是疱疹病毒科的成员之一,在全球范围内广泛流行。HCMV通常无症状,但会在免疫功能低下的患者或先天性感染的婴儿中引发严重疾病。测序技术的最新进展导致HCMV基因数据库迅速扩展,为研究病毒遗传学提供了全面的资源。尽管欧洲国家已经大力开展了基因研究,但东亚地区HCMV全基因组序列的信息仍然有限。在本研究中,我们测定了在日本流行的两株HCMV临床分离株的全基因组序列。还使用另外七株临床分离株鉴定了UL/b'区域中26个基因的部分基因组序列。对UL148基因的系统发育分析揭示了一个特征性的遗传分支,主要由来自日本和中国的HCMV分离株构成,这表明东亚地区存在地理基因结构。我们认为这项研究将有助于扩大HCMV的基因数据库,并揭示亚洲地区HCMV的新遗传特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/eb1470ac948f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/c7bad67aba27/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/f4a616123957/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/eb1470ac948f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/c7bad67aba27/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/f4a616123957/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a5e/11846927/eb1470ac948f/gr3.jpg

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本文引用的文献

1
Human Cytomegalovirus (HCMV) Genetic Diversity, Drug Resistance Testing and Prevalence of the Resistance Mutations: A Literature Review.人类巨细胞病毒(HCMV)的遗传多样性、耐药性检测及耐药突变的流行情况:文献综述
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中国河北省汉城病毒的遗传多样性和分子进化。
Infect Genet Evol. 2023 Oct;114:105503. doi: 10.1016/j.meegid.2023.105503. Epub 2023 Sep 16.
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Genomic and geographical structure of human cytomegalovirus.人类巨细胞病毒的基因组和地理结构。
Proc Natl Acad Sci U S A. 2023 Jul 25;120(30):e2221797120. doi: 10.1073/pnas.2221797120. Epub 2023 Jul 17.
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Direct Nanopore Sequencing of Human Cytomegalovirus Genomes from High-Viral-Load Clinical Samples.直接从高病毒载量临床样本中对人类巨细胞病毒基因组进行纳米孔测序。
Viruses. 2023 May 26;15(6):1248. doi: 10.3390/v15061248.
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Nanopore adaptive sampling: a tool for enrichment of low abundance species in metagenomic samples.纳米孔自适应采样:一种用于宏基因组样本中低丰度物种富集的工具。
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MEGA11: Molecular Evolutionary Genetics Analysis Version 11.MEGA11:分子进化遗传学分析版本 11。
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Congenital Cytomegalovirus Infection: Update on Diagnosis and Treatment.先天性巨细胞病毒感染:诊断与治疗的最新进展
Microorganisms. 2020 Oct 1;8(10):1516. doi: 10.3390/microorganisms8101516.
9
Human cytomegalovirus haplotype reconstruction reveals high diversity due to superinfection and evidence of within-host recombination.人类巨细胞病毒单倍型重建揭示了由于超感染和宿主内重组的证据而导致的高度多样性。
Proc Natl Acad Sci U S A. 2019 Mar 19;116(12):5693-5698. doi: 10.1073/pnas.1818130116. Epub 2019 Feb 28.
10
Estimation of the worldwide seroprevalence of cytomegalovirus: A systematic review and meta-analysis.估算全球巨细胞病毒的血清流行率:系统综述和荟萃分析。
Rev Med Virol. 2019 May;29(3):e2034. doi: 10.1002/rmv.2034. Epub 2019 Jan 31.