Limits and patterns of cytomegalovirus genomic diversity in humans

被引:95
作者
Renzette, Nicholas [1 ]
Pokalyuk, Cornelia [2 ,3 ]
Gibson, Laura [4 ,5 ]
Bhattacharjee, Bornali [1 ]
Schleiss, Mark R. [6 ,7 ]
Hamprecht, Klaus [8 ]
Yamamoto, Aparecida Y. [9 ]
Mussi-Pinhata, Marisa M. [9 ]
Britt, William J. [10 ]
Jensen, Jeffrey D. [3 ,11 ]
Kowalik, Timothy F. [1 ,12 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA 01655 USA
[2] Goethe Univ Frankfurt, Inst Stochast, D-60325 Frankfurt, Germany
[3] Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
[4] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA 01605 USA
[5] Univ Massachusetts, Sch Med, Dept Med, Div Infect Dis & Immunol, Worcester, MA 01655 USA
[6] Univ Minnesota, Sch Med, Ctr Infect Dis & Microbiol Translat Res, Minneapolis, MN 55455 USA
[7] Univ Minnesota, Sch Med, Dept Pediat, Div Pediat Infect Dis, Minneapolis, MN 55455 USA
[8] Univ Tubingen Hosp, Inst Med Virol, D-72076 Tubingen, Germany
[9] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pediat, BR-14048900 Ribeirao Preto, SP, Brazil
[10] Univ Alabama Birmingham, Sch Med, Dept Pediat, Birmingham, AL 35294 USA
[11] Ecole Polytech Fed Lausanne, Sch Life Sci, CH-1015 Lausanne, Switzerland
[12] Univ Massachusetts, Sch Med, Immunol & Virol Program, Worcester, MA 01655 USA
基金
欧洲研究理事会; 瑞士国家科学基金会; 美国国家卫生研究院;
关键词
human cytomegalovirus; HCMV; congenital CMV; virology; evolution; T-CELL RESPONSES; POLYMERASE SUBUNIT UL44; MUTATION-RATES; SIMULTANEOUS INFECTION; BACKGROUND SELECTION; GENETIC HITCHHIKING; HOMOSEXUAL-MEN; WIDE VIEW; STRAINS; GENOTYPES;
D O I
10.1073/pnas.1501880112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human cytomegalovirus (HCMV) exhibits surprisingly high genomic diversity during natural infection although little is known about the limits or patterns of HCMV diversity among humans. To address this deficiency, we analyzed genomic diversity among congenitally infected infants. We show that there is an upper limit to HCMV genomic diversity in these patient samples, with similar to 25% of the genome being devoid of polymorphisms. These low diversity regions were distributed across 26 loci that were preferentially located in DNA-processing genes. Furthermore, by developing, to our knowledge, the first genome-wide mutation and recombination rate maps for HCMV, we show that genomic diversity is positively correlated with these two rates. In contrast, median levels of viral genomic diversity did not vary between putatively single or mixed strain infections. We also provide evidence that HCMV populations isolated from vascular compartments of hosts from different continents are genetically similar and that polymorphisms in glycoproteins and regulatory proteins are enriched in these viral populations. This analysis provides the most highly detailed map of HCMV genomic diversity in human hosts to date and informs our understanding of the distribution of HCMV genomic diversity within human hosts.
引用
收藏
页码:E4120 / E4128
页数:9
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