History and genomic sequence analysis of the herpes simplex virus 1 KOS and KOS1.1 sub-strains

被引:29
作者
Colgrove, Robert C. [1 ,2 ]
Liu, Xueqiao [1 ]
Griffiths, Anthony [3 ]
Raja, Priya [1 ]
Deluca, Neal A. [4 ]
Newman, Ruchi M. [5 ]
Coen, Donald M. [3 ]
Knipe, David M. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA 02114 USA
[2] Mt Auburn Hosp, Cambridge, MA USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Univ Pittsburgh, Dept Microbiol & Mol Genet, Pittsburgh, PA USA
[5] Broad Inst Harvard & MIT, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
HSV history; HSV genome sequence; KOS sequence; KOS1.1; sequence; Herpes simplex virus; HSV; KOS; LATENCY-ASSOCIATED TRANSCRIPT; TEMPERATURE-SENSITIVE MUTANTS; DNA-POLYMERASE; CRYSTAL-STRUCTURE; GENETIC-EVIDENCE; GLYCOPROTEIN-B; TYPE-1; INFECTION; GANGLIA; REACTIVATION;
D O I
10.1016/j.virol.2015.09.026
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A collection of genomic DNA sequences of herpes simplex virus (HSV) strains has been defined and analyzed, and some information is available about genomic stability upon limited passage of viruses in culture. The nature of genomic change upon extensive laboratory passage remains to be determined. In this report we review the history of the HSV-1 KOS laboratory strain and the related KOS1.1 laboratory sub-strain, also called KOS (M), and determine the complete genomic sequence of an early passage stock of the KOS laboratory sub-strain and a laboratory stock of the KOS1.1 sub-strain. The genomes of the two sub-strains are highly similar with only five coding changes, 20 non-coding changes, and about twenty non-ORF sequence changes. The coding changes could potentially explain the KOS1.1 phenotypic properties of increased replication at high temperature and reduced neuroinvasiveness. The study also provides sequence markers to define the provenance of specific laboratory KOS virus stocks. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:215 / 221
页数:7
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