Length variability of telomeric repeat sequences of human herpesvirus 6 DNA

被引:26
作者
Achour, Abla
Malet, Isabelle
Deback, Claire
Bonnafous, Pascale
Boutolleau, David
Gautheret-Dejean, Agnes [2 ]
Agut, Henri [1 ]
机构
[1] Univ Paris 06, CERVI, Serv Virol, Grp Hosp Pitie Salpetriere,EA2387,Lab Virol,AP HP, F-75013 Paris, France
[2] Univ Paris 05, Microbiol Lab, Fac Sci Pharmaceut & Biol, Paris, France
关键词
Human herpesvirus-6; Human herpesvirus-6 variant; Genetic variability; Telomeric repeat sequence; Mixed infection; HUMAN CYTOMEGALOVIRUS; IDENTIFICATION; POLYMORPHISMS; STRAINS; PCR;
D O I
10.1016/j.jviromet.2009.03.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The telomeric repeat sequences (TRS) located near both ends of human herpesvirus 6 (HHV-6) genome are unique structures of unknown function among human herpesviruses. The goal of the present study was to investigate the variability of TRS copy number among different laboratory strains and HHV-6-infected clinical specimens regarding the two variants A and B of HHV-6. DNA obtained from infected cells was submitted to a PCR assay designed to amplify the part of genome containing TRS specifically either for HHV-6A or HHV-6B. Amplicons were analyzed by electrophoresis on agarose gel with ethidium bromide staining and nucleotide sequencing. The number of TRS copies was highly variable among the distinct laboratory strains and clinical specimens studied, ranging from 15 up to more than 180. However, this number was constant for a given strain after serial propagation in cell cultures as well as in different samples from the same subject. This permitted to detect a mixed infection with two distinct strains of HHV-6A within the same patient. The PCR-based analysis of HHV-6 TRS has a limited sensitivity but is highly specific, which provides the opportunity to include it in the set of molecular tools dedicated to the study of HHV-6 epidemiology. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 130
页数:4
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