Prevalence and Quantitation of Adenovirus DNA From Human Tonsil and Adenoid Tissues

被引:24
作者
Alkhalaf, Moustafa Alissa [1 ]
Guiver, Malcolm [2 ]
Cooper, Robert J. [1 ]
机构
[1] Univ Manchester, Virol Unit, Inst Inflammat & Repair, Manchester, Lancs, England
[2] Hlth Protect Agcy, Manchester, Lancs, England
关键词
adenovirus latency; sequence typing; adenoids; methylation; SPECIES-C; CYTOSINE METHYLATION; PERSISTENT INFECTION; SEQUENCE ALIGNMENT; CELLS; PROMOTER; CHILDREN; VIRUSES; HEXON; PCR;
D O I
10.1002/jmv.23678
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study, real-time PCR was used to quantify adenovirus DNA in cell suspensions prepared from 106 right and left tonsils and 10 adenoids obtained from 57 patients who underwent routine tonsillectomies and/or adenoidectomies. Eighty-four (72.4%) tonsils and adenoids samples were positive for HAdV by real-time PCR. The viral load ranged from 2.8x10(2) to 2.6x10(6)copies/10(7) cells and varied up to sixfold between the right and left tonsils. In some cases, only one tonsil was positive and the viral load was lower in older children. Seventy-eight of 84 positive samples could be typed by sequencing of the hexon L1 region. Species C (types 1, 2, and 5) were detected in 84.1% of the patients followed by types 3 and 7 of species B (6.8%), HAdV-E4 (6.8%), and HAdV-F41 (2.3%). In one patient adenovirus C2 was found in the left tonsil and adenovirus C5 in the right tonsil. No DNA methylation was detected in either the E1A promoter or the major late promoter region of adenovirus DNA from six tonsils and adenoids samples and two clinical isolates. J Med. Virol. 85:1947-1954, 2013.. (c) 2013 Wiley Periodicals, Inc.
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页码:1947 / 1954
页数:8
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