Human papillomavirus type 16 long control region and E6 variants stratified by cervical disease stage

被引:14
|
作者
Marongiu, Luigi [1 ]
Godi, Anna [1 ]
Parry, John V. [1 ]
Beddows, Simon [1 ]
机构
[1] Publ Hlth England, Virus Reference Dept, London NW9 5EQ, England
关键词
Human papillomavirus; Cervical cancer; HPV16; Variants; LCR; E6; HPV; 16; E6; INTRAEPITHELIAL NEOPLASIA; SEQUENCE VARIATION; MOLECULAR VARIANTS; RISK; LINEAGES; VIRUS; IMMORTALIZATION; PERSISTENCE; CYTOLOGY;
D O I
10.1016/j.meegid.2014.05.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objective: Certain intra-type variants of HPV16 have been shown to be associated with an increased risk of developing high grade cervical disease, but their potential association is confounded by apparent geographic and phylogenetic lineage dependency. The objective of this study was to evaluate the relationship between HPV16 sequence variants and cervical disease stage in monospecific infection samples from a single lineage (European, EUR) in England. Methods: One hundred and twelve women singly infected with HPV16 and displaying normal and abnormal cytology grades were selected. An 1187 bp fragment encompassing the entire LCR and a portion of the E6 open reading frame was sequenced to identify intra-type variants. Intra-type diversity was estimated using Shannon entropy. Results: Almost all samples (110/112; 98%) were assigned to the EUR lineage, one sample was classified as European-Asian (EAS) and another African (Afr1a). The mean pairwise distance of the EUR sequences in this study was low (0.29%; 95% CI 0.13-0.45%) but there were nevertheless several sites in the LCR (n = 5) and E6 (n = 2) that exhibited a high degree of entropy. None of these sites, however, including the T350G non-synonymous (L83V) substitution in E6, alone or in combination, were found to be associated with cervical disease stage. Conclusions: Despite using single infection samples and samples from a single variant lineage, intra-type variants of HPV16 were not differentially associated with cervical disease. Monitoring intra-lineage, sitespecific variants, such as T350G, is unlikely to be of diagnostic value. Crown Copyright (C) 2014 Published by Elsevier B. V. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/3.0/).
引用
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页码:8 / 13
页数:6
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