Phylogenetic analysis of the complete genome of 11 BKV isolates obtained from allogenic stem cell transplant recipients in Ireland

被引:14
作者
Drew, Richard John [1 ]
Walsh, Anne [2 ]
Laoi, Bairbre Ni [2 ]
Crowley, Brendan [2 ]
机构
[1] Trinity Coll Dublin, Sir Patrick Dun Translat Res Lab, Dublin, Ireland
[2] St James Hosp, Dept Microbiol, Dublin, Ireland
关键词
polyomavirus; hemorrhagic cystitis; transplant; BK; TRANSCRIPTIONAL CONTROL REGION; NONCODING CONTROL REGION; HUMAN POLYOMAVIRUS BK; INTERSTITIAL NEPHRITIS; DISTRIBUTION PATTERNS; HEMORRHAGIC CYSTITIS; REGULATORY REGIONS; VIRUS VARIANTS; SEQUENCE; EVOLUTION;
D O I
10.1002/jmv.23240
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
BK polyomavirus (family Polyomaviridae) may cause hemorrhagic cystitis (BKV-HC) in hematopoietic stem cell transplant recipients. Eleven complete BKV genomes (GenBank accession numbers: JN192431-JN192441) were sequenced from urine samples of allogenic hematopoietic stem cell transplant recipients and compared to complete BKV genomes in the published literature. Of the 11 isolates, seven (64%) were subgroup Ib-1, three (27%) isolates belonged to subgroup Ib-2 and a single isolate belonged to subtype III. The analysis of single-nucleotide polymorphisms in this study showed that isolates could be subclassified into subtypes IIV and subgroups Ib-1 and Ib-2 on the basis of VP1 of the first part of the Large T-antigen (LTag). The non-coding control region (NCCR) of the 11 isolates was also sequenced. These sequences showed that there was consistent sequence homology within subgroups Ib-1 and Ib-2. Two new mutations were described in the isolates, G?C at O84 in isolate SJH-LG-310, and a deletion at R2-7 in isolate SJH-LG-309. No known transcription factor is thought to be present at the site of either of these mutations. There were no rearrangements seen in isolates and this may be because the patients were not followed up over time. There were five nucleotide positions at which subgroup Ib-1 isolated differed from subgroup Ib-2 isolates in the NCCR sequence, O41, P18, P31, R4, and S18. The mutation O41 is present in the promoter granulocyte/macrophage stimulating factor) gene and the P31 mutation is present in the NF-1 gene. J. Med. Virol. 84: 10371048, 2012. (C) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1037 / 1048
页数:12
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