BK VIRUS AND A NEW-TYPE OF JC VIRUS EXCRETED BY HIV-1 POSITIVE PATIENTS IN RURAL TANZANIA

被引:72
作者
AGOSTINI, HT
BRUBAKER, GR
SHAO, J
LEVIN, A
RYSHKEWITSCH, CF
BLATTNER, WA
STONER, GL
机构
[1] NATL INST HLTH, NINDS, EXPTL NEUROPATHOL LAB, BETHESDA, MD 20892 USA
[2] UNIV DAR ES SALAAM, MUHIMBILI MED CTR, DAR ES SALAAM, TANZANIA
[3] SHIRATI HOSP, SHIRATI, TANZANIA
[4] NATL INST HLTH, NATL CANC INST, VIRAL EPIDEMIOL BRANCH, BETHESDA, MD 20892 USA
[5] ST BARTHOLOMEWS HOSP, COLL MED, RES TRIANGLE INST, RTI UNIT, LONDON, ENGLAND
关键词
D O I
10.1007/BF01322682
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HIV-1 positive patients from Tanzanian villages near Shirati were examined for urinary excretion of the human polyomaviruses JC and BK using the polymerase chain reaction (PCR). BK virus (BKV) was detected in 11 of 23 individuals tested. The BKV DNA sequences were all closely related to prototype Gardner strain and BKV (DUN). In contrast, a new type of JCV, termed Type 3 [or JCV (Shi)], was identified in seven of these same 23 individuals by comparison with Type 1 and Type 2 sequences of the VP1/intergenic/T antigen region of U.S., European and Asian strains. This suggests that JCV and BKV, although closely related, have different evolutionary histories within the African population. The six BKV regulatory regions amplified all showed the archetypal configuration. However, two of the seven JCV regulatory regions showed rearrangements: a small deletion and an inverted repeat. JCV causes a fatal demyelinating disease, progressive multifocal leukoencephalopathy (PML), in about 5% of AIDS patients in Europe and the U.S.A., but only one case has been reported in Africa. Our results suggest that this rarity of PML is not due to the absence of JCV in the African population.
引用
收藏
页码:1919 / 1934
页数:16
相关论文
共 47 条