Knowles W A, Gibson P E, Gardner S D
Virus Reference Laboratory, Central Public Health Laboratory, Colindale, London, England.
J Med Virol. 1989 Jun;28(2):118-23. doi: 10.1002/jmv.1890280212.
Human polyomavirus BK-like isolates were subjected to restriction endonuclease analysis with the enzymes EcoRI and Hind III. End-point dilution was used to obtain homogeneous virus pools for DNA analysis and to remove JC virus from a mixed stock. The results of Hind III digestion suggested that two subgroups could be distinguished. Several BK-like isolates were purified and rabbit antisera raised. The isolates were compared with each other and with BK and JC viruses by haemagglutination-inhibition (HI) and by neutralisation. JC virus was serologically distinct, but all the other isolates showed some cross-reactivity. Two subgroups were again evident: GS and PG were with prototype BK in subgroup 1, and MG and IV were in subgroup 2. Two isolates, AS and SB, reacted with isolates of both subgroups 1 and 2 but were distinct from one another: their genome was similar to subgroup 1 isolates. Typing by HI or by neutralisation may form a basis for grouping BK-like polyomavirus isolates.
对人多瘤病毒BK样分离株使用EcoRI和Hind III酶进行限制性内切酶分析。采用终点稀释法获得用于DNA分析的均匀病毒库,并从混合毒株中去除JC病毒。Hind III消化结果表明可区分出两个亚组。纯化了几株BK样分离株并制备了兔抗血清。通过血凝抑制(HI)和中和试验将这些分离株相互比较,并与BK病毒和JC病毒进行比较。JC病毒在血清学上是独特的,但所有其他分离株都表现出一些交叉反应性。两个亚组再次显现:GS和PG与亚组1中的原型BK病毒在一起,MG和IV在亚组2中。两株分离株AS和SB与亚组1和2的分离株都有反应,但彼此不同:它们的基因组与亚组1分离株相似。通过HI或中和试验进行分型可为BK样多瘤病毒分离株的分组提供依据。