Ward R L, Clemens J D, Sack D A, Knowlton D R, McNeal M M, Huda N, Ahmed F, Rao M, Schiff G M
Division of Clinical Virology, James N. Gamble Institute of Medical Research, Cincinnati, Ohio 45219.
J Clin Microbiol. 1991 Sep;29(9):1915-23. doi: 10.1128/jcm.29.9.1915-1923.1991.
Group A rotaviruses collected between 1985 and 1986 during comprehensive surveillance of treated diarrheal episodes occurring in a rural Bangladesh population were culture adapted and characterized by electropherotype, serotype, and subgroup. Of 454 episodes of rotavirus-associated diarrhea, rotaviruses were culture adapted from 381 (84%), and 335 contained 11 electrophoretically identical segments in unpassaged and cultured preparations. These 335 comprised 69 different electropherotypes with between 1 (32 isolates) and 79 representatives. The persistence of specific rotavirus strains within the study population, as defined by the detection of viruses with particular electropherotypes, was generally limited to a period of only a few months. All 335 isolates were serotyped by neutralization with hyperimmune antisera to prototype rotavirus strains representative of serotypes 1 to 4, i.e., Wa, DS-1, P, and ST-3. It was found that 80, 48, 119, and 88 isolates belonged to serotypes 1 to 4, respectively. The concentrations of hyperimmune antisera required to neutralize these isolates, however, were at least threefold greater than those needed to neutralize the homologous strains. Therefore, the isolates appeared to have altered neutralization epitopes from their prototype strains. Furthermore, the serotype 4 isolates were consistently shown to be much more closely related to the serotype 4B VA70 strain than the serotype 4A ST-3 strain. All but two isolates identified as serotypes 1, 3, or 4 had long electropherotypes and were subgroup II, and all but one serotype 2 isolate were subgroup I and had short electropherotypes. The three disparate strains appeared to be genetic reassortants. Evidence is presented that dual infections required for reassortant formation were not uncommon. Thus, formation of multiple reassortants may have been a cause for the observed rapid shift in viral strains within the study population.
1985年至1986年期间,在对孟加拉国农村地区治疗的腹泻病例进行全面监测时收集的A组轮状病毒,经过培养适应,并通过电泳型、血清型和亚组进行了特征分析。在454例轮状病毒相关性腹泻病例中,381例(84%)的轮状病毒经过了培养适应,335例在未传代和培养的制剂中含有11个电泳相同的片段。这335例包括69种不同的电泳型,每种电泳型有1个(32株分离株)至79个代表株。根据具有特定电泳型的病毒检测所定义,特定轮状病毒株在研究人群中的持续存在通常仅限于几个月的时间。所有335株分离株都用针对血清型1至4的原型轮状病毒株(即Wa、DS-1、P和ST-3)的超免疫抗血清进行中和血清分型。结果发现,分别有80、48、119和88株分离株属于血清型1至4。然而,中和这些分离株所需的超免疫抗血清浓度至少是中和同源株所需浓度的三倍。因此,这些分离株的中和表位似乎与其原型株有所不同。此外,血清型4的分离株始终显示与血清型4B的VA70株比血清型4A的ST-3株关系更为密切。除两株外,所有鉴定为血清型1、3或4的分离株都具有长电泳型,属于亚组II,除一株血清型2的分离株外,所有血清型2的分离株都属于亚组I,具有短电泳型。这三株不同的毒株似乎是基因重配株。有证据表明,重配株形成所需的双重感染并不罕见。因此,多个重配株的形成可能是研究人群中观察到的病毒株快速变化的一个原因。