首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Single gene substitution rotavirus reassortants containing the major neutralization protein (VP7) of human rotavirus serotype 4.
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Single gene substitution rotavirus reassortants containing the major neutralization protein (VP7) of human rotavirus serotype 4.

机译:包含人类轮状病毒血清型4的主要中和蛋白(VP7)的单基因替代轮状病毒重配子。

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摘要

A series of reassortants was isolated from coinfection of cell cultures with wild-type bovine rotavirus (UK strain [serotype 6]) or rhesus rotavirus (strain MMU18006 [serotype 3]) and a tissue culture-adapted human rotavirus strain, ST3 (serotype 4). Monospecific antiserum or a set of monoclonal antibodies to the major outer capsid neutralization glycoprotein, VP7, of the animal rotavirus parent was used to select for reassortants with human rotavirus serotype 4 neutralization specificity. The majority of reassortants contained only gene 9 of the human rotavirus parent, ST3, whereas the remaining genes were derived from the animal rotavirus parent. These single human rotavirus gene substitution reassortants were neutralized to high titer by hyperimmune serum directed at ST3, thus demonstrating that gene 9 of ST3 codes for the major neutralization protein of this strain. Moreover, these single gene substitution, reassortants were also neutralized to low titer by antiserum directed at their animal rotavirus parent, probably because they derived gene 4, which codes for another outer capsid protein, VP3, from their animal rotavirus parent. None of the reassortants derived gene 4, which had previously been shown to be responsible for host range restriction of human rotaviruses in tissue culture, from ST3, despite the fact that the ST3 strain used for gene reassortment had been tissue culture adapted.
机译:从野生型牛轮状病毒(UK菌株[血清型6])或恒河猴轮状病毒(MMU18006 [血清型3])和组织培养适应性人轮状病毒株ST3(血清型4)共同感染的细胞培养物中分离出一系列重组子。 )。使用针对动物轮状病毒亲本的主要外衣壳中和糖蛋白VP7的单特异性抗血清或一组单克隆抗体来选择具有人轮状病毒血清型4中和特异性的重配子。大多数重配体仅包含人类轮状病毒亲本ST3的基因9,而其余基因则来自动物轮状病毒亲本。这些单一的人轮状病毒基因取代重配体被针对ST3的超免疫血清中和至高滴度,因此证明ST3的基因9编码该菌株的主要中和蛋白。而且,这些单基因取代重配体也被针对其动物轮状病毒亲本的抗血清中和至低滴度,可能是因为它们从其动物轮状病毒亲本衍生了编码另一外衣壳蛋白VP3的基因4。尽管用于基因重组的ST3菌株已经适应了组织培养的事实,但重组子均未从ST3衍生出基因4,该基因先前已被证明负责组织培养中人类轮状病毒的宿主范围。

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