首页> 外文期刊>The Journal of Infectious Diseases >Human cytomegalovirus-encoded alpha -chemokines exhibit high sequence variability in congenitally infected newborns.
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Human cytomegalovirus-encoded alpha -chemokines exhibit high sequence variability in congenitally infected newborns.

机译:人类巨细胞病毒编码的α-趋化因子在先天感染的新生儿中表现出高序列变异性。

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摘要

Most congenital human cytomegalovirus (HCMV) infections are asymptomatic, but some lead to severe disease. We hypothesized that differences in disease manifestations may be partially explained by differences in viral strains. We recently reported an association between unique long (UL) 144 gene polymorphisms and clinical disease. We now report on the sequence heterogeneity of 2 potential HCMV virulence genes that encode alpha -chemokines: UL146 and UL147. These 2 genes were highly divergent in cultured isolates obtained from 23 newborns with congenital HCMV infection and were difficult to categorize. Unlike our findings for the contiguous UL144 gene, no specific UL146 or UL147 genotype was associated with disease outcome.
机译:大多数先天性人类巨细胞病毒(HCMV)感染无症状,但有些会导致严重疾病。我们假设疾病表现的差异可能部分由病毒株的差异解释。我们最近报道了独特的长(UL)144基因多态性与临床疾病之间的关联。现在,我们报告编码α-趋化因子的两个潜在HCMV毒力基因:UL146和UL147的序列异质性。这两个基因在从23名先天性HCMV感染的新生儿中分离得到的培养分离物中高度不同,并且难以分类。与我们对连续UL144基因的发现不同,没有特定的UL146或UL147基因型与疾病结局相关。

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