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巨细胞病毒糖蛋白B基因型与垂直传播结局:对先天性感染婴儿干血斑的研究

CMV gB genotypes and outcome of vertical transmission: study on dried blood spots of congenitally infected babies.

作者信息

Barbi M, Binda S, Caroppo S, Primache V, Didò P, Guidotti P, Corbetta C, Melotti D

机构信息

Institute of Virology, University of Milan, Via C. Pascal 38, 20133 Milan, Italy.

出版信息

J Clin Virol. 2001 Apr;21(1):75-9. doi: 10.1016/s1386-6532(00)00188-8.

Abstract

BACKGROUND

The role of the virulence of the infecting cytomegalovirus (CMV) strain in the transmission of the virus from mother to fetus and the outcome of the fetal infection has not received much attention yet. Molecular analysis of the gene coding for the surface glycoprotein B (gB) has been used to investigate the relationship between genotype and virulence in groups of immunosuppressed patients.

OBJECTIVES

(1) to assess the prevalence of different gB genotypes in babies with congenital CMV infection; (2) to investigate the possible relationship between genotype and severity of congenital CMV disease; (3) to evaluate the possibility of using dried blood on Guthrie cards (DBS) for genotyping.

STUDY DESIGN

CMV DNA was extracted from DBS and from urine/saliva samples collected in the first two weeks of life of 98 congenitally infected babies, half of which were symptomatic at birth. Genotyping was performed through RFLP analysis of the region corresponding to the cleavage site of the gB protein.

RESULTS

The most prevalent genotype was gB1 (42%) followed by gB3 (26%), gB2 (19%) and gB4 (13%). Rates of disease and CNS damages were higher among children infected by gB1 (35%, 17%) and gB3 (31%, 28%) than in those infected by gB2 and gB4 (20%, 17% and 13%, 15%, respectively). These differences however did not reach the statistical significance. The parallel typing of DBS and urine/saliva strains gave a full concordance of results.

CONCLUSIONS

All four major CMV gB genotypes (gB1-4) can cause a congenital infection but none seems to be associated to the development and the severity of disease. The possibility of using the neonatal DBS for genotyping opens a way to the examination of large numbers of cases of congenital CMV infection.

摘要

背景

感染性巨细胞病毒(CMV)毒株的毒力在病毒从母亲传播至胎儿以及胎儿感染结局中的作用尚未得到足够关注。对编码表面糖蛋白B(gB)的基因进行分子分析已被用于研究免疫抑制患者群体中基因型与毒力之间的关系。

目的

(1)评估先天性CMV感染婴儿中不同gB基因型的流行率;(2)研究基因型与先天性CMV疾病严重程度之间的可能关系;(3)评估使用Guthrie卡片上的干血斑(DBS)进行基因分型的可能性。

研究设计

从98例先天性感染婴儿出生后前两周采集的DBS以及尿液/唾液样本中提取CMV DNA,其中一半婴儿出生时出现症状。通过对与gB蛋白切割位点相对应区域的限制性片段长度多态性(RFLP)分析进行基因分型。

结果

最常见的基因型是gB1(42%),其次是gB3(26%)、gB2(19%)和gB4(13%)。gB1(35%,17%)和gB3(31%,28%)感染的儿童中疾病和中枢神经系统损害的发生率高于gB2和gB4感染的儿童(分别为20%,17%和13%,15%)。然而,这些差异未达到统计学意义。DBS和尿液/唾液毒株的平行分型结果完全一致。

结论

所有四种主要的CMV gB基因型(gB1 - 4)均可导致先天性感染,但似乎均与疾病的发生和严重程度无关。使用新生儿DBS进行基因分型的可能性为大量先天性CMV感染病例的检测开辟了一条途径。

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