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[从波兰南部住院新生儿和婴儿中分离出的巨细胞病毒株的 UL55 基因型多样性]

[UL55 genotype diversity of cytomegalovirus strains isolated from newborns and infants hospitalized in southern Poland].

作者信息

Zawilińska Barbara, Szostek Sława, Kopeć Jolanta, Koprynia Małgorzata, Kosz-Vnenchak Magdalena

机构信息

Zakład Wirusologii Katedry Mikrobiologii, Uniwersytetu Jagiellońskiego, Collegium Medicum w Krakowie.

出版信息

Przegl Epidemiol. 2011;65(3):409-13.

Abstract

Studies on cytomegalovirus (HCMV) infections more often draw attention to the differences in tropism, pathogenicity and virulence of the virus depending on its genotype. The aim of this study was to assess the individual gB genotypes which are encoded in UL55 region of HCMV genome in a population of newborns and infants from Southern Poland. Genotypic analysis was carried out on 53 children (16 newborns and 37 neonates) with confirmed HCMV infection. The children were tested several times. A total of 101 samples, mainly urine, less blood, swabs from the upper respiratory tract, in justified cases, the cerebrospinal fluid were used in our study. Both genotyping and quantitative assessment of HCMV were performed using real time-PCR (rt-PCR). For identification of four major gB genotypes in one reaction, a modification of multiplex rt-PCR was used. Studies confirmed the presence of all major genotypes: gB1, gB2, gB3 and gB4 in the examined groups of children. Only in one case, the genotype could not be determined, perhaps it belonged to subtypes outside the detectable majority ofgB genotypes. Genotype gB1 (63.5%) which was slightly more frequent in infants than in neonates, dominated in our studies. The other genotypes occurred at a rate: gB2 - 15.4%, gB3 - 21.2%, gB4 - 28.8%, respectively. Mixed infections, caused by two genotypes were found in 16 (31%) children, mainly in older infants. There were no statistically significant differences in viral load when comparing a group of newborns with infants and single vs. mixed infection, as well as individual genotypes. The observed differences in the proportional occurrence of different gB genotypes in the two study groups of children may suggest various preferences of particular HCMV genotypes in congenital and acquired infections. Moreover, by monitoring of HCMV infection and determination the genotypes in consecutive samples, it could be identified infection acquired during hospitalization in three children.

摘要

关于巨细胞病毒(HCMV)感染的研究更多地关注该病毒在嗜性、致病性和毒力方面因基因型不同而存在的差异。本研究的目的是评估波兰南部新生儿和婴儿群体中,HCMV基因组UL55区域编码的gB各基因型。对53例确诊为HCMV感染的儿童(16例新生儿和37例婴儿)进行了基因分型分析。对这些儿童进行了多次检测。本研究共使用了101份样本,主要是尿液,少量血液,上呼吸道拭子,在合理情况下,还使用了脑脊液。HCMV的基因分型和定量评估均采用实时荧光定量PCR(rt-PCR)。为了在一个反应中鉴定四种主要的gB基因型,采用了多重rt-PCR的改良方法。研究证实,在所检测的儿童组中存在所有主要基因型:gB1、gB2、gB3和gB4。仅在1例中无法确定基因型,可能它属于可检测到的大多数gB基因型之外的亚型。在我们的研究中,gB1基因型(63.5%)占主导,在婴儿中比在新生儿中略为常见。其他基因型的出现率分别为:gB2 - 15.4%,gB3 - 21.2%,gB4 - 28.8%。在16例(31%)儿童中发现了由两种基因型引起的混合感染,主要发生在较大的婴儿中。比较新生儿组与婴儿组、单一感染与混合感染以及各基因型之间的病毒载量时,未发现统计学上的显著差异。在两个儿童研究组中观察到的不同gB基因型比例出现的差异,可能表明特定HCMV基因型在先天性和获得性感染中有不同偏好。此外,通过监测HCMV感染并确定连续样本中的基因型,可以识别出3例儿童在住院期间获得的感染。

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