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Genotypes of varicella-zoster virus wild-type strains in Germany.

机译:德国水痘带状疱疹病毒野生型菌株的基因型。

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摘要

Surveillance of varicella-zoster virus (VZV) genotypes is indicated in Germany after implementation of universal varicella vaccination. This article reports genotyping data of 77 VZV strains obtained from 54 patients with varicella, 1 newborn with congenital varicella syndrome, 2 fetuses with intrauterine VZV infection and 20 cases with zoster. Fragments of the open reading frames (ORF) 1, 21, 22, 37, 50, 54, and 60 were analyzed by sequencing. In addition, the PstI polymorphism of the ORF 38 was characterized. Thirty strains, 22 from varicella and 8 from zoster, had the genetic markers of genotype E2, 2 of them carried new single nucleotide polymorphisms (SNP). Twenty-nine VZV isolates, 17 from varicella, and 12 from zoster, could be analyzed as E1 strains, 6 of them as E1 variants containing individual SNPs. Finally, 17 strains taken from primary VZV infection were classified as genotype M1, 13 of which belonged to the M1 subtype 1, 3 to the M1 subtype 2, and 1 to the M1 subtype 3. One strain was regarded as potential E2/J recombinant. In conclusion, VZV genotypes E2, E1, and M1 can be found in nearly equal incidence in varicella in Germany. The most frequent group is attributed to the genotype E2. Genotype M1 strains can only be detected after primary VZV infection and not in zoster cases. The possible recombinant could not be classified definitely by the scattered SNP method used and, therefore, has to be confirmed by full-genome sequencing studies.
机译:在德国实施水痘通用疫苗接种后,对水痘带状疱疹病毒(VZV)基因型进行了监测。本文报道了54例水痘患者,1例先天性水痘综合征新生儿,2例宫内VZV感染胎儿和20例带状疱疹患者获得的77株VZV菌株的基因型数据。通过测序分析开放阅读框(ORF)1、21、22、37、50、54和60的片段。另外,表征了ORF 38的PstI多态性。 30个菌株,来自水痘的22个和带状疱疹的8个,具有E2基因型的遗传标记,其中2个带有新的单核苷酸多态性(SNP)。可以将29个VZV分离株(来自水痘的17个,带状疱疹的12个)分析为E1菌株,其中6个为包含单个SNP的E1变异体。最后,从原发性VZV感染中分离出的17个菌株被归为M1基因型,其中13个属于M1亚型1、3属于M1亚型2,并且属于M1亚型3。1个菌株被认为是潜在的E2 / J重组体。总之,在德国的水痘中,VZV基因型E2,E1和M1的发病率几乎相等。最常见的人群归因于基因型E2。 M1基因型菌株只能在原发性VZV感染后检测到,而在带状疱疹病例中则不能检测到。可能的重组子不能通过所使用的分散SNP方法进行明确分类,因此,必须通过全基因组测序研究加以证实。

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