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本文引用的文献

1
Genetic variability among serotype G6 human rotaviruses: identification of a novel lineage isolated in Hungary.G6型人类轮状病毒的遗传变异性:在匈牙利分离出的一个新谱系的鉴定。
J Med Virol. 2003 Sep;71(1):124-34. doi: 10.1002/jmv.10462.
2
Detection of human rotavirus serotype G6 in Hungary.匈牙利人轮状病毒G6血清型的检测
Epidemiol Infect. 2003 Feb;130(1):107-12. doi: 10.1017/s0950268802007975.
3
Characterization of nontypeable rotavirus strains from the United States: identification of a new rotavirus reassortant (P2A[6],G12) and rare P3[9] strains related to bovine rotaviruses.美国非典型轮状病毒株的特征分析:鉴定一种新型轮状病毒重配株(P2A[6],G12)以及与牛轮状病毒相关的罕见P3[9]株。
Virology. 2002 Mar 15;294(2):256-69. doi: 10.1006/viro.2001.1333.
4
Expanding global distribution of rotavirus serotype G9: detection in Libya, Kenya, and Cuba.轮状病毒G9血清型在全球分布范围的扩大:在利比亚、肯尼亚和古巴的检测情况
Emerg Infect Dis. 2001 Sep-Oct;7(5):890-2. doi: 10.3201/eid0705.017521.
5
Amino acid substitution within the VP7 protein of G2 rotavirus strains associated with failure to serotype.与血清分型失败相关的G2轮状病毒株VP7蛋白内的氨基酸替换。
J Clin Microbiol. 2001 Oct;39(10):3796-8. doi: 10.1128/JCM.39.10.3796-3798.2001.
6
Safety and immunogenicity of live attenuated quadrivalent human-bovine (UK) reassortant rotavirus vaccine administered with childhood vaccines to infants.与儿童期疫苗同时接种给婴儿的减毒活四价人-牛(英国)重配轮状病毒疫苗的安全性和免疫原性。
Vaccine. 2001 Sep 14;19(32):4676-84. doi: 10.1016/s0264-410x(01)00242-0.
7
Direct evidence for genome segment reassortment between concurrently-circulating human rotavirus strains.同时流行的人类轮状病毒株之间基因组片段重配的直接证据。
Arch Virol. 2001;146(3):557-70. doi: 10.1007/s007050170162.
8
Rotavirus genotypes P[4]G9, P[6]G9, and P[8]G9 in hospitalized children with acute gastroenteritis in Rio de Janeiro, Brazil.巴西里约热内卢住院急性胃肠炎儿童中的轮状病毒基因型P[4]G9、P[6]G9和P[8]G9
J Clin Microbiol. 2001 May;39(5):1999-2001. doi: 10.1128/JCM.39.5.1999-2001.2001.
9
Circulation of group A rotavirus subgroups and serotypes in Pune, India, 1990-1997.1990 - 1997年印度浦那A组轮状病毒亚组和血清型的流行情况
J Health Popul Nutr. 2000 Dec;18(3):163-70.
10
Rotavirus strain diversity in Blantyre, Malawi, from 1997 to 1999.1997年至1999年马拉维布兰太尔的轮状病毒株多样性
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对人类轮状病毒株的八年调查表明,匈牙利存在不寻常的G型和P型毒株的传播。

Eight-year survey of human rotavirus strains demonstrates circulation of unusual G and P types in Hungary.

作者信息

Bányai Krisztián, Gentsch Jon R, Glass Roger I, Uj Mária, Mihály Ilona, Szücs György

机构信息

Regional Laboratory of Virology, Baranya County Institute of State Public Health Service, Pécs, Hungary.

出版信息

J Clin Microbiol. 2004 Jan;42(1):393-7. doi: 10.1128/JCM.42.1.393-397.2004.

DOI:10.1128/JCM.42.1.393-397.2004
PMID:14715788
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC321674/
Abstract

Between 1992 and 2000, a total of 4173 rotavirus-positive samples were collected from two areas of Hungary. Of these, 2020 specimens (48.4%) were analyzed for G serotype, using monoclonal antibody-based immunoassay and reverse transcription-PCR. By the two methods, 1789 samples were specified as G1 (62%), G2 (12.2%), G3 (1.4%), G4 (6.4%), G6 (1.0%), G9 (2.9%), or mixed infection (2.6%), and the remaining 231 (11.4%) could not be G typed. The linkage between G and P type, subgroup specificity, and RNA profile was investigated with a sample subset. Among these specimens, we identified both the four globally common strains (P[8],G1 subgroup II (sgII); P[4],G2 sgI; P[8],G3 sgII; and P[8],G4 sgII) and six uncommon strains (P[6],G4 sgII; P[9],G3 sgI; P[9],G6 sgI; P[14],G6 sgI; P[8],G9 sgII; and P[8],G9 sgI). All strains with P[8], P[6], P[9], and P[14] specificities had a long electropherotype, whereas most of those carrying a P[4] specificity were associated with a short electropherotype. Although once considered to be rare, P[9],G6 and P[8],G9 rotavirus strains represent potentially important new serotypes in Hungary.

摘要

1992年至2000年间,匈牙利两个地区共采集了4173份轮状病毒阳性样本。其中,2020份样本(48.4%)采用基于单克隆抗体的免疫测定和逆转录聚合酶链反应分析G血清型。通过这两种方法,1789份样本被鉴定为G1(62%)、G2(12.2%)、G3(1.4%)、G4(6.4%)、G6(1.0%)、G9(2.9%)或混合感染(2.6%),其余231份(11.4%)无法进行G分型。使用样本子集研究了G型和P型之间的关联、亚组特异性和RNA图谱。在这些样本中,我们鉴定出了四种全球常见毒株(P[8],G1亚组II(sgII);P[4],G2 sgI;P[8],G3 sgII;以及P[8],G4 sgII)和六种不常见毒株(P[6],G4 sgII;P[9],G3 sgI;P[9],G6 sgI;P[14],G6 sgI;P[8],G9 sgII;以及P[8],G9 sgI)。所有具有P[8]、P[6]、P[9]和P[14]特异性的毒株都具有长电泳型,而大多数携带P[4]特异性的毒株则与短电泳型相关。尽管P[9],G6和P[8],G9轮状病毒毒株曾被认为很罕见,但它们在匈牙利代表了潜在重要的新血清型。