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印度爆发高死亡率乙型肝炎:与前核心、基本核心启动子突变体和未正确消毒的注射器有关。

An outbreak of hepatitis B with high mortality in India: association with precore, basal core promoter mutants and improperly sterilized syringes.

机构信息

National Institute of Virology, Pune, Maharashtra, India.

出版信息

J Viral Hepat. 2011 Apr;18(4):e20-8. doi: 10.1111/j.1365-2893.2010.01391.x. Epub 2010 Nov 26.

Abstract

In 2009, an outbreak of hepatitis B with high mortality was observed in Sabarkantha district, Gujarat state, India with 456 cases and 89 deaths. Hospitalized patients with self-limiting disease (152, AVH)) and fulminant hepatic failure (39, FHF including 27 fatal and 12 survivals) were investigated. These were screened for diagnostic markers for hepatitis viruses, hepatitis B virus (HBV) genotyping and mutant analysis. Complete HBV genomes from 22 FHF and 17 AVH cases were sequenced. Serosurveys were carried out in the most and least affected blocks for the prevalence of HBV and identification of mutants. History of injection from a physician was associated with FHF and AVH cases. Co-infection with other hepatitis viruses or higher HBV DNA load was not responsible for mortality. Four blocks contributed to 85.7% (391/456) of the cases and 95.5% (85/89) mortality while two adjacent blocks had negligible mortality. Sequence analysis showed the presence of pre-core and basal core promoter mutants and 4 amino acid substitutions exclusively among FHF cases. None of the self-limiting patients exhibited these dual mutations. Genotype D was predominant, D1 being present in all FHF cases while D2 was most prevalent in AVH cases. Probably due to violation of accepted infection control procedures by the qualified medical practitioners, HBV prevalence was higher in the affected blocks before the outbreak. Gross and continued use of HBV contaminated (mutant and wild viruses) injection devices led to an explosive outbreak with high mortality with a striking association with pre-C/BCP mutants and D1 genotype.

摘要

2009 年,印度古吉拉特邦萨巴尔卡坦地区爆发了乙型肝炎疫情,共有 456 例病例和 89 例死亡。对患有自限性疾病(152 例,AVH)和暴发性肝衰竭(39 例,包括 27 例死亡和 12 例存活,FHF)的住院患者进行了调查。对这些患者进行了诊断标志物、乙型肝炎病毒(HBV)基因分型和突变分析检测。对 22 例 FHF 和 17 例 AVH 病例的完整 HBV 基因组进行了测序。在受影响最严重和最不严重的街区进行了 HBV 患病率和突变体鉴定血清学调查。来自医生的注射史与 FHF 和 AVH 病例有关。其他肝炎病毒的合并感染或更高的 HBV DNA 载量与死亡率无关。四个街区导致了 85.7%(391/456)的病例和 95.5%(89/89)的死亡,而两个相邻街区的死亡率可以忽略不计。序列分析显示,在 FHF 病例中仅存在前核心和基本核心启动子突变体和 4 个氨基酸替换。没有一个自限性患者表现出这两种突变。基因型 D 占主导地位,所有 FHF 病例中均存在 D1,而 D2 在 AVH 病例中最为普遍。可能是由于合格医务人员违反了公认的感染控制程序,在疫情爆发前,受影响街区的 HBV 流行率更高。大规模且持续使用 HBV 污染(突变和野生病毒)的注射装置导致了高死亡率的爆发性疫情,与前 C/BCP 突变体和 D1 基因型存在显著关联。

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