| 南京地区戊型肝炎病毒基因型鉴定和变异分析 |
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| 引用本文： | 程险峰,戴星,孟继鸿,张红梅,周镇先,丁福,梁久红,耿全林.南京地区戊型肝炎病毒基因型鉴定和变异分析[J].Virologica Sinica,2005,20(5):468-471. |
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| 作者姓名： | 程险峰 戴星 孟继鸿 张红梅 周镇先 丁福 梁久红 耿全林 |
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| 作者单位： | 东南大学医学院病原生物学与免疫学系 江苏南京210009
(程险峰，孟继鸿，张红梅，丁福，梁久红)，东南大学医学院附属中大医院皮肤科 江苏南京210009
(戴星)，东南大学医学院附属南京市第二医院检验科 江苏南京210003
(周镇先)，东南大学医学院附属南京市第二医院检验科 江苏南京210003(耿全林) |
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| 基金项目： | 国家自然科学基金(30271231,30271212)，江苏省自然科学基金(KB2002053)，江苏省社会发展科技指导性计划(BS2004506)资助项目 |
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| 摘 要： | 为了解南京地区戊型肝炎病毒(Hepatitis E virus,HEV)基因型的分布以及变异状况,本研究采用逆转录套式聚合酶反应(RT-nPCR)的方法检测南京地区40份急性散发性戊型肝炎患者的粪便标本,对PCR产物进行测序,利用生物信息学软件比较核苷酸的同源性、遗传距离,进行基因分型和变异分析。40份粪便标本中检测到14份阳性HEV、RNA,检出率为35%,基因分型均为HEV IV型,且分属2个不同的亚型;利用生物信息学软件对国内I型和IV型毒株加以比较,发现HEV IV型毒株比I型变异程度高,不同年份的HEV IV型毒株变异更大,有新的亚型出现,且变异有随时间推移而增大的趋势。
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| 关 键 词： | 戊型肝炎病毒 基因型 序列分析 逆转录套式聚合酶链反应 |
| 收稿时间： | 2005-03-21 |
| 修稿时间： | 2005-05-18 |
Genotype Identification and Variation Analysis of Hepatitis E Virus Isolated in Nanjing, China |
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| CHENG Xian-feng , DAI Xing , MENG Ji-hong , ZHANG Hong-mei , ZHOU Zhen-xian , DING Fu , LIANG Jiu-hong , GENG Quan-lin.Genotype Identification and Variation Analysis of Hepatitis E Virus Isolated in Nanjing, China[J].中国病毒学(英文版),2005,20(5):468-471. |
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| Authors: | CHENG Xian-feng DAI Xing MENG Ji-hong ZHANG Hong-mei ZHOU Zhen-xian DING Fu LIANG Jiu-hong GENG Quan-lin |
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| Institution: | 1. Department of Microbiology and Immunology, Medical College, Southeast University, Nanjing 210009,China; 2. Zhongda Hospital, Medical College ,Southeast University, Nanjing 210009,China; 3.The Affiliated Second Hospital of Nanjing, Medical College,Southeast University, Nanjing 210003,China |
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| Abstract: | The objective of this study was to identify and analyze genotype distribution and genetic variation of Hepatitis E virus(HEV) isolated in Nanjing,China.RT-nPCR based on universal primers for multiple HEV genotypes was used to detect HEV RNA in 40 samples collected from patients with acute sporadic hepatitis E.PCR products were sequenced and analyzed with the LASERGENE and PHYLIP softwares.Fourteen out of the 40 samples were positive for RT-nPCR.The positive rate was 35%.All of the fourteen isolates were clustered into HEV genotype IV and were separated into two different sub-genotypes.The nucleotide sequences of the HEV isolates of genotype IV presented higher variability when compared with the sequences of the Chinese isolates of HEV genotype I.Moreover,a new subtype of HEV genotype IV was discovered in this study. |
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| Keywords: | Hepatitis E virus Genotype Sequence analysis RT-nPCR |
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