| 周济华,张海林,王静林,杨卫红,米竹青,张云智,章域震,宋先毅,胡秋凌,董应宽,普文华,胡海梅,高丽芬,袁庆虹,亚红祥,冯云.云南省楚雄州汉坦病毒宿主动物及分子流行病学研究[J].中华流行病学杂志,2009,30(3):239-242 |
| 云南省楚雄州汉坦病毒宿主动物及分子流行病学研究 |
| Survey on host animal and molecular epidemiology of hantavirus in Chuxiong prefecture, Yunnan province |
| 收稿日期:2008-10-26 出版日期:2014-09-11 |
| DOI：10.3760/cma.j.issn.0254-6450.2009.03.009 |
| 中文关键词: 汉坦病毒 汉城型 宿主动物 分子流行病学 |
| 英文关键词: Hantavirus Seoul type Host animal Molecular epidemiology? |
| 基金项目: |
| 作者 | 单位 | E-mail | | 周济华 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 张海林 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | zhangHL715@163.com | | 王静林 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 杨卫红 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 米竹青 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 张云智 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 章域震 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 宋先毅 | 云南省楚雄州疾病预防控制中心 | | | 胡秋凌 | 云南省楚雄州疾病预防控制中心 | | | 董应宽 | 楚雄州卫生局 | | | 普文华 | 云南省楚雄州疾病预防控制中心 | | | 胡海梅 | 云南省楚雄州疾病预防控制中心 | | | 高丽芬 | 云南省楚雄州疾病预防控制中心 | | | 袁庆虹 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 亚红祥 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | | | 冯云 | 云南省地方病防治所/云南省病毒立克次体研究中心, 大理 671000 | |
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| 中文摘要: |
| 目的 掌握汉坦病毒(HV)在云南省啮齿动物中的流行情况及其遗传特征. 方法 采用笼夜法捕鼠, 鼠肺标本用直接免疫荧光法检测HV抗原, 用RT-PCR法检测HV核酸及分型, 对产物进行序列测定, 用PHYLIP软件包进行系统发生分析. 结果 2005-2006年在云南省楚雄州10个县(市)居民区共捕获鼠类4属8种1421只, 其中褐家鼠1056只, 构成比高达74. 31%, 其次为黄胸鼠(19. 70%). 检测鼠肺组织1029份, HV抗原阳性53份, 总带病毒率为5. 15%, 带病毒鼠种为褐家鼠(5. 08%, 38/748))、黄胸鼠(5. 97%, 12/201)、大足鼠(7. 69%, 2/26)和斯氏家鼠(6. 25%, 1/16). HV汉城型(SEO)核酸检测阳性21份(褐家鼠15份, 黄胸鼠4份, 大足鼠2份). 获得的12个病毒S片段核苷酸序列与GenBank中国SEO型病毒R22、L99和HLD65株同源性较高, 为87. 1%～99. 7%;与汉滩型(HTN)76-118株同源性仅为64. 4%～69. 1%. 系统进化分析显示, 楚雄州12个病毒S片段核苷酸序列与SEO型亲缘关系较近, 与HTN型及其他型HV相距较远, 证实这12份病毒标本均为SEO型病毒, 并可分S1和S3两个亚型. 结论 首次证实楚雄州10个县(市)广泛存在以褐家鼠为主要传染源的HFRS家鼠型疫源地及SEO型病毒的流行. 分析发现SEO型不同亚型病毒的分布有其地域特点和独立性. |
| 英文摘要: |
| Objective To determine the hosts of hantavirus(HV)and its molecular epidemiological characteristics, to provide evidence for prevention and control on hemorrhagic fever with renal syndrome(HFRS). Methods Rodents were captured by a special trap within the residential area. The antigens of HV in lung tissues were detected by direct immuno-fluorescence assay(DFA). Nucleotide sequences of HV were amplified by RT-PCR with HV genotype-specific primer. The amplified genes were then sequenced. Phylogenetic tree were built on nucleotide sequence with Clusta1X 1. 83 software. Results 1421 rodents were captured and classified into 8 species of 4 Genera in the epidemic area within 10 counties of Chuxiong prefecture, Yunnan province, between 2005 and 2006. Out of the 1421 rodents, 1056(74. 31%)of them were Rattus norvegicas and 280(19. 70%)belonged to Rattus flavipectus. The antigens of HV were detected by DFA in lung tissues and the total positive rate of HV was 5. 15%(53/ 1029). After applying the sequencing nucleotide method to the 53 positive specimens, data showed that 21 specimens were positive and all of them belonged to Seoul type( 15 samples were from Rattus norvegicus, 4 samples Rattasflavipectas, 2 samples Rattus nitidas). The partial S segments from 12 specimens were sequenced which appeared homologic with R22, L99 and HLD65 from GenBank in relatively high level(87. 1%-99. 7%). When compared to 76-118 strain of Hantaan type, their homologic degree was only 64. 4%-69. 1%. Results from Phylogenetic analysis showed that 12 specimens belonged to Seoul type. As for their homology, they were significantly similar to Seoul type and could be tentatively divided into two subtypes S1 and S3. Conclusion It was confirmed that the Seoul type virus, as HFRS's pathogenetic agent mainly carried by rats, prevailed widely in Chuxiong prefecture. Owing to the local ecological environment, we also noticed the characteristics of different HV subtypes among Seoul type. |
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