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快速获取55型腺病毒基因组序列的方法
引用本文:刘媛,王文博,邹自英,冯子良,范泉水,熊杰.快速获取55型腺病毒基因组序列的方法[J].微生物学通报,2017,44(11):2708-2713.
作者姓名:刘媛  王文博  邹自英  冯子良  范泉水  熊杰
作者单位:1. 成都军区总医院检验科 四川 成都 610083,2. 成都军区疾病预防控制中心 四川 成都 610021,1. 成都军区总医院检验科 四川 成都 610083,2. 成都军区疾病预防控制中心 四川 成都 610021,2. 成都军区疾病预防控制中心 四川 成都 610021,1. 成都军区总医院检验科 四川 成都 610083
基金项目:国家自然科学基金青年项目(No. 81301445);全军后勤“十二五”重大专项(No. AWS11L009);全军医学科技青年培育项目(No. 14QNP057);上海市医学生物防护重点实验室开放课题(No. SKLM1401)
摘    要:【目的】建立快速获取55型腺病毒的全长基因组序列的方法。【方法】根据55型腺病毒的基因组特点,设计覆盖55型腺病毒基因组序列的12对引物,分别以55型腺病毒DNA为模板,扩增得到12个PCR产物,通过对12个PCR产物测序及序列拼接,获得55型腺病毒的全长基因组序列。【结果】从本院急性上呼吸道感染者咽拭子标本中分离得到一株55型腺病毒毒株SF04/SC/2016,以其DNA为模板扩增成功获得12个PCR产物,对其进行测序,并对12段序列进行拼接得到55型腺病毒的全长基因组序列,与已报到的各型腺病毒序列进行比对,采用邻位相连法构建系统发育进化树,所得序列与55型腺病毒处于同一分支,进一步确认该病原体为55型腺病毒。【结论】研究公布的序列和方法,能够实现更方便对腺病毒的快速测序,为揭示55型腺病毒的进化特点及制订疾病防控策略提供了有效手段。

关 键 词:55型腺病毒,病原分离,全基因测序,序列拼接

Rapid acquisition of complete viral genome sequence of human adenovirus type 55
LIU Yuan,WANG Wen-bo,ZOU Zi-Ying,FENG Zi-Liang,FAN Quan-Shui and XIONG Jie.Rapid acquisition of complete viral genome sequence of human adenovirus type 55[J].Microbiology,2017,44(11):2708-2713.
Authors:LIU Yuan  WANG Wen-bo  ZOU Zi-Ying  FENG Zi-Liang  FAN Quan-Shui and XIONG Jie
Institution:1. Department of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan 610083, China,2. Center for Disease Control and Prevention of Chengdu Military Region, Chengdu, Sichuan 610021, China,1. Department of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan 610083, China,2. Center for Disease Control and Prevention of Chengdu Military Region, Chengdu, Sichuan 610021, China,2. Center for Disease Control and Prevention of Chengdu Military Region, Chengdu, Sichuan 610021, China and 1. Department of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan 610083, China
Abstract:Objective] To build a simple method for rapidly obtaining the full-length genome sequence of adenovirus type 55 (HAdV-55). Methods] 12 pairs of primers were designed which covered the whole genome sequence of HAdV-55. HAdV-55 DNA was used as the template for PCR and twelve PCR products were obtained, which were sequenced respectively. Resulting sequences were assembled together and then the whole gene sequence was obtained. Results] A strain of HAdV-55 (SF04/SC/2016) was isolated from throat swab specimens of a patient with acute upper respiratory tract infection. Twelve PCR products and their sequences were obtained. The sequences were assembled which yield the full-length genomic sequence. Sequence analysis was performed between this HAdV-55 strain and previous reported HAdV-55 virus in China. Phylogenetic tree was constructed by neighbor-joining method and this virus is in the same branch with previous reported HAdV-55 strains, which confirmed that this pathogen is HAdV-55. Conclusion] The primer sequences and methods published in this study could facilitate the rapid sequencing of adenovirus, which will be contribute to reveal the evolutionary characteristics of HAdV-55 and the prevention and control of adenovirus type 55 related disease.
Keywords:Adenovirus type 55  pathogen isolation  whole genome sequencing  sequence assembly
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