检测小鼠肝炎病毒的SNaPshot分型技术及其应用
作者单位:

湖北医药学院,重庆医科大学,重庆医科大学,重庆医科大学,重庆医科大学,重庆医科大学,重庆医科大学

基金项目:

重庆市科委应用开发项目(No. CSTC2014YYKFA110033)


Typing Mouse Hepatitis Viruses Using SNaPshot Assay
Author:
Affiliation:

Chongqing Medical University,Chongqing Medical University,Chongqing Medical University,Chongqing Medical University,Chongqing Medical University,Chongqing Medical University

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    摘要:

    建立一种能对MHV1、MHV3、JHM、A59 4种常见小鼠肝炎病毒(Murine Hepatitis Virus,MHV)进行分型检测的SNaPshot新方法。根据MHV 4种常见毒株基因序列比对结果,设计内外两对PCR通用引物和4个单碱基延伸引物,提取MHV 4种常见毒株RNA,逆转录后进行PCR扩增,纯化扩增产物,用SNaPshot方法进行单碱基延伸,将产物进行毛细管凝胶电泳,根据电泳结果分析毒株基因型。优化SNaPshot分析条件,进行灵敏度、特异性分析。用ELISA法和SNaPshot方法检测41例小鼠(Mus musculus)血清样本,将阳性样本进行克隆测序检测。当T1 ~ T4引物修饰的poly T的数量分别为0、3、10和15,其浓度比为4︰6︰5︰10,引物大小分别为16 bp、19 bp、26 bp和31 bp时,SNaPhot分型检测MHV cDNA的最低浓度为1.25 mg/L,特异性为100%,与ELISA和T-克隆测序比较,其准确性为100%(41/41),阳性样本均为JHM毒株。实验结果说明,所建立的SNaPshot检测方法能对MHV1、MHV3、JHM、A59进行分型检测,并且具有灵敏、特异、准确的优点。

    Abstract:

    SNaPshot assay is a single base extension assay which, by extending a base after four primers, displays color of the base through capillary gel electrophoresis to judge the genotype of samples. We aimed to establish a SNaPshot assay to type mouse hepatitis viruses (MHV), including MHV1, MHV3, JHM, and A59. The SNaPshot assay was developed after polymerase chain reaction (PCR) using cDNA from MHV strains two pairs of universal PCR primers and four single-base primers that were designed according to the conserved sequence of the four strains. The PCR products were analyzed by capillary gel electrophoresis. The sensitivity and specificity of the SNaPshot assay were analyzed using gradient dilution method and compared with human Hepatitis B virus (HBV). The accuracy of the SNaPshot assay was analyzed using 41 murine (Mus musculus) serum samples by comparing with ELISA and sequencing the samples containing MHVs. The optimal conditions of SNaPshot assay were that T1﹣T4 primers were 0, 3, 10, and 15 Ts in modification, 4︰6︰5︰10 in concentration, and 16 bp, 19 bp, 26 bp and 31 bp in length. The sensitivity of the SNaPShot assay was 1.25 mg/L (MHV cDNA) (Fig. 3), the specificity was 100% (Fig. 4), and the accuracy was 100% (41/41, Table 3), which was confirmed by ELISA, and the sequencing data. The SNaPshot assay is a sensitive, specific, and accurate method for typing MHV1, MHV3, JHM, and A59.

    参考文献
    Carolyn DH, Tahlita CZ, Christian H, at al. 2009. A SNaPshot assay for the rapid and simple detection of four common hotspot codon mutations in the PIK3CA gene [J]. BMC Research Notes, 2:1-6.
    Wang HX, Yue J, Han M, et al. 2010. Rapid Method for Identification of Six Common Species of Mycobacteria Based on Multiplex SNP Analysis[J]. Journal of Clinical Microbiology, 48:247-250.
    F.M.奥斯伯, R.E.金斯顿, J.G.塞德曼, 等. 2005. 精编分子生物学实验指南[M].第四版. 北京: 科学出版社, 1-27.
    吴迪, 王洪武, 宁琴. 2012. TGF-β1在MHV-3诱导的小鼠爆发型肝炎模型中的表达研究[J]. 基础医学, 2(7):28-30.
    陆玉蕾,林有智, 王晓晶, 等. 2012. TNF-α在MHV-3诱导的小鼠病毒性肝炎模型肾脏中的表达及意义[J]. 基础医学, 2(6):22-23.
    甘露, 张哲, 郭进强, 等. 2012. 小鼠慢性病毒性肝炎诱发肝脂肪变性模型的构建[J]. 南方医科大学学报, 32(12):1722-1726.
    苏丽贤, 汤朝晖, 万为人, 等. 2011. 藏茵陈对MHV-A59病毒感染湿热证小鼠肝脏损伤的干预作用[J]. 时珍国医国药, 22(8):1822-1824.
    周艳. 2008.小鼠肝炎病毒N基因的表达与间接ELISA检测方法的建立与应用 [D].扬州大学硕士学位论文.
    孙亚男, 李安, 史斌, 等. 2013. SNaPshot技术检测Y-SNP位点O3-M122单倍群的应用[J]. 中国法医学杂志, 28(1):1-4.
    胡抗, 袁东亚, 贺学, 等. 2013. 分子人类学中的单核苷酸突变检测方法的研究进展[J]. 生命科学, 25(1):119-125.
    刘小琦. 2013. 采用SNaPshot方法对中国老年黄斑变性与C2和C3基因单核苷酸多态性进行相关性研究[J]. 国际检验医学杂志, 34(3): 285-290.
    张成才, 谭礼强, 王丽鸳, 等. 2014. SNaPshot技术检测茶树SNP研究[J]. 茶叶科学, 34(2): 180-187.
    谢雯, 鲍世民, 谢建云, 等. 2012. 基于PCR-LDR平台的近交系小鼠遗传质量快速检测方法[J]. 中国实验动物学报, 20(4): 1-8.
    王玉珏, 岳敏, 顾阳, 等. 2015. 西藏小型猪GH基因部分序列的SNP分析[J]. 中国比较医学杂志, 25(1): 50-54.
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赵婷婷,王会娟,王蕾,谭毅,王胜,张道华,赖国旗.2016.检测小鼠肝炎病毒的SNaPshot分型技术及其应用.动物学杂志,51(6):1084-1091.

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  • 收稿日期:2015-06-16
  • 最后修改日期:2016-08-23
  • 录用日期:2016-08-14
  • 在线发布日期: 2016-11-28