期刊文献+

逆转录-聚合酶链反应-酶联夹心杂交法检测呼吸道合胞病毒及其亚型感染 被引量:1

The study of identification of RSV subgroups A and B by reverse transcription polymerase chain reaction enzyme linked sandwich hybridization assay
下载PDF
导出
摘要 目的:建立一种呼吸道合胞病毒(RSV)及其亚型核酸检测方法并初步应用于临床,检测浙南地区RSV及其亚型的流行情况。方法:根据RSVG蛋白基因核苷酸序列设计引物和探针,通过逆转录-聚合酶链反应-酶联夹心杂交法(RT-PCR-ELSH)随机检测了浙南地区连续两年冬春季期间202例急性下呼吸道感染的婴幼儿鼻咽部分泌物中RSV及其亚型的病毒核酸;与病毒分离培养、直接免疫荧光法(DFA)、OligoDetect试剂盒比较探讨其临床实用性。结果:202例标本中RSV阳性123例,阳性检出率为60.9%,2002~2003年和2003~2004年冬春季分别为68.2%和52.6%;两个冬春季都以RSVA亚型为主,占78.9%,2002~2003年冬春季A亚型占RSV阳性标本中的76.7%,2003~2004年A亚型占82.0%;RT-PCR-ELSH阳性检出率与其他三种方法的阳性检出率差异无显著性(P>0.05)。结论:RT-PCR-ELSH法用于检测RSV及其亚型,是一种灵敏度高、特异性强,方便、快速的方法,非常适用于临床标本的大批量检测和流行病学调查;RSV是引起浙南地区冬春季婴幼儿急性下呼吸道感染的最主要的病原体,并以A亚型为主。 Objective: To establish a RT-PCR-enzyme-linked sandwich hybridization(RT- PCR-ELSH)method for the identification of RSV subgroups A and B and to analyze the epidemics and distributive situations of RSV subgroups A and B in infants with acute lower respiratory tract infections in the southern area of Zhejiang province. Methods:Primers and probes to RSV G protein genes were designed based on published sequence database from NCBI GeneBank. The nucleic acid(RNA)of RSV in the nasopharyngeal aspirates(NPAs)obtained from 202 infants with acute lower respiratory tract infection at Children’s Hospital of Wenzhou Medical College over two consecutive winters and springs from 2002~2003 and 2003~ 2004 were randomly detected with RT-PCR-ELSH,to analyze the diseased situation of RSV and its subgroups in the southern area of Zhejiang province. The value and feasibility of RT- PCR-ELSH were assessed by comparing with virus isolation in cell culture, DFA and OligoDetect Kit obtained from Chemicon International. Results:Of the 202 samples,123(60.9%)were positive for RSV with RT-PCR-ELSH. In winters and springs of 2002~2003 and 2003~2004 RSV accounted for 68.2% and 52.6%, respectively. RSV subgroup A(78.9%)predominated in this two consecutive winters and springs of 2002~2003 and 2003~2004 (76.7%,82.0% of RSV positive samples,respectively). The sensitivity of RT-PCR-ELSH was the same as the other three measurement ways. Conclusions:RT-PCR-ELSH,with high sensitivity,specificity,convenience and rapidity, was an alternative for detection of RSV nucleic acid, especially used in the epidemiological survey and routine diagnosis of samples in batch. RSV is the major pathogen of acute lower respiratory tract infections among infants in winter and spring in the southern area of Zhejiang province. And RSV subgroup A predominated during the two consecutive winters and springs of 2002~2003 and 2003~2004.
出处 《温州医学院学报》 CAS 2005年第3期201-206,共6页 Journal of Wenzhou Medical College
基金 温州市科技局科研基金资助项目(Y2003A059)
关键词 逆转录-聚合酶链反应 酶联夹心杂交 呼吸道合胞病毒 reverse transcription polymerase chain reaction(RT-PCR) enzyme-linked sandwich hybridization respiratory syncytial virus (RSV)
  • 相关文献

参考文献14

  • 1Garenne M, Ronsmans C, Campbell H. The magnitude of mortality from acute respiratory infections in children under 5 years in developing countries[J]. World Health Stat Q,1992,45(2-3):180-191.
  • 2Abels S, D Nadal, A Stroehle, et al. Reliable detection of respiratory syncytial virus infection in children for adequate hospital infection control management[J]. J Clin Microbiol, 2001, 39(9): 3135-3139.
  • 3Falsey AR, MA Formica, EE Walsh. Diagnosis of respiratory syncytial virus infection: comparison of reverse transcriptionPCR to viral culture and serology in adults with respiratory illness[J]. J Clin Microbiol, 2002, 40(3): 817-820.
  • 4池永斌,吕建新,陆永绥.微量酶联夹心杂交法定量检测TNF-α mRNA[J].中国病理生理杂志,2003,19(9):1289-1291. 被引量:1
  • 5Freymuth F, G Eugene, A Vabret, et al. Detection of respiratory syncytial virus by reverse transcription-PCR and hybridization with a DNA enzyme immunoassay[J]. J Clin Microbiol, 1995,33(12): 3352-3355.
  • 6Yi-Wei Tang, Paul N Rys, Barbara J. Rutledge,et al. Comparative evaluation of colorimetric microtiter plate systems for detection of herpes simplex virus in cerebrospinal fluid[J]. J Clin Microbiol, 1998, 36(9): 2714-2717.
  • 7Britta Grondahl, Wolfram Puppe, Andrea Hoppe,et al. Rapid identification of nine microorganisms causing acute respiratory tract infections by single-tube multiplex reverse transcriptionPCR: Feasibility study[J]. J Clin Microbiol, 1999,37(1): 1-7.
  • 8Sullender WM, L Sun, LJ Anderson. Analysis of respiratory syncytial virus genetic variability with amplified cDNAs[J]. J Clin Microbiol, 1993,31(5): 1224-1231.
  • 9陈小芳,董琳,周晓聪,郑雯洁,王秀娣,李昌崇.306例儿童急性呼吸道感染鼻咽分泌物病毒病原检测[J].温州医学院学报,2004,34(2):108-110. 被引量:22
  • 10Mlinaric-Galinovic G,Ugrcic I,Detic D,et al. Epidemiological picture of respiratory viral infection in Croatia[J]. Acta med Iugosl 1991, 45(3):203-211.

二级参考文献21

  • 1Nathalie JS 顾方舟等(译).病毒、立克次体及衣原体疾病诊断技术[M].北京:北京医科大学,中国协和医大联合出版社,1993.561-570.
  • 2Takahashi M, Funato T, Ishii KK, et al. Measurement of tumor necrosis factor- alpha messenger RNA in synovial fibroblasts by real- time quantitative reverse transcriptase- polymerase chain reaction[J]. J Lab Clin Med , 2001, 137(2) : 101 - 106.
  • 3Herminger HP, Hoffmann R, Grewe M, et al. Purification and quantitative analysis of nucleic acids by anion - exchange high - performance liquid chromatography [ J ]. Biol Chem,1993, 374(8) :625 - 634.
  • 4Motmans D, Raus J, Vandevyver C. Quantification of cytokine messenger RNA in transfected human T cells by RT-PCR and an automated electrochemiluminescence- based post-PCR detection system[J]. J Immunol Methods, 1996,190(1):107- 116.
  • 5Leutenegger CM, Alluwaimi AM, Smith WL, et al. Quantitation of bovine cytokine mRNA in milk cells of healthy cattle by real- time TaqMan(R)polymerase chain reaction[J]. Vet Immunol Immunopathol, 2000,77(3 -4) :275- 287.
  • 6K Actor J, Kuffner T, C Dezzutti S, et al. A flash - type bioluminescent immunoassay that is more sensitive than radioimaging : quantitative detection of cytokine cDNA in activated and resting human cells[J]. J Immunol Methods, 1998,211(1- 2) :65- 77.
  • 7Andreoletti L, Lesay M, Deschildre A, et al. Differential detection of rhinoviruses and enterovirusese RNA sequences associated with classial immunofluorescence assay detection of respiratory virus antigens in nasopharyngeal seabs from infant with bronchiolitis [ J]. J Med Virol 2000,61(3) :341 - 346.
  • 8Mlinaric-Cndinovic G, Ugrcic I, Detic D, et al. Epidemiological picture of respiratory viral infection in Croatia[J]. Acta Med Iugosl, 1991 ;45(3) :203 - 211.
  • 9Cram JE. Mechanisms of virus-induced asthma[J]. J Pediatr, 2003,142(2 Suppl) :S9- 14.
  • 10Isaacs D, Joshi P. Respiratory infections and asthma[J] .Med J Aust,2002,177(Suppl) : S50 - 51.

共引文献120

同被引文献3

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部