[1]伊 洁a,解宏杰a,刘文静a,等.多重核酸检测技术和传统检测方法对胃肠道感染性病原体检测的比较[J].现代检验医学杂志,2017,32(05):118-121.[doi:10.3969/j.issn.1671-7414.2017.05.017]
 YI Jiea,XIE Hong-jiea,LIU Wen-jinga,et al.Comparation of Pathogens in Infectious Gastroenteritis Cases Using Multiplex Ncleic Acid Amplification Testing and Conventional Laboratory Diagnostic Tools[J].Journal of Modern Laboratory Medicine,2017,32(05):118-121.[doi:10.3969/j.issn.1671-7414.2017.05.017]
点击复制

多重核酸检测技术和传统检测方法对胃肠道感染性病原体检测的比较()
分享到:

《现代检验医学杂志》[ISSN:/CN:]

卷:
第32卷
期数:
2017年05期
页码:
118-121
栏目:
研究简报·实验技术
出版日期:
2017-11-02

文章信息/Info

Title:
Comparation of Pathogens in Infectious Gastroenteritis Cases Using Multiplex Ncleic Acid Amplification Testing and Conventional Laboratory Diagnostic Tools
文章编号:
1671-7414(2017)05-118-04
作者:
伊 洁a解宏杰a刘文静a赵玉沛b徐英春a
中国医学科学院北京协和医院a.检验科; b.基本外科,北京 100730
Author(s):
YI JieaXIE Hong-jieaLIU Wen-jingaZHAO Yu-peibXU Ying-chuna
a.Department of Clinical Laboratory; b.Department of General Surgery,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences,Beijing 100730,China
关键词:
胃肠道感染性疾病 多重核酸检测技术 传统检测技术
分类号:
Q503; R378
DOI:
10.3969/j.issn.1671-7414.2017.05.017
文献标志码:
A
摘要:
目的 比较一种商品化的多重核酸检测试剂盒和传统检测方法对胃肠道感染性病原体检测的性能。方法 收集135例有胃肠道感染症状患者的135份粪便标本,分别用多重核酸检测技术和传统检测方法进行检测。结果 多重核酸检测技术和传统检测方法检出至少一种病原体的检出率分别是81.5%和33.3%,其中多重核酸检测技术可检出12种病原体,传统检测方法可检出5种病原体; 传统方法检测的阴性标本中,用多重核酸检测技术可以检出48.1%的阳性标本; 多重核酸检测技术和传统检测方法分别检出31.1%和0的混合感染标本; 多重核酸检测技术检测的结果中,门诊、住院和急诊患者标本中病毒的阳性检出率均是最高,分别是15.6%,31.1%和3.7%。传统检测方法和多重核酸检测技术方法对住院的标本中病原体的检出率均高于急诊和门诊患者。采用配对资料χ2检验进行统计学分析,两种方法的阳性检出率,混合感染标本的阳性检出率及不同环境中阳性标本检出率,差异均具有统计学意义(χ2=45.57~58.887,P<0.01)。结论 多重核酸检测技术相对于传统检测方法阳性检出率更高,为临床上诊断胃肠道感染提供一种可能有效的检测方法。
Abstract:
Abstract:Objective To compare the performance of a commercial multiplex nucleic acid amplification test(MultiplexNAT)and the conventional microbiological testing for etiologic pathogens of gastroenteritis.Methods 135 stool specimens from 135 patients showing gastroenteritis symptoms were collected and detected by both the MultiplexNAT and the conventional testing.Results The detection rates of at least one potential etiologic agent was 81.5% and 33.3% by the MultiplexNAT and conventional testing, respectively.12 pathogens could be detected by the MultiplexNAT while 5 pathogens could be detected by the conventional testing. Of the negative samples from conventional testing,48.1% were positive with the MultiplexNAT.Furthermore, 31.1% and none of the stool specimens showed coinfection by MultiplexNAT and conventional testing,respectively.Using MultiplexNAT,the positive detection rates of viruses were highest in the outpatient settings,emergency and inpatient settings,which were 15.6%,31.1% and 3.7% respectively.The overall proportion of pathogen-positive samples was higher for outpatientsettings than for emergency and inpatient settings using both conventional testing and the MultiplexNAT.χ2 test for paired data for statistical analysis:positive detection rates,coinfection positive detection rates and three settings positive detection rates using two methods was statistically significantrespectively(χ2=45.57~58.887,P<0.01).Conclusion The MultiplexNAT significantly has more postivie detection rates compared to the conventional testing,and could be a possible method in the diagnosis of infectious gastroenteritis diseases.

参考文献/References:

[1] Wang X,Wang J,Sun H,et al.Etiology of childhood infectious diarrhea in a developed region of China:compared to childhood diarrhea in a developing region and adult diarrhea in a developed region[J].PLoS One,2015,10(11):e0142136.
[2] Walker CL,Rudan I,Liu L,et al.Global burden of childhood pneumonia and diarrhoea[J].Lancet,2013,381(9875):1405-1416.
[3] Qu M,Deng Y,Zhang X,et al.Etiology of acute diarrhea due to enteropathogenic bacteria in Beijing,China[J].J Infect,2012,65(3):214-222.
[4] 任 强,常文辉,张梦妍,等.2009~2014年陕西省艾滋病哨点监测重点人群HIV感染和新发感染检测分析[J].现代检验医学杂志,2015,30(3):56-59. Ren Q,Chang WH,Zhang MY,et al.Analysis of HIV infection and newinfections detection of AIDS sentinel surveillance focus groups in Shaanxi province 2009~2014[J].Journal of Modern Laboratory Medicine,2015,30(3):56-59.
[5] 肖海军,殷晓晴,张慧莲,等.深圳地区儿童A群致病性链球菌感染流行现状及M蛋白基因分型分析[J].现代检验医学杂志,2016,31(6):51-54. Xiao HJ,Yin XQ,Zhang HL,et al.Analysis of the prevalence statusand M protein gene classification of A group pathogenic Streptococcus infection of children in Shenzhen area[J].Journal of Modern Laboratory Medicine,2016,31(6):51-54.
[6] Zhang H,Morrison S,Tang YW.Multiplex polymerase chain reaction tests for detection of pathogens associated with gastroenteritis[J].Clin Lab Med,2015,35(2):461-486.
[7] Liu J,Gratz J,Amour C,et al.A laboratory-developed TaqMan Array Cardfor simultaneous detection of 19 enteropathogens[J].J Clin Microbiol,2013,51(2):472-480.
[8] Coste JF,Vuiblet V,Moustapha B,et al.Microbiological diagnosis of severe diarrhea in kidney transplant recipients by use of multiplex PCR assays[J].J Clin Microbiol,2013,51(6):1841-1849.
[9] Amar CF,East CL,Gray J,et al.Detection by PCR of eight groups of enteric pathogens in 4 627 faecal samples:re-examination of the English case-control Infectious Intestinal Disease Study(1993~1996)[J]. Eur J Clin MicrobiolInfect Dis,2007,26(5):311-323.
[10] Maes B,Hadaya K,de Moor B,et al.Severe diarrhea in renal transplant patients:results of the DIDACT study[J].Am J Transplant,2006,6(6):1466-1472.
[11] Atmar RL,Estes MK.The epidemiologic and clinical importance of norovirus infection[J].Gastroenterol Clin North Am,2006,35(2):275-290,viii.
[12] Mai H,Jin M,Guo X,et al.Clinical and epidemiologic characteristics of norovirus GII.4 Sydney during winter 2012-13 in Beijing,China following itsglobal emergence[J].PLoS One,2013,8(8):e71483.
[13] Halligan E,Edgeworth J,Bisnauthsing K,et al.Multiplex molecular testing for management of infectious gastroenteritis in a hospital setting:a comparative diagnostic and clinical utility study[J].Clin Microbiol Infect,2014,20(8):O460-O467.
[14] Patel A,Navidad J,Bhattacharyya S.Site-specific cli-nical evaluation of the Luminex xTAG gastrointestinal pathogen panel for detection of infectious gastroenteritis in fecal specimens[J].J Clin Microbiol,2014,52(8):3068-3071.
[15] Sammons JS,Toltzis P,Zaoutis TE.Clostridium difficile lnfection in children[J].JAMA Pediatr,2013,167(6):567-573.
[16] Muhsen K,Levine MM.A systematic review and meta-analysis of the association between Giardia lamblia and endemic pediatric diarrhea in developing countries[J].Clin Infect Dis,2012,55(4):S271-S293.
[17] Verweij JJ,Stensvold CR.Molecular testing for clinical diagnosis and epidemiological investigations of intestinal parasitic infections[J].Clin Microbiol Rev,2014,27(2):371-418.
[18] Lu L,Jia R,Zhong H,et al.Molecular characterization and multiple infections of rotavirus,norovirus,sapovirus,astrovirus and adenovirus in outpatients with sporadic gastroenteritis in Shanghai,China,2010~2011[J].Arch Virol,2015,160(5):1229-1238.
[19] Jia LP,Qian Y,Zhang Y,et al.Prevalence and genetic diversity of noroviruses in outpatient pediatric clinics in Beijing,China 2010~2012[J].Infect Genet Evol,2014(28):71-77

备注/Memo

备注/Memo:
基金项目:卫生部公益性行业科研专项(项目编号:201402001)。 作者简介:伊 洁(1983-),女,博士,助理研究员,主要从事病原微生物和肿瘤分子检测,E-mail:yijie0908@126.com。 通讯作者:徐英春(1964-),男,本科,研究员,博士生导师,主要从事临床微生物研究,E-mail:xycpumch@139.com。
更新日期/Last Update: 1900-01-01