Abstract
周永明,陈秀华,徐闻,金汇明,李超群,梁未丽,王多春,阎梅英,娄静,阚飙,冉陆,崔志刚,王树坤,许学斌.沙门菌常规检测方法分段控制技术在网络实验室构建中基础作用的评估[J].Chinese journal of Epidemiology,2013,34(11):1105-1110
沙门菌常规检测方法分段控制技术在网络实验室构建中基础作用的评估
The fundamental role of Stage Control Technology on the detectability for Salmonellanetworking laboratory
Received:June 05, 2013  
DOI:10.3760/cma.j.issn.0254-6450.2013.011.014
KeyWord: 评估  伤寒与非伤寒沙门菌  常规检测  阳性率  网络实验室
English Key Word: Assessment  Typhoid and non-typhoid Salmonella  Conventional detection  Positive rates:Network laboratory
FundProject:中美新发和再发传染病合作项目子项目6;国家“十-五”重大专项(2008ZXl0004-008);国家“十二五”重大专项(2012ZXl0004215-003);国家“863”项目(2012AAl01601);中日亚洲传染病实验室合作网络H23-shinkou-shifei-020子课题
Author NameAffiliationE-mail
ZHOU Yong-ming Yunnan Provincial Center for Disease Control and Prevention, Ynnnan650022, China  
CHEN Xiu-hua Shanghai Minhang District Center for Disease Control arid Prevention  
XU Wen Yunnan Provincial Center for Disease Control and Prevention, Ynnnan650022, China  
JIN Hui-ming Shanghai Municipal Center for Disease Control and Prevention  
Ll Chao-gun Yunnan Provincial Center for Disease Control and Prevention, Ynnnan650022, China  
LIANG Wei-li China Center for Disease Control and Prevention  
WANG Duo-chun China Center for Disease Control and Prevention  
YAN Mei-yiing China Center for Disease Control and Prevention  
LOU Jing China Center for Disease Control and Prevention  
KAN Biao China Center for Disease Control and Prevention  
RAN Lu0 China Center for Disease Control and Prevention  
CUl Zhi-gang China Center for Disease Control and Prevention  
WANG Shu-kuns Yunnan Yuxi Citv Center for Disease Control and Prevention ynyxwsk@163.Com 
XU Xue-bin Shanghai Municipal Center for Disease Control and Prevention xbxu@scdc.sh.cn 
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Abstract:
      目的评估沙门菌常规检测方法分段控制技术在网络实验室建设中的基础性作用。方法建立经过关键点技术控制评价的沙门菌检测方法,评估上海市参加世界卫生组织一全球沙门菌监测项目(WHO-GSS)、中美新发和再发传染病项目(GFN)网络实验室的实施,培训云南省玉溪市疾病预防控制中心腹泻标本沙门菌常规检测能力,收集2006-2012年省级GSS-GFN监测点年度沙门菌监测阳性率。结果基于分段控制技术设计的沙门菌分离、鉴定和种属鉴定、血清分群方法,能同时满足网络实验室对伤寒、非伤寒沙门菌检测敏感性需求;上海市网络实验室建设从2006年的5个公共卫生实验室和8个临床实验室发展到2011年的9和22个,伤寒、非伤寒沙门菌临床分离菌株从2006年的196株增加到2011年1442株;2012年云南省玉溪市临床腹泻病例沙门菌阳性率为2.4%;除上海外还有3个省级监测点将亚硒酸盐磺绿增菌液(SBG)作为沙门菌选择性增菌液,以上海市沙门菌监测基线最稳定。结论常规沙门菌检测分段优化的方法是构建区域网络实验室的基础,由此可上升为具有精确表型鉴定和分子分型能力的国家网络实验室。
English Abstract:
      Objective To evaluated the fundamental role of stage control technology(SCT)on the detectability for Salmonella networking laboratories.Methotis Appropriate Salmonella detection methods after key point control being evaluated.were establishment and optimized.Ourtraining and evaluation networking laboratories participated in the World Health Organization-Global Salmonella Surveillance Project(WHO.GSS)and China-U.S.Collaborative Program on Emergingand Re.emerging infectious diseases Project(GFN)in Shanghai.Stafr members from the YunnanYuxi city Center for Disease Control and Prevention were trained on Salmonella isolation fromdiarrhea specimens.Data on annual Salmonella positive rates was collected from the provincial.monitoring sites to be part of the GSS and GFN projects from 2006 to 20 1 2.Results Themethodology was designed based on the conventional detection procedure of Salmonella whichinvolved the processes as enrichment.isolation.species identification and sero.typing.These methodswere simultaneously used to satisfy the sensitivity requirements on non.typhoid Salmonella detectionfor networking laboratories.Public Health Laboratories in Shanghai had developed from 5 in 2006 to 9 in 20 1l,and Clinicallaboratories from 8 to 22.Number of clinicalisolates.including typhoid andnon-typhoid Salmonella increased from l96 in 2006 to 1 442 in 20 11.The positive rate of Salmonellaisolated from the clinical diarrhea cases was 24%in Yuxi county.in 20l2.At present.three otherprovincial monitoring sites were using the SBG technique as selectivity enrichment broth for Salmonella isolation,with Shanghai having the most stable positive baseline.Conclusion Themethod of SCT was proved the premise of the network laboratory construction.Based on this,theimprovement of precise phenotypic identification and molecular typing capabilities could reach thelevel equivalent to the national networking laboratory.1evel
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