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牛羊猪种布鲁氏菌快速鉴别PCR方法的建立及评价
引用本文:刘志国,塔娜,李晓燕,王妙,赵鸿雁,朴东日,蔚瑞平,米景川,李振军.牛羊猪种布鲁氏菌快速鉴别PCR方法的建立及评价[J].中国人兽共患病杂志,2019,35(5):399-403.
作者姓名:刘志国  塔娜  李晓燕  王妙  赵鸿雁  朴东日  蔚瑞平  米景川  李振军
作者单位:1.中国疾病预防控制中心传染病预防控制所,传染病预防控制国家重点实验室,北京 102206;
2.内蒙古自治区综合疾病预防控制中心,呼和浩特 010031;
3.乌兰察布市地方病防治中心,乌兰察布 012000
基金项目:内蒙古自治区自然科学基金项目(No.2018MS08004),传染病重大专项(No.2017ZX10303401),生物安全重点专项(No.2017YFC1200303),生物安全重点专项(No.2016YFC1200701)联合资助
摘    要:目的建立一种可在一个反应体系中同时鉴别布鲁氏菌及牛羊猪种布鲁氏菌的快速PCR鉴别方法。方法将布鲁氏菌及牛羊猪种布鲁氏菌的扩增引物进行优化组合,建立全新的BAMS-PCR方法;随后对该方法的特异性和灵敏度进行评价,并对现场分离的219株布鲁氏菌进行鉴别,评价其在布鲁氏菌鉴别中的应用价值。最后,用该方法对临床标本中布鲁氏菌的DNA进行扩增,评价其在临床诊断中的实用性。结果 BAMS-PCR方法可在同一反应中同时鉴别布鲁氏菌及牛种(1,2,4型),羊种(1,2和3型)和猪种(1型)布鲁氏菌,并有较好的特异性和敏感性。布鲁氏菌属,牛种,猪种和羊种布鲁氏菌引物的检测灵敏度分别为10 pg/μL,100 pg/μL, 10 pg/μL和100 pg/μL。BAMS-PCR对219株临床分离菌株的鉴定结果和常规生物分型方法的鉴定符合率为100%。经BAMS-PCR检测,97份临床血清样本仅6份为阳性,全血和组织(羊脾)样本全部为阴性。结论 BAMS-PCR是一种简便、快速、高效、准确的布鲁氏菌鉴别方法,可作为临床分离菌株的首选鉴别方法。

关 键 词:布鲁氏菌  聚合酶链式反应  鉴别  评价
收稿时间:2018-12-17

Establishment and evaluation of rapid discriminate PCR assay for Brucella abortus,Brucella melitensis and Brucella suis
LIU Zhi-guo,TA Na,LI Xiao-yan,WANG Miao,ZHAO Hong-yan,PIAO Dong-ri,YU Rui-ping,MI Jing-chuan,LI Zhen-jun.Establishment and evaluation of rapid discriminate PCR assay for Brucella abortus,Brucella melitensis and Brucella suis[J].Chinese Journal of Zoonoses,2019,35(5):399-403.
Authors:LIU Zhi-guo  TA Na  LI Xiao-yan  WANG Miao  ZHAO Hong-yan  PIAO Dong-ri  YU Rui-ping  MI Jing-chuan  LI Zhen-jun
Institution:1. National Institute of Infectious Diseases Control and Prevention, Chinese Center for Disease Control and Prevention/Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, Beijing 102206, China;2. Inner Mongolia Autonomous Region Central for Comprehensive Disease Control and Prevention, Huhhot 010031, China;3.Ulanqab Center for Endemic Disease Control and Prevention, Ulanqab 012000, China
Abstract:The aim of this study is to establish a rapid PCR discriminate assay for simultaneous identified Brucella genus, B. abortus, B. melitensis and B. suis in single reaction system. Amplification primers of Brucella genus and B. abortus, B. melitensis, and B. suis were combined and optimizated, a kind of novelty BAMS-PCR was established. Subsequently, specificity and sensitivity of BAMS-PCR were evaluated. In present study, 219 Brucella spp. were identified for assessed practicable of BAMS-PCR. Finally, DNA of Brucella clinical sample were detected by BAMS-PCR for evaluated using valuable in clinical diagnosis of Brucellosis. BAMS-PCR can simultaneous identified Brucella genus, B. abortus (bv.1,2 and 4), B. melitensis (bv.1-3) and B. suis (bv.1) in single reaction system, and this method had very higher specificity and sensitivity, detecting sensitivity of primers of Brucella genus, B. abortus, B. melitensis and B. suis with 10 pg/μL,100 pg/μL, 10 pg/μL and 100 pg/μL, respectively. There were 100% identification coincidence rate between BAMS-PCR and convention biotypes testing based on amplificated results of 219 Brucella spp. BAMS-PCR detected showing that there were only 6 serum samples were positive, others (whole blood and tissues (sheep spleen)) samples were all negative. BAMS-PCR was a simple, rapid, high efficiency and accuracy identification assay for Bruclla spp., could as first choice discriminate method of clinical isolates Bruclla spp.
Keywords:Brucella spp    PCR  discriminate  evaluation  
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