中国媒介生物学及控制杂志 ›› 2012, Vol. 23 ›› Issue (3): 231-233.

• 论著 • 上一篇    下一篇

一起炭疽疫情中炭疽病原检测方法的应用与评价

张慧娟1, 梁旭东1, 海岩2, 李忠延3, 袁海涛3, 郭长山4, 东晓晖5, 魏建春1   

  1. 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 内蒙古自治区疾病预防控制中心;
    3 兴安盟疾病预防控制中心;
    4 科尔沁右翼前旗疾病预防控制中心;
    5 扎赉特旗疾病预防控制中心
  • 收稿日期:2012-02-10 出版日期:2012-06-20 发布日期:2012-06-20
  • 通讯作者: 魏建春,Email: weijianchun@icdc.cn
  • 基金资助:
    国家科技重大专项课题(2008ZX10004-008)

Evaluation of the methods applied for the detection of Bacillus anthracis in anthrax outbreak

ZHANG Hui-juan1, LIANG Xu-dong1, HAI Yan2, LI Zhong-yan3, YUAN Hai-tao3, GUO Chang-shan4, DONG Xiao-hui5, WEI Jian-chun1   

  1. 1 State Key Laboratory for Infectious Diseases Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China;
    2 Inner Mongolia Autonomous Region Center for Disease Control and Prevention;
    3 Xing’an League Center for Disease Control and Prevention;
    4 Keyouqian Banner Center for Disease Control and Prevention;
    5 Zhalaite Town Center for Disease Control and Prevention
  • Received:2012-02-10 Online:2012-06-20 Published:2012-06-20
  • Supported by:
    Supported by the Major National Science and Technology Projects of China(No. 2008ZX10004-008)

摘要: 目的 分析总结一起炭疽疫情中应急检测的经验与问题,为炭疽疾病预防控制提供参考依据。方法 采集报告的疑似皮肤炭疽患者皮损渗出液和静脉血标本,与病例相关的病死动物和土壤标本,渗出液采集采用载玻片直接蘸取和无菌棉签擦取2种方法,用涂片镜检、直接分离培养和肉汤增菌后分离培养细菌以及炭疽芽胞杆菌毒力基因PCR扩增方法检测病原,分析检测结果。结果 共采集标本57份,病例标本占91.23%,病死牛肉及剖牛处土壤标本占8.77%。病例标本采集时间距发病时间最短1 d,最长23 d,平均6.62 d。29例疑似皮肤炭疽患者在采样时其中16例(占55.17%)已使用抗生素类药物治疗,4例(占13.79%)未曾使用抗生素。从2例未使用抗生素的患者皮损渗出液和1份病死牛肉中分离到炭疽芽胞杆菌,分离阳性率为5.26%;其中1例患者皮损渗出液涂片镜检阳性;全部标本PCR扩增结果均为阴性。结论 标本炭疽芽胞杆菌阳性检出率较低,与采样方法和采样时机关系较大,应加强部门间的沟通协作和人群的健康教育,做到疫情早报告、早确诊、早控制。

关键词: 炭疽, 疫情, 应急检测

Abstract: Objective To analyze and summarize the experience and problems in emergent detection of Bacillus anthracis in anthrax outbreak for providing a basis for anthrax prevention and control. Methods The study collected lesions exudates and blood samples from suspected cases, as well as related animal samples and soil samples. The lesions were collected by slides and sterile cotton swabs. Smear microscopy, direct culture and broth enrichment were used to isolate and foster virulence genes. The virulence genes were amplified by PCR for detection of pathogens. Results Fifty-seven specimens were collected. 91.23% of the specimens came from B. anthracis cases and the other 8.77% came from cattle and soil. The time window between disease outbreak and collection of case specimens was 1 day at least and 23 days at most, with an average of 6.62 days. 16 (55.17%) of 29 suspected cases had received antibiotic treatment before their specimens were collected while 4 (13.79%) suspected cases had never received any antibiotic treatment. B. anthracis was isolated from lesions of 2 suspected cases who did not receive antibiotic treatment and 1 dead cattle, with 5.26% of positive isolation rate. Lesions from 1 patient had positive result under smear microscopy. All the specimens were tested negative after PCR amplification. Conclusion Low detection rate of B. anthracis is closely associated with the methods and time window of sample collection. Therefore, we should enhance interdepartmental communication and coordination and public education for early reporting, diagnosis and control of the pandemic.

Key words: Anthrax, Outbreak, Emergent detection

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