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中国防痨杂志 ›› 2023, Vol. 45 ›› Issue (1): 31-37.doi: 10.19982/j.issn.1000-6621.20220319

• 论著 • 上一篇    下一篇

肺结核患儿胃液样本结核分枝杆菌培养阳性率提高方法的探讨

李桂莲1, 方敏2, 姜靖伟1, 王瑞欢1, 钱程宇1,3, 于晋杰1,4, 曹滨1,4, 许达1, 赵秀芹1, 李马超1, 刘海灿1(), 孙琳5(), 朱渝6(), 万康林1()   

  1. 1中国疾病预防控制中心传染病预防控制所结核病控制室/传染病预防控制国家重点实验室/感染性疾病诊治协同创新中心,北京 102206
    2四川省凉山彝族自治州第一人民医院儿科,凉山 615099
    3温州医科大学检验医学院,温州 325035
    4南华大学公共卫生学院,衡阳 421001
    5首都医科大学附属北京儿童医院呼吸疾病研究室/北京市儿科研究所/儿科学国家重点学科/教育部儿科重大疾病研究重点实验室/儿童呼吸道感染性疾病研究北京市重点实验室,北京 100045
    6四川大学华西第二医院感染科,成都 610044
  • 收稿日期:2022-08-17 出版日期:2023-01-10 发布日期:2022-12-30
  • 通信作者: 刘海灿,孙琳,朱渝,万康林 E-mail:liuhaican@icdc.cn;chinatka@163.com;zhuyu_wj@163.com;wankanglin@icdc.cn
  • 基金资助:
    “十三五”国家科技重大专项(2018ZX10103001-003-012)

Exploration for improving the culture-positive rate of Mycobacterium tuberculosis in gastric fluid specimens from pediatric patients with pulmonary tuberculosis

Li Guilian1, Fang Min2, Jiang Jingwei1, Wang Ruihuan1, Qian Chengyu1,3, Yu Jinjie1,4, Cao Bin1,4, Xu Da1, Zhao Xiuqin1, Li Machao1, Liu Haican1(), Sun Lin5(), Zhu Yu6(), Wan Kanglin1()   

  1. 1State Key Laboratory for Infectious Disease Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China
    2Department of Pediatrics, the First People’s Hospital of Liangshan Yizu Autonomous Prefecture, Sichuan Province, Liangshan 615099, China
    3School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Zhejiang Province, Wenzhou 325035, China
    4School of Public Health, University of South China, Hunan Province, Hengyang 421001, China
    5Key Laboratory of Major Diseases in Children and National Key Discipline of Pediatrics (Capital Medical University), Ministry of Education, Beijing Key Laboratory of Pediatric Respiratory Infection Diseases, Beijing Pediatric Research Institute, Beijing Children’s Hospital, Capital Medical University, Beijing 100045, China
    6Department of Infection, West China Second Hospital, Sichuan University, Chengdu 610044, China
  • Received:2022-08-17 Online:2023-01-10 Published:2022-12-30
  • Contact: Liu Haican,Sun Lin,Zhu Yu,Wan Kanglin E-mail:liuhaican@icdc.cn;chinatka@163.com;zhuyu_wj@163.com;wankanglin@icdc.cn
  • Supported by:
    National Science and Technology Mega Project during the 13th Five-year Plan Period(2018ZX10103001-003-012)

摘要:

目的: 建立提高肺结核患儿胃液样本结核分枝杆菌(Mycobacterium tuberculosis,MTB)培养阳性率的方法,同时,探讨培养液的pH值对MTB抗原-胶体金检测试剂正确判读结果的影响和磷酸盐缓冲液(phosphate buffer solution,PBS)对结核样本前处理液pH值的调节作用。方法: 将70份疑似肺结核患儿胃液样本同时用两步培养法、传统培养法和Xpert Ultra进行检测。两步培养法为先将胃液样本直接接种到罗氏培养基上,约20~30d后收集可疑MTB菌落再行常规的碱处理-中和离心法处理进行分离培养(传统培养法)。比较传统培养法和两步法阳性检出率的差异;以样本的Xpert Ultra检测结果作为菌载量标准,分析两步法在不同菌载量样本中的阳性检出率差异。同时,配制系列pH值梯度的溶液,确定MTB抗原-胶体金检测试剂获得最佳显示结果的最适pH值范围;用系列体积的PBS缓冲液(pH=6.8)中和3%或4%NaOH与等体积样本的混合液,确定pH值至7~9时所需的体积稀释倍数。结果: 传统培养法阳性检出率为26.5%(18/68),两步法阳性检出率为23.1%(15/65),未发现两种方法的阳性检出率差异有统计学意义(χ2=0.125,P>0.05)。两步法在传统培养法的基础上将阳性检出率从26.5%(18/68)提高到32.4%(22/68)。两步法在菌载量低级及以上分级样本中的阳性检出比例(44.0%,11/25)明显高于菌载量极低级及以下标本的阳性检出比例(11.8%,4/34),差异有统计学意义(χ2=7.896,P=0.005)。本研究所选用的MTB抗原-胶体金检测试剂最适pH值范围为6~9。胃液模拟样本经3%或4%的NaOH处理后,调节pH值至7~9时需用PBS缓冲液(pH=6.8)稀释至少10或14倍,而痰液模拟样本经3%或4%的NaOH处理后,调节pH值至7~9时需用PBS缓冲液(pH=6.8)稀释至少12或16倍。结论: 分离培养两步法的阳性检出率未优于传统培养法,可作为传统培养法的补充,推荐对难以确诊的高度可疑肺结核患儿使用该方法进行检测。此外,本研究确定了MTB抗原-胶体金检测试剂使用的最适pH值范围及用PBS缓冲液(pH=6.8)调节NaOH-样本混合液pH值需要的稀释比例,可为规范MTB的分离培养提供科学依据。

关键词: 儿童, 结核,肺, 胃液, 诊断技术和方法

Abstract:

Objective: To establish a method to improve the positive rate of culture for Mycobacterium tuberculosis (MTB) in gastric fluid specimens from pediatric patients with pulmonary tuberculosis, and to investigate the effect of culture medium pH on the correct interpretation of a tuberculosis antigen-colloidal gold assay and the effect of phosphate buffer solution (PBS) buffer on the pH of the NaOH-sample mix-solution. Methods: Seventy gastric juice samples received from suspected tuberculosis children were detected by self-established two-step culture method, traditional culture method and Xpert Ultra at the same time. The two-step culture method was to inoculate the gastric fluid specimens directly on the Lowenstein-Jensen (L-J) media first, and then, collect the suspected MTB colonies after about 20 to 30 days and treat them with sodium hydroxide-neutralization-centrifugation (traditional method) for MTB isolation. The difference of positive detection rate between traditional culture method and two-step method was compared. Take the Xpert Ultra test results of the sample as the bacterial load standard, the difference of positive detection rate of the two-step method in different bacterial load samples was analyzed. Meanwhile, a series of solutions with gradient pH were prepared to determine the optimal pH value for MTB antigen-colloidal gold diagnosis kit; the mixture of 3% or 4% NaOH and equal volume sample were neutralized with PBS buffer (pH=6.8) of a series of volumes, and the volume dilution ratio required when the pH value reaches 7-9 were determined. Results: The MTB positive rates were 26.5% (18/68) by the traditional method and 23.1% (15/65) by the two-step culture method, there was no statistically significant difference (χ2=0.125, P>0.05). The two-step method raised the positive detection rate from 26.5% (18/68) to 32.4% (22/68) based on the traditional method. The positive isolation rate of the two-step method in samples with bacterial load ≥low grade (44.0%, 11/25) was significantly higher than that in samples with load ≤very low grade (11.8%, 4/34) (χ2=7.896, P=0.005). The optimal pH range for the chosen tuberculosis antigen-colloidal gold diagnosis kit was 6-9. After being treated with 3% or 4% NaOH, adjustment of pH to 7-9 required at least 10- or 14-fold dilution with PBS buffer (pH=6.8) for gastric fluid simulative samples, and at least 12- or 16-fold dilution for sputum simulative samples. Conclusion: The positive detection rate of the two-step isolation culture method was not found better than the traditional method, however, it could be used as a supplement to the conventional method to improve the overall positive isolation rate of gastric fluid samples, and was especially recommended for the MTB detection in children with highly suspected but difficultly diagnosed pulmonary tuberculosis. In addition, this study investigated the optimal pH range for the use of MTB antigen-colloidal gold diagnosis kit and the optimal dilution ratio of neutralizing the NaOH-sample solution with PBS (pH=6.8), which could provide scientific basis for standardizing the isolation of MTB in China.

Key words: Child, Tuberculosis, pulmonary, Gastric juice, Diagnostic techniques and procedures

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