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本文引用的文献

1
Cross-contamination of specimens with Mycobacterium tuberculosis: clinical significance, causes, and prevention.结核分枝杆菌对标本的交叉污染:临床意义、原因及预防
Am J Clin Pathol. 1998 Mar;109(3):324-30. doi: 10.1093/ajcp/109.3.324.
2
False-positive results from cultures of Mycobacterium tuberculosis due to laboratory cross-contamination confirmed by restriction fragment length polymorphism.通过限制性片段长度多态性确认的因实验室交叉污染导致的结核分枝杆菌培养假阳性结果。
J Clin Microbiol. 1997 Apr;35(4):988-91. doi: 10.1128/jcm.35.4.988-991.1997.
3
Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology.同时检测结核分枝杆菌并进行菌株鉴别以用于诊断和流行病学研究。
J Clin Microbiol. 1997 Apr;35(4):907-14. doi: 10.1128/jcm.35.4.907-914.1997.
4
Retrospective detection of laboratory cross-contamination of Mycobacterium tuberculosis cultures with use of DNA fingerprint analysis.运用DNA指纹分析对结核分枝杆菌培养物实验室交叉污染进行回顾性检测。
Clin Infect Dis. 1997 Jan;24(1):35-40. doi: 10.1093/clinids/24.1.35.
5
Specimen contamination in mycobacteriology laboratory detected by pseudo-outbreak of multidrug-resistant tuberculosis: analysis by routine epidemiology and confirmation by molecular technique.通过耐多药结核病假性暴发检测分枝杆菌实验室中的标本污染:常规流行病学分析及分子技术确认
J Clin Microbiol. 1996 Apr;34(4):1017-9. doi: 10.1128/jcm.34.4.1017-1019.1996.
6
Tuberculosis notification update.
Wkly Epidemiol Rec. 1996 Mar 1;71(9):65-9.
7
Strain identification of Mycobacterium tuberculosis by DNA fingerprinting: recommendations for a standardized methodology.通过DNA指纹图谱技术进行结核分枝杆菌菌株鉴定:标准化方法建议
J Clin Microbiol. 1993 Feb;31(2):406-9. doi: 10.1128/jcm.31.2.406-409.1993.
8
Molecular strain typing of Mycobacterium tuberculosis to confirm cross-contamination in the mycobacteriology laboratory and modification of procedures to minimize occurrence of false-positive cultures.结核分枝杆菌的分子菌株分型,以确认分枝杆菌实验室中的交叉污染,并修改程序以尽量减少假阳性培养物的出现。
J Clin Microbiol. 1993 Jul;31(7):1677-82. doi: 10.1128/jcm.31.7.1677-1682.1993.
9
Nature of DNA polymorphism in the direct repeat cluster of Mycobacterium tuberculosis; application for strain differentiation by a novel typing method.结核分枝杆菌直接重复序列簇中DNA多态性的性质;通过一种新型分型方法用于菌株鉴别
Mol Microbiol. 1993 Dec;10(5):1057-65. doi: 10.1111/j.1365-2958.1993.tb00976.x.
10
Laboratory contamination of Mycobacterium tuberculosis cultures.结核分枝杆菌培养物的实验室污染
Am J Respir Crit Care Med. 1995 Nov;152(5 Pt 1):1702-4. doi: 10.1164/ajrccm.152.5.7582316.

一家参考实验室中结核分枝杆菌对标本的广泛交叉污染。

Extensive cross-contamination of specimens with Mycobacterium tuberculosis in a reference laboratory.

作者信息

de C Ramos M, Soini H, Roscanni G C, Jaques M, Villares M C, Musser J M

机构信息

Faculdade de Ciencias Medicas, Universidade Estadual de Campinas (UNICAMP), Campinas, Sao Paulo State, Brazil.

出版信息

J Clin Microbiol. 1999 Apr;37(4):916-9. doi: 10.1128/JCM.37.4.916-919.1999.

DOI:10.1128/JCM.37.4.916-919.1999
PMID:10074501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC88624/
Abstract

A striking increase in the numbers of cultures positive for Mycobacterium tuberculosis was noticed in a mycobacterial reference laboratory in Campinas, Sao Paulo State, Brazil, in May 1995. A contaminated bronchoscope was the suspected cause of the increase. All 91 M. tuberculosis isolates grown from samples from patients between 8 May and 18 July 1995 were characterized by spoligotyping and IS6110 fingerprinting. Sixty-one of the 91 isolates had identical spoligotype patterns, and the pattern was arbitrarily designated S36. The 61 specimens containing these isolates had been processed and cultured in a 21-day period ending on 1 June 1995, but only 1 sample was smear positive for acid-fast bacilli. The patient from whom this sample was obtained was considered to be the index case patient and had a 4+ smear-positive lymph node aspirate that had been sent to the laboratory on 10 May. Virtually all organisms with spoligotype S36 had the same IS6110 fingerprint pattern. Extensive review of the patients' charts and investigation of laboratory procedures revealed that cross-contamination of specimens had occurred. Because the same strain was grown from all types of specimens, the bronchoscope was ruled out as the outbreak source. The most likely source of contamination was a multiple-use reagent used for specimen processing. The organism was cultured from two of the solutions 3 weeks after mock contamination. This investigation strongly supports the idea that M. tuberculosis grown from smear-negative specimens should be analyzed by rapid and reliable strain differentiation techniques, such as spoligotyping, to help rule out laboratory contamination.

摘要

1995年5月,巴西圣保罗州坎皮纳斯的一家分枝杆菌参考实验室注意到结核分枝杆菌培养阳性数量显著增加。怀疑污染源是一台受污染的支气管镜。对1995年5月8日至7月18日期间从患者样本中培养出的所有91株结核分枝杆菌进行了间隔寡核苷酸分型(spoligotyping)和IS6110指纹分析。91株分离株中有61株具有相同的间隔寡核苷酸分型模式,该模式被任意指定为S36。含有这些分离株的61份标本在截至1995年6月1日的21天内进行了处理和培养,但只有1份样本抗酸杆菌涂片呈阳性。获得该样本的患者被视为索引病例患者,其淋巴结穿刺液涂片4+阳性,于5月10日送检实验室。几乎所有具有间隔寡核苷酸分型S36的菌株都具有相同的IS6110指纹模式。对患者病历的广泛审查和实验室操作调查显示,标本发生了交叉污染。由于所有类型的标本都培养出了相同的菌株,因此排除支气管镜作为暴发源。最可能的污染源是用于标本处理的一种多用途试剂。模拟污染3周后,从两种溶液中培养出了该菌株。这项调查有力地支持了这样一种观点,即对于从涂片阴性标本中培养出的结核分枝杆菌,应通过快速可靠的菌株鉴别技术(如间隔寡核苷酸分型)进行分析,以帮助排除实验室污染。