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Performance of solid and liquid culture media for the detection of Mycobacterium tuberculosis in clinical materials: meta-analysis of recent studies.固体和液体培养基在临床材料中检测结核分枝杆菌的性能:近期研究的荟萃分析
Eur J Clin Microbiol Infect Dis. 2014 Jun;33(6):867-70. doi: 10.1007/s10096-014-2105-z. Epub 2014 Apr 24.
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Liquid vs. solid culture for tuberculosis: performance and cost in a resource-constrained setting.液体与固体培养法诊断结核病:在资源有限环境下的表现与成本。
Int J Tuberc Lung Dis. 2010 Aug;14(8):1024-31.
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Cost-effectiveness of blood agar for isolation of mycobacteria.血琼脂用于分枝杆菌分离的成本效益。
PLoS Negl Trop Dis. 2007 Nov 28;1(2):e83. doi: 10.1371/journal.pntd.0000083.
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The new mycobacteria: an update.新型分枝杆菌:最新进展
FEMS Immunol Med Microbiol. 2006 Nov;48(2):159-78. doi: 10.1111/j.1574-695X.2006.00123.x.
5
The new mycobacterial species--emerging or newly distinguished pathogens.新型分枝杆菌物种——新出现的或新鉴定的病原体。
Clin Lab Med. 2004 Sep;24(3):651-90, vi. doi: 10.1016/j.cll.2004.05.011.
6
Evaluation of the MicroSeq system for identification of mycobacteria by 16S ribosomal DNA sequencing and its integration into a routine clinical mycobacteriology laboratory.通过16S核糖体DNA测序评估用于鉴定分枝杆菌的MicroSeq系统及其在常规临床分枝杆菌学实验室中的整合。
J Clin Microbiol. 2003 Apr;41(4):1447-53. doi: 10.1128/JCM.41.4.1447-1453.2003.
7
Comparison of the Automated Mycobacteria Growth Indicator Tube System (BACTEC 960/MGIT) with Löwenstein-Jensen medium for recovery of mycobacteria from clinical specimens.用于从临床标本中分离分枝杆菌的自动化分枝杆菌生长指示管系统(BACTEC 960/MGIT)与洛温斯坦-詹森培养基的比较
Am J Clin Pathol. 2002 Oct;118(4):542-5. doi: 10.1309/65KN-2M7E-7MNN-X0TA.
8
Comparison of the BACTEC MGIT 960 and ESP culture system II for growth and detection of mycobacteria.用于分枝杆菌生长和检测的BACTEC MGIT 960与ESP培养系统II的比较
J Clin Microbiol. 2000 Nov;38(11):4167-70. doi: 10.1128/JCM.38.11.4167-4170.2000.
9
Comparison of the BACTEC MGIT 960 with Löwenstein-Jensen medium for recovery of mycobacteria from clinical specimens.BACTEC MGIT 960与罗氏培养基从临床标本中分离分枝杆菌的比较。
Int J Tuberc Lung Dis. 2000 Sep;4(9):866-70.
10
Löwenstein-Jensen media. No longer necessary for mycobacterial isolation.罗-琴培养基。不再是分离分枝杆菌所必需的。
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分枝杆菌和好氧放线菌培养:是否需要两种培养基类型及延长培养时间?

Mycobacterium and Aerobic Actinomycete Culture: Are Two Medium Types and Extended Incubation Times Necessary?

作者信息

Simner Patricia J, Doerr Kelly A, Steinmetz Lory K, Wengenack Nancy L

机构信息

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA

出版信息

J Clin Microbiol. 2016 Apr;54(4):1089-93. doi: 10.1128/JCM.02838-15. Epub 2016 Feb 10.

DOI:10.1128/JCM.02838-15
PMID:26865689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4809932/
Abstract

Mycobacterial cultures are historically performed using a liquid medium and a solid agar medium with an incubation period of up to 60 days. We performed a retrospective analysis of 21,494 mycobacterial and aerobic actinomycetes cultures performed over 10 months to determine whether two medium types remain necessary and to investigate whether culture incubation length can be shortened. Specimens were cultured using Bactec MGIT liquid medium and Middlebrook 7H11/S7H11 solid medium with incubation periods of 42 and 60 days, respectively. Time-to-positivity and the identity of isolates recovered from each medium were evaluated. A total of 1,205/21,494 cultures (6%) were positive on at least one medium. Of the 1,353 isolates recovered, 1,110 (82%) were nontuberculous mycobacteria, 145 (11%) were aerobic actinomycetes, and 98 (7%) wereMycobacterium tuberculosiscomplex. Assessing medium types, 1,121 isolates were recovered from solid medium cultures, 922 isolates were recovered from liquid medium cultures, and 690 isolates were recovered on both media. Liquid cultures were positive an average of 10 days before solid cultures when the two medium types were positive (P< 0.0001). Isolates detected on solid medium after 6 weeks of incubation included 65 (5%) nontuberculous mycobacteria, 4 (0.3%) aerobic actinomycetes, and 2 (0.2%) isolates from theM. tuberculosiscomplex. Medical chart review suggested that most of these later-growing isolates were insignificant, as the diagnosis was already known, or they were considered colonizers/contaminants. This study reaffirms the need for both liquid medium and solid medium for mycobacterial and aerobic actinomycetes culture and demonstrates that solid medium incubation times may be reduced to 6 weeks without significantly impacting sensitivity.

摘要

传统上,分枝杆菌培养采用液体培养基和固体琼脂培养基,培养期长达60天。我们对10个月内进行的21494例分枝杆菌和好氧放线菌培养进行了回顾性分析,以确定是否仍需要两种培养基类型,并研究培养孵育时间是否可以缩短。使用Bactec MGIT液体培养基和Middlebrook 7H11/S7H11固体培养基分别在42天和60天的孵育期内对标本进行培养。评估了每种培养基的阳性时间和分离株的鉴定结果。在21494例培养物中,共有1205例(6%)在至少一种培养基上呈阳性。在回收的1353株分离株中,1110株(82%)为非结核分枝杆菌,145株(11%)为好氧放线菌,98株(7%)为结核分枝杆菌复合群。评估培养基类型,从固体培养基培养物中回收了1121株分离株,从液体培养基培养物中回收了922株分离株,两种培养基上均回收了690株分离株。当两种培养基类型均呈阳性时,液体培养物比固体培养物平均早10天呈阳性(P<0.0001)。孵育6周后在固体培养基上检测到的分离株包括65株(5%)非结核分枝杆菌、4株(0.3%)好氧放线菌和2株(0.2%)结核分枝杆菌复合群分离株。病历审查表明,这些后期生长的分离株大多无意义,因为诊断已经明确,或者它们被视为定植菌/污染物。本研究再次证实了分枝杆菌和好氧放线菌培养需要液体培养基和固体培养基,并表明固体培养基孵育时间可缩短至6周,而不会显著影响敏感性。