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Development and clinical evaluation of a new multiplex PCR assay for a simultaneous diagnosis of tuberculous and nontuberculous mycobacteria.一种新的多重 PCR 检测方法的开发和临床评估,用于同时诊断结核分枝杆菌和非结核分枝杆菌。
EBioMedicine. 2021 Aug;70:103527. doi: 10.1016/j.ebiom.2021.103527. Epub 2021 Aug 11.
2
Treatment of Nontuberculous Mycobacterial Pulmonary Disease: An Official ATS/ERS/ESCMID/IDSA Clinical Practice Guideline.非结核分枝杆菌肺病治疗:美国胸科学会/欧洲呼吸学会/欧洲临床微生物学和传染病学会/美国感染病学会临床实践指南。
Clin Infect Dis. 2020 Aug 14;71(4):905-913. doi: 10.1093/cid/ciaa1125.
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Advances in Molecular Diagnosis of Tuberculosis.结核病分子诊断的进展
J Clin Microbiol. 2020 Sep 22;58(10). doi: 10.1128/JCM.01582-19.
4
Prolongation of incubation time improves clinical diagnosis of Mycobacterium xenopi infection and allows susceptibility testing of mycobacterial strains against multiple antibiotics.延长潜伏期可改善对分枝杆菌属 Xenopi 感染的临床诊断,并允许对分枝杆菌菌株进行多种抗生素的药敏试验。
J Glob Antimicrob Resist. 2020 Sep;22:533-537. doi: 10.1016/j.jgar.2020.04.028. Epub 2020 May 5.
5
The Rise of Non-Tuberculosis Mycobacterial Lung Disease.非结核分枝杆菌肺病的兴起。
Front Immunol. 2020 Mar 3;11:303. doi: 10.3389/fimmu.2020.00303. eCollection 2020.
6
Diagnostic Performance of the GENEDIA MTB/NTM Detection Kit for Detecting and Nontuberculous Mycobacteria With Sputum Specimens.GENEDIA MTB/NTM 检测试剂盒检测痰液标本中结核分枝杆菌和非结核分枝杆菌的诊断性能。
Ann Lab Med. 2020 Mar;40(2):169-173. doi: 10.3343/alm.2020.40.2.169.
7
Evaluation of the performance of two real-time PCR assays for detecting Mycobacterium species.两种用于检测分枝杆菌属的实时荧光定量PCR检测方法的性能评估。
J Clin Lab Anal. 2019 Jan;33(1):e22645. doi: 10.1002/jcla.22645. Epub 2018 Aug 13.
8
Increasing nontuberculous mycobacteria reporting rates and species diversity identified in clinical laboratory reports.提高临床实验室报告中报告的非结核分枝杆菌的检出率和物种多样性。
BMC Infect Dis. 2018 Apr 10;18(1):163. doi: 10.1186/s12879-018-3043-7.
9
Paradigm for diagnosing mycobacterial disease: direct detection and differentiation of complex and non-tuberculous mycobacteria in clinical specimens using multiplex real-time PCR.用于诊断分枝杆菌病的模式:使用多重实时 PCR 直接检测和区分临床标本中的复杂和非结核分枝杆菌。
J Clin Pathol. 2018 Sep;71(9):774-780. doi: 10.1136/jclinpath-2017-204945. Epub 2018 Mar 20.
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British Thoracic Society guidelines for the management of non-tuberculous mycobacterial pulmonary disease (NTM-PD).英国胸科学会非结核分枝杆菌肺病(NTM-PD)管理指南。
Thorax. 2017 Nov;72(Suppl 2):ii1-ii64. doi: 10.1136/thoraxjnl-2017-210927.

用于从临床标本中快速鉴定分枝杆菌的GenoType CM Direct和VisionArray Myco检测系统

GenoType CM Direct and VisionArray Myco for the Rapid Identification of Mycobacteria from Clinical Specimens.

作者信息

Schildhaus Hans-Ulrich, Steindor Mathis, Kölsch Bernd, Herold Thomas, Buer Jan, Kehrmann Jan

机构信息

Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, 45147 Essen, Germany.

Department of Pediatric Pulmonology and Sleep Medicine, Children's Hospital, University of Duisburg-Essen, 45147 Essen, Germany.

出版信息

J Clin Med. 2022 Apr 25;11(9):2404. doi: 10.3390/jcm11092404.

DOI:10.3390/jcm11092404
PMID:35566531
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9103381/
Abstract

is the single infectious agent responsible for most deaths worldwide outside of pandemics. Diseases due to non-tuberculous mycobacteria (NTM) are increasing in many regions of the world. The two molecular assays GenoType CM direct (GTCMd) (Bruker, Billerica, MA, USA) and VisionArray Myco (VAM) (ZytoVision, Bremerhaven, Germany) are based on the DNA/DNA hybridization technique, and allow for the identification of tuberculous and the most clinically relevant non-tuberculous mycobacterial species from clinical specimens. We evaluated the performance of both assays for the identification of mycobacteria from 65 clinical specimens of 65 patients and compared it with the results of conventional culture. Based on conventional culture that recovered 37 mycobacterial isolates including 11 tuberculous and 26 NTM isolates, sensitivity, specificity, positive predictive value and negative predictive value were 89.2%, 81.5%, 86.8% and 84.6% for GTCMd and 73.0%, 96.3%, 96.4% and 72.2% for VAM. Additionally, GTCMd identified mycobacteria from five and VAM from one culture-negative sample. Both assays identified a mycobacterium in one sample overgrown by other microorganisms. Two subsp. isolates grown from culture were identified as by GTCMd assay. In conclusion, both assays improve the rapid identification of mycobacteria directly from clinical specimens.

摘要

是全球除大流行外导致大多数死亡的单一传染源。在世界许多地区,非结核分枝杆菌(NTM)引起的疾病正在增加。两种分子检测方法,即GenoType CM direct(GTCMd)(美国马萨诸塞州比勒里卡的布鲁克公司)和VisionArray Myco(VAM)(德国不来梅港的ZytoVision公司),基于DNA/DNA杂交技术,可从临床标本中鉴定结核分枝杆菌和临床上最相关的非结核分枝杆菌菌种。我们评估了这两种检测方法从65例患者的65份临床标本中鉴定分枝杆菌的性能,并将其与传统培养结果进行比较。基于传统培养法分离出37株分枝杆菌,其中包括11株结核分枝杆菌和26株NTM菌株,GTCMd的敏感性、特异性、阳性预测值和阴性预测值分别为89.2%、81.5%、86.8%和84.6%,VAM的分别为73.0%、96.3%、96.4%和72.2%。此外,GTCMd从5份培养阴性样本中鉴定出分枝杆菌,VAM从1份培养阴性样本中鉴定出分枝杆菌。两种检测方法都在一个被其他微生物过度生长的样本中鉴定出一种分枝杆菌。通过GTCMd检测,从培养物中生长的两株亚种分离株被鉴定为 。总之,这两种检测方法都提高了直接从临床标本中快速鉴定分枝杆菌的能力。