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评估GenoType分枝杆菌直接检测法在涂片阳性呼吸道标本中同时检测结核分枝杆菌复合群和四种非结核分枝杆菌的性能。

Evaluation of the GenoType Mycobacteria Direct assay for the simultaneous detection of the Mycobacterium tuberculosis complex and four atypical mycobacterial species in smear-positive respiratory specimens.

作者信息

Seagar A-Louise, Prendergast Carmel, Emmanuel F Xavier, Rayner Alan, Thomson Susan, Laurenson Ian F

机构信息

Scottish Mycobacteria Reference Laboratory, Department of Laboratory Medicine, Royal Infirmary of Edinburgh, 51 Little France Crescent, Edinburgh EH16 4SA, UK.

Microbiology Department, Royal Brompton Hospital, Sydney Street, London SW3 6NP, UK.

出版信息

J Med Microbiol. 2008 May;57(Pt 5):605-611. doi: 10.1099/jmm.0.47484-0.

Abstract

A novel, commercially available reverse hybridization assay [GenoType Mycobacteria Direct (GTMD), version 2.0; Hain Lifescience] was evaluated for the direct detection of five clinically relevant mycobacterial species [Mycobacterium tuberculosis complex (MTBC), Mycobacterium avium, Mycobacterium malmoense, Mycobacterium kansasii and Mycobacterium intracellulare] from 54 smear-positive respiratory specimens and the findings were compared with culture results. Three approaches were used for specimen preparation using either whole or 'split' sample volumes and N-acetyl-l-cysteine/3 % NaOH or 4 % NaOH as decontamination chemicals. Forty-three out of 52 samples in which RNA amplification was successful gave GTMD results that concurred with the identification of the cultured isolate. All cases of MTBC were detected. Twenty-two samples contained M. tuberculosis complex, seven had M. kansasii, four had M. malmoense, seven contained atypical mycobacteria other than those detectable using the GTMD assay and three specimens contained no viable mycobacteria. The assay is easy to use and can be completed in one working day. Results interpretation is facilitated by the inclusion of an internal amplification control with each sample to allow identification of specimens containing amplification inhibitors. A positive GTMD result will quickly identify patients with MTBC infection or provide specific identification of four other atypical mycobacteria from the same specimen. This allows more rapid drug susceptibility testing, treatment, and public health and infection control decisions.

摘要

对一种新型的、市售的反向杂交检测方法[基因分型分枝杆菌直接检测法(GTMD),第2版;海因生命科学公司]进行了评估,以直接检测54份涂片阳性呼吸道标本中的5种临床相关分枝杆菌[结核分枝杆菌复合群(MTBC)、鸟分枝杆菌、马尔默分枝杆菌、堪萨斯分枝杆菌和胞内分枝杆菌],并将结果与培养结果进行比较。使用了三种方法进行标本制备,采用全量或“分割”样本量,并使用N-乙酰-L-半胱氨酸/3%氢氧化钠或4%氢氧化钠作为去污剂。在52份RNA扩增成功的样本中,有43份的GTMD结果与培养分离株的鉴定结果一致。所有MTBC病例均被检测到。22份样本含有结核分枝杆菌复合群,7份含有堪萨斯分枝杆菌,4份含有马尔默分枝杆菌,7份含有GTMD检测法无法检测到的非典型分枝杆菌,3份标本不含活的分枝杆菌。该检测方法易于使用,可在一个工作日内完成。每个样本都包含一个内部扩增对照,便于结果解读,以识别含有扩增抑制剂的标本。GTMD检测结果呈阳性将快速识别MTBC感染患者,或从同一份标本中对其他四种非典型分枝杆菌进行特异性鉴定。这使得药物敏感性检测、治疗以及公共卫生和感染控制决策能够更快地做出。

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