Garima Kushal, Varma-Basil Mandira, Pathak Rakesh, Kumar Sujeet, Narang Anshika, Rawat Khushal Singh, Chaudhry Anil, Nair Deepthi, Ramachandran V G, Bose Mridula
Department of Microbiology, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi 110007, India.
Department of Microbiology, Guru Teg Bahadur Hospital, New Delhi 110095, India.
Int J Mycobacteriol. 2012 Dec;1(4):207-11. doi: 10.1016/j.ijmyco.2012.10.005. Epub 2012 Nov 6.
A large number of potentially pathogenic non-tuberculous mycobacteria (NTM) encountered in the clinical laboratory makes it necessary to identify their species to ensure appropriate treatment. However, labor-intensive conventional methods of speciation are not used in every laboratory, and hence NTM infections are often ignored. Polymerase chain reaction (PCR) restriction analysis (PRA) was applied in this study for early identification and speciation of mycobacterial species on 306 cultures of acid-fast bacilli isolated from patients suspected of suffering from tuberculosis. Mycobacterium tuberculosis was identified in 85.6% of the isolates. The NTM isolated most commonly was Mycobacterium kansasii/gastri group (3.5%), followed by Mycobacterium fortuitum (3.2%). Four of the M. fortuitum were grown from cultures obtained on the same day, but from samples from different patients and were probably laboratory contaminants. Mycobacterium intracellulare and Mycobacterium avium were identified in 2.94% and 2.28% of the isolates, respectively. Three isolates of M. avium and two isolates of M. intracellulare were obtained in repeated cultures from sputum samples of the same patients and were thus pathogenic. A single isolate of Mycobacterium abscessus was obtained from a breast abscess. A rare pathogen Mycobacterium phocaicum was isolated from one patient with epididymitis. However, whether it was the causative agent of epididymitis in this patient remains doubtful. The results of this study highlight the importance of speciation of mycobacteria for appropriate diagnosis and the importance of including molecular assays to augment conventional methods of diagnosis of mycobacterial diseases for rapid identification of NTM so that these potential pathogens are not overlooked in routine diagnostic procedures.
临床实验室中遇到大量具有潜在致病性的非结核分枝杆菌(NTM),因此有必要鉴定其菌种以确保进行适当治疗。然而,并非每个实验室都采用劳动强度大的传统菌种鉴定方法,因此NTM感染常常被忽视。本研究应用聚合酶链反应(PCR)限制性分析(PRA)对从疑似结核病患者分离出的306株抗酸杆菌培养物进行分枝杆菌菌种的早期鉴定和分类。在85.6%的分离株中鉴定出结核分枝杆菌。最常分离出的NTM是堪萨斯/胃分枝杆菌群(3.5%),其次是偶然分枝杆菌(3.2%)。4株偶然分枝杆菌是从同一天获得的培养物中生长出来的,但来自不同患者的样本,可能是实验室污染物。胞内分枝杆菌和鸟分枝杆菌分别在2.94%和2.28%的分离株中被鉴定出来。3株鸟分枝杆菌分离株和2株胞内分枝杆菌分离株是从同一患者的痰标本重复培养中获得的,因此具有致病性。从乳腺脓肿中获得1株脓肿分枝杆菌分离株。从1例附睾炎患者中分离出一种罕见病原体海豹分枝杆菌。然而,它是否是该患者附睾炎的病原体仍存疑问。本研究结果突出了分枝杆菌菌种鉴定对于正确诊断的重要性,以及纳入分子检测以加强分枝杆菌病传统诊断方法对快速鉴定NTM的重要性,从而使这些潜在病原体在常规诊断程序中不被忽视。