Multiplex PCR assay for simultaneous detection and differentiation of Mycobacterium tuberculosis, Mycobacterium avium complexes and other Mycobacterial species directly from clinical specimens

被引:81
作者
Gopinath, K. [1 ]
Singh, S. [1 ]
机构
[1] All India Inst Med Sci, Div Clin Microbiol, Dept Lab Med, New Delhi 110029, India
关键词
HIV; Mycobacterium avium; mixed infection; multiplex PCR; tuberculosis; POLYMERASE-CHAIN-REACTION; HIV-INFECTED PATIENTS; RAPID IDENTIFICATION; RECOVERY; SAMPLES; BOVIS; AIDS; DNA;
D O I
10.1111/j.1365-2672.2009.04218.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: Polymerase chain reaction ( PCR) is the most rapid and sensitive method for diagnosing mycobacterial infections and identifying the aetiological Mycobacterial species in order to administer the appropriate therapy and for better patient management. Methods and Results: Two hundred and thirty-five samples from 145 clinically suspected cases of tuberculosis were processed for the detection of Mycobacterial infections by ZN (Ziehl Neelsen) smear examination, L-J & BACTEC (TM) MGIT-960 culture and multiplex PCR tests. The multiplex PCR comprised of genus-specific primers targeting hsp65 gene, Mycobacterium tuberculosis complex-specific primer targeting cfp10 (Rv3875, esxB) region and Mycobacterium avium complex-specific primer pairs targeting 16S-23S Internal Transcribed Spacer sequences. The multiplex PCR developed had an analytical sensitivity of 10 fg (3-4 cells) of mycobacterial DNA. The multiplex PCR test showed the highest (77.24%) detection rate, while ZN smear examination had the lowest (20%) detection rate, which was bettered by L-J culture (34.4%) and BACTEC (TM) MGIT-960 culture (50.34%) methods. The mean isolation time for M. tuberculosis was 19.03 days in L-J culture and 8.7 days in BACTEC (TM) MGIT-960 culture. Using the multiplex PCR, we could establish M. tuberculosis + M. avium co-infection in 1.3% HIV-negative and 2.9% HIV-positive patients. The multiplex PCR was also highly useful in diagnosing mycobacteraemia in 38.09% HIV-positive and 15.38% HIV-negative cases. Conclusions: The developed in-house multiplex PCR could identify and differentiate the M. tuberculosis and M. avium complexes from other Mycobacterial species directly from clinical specimens. Significance and Impact of the Study: The triplex PCR developed by us could be used to detect and differentiate M. tuberculosis, M. avium and other mycobacteria in a single reaction tube.
引用
收藏
页码:425 / 435
页数:11
相关论文
共 43 条
[1]  
[Anonymous], 2003, AM J RESP CRIT CARE, V167, P603
[2]  
[Anonymous], 2008, GLOBAL TUBERCULOSIS
[3]  
[Anonymous], 1989, Molecular Cloning: A Laboratory Manual
[4]  
AUSUBEL FM, 1998, PREPARATION GENOMIC, P1129
[5]  
Benson Constance A., 2004, Morbidity and Mortality Weekly Report, V53, P1
[6]  
*CDCP, 2002, MMWR-MORBID MORTAL W, V51, P501
[7]  
Collier L., 1998, TOPLEY WILSONS MICRO
[8]   Controlled comparison of BACTEC 13A, MYCO/F LYTIC, BacT/ALERT MB, and ISOLATOR 10 systems for detection of mycobacteremia [J].
Crump, JA ;
Tanner, DC ;
Mirrett, S ;
McKnight, CM ;
Reller, LB .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) :1987-1990
[9]   A case of mycobacterium tuberculosis (MTB) and mycobacterium avium-complex (MAC) co-infection in an immunocompetent host: A pathogen and a colonizer or two pathogens in the same host? [J].
Damian, JB ;
Coellio-D'Costa, VE ;
Iqbal, J ;
Mannheimer, S ;
Schicchi, JS ;
Nachman, S .
CHEST, 2004, 126 (04) :985S-986S
[10]   Diagnostic standards and classification of tuberculosis in adults and children [J].
Dunlap, NE ;
Bass, J ;
Fujiwara, P ;
Hopewell, P ;
Horsburgh, CR ;
Salfinger, M ;
Simone, PM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (04) :1376-1395