Direct and early detection of Mycobacterium tuberculosis complex and rifampicin resistance from sputum smears

被引:8
作者
Bhutia, R. [1 ]
Narain, K. [1 ]
Devi, K. R. [1 ]
Singh, T. S. K. [2 ]
Mahanta, J. [1 ]
机构
[1] Indian Council Med Res, Reg Med Res Ctr, Dibrugarh, Assam, India
[2] Sikkim Manipal Univ, Sikkim Manipal Inst Med Sci, Dept Microbiol, Gangtok, India
关键词
Mycobacterium tuberculosis complex; rifampicin resistance; sputum smears; INNO-LiPA Rif.TB assay; RAPID DETECTION; MUTATIONS;
D O I
10.5588/ijtld.12.0452
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
SETTING: Four district DOTS centres in Sikkim, India. OBJECTIVE: Direct and early detection of Mycobacterium tuberculosis complex and rifampicin (RMP) susceptibility using the INNO-LiPA Rif.TB assay. DESIGN: DNA was extracted from 44 inactivated acid-fast bacilli-positive sputum slides using the Gen Elute bacterial genomic DNA kit. Eluted DNA were ethanol precipitated. The LiPA kit detected RMP susceptibility by detection of mutation in the 81 base pair (bp) rpoB gene. Culture of sputum from the same person was used for drug susceptibility testing for RMP using the proportion method. RESULTS: Amplification of 88.6% (39 slides) was achieved from DNA extracted using kits (66.7% for 1+, 81.8% for 2+ and 100% for 3+ slides). Hybridisation using the LiPA kit was applied to 31 amplified products. There was a concordance of 96.8% (24 RMP-resistant and 6 RMP-susceptible samples) and discordance of 3.2% (one sample resistant using the proportion method and susceptible on LiPA) between LiPA and the proportion method. CONCLUSION: LiPA proved useful on DNA extracted from smear-positive slides. Appropriate treatment regimen could be decided early. Slide smear preparation could replace sputum transport in cetylpyridinium chloride, reducing biohazard and thereby controlling the transmission of multidrug-resistant tuberculosis in the community.
引用
收藏
页码:258 / 261
页数:4
相关论文
共 12 条
[1]  
Cheong S F, 2003, KUAL LUMP MAL PROS S, P1
[2]  
Revised National Tuberculosis Control Programme, 2005, MOD LAB TECHN
[3]  
Revised National Tuberculosis Control Programme, 2009, TRAIN MAN MYC TUB CU
[4]  
Sharma M, 2003, INDIAN J MED RES, V117, P76
[5]  
Srivastava K, 2004, INDIAN J MED RES, V120, P100
[6]   Rapid detection of rifampin-resistant Mycobacterium tuberculosis directly from stained sputum smears using single-tube nested polymerase chain reaction deoxyribonucleic acid sequencing [J].
Suresh, Naga ;
Singh, Urvashi Balbir ;
Gupta, Chhavi ;
Arora, Jyoti ;
Rana, Tanu ;
Samantaray, Jyotish Chandra .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2007, 58 (02) :217-222
[7]   DETECTION OF RIFAMPICIN-RESISTANCE MUTATIONS IN MYCOBACTERIUM-TUBERCULOSIS [J].
TELENTI, A ;
IMBODEN, P ;
MARCHESI, F ;
LOWRIE, D ;
COLE, S ;
COLSTON, MJ ;
MATTER, L ;
SCHOPFER, K ;
BODMER, T .
LANCET, 1993, 341 (8846) :647-650
[8]   Simultaneous detection and strain differentiation of Mycobacterium tuberculosis complex in paraffin wax embedded tissues and in stained microscopic preparations [J].
van der Zanden, AGM ;
Hoentjen, AH ;
Heilmann, FGC ;
Weltevreden, EF ;
Schouls, LM ;
van Embden, JDA .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 1998, 51 (04) :209-214
[9]   Use of DNA extracts from Ziehl-Neelsen-stained slides for molecular detection of rifampin resistance and spoligotyping of Mycobacterium tuberculosis [J].
Van Der Zanden, AGM ;
Koppele-Vije, EMT ;
Bhanu, NV ;
Van Soolingen, D ;
Schouls, LM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (03) :1101-1108
[10]   Tuberculosis 4 Biomarkers and diagnostics for tuberculosis: progress, needs, and translation into practice [J].
Wallis, Robert S. ;
Pai, Madhukar ;
Menzies, Dick ;
Doherty, T. Mark ;
Walzl, Gerhard ;
Perkins, Mark D. ;
Zumla, Alimuddin .
LANCET, 2010, 375 (9729) :1920-1937