Comparative evaluation of ligation-mediated PCR and spoligotyping as screening methods for genotyping of Mycobacterium tuberculosis strains

被引:20
作者
Bonora, S
Gutierrez, MC
di Perri, G
Brunello, F
Allegranzi, B
Ligozzi, M
Fontana, R
Concia, E
Vincent, V
机构
[1] Univ Verona, Inst Immunol & Infect Dis, I-37126 Verona, Italy
[2] Univ Verona, Inst Microbiol, I-37126 Verona, Italy
[3] Ctr Natl Reference Mycobacteries, Inst Pasteur, F-75724 Paris, France
关键词
D O I
10.1128/JCM.37.10.3118-3123.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Spoligotyping has been suggested as a screening test in multistep genotyping of Mycobacterium tuberculosis strains. Relying on restriction fragment length polymorphism (RFLP) analysis with IS6110 (IS6110 RFLP analysis) as a "gold standard," we performed a comparative evaluation of spoligotyping and ligation-mediated PCR (LMPCR), a recently described PCR-based typing method, as rapid screening tests for fingerprinting of 158 M. tuberculosis strains collected in Verona, Italy. LMPCR seemed to be comparable to spoligotyping in terms both of feasibility with rapidly extracted DNA and of generation of software-analyzable images. Moreover, LMPCR grouped considerably fen er strains than spoligotyping (38 versus 67%) and was found to reduce the cluster overestimation rate (26.3 versus 58%) and to give a better discriminatory index (0.992 versus 0.970) compared to spoligotyping, In our geographical region, where there was no evidence of clustered strains carrying fewer than six IS6110 copies, LMPCR was found to be more discriminatory than spoligotyping, We also evaluated two models of three-step typing strategies, involving the use of spoligotyping and LMPCR as screening methods and IS6110 RFLP analysis as a further supporting test. LMPCR proved, to be a more effective first-step test than spoligotyping, significantly reducing the need for subtyping, LMPCR should be considered an alternative to spoligotyping as a rapid screening method for M. tuberculosis fingerprinting, particularly in areas with a low prevalence of M. tuberculosis strains carrying few copies of IS6110.
引用
收藏
页码:3118 / 3123
页数:6
相关论文
共 27 条
[21]   IS6110, AN IS-LIKE ELEMENT OF MYCOBACTERIUM-TUBERCULOSIS COMPLEX [J].
THIERRY, D ;
CAVE, MD ;
EISENACH, KD ;
CRAWFORD, JT ;
BATES, JH ;
GICQUEL, B ;
GUESDON, JL .
NUCLEIC ACIDS RESEARCH, 1990, 18 (01) :188-188
[22]   Evaluation of tuberculosis transmission in a community by 1 year of systematic typing of Mycobacterium tuberculosis clinical isolates [J].
Torrea, G ;
Offredo, C ;
Simonet, M ;
Gicquel, B ;
Berche, P ;
PierreAudigier, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (05) :1043-1049
[23]   Utility of molecular epidemiology of tuberculosis [J].
van Soolingen, D .
EUROPEAN RESPIRATORY JOURNAL, 1998, 11 (04) :795-797
[24]   STRAIN IDENTIFICATION OF MYCOBACTERIUM-TUBERCULOSIS BY DNA FINGERPRINTING - RECOMMENDATIONS FOR A STANDARDIZED METHODOLOGY [J].
VANEMBDEN, JDA ;
CAVE, MD ;
CRAWFORD, JT ;
DALE, JW ;
EISENACH, KD ;
GICQUEL, B ;
HERMANS, P ;
MARTIN, C ;
MCADAM, R ;
SHINNICK, TM ;
SMALL, PM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (02) :406-409
[25]   OCCURRENCE AND STABILITY OF INSERTION SEQUENCES IN MYCOBACTERIUM-TUBERCULOSIS COMPLEX STRAINS - EVALUATION OF AN INSERTION SEQUENCE-DEPENDENT DNA POLYMORPHISM AS A TOOL IN THE EPIDEMIOLOGY OF TUBERCULOSIS [J].
VANSOOLINGEN, D ;
HERMANS, PWM ;
DEHAAS, PEW ;
SOLL, DR ;
VANEMBDEN, JDA .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (11) :2578-2586
[26]   Evaluation of strategies for molecular fingerprinting for use in the routine work of a mycobacterium reference unit [J].
Wilson, SM ;
Goss, S ;
Drobniewski, F .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (11) :3385-3388
[27]   CHARACTERIZATION OF MYCOBACTERIUM-TUBERCULOSIS STRAINS FROM VIETNAMESE PATIENTS BY SOUTHERN BLOT HYBRIDIZATION [J].
YUEN, LKW ;
ROSS, BC ;
JACKSON, KM ;
DWYER, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) :1615-1618