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

Citation
S. Bonora et al., Comparative evaluation of ligation-mediated PCR and spoligotyping as screening methods for genotyping of Mycobacterium tuberculosis strains, J CLIN MICR, 37(10), 1999, pp. 3118-3123
Citations number
27
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
37
Issue
10
Year of publication
1999
Pages
3118 - 3123
Database
ISI
SICI code
0095-1137(199910)37:10<3118:CEOLPA>2.0.ZU;2-G
Abstract
Spoligotyping has been suggested as a screening test in multistep genotypin g of Mycobacterium tuberculosis strains. Relying on restriction fragment le ngth 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 strain s collected in Verona, Italy. LMPCR seemed to be comparable to spoligotypin g 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 clu ster overestimation rate (26.3 versus 58%) and to give a better discriminat ory index (0.992 versus 0.970) compared to spoligotyping, In our geographic al region, where there was no evidence of clustered strains carrying fewer than six IS6110 copies, LMPCR was found to be more discriminatory than spol igotyping, We also evaluated two models of three-step typing strategies, in volving the use of spoligotyping and LMPCR as screening methods and IS6110 RFLP analysis as a further supporting test. LMPCR proved, to be a more effe ctive first-step test than spoligotyping, significantly reducing the need f or 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 copi es of IS6110.