Evaluation of the new advanced 15-loci MIRU-VNTR genotyping tool in Mycobacterium tuberculosis molecular epidemiology studies

被引:66
作者
Alonso-Rodriguez, Noelia [1 ]
Martinez-Lirola, Miguel [2 ]
Herranz, Marta [1 ]
Sanchez-Benitez, Marisa [3 ]
Barroso, Pilar [4 ]
Bouza, Emilio [1 ]
Garcia de Viedma, Dario [1 ]
机构
[1] Univ Complutense, Hosp Gregorio Maranon, Serv Microbiol & Enfermedades Infecciosas, CIBER Enfermedades Resp CIBERES, E-28040 Madrid, Spain
[2] Complejo Hosp Torrecardenas, Almeria, Spain
[3] Univ TB Poniente, Almeria, Spain
[4] Delegac Salud Dist Levante, Almeria, Spain
关键词
D O I
10.1186/1471-2180-8-34
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: During the last few years, PCR-based methods have been developed to simplify and reduce the time required for genotyping Mycobacterium tuberculosis (MTB) by standard approaches based on IS6110-Restriction Fragment Length Polymorphism (RFLP). Of these, MIRU-12-VNTR (Mycobacterial interspersed repetitive units- variable number of tandem repeats) (MIRU-12) has been considered a good alternative. Nevertheless, some limitations and discrepancies with RFLP, which are minimized if the technique is complemented with spoligotyping, have been found. Recently, a new version of MIRU-VNTR targeting 15 loci (MIRU-15) has been proposed to improve the MIRU-12 format. Results: We evaluated the new MIRU-15 tool in two different samples. First, we analyzed the same convenience sample that had been used to evaluate MIRU-12 in a previous study, and the new 15-loci version offered higher discriminatory power (Hunter-Gaston discriminatory index [HGDI]: 0.995 vs 0.978; 34.4% of clustered cases vs 57.5%) and better correlation (full or high correlation with RFLP for 82% of the clusters vs 47%). Second, we evaluated MIRU-15 on a population-based sample and, once again, good correlation with the RFLP clustering data was observed (for 83% of the RFLP clusters). To understand the meaning of the discrepancies still found between MIRU-15 and RFLP, we analyzed the epidemiological data for the clustered patients. In most cases, splitting of RFLP-clustered patients by MIRU-15 occurred for those without epidemiological links, and RFLP-clustered patients with epidemiological links were also clustered by MIRU-15, suggesting a good epidemiological background for clustering defined by MIRU-15. Conclusion: The data obtained by MIRU-15 suggest that the new design is very efficient at assigning clusters confirmed by epidemiological data. If we add this to the speed with which it provides results, MIRU-15 could be considered a suitable tool for real-time genotyping.
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