A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping

被引:36
作者
Haguenoer, Eve [1 ,2 ]
Baty, Gaelle [2 ]
Pourcel, Christine [3 ]
Lartigue, Marie-Frederique [1 ,4 ]
Domelier, Anne-Sophie [1 ,4 ]
Rosenau, Agnes [1 ]
Quentin, Roland [1 ,4 ]
Mereghetti, Laurent [1 ,2 ]
Lanotte, Philippe [1 ,2 ]
机构
[1] Univ Tours, UFR Med, Inst Federatif Rech Agents Transmissibles & Infec, EA Bacteries & Risque Materno Foetal 3854, Tours, France
[2] CHRU Tours, Serv Bacteriol Virol, Tours, France
[3] Univ Paris 11, CNRS, UMR 8621, Inst Genet & Microbiol, F-91405 Orsay, France
[4] CHRU Tours, Serv Bacteriol & Hyg Hosp Tours, Tours, France
关键词
GROUP-B STREPTOCOCCUS; ALPHA-C-PROTEIN; INVASIVE NEONATAL DISEASE; MYCOBACTERIUM-TUBERCULOSIS; GENETIC DIVERSITY; MOLECULAR EPIDEMIOLOGY; BACILLUS-ANTHRACIS; REPETITIVE UNITS; STRAINS; SEQUENCE;
D O I
10.1186/1471-2180-11-171
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Multilocus sequence typing (MLST) is currently the reference method for genotyping Streptococcus agalactiae strains, the leading cause of infectious disease in newborns and a major cause of disease in immunocompromised children and adults. We describe here a genotyping method based on multiple locus variable number of tandem repeat (VNTR) analysis (MLVA) applied to a population of S. agalactiae strains of various origins characterized by MLST and serotyping. Results: We studied a collection of 186 strains isolated from humans and cattle and three reference strains (A909, NEM316 and 2603 V/R). Among 34 VNTRs, 6 polymorphic VNTRs loci were selected for use in genotyping of the bacterial population. The MLVA profile consists of a series of allele numbers, corresponding to the number of repeats at each VNTR locus. 98 MLVA genotypes were obtained compared to 51 sequences types generated by MLST. The MLVA scheme generated clusters which corresponded well to the main clonal complexes obtained by MLST. However it provided a higher discriminatory power. The diversity index obtained with MLVA was 0.960 compared to 0.881 with MLST for this population of strains. Conclusions: The MLVA scheme proposed here is a rapid, cheap and easy genotyping method generating results suitable for exchange and comparison between different laboratories and for the epidemiologic surveillance of S. agalactiae and analyses of outbreaks.
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