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

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 mu...

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Autores principales: Haguenoer, Eve, Baty, Gaelle, Pourcel, Christine, Lartigue, Marie-Frédérique, Domelier, Anne-Sophie, Rosenau, Agnès, Quentin, Roland, Mereghetti, Laurent, Lanotte, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163538/
https://www.ncbi.nlm.nih.gov/pubmed/21794143
http://dx.doi.org/10.1186/1471-2180-11-171
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author Haguenoer, Eve
Baty, Gaelle
Pourcel, Christine
Lartigue, Marie-Frédérique
Domelier, Anne-Sophie
Rosenau, Agnès
Quentin, Roland
Mereghetti, Laurent
Lanotte, Philippe
author_facet Haguenoer, Eve
Baty, Gaelle
Pourcel, Christine
Lartigue, Marie-Frédérique
Domelier, Anne-Sophie
Rosenau, Agnès
Quentin, Roland
Mereghetti, Laurent
Lanotte, Philippe
author_sort Haguenoer, Eve
collection PubMed
description 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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spelling pubmed-31635382011-08-30 A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping Haguenoer, Eve Baty, Gaelle Pourcel, Christine Lartigue, Marie-Frédérique Domelier, Anne-Sophie Rosenau, Agnès Quentin, Roland Mereghetti, Laurent Lanotte, Philippe BMC Microbiol Research Article 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. BioMed Central 2011-07-27 /pmc/articles/PMC3163538/ /pubmed/21794143 http://dx.doi.org/10.1186/1471-2180-11-171 Text en Copyright ©2011 Haguenoer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Haguenoer, Eve
Baty, Gaelle
Pourcel, Christine
Lartigue, Marie-Frédérique
Domelier, Anne-Sophie
Rosenau, Agnès
Quentin, Roland
Mereghetti, Laurent
Lanotte, Philippe
A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title_full A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title_fullStr A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title_full_unstemmed A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title_short A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping
title_sort multi locus variable number of tandem repeat analysis (mlva) scheme for streptococcus agalactiae genotyping
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163538/
https://www.ncbi.nlm.nih.gov/pubmed/21794143
http://dx.doi.org/10.1186/1471-2180-11-171
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