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Identification of rickettsial isolates at the species level using multi-spacer typing

BACKGROUND: In order to estimate whether multi-spacer typing (MST), based on the sequencing of variable intergenic spacers, could serve for the identification of Rickettsia at the species level, we applied it to 108 rickettsial isolates or arthropod amplicons that include representatives of 23 valid...

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Autores principales: Fournier, Pierre-Edouard, Raoult, Didier
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950309/
https://www.ncbi.nlm.nih.gov/pubmed/17662158
http://dx.doi.org/10.1186/1471-2180-7-72
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author Fournier, Pierre-Edouard
Raoult, Didier
author_facet Fournier, Pierre-Edouard
Raoult, Didier
author_sort Fournier, Pierre-Edouard
collection PubMed
description BACKGROUND: In order to estimate whether multi-spacer typing (MST), based on the sequencing of variable intergenic spacers, could serve for the identification of Rickettsia at the species level, we applied it to 108 rickettsial isolates or arthropod amplicons that include representatives of 23 valid Rickettsia species. RESULTS: MST combining the dksA-xerC, mppA-purC, and rpmE-tRNA(fMet )spacer sequences identified 61 genotypes, allowing the differentiation of each species by at least one distinct genotype. In addition, MST was discriminatory at the strain level in six species for which several isolates or arthropod amplicons were available. CONCLUSION: MST proved to be a reproducible and high-resolution genotyping method allowing clear identification of rickettsial isolates at the species level and further additional differentiation of strains within some species.
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spelling pubmed-19503092007-08-21 Identification of rickettsial isolates at the species level using multi-spacer typing Fournier, Pierre-Edouard Raoult, Didier BMC Microbiol Research Article BACKGROUND: In order to estimate whether multi-spacer typing (MST), based on the sequencing of variable intergenic spacers, could serve for the identification of Rickettsia at the species level, we applied it to 108 rickettsial isolates or arthropod amplicons that include representatives of 23 valid Rickettsia species. RESULTS: MST combining the dksA-xerC, mppA-purC, and rpmE-tRNA(fMet )spacer sequences identified 61 genotypes, allowing the differentiation of each species by at least one distinct genotype. In addition, MST was discriminatory at the strain level in six species for which several isolates or arthropod amplicons were available. CONCLUSION: MST proved to be a reproducible and high-resolution genotyping method allowing clear identification of rickettsial isolates at the species level and further additional differentiation of strains within some species. BioMed Central 2007-07-30 /pmc/articles/PMC1950309/ /pubmed/17662158 http://dx.doi.org/10.1186/1471-2180-7-72 Text en Copyright © 2007 Fournier and Raoult; 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
Fournier, Pierre-Edouard
Raoult, Didier
Identification of rickettsial isolates at the species level using multi-spacer typing
title Identification of rickettsial isolates at the species level using multi-spacer typing
title_full Identification of rickettsial isolates at the species level using multi-spacer typing
title_fullStr Identification of rickettsial isolates at the species level using multi-spacer typing
title_full_unstemmed Identification of rickettsial isolates at the species level using multi-spacer typing
title_short Identification of rickettsial isolates at the species level using multi-spacer typing
title_sort identification of rickettsial isolates at the species level using multi-spacer typing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950309/
https://www.ncbi.nlm.nih.gov/pubmed/17662158
http://dx.doi.org/10.1186/1471-2180-7-72
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