Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains

Detalhes bibliográficos
Autor(a) principal: Macheras, Edouard
Data de Publicação: 2011
Outros Autores: Roux, Anne-Laure, Bastian, Sylvaine, Leao, Sylvia Cardoso [UNIFESP], Palaci, Moises, Sivadon-Tardy, Valerie, Gutierrez, Cristina, Richter, Elvira, Ruesch-Gerdes, Sabine, Pfyffer, Gaby, Bodmer, Thomas, Cambau, Emmanuelle, Gaillard, Jean-Louis, Heym, Beate
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/33394
http://dx.doi.org/10.1128/JCM.01274-10
Resumo: Mycobacterium abscessus, Mycobacterium bolletii, and Mycobacterium massiliense (Mycobacterium abscessus sensu lato) are closely related species that currently are identified by the sequencing of the rpoB gene. However, recent studies show that rpoB sequencing alone is insufficient to discriminate between these species, and some authors have questioned their current taxonomic classification. We studied here a large collection of M. abscessus (sensu lato) strains by partial rpoB sequencing (752 bp) and multilocus sequence analysis (MLSA). the final MLSA scheme developed was based on the partial sequences of eight housekeeping genes: argH, cya, glpK, gnd, murC, pgm, pta, and purH. the strains studied included the three type strains (M. abscessus CIP 104536T, M. massiliense CIP 108297(T), and M. bolletii CIP 108541(T)) and 120 isolates recovered between 1997 and 2007 in France, Germany, Switzerland, and Brazil. the rpoB phylogenetic tree confirmed the existence of three main clusters, each comprising the type strain of one species. However, divergence values between the M. massiliense and M. bolletii clusters all were below 3% and between the M. abscessus and M. massiliense clusters were from 2.66 to 3.59%. the tree produced using the concatenated MLSA gene sequences (4,071 bp) also showed three main clusters, each comprising the type strain of one species. the M. abscessus cluster had a bootstrap value of 100% and was mostly compact. Bootstrap values for the M. massiliense and M. bolletii branches were much lower (71 and 61%, respectively), with the M. massiliense cluster having a fuzzy aspect. Mean (range) divergence values were 2.17% (1.13 to 2.58%) between the M. abscessus and M. massiliense clusters, 2.37% (1.5 to 2.85%) between the M. abscessus and M. bolletii clusters, and 2.28% (0.86 to 2.68%) between the M. massiliense and M. bolletii clusters. Adding the rpoB sequence to the MLSA-concatenated sequence (total sequence, 4,823 bp) had little effect on the clustering of strains. We found 10/120 (8.3%) isolates for which the concatenated MLSA gene sequence and rpoB sequence were discordant (e. g., M. massiliense MLSA sequence and M. abscessus rpoB sequence), suggesting the intergroup lateral transfers of rpoB. in conclusion, our study strongly supports the recent proposal that M. abscessus, M. massiliense, and M. bolletii should constitute a single species. Our findings also indicate that there has been a horizontal transfer of rpoB sequences between these subgroups, precluding the use of rpoB sequencing alone for the accurate identification of the two proposed M. abscessus subspecies.
id UFSP_9435ae29202ffcc4ca6b669a1a40427c
oai_identifier_str oai:repositorio.unifesp.br:11600/33394
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Macheras, EdouardRoux, Anne-LaureBastian, SylvaineLeao, Sylvia Cardoso [UNIFESP]Palaci, MoisesSivadon-Tardy, ValerieGutierrez, CristinaRichter, ElviraRuesch-Gerdes, SabinePfyffer, GabyBodmer, ThomasCambau, EmmanuelleGaillard, Jean-LouisHeym, BeateHop Ambroise PareHop Raymond PoincareUniv Versailles St Quentin En YvelinesGrp Hosp Pitie SalpetriereUniversidade Federal de São Paulo (UNIFESP)Univ Fed Espirito SantoFINDForschungszentrum BorstelLuzerner KantonsspitalUniv BernGrp Hosp St Louis Lariboisiere2016-01-24T14:06:06Z2016-01-24T14:06:06Z2011-02-01Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 49, n. 2, p. 491-499, 2011.0095-1137http://repositorio.unifesp.br/handle/11600/33394http://dx.doi.org/10.1128/JCM.01274-10WOS000286977500003.pdf10.1128/JCM.01274-10WOS:000286977500003Mycobacterium abscessus, Mycobacterium bolletii, and Mycobacterium massiliense (Mycobacterium abscessus sensu lato) are closely related species that currently are identified by the sequencing of the rpoB gene. However, recent studies show that rpoB sequencing alone is insufficient to discriminate between these species, and some authors have questioned their current taxonomic classification. We studied here a large collection of M. abscessus (sensu lato) strains by partial rpoB sequencing (752 bp) and multilocus sequence analysis (MLSA). the final MLSA scheme developed was based on the partial sequences of eight housekeeping genes: argH, cya, glpK, gnd, murC, pgm, pta, and purH. the strains studied included the three type strains (M. abscessus CIP 104536T, M. massiliense CIP 108297(T), and M. bolletii CIP 108541(T)) and 120 isolates recovered between 1997 and 2007 in France, Germany, Switzerland, and Brazil. the rpoB phylogenetic tree confirmed the existence of three main clusters, each comprising the type strain of one species. However, divergence values between the M. massiliense and M. bolletii clusters all were below 3% and between the M. abscessus and M. massiliense clusters were from 2.66 to 3.59%. the tree produced using the concatenated MLSA gene sequences (4,071 bp) also showed three main clusters, each comprising the type strain of one species. the M. abscessus cluster had a bootstrap value of 100% and was mostly compact. Bootstrap values for the M. massiliense and M. bolletii branches were much lower (71 and 61%, respectively), with the M. massiliense cluster having a fuzzy aspect. Mean (range) divergence values were 2.17% (1.13 to 2.58%) between the M. abscessus and M. massiliense clusters, 2.37% (1.5 to 2.85%) between the M. abscessus and M. bolletii clusters, and 2.28% (0.86 to 2.68%) between the M. massiliense and M. bolletii clusters. Adding the rpoB sequence to the MLSA-concatenated sequence (total sequence, 4,823 bp) had little effect on the clustering of strains. We found 10/120 (8.3%) isolates for which the concatenated MLSA gene sequence and rpoB sequence were discordant (e. g., M. massiliense MLSA sequence and M. abscessus rpoB sequence), suggesting the intergroup lateral transfers of rpoB. in conclusion, our study strongly supports the recent proposal that M. abscessus, M. massiliense, and M. bolletii should constitute a single species. Our findings also indicate that there has been a horizontal transfer of rpoB sequences between these subgroups, precluding the use of rpoB sequencing alone for the accurate identification of the two proposed M. abscessus subspecies.Vaincre la MucoviscidoseHop Ambroise Pare, AP HP, Serv Microbiol Hyg, Boulogne, FranceHop Raymond Poincare, AP HP, Microbiol Lab, Garches, FranceUniv Versailles St Quentin En Yvelines, EA 3647, Garches, FranceGrp Hosp Pitie Salpetriere, Ctr Natl Reference Mycobacteries & Resistance Myc, Lab Bacteriol Hyg, F-75634 Paris, FranceUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, São Paulo, BrazilUniv Fed Espirito Santo, Nucleo Doencas Infecciosas, Vitoria, ES, BrazilFIND, Geneva, SwitzerlandForschungszentrum Borstel, Natl Reference Ctr Mycobacteria, Borstel, GermanyLuzerner Kantonsspital, Inst Med Mikrobiol, Zentrum LaborMed, Luzern, SwitzerlandUniv Bern, Inst Infekt Krankheiten, Bern, SwitzerlandGrp Hosp St Louis Lariboisiere, Ctr Natl Reference Mycobacteries & Resistance Myc, Lab Associe, Paris, FranceUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, São Paulo, BrazilWeb of Science491-499engAmer Soc MicrobiologyJournal of Clinical MicrobiologyMultilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strainsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000286977500003.pdfapplication/pdf859741${dspace.ui.url}/bitstream/11600/33394/1/WOS000286977500003.pdfd9f7d6e03f518eb75bed7fb0ba563f3dMD51open accessTEXTWOS000286977500003.pdf.txtWOS000286977500003.pdf.txtExtracted texttext/plain48011${dspace.ui.url}/bitstream/11600/33394/2/WOS000286977500003.pdf.txtf2d2b8f30da8f3d64a927a19c605e1ddMD52open access11600/333942023-01-30 22:17:47.122open accessoai:repositorio.unifesp.br:11600/33394Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-01-31T01:17:47Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
title Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
spellingShingle Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
Macheras, Edouard
title_short Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
title_full Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
title_fullStr Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
title_full_unstemmed Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
title_sort Multilocus Sequence Analysis and rpoB Sequencing of Mycobacterium abscessus (Sensu Lato) Strains
author Macheras, Edouard
author_facet Macheras, Edouard
Roux, Anne-Laure
Bastian, Sylvaine
Leao, Sylvia Cardoso [UNIFESP]
Palaci, Moises
Sivadon-Tardy, Valerie
Gutierrez, Cristina
Richter, Elvira
Ruesch-Gerdes, Sabine
Pfyffer, Gaby
Bodmer, Thomas
Cambau, Emmanuelle
Gaillard, Jean-Louis
Heym, Beate
author_role author
author2 Roux, Anne-Laure
Bastian, Sylvaine
Leao, Sylvia Cardoso [UNIFESP]
Palaci, Moises
Sivadon-Tardy, Valerie
Gutierrez, Cristina
Richter, Elvira
Ruesch-Gerdes, Sabine
Pfyffer, Gaby
Bodmer, Thomas
Cambau, Emmanuelle
Gaillard, Jean-Louis
Heym, Beate
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Hop Ambroise Pare
Hop Raymond Poincare
Univ Versailles St Quentin En Yvelines
Grp Hosp Pitie Salpetriere
Universidade Federal de São Paulo (UNIFESP)
Univ Fed Espirito Santo
FIND
Forschungszentrum Borstel
Luzerner Kantonsspital
Univ Bern
Grp Hosp St Louis Lariboisiere
dc.contributor.author.fl_str_mv Macheras, Edouard
Roux, Anne-Laure
Bastian, Sylvaine
Leao, Sylvia Cardoso [UNIFESP]
Palaci, Moises
Sivadon-Tardy, Valerie
Gutierrez, Cristina
Richter, Elvira
Ruesch-Gerdes, Sabine
Pfyffer, Gaby
Bodmer, Thomas
Cambau, Emmanuelle
Gaillard, Jean-Louis
Heym, Beate
description Mycobacterium abscessus, Mycobacterium bolletii, and Mycobacterium massiliense (Mycobacterium abscessus sensu lato) are closely related species that currently are identified by the sequencing of the rpoB gene. However, recent studies show that rpoB sequencing alone is insufficient to discriminate between these species, and some authors have questioned their current taxonomic classification. We studied here a large collection of M. abscessus (sensu lato) strains by partial rpoB sequencing (752 bp) and multilocus sequence analysis (MLSA). the final MLSA scheme developed was based on the partial sequences of eight housekeeping genes: argH, cya, glpK, gnd, murC, pgm, pta, and purH. the strains studied included the three type strains (M. abscessus CIP 104536T, M. massiliense CIP 108297(T), and M. bolletii CIP 108541(T)) and 120 isolates recovered between 1997 and 2007 in France, Germany, Switzerland, and Brazil. the rpoB phylogenetic tree confirmed the existence of three main clusters, each comprising the type strain of one species. However, divergence values between the M. massiliense and M. bolletii clusters all were below 3% and between the M. abscessus and M. massiliense clusters were from 2.66 to 3.59%. the tree produced using the concatenated MLSA gene sequences (4,071 bp) also showed three main clusters, each comprising the type strain of one species. the M. abscessus cluster had a bootstrap value of 100% and was mostly compact. Bootstrap values for the M. massiliense and M. bolletii branches were much lower (71 and 61%, respectively), with the M. massiliense cluster having a fuzzy aspect. Mean (range) divergence values were 2.17% (1.13 to 2.58%) between the M. abscessus and M. massiliense clusters, 2.37% (1.5 to 2.85%) between the M. abscessus and M. bolletii clusters, and 2.28% (0.86 to 2.68%) between the M. massiliense and M. bolletii clusters. Adding the rpoB sequence to the MLSA-concatenated sequence (total sequence, 4,823 bp) had little effect on the clustering of strains. We found 10/120 (8.3%) isolates for which the concatenated MLSA gene sequence and rpoB sequence were discordant (e. g., M. massiliense MLSA sequence and M. abscessus rpoB sequence), suggesting the intergroup lateral transfers of rpoB. in conclusion, our study strongly supports the recent proposal that M. abscessus, M. massiliense, and M. bolletii should constitute a single species. Our findings also indicate that there has been a horizontal transfer of rpoB sequences between these subgroups, precluding the use of rpoB sequencing alone for the accurate identification of the two proposed M. abscessus subspecies.
publishDate 2011
dc.date.issued.fl_str_mv 2011-02-01
dc.date.accessioned.fl_str_mv 2016-01-24T14:06:06Z
dc.date.available.fl_str_mv 2016-01-24T14:06:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 49, n. 2, p. 491-499, 2011.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/33394
http://dx.doi.org/10.1128/JCM.01274-10
dc.identifier.issn.none.fl_str_mv 0095-1137
dc.identifier.file.none.fl_str_mv WOS000286977500003.pdf
dc.identifier.doi.none.fl_str_mv 10.1128/JCM.01274-10
dc.identifier.wos.none.fl_str_mv WOS:000286977500003
identifier_str_mv Journal of Clinical Microbiology. Washington: Amer Soc Microbiology, v. 49, n. 2, p. 491-499, 2011.
0095-1137
WOS000286977500003.pdf
10.1128/JCM.01274-10
WOS:000286977500003
url http://repositorio.unifesp.br/handle/11600/33394
http://dx.doi.org/10.1128/JCM.01274-10
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Journal of Clinical Microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 491-499
dc.publisher.none.fl_str_mv Amer Soc Microbiology
publisher.none.fl_str_mv Amer Soc Microbiology
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
bitstream.url.fl_str_mv ${dspace.ui.url}/bitstream/11600/33394/1/WOS000286977500003.pdf
${dspace.ui.url}/bitstream/11600/33394/2/WOS000286977500003.pdf.txt
bitstream.checksum.fl_str_mv d9f7d6e03f518eb75bed7fb0ba563f3d
f2d2b8f30da8f3d64a927a19c605e1dd
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
_version_ 1802764278902554624