Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Microbiology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000100200 |
Resumo: | ABSTRACT Bacteroides fragilis is the strict anaerobic bacteria most commonly found in human infections, and has a high mortality rate. Among other virulence factors, the remarkable ability to acquire resistance to a variety of antimicrobial agents and to tolerate nanomolar concentrations of oxygen explains in part their success in causing infection and colonizing the mucosa. Much attention has been given to genes related to multiple drug resistance derived from plasmids, integrons or transposon, but such genes are also detected in chromosomal systems, like the mar (multiple antibiotic resistance) locus, that confer resistance to a range of drugs. Regulators like MarR, that control expression of the locus mar, also regulate resistance to organic solvents, disinfectants and oxygen reactive species are important players in these events. Strains derived from the parental strain 638R, with mutations in the genes hereby known as marRI (BF638R_3159) and marRII (BF638R_3706) were constructed by gene disruption using a suicide plasmid. Phenotypic response of the mutant strains to hydrogen peroxide, cell survival assay against exposure to oxygen, biofilm formation, resistance to bile salts and resistance to antibiotics was evaluated. The results showed that the mutant strains exhibit statistically significant differences in their response to oxygen stress, but no changes were observed in survival when exposed to bile salts. Biofilm formation was not affected by either gene disruption. Both mutant strains however, became more sensitive to multiple antimicrobial drugs tested. This indicates that as observed in other bacterial species, MarR are an important resistance mechanism in B. fragilis. |
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Brazilian Journal of Microbiology |
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Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilisBacteroides fragilisAnaerobic bacteriaMulti-drug resistanceOxidative stress resistanceABSTRACT Bacteroides fragilis is the strict anaerobic bacteria most commonly found in human infections, and has a high mortality rate. Among other virulence factors, the remarkable ability to acquire resistance to a variety of antimicrobial agents and to tolerate nanomolar concentrations of oxygen explains in part their success in causing infection and colonizing the mucosa. Much attention has been given to genes related to multiple drug resistance derived from plasmids, integrons or transposon, but such genes are also detected in chromosomal systems, like the mar (multiple antibiotic resistance) locus, that confer resistance to a range of drugs. Regulators like MarR, that control expression of the locus mar, also regulate resistance to organic solvents, disinfectants and oxygen reactive species are important players in these events. Strains derived from the parental strain 638R, with mutations in the genes hereby known as marRI (BF638R_3159) and marRII (BF638R_3706) were constructed by gene disruption using a suicide plasmid. Phenotypic response of the mutant strains to hydrogen peroxide, cell survival assay against exposure to oxygen, biofilm formation, resistance to bile salts and resistance to antibiotics was evaluated. The results showed that the mutant strains exhibit statistically significant differences in their response to oxygen stress, but no changes were observed in survival when exposed to bile salts. Biofilm formation was not affected by either gene disruption. Both mutant strains however, became more sensitive to multiple antimicrobial drugs tested. This indicates that as observed in other bacterial species, MarR are an important resistance mechanism in B. fragilis.Sociedade Brasileira de Microbiologia2018-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000100200Brazilian Journal of Microbiology v.49 n.1 2018reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1016/j.bjm.2017.05.005info:eu-repo/semantics/openAccessSilva,Clara Maria GuimarãesSilva,Déborah Nascimento dos SantosCosta,Scarlathe Bezerra daAlmeida,Juliana Soares de SáBoente,Renata FerreiraTeixeira,Felipe LopesDomingues,Regina Maria Cavalcanti PilottoLobo,Leandro Araujoeng2018-02-20T00:00:00Zoai:scielo:S1517-83822018000100200Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2018-02-20T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false |
dc.title.none.fl_str_mv |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
title |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
spellingShingle |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis Silva,Clara Maria Guimarães Bacteroides fragilis Anaerobic bacteria Multi-drug resistance Oxidative stress resistance |
title_short |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
title_full |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
title_fullStr |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
title_full_unstemmed |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
title_sort |
Inactivation of MarR gene homologs increases susceptibility to antimicrobials in Bacteroides fragilis |
author |
Silva,Clara Maria Guimarães |
author_facet |
Silva,Clara Maria Guimarães Silva,Déborah Nascimento dos Santos Costa,Scarlathe Bezerra da Almeida,Juliana Soares de Sá Boente,Renata Ferreira Teixeira,Felipe Lopes Domingues,Regina Maria Cavalcanti Pilotto Lobo,Leandro Araujo |
author_role |
author |
author2 |
Silva,Déborah Nascimento dos Santos Costa,Scarlathe Bezerra da Almeida,Juliana Soares de Sá Boente,Renata Ferreira Teixeira,Felipe Lopes Domingues,Regina Maria Cavalcanti Pilotto Lobo,Leandro Araujo |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Silva,Clara Maria Guimarães Silva,Déborah Nascimento dos Santos Costa,Scarlathe Bezerra da Almeida,Juliana Soares de Sá Boente,Renata Ferreira Teixeira,Felipe Lopes Domingues,Regina Maria Cavalcanti Pilotto Lobo,Leandro Araujo |
dc.subject.por.fl_str_mv |
Bacteroides fragilis Anaerobic bacteria Multi-drug resistance Oxidative stress resistance |
topic |
Bacteroides fragilis Anaerobic bacteria Multi-drug resistance Oxidative stress resistance |
description |
ABSTRACT Bacteroides fragilis is the strict anaerobic bacteria most commonly found in human infections, and has a high mortality rate. Among other virulence factors, the remarkable ability to acquire resistance to a variety of antimicrobial agents and to tolerate nanomolar concentrations of oxygen explains in part their success in causing infection and colonizing the mucosa. Much attention has been given to genes related to multiple drug resistance derived from plasmids, integrons or transposon, but such genes are also detected in chromosomal systems, like the mar (multiple antibiotic resistance) locus, that confer resistance to a range of drugs. Regulators like MarR, that control expression of the locus mar, also regulate resistance to organic solvents, disinfectants and oxygen reactive species are important players in these events. Strains derived from the parental strain 638R, with mutations in the genes hereby known as marRI (BF638R_3159) and marRII (BF638R_3706) were constructed by gene disruption using a suicide plasmid. Phenotypic response of the mutant strains to hydrogen peroxide, cell survival assay against exposure to oxygen, biofilm formation, resistance to bile salts and resistance to antibiotics was evaluated. The results showed that the mutant strains exhibit statistically significant differences in their response to oxygen stress, but no changes were observed in survival when exposed to bile salts. Biofilm formation was not affected by either gene disruption. Both mutant strains however, became more sensitive to multiple antimicrobial drugs tested. This indicates that as observed in other bacterial species, MarR are an important resistance mechanism in B. fragilis. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-03-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000100200 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822018000100200 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.bjm.2017.05.005 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Microbiologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Microbiologia |
dc.source.none.fl_str_mv |
Brazilian Journal of Microbiology v.49 n.1 2018 reponame:Brazilian Journal of Microbiology instname:Sociedade Brasileira de Microbiologia (SBM) instacron:SBM |
instname_str |
Sociedade Brasileira de Microbiologia (SBM) |
instacron_str |
SBM |
institution |
SBM |
reponame_str |
Brazilian Journal of Microbiology |
collection |
Brazilian Journal of Microbiology |
repository.name.fl_str_mv |
Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM) |
repository.mail.fl_str_mv |
bjm@sbmicrobiologia.org.br||mbmartin@usp.br |
_version_ |
1752122209325809664 |