The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence

Brucella spp., like other pathogens, must cope with the environment of diverse host niches during the infection process. In doing this, pathogens evolved different type of transport systems to help them survive and disseminate within the host. Members of the TolC family have been shown to be involve...

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Autores principales: Posadas, D.M., Martín, F.A., Sabio Y Garcïa, J.V., Spera, J.M., Delpino, M.V., Baldi, P., Campos, E., Cravero, S.L., Zorreguieta, A.
Formato: Artículo publishedVersion
Lenguaje:Inglés
Publicado: 2007
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00199567_v75_n1_p379_Posadas
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spelling paperaa:paper_00199567_v75_n1_p379_Posadas2023-06-12T16:42:06Z The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence Infect. Immun. 2007;75(1):379-389 Posadas, D.M. Martín, F.A. Sabio Y Garcïa, J.V. Spera, J.M. Delpino, M.V. Baldi, P. Campos, E. Cravero, S.L. Zorreguieta, A. acriflavine amikacin ampicillin antiinfective agent berberine bile salt carbenicillin cetrimide chloramphenicol deoxycholate sodium erythromycin ethidium bromide hemolysin nalidixic acid norfloxacin rhodamine rifampicin spectinomycin tetracycline TolC protein animal cell antibiotic resistance article bacterial gene bacterial mutation bacterial survival bacterial virulence BepC gene Brucella suis controlled study environmental factor Escherichia coli female gene disruption gene expression regulation gene insertion molecular cloning mouse nonhuman phenotype phylogeny priority journal protein analysis protein family Animals Anti-Infective Agents Bacterial Outer Membrane Proteins Brucella suis Cloning, Molecular Drug Resistance Female Membrane Transport Proteins Mice Mice, Inbred BALB C Phylogeny Polymerase Chain Reaction Virulence Brucella spp., like other pathogens, must cope with the environment of diverse host niches during the infection process. In doing this, pathogens evolved different type of transport systems to help them survive and disseminate within the host. Members of the TolC family have been shown to be involved in the export of chemically diverse molecules ranging from large protein toxins to small toxic compounds. The role of proteins from the TolC family in Brucella and other α-2-proteobacteria has been explored little. The gene encoding the unique member of the TolC family from Brucella suis (BepC) was cloned and expressed in an Escherichia coli mutant disrupted in the gene encoding TolC, which has the peculiarity of being involved in diverse transport functions. BepC fully complemented the resistance to drugs such as chloramphenicol and acriflavine but was incapable of restoring hemolysin secretion in the tolC mutant of & coli. An insertional mutation in the bepC gene strongly affected the resistance phenotype of B. suis to bile salts and toxic chemicals such as ethidium bromide and rhodamine and significantly decreased the resistance to antibiotics such as erythromycin, ampicillin, tetracycline, and norfloxacin. Moreover, the B. suis bepC mutant was attenuated in the mouse model of infection. Taken together, these results suggest that BepC-dependent efflux processes of toxic compounds contribute to B. suis survival inside the host. Copyright © 2007, American Society for Microbiology. All Rights Reserved. Fil:Posadas, D.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Martín, F.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sabio Y Garcïa, J.V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Campos, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Zorreguieta, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2007 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00199567_v75_n1_p379_Posadas
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language Inglés
orig_language_str_mv eng
topic acriflavine
amikacin
ampicillin
antiinfective agent
berberine
bile salt
carbenicillin
cetrimide
chloramphenicol
deoxycholate sodium
erythromycin
ethidium bromide
hemolysin
nalidixic acid
norfloxacin
rhodamine
rifampicin
spectinomycin
tetracycline
TolC protein
animal cell
antibiotic resistance
article
bacterial gene
bacterial mutation
bacterial survival
bacterial virulence
BepC gene
Brucella suis
controlled study
environmental factor
Escherichia coli
female
gene disruption
gene expression regulation
gene insertion
molecular cloning
mouse
nonhuman
phenotype
phylogeny
priority journal
protein analysis
protein family
Animals
Anti-Infective Agents
Bacterial Outer Membrane Proteins
Brucella suis
Cloning, Molecular
Drug Resistance
Female
Membrane Transport Proteins
Mice
Mice, Inbred BALB C
Phylogeny
Polymerase Chain Reaction
Virulence
spellingShingle acriflavine
amikacin
ampicillin
antiinfective agent
berberine
bile salt
carbenicillin
cetrimide
chloramphenicol
deoxycholate sodium
erythromycin
ethidium bromide
hemolysin
nalidixic acid
norfloxacin
rhodamine
rifampicin
spectinomycin
tetracycline
TolC protein
animal cell
antibiotic resistance
article
bacterial gene
bacterial mutation
bacterial survival
bacterial virulence
BepC gene
Brucella suis
controlled study
environmental factor
Escherichia coli
female
gene disruption
gene expression regulation
gene insertion
molecular cloning
mouse
nonhuman
phenotype
phylogeny
priority journal
protein analysis
protein family
Animals
Anti-Infective Agents
Bacterial Outer Membrane Proteins
Brucella suis
Cloning, Molecular
Drug Resistance
Female
Membrane Transport Proteins
Mice
Mice, Inbred BALB C
Phylogeny
Polymerase Chain Reaction
Virulence
Posadas, D.M.
Martín, F.A.
Sabio Y Garcïa, J.V.
Spera, J.M.
Delpino, M.V.
Baldi, P.
Campos, E.
Cravero, S.L.
Zorreguieta, A.
The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
topic_facet acriflavine
amikacin
ampicillin
antiinfective agent
berberine
bile salt
carbenicillin
cetrimide
chloramphenicol
deoxycholate sodium
erythromycin
ethidium bromide
hemolysin
nalidixic acid
norfloxacin
rhodamine
rifampicin
spectinomycin
tetracycline
TolC protein
animal cell
antibiotic resistance
article
bacterial gene
bacterial mutation
bacterial survival
bacterial virulence
BepC gene
Brucella suis
controlled study
environmental factor
Escherichia coli
female
gene disruption
gene expression regulation
gene insertion
molecular cloning
mouse
nonhuman
phenotype
phylogeny
priority journal
protein analysis
protein family
Animals
Anti-Infective Agents
Bacterial Outer Membrane Proteins
Brucella suis
Cloning, Molecular
Drug Resistance
Female
Membrane Transport Proteins
Mice
Mice, Inbred BALB C
Phylogeny
Polymerase Chain Reaction
Virulence
description Brucella spp., like other pathogens, must cope with the environment of diverse host niches during the infection process. In doing this, pathogens evolved different type of transport systems to help them survive and disseminate within the host. Members of the TolC family have been shown to be involved in the export of chemically diverse molecules ranging from large protein toxins to small toxic compounds. The role of proteins from the TolC family in Brucella and other α-2-proteobacteria has been explored little. The gene encoding the unique member of the TolC family from Brucella suis (BepC) was cloned and expressed in an Escherichia coli mutant disrupted in the gene encoding TolC, which has the peculiarity of being involved in diverse transport functions. BepC fully complemented the resistance to drugs such as chloramphenicol and acriflavine but was incapable of restoring hemolysin secretion in the tolC mutant of & coli. An insertional mutation in the bepC gene strongly affected the resistance phenotype of B. suis to bile salts and toxic chemicals such as ethidium bromide and rhodamine and significantly decreased the resistance to antibiotics such as erythromycin, ampicillin, tetracycline, and norfloxacin. Moreover, the B. suis bepC mutant was attenuated in the mouse model of infection. Taken together, these results suggest that BepC-dependent efflux processes of toxic compounds contribute to B. suis survival inside the host. Copyright © 2007, American Society for Microbiology. All Rights Reserved.
format Artículo
Artículo
publishedVersion
author Posadas, D.M.
Martín, F.A.
Sabio Y Garcïa, J.V.
Spera, J.M.
Delpino, M.V.
Baldi, P.
Campos, E.
Cravero, S.L.
Zorreguieta, A.
author_facet Posadas, D.M.
Martín, F.A.
Sabio Y Garcïa, J.V.
Spera, J.M.
Delpino, M.V.
Baldi, P.
Campos, E.
Cravero, S.L.
Zorreguieta, A.
author_sort Posadas, D.M.
title The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
title_short The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
title_full The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
title_fullStr The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
title_full_unstemmed The TolC homologue of Brucella suis is involved in resistance to antimicrobial compounds and virulence
title_sort tolc homologue of brucella suis is involved in resistance to antimicrobial compounds and virulence
publishDate 2007
url http://hdl.handle.net/20.500.12110/paper_00199567_v75_n1_p379_Posadas
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