Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon

Autores
Sieira, R.; Comerci, D.J.; Pietrasanta, L.I.; Ugalde, R.A.
Año de publicación
2004
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Type IV secretion systems (T4SSs) are multicomponent machineries that play an essential role in pathogenicity of many facultative intracellular bacteria. The virB operon of Brucella abortus codes for a T4SS essential for virulence and intracellular multiplication. Here, virB expression analyses carried out using lacZ transcriptional fusions showed that virB promoter (PvirB) is temporally activated within J774 cells. Primer extension experiments revealed that virB transcription starts at 27 bp upstream of the first gene of the virB operon. Structural analyses showed that PvirB and regulatory sequences involved in intracellular regulation span 430 bp upstream of the transcription start site. A protein able to bind PvirB was isolated and identified. This protein, homologue to integration host factor (IHF), specifically interacts with PvirB and induces a DNA bending with an angle of 50.36°. DNAse I footprinting experiments showed that IHF protects a 51 bp region that contains two overlapped IHF binding consensus motifs. VirB expression experiments carried out with PvirB-lacZ fusions showed that in B. abortus IHF participates in the regulation of PvirB activity during the intracellular and vegetative growth in different media. A mutant strain with a 20 bp IHF binding site replacement failed to turn on the virB operon during the initial stages of macrophage infection and displayed severe intracellular multiplication defects. These data indicate that IHF plays a key role during intracellular virB operon expression being required for the biogenesis of the endoplasmic reticulum-derived replicative vacuole.
Fil:Ugalde, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Mol. Microbiol. 2004;54(3):808-822
Materia
beta galactosidase
curved DNA
deoxyribonuclease I
integration host factor
VirB protein
animal cell
article
bacterial strain
bacterial virulence
bacterium mutant
binding site
Brucella abortus
cell vacuole
consensus sequence
endoplasmic reticulum
gene overexpression
gene replication
genetic transcription
macrophage
mouse
nonhuman
operon
pathogenicity
priority journal
promoter region
protein binding
protein protein interaction
regulatory sequence
transcription initiation site
transcription regulation
Animals
Bacterial Proteins
Base Sequence
Binding Sites
Brucella abortus
Cell Line
Gene Expression Regulation, Bacterial
Genes, Reporter
Integration Host Factors
Macrophages
Mice
Operon
Promoter Regions (Genetics)
Recombinant Fusion Proteins
Transcription Factors
Transcription, Genetic
Animalia
Bacteria (microorganisms)
Brucella
Brucella melitensis biovar Abortus
Negibacteria
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_0950382X_v54_n3_p808_Sieira

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oai_identifier_str paperaa:paper_0950382X_v54_n3_p808_Sieira
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operonSieira, R.Comerci, D.J.Pietrasanta, L.I.Ugalde, R.A.beta galactosidasecurved DNAdeoxyribonuclease Iintegration host factorVirB proteinanimal cellarticlebacterial strainbacterial virulencebacterium mutantbinding siteBrucella abortuscell vacuoleconsensus sequenceendoplasmic reticulumgene overexpressiongene replicationgenetic transcriptionmacrophagemousenonhumanoperonpathogenicitypriority journalpromoter regionprotein bindingprotein protein interactionregulatory sequencetranscription initiation sitetranscription regulationAnimalsBacterial ProteinsBase SequenceBinding SitesBrucella abortusCell LineGene Expression Regulation, BacterialGenes, ReporterIntegration Host FactorsMacrophagesMiceOperonPromoter Regions (Genetics)Recombinant Fusion ProteinsTranscription FactorsTranscription, GeneticAnimaliaBacteria (microorganisms)BrucellaBrucella melitensis biovar AbortusNegibacteriaType IV secretion systems (T4SSs) are multicomponent machineries that play an essential role in pathogenicity of many facultative intracellular bacteria. The virB operon of Brucella abortus codes for a T4SS essential for virulence and intracellular multiplication. Here, virB expression analyses carried out using lacZ transcriptional fusions showed that virB promoter (PvirB) is temporally activated within J774 cells. Primer extension experiments revealed that virB transcription starts at 27 bp upstream of the first gene of the virB operon. Structural analyses showed that PvirB and regulatory sequences involved in intracellular regulation span 430 bp upstream of the transcription start site. A protein able to bind PvirB was isolated and identified. This protein, homologue to integration host factor (IHF), specifically interacts with PvirB and induces a DNA bending with an angle of 50.36°. DNAse I footprinting experiments showed that IHF protects a 51 bp region that contains two overlapped IHF binding consensus motifs. VirB expression experiments carried out with PvirB-lacZ fusions showed that in B. abortus IHF participates in the regulation of PvirB activity during the intracellular and vegetative growth in different media. A mutant strain with a 20 bp IHF binding site replacement failed to turn on the virB operon during the initial stages of macrophage infection and displayed severe intracellular multiplication defects. These data indicate that IHF plays a key role during intracellular virB operon expression being required for the biogenesis of the endoplasmic reticulum-derived replicative vacuole.Fil:Ugalde, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2004info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_0950382X_v54_n3_p808_SieiraMol. Microbiol. 2004;54(3):808-822reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-04T09:48:38Zpaperaa:paper_0950382X_v54_n3_p808_SieiraInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-04 09:48:39.449Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
title Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
spellingShingle Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
Sieira, R.
beta galactosidase
curved DNA
deoxyribonuclease I
integration host factor
VirB protein
animal cell
article
bacterial strain
bacterial virulence
bacterium mutant
binding site
Brucella abortus
cell vacuole
consensus sequence
endoplasmic reticulum
gene overexpression
gene replication
genetic transcription
macrophage
mouse
nonhuman
operon
pathogenicity
priority journal
promoter region
protein binding
protein protein interaction
regulatory sequence
transcription initiation site
transcription regulation
Animals
Bacterial Proteins
Base Sequence
Binding Sites
Brucella abortus
Cell Line
Gene Expression Regulation, Bacterial
Genes, Reporter
Integration Host Factors
Macrophages
Mice
Operon
Promoter Regions (Genetics)
Recombinant Fusion Proteins
Transcription Factors
Transcription, Genetic
Animalia
Bacteria (microorganisms)
Brucella
Brucella melitensis biovar Abortus
Negibacteria
title_short Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
title_full Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
title_fullStr Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
title_full_unstemmed Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
title_sort Integration host factor is involved in transcriptional regulation of the Brucella abortus virB operon
dc.creator.none.fl_str_mv Sieira, R.
Comerci, D.J.
Pietrasanta, L.I.
Ugalde, R.A.
author Sieira, R.
author_facet Sieira, R.
Comerci, D.J.
Pietrasanta, L.I.
Ugalde, R.A.
author_role author
author2 Comerci, D.J.
Pietrasanta, L.I.
Ugalde, R.A.
author2_role author
author
author
dc.subject.none.fl_str_mv beta galactosidase
curved DNA
deoxyribonuclease I
integration host factor
VirB protein
animal cell
article
bacterial strain
bacterial virulence
bacterium mutant
binding site
Brucella abortus
cell vacuole
consensus sequence
endoplasmic reticulum
gene overexpression
gene replication
genetic transcription
macrophage
mouse
nonhuman
operon
pathogenicity
priority journal
promoter region
protein binding
protein protein interaction
regulatory sequence
transcription initiation site
transcription regulation
Animals
Bacterial Proteins
Base Sequence
Binding Sites
Brucella abortus
Cell Line
Gene Expression Regulation, Bacterial
Genes, Reporter
Integration Host Factors
Macrophages
Mice
Operon
Promoter Regions (Genetics)
Recombinant Fusion Proteins
Transcription Factors
Transcription, Genetic
Animalia
Bacteria (microorganisms)
Brucella
Brucella melitensis biovar Abortus
Negibacteria
topic beta galactosidase
curved DNA
deoxyribonuclease I
integration host factor
VirB protein
animal cell
article
bacterial strain
bacterial virulence
bacterium mutant
binding site
Brucella abortus
cell vacuole
consensus sequence
endoplasmic reticulum
gene overexpression
gene replication
genetic transcription
macrophage
mouse
nonhuman
operon
pathogenicity
priority journal
promoter region
protein binding
protein protein interaction
regulatory sequence
transcription initiation site
transcription regulation
Animals
Bacterial Proteins
Base Sequence
Binding Sites
Brucella abortus
Cell Line
Gene Expression Regulation, Bacterial
Genes, Reporter
Integration Host Factors
Macrophages
Mice
Operon
Promoter Regions (Genetics)
Recombinant Fusion Proteins
Transcription Factors
Transcription, Genetic
Animalia
Bacteria (microorganisms)
Brucella
Brucella melitensis biovar Abortus
Negibacteria
dc.description.none.fl_txt_mv Type IV secretion systems (T4SSs) are multicomponent machineries that play an essential role in pathogenicity of many facultative intracellular bacteria. The virB operon of Brucella abortus codes for a T4SS essential for virulence and intracellular multiplication. Here, virB expression analyses carried out using lacZ transcriptional fusions showed that virB promoter (PvirB) is temporally activated within J774 cells. Primer extension experiments revealed that virB transcription starts at 27 bp upstream of the first gene of the virB operon. Structural analyses showed that PvirB and regulatory sequences involved in intracellular regulation span 430 bp upstream of the transcription start site. A protein able to bind PvirB was isolated and identified. This protein, homologue to integration host factor (IHF), specifically interacts with PvirB and induces a DNA bending with an angle of 50.36°. DNAse I footprinting experiments showed that IHF protects a 51 bp region that contains two overlapped IHF binding consensus motifs. VirB expression experiments carried out with PvirB-lacZ fusions showed that in B. abortus IHF participates in the regulation of PvirB activity during the intracellular and vegetative growth in different media. A mutant strain with a 20 bp IHF binding site replacement failed to turn on the virB operon during the initial stages of macrophage infection and displayed severe intracellular multiplication defects. These data indicate that IHF plays a key role during intracellular virB operon expression being required for the biogenesis of the endoplasmic reticulum-derived replicative vacuole.
Fil:Ugalde, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description Type IV secretion systems (T4SSs) are multicomponent machineries that play an essential role in pathogenicity of many facultative intracellular bacteria. The virB operon of Brucella abortus codes for a T4SS essential for virulence and intracellular multiplication. Here, virB expression analyses carried out using lacZ transcriptional fusions showed that virB promoter (PvirB) is temporally activated within J774 cells. Primer extension experiments revealed that virB transcription starts at 27 bp upstream of the first gene of the virB operon. Structural analyses showed that PvirB and regulatory sequences involved in intracellular regulation span 430 bp upstream of the transcription start site. A protein able to bind PvirB was isolated and identified. This protein, homologue to integration host factor (IHF), specifically interacts with PvirB and induces a DNA bending with an angle of 50.36°. DNAse I footprinting experiments showed that IHF protects a 51 bp region that contains two overlapped IHF binding consensus motifs. VirB expression experiments carried out with PvirB-lacZ fusions showed that in B. abortus IHF participates in the regulation of PvirB activity during the intracellular and vegetative growth in different media. A mutant strain with a 20 bp IHF binding site replacement failed to turn on the virB operon during the initial stages of macrophage infection and displayed severe intracellular multiplication defects. These data indicate that IHF plays a key role during intracellular virB operon expression being required for the biogenesis of the endoplasmic reticulum-derived replicative vacuole.
publishDate 2004
dc.date.none.fl_str_mv 2004
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_0950382X_v54_n3_p808_Sieira
url http://hdl.handle.net/20.500.12110/paper_0950382X_v54_n3_p808_Sieira
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Mol. Microbiol. 2004;54(3):808-822
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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