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
- 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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paperaa:paper_0950382X_v54_n3_p808_Sieira |
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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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1842340705312178177 |
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12.623145 |