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1.
J Bacteriol ; 198(19): 2643-50, 2016 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-27068594

RESUMEN

UNLABELLED: Members of the genus Burkholderia are known to be adept at biofilm formation, which presumably assists in the survival of these organisms in the environment and the host. Biofilm formation has been linked to quorum sensing (QS) in several bacterial species. In this study, we characterized Burkholderia thailandensis biofilm development under flow conditions and sought to determine whether QS contributes to this process. B. thailandensis biofilm formation exhibited an unusual pattern: the cells formed small aggregates and then proceeded to produce mature biofilms characterized by "dome" structures filled with biofilm matrix material. We showed that this process was dependent on QS. B. thailandensis has three acyl-homoserine lactone (AHL) QS systems (QS-1, QS-2, and QS-3). An AHL-negative strain produced biofilms consisting of cell aggregates but lacking the matrix-filled dome structures. This phenotype was rescued via exogenous addition of the three AHL signals. Of the three B. thailandensis QS systems, we show that QS-1 is required for proper biofilm development, since a btaR1 mutant, which is defective in QS-1 regulation, forms biofilms without these dome structures. Furthermore, our data show that the wild-type biofilm biomass, as well as the material inside the domes, stains with a fucose-binding lectin. The btaR1 mutant biofilms, however, are negative for fucose staining. This suggests that the QS-1 system regulates the production of a fucose-containing exopolysaccharide in wild-type biofilms. Finally, we present data showing that QS ability during biofilm development produces a biofilm that is resistant to dispersion under stress conditions. IMPORTANCE: The saprophyte Burkholderia thailandensis is a close relative of the pathogenic bacterium Burkholderia pseudomallei, the causative agent of melioidosis, which is contracted from its environmental reservoir. Since most bacteria in the environment reside in biofilms, B. thailandensis is an ideal model organism for investigating questions in Burkholderia physiology. In this study, we characterized B. thailandensis biofilm development and sought to determine if quorum sensing (QS) contributes to this process. Our work shows that B. thailandensis produces biofilms with unusual dome structures under flow conditions. Our findings suggest that these dome structures are filled with a QS-regulated, fucose-containing exopolysaccharide that may be involved in the resilience of B. thailandensis biofilms against changes in the nutritional environment.


Asunto(s)
Biopelículas/crecimiento & desarrollo , Burkholderia/fisiología , Percepción de Quorum/fisiología , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Fucosa/química , Regulación Bacteriana de la Expresión Génica/fisiología , Polisacáridos Bacterianos/química
2.
Proc Natl Acad Sci U S A ; 109(48): 19775-80, 2012 Nov 27.
Artículo en Inglés | MEDLINE | ID: mdl-23150539

RESUMEN

Acyl-homoserine lactone-mediated quorum sensing (QS) regulates diverse activities in many species of Proteobacteria. QS-controlled genes commonly code for production of secreted or excreted public goods. The acyl-homoserine lactones are synthesized by members of the LuxI signal synthase family and are detected by cognate members of the LuxR family of transcriptional regulators. QS affords a means of population density-dependent gene regulation. Control of public goods via QS provides a fitness benefit. Another potential role for QS is to anticipate overcrowding. As population density increases and stationary phase approaches, QS might induce functions important for existence in stationary phase. Here we provide evidence that in three related species of the genus Burkholderia QS allows individuals to anticipate and survive stationary-phase stress. Survival requires QS-dependent activation of cellular enzymes required for production of excreted oxalate, which serves to counteract ammonia-mediated alkaline toxicity during stationary phase. Our findings provide an example of QS serving as a means to anticipate stationary phase or life at the carrying capacity of a population by activating the expression of cytoplasmic enzymes, altering cellular metabolism, and producing a shared resource or public good, oxalate.


Asunto(s)
Burkholderia/fisiología , Percepción de Quorum , Burkholderia/genética , Regulación Bacteriana de la Expresión Génica , Genes Bacterianos , Concentración de Iones de Hidrógeno , Mutación , Oxalatos/metabolismo
3.
J Bacteriol ; 196(22): 3862-71, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25182491

RESUMEN

Burkholderia pseudomallei, Burkholderia thailandensis, and Burkholderia mallei (the Bptm group) are close relatives with very different lifestyles: B. pseudomallei is an opportunistic pathogen, B. thailandensis is a nonpathogenic saprophyte, and B. mallei is a host-restricted pathogen. The acyl-homoserine lactone quorum-sensing (QS) systems of these three species show a high level of conservation. We used transcriptome sequencing (RNA-seq) to define the quorum-sensing regulon in each species, and we performed a cross-species analysis of the QS-controlled orthologs. Our analysis revealed a core set of QS-regulated genes in all three species, as well as QS-controlled factors shared by only two species or unique to a given species. This global survey of the QS regulons of B. pseudomallei, B. thailandensis, and B. mallei serves as a platform for predicting which QS-controlled processes might be important in different bacterial niches and contribute to the pathogenesis of B. pseudomallei and B. mallei.


Asunto(s)
Burkholderia/genética , Burkholderia/fisiología , Percepción de Quorum/fisiología , Regulón/fisiología , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Burkholderia/clasificación , Burkholderia mallei/clasificación , Burkholderia mallei/genética , Burkholderia mallei/fisiología , Burkholderia pseudomallei/clasificación , Burkholderia pseudomallei/genética , Burkholderia pseudomallei/fisiología , Regulación Bacteriana de la Expresión Génica/fisiología , Especificidad de la Especie
4.
J Bacteriol ; 192(11): 2861-77, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20363936

RESUMEN

More than 200 direct CodY target genes in Staphylococcus aureus were identified by genome-wide analysis of in vitro DNA binding. This analysis, which was confirmed for some genes by DNase I footprinting assays, revealed that CodY is a direct regulator of numerous transcription units associated with amino acid biosynthesis, transport of macromolecules, and virulence. The virulence genes regulated by CodY fell into three groups. One group was dependent on the Agr system for its expression; these genes were indirectly regulated by CodY through its repression of the agr locus. A second group was regulated directly by CodY. The third group, which includes genes for alpha-toxin and capsule synthesis, was regulated by CodY in two ways, i.e., by direct repression and by repression of the agr locus. Since S. aureus CodY was activated in vitro by the branched chain amino acids and GTP, CodY appears to link changes in intracellular metabolite pools with the induction of numerous adaptive responses, including virulence.


Asunto(s)
Proteínas Bacterianas/metabolismo , Proteínas Represoras/metabolismo , Staphylococcus aureus/metabolismo , Proteínas Bacterianas/genética , Sitios de Unión/genética , Huella de ADN , Ensayo de Cambio de Movilidad Electroforética , Regulación Bacteriana de la Expresión Génica/genética , Regulación Bacteriana de la Expresión Génica/fisiología , Modelos Biológicos , Análisis de Secuencia por Matrices de Oligonucleótidos , Regiones Promotoras Genéticas/genética , Unión Proteica/genética , Regulón/genética , Proteínas Represoras/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Staphylococcus aureus/genética , Transactivadores/genética , Transactivadores/metabolismo , Virulencia/genética , Virulencia/fisiología
5.
J Bacteriol ; 190(7): 2257-65, 2008 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-18156263

RESUMEN

CodY is a global regulatory protein that was first discovered in Bacillus subtilis, where it couples gene expression to changes in the pools of critical metabolites through its activation by GTP and branched-chain amino acids. Homologs of CodY can be found encoded in the genomes of nearly all low-G+C gram-positive bacteria, including Staphylococcus aureus. The introduction of a codY-null mutation into two S. aureus clinical isolates, SA564 and UAMS-1, through allelic replacement, resulted in the overexpression of several virulence genes. The mutant strains had higher levels of hemolytic activity toward rabbit erythrocytes in their culture fluid, produced more polysaccharide intercellular adhesin (PIA), and formed more robust biofilms than did their isogenic parent strains. These phenotypes were associated with derepressed levels of RNA for the hemolytic alpha-toxin (hla), the accessory gene regulator (agr) (RNAII and RNAIII/hld), and the operon responsible for the production of PIA (icaADBC). These data suggest that CodY represses, either directly or indirectly, the synthesis of a number of virulence factors of S. aureus.


Asunto(s)
Proteínas Bacterianas/genética , Regulación Bacteriana de la Expresión Génica , Proteínas Represoras/genética , Staphylococcus aureus/genética , Animales , Proteínas Bacterianas/metabolismo , Proteínas Bacterianas/fisiología , Biopelículas/crecimiento & desarrollo , Western Blotting , Eritrocitos/microbiología , Prueba de Complementación Genética , Hemólisis , Mutación , Conejos , Proteínas Represoras/metabolismo , Proteínas Represoras/fisiología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Staphylococcus aureus/crecimiento & desarrollo , Staphylococcus aureus/patogenicidad , Transcripción Genética/genética , Virulencia/genética
6.
Methods Mol Biol ; 1673: 177-192, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29130173

RESUMEN

RNA sequencing (RNAseq) enables transcriptional profiling of many organisms. This chapter describes the use of RNAseq in prokaryotes to identify quorum sensing (QS)-controlled transcripts by comparing samples from QS-induced and -uninduced conditions. Briefly, each RNA sample is converted to ds-cDNA in a method that limits amplification of ribosomal RNA species. The ds-cDNA contains adapters that enable sequencing and quantification by next-generation sequencing (NGS).


Asunto(s)
Perfilación de la Expresión Génica/métodos , Regulación Bacteriana de la Expresión Génica , Percepción de Quorum/genética , Análisis de Secuencia de ARN/métodos , Electroforesis en Gel de Agar , Biblioteca de Genes
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