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1.
BMC Genomics ; 17: 661, 2016 08 20.
Article in English | MEDLINE | ID: mdl-27543103

ABSTRACT

BACKGROUND: Agrobacterium tumefaciens strain P4 is atypical, as the strain is not pathogenic and produces a for this species unusual quorum sensing signal, identified as N-(3-hydroxy-octanoyl)-homoserine lactone (3OH,C8-HSL). RESULTS: By sequence analysis and cloning, a functional luxI-like gene, named cinI, has been identified on the At plasmid of A. tumefaciens strain P4. Insertion mutagenesis in the cinI gene and transcriptome analyses permitted the identification of 32 cinI-regulated genes in this strain, most of them encoding proteins responsible for the conjugative transfer of pAtP4. Among these genes were the avhB genes that encode a type 4 secretion system (T4SS) involved in the formation of the conjugation apparatus, the tra genes that encode the DNA transfer and replication (Dtr) machinery and cinI and two luxR orthologs. These last two genes, cinR and cinX, exhibit an unusual organization, with the cinI gene surrounded by the two luxR orthologs. Conjugation experiments confirmed that the conjugative transfer of pAtP4 is regulated by 3OH,C8-HSL. Root colonization experiments indicated that the quorum sensing regulation of the conjugation of the pAtP4 does not confer a gain or a loss of fitness to the bacterial host in the tomato plant rhizosphere. CONCLUSION: This work is the first identification of the occurrence of a quorum sensing regulation of the pAt conjugation phenomenon in Agrobacterium.


Subject(s)
Agrobacterium tumefaciens/physiology , Gene Expression Profiling/methods , Plasmids/genetics , Quorum Sensing , Sequence Analysis, RNA/methods , Agrobacterium tumefaciens/genetics , Bacterial Proteins/genetics , Cloning, Molecular , Conjugation, Genetic , Gene Expression Regulation, Bacterial , Genetic Fitness , Solanum lycopersicum/microbiology , Phylogeny , Plant Roots/microbiology
2.
BMC Evol Biol ; 11: 67, 2011 Mar 11.
Article in English | MEDLINE | ID: mdl-21396107

ABSTRACT

BACKGROUND: Bacterial plant pathogens belonging to the Xanthomonas genus are tightly adapted to their host plants and are not known to colonise other environments. The host range of each strain is usually restricted to a few host plant species. Bacterial strains responsible for the same type of symptoms on the same host range cluster in a pathovar. The phyllosphere is a highly stressful environment, but it provides a selective habitat and a source of substrates for these bacteria. Xanthomonads colonise host phylloplane before entering leaf tissues and engaging in an invasive pathogenic phase. Hence, these bacteria are likely to have evolved strategies to adapt to life in this environment. We hypothesised that determinants responsible for bacterial host adaptation are expressed starting from the establishment of chemotactic attraction and adhesion on host tissue. RESULTS: We established the distribution of 70 genes coding sensors and adhesins in a large collection of xanthomonad strains. These 173 strains belong to different pathovars of Xanthomonas spp and display different host ranges. Candidate genes are involved in chemotactic attraction (25 genes), chemical environment sensing (35 genes), and adhesion (10 genes). Our study revealed that candidate gene repertoires comprised core and variable gene suites that likely have distinct roles in host adaptation. Most pathovars were characterized by unique repertoires of candidate genes, highlighting a correspondence between pathovar clustering and repertoires of sensors and adhesins. To further challenge our hypothesis, we tested for molecular signatures of selection on candidate genes extracted from sequenced genomes of strains belonging to different pathovars. We found strong evidence of adaptive divergence acting on most candidate genes. CONCLUSIONS: These data provide insight into the potential role played by sensors and adhesins in the adaptation of xanthomonads to their host plants. The correspondence between repertoires of sensor and adhesin genes and pathovars and the rapid evolution of sensors and adhesins shows that, for plant pathogenic xanthomonads, events leading to host specificity may occur as early as chemotactic attraction by host and adhesion to tissues.


Subject(s)
Adaptation, Physiological/genetics , Bacterial Adhesion , Chemotaxis/genetics , Xanthomonas/physiology , Adhesins, Bacterial/genetics , DNA, Bacterial/genetics , Data Mining , Genes, Bacterial , Plants/microbiology , Selection, Genetic , Sequence Alignment , Xanthomonas/genetics , Xanthomonas/pathogenicity
3.
Environ Microbiol ; 13(11): 2901-14, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21906221

ABSTRACT

Successful infection of a pathogen relies on the coordinated expression of numerous virulence factor-encoding genes. In plant-bacteria interactions, this control is very often achieved through the integration of several regulatory circuits controlling cell-cell communication or sensing environmental conditions. Dickeya dadantii (formerly Erwinia chrysanthemi), the causal agent of soft rot on many crops and ornamentals, provokes maceration of infected plants mainly by producing and secreting a battery of plant cell wall-degrading enzymes. However, several other virulence factors have also been characterized. During Arabidopsis infection, most D. dadantii virulence gene transcripts accumulated in a coordinated manner during infection. This activation requires a functional GacA-GacS two-component regulatory system but the Gac system is not involved in the growth phase dependence of virulence gene expression. Here we show that, contrary to Pectobacterium, the AHL-mediated ExpIR quorum-sensing system does not play a major role in the growth phase-dependent control of D. dadantii virulence genes. On the other hand, the global regulator PecS participates in this coordinated expression since, in a pecS mutant, an early activation of virulence genes is observed both in vitro and in planta. This correlated with the known hypervirulence phenotype of the pecS mutant. Analysis of the relationship between the regulatory circuits governed by the PecS and GacA global regulators indicates that these two regulators act independently. PecS prevents a premature expression of virulence genes in the first stages of colonization whereas GacA, presumably in conjunction with other regulators, is required for the activation of virulence genes at the onset of symptom occurrence.


Subject(s)
Bacterial Proteins/metabolism , Dickeya chrysanthemi/genetics , Genes, Regulator , Plants/microbiology , Repressor Proteins/metabolism , Bacterial Proteins/genetics , Dickeya chrysanthemi/pathogenicity , Gene Regulatory Networks , Genes, Bacterial , Mutation , Quorum Sensing , Repressor Proteins/genetics , Virulence , Virulence Factors/genetics , Virulence Factors/metabolism
4.
Adv Exp Med Biol ; 715: 71-89, 2011.
Article in English | MEDLINE | ID: mdl-21557058

ABSTRACT

The family Xanthomonadaceae is a wide-spread family of bacteria belonging to the gamma subdivision of the Gram-negative proteobacteria, including the two plant-pathogenic genera Xanthomonas and Xylella, and the related genus Stenotrophomonas. Adhesion is a widely conserved virulence mechanism among Gram-negative bacteria, no matter whether they are human, animal or plant pathogens, since attachment to the host tissue is one of the key early steps of the bacterial infection process. Bacterial attachment to surfaces is mediated by surface structures that are anchored in the bacterial outer membrane and cover a broad group of fimbrial and non-fimbrial structures, commonly known as adhesins. In this chapter, we discuss recent findings on candidate adhesins of plant-pathogenic Xanthomonadaceae, including polysaccharidic (lipopolysaccharides, exopolysaccharides) and proteineous structures (chaperone/usher pili, type IV pili, autotransporters, two-partner-secreted and other outer membrane adhesins), their involvement in the formation of biofilms and their mode of regulation via quorum sensing. We then compare the arsenals of adhesins among different Xanthomonas strains and evaluate their mode of selection. Finally, we summarize the sparse knowledge on specific adhesin receptors in plants and the possible role of RGD motifs in binding to integrin-like plant molecules.


Subject(s)
Bacterial Adhesion/physiology , Plants/microbiology , Xanthomonadaceae/physiology , Xanthomonadaceae/pathogenicity , Adhesins, Bacterial/physiology , Fimbriae, Bacterial/physiology , Gram-Negative Bacterial Infections/microbiology , Host-Pathogen Interactions/physiology , Plant Diseases/microbiology , Polysaccharides, Bacterial/physiology , Receptors, Immunologic/physiology , Virulence/physiology
5.
Sci Rep ; 9(1): 5398, 2019 04 01.
Article in English | MEDLINE | ID: mdl-30931953

ABSTRACT

The gut barrier plays an important role in human health. When barrier function is impaired, altered permeability and barrier dysfunction can occur, leading to inflammatory bowel diseases, irritable bowel syndrome or obesity. Several bacteria, including pathogens and commensals, have been found to directly or indirectly modulate intestinal barrier function. The use of probiotic strains could be an important landmark in the management of gut dysfunction with a clear impact on the general population. Previously, we found that Lactobacillus rhamnosus CNCM I-3690 can protect intestinal barrier functions in mice inflammation model. Here, we investigated its mechanism of action. Our results show that CNCM I-3690 can (i) physically maintain modulated goblet cells and the mucus layer and (ii) counteract changes in local and systemic lymphocytes. Furthermore, mice colonic transcriptome analysis revealed that CNCM I-3690 enhances the expression of genes related to healthy gut permeability: motility and absorption, cell proliferation; and protective functions by inhibiting endogenous proteases. Finally, SpaFED pili are clearly important effectors since an L. rhamnosus ΔspaF mutant failed to provide the same benefits as the wild type strain. Taken together, our data suggest that CNCM I-3690 restores impaired intestinal barrier functions via anti-inflammatory and cytoprotective responses.


Subject(s)
Intestinal Mucosa/metabolism , Intestines/drug effects , Lacticaseibacillus rhamnosus/physiology , Mucus/metabolism , Probiotics/pharmacology , Animals , Caco-2 Cells , Colon/drug effects , Colon/metabolism , Colon/pathology , Cytoprotection/drug effects , Dinitrofluorobenzene/analogs & derivatives , Gene Expression Profiling/methods , Goblet Cells/drug effects , Goblet Cells/metabolism , HEK293 Cells , HT29 Cells , Humans , Inflammation/chemically induced , Inflammation/genetics , Inflammation/metabolism , Intestines/microbiology , Intestines/physiology , Lacticaseibacillus rhamnosus/genetics , Mice , Mutation , Permeability/drug effects , Protective Agents/pharmacology
6.
PLoS One ; 8(3): e58474, 2013.
Article in English | MEDLINE | ID: mdl-23505513

ABSTRACT

Deciphering mechanisms shaping bacterial diversity should help to build tools to predict the emergence of infectious diseases. Xanthomonads are plant pathogenic bacteria found worldwide. Xanthomonas axonopodis is a genetically heterogeneous species clustering, into six groups, strains that are collectively pathogenic on a large number of plants. However, each strain displays a narrow host range. We address the question of the nature of the evolutionary processes--geographical and ecological speciation--that shaped this diversity. We assembled a large collection of X. axonopodis strains that were isolated over a long period, over continents, and from various hosts. Based on the sequence analysis of seven housekeeping genes, we found that recombination occurred as frequently as point mutation in the evolutionary history of X. axonopodis. However, the impact of recombination was about three times greater than the impact of mutation on the diversity observed in the whole dataset. We then reconstructed the clonal genealogy of the strains using coalescent and genealogy approaches and we studied the diversification of the pathogen using a model of divergence with migration. The suggested scenario involves a first step of generalist diversification that spanned over the last 25,000 years. A second step of ecology-driven specialization occurred during the past two centuries. Eventually, secondary contacts between host-specialized strains probably occurred as a result of agricultural development and intensification, allowing genetic exchanges of virulence-associated genes. These transfers may have favored the emergence of novel pathotypes. Finally, we argue that the largest ecological entity within X. axonopodis is the pathovar.


Subject(s)
Biological Evolution , Xanthomonas axonopodis/genetics , Xanthomonas axonopodis/pathogenicity , Cluster Analysis , Evolution, Molecular , Gene Flow , Genes, Bacterial , Genes, Essential , Genetic Drift , Multilocus Sequence Typing , Mutation , Mutation Rate , Phylogeny , Plant Diseases/microbiology , Recombination, Genetic , Virulence/genetics , Xanthomonas , Xanthomonas axonopodis/classification
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