scholarly article | Q13442814 |
P819 | ADS bibcode | 2009PLoSO...4.6632H |
P356 | DOI | 10.1371/JOURNAL.PONE.0006632 |
P932 | PMC publication ID | 2722093 |
P698 | PubMed publication ID | 19680562 |
P5875 | ResearchGate publication ID | 26741842 |
P50 | author | Charles Manceau | Q56860157 |
Ahmed Hajri | Q56860269 | ||
Frédéric Lardeux | Q59698429 | ||
Tristan Boureau | Q90750415 | ||
Stéphane Poussier | Q104129895 | ||
Chrystelle Brin | Q117282764 | ||
P2093 | author name string | Christophe Lemaire | |
Gilles Hunault | |||
P2860 | cites work | Evolutionary origins of genomic repertoires in bacteria | Q21146363 |
Insights into Genome Plasticity and Pathogenicity of the Plant Pathogenic Bacterium Xanthomonas campestris pv. vesicatoria Revealed by the Complete Genome Sequence | Q22065447 | ||
Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris | Q22065748 | ||
Pathogenic and Genetic Relatedness Among Xanthomonas axonopodis pv. allii and Other Pathovars of X. axonopodis. | Q49167125 | ||
Pseudomonas syringae pv. tomato DC3000 HopPtoM (CEL ORF3) is important for lesion formation but not growth in tomato and is secreted and translocated by the Hrp type III secretion system in a chaperone-dependent manner. | Q51831885 | ||
Multiple approaches to a complete inventory of Pseudomonas syringae pv. tomato DC3000 type III secretion system effector proteins. | Q52574657 | ||
Layered basal defenses underlie non-host resistance of Arabidopsis to Pseudomonas syringae pv. phaseolicola. | Q52579853 | ||
A comprehensive species to strain taxonomic framework for xanthomonas. | Q54511272 | ||
Diverse members of the AvrBs3/PthA family of type III effectors are major virulence determinants in bacterial blight disease of rice | Q57213998 | ||
The Evolutionary Origin of Xanthomonadales Genomes and the Nature of the Horizontal Gene Transfer Process | Q58039212 | ||
Molecular basis for evasion of plant host defence in bacterial spot disease of pepper | Q59065358 | ||
Non-Gamma-Proteobacteria Gene Islands Contribute to the Xanthomonas Genome | Q61268357 | ||
Pathoadaptive mutations: gene loss and variation in bacterial pathogens | Q77830302 | ||
Characterization of pathogenic and nonpathogenic strains of Xanthomonas axonopodis pv. manihotis by PCR-based DNA fingerprinting techniques | Q78409387 | ||
The type III secretion effector XopXccN of Xanthomonas campestris pv. campestris is required for full virulence | Q80722375 | ||
Mutagenesis of all eight avr genes in Xanthomonas campestris pv. campestris had no detected effect on pathogenicity, but one avr gene affected race specificity | Q82550802 | ||
A Pseudomonas syringae pv. tomato avrE1/hopM1 mutant is severely reduced in growth and lesion formation in tomato | Q82788030 | ||
Suppression of defense response in plants by the avrBs3/pthA gene family of Xanthomonas spp | Q82999721 | ||
Reduced genetic variation occurs among genes of the highly clonal plant pathogen Xanthomonas axonopodis pv. vesicatoria, including the effector gene avrBs2 | Q42186152 | ||
A functional screen for the type III (Hrp) secretome of the plant pathogen Pseudomonas syringae. | Q42671228 | ||
A race-specific insertion of transposable element IS801 in Pseudomonas syringae pv. phaseolicola | Q42677093 | ||
Characterization of ISXax1, a novel insertion sequence restricted to Xanthomonas axonopodis pv. phaseoli (variants fuscans and non-fuscans) and Xanthomonas axonopodis pv. vesicatoria. | Q42913065 | ||
Genetic Diversity and Pathogenic Variation of Common Blight Bacteria (Xanthomonas campestris pv. phaseoli and X. campestris pv. phaseoli var. fuscans) Suggests Pathogen Coevolution with the Common Bean | Q43943920 | ||
Pathological Variations Within Xanthomonas campestris pv. mangiferaeindicae Support Its Separation Into Three Distinct Pathovars that Can Be Distinguished by Amplified Fragment Length Polymorphism | Q44468061 | ||
Measuring the Genetic Diversity of Xanthomonas axonopodis pv. manihotis Within Different Fields in Colombia | Q44775930 | ||
The type III effector repertoire of Pseudomonas syringae pv. syringae B728a and its role in survival and disease on host and non-host plants. | Q44922944 | ||
HopPtoN is a Pseudomonas syringae Hrp (type III secretion system) cysteine protease effector that suppresses pathogen-induced necrosis associated with both compatible and incompatible plant interactions | Q45094178 | ||
Reclassification of Xanthomonas | Q45312520 | ||
Comparison of AFLP and rep-PCR genomic fingerprinting with DNA--DNA homology studies: Xanthomonas as a model system | Q45314468 | ||
Widespread distribution and fitness contribution of Xanthomonas campestris avirulence gene avrBs2. | Q45938707 | ||
The conserved Xanthomonas campestris pv. vesicatoria effector protein XopX is a virulence factor and suppresses host defense in Nicotiana benthamiana | Q46209108 | ||
Allelic variants of the Pseudomonas syringae type III effector HopZ1 are differentially recognized by plant resistance systems | Q46737344 | ||
Non-host resistance in plants: new insights into an old phenomenon | Q47277708 | ||
Adhesion and fitness in the bean phyllosphere and transmission to seed of Xanthomonas fuscans subsp. fuscans | Q47792160 | ||
Antagonistic action of harpin proteins: HrpWea from Erwinia amylovora suppresses HrpNea-induced cell death in Arabidopsis thaliana | Q47837832 | ||
Diversity among xanthomonads pathogenic on pepper and tomato | Q47974062 | ||
Exposure to host resistance mechanisms drives evolution of bacterial virulence in plants | Q48108253 | ||
Avoidance of host recognition by alterations in the repetitive and C-terminal regions of AvrXa7, a type III effector of Xanthomonas oryzae pv. oryzae | Q48149879 | ||
Identification of Pseudomonas syringae type III effectors that can suppress programmed cell death in plants and yeast | Q48207372 | ||
Xanthomonas citri: breaking the surface. | Q48723776 | ||
The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice | Q22065983 | ||
Comparison of the complete genome sequences of Pseudomonas syringae pv. syringae B728a and pv. tomato DC3000 | Q22066353 | ||
Comparison of the genomes of two Xanthomonas pathogens with differing host specificities | Q22122346 | ||
Integrons in Xanthomonas: a source of species genome diversity | Q24555753 | ||
Multilocus sequence typing: a portable approach to the identification of clones within populations of pathogenic microorganisms | Q24685491 | ||
MODELTEST: testing the model of DNA substitution | Q26778437 | ||
The plant immune system | Q28131801 | ||
Specific binding of the Xanthomonas campestris pv. vesicatoria AraC-type transcriptional activator HrpX to plant-inducible promoter boxes | Q29346553 | ||
The Staden package, 1998 | Q29614998 | ||
Insertion sequences | Q29617579 | ||
The type III secretion injectisome | Q29617944 | ||
How Xanthomonas type III effectors manipulate the host plant | Q30319160 | ||
XopC and XopJ, two novel type III effector proteins from Xanthomonas campestris pv. vesicatoria | Q30320542 | ||
Xv4-vrxv4: a new gene-for-gene interaction identified between Xanthomonas campestris pv. vesicatoria race T3 and wild tomato relative Lycopersicon pennellii | Q30620575 | ||
Resistance of tomato and pepper to T3 strains of Xanthomonas campestris pv. vesicatoria is specified by a plant-inducible avirulence gene | Q30919413 | ||
The avrRxo1 gene from the rice pathogen Xanthomonas oryzae pv. oryzicola confers a nonhost defense reaction on maize with resistance gene Rxo1. | Q31089859 | ||
Distribution and sequence analysis of a family of type ill-dependent effectors correlate with the phylogeny of Ralstonia solanacearum strains. | Q33205781 | ||
Genetic differences between blight-causing Erwinia species with differing host specificities, identified by suppression subtractive hybridization | Q33256962 | ||
Terminal reassortment drives the quantum evolution of type III effectors in bacterial pathogens | Q33260347 | ||
Genomic structure and phylogeny of the plant pathogen Ralstonia solanacearum inferred from gene distribution analysis. | Q33262738 | ||
Type III effector diversification via both pathoadaptation and horizontal transfer in response to a coevolutionary arms race | Q33267844 | ||
Common and specific genomic sequences of avian and human extraintestinal pathogenic Escherichia coli as determined by genomic subtractive hybridization | Q33296100 | ||
Salmonella type III effector AvrA stabilizes cell tight junctions to inhibit inflammation in intestinal epithelial cells | Q33340305 | ||
A multilocus sequence analysis of the genus Xanthomonas | Q33368516 | ||
Acquisition and evolution of plant pathogenesis-associated gene clusters and candidate determinants of tissue-specificity in xanthomonas | Q33388256 | ||
The Plant-Associated Microbe Gene Ontology (PAMGO) Consortium: community development of new Gene Ontology terms describing biological processes involved in microbe-host interactions | Q33417106 | ||
Gene Ontology annotation highlights shared and divergent pathogenic strategies of type III effector proteins deployed by the plant pathogen Pseudomonas syringae pv tomato DC3000 and animal pathogenic Escherichia coli strains | Q33417110 | ||
Deletions in the repertoire of Pseudomonas syringae pv. tomato DC3000 type III secretion effector genes reveal functional overlap among effectors | Q33432683 | ||
Extensive gene diversity in septicemic Escherichia coli strains | Q33593077 | ||
Erwinia amylovora secretes DspE, a pathogenicity factor and functional AvrE homolog, through the Hrp (type III secretion) pathway | Q33729324 | ||
Multilocus sequence typing | Q33798073 | ||
A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae | Q33850561 | ||
Changes in race-specific virulence in Pseudomonas syringae pv. phaseolicola are associated with a chimeric transposable element and rare deletion events in a plasmid-borne pathogenicity island | Q33884633 | ||
Pathogenicity islands and the evolution of microbes | Q33920183 | ||
Genes lost and genes found: evolution of bacterial pathogenesis and symbiosis | Q34250498 | ||
Multi-locus sequence typing: a tool for global epidemiology | Q34269596 | ||
Type III secretion system effector proteins: double agents in bacterial disease and plant defense | Q34337243 | ||
Specific detection of Xanthomonas axonopodis pv. dieffenbachiae in anthurium (Anthurium andreanum) tissues by nested PCR | Q34431505 | ||
Pathogen fitness penalty as a predictor of durability of disease resistance genes. | Q34433601 | ||
Diverse evolutionary mechanisms shape the type III effector virulence factor repertoire in the plant pathogen Pseudomonas syringae | Q34645388 | ||
Chemotaxis is required for virulence and competitive fitness of the bacterial wilt pathogen Ralstonia solanacearum | Q34696759 | ||
Bacterial pathogenomics | Q34702436 | ||
Pathogenomics: an updated European Research Agenda. | Q34758896 | ||
Comparative genomics of host-specific virulence in Pseudomonas syringae | Q35082974 | ||
Identification of a pathogenicity island, which contains genes for virulence and avirulence, on a large native plasmid in the bean pathogen Pseudomonas syringae pathovar phaseolicola | Q35635473 | ||
The Pseudomonas syringae Hrp pathogenicity island has a tripartite mosaic structure composed of a cluster of type III secretion genes bounded by exchangeable effector and conserved effector loci that contribute to parasitic fitness and pathogenicity | Q35699642 | ||
Cysteine proteases in phytopathogenic bacteria: identification of plant targets and activation of innate immunity | Q35825006 | ||
Characterization of Xanthomonas campestris Pathovars by rRNA Gene Restriction Patterns | Q36064479 | ||
Characterization of IS476 and its role in bacterial spot disease of tomato and pepper | Q36156199 | ||
Virulence factors of septicemic Escherichia coli strains | Q36291985 | ||
Host specificity of septicemic Escherichia coli: human and avian pathogens | Q36356385 | ||
Type III effector proteins from the plant pathogen Xanthomonas and their role in the interaction with the host plant | Q36357133 | ||
AvrAC(Xcc8004), a type III effector with a leucine-rich repeat domain from Xanthomonas campestris pathovar campestris confers avirulence in vascular tissues of Arabidopsis thaliana ecotype Col-0. | Q36422269 | ||
Comparative and functional genomics reveals genetic diversity and determinants of host specificity among reference strains and a large collection of Chinese isolates of the phytopathogen Xanthomonas campestris pv. campestris | Q36465631 | ||
Subterfuge and manipulation: type III effector proteins of phytopathogenic bacteria | Q36497116 | ||
Closing the circle on the discovery of genes encoding Hrp regulon members and type III secretion system effectors in the genomes of three model Pseudomonas syringae strains | Q36638315 | ||
Genomic insights into the contribution of phytopathogenic bacterial plasmids to the evolutionary history of their hosts | Q36762465 | ||
Evolution of microbial virulence: the benefits of stress | Q36791805 | ||
Defense suppression by virulence effectors of bacterial phytopathogens | Q36878209 | ||
Host-pathogen interplay and the evolution of bacterial effectors | Q37012231 | ||
Synopsis on the taxonomy of the genus xanthomonas. | Q37305993 | ||
A genetic screen to isolate type III effectors translocated into pepper cells during Xanthomonas infection | Q37692988 | ||
The Type III secretion system of Xanthomonas fuscans subsp. fuscans is involved in the phyllosphere colonization process and in transmission to seeds of susceptible beans. | Q38607433 | ||
Assessment of the genetic diversity of Xanthomonas axonopodis pv. phaseoli and Xanthomonas fuscans subsp. fuscans as a basis to identify putative pathogenicity genes and a type III secretion system of the SPI-1 family by multiple suppression subtrac | Q38607877 | ||
Polyphasic characterization of xanthomonads isolated from onion, garlic and Welsh onion (Allium spp.) and their relatedness to different Xanthomonas species | Q39411408 | ||
Intragenic recombination of a single plant pathogen gene provides a mechanism for the evolution of new host specificities | Q39838132 | ||
Evolution of the core genome of Pseudomonas syringae, a highly clonal, endemic plant pathogen | Q40744160 | ||
Regulation of expression of avirulence gene avrRxv and identification of a family of host interaction factors by sequence analysis of avrBsT. | Q41484075 | ||
DspA, an essential pathogenicity factor of Erwinia amylovora showing homology with AvrE of Pseudomonas syringae, is secreted via the Hrp secretion pathway in a DspB-dependent way. | Q41487148 | ||
Xanthomonas axonopodis pv. phaseoli var. fuscans is aggregated in stable biofilm population sizes in the phyllosphere of field-grown beans | Q41779844 | ||
Extraintestinal pathogenic Escherichia coli strains of avian and human origin: link between phylogenetic relationships and common virulence patterns | Q41821724 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | host tropism | Q1536273 |
P304 | page(s) | e6632 | |
P577 | publication date | 2009-08-14 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | A "repertoire for repertoire" hypothesis: repertoires of type three effectors are candidate determinants of host specificity in Xanthomonas | |
P478 | volume | 4 |
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