Gene_locus Report for: xanax-XAC2541

ESTHER: Moreira_2010_BMC.Genomics_11_238
PubMedSearch: Moreira 2010 BMC.Genomics 11 238
PubMedID: 20388224
Gene_locus related to this paper: xanax-CATD, xanax-ENTF2, xanax-estA1, xanax-GAA, xanax-PTRB, xanax-XAC0198, xanax-XAC0515, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC1213, xanax-XAC1713, xanax-XAC1752, xanax-XAC2393, xanax-XAC2532, xanax-XAC2541, xanax-XAC2987, xanax-XAC3315, xanax-XAC3371, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XYNB, xanc5-q3bqi2, xanca-impep, xanca-XCC1105, xanca-XCC2566, xanca-XCC2722, xanor-acvB, xanor-metx, 9xant-a0a0g8v5k2

Abstract

BACKGROUND: Citrus canker is a disease that has severe economic impact on the citrus industry worldwide. There are three types of canker, called A, B, and C. The three types have different phenotypes and affect different citrus species. The causative agent for type A is Xanthomonas citri subsp. citri, whose genome sequence was made available in 2002. Xanthomonas fuscans subsp. aurantifolii strain B causes canker B and Xanthomonas fuscans subsp. aurantifolii strain C causes canker C.
RESULTS: We have sequenced the genomes of strains B and C to draft status. We have compared their genomic content to X. citri subsp. citri and to other Xanthomonas genomes, with special emphasis on type III secreted effector repertoires. In addition to pthA, already known to be present in all three citrus canker strains, two additional effector genes, xopE3 and xopAI, are also present in all three strains and are both located on the same putative genomic island. These two effector genes, along with one other effector-like gene in the same region, are thus good candidates for being pathogenicity factors on citrus. Numerous gene content differences also exist between the three cankers strains, which can be correlated with their different virulence and host range. Particular attention was placed on the analysis of genes involved in biofilm formation and quorum sensing, type IV secretion, flagellum synthesis and motility, lipopolysacharide synthesis, and on the gene xacPNP, which codes for a natriuretic protein. CONCLUSION: We have uncovered numerous commonalities and differences in gene content between the genomes of the pathogenic agents causing citrus canker A, B, and C and other Xanthomonas genomes. Molecular genetics can now be employed to determine the role of these genes in plant-microbe interactions. The gained knowledge will be instrumental for improving citrus canker control.

ESTHER: Thieme_2005_J.Bacteriol_187_7254
PubMedSearch: Thieme 2005 J.Bacteriol 187 7254
PubMedID: 16237009
Gene_locus related to this paper: xanac-q8pmm6, xanax-ACVB, xanax-BIOH, xanax-CATD, xanax-CPO, xanax-DHAA, xanax-ENTF2, xanax-GAA, xanax-META, xanax-METX, xanax-PCAD, xanax-PHBC, xanax-PTRB, xanax-Q8PMQ8, xanax-XAC0198, xanax-XAC0262, xanax-XAC0319, xanax-XAC0372, xanax-XAC0375, xanax-XAC0515, xanax-XAC0574, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC0874, xanax-XAC1200, xanax-XAC1213, xanax-XAC1713, xanax-XAC2532, xanax-XAC2541, xanax-XAC2907, xanax-XAC2981, xanax-XAC2990, xanax-XAC3037, xanax-XAC3053, xanax-XAC3152, xanax-XAC3770, xanax-XAC3999, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XAC4221, xanax-XAC4316, xanax-XYNB, xanc5-q3bqi2, xanc5-q3bst4, xanc5-q3btn4, xanc5-q3bup9, xanc5-q3byx0, xanca-estA1, xanca-impep, xanca-XCC1105, xanca-XCC2285, xanca-XCC2566, xanca-XCC2722, xanca-XCC3164, xanca-XCC3555, xanor-q5h3e8

Abstract

The gram-negative plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria is the causative agent of bacterial spot disease in pepper and tomato plants, which leads to economically important yield losses. This pathosystem has become a well-established model for studying bacterial infection strategies. Here, we present the whole-genome sequence of the pepper-pathogenic Xanthomonas campestris pv. vesicatoria strain 85-10, which comprises a 5.17-Mb circular chromosome and four plasmids. The genome has a high G+C content (64.75%) and signatures of extensive genome plasticity. Whole-genome comparisons revealed a gene order similar to both Xanthomonas axonopodis pv. citri and Xanthomonas campestris pv. campestris and a structure completely different from Xanthomonas oryzae pv. oryzae. A total of 548 coding sequences (12.2%) are unique to X. campestris pv. vesicatoria. In addition to a type III secretion system, which is essential for pathogenicity, the genome of strain 85-10 encodes all other types of protein secretion systems described so far in gram-negative bacteria. Remarkably, one of the putative type IV secretion systems encoded on the largest plasmid is similar to the Icm/Dot systems of the human pathogens Legionella pneumophila and Coxiella burnetii. Comparisons with other completely sequenced plant pathogens predicted six novel type III effector proteins and several other virulence factors, including adhesins, cell wall-degrading enzymes, and extracellular polysaccharides.

ESTHER: da Silva_2002_Nature_417_459
PubMedSearch: da Silva 2002 Nature 417 459
PubMedID: 12024217
Gene_locus related to this paper: xanac-q8phx9, xanac-q8pmm6, xanax-ACVB, xanax-BIOH, xanax-CATD, xanax-CPO, xanax-DHAA, xancp-OleB, xanax-ENTF2, xanax-estA1, xanax-GAA, xanax-META, xanax-METX, xanax-PCAD, xanax-PHBC, xanax-PTRB, xanax-Q8PMQ8, xanax-Q8PQP0, xanax-XAC0198, xanax-XAC0262, xanax-XAC0279, xanax-XAC0319, xanax-XAC0372, xanax-XAC0375, xanax-XAC0501, xanax-XAC0515, xanax-XAC0574, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC0874, xanax-XAC0916, xanax-XAC1200, xanax-XAC1213, xanax-XAC1591, xanax-XAC1713, xanax-XAC1752, xanax-XAC2126, xanax-XAC2393, xanax-XAC2532, xanax-XAC2541, xanax-XAC2907, xanax-XAC2981, xanax-XAC2987, xanax-XAC2990, xanax-XAC3037, xanax-XAC3053, xanax-XAC3152, xanax-XAC3173, xanax-XAC3315, xanax-XAC3371, xanax-XAC3619, xanax-XAC3674, xanax-XAC3770, xanax-XAC3967, xanax-XAC3999, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XAC4221, xanax-XAC4316, xanax-XYNB, xanca-acvB, xanca-BIOH, xanca-CATD, xanca-CPO, xanca-estA1, xanca-impep, xanca-META, xanca-METX, xanca-PCAD, xanca-PHBC, xanca-Q8PB04, xanca-W78, xanca-XCC0080, xanca-XCC0180, xanca-XCC0243, xanca-XCC0260, xanca-XCC0266, xanca-XCC0372, xanca-XCC0375, xanca-XCC0753, xanca-XCC0757, xanca-XCC0800, xanca-XCC0843, xanca-XCC1105, xanca-XCC1541, xanca-XCC1734, xanca-XCC2285, xanca-XCC2374, xanca-XCC2397, xanca-XCC2405, xanca-XCC2566, xanca-XCC2722, xanca-XCC2737, xanca-XCC2811, xanca-XCC2817, xanca-XCC2854, xanca-XCC2869, xanca-XCC2957, xanca-XCC3028, xanca-XCC3164, xanca-XCC3219, xanca-XCC3296, xanca-XCC3300, xanca-XCC3308, xanca-XCC3320, xanca-XCC3514, xanca-XCC3548, xanca-XCC3555, xanca-XCC3623, xanca-XCC3885, xanca-XCC3915, xanca-XCC3961, xanca-XCC3970, xanca-XCC4016, xanca-XCC4096, xanca-XCC4180, xanca-XYNB, xanca-XYNB2, xancb-b0rq23, xancp-q8pax3, xancp-y2094

Abstract

The genus Xanthomonas is a diverse and economically important group of bacterial phytopathogens, belonging to the gamma-subdivision of the Proteobacteria. Xanthomonas axonopodis pv. citri (Xac) causes citrus canker, which affects most commercial citrus cultivars, resulting in significant losses worldwide. Symptoms include canker lesions, leading to abscission of fruit and leaves and general tree decline. Xanthomonas campestris pv. campestris (Xcc) causes black rot, which affects crucifers such as Brassica and Arabidopsis. Symptoms include marginal leaf chlorosis and darkening of vascular tissue, accompanied by extensive wilting and necrosis. Xanthomonas campestris pv. campestris is grown commercially to produce the exopolysaccharide xanthan gum, which is used as a viscosifying and stabilizing agent in many industries. Here we report and compare the complete genome sequences of Xac and Xcc. Their distinct disease phenotypes and host ranges belie a high degree of similarity at the genomic level. More than 80% of genes are shared, and gene order is conserved along most of their respective chromosomes. We identified several groups of strain-specific genes, and on the basis of these groups we propose mechanisms that may explain the differing host specificities and pathogenic processes.

ESTHER: Potnis_2011_BMC.Genomics_12_146
PubMedSearch: Potnis 2011 BMC.Genomics 12 146
PubMedID: 21396108
Gene_locus related to this paper: 9xant-f0bam8, 9xant-f0bb73, 9xant-f0bea2, 9xant-f0bfp7, 9xant-f0c1j5, 9xant-f0c9f8, 9xant-f0c729, xanax-CATD, xanax-CPO, xanax-ENTF2, xanax-estA1, xanax-GAA, xanax-PTRB, xanax-XAC0198, xanax-XAC0262, xanax-XAC0515, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC1213, xanax-XAC1713, xanax-XAC2532, xanax-XAC2541, xanax-XAC2987, xanax-XAC2990, xanax-XAC3315, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XAC4316, xanc5-q3bqi2, xanca-impep, xanca-XCC0266, xanca-XCC1105, xanca-XCC2566, xanca-XCC2722, xanca-XCC3296, xanca-XCC3961, xanor-acvB, xanor-metx, 9xant-f0bgj0, 9xant-f0cdj1, 9xant-a0a0g8v5k2, 9xant-f0cdg7

Abstract

BACKGROUND: Bacterial spot of tomato and pepper is caused by four Xanthomonas species and is a major plant disease in warm humid climates. The four species are distinct from each other based on physiological and molecular characteristics. The genome sequence of strain 85-10, a member of one of the species, Xanthomonas euvesicatoria (Xcv) has been previously reported. To determine the relationship of the four species at the genome level and to investigate the molecular basis of their virulence and differing host ranges, draft genomic sequences of members of the other three species were determined and compared to strain 85-10.
RESULTS: We sequenced the genomes of X. vesicatoria (Xv) strain 1111 (ATCC 35937), X. perforans (Xp) strain 91-118 and X. gardneri (Xg) strain 101 (ATCC 19865). The genomes were compared with each other and with the previously sequenced Xcv strain 85-10. In addition, the molecular features were predicted that may be required for pathogenicity including the type III secretion apparatus, type III effectors, other secretion systems, quorum sensing systems, adhesins, extracellular polysaccharide, and lipopolysaccharide determinants. Several novel type III effectors from Xg strain 101 and Xv strain 1111 genomes were computationally identified and their translocation was validated using a reporter gene assay. A homolog to Ax21, the elicitor of XA21-mediated resistance in rice, and a functional Ax21 sulfation system were identified in Xcv. Genes encoding proteins with functions mediated by type II and type IV secretion systems have also been compared, including enzymes involved in cell wall deconstruction, as contributors to pathogenicity.
CONCLUSIONS: Comparative genomic analyses revealed considerable diversity among bacterial spot pathogens, providing new insights into differences and similarities that may explain the diverse nature of these strains. Genes specific to pepper pathogens, such as the O-antigen of the lipopolysaccharide cluster, and genes unique to individual strains, such as novel type III effectors and bacteriocin genes, have been identified providing new clues for our understanding of pathogen virulence, aggressiveness, and host preference. These analyses will aid in efforts towards breeding for broad and durable resistance in economically important tomato and pepper cultivars.

ESTHER: Moreira_2010_BMC.Genomics_11_238
PubMedSearch: Moreira 2010 BMC.Genomics 11 238
PubMedID: 20388224
Gene_locus related to this paper: xanax-CATD, xanax-ENTF2, xanax-estA1, xanax-GAA, xanax-PTRB, xanax-XAC0198, xanax-XAC0515, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC1213, xanax-XAC1713, xanax-XAC1752, xanax-XAC2393, xanax-XAC2532, xanax-XAC2541, xanax-XAC2987, xanax-XAC3315, xanax-XAC3371, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XYNB, xanc5-q3bqi2, xanca-impep, xanca-XCC1105, xanca-XCC2566, xanca-XCC2722, xanor-acvB, xanor-metx, 9xant-a0a0g8v5k2

Abstract

BACKGROUND: Citrus canker is a disease that has severe economic impact on the citrus industry worldwide. There are three types of canker, called A, B, and C. The three types have different phenotypes and affect different citrus species. The causative agent for type A is Xanthomonas citri subsp. citri, whose genome sequence was made available in 2002. Xanthomonas fuscans subsp. aurantifolii strain B causes canker B and Xanthomonas fuscans subsp. aurantifolii strain C causes canker C.
RESULTS: We have sequenced the genomes of strains B and C to draft status. We have compared their genomic content to X. citri subsp. citri and to other Xanthomonas genomes, with special emphasis on type III secreted effector repertoires. In addition to pthA, already known to be present in all three citrus canker strains, two additional effector genes, xopE3 and xopAI, are also present in all three strains and are both located on the same putative genomic island. These two effector genes, along with one other effector-like gene in the same region, are thus good candidates for being pathogenicity factors on citrus. Numerous gene content differences also exist between the three cankers strains, which can be correlated with their different virulence and host range. Particular attention was placed on the analysis of genes involved in biofilm formation and quorum sensing, type IV secretion, flagellum synthesis and motility, lipopolysacharide synthesis, and on the gene xacPNP, which codes for a natriuretic protein. CONCLUSION: We have uncovered numerous commonalities and differences in gene content between the genomes of the pathogenic agents causing citrus canker A, B, and C and other Xanthomonas genomes. Molecular genetics can now be employed to determine the role of these genes in plant-microbe interactions. The gained knowledge will be instrumental for improving citrus canker control.

ESTHER: Thieme_2005_J.Bacteriol_187_7254
PubMedSearch: Thieme 2005 J.Bacteriol 187 7254
PubMedID: 16237009
Gene_locus related to this paper: xanac-q8pmm6, xanax-ACVB, xanax-BIOH, xanax-CATD, xanax-CPO, xanax-DHAA, xanax-ENTF2, xanax-GAA, xanax-META, xanax-METX, xanax-PCAD, xanax-PHBC, xanax-PTRB, xanax-Q8PMQ8, xanax-XAC0198, xanax-XAC0262, xanax-XAC0319, xanax-XAC0372, xanax-XAC0375, xanax-XAC0515, xanax-XAC0574, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC0874, xanax-XAC1200, xanax-XAC1213, xanax-XAC1713, xanax-XAC2532, xanax-XAC2541, xanax-XAC2907, xanax-XAC2981, xanax-XAC2990, xanax-XAC3037, xanax-XAC3053, xanax-XAC3152, xanax-XAC3770, xanax-XAC3999, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XAC4221, xanax-XAC4316, xanax-XYNB, xanc5-q3bqi2, xanc5-q3bst4, xanc5-q3btn4, xanc5-q3bup9, xanc5-q3byx0, xanca-estA1, xanca-impep, xanca-XCC1105, xanca-XCC2285, xanca-XCC2566, xanca-XCC2722, xanca-XCC3164, xanca-XCC3555, xanor-q5h3e8

Abstract

The gram-negative plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria is the causative agent of bacterial spot disease in pepper and tomato plants, which leads to economically important yield losses. This pathosystem has become a well-established model for studying bacterial infection strategies. Here, we present the whole-genome sequence of the pepper-pathogenic Xanthomonas campestris pv. vesicatoria strain 85-10, which comprises a 5.17-Mb circular chromosome and four plasmids. The genome has a high G+C content (64.75%) and signatures of extensive genome plasticity. Whole-genome comparisons revealed a gene order similar to both Xanthomonas axonopodis pv. citri and Xanthomonas campestris pv. campestris and a structure completely different from Xanthomonas oryzae pv. oryzae. A total of 548 coding sequences (12.2%) are unique to X. campestris pv. vesicatoria. In addition to a type III secretion system, which is essential for pathogenicity, the genome of strain 85-10 encodes all other types of protein secretion systems described so far in gram-negative bacteria. Remarkably, one of the putative type IV secretion systems encoded on the largest plasmid is similar to the Icm/Dot systems of the human pathogens Legionella pneumophila and Coxiella burnetii. Comparisons with other completely sequenced plant pathogens predicted six novel type III effector proteins and several other virulence factors, including adhesins, cell wall-degrading enzymes, and extracellular polysaccharides.

ESTHER: da Silva_2002_Nature_417_459
PubMedSearch: da Silva 2002 Nature 417 459
PubMedID: 12024217
Gene_locus related to this paper: xanac-q8phx9, xanac-q8pmm6, xanax-ACVB, xanax-BIOH, xanax-CATD, xanax-CPO, xanax-DHAA, xancp-OleB, xanax-ENTF2, xanax-estA1, xanax-GAA, xanax-META, xanax-METX, xanax-PCAD, xanax-PHBC, xanax-PTRB, xanax-Q8PMQ8, xanax-Q8PQP0, xanax-XAC0198, xanax-XAC0262, xanax-XAC0279, xanax-XAC0319, xanax-XAC0372, xanax-XAC0375, xanax-XAC0501, xanax-XAC0515, xanax-XAC0574, xanax-XAC0591, xanax-XAC0619, xanax-XAC0628, xanax-XAC0736, xanax-XAC0753, xanax-XAC0805, xanax-XAC0874, xanax-XAC0916, xanax-XAC1200, xanax-XAC1213, xanax-XAC1591, xanax-XAC1713, xanax-XAC1752, xanax-XAC2126, xanax-XAC2393, xanax-XAC2532, xanax-XAC2541, xanax-XAC2907, xanax-XAC2981, xanax-XAC2987, xanax-XAC2990, xanax-XAC3037, xanax-XAC3053, xanax-XAC3152, xanax-XAC3173, xanax-XAC3315, xanax-XAC3371, xanax-XAC3619, xanax-XAC3674, xanax-XAC3770, xanax-XAC3967, xanax-XAC3999, xanax-XAC4046, xanax-XAC4055, xanax-XAC4106, xanax-XAC4221, xanax-XAC4316, xanax-XYNB, xanca-acvB, xanca-BIOH, xanca-CATD, xanca-CPO, xanca-estA1, xanca-impep, xanca-META, xanca-METX, xanca-PCAD, xanca-PHBC, xanca-Q8PB04, xanca-W78, xanca-XCC0080, xanca-XCC0180, xanca-XCC0243, xanca-XCC0260, xanca-XCC0266, xanca-XCC0372, xanca-XCC0375, xanca-XCC0753, xanca-XCC0757, xanca-XCC0800, xanca-XCC0843, xanca-XCC1105, xanca-XCC1541, xanca-XCC1734, xanca-XCC2285, xanca-XCC2374, xanca-XCC2397, xanca-XCC2405, xanca-XCC2566, xanca-XCC2722, xanca-XCC2737, xanca-XCC2811, xanca-XCC2817, xanca-XCC2854, xanca-XCC2869, xanca-XCC2957, xanca-XCC3028, xanca-XCC3164, xanca-XCC3219, xanca-XCC3296, xanca-XCC3300, xanca-XCC3308, xanca-XCC3320, xanca-XCC3514, xanca-XCC3548, xanca-XCC3555, xanca-XCC3623, xanca-XCC3885, xanca-XCC3915, xanca-XCC3961, xanca-XCC3970, xanca-XCC4016, xanca-XCC4096, xanca-XCC4180, xanca-XYNB, xanca-XYNB2, xancb-b0rq23, xancp-q8pax3, xancp-y2094

Abstract

The genus Xanthomonas is a diverse and economically important group of bacterial phytopathogens, belonging to the gamma-subdivision of the Proteobacteria. Xanthomonas axonopodis pv. citri (Xac) causes citrus canker, which affects most commercial citrus cultivars, resulting in significant losses worldwide. Symptoms include canker lesions, leading to abscission of fruit and leaves and general tree decline. Xanthomonas campestris pv. campestris (Xcc) causes black rot, which affects crucifers such as Brassica and Arabidopsis. Symptoms include marginal leaf chlorosis and darkening of vascular tissue, accompanied by extensive wilting and necrosis. Xanthomonas campestris pv. campestris is grown commercially to produce the exopolysaccharide xanthan gum, which is used as a viscosifying and stabilizing agent in many industries. Here we report and compare the complete genome sequences of Xac and Xcc. Their distinct disease phenotypes and host ranges belie a high degree of similarity at the genomic level. More than 80% of genes are shared, and gene order is conserved along most of their respective chromosomes. We identified several groups of strain-specific genes, and on the basis of these groups we propose mechanisms that may explain the differing host specificities and pathogenic processes.