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http://purl.uniprot.org/citations/21592381http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21592381http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21592381http://www.w3.org/2000/01/rdf-schema#comment"

Background

Some microorganisms can produce pigments such as melanin, which has been associated with virulence in the host and with a survival advantage in the environment. In Vibrio cholerae, studies have shown that pigment-producing mutants are more virulent than the parental strain in terms of increased UV resistance, production of major virulence factors, and colonization. To date, almost all of the pigmented V. cholerae strains investigated have been induced by chemicals, culture stress, or transposon mutagenesis. However, during our cholera surveillance, some nontoxigenic serogroup O139 strains and one toxigenic O1 strain, which can produce pigment steadily under the commonly used experimental growth conditions, were obtained in different years and from different areas. The genes VC1344 to VC1347, which correspond to the El Tor strain N16961 genome and which comprise an operon in the tyrosine catabolic pathway, have been confirmed to be associated with a pigmented phenotype. In the present study, we investigated the mechanism of pigment production in these strains.

Results

Sequencing of the VC1344, VC1345, VC1346, and VC1347 genes in these pigmented strains suggested that a deletion mutation in the homogentisate oxygenase gene (VC1345) may be associated with the pigmented phenotype, and gene complementation confirmed the role of this gene in pigment production. An identical 15-bp deletion was found in the VC1345 gene of all six O139 pigment-producing strains examined, and a 10-bp deletion was found in the VC1345 gene of the O1 strain. Strict sequence conservation in the VC1344 gene but higher variance in the other three genes of this operon were observed, indicating the different stress response functions of these genes in environmental adaption and selection. On the basis of pulsed-field gel electrophoresis typing, the pigment-producing O139 strains showed high clonality, even though they were isolated in different years and from different regions. Additionally all these O139 strains belong to the rb4 ribotype, which contains the O139 strains isolated from diarrheal patients, although these strains are cholera toxin negative.

Conclusion

Dysfunction of homogentisate oxygenase (VC1345) causes homogentisate accumulation and pigment formation in naturally pigmented strains of V. cholerae. The high clonality of these strains may correlate to an environmental survival advantage in the V. cholerae community due to their pigment production, and may imply a potential protective function of melanin in environmental survival of such strains."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.org/dc/terms/identifier"doi:10.1186/1471-2180-11-109"xsd:string
http://purl.uniprot.org/citations/21592381http://purl.org/dc/terms/identifier"doi:10.1186/1471-2180-11-109"xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Kan B."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Kan B."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Zhou H."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Zhou H."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang H."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang H."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang R."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Wang R."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Yue J."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Yue J."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Diao B."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/author"Diao B."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/name"BMC Microbiol."xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/name"BMC Microbiol"xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/pages"109"xsd:string
http://purl.uniprot.org/citations/21592381http://purl.uniprot.org/core/pages"109"xsd:string
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