Molecular cloning of the ViaB region of Salmonella typhi

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Complete nucleotide sequence and molecular characterization of ViaB region encoding Vi antigen in Salmonella typhi.

Plasmid pGBM124, which contains a 14-kb Salmonella typhi chromosomal DNA fragment capable of producing the Vi antigen in Escherichia coli HB101 and ViaB-deleted S. typhi GIFU 10007-3, was studied. We determined the complete nucleotide sequence of this fragment and found 11 open reading frames. Mutagenesis, subcloning, and complementation analysis showed that three genes (vipA, vipB, and vipC) a...

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The Vi antigen of Salmonella typhi: molecular analysis of the viaB locus.

Strains of Salmonella typhi isolated from the blood of patients with typhoid fever invariably express a capsular polysaccharide, termed the Vi antigen. Vi antigen expression is controlled by two separate chromosomal loci, viaA and viaB. The viaA locus is commonly found in enteric bacteria. In contrast, the viaB locus appears to be specific to Vi-expressing strains of Salmonella and Citrobacter....

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Molecular Characterization of the viaB Locus Encoding the Biosynthetic Machinery for Vi Capsule Formation in Salmonella Typhi

The Vi capsular polysaccharide (CPS) of Salmonella enterica serovar Typhi, the cause of human typhoid, is important for infectivity and virulence. The Vi biosynthetic machinery is encoded within the viaB locus composed of 10 genes involved in regulation of expression (tviA), polymer synthesis (tviB-tviE), and cell surface localization of the CPS (vexA-vexE). We cloned the viaB locus from S. Typ...

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By using nested PCR based on the nucleotide sequence encoding the Vi antigen, the ViaB region of Salmonella typhi, it has been possible to detect Salmonella typhi at the single-cell level. Amplification with two primer sets, R1, which amplified 599 bp of DNA (nucleotides 745 to 1343), and R2, which amplified 307 bp (nucleotides 877 to 1183), was associated with highly specific results for S. ty...

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ژورنال

عنوان ژورنال: FEMS Microbiology Letters

سال: 1991

ISSN: 0378-1097

DOI: 10.1016/0378-1097(91)90645-q