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Volume 8, Number 4—April 2002

Dispatch

Salmonella enterica Serotype Typhimurium DT 104 Antibiotic Resistance Genomic Island I in Serotype Paratyphi B

Danièle Meunier*, David Boyd†, Michael R. Mulvey†, Sylvie Baucheron*, Caterina Mammina‡, Antonino Nastasi§, Elisabeth Chaslus-Dancla*, and Axel Cloeckaert*Comments to Author 
Author affiliations: *Institut National de la Recherche Agronomique, Nouzilly, France; †Health Canada, Winnipeg, Manitoba, Canada; ‡University of Palermo, Palermo, Italy; §University of Florence, Florence, Italy;

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Figure 1

Genetic organization of the antibiotic-resistance gene cluster of SGI1 of Salmonella enterica serotype Typhimurium DT 104. DR-L and DR-R are the left and right direct repeats, respectively, bracketing SGI1. Polymerase chain reactions (PCRs) used to assess the genetic organization of the antibiotic-resistance genes (PCRs floR, A, B, C, D, and E) and the SGI1 junctions to the chromosome (PCRs LJ and RJ for left and right junctions, respectively) are indicated. Abbreviations for restriction sites: X, XbaI; H, HindIII; Xh, XhoI.

Figure 1. Genetic organization of the antibiotic-resistance gene cluster of SGI1 of Salmonella enterica serotype Typhimurium DT 104. DR-L and DR-R are the left and right direct repeats, respectively, bracketing SGI1. Polymerase chain reactions (PCRs) used to assess the genetic organization of the antibiotic-resistance genes (PCRs floR, A, B, C, D, and E) and the SGI1 junctions to the chromosome (PCRs LJ and RJ for left and right junctions, respectively) are indicated. Abbreviations for restriction sites: X, XbaI; H, HindIII; Xh, XhoI.

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