Complete Nucleotide Sequence of a 43-Kilobase Genomic Island Associated with the Multidrug Resistance Region of Salmonella enterica Serovar Typhimurium DT104 and Its Identification in Phage Type DT120 and Serovar Agona

Author:

Boyd David1,Peters Geoffrey A.1,Cloeckaert Axel2,Boumedine Karim Sidi2,Chaslus-Dancla Elisabeth2,Imberechts Hein3,Mulvey Michael R.1

Affiliation:

1. National Microbiology Laboratory, Health Canada, Winnipeg, Manitoba R3E 3R2, Canada1;

2. Station de Pathologie Aviaire et Parasitologie, Institut National de la Recherche Agronomique, 37380 Nouzilly, France2; and

3. Centre d'Etude et de Recherches Vétérinaires et Agrochimiques, B-1180 Brussels, Belgium3

Abstract

ABSTRACT This study describes the characterization of the recently described Salmonella genomic island 1 (SGI1) (D. A. Boyd, G. A. Peters, L.-K. Ng, and M. R. Mulvey, FEMS Microbiol. Lett. 189:285–291, 2000), which harbors the genes associated with the ACSSuT phenotype in a Canadian isolate of Salmonella enterica serovar Typhimurium DT104. A 43-kb region has been completely sequenced and found to contain 44 predicted open reading frames (ORFs) which comprised ∼87% of the total sequence. Fifteen ORFs did not show any significant homology to known gene sequences. A number of ORFs show significant homology to plasmid-related genes, suggesting, at least in part, a plasmid origin for the SGI1, although some with homology to phage-related genes were identified. The SGI1 was identified in a number of multidrug-resistant DT120 and S. enterica serovar Agona strains with similar antibiotic-resistant phenotypes. The G+C content suggests a potential mosaic structure for the SGI1. Emergence of the SGI1 in serovar Agona strains is discussed.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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