Affiliation:
1. Poultry Microbiological Safety Research Unit, Richard B. Russell Agricultural Research Center, USDA Agricultural Research Services, Athens, Georgia 30604-5677,1and
2. Department of Medical Microbiology and Parasitology2 and
3. Department of Avian Medicine,3 The University of Georgia, Athens, Georgia 30602
Abstract
ABSTRACT
Salmonella enterica
serotype
typhimurium
(
S. typhimurium
) DT104 (DT104) first emerged as a major pathogen in Europe and is characterized by its pentadrug-resistant pattern. It has also been associated with outbreaks in the United States. The organism typically carries resistance to ampicillin, chloramphenicol, streptomycin, sulfonamides, and tetracycline. The mechanism of chloramphenicol resistance in DT104 was determined by producing antibiotic-resistant
Escherichia coli
host strain clones from DT104 DNA. DNA from chloramphenicol-resistant clones was sequenced, and probes specific for the genes
flo
S. typhimurium
(
flo
St
),
int
,
invA
, and
spvC
were produced for colony blot hybridizations. One hundred nine
Salmonella
isolates, including 44 multidrug-resistant DT104 isolates, were tested to evaluate the specificities of the probes. The gene
flo
St
, reported in this study, confers chloramphenicol and florfenicol resistance on
S. typhimurium
DT104. Florfenicol resistance is unique to
S. typhimurium
DT104 and multidrug-resistant
S. typhimurium
isolates with the same drug resistance profile among all isolates evaluated. Of 44 DT104 isolates tested, 98% were detected based on phenotypic florfenicol resistance and 100% had the
flo
St
-positive genotype. Resistances to florfenicol and chloramphenicol are conferred by the gene
flo
St
, described in this paper. Presumptive identification of
S. typhimurium
DT104 can be made rapidly based on the presence of the
flo
St
gene or its resulting phenotype.
Publisher
American Society for Microbiology
Cited by
123 articles.
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