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Novel trimethoprim resistance gene dfrA34 identified in Salmonella Heidelberg in the USA
Author(s) -
Kaitlin A. Tagg,
Louise Francois Watkins,
Matthew D. Moore,
Christy Bennett,
Yoo Jin Joung,
Jessica C. Chen,
Jason P. Folster
Publication year - 2018
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dky373
Subject(s) - sulfamethoxazole , trimethoprim , salmonella , microbiology and biotechnology , salmonella enterica , serotype , gene , biology , antibiotic resistance , enterobacteriaceae , antibiotics , virology , escherichia coli , bacteria , genetics
Trimethoprim/sulfamethoxazole is a synthetic antibiotic combination recommended for the treatment of complicated non-typhoidal Salmonella infections in humans. Resistance to trimethoprim/sulfamethoxazole is mediated by the acquisition of mobile genes, requiring both a dfr gene (trimethoprim resistance) and a sul gene (sulfamethoxazole resistance) for a clinical resistance phenotype (MIC ≥4/76 mg/L). In 2017, the CDC investigated a multistate outbreak caused by a Salmonella enterica serotype Heidelberg strain with trimethoprim/sulfamethoxazole resistance, in which sul genes but no known dfr genes were detected.

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