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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom