Journal of Antimicrobial Chemotherapy · 2017 · 76 citations · 38 references
Life SciencesInfectious DiseasesMicrobiologyAntimicrobial ResistanceMedical MicrobiologyMicrobial GeneticsAntibiotic ResistanceAntibiotic Resistance GeneticsAntibiotic Resistance MechanismsAntimicrobial Resistance GenomicsPlasmid-mediated ResistanceResistance GenesAntibiotic Resistance GenesAntibiotic Resistance In WastewaterAntibiotic Resistance PlasmidsAntimicrobial Resistance Gene DetectionEnterococciOxazolidinone AntibioticsOxazolidinone ResistanceResistance Mechanisms In Enterococci
OBJECTIVES: Oxazolidinone resistance is a serious limitation in the treatment of MDR Enterococcus infections. Plasmid-mediated oxazolidinone resistance has been strongly linked to animals where the use of phenicols might co-select resistance to both antibiotic families. Our goal was to assess the diversity of genes conferring phenicol/oxazolidinone resistance among diverse enterococci and to characterize the optrA genetic environment. METHODS: Chloramphenicol-resistant isolates (>16 mg/L, n = 245) from different sources (hospitals/healthy humans/wastewaters/animals) in Portugal, Angola and Tunisia (1996-2016) were selected. Phenicol (eight cat variants, fexA, fexB) or phenicol + oxazolidinone [cfr, cfr(B), optrA] resistance genes were searched for by PCR. Susceptibility (disc diffusion/microdilution), filter mating, stability of antibiotic resistance (500 bacterial generations), plasmid typing (S1-PFGE/hybridization), MLST and WGS (Illumina-HiSeq) were performed for optrA-positive isolates. RESULTS: Resistance to phenicols (n = 181, 74%) and phenicols + oxazolidinones (n = 2, 1%) was associated with the presence of cat(A-8) (40%, predominant in hospitals and swine), cat(A-7) (29%, predominant in poultry and healthy humans), cat(A-9) (2%), fexB (2%) and fexA + optrA (1%). fexA and optrA genes were co-located in a transferable plasmid (pAF379, 72 918 bp) of two ST86 MDR Tunisian Enterococcus faecalis (wastewaters) carrying several putative virulence genes. MICs of chloramphenicol, linezolid and tedizolid were stably maintained at 64, 4 and 1 mg/L, respectively. The chimeric pAF379 comprised relics of genetic elements from different Gram-positive bacteria and origins (human/porcine). CONCLUSIONS: To the best of our knowledge, we report the first detection of optrA in an African country (Tunisia) within a transferable mosaic plasmid of different origins. Its identification in isolates from environmental sources is worrisome and alerts for the need of a concerted global surveillance on the occurrence and spread of optrA.
38
Prokka: rapid prokaryotic genome annotation
Torsten Seemann · Bioinformatics · 2014 · 19.6K citations
Easyfig: a genome comparison visualizer
Mitchell J. Sullivan, Nicola K. Petty, Scott A. Beatson · Bioinformatics · 2011 · 3.7K citations · Full text
Enterococci: From Commensals to Leading Causes of Drug Resistant Infection
Gilmore Ms, Clewell Db, Yasuyoshi Ike et al. · 2014 · 824 citations
Yang Wang, Yuan Lv, Jiachang Cai et al. · Journal of Antimicrobial Chemotherapy · 2015 · 554 citations
Frank M. Aarestrup, Peter Gerner‐Smidt, M. Madsen et al. · Diagnostic Microbiology and Infectious Disease · 2000 · 488 citations