Some species, potentially pathogenic for humans, are known to express up to three different classes of chromosomal β-lactamases, which may become hyperproduced and cause treatment failure. The aim of this study was to assess the utility of these species-specific β-lactamase genes as phylogenetic markers using whole-genome sequencing data. Core-genome alignments were generated for 36 genomes from seven different species and scanned for antimicrobial resistance genes. Core-genome alignment confirmed the MALDI-TOF identification of most of the isolates and re-identified an isolate as . Three (B, C and D) of the four Ambler classes of β-lactamase genes were found in and ( and ). only showed class-B- and class-D-like matches ( and ), whereas those for and were class C and D (, and ). The phylogenetic tree derived from concatenated sequences of β-lactamase genes successfully clustered each species. Some isolates also had resistance to sulfonamides, quinolones and aminoglycosides. Whole-genome sequencing proved to be a useful method to identify at the species level, which led to the unexpected identification of and . and revealed the resistome of each isolate.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065696 | PMC |
http://dx.doi.org/10.3390/antibiotics10040354 | DOI Listing |
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