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Genomic Background and Phylogeny of cfiA-Positive Bacteroides fragilis Strains Resistant to Meropenem-EDTA

Authors :
María J. Medina-Pascual
Sylvia Valdezate
Sara Monzón
Fernando Cobo
Isabel Cuesta
Silvia Pino-Rosa
Pilar Villalón
Ángel Zaballos
Source :
Antibiotics, Volume 10, Issue 3, Antibiotics, Vol 10, Iss 304, p 304 (2021), Repisalud, Instituto de Salud Carlos III (ISCIII)
Publication Year :
2021
Publisher :
Multidisciplinary Digital Publishing Institute, 2021.

Abstract

Background: Bacteroides fragilis shows high antimicrobial resistance (AMR) rates and possesses numerous AMR mechanisms. Its carbapenem-resistant strains (metallo-β-lactamase cfiA-positive) appear as an emergent, evolving clade. Methods: This work examines the genomes, taxonomy, and phylogenetic relationships with respect to other B. fragilis genomes of two B. fragilis strains (CNM20180471 and CNM20200206) resistant to meropenem+EDTA and other antimicrobial agents. Results: Both strains possessed cfiA genes (cfiA14b and the new cfiA28), along with other AMR mechanisms. The presence of other efflux-pump genes, mexAB/mexJK/mexXY-oprM, acrEF/mdtEF-tolC, and especially cusR, which reduces the entry of carbapenem via the repression of porin OprD, may be related to meropenem–EDTA resistance. None of the detected insertion sequences were located upstream of cfiA. The genomes of these and other B. fragilis strains that clustered together in phylogenetic analyses did not meet the condition of &gt<br />95% average nucleotide/amino acid identity, or &gt<br />70% in silico genome-to-genome hybridization similarity, to be deemed members of the same species, although &lt<br />1% difference in the genomic G+C content was seen with respect to the reference genome B. fragilis NCTC 9343T. Conclusions: Carbapenem-resistant strains may be considered a distinct clonal entity, and their surveillance is recommended given the ease with which they appear to acquire AMR.

Details

Language :
English
ISSN :
20796382
Database :
OpenAIRE
Journal :
Antibiotics
Accession number :
edsair.doi.dedup.....67f0a21ca9d45d4122696cd586cfde34
Full Text :
https://doi.org/10.3390/antibiotics10030304