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Genomic diversity of prevalentStaphylococcus epidermidismultidrug-resistant strains isolated from a Children’s Hospital in México City in an eight-years survey
Author(s) -
Roberto Cabrera-Contreras,
Rosa I. Santamaría,
Patricia Bustos,
Irma MartínezFlores,
Enrique Meléndez-Herrada,
Rubén Morelos-Ramírez,
Martín Barbosa-Amezcua,
Vanessa González-Covarrubias,
Eugenia SilvaHerzog,
Xavier Soberón,
Víctor González
Publication year - 2019
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.8068
Subject(s) - staphylococcus epidermidis , biology , virulence , multilocus sequence typing , multiple drug resistance , microbiology and biotechnology , antibiotic resistance , operon , genetics , gene , horizontal gene transfer , mobile genetic elements , genome , genotype , drug resistance , antibiotics , staphylococcus aureus , bacteria , escherichia coli
Staphylococcus epidermidis is a human commensal and pathogen worldwide distributed. In this work, we surveyed for multi-resistant S. epidermidis strains in eight years at a children’s health-care unit in México City. Multidrug-resistant S. epidermidis were present in all years of the study, including resistance to methicillin, beta-lactams, fluoroquinolones, and macrolides. To understand the genetic basis of antibiotic resistance and its association with virulence and gene exchange, we sequenced the genomes of 17 S. epidermidis isolates. Whole-genome nucleotide identities between all the pairs of S. epidermidis strains were about 97% to 99%. We inferred a clonal structure and eight Multilocus Sequence Types (MLSTs) in the S. epidermidis sequenced collection. The profile of virulence includes genes involved in biofilm formation and phenol-soluble modulins (PSMs). Half of the S. epidermidis analyzed lacked the ica operon for biofilm formation. Likely, they are commensal S. epidermidis strains but multi-antibiotic resistant. Uneven distribution of insertion sequences, phages, and CRISPR-Cas immunity phage systems suggest frequent horizontal gene transfer. Rates of recombination between S. epidermidis strains were more prevalent than the mutation rate and affected the whole genome. Therefore, the multidrug resistance, independently of the pathogenic traits, might explain the persistence of specific highly adapted S. epidermidis clonal lineages in nosocomial settings.

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