Methicillin resistance and virulence genes in invasive and nasal Staphylococcus epidermidis isolates from neonates

Vivian Carolina Salgueiro1, Natalia Lopes Pontes Iorio2, Marcelle Cristina Ferreira1

  • 1Departamento de Microbiologia Médica, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Av Carlos Chagas Filho, no 373, CCS, Bloco I, Sala 010, Cidade Universitária, Rio de Janeiro, Brazil.

BMC Microbiology
|January 15, 2017
PubMed
Abstract

Insights

Staphylococcus epidermidis bloodstream infection isolates from neonates more frequently carried specific adhesin genes (sdrF, sesI) and SCCmec type IV, suggesting increased pathogenicity compared to nasal isolates.

Area of Science:

  • Microbiology
  • Infectious Diseases
  • Genetics

Background:

  • Staphylococcus epidermidis is a key cause of hospital-acquired infections, especially those linked to medical devices.
  • Neonatal bloodstream infections (BSIs) and nasal colonization by S. epidermidis are significant clinical concerns.
  • Understanding virulence factors is crucial for predicting S. epidermidis pathogenicity.

Purpose of the Study:

  • To characterize S. epidermidis isolates from neonatal BSIs and nares.
  • To investigate the association of staphylococcal chromosomal cassette mec (SCCmec) type, biofilm production, and arginine catabolic mobile elements (ACME) with infection source.
  • To identify virulence factors differentiating invasive S. epidermidis isolates.

Main Methods:

  • Genomic analysis of 50 genetically distinct S. epidermidis isolates from neonatal BSIs (n=31) and nares (n=19).
  • Assessment of staphylococcal chromosomal cassette mec (SCCmec) types, biofilm production, and arginine catabolic mobile elements (ACME).
  • Detection of specific virulence genes including sdrF, sesI, and aap.

Main Results:

  • No significant differences in biofilm production or ACME genes between BSI and nasal isolates.
  • BSI isolates more frequently harbored sdrF and sesI genes (p<0.05).
  • SCCmec type IV and ccr2 complex were associated with BSI isolates; 83% of nasal isolates were non-typeable for SCCmec.

Conclusions:

  • Neonatal S. epidermidis isolates exhibit significant clonal diversity.
  • The presence of sdrF and sesI adhesin genes in BSI isolates may contribute to increased pathogenicity.
  • Variability in SCCmec composition of nasal isolates warrants further investigation.

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