Characterization of Multidrug-Resistant Staphylococcus aureus Isolates and Comparison of Methods of Susceptibility to Vancomycin.
Danillo S RosaSamily A S OliveiraRenata F S SouzaAmaro A S NetoLetícia S B CunhaAntônio Wilton Cavalcante FernandesIanka F S SoaresSarah K R TeixeiraSamuel Ricarte de AquinoGisele Veneroni GouveiaJackson Roberto Guedes da Silva AlmeidaCarlos Henrique A DiasMateus Matiuzzi da CostaPublished in: Current microbiology (2022)
S. aureus are among the main bacteria causing problems related to multidrug resistance in nosocomial infections. Therefore, it is necessary to carry out a reliable and rapid diagnosis for the identification of the bacteria and characterization of its susceptibility profile, especially vancomycin, which is an alternative treatment against multidrug-resistant (MDR) S. aureus. Thus, the goal of this study was to characterize isolates of S. aureus regarding the resistance and virulence and to check the susceptibility to vancomycin, through different methods, for comparative purposes. Seventeen antimicrobials were tested to assess the susceptibility profile. It was evaluated the presence of identification (nuc), resistance (mecA and blaZ), biofilm (icaA and icaD) and siderophore (sfaD and sbnD) genes. The susceptibility to vancomycin was evaluated by Minimum Inhibitory Concentration (MIC) by broth microdilution (BMD), E-test, commercial panel (Kit), and Phoenix equipment. Most S. aureus (93,33%) was classified as MDR. These isolates were 100% positive for nuc, mecA, icaA, icaD, and sfaD genes; 96.67% for sbnD and 33.33% for blaZ. In relation to BMD, all methods correctly classified the susceptibility of the isolates; however, regarding the exact MIC value for vancomycin, Phoenix showed agreement of 63.33%, E-test (33.33%) and Kit (26.66%). In conclusion, most of S. aureus was considered MDR. Also, they presented resistance, biofilm production, and siderophores genes, showing the pathogenic potential of these bacteria. Besides, the Phoenix test was considered the most effective, as it presents advantages, such as identification of the microorganism and a greater number of antimicrobials tested at a time.
Keyphrases
- multidrug resistant
- staphylococcus aureus
- methicillin resistant staphylococcus aureus
- bioinformatics analysis
- acinetobacter baumannii
- pseudomonas aeruginosa
- drug resistant
- biofilm formation
- gram negative
- klebsiella pneumoniae
- genome wide
- genetic diversity
- mental health
- gene expression
- dna methylation
- transcription factor
- risk assessment
- genome wide identification
- replacement therapy
- climate change
- loop mediated isothermal amplification