4.5 Article

Exploring the Biofilm Formation Capacity in S. pseudintermedius and Coagulase-Negative Staphylococci Species

Journal

PATHOGENS
Volume 11, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens11060689

Keywords

biofilm; staphylococci; coagulase-negative staphylococci (CoNS)

Categories

Funding

  1. RD Project CAREBIO2: Comparative assessment of antimicrobial resistance in environmental biofilms through proteomics-towards innovative theranostic biomarkers - European Regional Development Fund (ERDF) through the Northern Regional Operational Program (N [NORTE-01-0145-FEDER-030101, PTDC/SAU-INF/30101/2017]
  2. Foundation for Science and Technology (FCT)
  3. Associate Laboratory for Green Chemistry-LAQV - FCT/MCTES [UIDB/50006/2020, UIDP/50006/2020]
  4. Portuguese Foundation for Science and Technology (FCT) [UIDB/CVT/00772/2020, LA/P/0059/2020]
  5. Ministerio de Ciencia, Innovacion y Universidades (Spain) [RTI2018-098267-R-C33]
  6. Junta de Castilla y Leon (Consejeria de Educacion, Spain) [LE018P20]
  7. FCT (Fundacao para a Ciencia e a Tecnologia) [SFRH/BD/137947/2018]

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This study evaluates the ability of biofilm formation in coagulase-negative staphylococci (CoNS) and S. pseudintermedius isolated from various animal species, and investigates the effect of conventional antimicrobials on reducing biofilm. The results show that all isolates can form biofilm, with S. urealyticus producing the most biomass and S. pseudintermedius producing the least biomass. Biofilm formation is positively associated with multidrug resistance and resistance to individual antimicrobials. Tetracycline and amikacin were unable to eradicate the biofilm, even at high concentrations.
The ability of biofilm formation seems to play an important role in the virulence of staphylococci. However, studies reporting biofilm formation of coagulase-negative staphylococci isolated from animals are still very scarce. Thus, we aimed to evaluate the biofilm-forming capacity of CoNS and S. pseudintermedius isolated from several animal species and to investigate the effect of conventional antimicrobials on biofilm reduction. A total of 35 S. pseudintermedius and 192 CoNS were included. Biofilm formation was accessed by the microtiter plate assay and the biofilms were stained by crystal violet. Association between biofilm formation and staphylococci species and antimicrobial resistance was also performed. Biofilm susceptibility testing was performed with tetracycline and amikacin at the minimum inhibitory concentration (MIC) and 10 x MIC. The metabolic activity of the biofilm cells after antimicrobial treatment was accessed by the XTT assay. All isolates formed biofilm, with S. urealyticus producing the most biofilm biomass and S. pseudintermedius producing the least biomass. There was a positive association between biofilm formation and multidrug resistance as well as resistance to individual antimicrobials. Neither tetracycline nor amikacin were able to eradicate the biofilm, not even at the highest concentration used. This study provides new insights into biofilm formation and the effects of antimicrobials on CoNS species.

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