alexa Methicillin Resistance, Biofilm Formation and Resistance to Benzalkonium Chloride in Staphylococcus aureus Clinical Isolates | OMICS International
ISSN: 2327-5073

Clinical Microbiology: Open Access
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Research Article

Methicillin Resistance, Biofilm Formation and Resistance to Benzalkonium Chloride in Staphylococcus aureus Clinical Isolates

Carla Raggi Perla Filippini Monica Monaco Annalisa Pantosti Roberta Creti Lucilla Baldassarri*

Dipartimento di Malattie Infettive, Parassitarie ed Immunomediate, Istituto Superiore di Sanita, Rome, Italy

*Corresponding Author:
Lucilla Baldassarri
Dipartimento di Malattie Infettive
Parassitarie ed Immunomediate
Istituto Superiore di Sanità, Rome, Italy
Tel: +39.06.4990.2333
E-mail: [email protected]

Received Date: June 17, 2013; Accepted Date: July 12, 2013; Published Date: July 15, 2013

Citation: Raggi C, Filippini P, Monaco M, Pantosti A, Creti R, et al, (2013) Methicillin Resistance, Biofilm Formation and Resistance to Benzalkonium Chloride in Staphylococcus aureus Clinical Isolates. Clin Microbial 2:121. doi: 10.4172/2327-5073.1000121

Copyright: © 2013 Raggi C, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Purpose: To examine the resistance to benzalkonium chloride (BKC) and the distribution of biocide-resistance genes in S.aureus clinical isolates and to determine whether any correlation may exist with antibiotic resistance pattern and biofilm formation.
Methods: MICs to BKC were determined in a collection of S.aureus (HA-MRSA, CA-MRSA and MSSA) both in suspension and on biofilm-embedded cells. Characteristic of the isolates (qac genes and biofilm formation) were determined by PCR and a plate assay, respectively.
Results: MICs to BKC were higher among MRSA than MSSA, where the CA-MRSA showed MIC levels closer to the MSSA group. qacA/B genes were found only among HA-MRSA and conferred higher resistance to the disinfectant while smr gene did not. MBC, but not MIC, were higher for biofilm embedded vs. planktonic cells, but no correlation was found with the ability to form biofilm.
Conclusion: We confirmed that presence of qacA/B but not smr confers higher resistance to BKC; MICs among MRSA were more spread compared to MSSA, suggesting that factors associated to the MR phenotype may confer resistance to BKC. Interestingly, MSSA showed higher biocide tolerance in both the planktonic and biofilm form according to the MIC/MBC fold change values. Although no correlation could be observed between biofilm thickness and biocide resistance, biofilm-embedded cells responded differently to disinfectants suggesting the current practices for efficacy testing of biocides may not be relevant in the evaluation of disinfectant efficacy against biofilm-embedded
microorganisms.

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