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A Platform of Anti-biofilm Assays Suited to the Exploration of Natural Compound Libraries
Published on: December 27, 2016
Promising Antibiofilm Agents: Recent Breakthrough against Biofilm Producing Methicillin-Resistant Staphylococcus
Marwa I Abd El-Hamid1, El-Sayed Y El-Naenaeey1, Toka M Kandeel2
1Department of Microbiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44511, Egypt.
Abstract:
Multidrug resistant (MDR) methicillin-resistant Staphylococcus aureus (MRSA) is a superbug pathogen that causes serious diseases. One of the main reasons for the lack of the effectiveness of antibiotic therapy against infections caused by this resistant pathogen is the recalcitrant nature of MRSA biofilms, which results in an increasingly serious situation worldwide. Consequently, the development of innovative biofilm inhibitors is urgently needed to control the biofilm formation by this pathogen. In this work, we thus sought to evaluate the biofilm inhibiting ability of some promising antibiofilm agents such as zinc oxide nanoparticles (Zno NPs), proteinase K, and hamamelitannin (HAM) in managing the MRSA biofilms. Different phenotypic and genotypic methods were used to identify the biofilm producing MDR MRSA isolates and the antibiofilm/antimicrobial activities of the used promising agents. Our study demonstrated strong antibiofilm activities of ZnO NPs, proteinase K, and HAM against MRSA biofilms along with their transcriptional modulation of biofilm (intercellular adhesion A, icaA) and quorum sensing (QS) (agr) genes. Interestingly, only ZnO NPs showed a powerful antimicrobial activity against this pathogen. Collectively, we observed overall positive correlations between the biofilm production and the antimicrobial resistance/agr genotypes II and IV. Meanwhile, there was no significant correlation between the toxin genes and the biofilm production. The ZnO NPs were recommended to be used alone as potent antimicrobial and antibiofilm agents against MDR MRSA and their biofilm-associated diseases. On the other hand, proteinase-K and HAM can be co-administrated with other antimicrobial agents to manage such types of infections.
Insights
Zinc oxide nanoparticles (ZnO NPs), proteinase K, and hamamelitannin (HAM) effectively inhibit multidrug-resistant Staphylococcus aureus (MRSA) biofilms. ZnO NPs also exhibit antimicrobial activity, offering a potent treatment option for MRSA infections.
Area of Science:
- Microbiology
- Nanotechnology
- Infectious Diseases
Background:
- Multidrug-resistant methicillin-resistant Staphylococcus aureus (MRSA) poses a significant global health threat due to its resistance to antibiotics.
- The recalcitrant nature of MRSA biofilms contributes to treatment failure, necessitating the development of novel antibiofilm strategies.
Purpose of the Study:
- To evaluate the antibiofilm efficacy of zinc oxide nanoparticles (ZnO NPs), proteinase K, and hamamelitannin (HAM) against MRSA biofilms.
- To investigate the impact of these agents on the expression of key biofilm and quorum sensing genes in MRSA.
- To assess the antimicrobial activity of the agents and their correlation with biofilm production and genotypic characteristics.
Main Methods:
- Phenotypic and genotypic methods were employed to identify biofilm-producing MDR MRSA isolates.
- Antimicrobial and antibiofilm activities of ZnO NPs, proteinase K, and HAM were assessed.
- Transcriptional modulation of biofilm (icaA) and quorum sensing (agr) genes was analyzed.
Main Results:
- ZnO NPs, proteinase K, and HAM demonstrated significant antibiofilm activity against MRSA biofilms.
- These agents modulated the transcription of icaA and agr genes.
- Only ZnO NPs exhibited potent antimicrobial activity against MRSA.
- Biofilm production positively correlated with antimicrobial resistance and agr genotypes II and IV.
Conclusions:
- ZnO NPs are recommended as standalone agents for their potent antimicrobial and antibiofilm properties against MDR MRSA.
- Proteinase K and HAM can be used as adjunct therapies, co-administered with other antimicrobials, to manage MRSA biofilm infections.
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