4.5 Review

Therapeutic Strategies To Counteract Antibiotic Resistance in MRSA Biofilm-Associated Infections

Journal

CHEMMEDCHEM
Volume 16, Issue 1, Pages 65-80

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.202000677

Keywords

MRSA; biofilms; antibiotic resistance; antivirulence; eradicating agents

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Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of persistent human infections, with the ability to colonize asymptomatically and cause moderate to severe infections. It is considered a superbug due to its high morbidity and mortality rates, as well as its resistance to most antibiotics on the market. Its formation of biofilms on various surfaces is believed to be the primary means of its antibiotic resistance and widespread presence. Development of new anti-virulence strategies is crucial in combating MRSA infections associated with biofilms.
Methicillin-resistant Staphylococcus aureus (MRSA) has emerged as one of the leading causes of persistent human infections. This pathogen is widespread and is able to colonize asymptomatically about a third of the population, causing moderate to severe infections. It is currently considered the most common cause of nosocomial infections and one of the main causes of death in hospitalized patients. Due to its high morbidity and mortality rate and its ability to resist most antibiotics on the market, it has been termed a superbug. Its ability to form biofilms on biotic and abiotic surfaces seems to be the primarily means of MRSA antibiotic resistance and pervasiveness. Importantly, more than 80 % of bacterial infections are biofilm-mediated. Biofilm formation on indwelling catheters, prosthetic devices and implants is recognized as the cause of serious chronic infections in hospital environments. In this review we discuss the most relevant literature of the last five years concerning the development of synthetic small molecules able to inhibit biofilm formation or to eradicate or disperse pre-formed biofilms in the fight against MRSA diseases. The aim is to provide guidelines for the development of new anti-virulence strategies based on the knowledge so far acquired, and, to identify the main flaws of this research field, which have hindered the generation of new market-approved anti-MRSA drugs that are able to act against biofilm-associated infections

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