» Articles » PMID: 26646248

Prevention and Treatment of Staphylococcus Aureus Biofilms

Overview
Date 2015 Dec 10
PMID 26646248
Citations 117
Authors
Affiliations
Soon will be listed here.
Abstract

S. aureus colonizes both artificial and tissue surfaces in humans causing chronic persistent infections that are difficult to cure. It is a notorious pathogen due to its antibiotic recalcitrance and phenotypic adaptability, both of which are facilitated by its ability to develop biofilms. S. aureus biofilms challenge conventional anti-infective approaches, most notably antibiotic therapy. Therefore there is an unmet need to develop and include parallel approaches that target S. aureus biofilm infections. This review discusses two broad anti-infective strategies: (1) preventative approaches (anti-biofilm surface coatings, the inclusion of biofilm-specific vaccine antigens); and (2) approaches aimed at eradicating established S. aureus biofilms, particularly those associated with implant infections. Advances in understanding the distinct nature of S. aureus biofilm development and pathogenesis have led to growing optimism in S. aureus biofilm targeted anti-infective strategies. Further research is needed however, to see the successful administration and validation of these approaches to the diverse types of infections caused by S. aureus biofilms from multiple clinical strains.

Citing Articles

Production and Potential Application of an Alkaline Serine Peptidase from Myceliophtora heterothallica for Biofilm Removal.

Barreto R, Ribeiro E, de Menezes C, Zaiter M, Boscolo M, da Silva R Curr Microbiol. 2025; 82(4):179.

PMID: 40057915 DOI: 10.1007/s00284-025-04149-6.


Antibacterial and antibiofilm activities of kaffir lime essential oils and their active constituents against focusing on sortase A.

Pontanayodsakorn C, Eurtivong C, Jiamboonsri P Heliyon. 2025; 11(2):e41977.

PMID: 40013263 PMC: 11862495. DOI: 10.1016/j.heliyon.2025.e41977.


Novel antibiotics against without detectable resistance by targeting proton motive force and FtsH.

Pengfei S, Yifan Y, Linhui L, Yimin L, Dan X, Shaowei G MedComm (2020). 2025; 6(1):e70046.

PMID: 39781293 PMC: 11707430. DOI: 10.1002/mco2.70046.


Infective Endocarditis by Biofilm-Producing Methicillin-Resistant -Pathogenesis, Diagnosis, and Management.

Kaushik A, Kest H, Sood M, Thieman C, Steussy B, Padomek M Antibiotics (Basel). 2025; 13(12.

PMID: 39766522 PMC: 11672591. DOI: 10.3390/antibiotics13121132.


Universal receptive system as a novel regulator of transcriptomic activity of Staphylococcus aureus.

Tetz G, Kardava K, Vecherkovskaya M, Khodadadi-Jamayran A, Tsirigos A, Tetz V Microb Cell Fact. 2025; 24(1):1.

PMID: 39754239 PMC: 11697845. DOI: 10.1186/s12934-024-02637-1.


References
1.
Park J, Jagasia R, Kaufmann G, Mathison J, Ruiz D, Moss J . Infection control by antibody disruption of bacterial quorum sensing signaling. Chem Biol. 2007; 14(10):1119-27. PMC: 2088803. DOI: 10.1016/j.chembiol.2007.08.013. View

2.
Fowler V, Allen K, Moreira E, Moustafa M, Isgro F, Boucher H . Effect of an investigational vaccine for preventing Staphylococcus aureus infections after cardiothoracic surgery: a randomized trial. JAMA. 2013; 309(13):1368-78. DOI: 10.1001/jama.2013.3010. View

3.
Brady R, Leid J, Camper A, Costerton J, Shirtliff M . Identification of Staphylococcus aureus proteins recognized by the antibody-mediated immune response to a biofilm infection. Infect Immun. 2006; 74(6):3415-26. PMC: 1479260. DOI: 10.1128/IAI.00392-06. View

4.
Fux C, Wilson S, Stoodley P . Detachment characteristics and oxacillin resistance of Staphyloccocus aureus biofilm emboli in an in vitro catheter infection model. J Bacteriol. 2004; 186(14):4486-91. PMC: 438612. DOI: 10.1128/JB.186.14.4486-4491.2004. View

5.
Percival S, Hill K, Malic S, Thomas D, Williams D . Antimicrobial tolerance and the significance of persister cells in recalcitrant chronic wound biofilms. Wound Repair Regen. 2011; 19(1):1-9. DOI: 10.1111/j.1524-475X.2010.00651.x. View