» Articles » PMID: 33573022

Staphylococcal Biofilms: Challenges and Novel Therapeutic Perspectives

Overview
Specialty Pharmacology
Date 2021 Feb 12
PMID 33573022
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

Staphylococci, like and , are common colonizers of the human microbiota. While being harmless in many cases, many virulence factors result in them being opportunistic pathogens and one of the major causes of hospital-acquired infections worldwide. One of these virulence factors is the ability to form biofilms-three-dimensional communities of microorganisms embedded in an extracellular polymeric matrix (EPS). The EPS is composed of polysaccharides, proteins and extracellular DNA, and is finely regulated in response to environmental conditions. This structured environment protects the embedded bacteria from the human immune system and decreases their susceptibility to antimicrobials, making infections caused by staphylococci particularly difficult to treat. With the rise of antibiotic-resistant staphylococci, together with difficulty in removing biofilms, there is a great need for new treatment strategies. The purpose of this review is to provide an overview of our current knowledge of the stages of biofilm development and what difficulties may arise when trying to eradicate staphylococcal biofilms. Furthermore, we look into promising targets and therapeutic methods, including bacteriocins and phage-derived antibiofilm approaches.

Citing Articles

Local Antimicrobial Potential of Bupivacaine and Tolfenamic Acid-Loaded Ultra-High Molecular Weight Polyethylene (UHMWPE) for Orthopedic Infection.

Sekar A, Inverardi N, Lekkala S, Thomson A, Daesety V, Trendafilova D Bioengineering (Basel). 2025; 12(2).

PMID: 40001692 PMC: 11851508. DOI: 10.3390/bioengineering12020173.


Structural characteristics, functions, and counteracting strategies of biofilms in .

Xia Y, Hu Z, Jin Q, Chen Q, Zhao C, Qiang R Comput Struct Biotechnol J. 2025; 27:488-500.

PMID: 39916696 PMC: 11799891. DOI: 10.1016/j.csbj.2025.01.021.


From Farm to Community: Dispersal of Potentially Pathogenic Staphylococcus and Mammaliicoccus Species and Antimicrobial Resistance Across Shared Environments.

Ahmad F, Martuchelle S, Andrade-Oliveira A, Lanes Viana V, Sousa M, da Silveira F Curr Microbiol. 2025; 82(3):104.

PMID: 39875692 DOI: 10.1007/s00284-025-04079-3.


Antibiofilm Activities of Multiple Halogenated Pyrimidines Against .

Sim M, Kim Y, Lee J, Lee J Int J Mol Sci. 2024; 25(23).

PMID: 39684543 PMC: 11641129. DOI: 10.3390/ijms252312830.


The clinical praxis of bacteriocins as natural anti-microbial therapeutics.

Nisar S, Shah A, Nazir R Arch Microbiol. 2024; 206(11):451.

PMID: 39476181 DOI: 10.1007/s00203-024-04152-8.


References
1.
Tenover F, Weigel L, Appelbaum P, McDougal L, Chaitram J, McAllister S . Vancomycin-resistant Staphylococcus aureus isolate from a patient in Pennsylvania. Antimicrob Agents Chemother. 2003; 48(1):275-80. PMC: 310200. DOI: 10.1128/AAC.48.1.275-280.2004. View

2.
Kiedrowski M, Crosby H, Hernandez F, Malone C, McNamara 2nd J, Horswill A . Staphylococcus aureus Nuc2 is a functional, surface-attached extracellular nuclease. PLoS One. 2014; 9(4):e95574. PMC: 3994088. DOI: 10.1371/journal.pone.0095574. View

3.
Breukink E, de Kruijff B . The lantibiotic nisin, a special case or not?. Biochim Biophys Acta. 1999; 1462(1-2):223-34. DOI: 10.1016/s0005-2736(99)00208-4. View

4.
Kobayashi S, Malachowa N, Whitney A, Braughton K, Gardner D, Long D . Comparative analysis of USA300 virulence determinants in a rabbit model of skin and soft tissue infection. J Infect Dis. 2011; 204(6):937-41. PMC: 3156927. DOI: 10.1093/infdis/jir441. View

5.
Balaban N, Giacometti A, Cirioni O, Gov Y, Ghiselli R, Mocchegiani F . Use of the quorum-sensing inhibitor RNAIII-inhibiting peptide to prevent biofilm formation in vivo by drug-resistant Staphylococcus epidermidis. J Infect Dis. 2003; 187(4):625-30. DOI: 10.1086/345879. View