Biochemistry of Bacterial Biofilm: Insights into Antibiotic Resistance Mechanisms and Therapeutic Intervention

被引:2
|
作者
Azeem, Kashish [1 ]
Fatima, Sadaf [1 ]
Ali, Asghar [1 ,2 ]
Ubaid, Ayesha [1 ]
Husain, Fohad Mabood [3 ]
Abid, Mohammad [1 ]
机构
[1] Jamia Millia Islamia, Dept Biosci, Med Chem Lab, New Delhi 110025, India
[2] Jamia Hamdard, Sch Chem & Life Sci, Dept Biochem, Clin Biochem Lab, New Delhi 110062, India
[3] King Saud Univ, Dept Food Sci & Nutr, Riyadh 11451, Saudi Arabia
来源
LIFE-BASEL | 2025年 / 15卷 / 01期
关键词
biofilms; antimicrobial resistance; quorum-sensing inhibitor; nanomaterials; immunomodulators; PSEUDOMONAS-AERUGINOSA; INFECTIONS;
D O I
10.3390/life15010049
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Biofilms, composed of structured communities of bacteria embedded in a self-produced extracellular matrix, pose a significant challenge due to their heightened resistance to antibiotics and immune responses. This review highlights the mechanisms underpinning antibiotic resistance within bacterial biofilms, elucidating the adaptive strategies employed by microorganisms to withstand conventional antimicrobial agents. This encompasses the role of the extracellular matrix, altered gene expression, and the formation of persister cells, contributing to the recalcitrance of biofilms to eradication. A comprehensive understanding of these resistance mechanisms provides a for exploring innovative therapeutic interventions. This study explores promising avenues for future research, emphasizing the necessity of uncovering the specific genetic and phenotypic adaptations occurring within biofilms. The identification of vulnerabilities in biofilm architecture and the elucidation of key biofilm-specific targets emerge as crucial focal points for the development of targeted therapeutic strategies. In addressing the limitations of traditional antibiotics, this review discusses innovative therapeutic approaches. Nanomaterials with inherent antimicrobial properties, quorum-sensing inhibitors disrupting bacterial communication, and bacteriophages as biofilm-specific viral agents are highlighted as potential alternatives. The exploration of combination therapies, involving antimicrobial agents, biofilm-disrupting enzymes, and immunomodulators, is emphasized to enhance the efficacy of existing treatments and overcome biofilm resilience.
引用
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页数:23
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