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Metabolomic profiling of bacterial biofilm: trends, challenges, and an emerging antibiofilm target

Biofilm-related infections substantially contribute to bacterial illnesses, with estimates indicating that at least 80% of such diseases are linked to biofilms. Biofilms exhibit unique metabolic patterns that set them apart from their planktonic counterparts, resulting in significant metabolic repro...

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Published in:World journal of microbiology & biotechnology 2023-08, Vol.39 (8), p.212-212, Article 212
Main Authors: Malviya, Jitendra, Alameri, Ameer A., Al-Janabi, Saif S., Fawzi, Omar Faridh, Azzawi, Ahmed L., Obaid, Rasha Fadhel, Alsudani, Ali A, Alkhayyat, Ameer S., Gupta, Jitendra, Mustafa, Yasser Fakri, Karampoor, Sajad, Mirzaei, Rasoul
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cited_by cdi_FETCH-LOGICAL-c375t-173f79524c20909c315b1680e09180ca43fcb6a78f55ab1d302db2ced50e0cfc3
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container_title World journal of microbiology & biotechnology
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creator Malviya, Jitendra
Alameri, Ameer A.
Al-Janabi, Saif S.
Fawzi, Omar Faridh
Azzawi, Ahmed L.
Obaid, Rasha Fadhel
Alsudani, Ali A
Alkhayyat, Ameer S.
Gupta, Jitendra
Mustafa, Yasser Fakri
Karampoor, Sajad
Mirzaei, Rasoul
description Biofilm-related infections substantially contribute to bacterial illnesses, with estimates indicating that at least 80% of such diseases are linked to biofilms. Biofilms exhibit unique metabolic patterns that set them apart from their planktonic counterparts, resulting in significant metabolic reprogramming during biofilm formation. Differential glycolytic enzymes suggest that central metabolic processes are markedly different in biofilms and planktonic cells. The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is highly expressed in Staphylococcus aureus biofilm progenitors, indicating that changes in glycolysis activity play a role in biofilm development. Notably, an important consideration is a correlation between elevated cyclic di-guanylate monophosphate (c-di-GMP) activity and biofilm formation in various bacteria. C-di-GMP plays a critical role in maintaining the persistence of Pseudomonas aeruginosa biofilms by regulating alginate production, a significant biofilm matrix component. Furthermore, it has been demonstrated that S. aureus biofilm development is initiated by several tricarboxylic acid (TCA) intermediates in a FnbA-dependent manner. Finally, Glucose 6-phosphatase (G6P) boosts the phosphorylation of histidine-containing protein (HPr) by increasing the activity of HPr kinase, enhancing its interaction with CcpA, and resulting in biofilm development through polysaccharide intercellular adhesion (PIA) accumulation and icaADBC transcription. Therefore, studying the metabolic changes associated with biofilm development is crucial for understanding the complex mechanisms involved in biofilm formation and identifying potential targets for intervention. Accordingly, this review aims to provide a comprehensive overview of recent advances in metabolomic profiling of biofilms, including emerging trends, prevailing challenges, and the identification of potential targets for anti-biofilm strategies.
doi_str_mv 10.1007/s11274-023-03651-y
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subjects Alginates
Alginic acid
Applied Microbiology
Bacteria
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Biochemistry
Biofilms
Biomedical and Life Sciences
Biotechnology
Cell adhesion
Environmental Engineering/Biotechnology
Extracellular Polymeric Substance Matrix - metabolism
Gene Expression Regulation, Bacterial
Glyceraldehyde-3-phosphate dehydrogenase
Glycolysis
Histidine
Intermediates
Kinases
Life Sciences
Metabolism
Metabolomics
Microbiology
Phosphorylation
Planktonic cells
Polysaccharides
Pseudomonas aeruginosa
Pseudomonas aeruginosa - genetics
Pseudomonas aeruginosa - metabolism
Review
Staphylococcus aureus
Staphylococcus aureus - metabolism
Trends
title Metabolomic profiling of bacterial biofilm: trends, challenges, and an emerging antibiofilm target
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