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      Benzalkonium chloride disinfectant residues stimulate biofilm formation and increase survival of Vibrio bacterial pathogens

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          Abstract

          Vibrio spp. are opportunistic human and animal pathogens found ubiquitously in marine environments. Globally, there is a predicted rise in the prevalence of Vibrio spp. due to increasing ocean temperatures, which carries significant implications for public health and the seafood industry. Consequently, there is an urgent need for enhanced strategies to control Vibrio spp. and prevent contamination, particularly in aquaculture and seafood processing facilities. Presently, these industries employ various disinfectants, including benzalkonium chloride (BAC), as part of their management strategies. While higher concentrations of BAC may be effective against these pathogens, inadequate rinsing post-disinfection could result in residual concentrations of BAC in the surrounding environment. This study aimed to investigate the adaptation and survival of Vibrio spp. exposed to varying concentrations of BAC residues. Results revealed that Vibrio bacteria, when exposed, exhibited a phenotypic adaptation characterized by an increase in biofilm biomass. Importantly, this effect was found to be strain-specific rather than species-specific. Exposure to BAC residues induced physiological changes in Vibrio biofilms, leading to an increase in the number of injured and alive cells within the biofilm. The exact nature of the “injured” bacteria remains unclear, but it is postulated that BAC might heighten the risk of viable but non-culturable (VBNC) bacteria development. These VBNC bacteria pose a significant threat, especially since they cannot be detected using the standard culture-based methods commonly employed for microbiological risk assessment in aquaculture and seafood industries. The undetected presence of VBNC bacteria could result in recurrent contamination events and subsequent disease outbreaks. This study provides evidence regarding the role of c-di-GMP signaling pathways in Vibrio adaptation mechanisms and suggests that c-di-GMP mediated repression is a potential avenue for further research. The findings underscore that the misuse and overuse of BAC may increase the risk of biofilm development and bacterial survival within the seafood processing chain.

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          The biofilm matrix.

          The microorganisms in biofilms live in a self-produced matrix of hydrated extracellular polymeric substances (EPS) that form their immediate environment. EPS are mainly polysaccharides, proteins, nucleic acids and lipids; they provide the mechanical stability of biofilms, mediate their adhesion to surfaces and form a cohesive, three-dimensional polymer network that interconnects and transiently immobilizes biofilm cells. In addition, the biofilm matrix acts as an external digestive system by keeping extracellular enzymes close to the cells, enabling them to metabolize dissolved, colloidal and solid biopolymers. Here we describe the functions, properties and constituents of the EPS matrix that make biofilms the most successful forms of life on earth.
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            Aminoglycoside antibiotics induce bacterial biofilm formation.

            Biofilms are adherent aggregates of bacterial cells that form on biotic and abiotic surfaces, including human tissues. Biofilms resist antibiotic treatment and contribute to bacterial persistence in chronic infections. Hence, the elucidation of the mechanisms by which biofilms are formed may assist in the treatment of chronic infections, such as Pseudomonas aeruginosa in the airways of patients with cystic fibrosis. Here we show that subinhibitory concentrations of aminoglycoside antibiotics induce biofilm formation in P. aeruginosa and Escherichia coli. In P. aeruginosa, a gene, which we designated aminoglycoside response regulator (arr), was essential for this induction and contributed to biofilm-specific aminoglycoside resistance. The arr gene is predicted to encode an inner-membrane phosphodiesterase whose substrate is cyclic di-guanosine monophosphate (c-di-GMP)-a bacterial second messenger that regulates cell surface adhesiveness. We found that membranes from arr mutants had diminished c-di-GMP phosphodiesterase activity, and P. aeruginosa cells with a mutation changing a predicted catalytic residue of Arr were defective in their biofilm response to tobramycin. Furthermore, tobramycin-inducible biofilm formation was inhibited by exogenous GTP, which is known to inhibit c-di-GMP phosphodiesterase activity. Our results demonstrate that biofilm formation can be a specific, defensive reaction to the presence of antibiotics, and indicate that the molecular basis of this response includes alterations in the level of c-di-GMP.
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              Critical review on biofilm methods.

              Biofilms are widespread in nature and constitute an important strategy implemented by microorganisms to survive in sometimes harsh environmental conditions. They can be beneficial or have a negative impact particularly when formed in industrial settings or on medical devices. As such, research into the formation and elimination of biofilms is important for many disciplines. Several new methodologies have been recently developed for, or adapted to, biofilm studies that have contributed to deeper knowledge on biofilm physiology, structure and composition. In this review, traditional and cutting-edge methods to study biofilm biomass, viability, structure, composition and physiology are addressed. Moreover, as there is a lack of consensus among the diversity of techniques used to grow and study biofilms. This review intends to remedy this, by giving a critical perspective, highlighting the advantages and limitations of several methods. Accordingly, this review aims at helping scientists in finding the most appropriate and up-to-date methods to study their biofilms.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/1100144/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                Role: Role:
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                Role:
                URI : https://loop.frontiersin.org/people/1277604/overviewRole: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/176610/overviewRole: Role: Role: Role:
                URI : https://loop.frontiersin.org/people/1188574/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                07 February 2024
                2023
                : 14
                : 1309032
                Affiliations
                [1] 1Department of Marine Sciences, University of Gothenburg , Gothenburg, Sweden
                [2] 2Bacteriology and Parasitology of Fishery and Aquaculture Products Unit, Laboratory for Food Safety, ANSES , Boulogne-sur-Mer, France
                [3] 3College of Science and Engineering, Flinders University , Adelaide, SA, Australia
                [4] 4ARC Training Centre for Biofilm Research and Innovation, Flinders University , Adelaide, SA, Australia
                [5] 5Flinders Institute for NanoScale Science and Technology, Flinders University , Adelaide, SA, Australia
                [6] 6Flinders Health and Medical Research Institute (FHMRI), College of Medicine and Public Health, Flinders University , Adelaide, SA, Australia
                [7] 7Agriculture and Agri-Food Canada, Kentville Research and Development Centre , Kentville, NS, Canada
                Author notes

                Edited by: Andrew Spiers, Abertay University, United Kingdom

                Reviewed by: Luis F. Melo, University of Porto, Portugal

                Srishti Baid, University of Michigan, United States

                *Correspondence: Thomas Brauge, thomas.brauge@ 123456anses.fr
                Article
                10.3389/fmicb.2023.1309032
                10897976
                38414711
                05ea1606-d90a-4848-8050-3b2b881276dc
                Copyright © 2024 Mougin, Midelet, Leterme, Best, Ells, Joyce, Whiley and Brauge.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 07 October 2023
                : 18 December 2023
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 57, Pages: 13, Words: 10383
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the embassy of France in Australia and Swedish Research Council FORMAS (Joyce 2017-00242). TB acknowledges the receipt of a fellowship from the OECD Co-operative Research Program: Sustainable Agricultural and Food Systems in 2023 (TAD/CRP PO 500120218). JM acknowledges the receipt of Swedish Foundation for International Cooperation in Research and Higher Education – Mobility Grant for Internationalization (STINT Mougin MG2022-9379).
                Categories
                Microbiology
                Original Research
                Custom metadata
                Infectious Agents and Disease

                Microbiology & Virology
                benzalkonium chloride,biocide,vibrio,biofilm,viability,c-di-gmp,seafood,aquaculture
                Microbiology & Virology
                benzalkonium chloride, biocide, vibrio, biofilm, viability, c-di-gmp, seafood, aquaculture

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