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      Antibiofilm assay for antimicrobial peptides combating the sulfate‐reducing bacteria Desulfovibrio vulgaris

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          Abstract

          In medical, environmental, and industrial processes, the accumulation of bacteria in biofilms can disrupt many processes. Antimicrobial peptides (AMPs) are receiving increasing attention in the development of new substances to avoid or reduce biofilm formation. There is a lack of parallel testing of the effect against biofilms in this area, as well as in the testing of other antibiofilm agents. In this paper, a high‐throughput screening was developed for the analysis of the antibiofilm activity of AMPs, differentiated into inhibition and removal of a biofilm. The sulfate‐reducing bacterium Desulfovibrio vulgaris was used as a model organism.  D. vulgaris represents an undesirable bacterium, which is considered one of the major triggers of microbiologically influenced corrosion. The application of a 96‐well plate and steel rivets as a growth surface realizes real‐life conditions and at the same time establishes a flexible, simple, fast, and cost‐effective assay. All peptides tested in this study demonstrated antibiofilm activity, although these peptides should be individually selected depending on the addressed aim. For biofilm inhibition, the peptide DASamP1 is the most suitable, with a sustained effect for up to 21 days. The preferred peptides for biofilm removal are S6L3‐33, in regard to bacteria reduction, and Bactenecin, regarding total biomass reduction.

          Abstract

          This study aimed to develop a fast and realistic antibiofilm assay for screening antimicrobial peptides (AMPs) for biocorrosive bacteria. Effective AMPs for both inhibition and removal of the biofilm could be identified and long‐term inhibition of biofilm was possible for up to 21 days.

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          Most cited references38

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          Antimicrobial Resistance in ESKAPE Pathogens

          Antimicrobial-resistant ESKAPE ( E nterococcus faecium , S taphylococcus aureus , K lebsiella pneumoniae , A cinetobacter baumannii , P seudomonas aeruginosa , and E nterobacter species) pathogens represent a global threat to human health. The acquisition of antimicrobial resistance genes by ESKAPE pathogens has reduced the treatment options for serious infections, increased the burden of disease, and increased death rates due to treatment failure and requires a coordinated global response for antimicrobial resistance surveillance. This looming health threat has restimulated interest in the development of new antimicrobial therapies, has demanded the need for better patient care, and has facilitated heightened governance over stewardship practices.
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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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              The Calgary Biofilm Device: new technology for rapid determination of antibiotic susceptibilities of bacterial biofilms.

              Determination of the MIC, based on the activities of antibiotics against planktonic bacteria, is the standard assay for antibiotic susceptibility testing. Adherent bacterial populations (biofilms) present with an innate lack of antibiotic susceptibility not seen in the same bacteria grown as planktonic populations. The Calgary Biofilm Device (CBD) is described as a new technology for the rapid and reproducible assay of biofilm susceptibilities to antibiotics. The CBD produces 96 equivalent biofilms for the assay of antibiotic susceptibilities by the standard 96-well technology. Biofilm formation was followed by quantitative microbiology and scanning electron microscopy. Susceptibility to a standard group of antibiotics was determined for National Committee for Clinical Laboratory Standards (NCCLS) reference strains: Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and Staphylococcus aureus ATCC 29213. Growth curves demonstrated that biofilms of a predetermined size could be formed on the CBD at specific time points and, furthermore, that no significant difference (P > 0.1) was seen between biofilms formed on each of the 96 pegs. The antibiotic susceptibilities for planktonic populations obtained by the NCCLS method or from the CBD were similar. Minimal biofilm eradication concentrations, derived by using the CBD, demonstrated that for biofilms of the same organisms, 100 to 1,000 times the concentration of a certain antibiotic were often required for the antibiotic to be effective, while other antibiotics were found to be effective at the MICs. The CBD offers a new technology for the rational selection of antibiotics effective against microbial biofilms and for the screening of new effective antibiotic compounds.
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                Author and article information

                Contributors
                dirk.holtmann@lse.thm.de
                Journal
                Microbiologyopen
                Microbiologyopen
                10.1002/(ISSN)2045-8827
                MBO3
                MicrobiologyOpen
                John Wiley and Sons Inc. (Hoboken )
                2045-8827
                21 August 2023
                August 2023
                : 12
                : 4 ( doiID: 10.1002/mbo3.v12.4 )
                : e1376
                Affiliations
                [ 1 ] Institute of Bioprocess Engineering and Pharmaceutical Technology University of Applied Sciences Mittelhessen Giessen Germany
                [ 2 ] Institute of Process Engineering in Life Sciences Karlsruhe Institute of Technology Karlsruhe Germany
                [ 3 ] Institute of Pharmaceutical Technology and Biopharmacy Philipps‐University Marburg Marburg Germany
                Author notes
                [*] [* ] Correspondence Dirk, Holtmann, Institute of Bioprocess Engineering and Pharmaceutical Technology, University of Applied Sciences Mittelhessen, Wiesenstraße 14, 35390 Giessen, Germany.

                Email: dirk.holtmann@ 123456lse.thm.de

                Author information
                http://orcid.org/0000-0001-5540-3550
                Article
                MBO31376
                10.1002/mbo3.1376
                10441178
                7c284b3f-b601-46b5-bffd-2d9f28b8a175
                © 2023 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 July 2023
                : 24 May 2023
                : 09 August 2023
                Page count
                Figures: 10, Tables: 4, Pages: 16, Words: 6604
                Funding
                Funded by: Allianz Industrie Forschung , doi 10.13039/501100002723;
                Award ID: IGF Number 21670N
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                August 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.3 mode:remove_FC converted:21.08.2023

                Microbiology & Virology
                antimicrobial peptides,biocorrosion,biofilm,biofilm monitoring,desulfovibrio vulgaris

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