A bacteriocin-based treatment option for Staphylococcus haemolyticus biofilms
العنوان: | A bacteriocin-based treatment option for Staphylococcus haemolyticus biofilms |
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المؤلفون: | Mikkel Brønner, Sofie S. Kristensen, Geir Mathiesen, Aparna Srikantam, Jorunn Pauline Cavanagh, Dzung B. Diep, Karolina T. Bartkiewicz, Christian Kranjec |
المصدر: | Scientific Reports Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021) |
سنة النشر: | 2021 |
مصطلحات موضوعية: | Molecular biology, medicine.medical_treatment, Science, Antimicrobial peptides, Microbial Sensitivity Tests, medicine.disease_cause, Models, Biological, Article, Microbiology, 03 medical and health sciences, Bacteriocin, Anti-Infective Agents, Bacteriocins, Drug Resistance, Bacterial, medicine, VDP::Medisinske Fag: 700, Amino Acid Sequence, 030304 developmental biology, 0303 health sciences, Multidisciplinary, Protease, biology, Whole Genome Sequencing, 030306 microbiology, Antimicrobials, Biofilm, Treatment options, food and beverages, biochemical phenomena, metabolism, and nutrition, biology.organism_classification, Staphylococcus haemolyticus, In vitro, VDP::Medical disciplines: 700, Genes, Bacterial, Biofilms, Mutation, Medicine, bacteria, Pathogens, Staphylococcus |
الوصف: | Bacteriocins are ribosomally-synthesized antimicrobial peptides, showing great potential as novel treatment options for multidrug-resistant pathogens. In this study, we designed a novel hybrid bacteriocin, Hybrid 1 (H1), by combing the N-terminal part and the C-terminal part of the related bacteriocins enterocin K1 (K1) and enterocin EJ97 (EJ97), respectively. Like the parental bacteriocins, H1 used the membrane-bound protease RseP as receptor, however, it differed from the others in the inhibition spectrum. Most notably, H1 showed a superior antimicrobial effect towards Staphylococcus haemolyticus—an important nosocomial pathogen. To avoid strain-dependency, we further evaluated H1 against 27 clinical and commensal S. haemolyticus strains, with H1 indeed showing high activity towards all strains. To curtail the rise of resistant mutants and further explore the potential of H1 as a therapeutic agent, we designed a bacteriocin-based formulation where H1 was used in combination with the broad-spectrum bacteriocins micrococcin P1 and garvicin KS. Unlike the individual bacteriocins, the three-component combination was highly effective against planktonic cells and completely eradicated biofilm-associated S. haemolyticus cells in vitro. Most importantly, the formulation efficiently prevented development of resistant mutants as well. These findings indicate the potential of a bacteriocins-based formulation as a treatment option for S. haemolyticus. |
وصف الملف: | application/pdf |
اللغة: | English |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93a5d7e36034e0cd3735b9311e2a6eb5 https://hdl.handle.net/11250/2774804 |
Rights: | OPEN |
رقم الانضمام: | edsair.doi.dedup.....93a5d7e36034e0cd3735b9311e2a6eb5 |
قاعدة البيانات: | OpenAIRE |
الوصف غير متاح. |