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Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections
Despite the progress in surgical techniques and antibiotic prophylaxis, opportunistic wound infections with Bacillus cereus remain a public health problem. Secreted toxins are one of the main factors contributing to B. cereus pathogenicity. A promising strategy to treat such infections is to target...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612511/ https://www.ncbi.nlm.nih.gov/pubmed/35310821 http://dx.doi.org/10.1002/adtp.202100222 |
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author | Alhayek, Alaa Khan, Essak S. Schönauer, Esther Däinghaus, Tobias Shafiei, Roya Voos, Katrin Han, Mitchell K.L. Ducho, Christian Posselt, Gernot Wessler, Silja Brandstetter, Hans Haupenthal, Jörg del Campo, Aránzazu Hirsch, Anna K.H. |
author_facet | Alhayek, Alaa Khan, Essak S. Schönauer, Esther Däinghaus, Tobias Shafiei, Roya Voos, Katrin Han, Mitchell K.L. Ducho, Christian Posselt, Gernot Wessler, Silja Brandstetter, Hans Haupenthal, Jörg del Campo, Aránzazu Hirsch, Anna K.H. |
author_sort | Alhayek, Alaa |
collection | PubMed |
description | Despite the progress in surgical techniques and antibiotic prophylaxis, opportunistic wound infections with Bacillus cereus remain a public health problem. Secreted toxins are one of the main factors contributing to B. cereus pathogenicity. A promising strategy to treat such infections is to target these toxins and not the bacteria. Although the exoenzymes produced by B. cereus are thoroughly investigated, little is known about the role of B. cereus collagenases in wound infections. In this report, the collagenolytic activity of secreted collagenases (Col) is characterized in the B. cereus culture supernatant (csn) and its isolated recombinantly produced ColQ1 is characterized. The data reveals that ColQ1 causes damage on dermal collagen (COL). This results in gaps in the tissue, which might facilitate the spread of bacteria. The importance of B. cereus collagenases is also demonstrated in disease promotion using two inhibitors. Compound 2 shows high efficacy in peptidolytic, gelatinolytic, and COL degradation assays. It also preserves the fibrillar COLs in skin tissue challenged with ColQ1, as well as the viability of skin cells treated with B. cereus csn. A Galleria mellonella model highlights the significance of collagenase inhibition in vivo. |
format | Online Article Text |
id | pubmed-7612511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76125112022-03-18 Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections Alhayek, Alaa Khan, Essak S. Schönauer, Esther Däinghaus, Tobias Shafiei, Roya Voos, Katrin Han, Mitchell K.L. Ducho, Christian Posselt, Gernot Wessler, Silja Brandstetter, Hans Haupenthal, Jörg del Campo, Aránzazu Hirsch, Anna K.H. Adv Ther (Weinh) Article Despite the progress in surgical techniques and antibiotic prophylaxis, opportunistic wound infections with Bacillus cereus remain a public health problem. Secreted toxins are one of the main factors contributing to B. cereus pathogenicity. A promising strategy to treat such infections is to target these toxins and not the bacteria. Although the exoenzymes produced by B. cereus are thoroughly investigated, little is known about the role of B. cereus collagenases in wound infections. In this report, the collagenolytic activity of secreted collagenases (Col) is characterized in the B. cereus culture supernatant (csn) and its isolated recombinantly produced ColQ1 is characterized. The data reveals that ColQ1 causes damage on dermal collagen (COL). This results in gaps in the tissue, which might facilitate the spread of bacteria. The importance of B. cereus collagenases is also demonstrated in disease promotion using two inhibitors. Compound 2 shows high efficacy in peptidolytic, gelatinolytic, and COL degradation assays. It also preserves the fibrillar COLs in skin tissue challenged with ColQ1, as well as the viability of skin cells treated with B. cereus csn. A Galleria mellonella model highlights the significance of collagenase inhibition in vivo. 2022-03 2022-01-15 /pmc/articles/PMC7612511/ /pubmed/35310821 http://dx.doi.org/10.1002/adtp.202100222 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Alhayek, Alaa Khan, Essak S. Schönauer, Esther Däinghaus, Tobias Shafiei, Roya Voos, Katrin Han, Mitchell K.L. Ducho, Christian Posselt, Gernot Wessler, Silja Brandstetter, Hans Haupenthal, Jörg del Campo, Aránzazu Hirsch, Anna K.H. Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title | Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title_full | Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title_fullStr | Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title_full_unstemmed | Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title_short | Inhibition of Collagenase Q1 of Bacillus cereus as a Novel Antivirulence Strategy for the Treatment of Skin-Wound Infections |
title_sort | inhibition of collagenase q1 of bacillus cereus as a novel antivirulence strategy for the treatment of skin-wound infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612511/ https://www.ncbi.nlm.nih.gov/pubmed/35310821 http://dx.doi.org/10.1002/adtp.202100222 |
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