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Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa

Combinations of human lysozyme (hLYS) and antimicrobial peptides (AMPs) are known to exhibit either additive or synergistic activity, and as a result, they have therapeutic potential for persistent and antibiotic‐resistant infections. We examined hLYS activity against Pseudomonas aeruginosa when com...

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Autores principales: Blumenthal, Ian, Davis, Lydia R., Berman, Chet M., Griswold, Karl E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931236/
https://www.ncbi.nlm.nih.gov/pubmed/33480189
http://dx.doi.org/10.1002/2211-5463.13094
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author Blumenthal, Ian
Davis, Lydia R.
Berman, Chet M.
Griswold, Karl E.
author_facet Blumenthal, Ian
Davis, Lydia R.
Berman, Chet M.
Griswold, Karl E.
author_sort Blumenthal, Ian
collection PubMed
description Combinations of human lysozyme (hLYS) and antimicrobial peptides (AMPs) are known to exhibit either additive or synergistic activity, and as a result, they have therapeutic potential for persistent and antibiotic‐resistant infections. We examined hLYS activity against Pseudomonas aeruginosa when combined with six different AMPs. In contrast to prior reports, we discovered that some therapeutically relevant AMPs manifest striking antagonistic interactions with hLYS across particular concentration ranges. We further found that the synthetic AMP Tet009 can inhibit hLYS‐mediated bacterial lysis. To the best of our knowledge, these results represent the first observations of antagonism between hLYS and AMPs, and they advise that future development of lytic enzyme and AMP combination therapies considers the potential for antagonistic interactions.
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spelling pubmed-79312362021-03-15 Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa Blumenthal, Ian Davis, Lydia R. Berman, Chet M. Griswold, Karl E. FEBS Open Bio Research Articles Combinations of human lysozyme (hLYS) and antimicrobial peptides (AMPs) are known to exhibit either additive or synergistic activity, and as a result, they have therapeutic potential for persistent and antibiotic‐resistant infections. We examined hLYS activity against Pseudomonas aeruginosa when combined with six different AMPs. In contrast to prior reports, we discovered that some therapeutically relevant AMPs manifest striking antagonistic interactions with hLYS across particular concentration ranges. We further found that the synthetic AMP Tet009 can inhibit hLYS‐mediated bacterial lysis. To the best of our knowledge, these results represent the first observations of antagonism between hLYS and AMPs, and they advise that future development of lytic enzyme and AMP combination therapies considers the potential for antagonistic interactions. John Wiley and Sons Inc. 2021-02-05 /pmc/articles/PMC7931236/ /pubmed/33480189 http://dx.doi.org/10.1002/2211-5463.13094 Text en © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. 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.
spellingShingle Research Articles
Blumenthal, Ian
Davis, Lydia R.
Berman, Chet M.
Griswold, Karl E.
Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title_full Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title_fullStr Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title_full_unstemmed Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title_short Nonclassical antagonism between human lysozyme and AMPs against Pseudomonas aeruginosa
title_sort nonclassical antagonism between human lysozyme and amps against pseudomonas aeruginosa
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931236/
https://www.ncbi.nlm.nih.gov/pubmed/33480189
http://dx.doi.org/10.1002/2211-5463.13094
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