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The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo

Staphylococcus aureus and Staphylococcus epidermidis are associated with life-threatening infections. Despite the best medical care, these infections frequently occur due to antibiotic resistance and the formation of biofilms of these two bacteria (i.e., clusters of bacteria embedded in a matrix). A...

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Autores principales: Kaul, Laurine, Abdo, Adrian I., Coenye, Tom, Krom, Bastiaan P., Hoogenkamp, Michel A., Zannettino, Andrew C. W., Süss, Regine, Richter, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500474/
https://www.ncbi.nlm.nih.gov/pubmed/36160243
http://dx.doi.org/10.3389/fmicb.2022.999893
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author Kaul, Laurine
Abdo, Adrian I.
Coenye, Tom
Krom, Bastiaan P.
Hoogenkamp, Michel A.
Zannettino, Andrew C. W.
Süss, Regine
Richter, Katharina
author_facet Kaul, Laurine
Abdo, Adrian I.
Coenye, Tom
Krom, Bastiaan P.
Hoogenkamp, Michel A.
Zannettino, Andrew C. W.
Süss, Regine
Richter, Katharina
author_sort Kaul, Laurine
collection PubMed
description Staphylococcus aureus and Staphylococcus epidermidis are associated with life-threatening infections. Despite the best medical care, these infections frequently occur due to antibiotic resistance and the formation of biofilms of these two bacteria (i.e., clusters of bacteria embedded in a matrix). As a consequence, there is an urgent need for effective anti-biofilm treatments. Here, we describe the antibacterial properties of a combination treatment of diethyldithiocarbamate (DDC) and copper ions (Cu(2+)) and their low toxicity in vitro and in vivo. The antibacterial activity of DDC and Cu(2+) was assessed in vitro against both planktonic and biofilm cultures of S. aureus and S. epidermidis using viability assays, microscopy, and attachment assays. Cytotoxicity of DDC and Cu(2+) (DDC-Cu(2+)) was determined using a human fibroblast cell line. In vivo antimicrobial activity and toxicity were monitored in Galleria mellonella larvae. DDC-Cu(2+) concentrations of 8 μg/ml DDC and 32 μg/ml Cu(2+) resulted in over 80% MRSA and S. epidermidis biofilm killing, showed synergistic and additive effects in both planktonic and biofilm cultures of S. aureus and S. epidermidis, and synergized multiple antibiotics. DDC-Cu(2+) inhibited MRSA and S. epidermidis attachment and biofilm formation in the xCELLigence and Bioflux systems. In vitro and in vivo toxicity of DDC, Cu(2+) and DDC-Cu(2+) resulted in > 70% fibroblast viability and > 90% G. mellonella survival. Treatment with DDC-Cu(2+) significantly increased the survival of infected larvae (87% survival of infected, treated larvae vs. 47% survival of infected, untreated larvae, p < 0.001). Therefore, DDC-Cu(2+) is a promising new antimicrobial with activity against planktonic and biofilm cultures of S. epidermidis and S. aureus and low cytotoxicity in vitro. This gives us high confidence to progress to mammalian animal studies, testing the antimicrobial efficacy and safety of DDC-Cu(2+).
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spelling pubmed-95004742022-09-24 The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo Kaul, Laurine Abdo, Adrian I. Coenye, Tom Krom, Bastiaan P. Hoogenkamp, Michel A. Zannettino, Andrew C. W. Süss, Regine Richter, Katharina Front Microbiol Microbiology Staphylococcus aureus and Staphylococcus epidermidis are associated with life-threatening infections. Despite the best medical care, these infections frequently occur due to antibiotic resistance and the formation of biofilms of these two bacteria (i.e., clusters of bacteria embedded in a matrix). As a consequence, there is an urgent need for effective anti-biofilm treatments. Here, we describe the antibacterial properties of a combination treatment of diethyldithiocarbamate (DDC) and copper ions (Cu(2+)) and their low toxicity in vitro and in vivo. The antibacterial activity of DDC and Cu(2+) was assessed in vitro against both planktonic and biofilm cultures of S. aureus and S. epidermidis using viability assays, microscopy, and attachment assays. Cytotoxicity of DDC and Cu(2+) (DDC-Cu(2+)) was determined using a human fibroblast cell line. In vivo antimicrobial activity and toxicity were monitored in Galleria mellonella larvae. DDC-Cu(2+) concentrations of 8 μg/ml DDC and 32 μg/ml Cu(2+) resulted in over 80% MRSA and S. epidermidis biofilm killing, showed synergistic and additive effects in both planktonic and biofilm cultures of S. aureus and S. epidermidis, and synergized multiple antibiotics. DDC-Cu(2+) inhibited MRSA and S. epidermidis attachment and biofilm formation in the xCELLigence and Bioflux systems. In vitro and in vivo toxicity of DDC, Cu(2+) and DDC-Cu(2+) resulted in > 70% fibroblast viability and > 90% G. mellonella survival. Treatment with DDC-Cu(2+) significantly increased the survival of infected larvae (87% survival of infected, treated larvae vs. 47% survival of infected, untreated larvae, p < 0.001). Therefore, DDC-Cu(2+) is a promising new antimicrobial with activity against planktonic and biofilm cultures of S. epidermidis and S. aureus and low cytotoxicity in vitro. This gives us high confidence to progress to mammalian animal studies, testing the antimicrobial efficacy and safety of DDC-Cu(2+). Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9500474/ /pubmed/36160243 http://dx.doi.org/10.3389/fmicb.2022.999893 Text en Copyright © 2022 Kaul, Abdo, Coenye, Krom, Hoogenkamp, Zannettino, Süss and Richter. https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Microbiology
Kaul, Laurine
Abdo, Adrian I.
Coenye, Tom
Krom, Bastiaan P.
Hoogenkamp, Michel A.
Zannettino, Andrew C. W.
Süss, Regine
Richter, Katharina
The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title_full The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title_fullStr The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title_full_unstemmed The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title_short The combination of diethyldithiocarbamate and copper ions is active against Staphylococcus aureus and Staphylococcus epidermidis biofilms in vitro and in vivo
title_sort combination of diethyldithiocarbamate and copper ions is active against staphylococcus aureus and staphylococcus epidermidis biofilms in vitro and in vivo
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9500474/
https://www.ncbi.nlm.nih.gov/pubmed/36160243
http://dx.doi.org/10.3389/fmicb.2022.999893
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