Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria
Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, c...
Ausführliche Beschreibung
Autor*in: |
Patrick R. Lennard [verfasserIn] Pieter S. Hiemstra [verfasserIn] Peter H. Nibbering [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Übergeordnetes Werk: |
In: Antibiotics - MDPI AG, 2013, 12(2023), 1518, p 1518 |
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Übergeordnetes Werk: |
volume:12 ; year:2023 ; number:1518, p 1518 |
Links: |
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DOI / URN: |
10.3390/antibiotics12101518 |
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Katalog-ID: |
DOAJ09318591X |
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10.3390/antibiotics12101518 doi (DE-627)DOAJ09318591X (DE-599)DOAJec6751889ac34d43b54f06de88c8bbf8 DE-627 ger DE-627 rakwb eng RM1-950 Patrick R. Lennard verfasserin aut Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. host defence peptide antimicrobial peptide antibiotics synergism antimicrobial resistance Therapeutics. Pharmacology Pieter S. Hiemstra verfasserin aut Peter H. Nibbering verfasserin aut In Antibiotics MDPI AG, 2013 12(2023), 1518, p 1518 (DE-627)726120596 (DE-600)2681345-2 20796382 nnns volume:12 year:2023 number:1518, p 1518 https://doi.org/10.3390/antibiotics12101518 kostenfrei https://doaj.org/article/ec6751889ac34d43b54f06de88c8bbf8 kostenfrei https://www.mdpi.com/2079-6382/12/10/1518 kostenfrei https://doaj.org/toc/2079-6382 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 1518, p 1518 |
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10.3390/antibiotics12101518 doi (DE-627)DOAJ09318591X (DE-599)DOAJec6751889ac34d43b54f06de88c8bbf8 DE-627 ger DE-627 rakwb eng RM1-950 Patrick R. Lennard verfasserin aut Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. host defence peptide antimicrobial peptide antibiotics synergism antimicrobial resistance Therapeutics. Pharmacology Pieter S. Hiemstra verfasserin aut Peter H. Nibbering verfasserin aut In Antibiotics MDPI AG, 2013 12(2023), 1518, p 1518 (DE-627)726120596 (DE-600)2681345-2 20796382 nnns volume:12 year:2023 number:1518, p 1518 https://doi.org/10.3390/antibiotics12101518 kostenfrei https://doaj.org/article/ec6751889ac34d43b54f06de88c8bbf8 kostenfrei https://www.mdpi.com/2079-6382/12/10/1518 kostenfrei https://doaj.org/toc/2079-6382 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 1518, p 1518 |
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10.3390/antibiotics12101518 doi (DE-627)DOAJ09318591X (DE-599)DOAJec6751889ac34d43b54f06de88c8bbf8 DE-627 ger DE-627 rakwb eng RM1-950 Patrick R. Lennard verfasserin aut Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. host defence peptide antimicrobial peptide antibiotics synergism antimicrobial resistance Therapeutics. Pharmacology Pieter S. Hiemstra verfasserin aut Peter H. Nibbering verfasserin aut In Antibiotics MDPI AG, 2013 12(2023), 1518, p 1518 (DE-627)726120596 (DE-600)2681345-2 20796382 nnns volume:12 year:2023 number:1518, p 1518 https://doi.org/10.3390/antibiotics12101518 kostenfrei https://doaj.org/article/ec6751889ac34d43b54f06de88c8bbf8 kostenfrei https://www.mdpi.com/2079-6382/12/10/1518 kostenfrei https://doaj.org/toc/2079-6382 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 1518, p 1518 |
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10.3390/antibiotics12101518 doi (DE-627)DOAJ09318591X (DE-599)DOAJec6751889ac34d43b54f06de88c8bbf8 DE-627 ger DE-627 rakwb eng RM1-950 Patrick R. Lennard verfasserin aut Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. host defence peptide antimicrobial peptide antibiotics synergism antimicrobial resistance Therapeutics. Pharmacology Pieter S. Hiemstra verfasserin aut Peter H. Nibbering verfasserin aut In Antibiotics MDPI AG, 2013 12(2023), 1518, p 1518 (DE-627)726120596 (DE-600)2681345-2 20796382 nnns volume:12 year:2023 number:1518, p 1518 https://doi.org/10.3390/antibiotics12101518 kostenfrei https://doaj.org/article/ec6751889ac34d43b54f06de88c8bbf8 kostenfrei https://www.mdpi.com/2079-6382/12/10/1518 kostenfrei https://doaj.org/toc/2079-6382 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 1518, p 1518 |
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Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria |
abstract |
Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. |
abstractGer |
Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. |
abstract_unstemmed |
Due to their ability to eliminate antimicrobial resistant (AMR) bacteria and to modulate the immune response, host defence peptides (HDPs) hold great promise for the clinical treatment of bacterial infections. Whereas monotherapy with HDPs is not likely to become an effective first-line treatment, combinations of such peptides with antibiotics can potentially provide a path to future therapies for AMR infections. Therefore, we critically reviewed the recent literature regarding the antibacterial activity of combinations of HDPs and antibiotics against AMR bacteria and the approaches taken in these studies. Of the 86 studies compiled, 56 featured a formal assessment of synergy between agents. Of the combinations assessed, synergistic and additive interactions between HDPs and antibiotics amounted to 84.9% of the records, while indifferent and antagonistic interactions accounted for 15.1%. Penicillin, aminoglycoside, fluoro/quinolone, and glycopeptide antibiotic classes were the most frequently documented as interacting with HDPs, and <i<Staphylococcus aureus</i<, <i<Pseudomonas aeruginosa</i<, <i<Escherichia coli</i<, and <i<Enterococcus faecium</i< were the most reported bacterial species. Few studies formally evaluated the effects of combinations of HDPs and antibiotics on bacteria, and even fewer assessed such combinations against bacteria within biofilms, in animal models, or in advanced tissue infection models. Despite the biases of the current literature, the studies suggest that effective combinations of HDPs and antibiotics hold promise for the future treatment of infections caused by AMR bacteria. |
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