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In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus

As d-amino acids play important roles in the physiological metabolism of bacteria, combination of d-amino acids with antibiotics may provide synergistic antibacterial activity. The aim of the study was to evaluate in vitro and in vivo activity of d-serine alone and in combination with β-lactams agai...

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Autores principales: Wang, Qing, Lv, Yuemeng, Pang, Jing, Li, Xue, Lu, Xi, Wang, Xiukun, Hu, Xinxin, Nie, Tongying, Yang, Xinyi, Xiong, Yan Q., Jiang, Jiandong, Li, Congran, You, Xuefu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543093/
https://www.ncbi.nlm.nih.gov/pubmed/31193801
http://dx.doi.org/10.1016/j.apsb.2019.01.017
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author Wang, Qing
Lv, Yuemeng
Pang, Jing
Li, Xue
Lu, Xi
Wang, Xiukun
Hu, Xinxin
Nie, Tongying
Yang, Xinyi
Xiong, Yan Q.
Jiang, Jiandong
Li, Congran
You, Xuefu
author_facet Wang, Qing
Lv, Yuemeng
Pang, Jing
Li, Xue
Lu, Xi
Wang, Xiukun
Hu, Xinxin
Nie, Tongying
Yang, Xinyi
Xiong, Yan Q.
Jiang, Jiandong
Li, Congran
You, Xuefu
author_sort Wang, Qing
collection PubMed
description As d-amino acids play important roles in the physiological metabolism of bacteria, combination of d-amino acids with antibiotics may provide synergistic antibacterial activity. The aim of the study was to evaluate in vitro and in vivo activity of d-serine alone and in combination with β-lactams against methicillin-resistant Staphylococcus aureus (MRSA) strains, and to explore the possible sensitization mechanisms. The activity of d-serine, β-lactams alone and in combinations was evaluated both in vitro by standard MICs, time–kill curves and checkerboard assays, and in vivo by murine systemic infection model as well as neutropenic thigh infection model. An in vitro synergistic effect was demonstrated with the combination of d-serine and β-lactams against MRSA standard and clinical strains. Importantly, the combinations enhanced the therapeutic efficacy in the animal models as compared to β-lactam alone groups. Initial mechanism study suggested possible revision of d-alanine-d-alanine residue to d-alanine-d-serine in peptidoglycan by adding of d-alanine in the medium, which may cause decreased affinity to PBPs during transpeptidation. In conclusion, d-serine had synergistic activity in combination with β-lactams against MRSA strains both in vitro and in vivo. Considering the relatively good safety of d-serine alone or in combination with β-lactams, d-serine is worth following up as new anti-MRSA infection strategies.
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spelling pubmed-65430932019-06-03 In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus Wang, Qing Lv, Yuemeng Pang, Jing Li, Xue Lu, Xi Wang, Xiukun Hu, Xinxin Nie, Tongying Yang, Xinyi Xiong, Yan Q. Jiang, Jiandong Li, Congran You, Xuefu Acta Pharm Sin B Original article As d-amino acids play important roles in the physiological metabolism of bacteria, combination of d-amino acids with antibiotics may provide synergistic antibacterial activity. The aim of the study was to evaluate in vitro and in vivo activity of d-serine alone and in combination with β-lactams against methicillin-resistant Staphylococcus aureus (MRSA) strains, and to explore the possible sensitization mechanisms. The activity of d-serine, β-lactams alone and in combinations was evaluated both in vitro by standard MICs, time–kill curves and checkerboard assays, and in vivo by murine systemic infection model as well as neutropenic thigh infection model. An in vitro synergistic effect was demonstrated with the combination of d-serine and β-lactams against MRSA standard and clinical strains. Importantly, the combinations enhanced the therapeutic efficacy in the animal models as compared to β-lactam alone groups. Initial mechanism study suggested possible revision of d-alanine-d-alanine residue to d-alanine-d-serine in peptidoglycan by adding of d-alanine in the medium, which may cause decreased affinity to PBPs during transpeptidation. In conclusion, d-serine had synergistic activity in combination with β-lactams against MRSA strains both in vitro and in vivo. Considering the relatively good safety of d-serine alone or in combination with β-lactams, d-serine is worth following up as new anti-MRSA infection strategies. Elsevier 2019-05 2019-01-31 /pmc/articles/PMC6543093/ /pubmed/31193801 http://dx.doi.org/10.1016/j.apsb.2019.01.017 Text en © 2019 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Wang, Qing
Lv, Yuemeng
Pang, Jing
Li, Xue
Lu, Xi
Wang, Xiukun
Hu, Xinxin
Nie, Tongying
Yang, Xinyi
Xiong, Yan Q.
Jiang, Jiandong
Li, Congran
You, Xuefu
In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title_full In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title_fullStr In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title_full_unstemmed In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title_short In vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant Staphylococcus aureus
title_sort in vitro and in vivo activity of d-serine in combination with β-lactam antibiotics against methicillin-resistant staphylococcus aureus
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543093/
https://www.ncbi.nlm.nih.gov/pubmed/31193801
http://dx.doi.org/10.1016/j.apsb.2019.01.017
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