DL-propargylglycine reverses beta-lactam resistance in Streptococcus agalactiae.

Fuente: PubMed
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Autores principales: Chen, Xuan-Wei, Zhang, Xiao-Lin, Wang, Zhi-Han, Wu, Jia-Yao, Tian, Si-Qi, Huang, Zi-Long, Peng, Bo
Formato: Artículo científico
Lenguaje:en
Publicado: Microbiological research 2026
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author Chen, Xuan-Wei
Zhang, Xiao-Lin
Wang, Zhi-Han
Wu, Jia-Yao
Tian, Si-Qi
Huang, Zi-Long
Peng, Bo
author_facet Chen, Xuan-Wei
Zhang, Xiao-Lin
Wang, Zhi-Han
Wu, Jia-Yao
Tian, Si-Qi
Huang, Zi-Long
Peng, Bo
Chen, Xuan-Wei
Zhang, Xiao-Lin
Wang, Zhi-Han
Wu, Jia-Yao
Tian, Si-Qi
Huang, Zi-Long
Peng, Bo
collection PubMed - marine biology
contents DL-propargylglycine reverses beta-lactam resistance in Streptococcus agalactiae. Chen, Xuan-Wei Zhang, Xiao-Lin Wang, Zhi-Han Wu, Jia-Yao Tian, Si-Qi Huang, Zi-Long Peng, Bo Alkynes Zebrafish Anti-Bacterial Agents Animals Streptococcus agalactiae beta-Lactam Resistance Glycine Biofilms Microbial Sensitivity Tests Streptococcal Infections beta-Lactams Cystathionine gamma-Lyase Drug Synergism Humans Streptococcus agalactiae (GBS) is a major pathogen causing severe infections in human and economic loss in animal farming, where β-lactams remain first-line therapy. However, emerging β-lactam resistance, including WHO-priority penicillin-resistant strains, threatens clinical efficacy, creating an urgent need for resistance-breaking adjuvants. In this study, we demonstrate that DL-Propargylglycine (PAG), an inhibitor of cystathionine-γ-lyase inhibitor, exclusively synergizes with β-lactams to reverse resistance in ampicillin-resistant GBS (AR-GBS) and other streptococci, overcoming tolerance in persisters and biofilms. Mechanistically, PAG potentiates antibiotic lethality through dual pathways: metabolic activation via enhanced central carbon metabolism for ROS production and cell envelope remodeling via concurrent downregulation of peptidoglycan biosynthesis genes and upregulation of capsular polysaccharide synthesis. This disrupts cell wall architecture, increases membrane permeability and accelerates antibiotic influx. While in vivo therapeutic efficacy in zebrafish was limited, PAG represents an adjuvant that overcomes β-lactam resistance through metabolic and membrane remodeling, paving the way for optimized derivatives.
format Artículo científico
id pubmed_41014824
institution PubMed
language en
publishDate 2026
publisher Microbiological research
record_format pubmed
spellingShingle DL-propargylglycine reverses beta-lactam resistance in Streptococcus agalactiae.
Chen, Xuan-Wei
Zhang, Xiao-Lin
Wang, Zhi-Han
Wu, Jia-Yao
Tian, Si-Qi
Huang, Zi-Long
Peng, Bo
Alkynes
Zebrafish
Anti-Bacterial Agents
Animals
Streptococcus agalactiae
beta-Lactam Resistance
Glycine
Biofilms
Microbial Sensitivity Tests
Streptococcal Infections
beta-Lactams
Cystathionine gamma-Lyase
Drug Synergism
Humans
DL-propargylglycine reverses beta-lactam resistance in Streptococcus agalactiae. Chen, Xuan-Wei Zhang, Xiao-Lin Wang, Zhi-Han Wu, Jia-Yao Tian, Si-Qi Huang, Zi-Long Peng, Bo Alkynes Zebrafish Anti-Bacterial Agents Animals Streptococcus agalactiae beta-Lactam Resistance Glycine Biofilms Microbial Sensitivity Tests Streptococcal Infections beta-Lactams Cystathionine gamma-Lyase Drug Synergism Humans Streptococcus agalactiae (GBS) is a major pathogen causing severe infections in human and economic loss in animal farming, where β-lactams remain first-line therapy. However, emerging β-lactam resistance, including WHO-priority penicillin-resistant strains, threatens clinical efficacy, creating an urgent need for resistance-breaking adjuvants. In this study, we demonstrate that DL-Propargylglycine (PAG), an inhibitor of cystathionine-γ-lyase inhibitor, exclusively synergizes with β-lactams to reverse resistance in ampicillin-resistant GBS (AR-GBS) and other streptococci, overcoming tolerance in persisters and biofilms. Mechanistically, PAG potentiates antibiotic lethality through dual pathways: metabolic activation via enhanced central carbon metabolism for ROS production and cell envelope remodeling via concurrent downregulation of peptidoglycan biosynthesis genes and upregulation of capsular polysaccharide synthesis. This disrupts cell wall architecture, increases membrane permeability and accelerates antibiotic influx. While in vivo therapeutic efficacy in zebrafish was limited, PAG represents an adjuvant that overcomes β-lactam resistance through metabolic and membrane remodeling, paving the way for optimized derivatives.
title DL-propargylglycine reverses beta-lactam resistance in Streptococcus agalactiae.
topic Alkynes
Zebrafish
Anti-Bacterial Agents
Animals
Streptococcus agalactiae
beta-Lactam Resistance
Glycine
Biofilms
Microbial Sensitivity Tests
Streptococcal Infections
beta-Lactams
Cystathionine gamma-Lyase
Drug Synergism
Humans
url https://pubmed.ncbi.nlm.nih.gov/41014824/