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<p>Diseases are emerging at unprecedented rates, prompting global efforts to understand factors shaping disease outcomes. Microbes associated with hosts and the environment influence disease by secreting antipathogenic metabolites, hindering pathogen success. However, antibiotic contamination and costs associated with microbial responses to antibiotics may reduce antipathogenic efficacy. We investigated how antibiotic tolerance influences the antipathogenic properties of metabolites produced by <i>Pseudomonas aeruginosa</i> using in vitro and in vivo experiments. We found that metabolites from antibiotic-non-tolerant <i>P. aeruginosa</i> strains retained their antipathogenic properties and inhibited the growth of <i>Batrachochytrium dendrobatidis</i> <i>(</i><i>Bd</i><i>)</i>, an amphibian fungal pathogen responsible for amphibian declines worldwide. In contrast, metabolites from <i>P. aeruginosa</i> strains that developed antibiotic tolerance promoted <i>Bd</i> growth and exacerbated infection severity. These patterns were consistent in vitro and in vivo. We also ran toxicological and small molecule analyses of microbial metabolites, and findings suggest the divergent experimental outcomes may stem from differences in metabolite toxicity and profiles between strains. These findings underscore the hidden consequences of interactions between microbial responses to environmental changes and pathogens on infectious disease dynamics and highlight the need to integrate environmental change and eco-evolutionary perspectives into disease research.</p>

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Microbial responses to antibiotics cryptically shift the direction of disease outcomes

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年7月2日

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  • Isabela Velasquez,
  • Kyra Ricci,
  • Eve Milusich,
  • Bryon F. Tuthill II,
  • Karin Sauer,
  • Obed Hernández-Gómez,
  • Jessica Hua

摘要

Diseases are emerging at unprecedented rates, prompting global efforts to understand factors shaping disease outcomes. Microbes associated with hosts and the environment influence disease by secreting antipathogenic metabolites, hindering pathogen success. However, antibiotic contamination and costs associated with microbial responses to antibiotics may reduce antipathogenic efficacy. We investigated how antibiotic tolerance influences the antipathogenic properties of metabolites produced by Pseudomonas aeruginosa using in vitro and in vivo experiments. We found that metabolites from antibiotic-non-tolerant P. aeruginosa strains retained their antipathogenic properties and inhibited the growth of Batrachochytrium dendrobatidis (Bd), an amphibian fungal pathogen responsible for amphibian declines worldwide. In contrast, metabolites from P. aeruginosa strains that developed antibiotic tolerance promoted Bd growth and exacerbated infection severity. These patterns were consistent in vitro and in vivo. We also ran toxicological and small molecule analyses of microbial metabolites, and findings suggest the divergent experimental outcomes may stem from differences in metabolite toxicity and profiles between strains. These findings underscore the hidden consequences of interactions between microbial responses to environmental changes and pathogens on infectious disease dynamics and highlight the need to integrate environmental change and eco-evolutionary perspectives into disease research.