Modulation of virulence and metabolic profiles in Klebsiella pneumoniae under indole-mediated stress response

Indole, a crucial bacterial signaling molecule, plays a fundamental role in regulating various physiological processes within bacteria, including growth, acid tolerance, biofilm development, motility, and other cellular functions. Its regulatory influence extends beyond indole-producing bacteria, significantly impacting the physiological activities in non-indole-producing species. In this study, we demonstrate that indole enhances the pathogenicity and viability of <i>Klebsiella pneumoniae</i> using the <i>Galleria mellonella</i> infection model and serum killing assay. Concurrently, indole has varying effects on biofilm formation in <i>K. pneumoniae</i>, with some strains showing enhanced biofilm formation ability. To elucidate the underlying molecular mechanisms, transcriptome analysis revealed that indole exposure in <i>K. pneumoniae</i> led to the upregulation of genes associated with pili formation and iron acquisition systems, while simultaneously inducing oxidative stress responses. Additionally, our analysis uncovered extensive metabolic remodeling. Specifically, we observed significant upregulation of genes involved in simple carbohydrate utilization pathways, including those responsible for galactose, mannose, and maltose metabolism, as well as enhanced expression of genes associated with pyrimidine biosynthesis. These findings collectively indicate that indole enhances the intestinal colonization and pathogenicity of <i>K. pneumoniae</i> primarily by modulation of fimbriae expression and metabolic pathway regulation.

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Publication Details

Journal
Frontiers in Cellular and Infection Microbiology
Published
2025-02-03
DOI
https://doi.org/10.3389/fcimb.2025.1546991
Citations
2
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
1.18

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article

Modulation of virulence and metabolic profiles in Klebsiella pneumoniae under indole-mediated stress response

Junqi Zhu, Yaping Hang, Xingwei Cao, Qiaoshi Zhong et al.
2 citations
Frontiers in Cellular and Infection Microbiology
Antibiotic Resistance in Bacteria
1.18
article

Modulation of virulence and metabolic profiles in Klebsiella pneumoniae under indole-mediated stress response

Junqi Zhu, Yaping Hang, Xingwei Cao, Qiaoshi Zhong, Xueyao Fang, Xiao Lin, Longhua Hu, Shumin Gu, Yanhui Chen, Hong Luo, Chuwen Zhao, Yanping Xiao
article en
2 citations

Abstract

Indole, a crucial bacterial signaling molecule, plays a fundamental role in regulating various physiological processes within bacteria, including growth, acid tolerance, biofilm development, motility, and other cellular functions. Its regulatory influence extends beyond indole-producing bacteria, significantly impacting the physiological activities in non-indole-producing species. In this study, we demonstrate that indole enhances the pathogenicity and viability of <i>Klebsiella pneumoniae</i> using the <i>Galleria mellonella</i> infection model and serum killing assay. Concurrently, indole has varying effects on biofilm formation in <i>K. pneumoniae</i>, with some strains showing enhanced biofilm formation ability. To elucidate the underlying molecular mechanisms, transcriptome analysis revealed that indole exposure in <i>K. pneumoniae</i> led to the upregulation of genes associated with pili formation and iron acquisition systems, while simultaneously inducing oxidative stress responses. Additionally, our analysis uncovered extensive metabolic remodeling. Specifically, we observed significant upregulation of genes involved in simple carbohydrate utilization pathways, including those responsible for galactose, mannose, and maltose metabolism, as well as enhanced expression of genes associated with pyrimidine biosynthesis. These findings collectively indicate that indole enhances the intestinal colonization and pathogenicity of <i>K. pneumoniae</i> primarily by modulation of fimbriae expression and metabolic pathway regulation.

Frontiers in Cellular and Infection MicrobiologyVol. 15
Nanchang University (CN), First Affiliated Hospital of Jiangxi Medical College (CN), Gansu Provincial Maternal and Child Health Hospital (CN)
National Taiwan University Hospital, Health Commission of Jiangxi Province
Life in Land
Openalex Percentile: Top 25%
Antibiotic Resistance in Bacteria
1.18
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