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Background <p>Butyrate and pyruvate are central metabolites in anaerobic microbial metabolism, with key roles in gastrointestinal physiology. We recently identified <i>Fusobacterium nucleatum</i> (<i>F. nucleatum</i>) and <i>Neisseria subflava</i> (<i>N. subflava</i>) as non-<i>Helicobacter pylori</i> (<i>H. pylori</i>) bacteria potentially involved in gastric cancer development. However, the metabolic pathways distinguishing <i>F. nucleatum</i>, <i>N. subflava</i>, and <i>H. pylori</i> remain poorly characterized.</p> Methods <p>We performed capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS) to profile the metabolic outputs of these three species under isolated culture conditions.</p> Results <p>Distinct metabolic signatures were observed: <i>F. nucleatum</i> predominantly synthesized butyrate via the acetyl-CoA pathway, whereas <i>N. subflava</i> produced high levels of pyruvate and employed a cyclical route regenerating pyruvate from acetyl-CoA. In contrast, <i>H. pylori</i> lacked significant production of either metabolite.</p> Conclusions <p>This study delineates species-specific metabolic programs among gastric cancer-associated bacteria and highlights unique butyrate and pyruvate metabolism as a potential axis of microbe–host and microbe–microbe interaction in the gastric environment.</p>

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Gastric cancer-associated bacteria exhibit distinct butyrate and pyruvate metabolism: a metabolomic analysis of F. nucleatum, N. subflava, and H. pylori

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月12日

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  • Ryota Niikura,
  • Yoku Hayakawa,
  • Takahiro Mukai,
  • Yoichi Kato,
  • Naofumi Yoshida,
  • Mitsuhiro Fujishiro

摘要

Background

Butyrate and pyruvate are central metabolites in anaerobic microbial metabolism, with key roles in gastrointestinal physiology. We recently identified Fusobacterium nucleatum (F. nucleatum) and Neisseria subflava (N. subflava) as non-Helicobacter pylori (H. pylori) bacteria potentially involved in gastric cancer development. However, the metabolic pathways distinguishing F. nucleatum, N. subflava, and H. pylori remain poorly characterized.

Methods

We performed capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS) to profile the metabolic outputs of these three species under isolated culture conditions.

Results

Distinct metabolic signatures were observed: F. nucleatum predominantly synthesized butyrate via the acetyl-CoA pathway, whereas N. subflava produced high levels of pyruvate and employed a cyclical route regenerating pyruvate from acetyl-CoA. In contrast, H. pylori lacked significant production of either metabolite.

Conclusions

This study delineates species-specific metabolic programs among gastric cancer-associated bacteria and highlights unique butyrate and pyruvate metabolism as a potential axis of microbe–host and microbe–microbe interaction in the gastric environment.