The role of dysbiotic gut mycobiota in modulating risk for abdominal aortic aneurysm

Guixiang Yao1, Xinjie Zhang2, Tongxue Zhang1

  • 1State Key Laboratory for Innovation and Transformation of Luobing Theory, Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education, Chinese National Health Commission and Chinese Academy of Medical Sciences, Department of Cardiology, Qilu Hospital of Shandong University, Jinan, China.

Microbiology Spectrum
|September 24, 2024
PubMed

Insights

Gut fungi play a key role in abdominal aortic aneurysm (AAA). Researchers found altered fungal communities in AAA patients, with beneficial yeast slowing disease progression in mice, suggesting new diagnostic and therapeutic strategies.

Area of Science:

  • Vascular Biology
  • Microbiome Research
  • Medical Mycology

Background:

  • Abdominal aortic aneurysm (AAA) is a life-threatening vascular disease with complex causes and limited treatments.
  • The role of the gut mycobiome (fungal community) in AAA pathogenesis is largely unknown.
  • Gut fungi are integral to the host microbiome, influencing various physiological processes.

Purpose of the Study:

  • To investigate the alterations in gut fungal communities associated with AAA.
  • To explore the potential diagnostic and therapeutic roles of gut fungi in AAA.
  • To determine if specific fungal species influence AAA development and progression.

Main Methods:

  • Metagenomic sequencing of fecal samples from 31 healthy individuals and 33 AAA patients.
  • Correlation analysis between fungal populations and clinical AAA indicators.
  • In vivo experiments using AAA mouse models supplemented with *Saccharomyces cerevisiae*.

Main Results:

  • Significant gut mycobiome dysbiosis observed in AAA patients compared to controls.
  • Increased abundance of pathogenic *Candida* species and decreased *Saccharomyces cerevisiae* in AAA patients.
  • *Saccharomyces cerevisiae* supplementation ameliorated pathological changes in AAA mouse models, indicating a protective effect.

Conclusions:

  • Gut fungal dysbiosis is strongly associated with AAA development and severity.
  • Specific gut fungi, like *Saccharomyces cerevisiae*, may offer protective benefits against AAA.
  • Modulating the gut mycobiome presents a potential novel non-surgical strategy for AAA diagnosis and treatment.

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