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Updated: Jun 12, 2025

Microbiota Analysis Using Two-step PCR and Next-generation 16S rRNA Gene Sequencing
Published on: October 15, 2019
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.
Abstract:
Abdominal aortic aneurysm (AAA) is a large-vessel disease with high mortality, characterized by complex pathogenic mechanisms. Current therapeutic approaches remain insufficient to halt its progression. Fungi are important members of the gut microbiota. However, their characteristic alterations and roles in AAA remain unclear. This study investigated the role of gut fungal communities in the development of AAA through metagenomic sequencing of fecal samples from 31 healthy individuals and 33 AAA patients. We observed significant dysbiosis in the gut mycobiomes of AAA patients compared to healthy individuals, characterized by an increase in pathogenic fungi like Candida species and a decrease in beneficial yeasts such as Saccharomyces cerevisiae. The changes in fungal populations correlated strongly with clinical indicators of AAA, highlighting their potential for diagnosing and predicting AAA progression. Furthermore, our animal experiments demonstrated that Saccharomyces cerevisiae significantly ameliorated pathological alterations in AAA mice, suggesting a protective role for specific yeast strains against AAA development. These findings underscore the significant impact of gut mycobiomes on AAA and suggest that modulating these fungal communities could offer a novel therapeutic approach. Our research advances the understanding of the influence of gut microbiome on vascular diseases and suggests potential non-surgical approaches for managing AAA. By elucidating the diagnostic and therapeutic potential of gut fungi in AAA, this study provided important clues for future clinical strategies and therapeutic developments in the field of vascular medicine.
Importance:
Our research highlights the crucial role of gut fungi in abdominal aortic aneurysm (AAA) development. By analyzing fecal samples from AAA patients and healthy controls, we discovered significant dysbiosis in gut fungal communities, characterized by an increase in harmful Candida species and a decrease in beneficial yeasts like Saccharomyces cerevisiae. This dysbiosis was correlated with the severity of AAA. Importantly, in animal experiments, supplementing with Saccharomyces cerevisiae significantly slowed AAA progression. These findings suggest that modulating gut fungi may offer a novel, non-surgical approach to the diagnosis and treatment of AAA, potentially reducing the need for invasive procedures.
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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