Bacterial-fungal interactions and their impact on microbial pathogenesis.
Jessie MacAlpineNicole RobbinsLeah E CowenPublished in: Molecular ecology (2022)
Microbial communities of the human microbiota exhibit diverse effects on human health and disease. Microbial homeostasis is important for normal physiological functions and changes to the microbiota are associated with many human diseases including diabetes, cancer, and colitis. In addition, there are many microorganisms that are either commensal or acquired from environmental reservoirs that can cause diverse pathologies. Importantly, the balance between health and disease is intricately connected to how members of the microbiota interact and affect one another's growth and pathogenicity. However, the mechanisms that govern these interactions are only beginning to be understood. In this review, we outline bacterial-fungal interactions in the human body, including examining the mechanisms by which bacteria govern fungal growth and virulence, as well as how fungi regulate bacterial pathogenesis. We summarize advances in the understanding of chemical, physical, and protein-based interactions, and their role in exacerbating or impeding human disease. We focus on the three fungal species responsible for the majority of systemic fungal infections in humans: Candida albicans, Cryptococcus neoformans, and Aspergillus fumigatus. We conclude by summarizing recent studies that have mined microbes for novel antimicrobials and antivirulence factors, highlighting the potential of the human microbiota as a rich resource for small molecule discovery.
Keyphrases
- endothelial cells
- small molecule
- human health
- induced pluripotent stem cells
- candida albicans
- healthcare
- pluripotent stem cells
- type diabetes
- public health
- biofilm formation
- microbial community
- metabolic syndrome
- squamous cell carcinoma
- staphylococcus aureus
- pseudomonas aeruginosa
- cardiovascular disease
- cystic fibrosis
- young adults
- adipose tissue
- glycemic control
- skeletal muscle
- social media
- life cycle
- genetic diversity