Abstract:Summary
Background
The role of the fungal microbiota in digestive diseases is poorly defined, but is becoming better understood due to advances in metagenomics.
Aim
To review the gastrointestinal fungal microbiota and its relationship with digestive diseases.
Methods
Search of the literature using PubMed and MEDLINE databases. Subject headings including ‘fungal‐bacterial interactions’, ‘mycotoxins’, ‘immunity to fungi’, ‘fungal infection’, ‘fungal microbiota’, ‘mycobiome’ and ‘digestive diseases’ were used.
Re… Show more
“…The predominant commensal fungal species in the human intestine are Candida species, Saccharomyces cerevisiae, and Malassezia species (9). Like commensal bacteria in the intestine, fungi interact with their host.…”
“…The predominant commensal fungal species in the human intestine are Candida species, Saccharomyces cerevisiae, and Malassezia species (9). Like commensal bacteria in the intestine, fungi interact with their host.…”
“…Specifically, whole-body perspectives of the human mycobiome are provided by Cui and colleagues, 10 Huffnagle and Noverr, 11 Seed, 12 and Underhill and Iliev, 13 while the gut mycobiota is reviewed by Ianiro and colleagues, 14 Kirschner and colleagues, 15 and Suhr and Hallen-Adams. 16 The role of the gut mycobiota in disease is reviewed by Moyes and Naglik, 17 Wang and colleagues, 18 Gouba and Drancourt, 19 Mukherjee and colleagues, 20 and Richard and colleagues. 21 In this paper, we focus on the gut mycobiome of healthy humans, with a particular emphasis on the relatively few fungi that are widely distributed in human gut samples.…”
Many species of fungi have been detected in the healthy human gut; however, nearly half of all taxa reported have only been found in one sample or one study. Fungi capable of growing in and colonizing the gut are limited to a small number of species, mostly Candida yeasts and yeasts in the family Dipodascaceae (Galactomyces, Geotrichum, Saprochaete). Malassezia and the filamentous fungus Cladosporium are potential colonizers; more work is needed to clarify their role. Other commonly-detected fungi come from the diet or environment but either cannot or do not colonize (Penicillium and Debaryomyces species, which are common on fermented foods but cannot grow at human body temperature), while still others have dietary or environmental sources (Saccharomyces cerevisiae, a fermentation agent and sometime probiotic; Aspergillus species, ubiquitous molds) yet are likely to impact gut ecology. The gut mycobiome appears less stable than the bacterial microbiome, and is likely subject to environmental factors.
“…Innate immune receptor activation by fungi may augment the development of colitis. The main pattern recognition receptors for fungi include Dectin-1, Dectin-2, DC-SIGN, mannose receptor, and mannose-binding lectin (29). Dectin-1 is a C-type lectin receptor, which recognizes β-glucans in the fungal cell wall.…”
Background
Inflammatory bowel disease (IBD) involves dysregulation of mucosal immunity in response to environmental factors such as the gut microbiota. The bacterial microbiota is often altered in IBD, but the connection to disease is not fully clarified, and gut fungi have recently been suggested to play a role as well. In this study, we compared microbes from all three domains of life–bacteria, archaea, and eukaryota–in pediatric patients with IBD and healthy controls.
Methods
A stool sample was collected from patients with IBD (n=34) or health control subjects (n=90), and bacterial, archaeal, and fungal communities were characterized by deep sequencing of rRNA gene segments specific to each domain.
Results
IBD patients (Crohn’s disease or ulcerative colitis) had lower bacterial diversity and distinctive fungal communities. Two lineages annotating as Candida were significantly more abundant in IBD patients (p = 0.0034 and p=0.00038, respectively) while a lineage annotating as Cladosporium was more abundant in healthy subjects (p=0.0025). There were no statistically significant differences in archaea, which were rare in pediatric samples compared to those from adults.
Conclusions
Pediatric IBD is associated with reduced diversity in both fungal and bacterial gut microbiota. Specific Candida taxa were increased in abundance in the IBD samples. These data emphasize the potential importance of fungal microbiota signatures as biomarkers of pediatric IBD, supporting their possible role in disease pathogenesis.
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