The Mycobiome

The largely overlooked resident fungal community plays a critical role in human health and disease.

By | February 1, 2016

© VEM/SCIENCE SOURCE

At a workshop held at the National Institutes of Health  (NIH) last September on the role of human microbiota in infectious disease, I was disheartened not to hear a single talk on the fungal community—the mycobiome. Disheartened, but not surprised. Ignoring the fungal kingdom is nothing new. More than five years ago, my colleague and I tried to draw attention to this issue in a letter published in Microbe, recommending that the Human Microbiome Project should investigate not just people’s bacterial inhabitants, but the fungal and viral commensal communities as well. While research on the human virome has increased in recent years, the scientific community has not heeded our advice with regard to the fungal components of the microbiome. As of November 2015, only 269 of more than 6,000 Web of Science search results for the term “microbiome” even mention “fungus,” and the scientific search engine returns only 55 papers pertaining to the “mycobiome.”

Despite this lack of attention, a handful of recent studies point to the importance of our commensal fungal inhabitants as critical players in human health and disease. The oral mycobiome of HIV-infected patients differs from that of uninfected controls, for example. Abundance of Candida and Saccharomyces species correlates with increased severity of hepatitis B infections. And an overabundance of the gut fungal pathogen Candida tropicalis aggravates inflammatory bowel disease. As widespread surveys of the mycobiome become available, such correlational data can be further explored by experimental manipulations in the lab. One day, perhaps, researchers will include fungal species in fecal transplants to treat infections by Clostridium difficile and other bacteria, and companies will begin to market probiotic products that contain live cultures of friendly fungi.

Characterization of the human mycobiome

THE HUMAN MYCOBIOME: Diverse fungal species live in and on the human body. Preliminary surveys have revealed several pathogenic species that may increase one’s risk of disease when the healthy microbiome is disrupted.
See full infographic: WEB | PDF
Aspergillus: MEDMYCO/WIKIMEDIA COMMONS; Candida: MICHAEL FRANCISCO/FLICKR; Fusarium: CDC/DR. LIBERO AJELLO; Malassezia :CDC/DR.LUCILLE K. GEORG
In 1974, my master’s advisor handed me a paper showing that rabbits treated with antibiotics to kill bacteria or with anti-inflammatory steroids to suppress the immune system developed the fungal infection candidiasis, commonly known as thrush.1 It made me realize that not only could fungi in the environment negatively impact our health, but fungal species also inhabit the mammalian body, alongside diverse commensal bacteria. And when one microbial community is knocked out, another can cause illness. If the communities are undisturbed, however, the fungal inhabitants appear to be harmless or perhaps even beneficial.

The medical mycology community didn’t attempt to define the fungal component of the human microbiome until 2010. My colleagues and I found a complex fungal commu­nity in the human oral cavity that went beyond Candida and Saccharomyces, fast growers that can be easily cultured. Across 20 volunteers, we identified 101 fungal species, each person harboring between 9 and 23 fungal species in their mouth. To eliminate transient fungi, we considered the core mycobiome to be those organisms that were present in at least four participants (20 percent of the population studied). This core included 15 genera, of which Candida species were the most fre­quent, followed by Cladosporium (a known allergen and trigger for asthmatic attacks), Aureobasidium (which can cause fungal infections in solid-organ transplant recipients), and genera of the order Saccharomycetales (which includes beneficial species, such as Saccharomyces boulardii, which has been suggested as a potential probiotic).2

We also found several pathogenic fungi, including Aspergillus (which can cause invasive and devastating fungal infections), Fusarium (which can cause superficial and systemic infections that are difficult to treat), and Cryptococcus (a major cause of meningitis in AIDS patients). These pathogens may render individ­uals at increased risk of infection, espe­cially if the host immune status is compromised, though such a link has yet to be demonstrated experimentally. Of the species we identified, more than a third could not be cultured, making it difficult to study their roles in health and disease.  

Investigators have started to look at the fungal communities residing in body sites other than the oral cavity. In 2012, a team in Japan profiled the distribution of Malassezia species, which can lead to a superficial skin disease, in the external auditory canal and on the sole of the foot. M. slooffiae, known to cause skin discoloration, was the most common species in both body sites, followed by M. restricta, which predominated in scalp dandruff. Despite some similarities to the mycobiomes of other body sites, however, the researchers found distinctive Malassezia communities present in the outer ear canal and on the sole.3

In 2013, Keisha Findley of the National Human Genome Research Institute and other NIH researchers characterized the mycobiome of the skin, which varied depending on the body part sampled.4 On 10 healthy adults, the research team found that fungi of the genus Malassezia dominated 11 torso and arm sites, while greater diversities of fungal genera were observed on the plantar heel, toenail, and toe web. Importantly, the researchers showed that while bacteria were grouped based on whether the skin was sebaceous, moist, or dry, the fungal community appeared to be determined by location—foot, arm, head, or torso.

Most recently, a group of French researchers characterized the mycobiome in the lungs and reported that environmental fungi such as Aspergillus dominate in healthy people.5 The lungs of patients with cystic fibrosis, pulmonary fibrosis, and other lung diseases, as well as of those suffering from cardiovascular disease or who had received a lung transplant, were dominated by Candida species such as C. albicans.

Collectively, these and other surveys have demonstrated the presence of diverse fungal communities throughout the human body, and suggest their importance in health and disease.

Fungi and disease

TWO-FACED FUNGUS: Candida tropicalis, a common species of the mammalian mycobiome, can exacerbate symptoms of inflammatory bowel disease in mice lacking the dectin-1 pattern recognition receptor typically found on the surface of innate immune cells.© WIKIMEDIA COMMONS/DJSPRINGIn 2014, to go beyond listing the fungal species found at various sites in the body and move towards mechanistic studies, my lab conducted an analysis of fungal-fungal and fungal-bacterial interactions in the oral cavity of HIV-infected patients.6 Among diverse microbial interactions, we discovered an antagonistic relationship between Pichia, a nonpathogenic yeast used as a biocontrol agent to protect crops from fungal growth, and pathogenic Candida: a decrease in Pichia abundance coincided with an increase in Candida colonization.
Growing these species in the lab, we found that Pichia released a growth inhibitory agent into culture media that was capable of limiting the growth of Candida, Aspergillus, and Fusarium. Moreover, adding Pichia cells or the medium they had been grown in (Pichia spent media, PSM) to Candida cultures significantly inhibited biofilm formation. And when immunosuppressed mice were challenged with C. albicans, those treated orally with PSM developed more-benign oral infections and had a decrease in the number of fungi invading the tongue mucosal tissues compared with untreated mice.6

Looking more closely at the fungal growth in PSM-treated mice, we found fewer hyphae growing on their tongues, and their oral mucosa appeared intact. Control mice, on the other hand, showed evidence of extensive fungal invasion of the tissue. Identification of the active Pichia component responsible for the inhibition of these pathogenic fungi is currently under investigation; preliminary studies suggest that it is a protein.  

Fungal species inhabit the mamma­lian body, alongside diverse commensal bacteria. And when one microbial community is knocked out, another can cause illness.
 

Recent work has also pointed to the importance of the mycobiome in gastrointestinal health. In 2008, Stephan Ott of Christian-Albrechts-University and the University Hospital Schleswig-Holstein in Kiel, Germany, and colleagues found that the fecal fungal community in patients with inflammatory bowel disease (IBD) was substantially different from that of healthy controls.7 And in a mouse model of colitis, David Underhill’s group at the Cedars-Sinai Medical Center in Los Angeles found that dectin-1, a pattern recognition receptor present on the cell surface of innate immune cells (e.g. macrophages, neutrophils, and dendritic cells) that mediates the biological effects of fungal wall polysaccharides called glucans, significantly influences the animals’ IBD symptoms.8 Specifically, Underhill and his colleagues found that mice deficient in dectin-1 suffered increased weight loss, histological alterations, and production of proinflam­matory cytokines compared with wild-type mice. Additional testing demonstrated that Candida tropicalis, a dominant species in the gut of wild-type mice, exploited the lack of dectin-1, and that treatment of dectin-1–deficient mice with the antifungal fluconazole attenuated disease severity.

Disruptions to the mycobiome can also exacerbate graft versus host disease (GVHD), a complex and multidirectional process that involves interactions between the host innate immune system, the gut micro­biota, and donor T cells. In 2000, Kieren Marr, then at the University of Washington and the Fred Hutchinson Cancer Research Center, and colleagues were among the first to show an association between treating candidiasis and improvement of GVHD. Specifically, they showed that bone marrow transplant patients undergoing long-term fluconazole treatment had decreased gastrointes­tinal GVHD, persistent protection against Candida infections and candidiasis-related death, and improved survival.9

Ten years later, Walter van der Velden of the Radboud University Nijmegen Medical Center in the Netherlands and colleagues examined whether Candida colonization and dectin-1 function had an effect on the development of GVHD through a retrospective analysis of patients who had undergone allogeneic stem cell transplanta­tion.10 The patients had been evaluated for Candida colonization in fecal and mouthwash samples. Van der Velden’s group found that Candida-colonized patients had a significantly higher rate of severe acute GVHD than those that were Candida free, and that colonization was the only factor they looked at that was associated with GVHD; stem cell source and the method by which the researchers depleted T cells had no significant impact. When treated with fluconazole, patients colonized with Candida had a lower likelihood of developing GVHD.

The composition of the human mycobiome may also influence much more common diseases, such as obesity. Last year, a group in Spain reported that the fungal community of obese people has an increased abundance of fungi belonging to the phylum Ascomycota, classes Saccharomycetes and Tremellomycetes, and families Dipodascaceae and Saccharomycetaceae compared with non-obese subjects.11 There was also a tendency towards decreased fungal diversity in obese individuals, which is consistent with published data on bacteria. Alterations in the mycobiome of obese subjects seemed to be associated with higher amounts of body fat and related metabolic disorders such as insulin resistance, high blood pressure, and inflammation.

The researchers found that Mucor was the most prevalent fungal genus in non-obese participants, and that the relative abundance of Mucor increased after weight loss in obese patients. Researchers have reported similar results with regard to Bacteroidetes bacteria, which tend to be associated with weight loss. The new finding may point to the potential use of Mucor with or without Bacteroidetes to combat obesity. Notably, similar to our findings of an antagonistic relationship between Candida and Pichia in the oral mycobiota of HIV-infected patients, the French group that surveyed the lung mycobiome found a significant negative association between the families Pichiaceae (which includes Pichia), and Dipodascaceae (which includes Candida) among nonobese subjects.5

Given that the field of mycobiome research is so young, these examples are undoubtedly but a few of many diseases in which our commensal fungi play significant roles. Already, additional links have been found between the fungal community and at least two such conditions, atopic dermatitis12 and allergic responses in the lung.13

Clearly, the human mycobiome has an influence on both health and disease. The scientific community must adopt an all-inclusive characterization of the human microbiome going forward; studies that focus solely on bacteria are myopic and doomed to failure, and they squander precious research funds. 

Mahmoud Ghannoum is the director of the Center for Medical Mycology at Case Western Reserve University and University Hospitals Case Medical Center and a tenured professor in the Department of Dermatology at the Case School of Medicine in Cleveland, Ohio. From 2011 to 2012, he served as president of the Medical Mycological Society of the Americas. 

References

  1. J.A. Montana, T.W. Sery, “Effect of fungistatic agents on corneal infections with Candida albicans,” AMA Arch Ophthalmol, 60:1-6, 1958.
  2. M.A. Ghannoum et al., “Characterization of the oral fungal microbiome (mycobiome) in healthy individuals,” PLOS Pathog, 6:e1000713, 2010.
  3. E. Zhang et al., “Characterization of Malassezia microbiota in the human external auditory canal and on the sole of the foot,” Microbiol Immunol, 56:238-44, 2012.
  4. K. Findley et al., “Topographic diversity of fungal and bacterial communities in human skin,” Nature, 498:367-70, 2013.
  5. L.D.N. Nguyen et al., “The lung mycobiome: An emerging field of the human respiratory microbiome,” Front Microbiol, 6:89, 2015.
  6. P.K. Mukherjee et al., “Oral mycobiome analysis of HIV-infected patients: Identification of Pichia as an antagonist of opportunistic fungi,” PLOS Pathog, 10:e1003996, 2014.
  7. S.J. Ott et al., “Fungi and inflammatory bowel diseases: Alterations of composition and diversity,” Scand J Gastroenterol, 43:831-41, 2008.
  8. I.D. Iliev et al., “Interactions between commensal fungi and the c-
  9. type lectin receptor dectin-1 influence colitis,” Science, 336:1314-17, 2012.
  10. K.A. Marr et al., “Prolonged fluconazole prophylaxis is associated with persistent protection against candidiasis-related death in allogeneic marrow transplant recipients: Long-term follow-up of a randomized, placebo-controlled trial,” Blood, 96:2055-61, 2000.
  11. W.J. van der Velden et al., “Role of the mycobiome in human acute graft-versus-host disease,” Biol Blood Marrow Transplant, 19:329-32, 2013.
  12. M.M. Rodríguez et al., “Obesity changes the human gut mycobiome,” Sci Rep, 5:14600, 2015.
  13. P.K. Mukherjee et al., “Disease-specific changes in skin bacteriome and mycobiome in atopic dermatitis (AD) patients,” Presented at the Society for Investigative Dermatology Meeting; Atlanta, Georgia, May 6–9, 2015.
  14. M.C. Noverr et al., “Development of allergic airway disease in mice following antibiotic therapy and fungal microbiota increase: Role of host genetics, antigen, and interleukin-13,” Infect Immun, 73:30-38, 2005.
     
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Avatar of: DaveSSI

DaveSSI

Posts: 9

February 1, 2016

I heard a presentatoin that claimed to have found that the fungal disease eliminating bats from many large geographic areas was associated with missing bacteria from the microbiota of those bats with evidence a balance normally existed between the particular bacteria and the fungal community.  With the balance upset the fungal community overwhelmed the bat.  We certainly need to understand much more about fungal communities.  Its potentially a factor elsewhere.  The pollinator crisis is one needing such  attention.

Avatar of: Natick4

Natick4

Posts: 4

February 1, 2016

Another great one - my nutrition classes are getting harder to teach.... all of these (bacteria, phages, fungi, viruses) modifiers of human health also respond to dietary practices and habits. 

Professor, what should I eat?

I have no idea - better yet, what should your entire biological population eat? That might be a better question. 

Avatar of: I-adore-pasteur

I-adore-pasteur

Posts: 6

February 6, 2016

Dear Sir,

I recently came across an articel about the communication between bacteria, fungi, and human cells who cooperate. It was published by a french lab. As soon as I can recall where it was stored I will publish the link here. 

Maybe you know this team already, if not you will like each other.

Thanks for your brilliant endeavour!

Cornelius

P.S.  if you have trouble cultivating fungi, feel free to ask me!

Avatar of: ironjustice

ironjustice

Posts: 43

February 11, 2016

A curious thing is, cystic fibrosis is hypothesised to be linked to hemochromatosis and they have a predominent candida overgrowth?

"Effect of trace iron levels and iron withdrawal by chelation on the growth of Candida albicans and Candida vini."

 

"Addition of iron enhance the multiplication of Candida species"
Avatar of: ironjustice

ironjustice

Posts: 43

February 11, 2016

"Survival in rhinocerebral mucormycosis: Is iron the key?"

  "Iron chelation is a promising, novel therapeutic strategy
for refractory mucormycosis infections."   "Invasive zygomycosis: notably in diabetes mellitus and iron overload"   "The availability of free iron in plasma and tissues is believed to be  crucial for the pathogenesis of these mycoses."   "development of iron chelators as adjunctive therapy for mucormycosis is warranted"    

 

Avatar of: ironjustice

ironjustice

Posts: 43

February 11, 2016

"iron homeostasis may be a viable therapeutic target for HIV"

  "the therapeutic benefit of venesection on HIV viral load"
Avatar of: I-adore-pasteur

I-adore-pasteur

Posts: 6

Replied to a comment from ironjustice made on February 11, 2016

February 12, 2016

Dear Sir, I am slightly confused by what you suggest and a possible different opinion expressed in the following article.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840956/

Maybe you can help me understand what one should deduct, or conclude.

 

Avatar of: I-adore-pasteur

I-adore-pasteur

Posts: 6

February 14, 2016

 

To ironjustice:

Dear Sir, I am slightly confused by what you suggest and a possible different opinion expressed in the following article.

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840956/

Maybe you can help me understand what one should deduct, or conclude.

 

 

 

 

 

Avatar of: JonRichfield

JonRichfield

Posts: 73

February 23, 2016

Well taken point with good illustrative material. Thank you.

Avatar of: ironjustice

ironjustice

Posts: 43

Replied to a comment from I-adore-pasteur made on February 14, 2016

February 25, 2016

Quote I-adore-pasteur

One has to choose carefully the method used to remove iron?

The only thing I can see is the fact he used desferoxamine. 

 

"Lactoferrin, ciclopirox and deferiprone inhibited whereas desferoxamine enhanced fungal growth."

 

http://www.ncbi.nlm.nih.gov/pubmed/20402789

 

 

 

 

 

To ironjustice:

 

 

 

Dear Sir, I am slightly confused by what you suggest and a possible different opinion expressed in the following article.

 

 

 

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840956/

 

 

 

Maybe you can help me understand what one should deduct, or conclude.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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