37 Trillion Invaders: We Are Not Alone
The adult
human body is made up of about 37 trillion cells. Microbes, mainly
bacteria, outnumber body cells by 10 to 1. This huge community of
microbes, called the microbiome, affects the health, development and
evolution of all multicellular organisms, including humans, according to
the latest craze in health supplement marketing and plenty of science
papers latching onto the fad.
Symbiotic microbes can help prevent infection by disease-causing
pathogens but sometimes the interaction goes the other way, with a
pathogen or disease disrupting the normal community of symbiotic
bacteria. In a new paper in the Proceedings of the National Academy of Sciences, a team of scientists from UC Santa Barbara say that a fungal pathogen of amphibians does just that.
Experiments with model organisms such as mice have shown that
infectious pathogens can disrupt the "normal" microbiome, but the extent
to which this process shapes symbiotic microbial communities during
disease outbreaks in nature is largely unknown.
This new work, conducted by Andrea Jani, a UCSB graduate student in
Cherie Briggs' lab in the Department of Ecology, Evolution and Marine
Biology (EEMB), addresses a fundamental gap in disease ecology and
microbiome research.
Co-authors Jani and Briggs -- also affiliated with UCSB's
Biomolecular Science and Engineering program -- found that the chytrid
fungus Batrachochytrium dendrobatidis (Bd) appears to drive dramatic
changes in symbiotic bacterial communities during natural disease
episodes in four populations of the endangered Sierra Nevada
yellow-legged frog (Rana sierrae). Chytridiomycosis, an
emerging infectious disease of amphibian skin caused by the Bd pathogen,
is a leading cause of amphibian biodiversity loss worldwide.
"In the California Sierra Nevada, this disease has led to the rapid
extirpation of frogs from hundreds of high-elevation lakes; however, in
other lakes, infected frogs of the same species are surviving and
persisting with the fungus," explained Briggs, who is the Duncan and
Suzanne Mellichamp Chair in Systems Biology. "Given that amphibian skin
is the organ infected by Bd, there has been a lot of interest in how
antifungal properties of some skin-associated bacteria may protect frogs
against this fungal pathogen. In this study we focused on the flip side
of this interaction -- that is, how infection with Bd can disrupt the
skin microbial community."
"We used next-generation DNA sequencing to document significant
shifts in skin-associated bacterial communities of the Sierra Nevada
yellow-legged frog during natural Bd outbreaks," Jani explained. "We
paired these field surveys with a laboratory infection experiment,
demonstrating a causal relationship in which Bd alters the Rana sierrae microbiome."
The researchers found a remarkable consistency in the response of the
microbiome to Bd infection among field populations and between the
field and laboratory. Several key taxa -- a group of one or more
populations of an organism or organisms -- consistently responded in the
same direction to Bd infection, suggesting some predictability in the
effect of Bd on the microbiome.
"What we found was that the severity of infection with Bd is strongly
correlated with the composition of bacterial communities on the skin of
frogs," Jani continued. "What was surprising was that across the
different frog populations there was pretty striking consistency in this
correlation with Bd. One of the frog populations crashed due to Bd
infection; the other three populations seemed to tolerate Bd infections.
So there are different disease dynamics going on, yet they have a
similar relationship between the microbiome and Bd."
Still, the underlying mechanism for Bd-induced changes in the
microbiome is not clear. The researchers hypothesize that the pathogen
might compete directly with certain bacteria for space or resources or
release compounds that negatively or positively affect certain bacterial
species. Alternatively, they say, some pathogens could control immune
responses of the host to favor their own growth and disrupt the normal
symbiotic bacterial community.
Jani noted that some promise exists for probiotic treatments as a
tool to fight the decline of frogs due to Bd, but she was careful to
qualify that statement by saying that there is still a lot that
scientists do not understand about either the environmental impact that
might have or what the interactions are between the natural bacteria
that exist on frogs and the pathogen. "We find that some taxa previously
identified as having anti-Bd properties are driven to low abundances by
Bd infection, which may limit their effectiveness as probiotic agents,"
she said.
"This study shows the importance of knowing how the many benign
microbes living on and in our bodies interact with those that cause
disease," said Sam Scheiner, National Science Foundation (NSF) director
for the joint NSF/National Institutes of Health/United States Department
of Agriculture Ecology and Evolution of Infectious Disease Program,
which funded the research. "The results are important for developing
responses to a disease causing amphibians to go extinct worldwide and
also have implications for future studies of human health."
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