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Title: The Oral and Skin Microbiomes of Captive Komodo Dragons Are Significantly Shared with Their Habitat

Journal Article · · mSystems
 [1];  [2]; ORCiD logo [3];  [4];  [1];  [5];  [6];  [7];  [8];  [9];  [10];  [11];  [12];
  1. Univ. of Colorado, Boulder, CO (United States). BioFrontiers Institute
  2. Univ. of Colorado, Boulder, CO (United States), Dept. of Computer Science
  3. Univ. of Colorado, Boulder, CO (United States). BioFrontiers Institute; Univ. of Colorado, Boulder, CO (United States). Dept. of Ecology and Evolutionary Biology
  4. Univ. of Colorado, Boulder, CO (United States). Dept. of Ecology and Evolutionary Biology
  5. Univ. of Chicago, IL (United States). Graduate Program in Biophysical Sciences
  6. Univ. of Colorado, Boulder, CO (United States). BioFrontiers Institute
  7. Department of Herpetology, Bronx Zoo/WCS, Bronx, New York, USA
  8. Denver Zoological Foundation, Denver, CO (United States)
  9. Zoo Atlanta, Atlanta, GA (United States); Georgia Inst. of Technology, Atlanta, GA (United States). School of Biology
  10. Department of Ecology and Evolutionary Biology, University of Colorado Boulder, Boulder, Colorado, USA
  11. Biosciences Department, Institute for Genomics and Systems Biology, Argonne National Laboratory, Argonne, Illinois, USA; Departments of Ecology and Evolution and Surgery, University of Chicago, Chicago, Illinois, USA
  12. BioFrontiers Institute, University of Colorado Boulder, Boulder, Colorado, USA; Departments of Chemistry and Biochemistry and Computer Science, University of Colorado Boulder, Boulder, Colorado, USA

Animals, including humans, have evolved in the context of exposure to a variety of microbial organisms present in the environment. Only recently have humans, and some animals, begun to spend a significant amount of time in enclosed artificial environments, rather than in the more natural spaces in which most of evolution took place. The consequences of this radical change in lifestyle likely extend to the microbes residing in and on our bodies and may have important implications for health and disease. A full characterization of host-microbe sharing in both closed and open environments will provide crucial information that may enable the improvement of health in humans and in captive animals, both of which experience a greater incidence of disease (including chronic illness) than counterparts living under more ecologically natural conditions. Examining the way in which animals, including those in captivity, interact with their environment is extremely important for studying ecological processes and developing sophisticated animal husbandry. Here we use the Komodo dragon (Varanus komodoensis) to quantify the degree of sharing of salivary, skin, and fecal microbiota with their environment in captivity. Both species richness and microbial community composition of most surfaces in the Komodo dragon’s environment are similar to the Komodo dragon’s salivary and skin microbiota but less similar to the stool-associated microbiota. We additionally compared host-environment microbiome sharing between captive Komodo dragons and their enclosures, humans and pets and their homes, and wild amphibians and their environments. We observed similar host-environment microbiome sharing patterns among humans and their pets and Komodo dragons, with high levels of human/pet- and Komodo dragon-associated microbes on home and enclosure surfaces. In contrast, only small amounts of amphibian-associated microbes were detected in the animals’ environments. We suggest that the degree of sharing between the Komodo dragon microbiota and its enclosure surfaces has important implications for animal health. These animals evolved in the context of constant exposure to a complex environmental microbiota, which likely shaped their physiological development; in captivity, these animals will not receive significant exposure to microbes not already in their enclosure, with unknown consequences for their health. Animals, including humans, have evolved in the context of exposure to a variety of microbial organisms present in the environment. Only recently have humans, and some animals, begun to spend a significant amount of time in enclosed artificial environments, rather than in the more natural spaces in which most of evolution took place. The consequences of this radical change in lifestyle likely extend to the microbes residing in and on our bodies and may have important implications for health and disease. A full characterization of host-microbe sharing in both closed and open environments will provide crucial information that may enable the improvement of health in humans and in captive animals, both of which experience a greater incidence of disease (including chronic illness) than counterparts living under more ecologically natural conditions.

Research Organization:
Argonne National Laboratory (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1626166
Journal Information:
mSystems, Vol. 1, Issue 4; ISSN 2379-5077
Publisher:
American Society for MicrobiologyCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 47 works
Citation information provided by
Web of Science

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Cited By (23)

Amphibian chytridiomycosis outbreak dynamics are linked with host skin bacterial community structure journal February 2018
Evaluating the impact of domestication and captivity on the horse gut microbiome journal November 2017
Habitat environments impacted the gut microbiome of long-distance migratory swan geese but central species conserved journal September 2018
Metagenomic analysis of dental calculus in ancient Egyptian baboons journal December 2019
The Effects of Captivity on the Mammalian Gut Microbiome journal August 2017
Conservation biology needs a microbial renaissance: a call for the consideration of host-associated microbiota in wildlife management practices journal January 2019
Host Microbiome Richness Predicts Resistance to Disturbance by Pathogenic Infection in a Vertebrate Host posted_content July 2017
The Skin Microbiome of Cohabiting Couples journal July 2017
Environmental Sources of Bacteria Differentially Influence Host-Associated Microbial Dynamics journal May 2018
Highly Reproducible 16S Sequencing Facilitates Measurement of Host Genetic Influences on the Stickleback Gut Microbiome journal August 2019
Engineering the microbiome for animal health and conservation journal February 2019
Skin and gut microbiomes of a wild mammal respond to different environmental cues journal November 2018
The skin microbiome of vertebrates journal May 2019
Looking like the locals - gut microbiome changes post-release in an endangered species journal October 2019
Bacterial Communities in Boreal Forest Mushrooms Are Shaped Both by Soil Parameters and Host Identity journal May 2017
One Health Relationships Between Human, Animal, and Environmental Microbiomes: A Mini-Review journal August 2018
Evaluating the impact of domestication and captivity on the horse gut microbiome. text January 2017
Highly reproducible 16S sequencing facilitates measurement of host genetic influences on the stickleback gut microbiome posted_content December 2018
Gut microbiome shifts with urbanization and potentially facilitates a zoonotic pathogen in a wading bird journal March 2020
Species abundance information improves sequence taxonomy classification accuracy text January 2019
Species abundance information improves sequence taxonomy classification accuracy journal October 2019
Gut Microbiomes of Endangered Przewalski’s Horse Populations in Short- and Long-Term Captivity: Implication for Species Reintroduction Based on the Soft-Release Strategy journal March 2020
Meta-SourceTracker: application of Bayesian source tracking to shotgun metagenomics journal March 2020