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The Effects of Captivity on the Mammalian Gut Microbiome.

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TLDR
Differences in gut bacterial beta diversity between the captive and wild state were observed for most of the taxa surveyed, except the even-toed ungulates, and beta diversity variation was also strongly influenced by host taxonomic group, diet type, and gut fermentation physiology.
Abstract
Recent studies increasingly note the effect of captivity or the built environment on the microbiome of humans and other animals. As symbiotic microbes are essential to many aspects of biology (e.g., digestive and immune functions), it is important to understand how lifestyle differences can impact the microbiome, and, consequently, the health of hosts. Animals living in captivity experience a range of changes that may influence the gut bacteria, such as diet changes, treatments, and reduced contact with other individuals, species and variable environmental substrates that act as sources of bacterial diversity. Thus far, initial results from previous studies point to a pattern of decreased bacterial diversity in captive animals. However, these studies are relatively limited in the scope of species that have been examined. Here we present a dataset that includes paired wild and captive samples from mammalian taxa across six Orders to investigate generalizable patterns of the effects captivity on mammalian gut bacteria. In comparing the wild to the captive condition, our results indicate that alpha diversity of the gut bacteria remains consistent in some mammalian hosts (bovids, giraffes, anteaters, and aardvarks), declines in the captive condition in some hosts (canids, primates, and equids), and increases in the captive condition in one host taxon (rhinoceros). Differences in gut bacterial beta diversity between the captive and wild state were observed for most of the taxa surveyed, except the even-toed ungulates (bovids and giraffes). Additionally, beta diversity variation was also strongly influenced by host taxonomic group, diet type, and gut fermentation physiology. Bacterial taxa that demonstrated larger shifts in relative abundance between the captive and wild states included members of the Firmicutes and Bacteroidetes. Overall, the patterns that we observe will inform a range of disciplines from veterinary practice to captive breeding efforts for biological conservation. Furthermore, bacterial taxa that persist in the captive state provide unique insight into symbiotic relationships with the host.

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The human gut bacteria Christensenellaceae are widespread, heritable, and associated with health

TL;DR: The Christensenellaceae, a recently described family in the phylum Firmicutes, is emerging as an important player in human health, with its relationship with BMI the most robust and reproducible link between the microbial ecology of the human gut and metabolic disease reported to date.
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Host diet and evolutionary history explain different aspects of gut microbiome diversity among vertebrate clades

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Conservation biology needs a microbial renaissance: a call for the consideration of host-associated microbiota in wildlife management practices

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Drivers of Microbiome Biodiversity: A Review of General Rules, Feces, and Ignorance.

TL;DR: It is demonstrated that both diet and body size affect diversity in the gut but that gut physiology (fermenter versus simple) is the most important driver.
References
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Journal ArticleDOI

Diet rapidly and reproducibly alters the human gut microbiome

TL;DR: Increases in the abundance and activity of Bilophila wadsworthia on the animal-based diet support a link between dietary fat, bile acids and the outgrowth of microorganisms capable of triggering inflammatory bowel disease.
Journal ArticleDOI

Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms

TL;DR: It is shown that the protocol developed for these instruments successfully recaptures known biological results, and additionally that biological conclusions are consistent across sequencing platforms (the HiSeq2000 versus the MiSeq) and across the sequenced regions of amplicons.
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