Evidence map›Paper›PMID 28874116›Full record

ArticleBMC genomics2017

Patterns of host gene expression associated with harboring a foregut microbial community.

Kevin D Kohl, Kelly F Oakeson, Diane Dunn, David K Meyerholz, Colin Dale, Robert B Weiss, M Denise Dearing

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Kevin D KohlDepartment of Biological Sciences, Vanderbilt University, 465 21st Ave South, Nashville, TN, 37235, USA. kevin.d.kohl@gmail.com.ORCID http://orcid.org/0000-0003-1126-2949
Kelly F OakesonDepartment of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT, 84112, USA.
Diane DunnDepartment of Human Genetics, University of Utah, 15 North 2030 East, Salt Lake City, 84112, USA.
David K MeyerholzDepartment of Pathology, University of Iowa, 200 Hawkins Dr, Iowa City, IA, 52242, USA.
Colin DaleDepartment of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT, 84112, USA.
Robert B WeissDepartment of Human Genetics, University of Utah, 15 North 2030 East, Salt Lake City, 84112, USA.
M Denise DearingDepartment of Biology, University of Utah, 257 South 1400 East, Salt Lake City, UT, 84112, USA.
University of Utah · USUniversity of Iowa · USVanderbilt University · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
TRAINING IN GASTROENTEROLOGYT32DK007673 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 1992 to 2026
$8.4M
NIDDK NIH HHS P30 DK054759NIDDK NIH HHS T32 DK007673
6 · The paper itself

Abstract

backgroundHarboring foregut microbial communities is considered a key innovation that allows herbivorous mammals to colonize new ecological niches. However, the functions of these chambers have only been well studied at the molecular level in ruminants. Here, we investigate gene expression in the foregut chamber of herbivorous rodents and ask whether these gene expression patterns are consistent with results in ruminants. We compared gene expression in foregut tissues of two rodent species: Stephen's woodrat (Neotoma stephensi), which harbors a dense foregut microbial community, and the lab rat (Rattus norvegicus), which lacks such a community.

resultsWe found that woodrats have higher abundances of transcripts associated with smooth muscle processes, specifically a higher expression of the smoothelin-like 1 gene, which may assist in contractile properties of this tissue to retain food material in the foregut chamber. The expression of genes associated with keratinization and cornification exhibited a complex pattern of differences between the two species, suggesting distinct molecular mechanisms. Lab rats exhibited higher abundances of transcripts associated with immune function, likely to inhibit microbial growth in the foregut of this species.

conclusionsSome of our results were consistent with previous findings in ruminants (high expression of facilitative glucose transporters, lower expression of B4galnt2), suggestive of possible convergent evolution, while other results were unclear, and perhaps represent novel host-microbe interactions in rodents. Overall, our results suggest that harboring a foregut microbiota is associated with changes to the functions and host-microbe interactions of the foregut tissues.

Indexed as

Gastrointestinal MicrobiomeGene Expression ProfilingGenomicsSymbiosisHerbivoreHost-microbe interactionsWoodrat

Identifiers

PMID28874116
PMCPMC5585965
OpenAlexW2753744112

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.