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Mapping gastrointestinal gene expression patterns in wild primates and humans via fecal RNA-seq
AK. Sharma, B. Pafčo, K. Vlčková, B. Červená, J. Kreisinger, S. Davison, K. Beeri, T. Fuh, SR. Leigh, MB. Burns, R. Blekhman, KJ. Petrželková, A. Gomez,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
LH15175
Czech - US cooperation project LH - KONTAKT II
NLK
BioMedCentral
od 2000-12-01
BioMedCentral Open Access
od 2000
Directory of Open Access Journals
od 2000
Free Medical Journals
od 2000
PubMed Central
od 2000
Europe PubMed Central
od 2000 do 2020
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2000-07-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2000-01-01
Medline Complete (EBSCOhost)
od 2000-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
Springer Nature OA/Free Journals
od 2000-12-01
- MeSH
- feces * MeSH
- gastrointestinální trakt metabolismus MeSH
- Gorilla gorilla genetika MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- poly A genetika MeSH
- sekvenování transkriptomu * MeSH
- stanovení celkové genové exprese * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Limited accessibility to intestinal epithelial tissue in wild animals and humans makes it challenging to study patterns of intestinal gene regulation, and hence to monitor physiological status and health in field conditions. To explore solutions to this limitation, we have used a noninvasive approach via fecal RNA-seq, for the quantification of gene expression markers in gastrointestinal cells of free-range primates and a forager human population. Thus, a combination of poly(A) mRNA enrichment and rRNA depletion methods was used in tandem with RNA-seq to quantify and compare gastrointestinal gene expression patterns in fecal samples of wild Gorilla gorilla gorilla (n = 9) and BaAka hunter-gatherers (n = 10) from The Dzanga Sangha Protected Areas, Central African Republic. RESULTS: Although only a small fraction (< 4.9%) of intestinal mRNA signals was recovered, the data was sufficient to detect significant functional differences between gorillas and humans, at the gene and pathway levels. These intestinal gene expression differences were specifically associated with metabolic and immune functions. Additionally, non-host RNA-seq reads were used to gain preliminary insights on the subjects' dietary habits, intestinal microbiomes, and infection prevalence, via identification of fungi, nematode, arthropod and plant RNA. CONCLUSIONS: Overall, the results suggest that fecal RNA-seq, targeting gastrointestinal epithelial cells can be used to evaluate primate intestinal physiology and gut gene regulation, in samples obtained in challenging conditions in situ. The approach used herein may be useful to obtain information on primate intestinal health, while revealing preliminary insights into foraging ecology, microbiome, and diet.
Department of Animal Science University of Minnesota Twin Cities USA
Department of Anthropology University of Colorado Boulder CO USA
Loyola University Chicago Quinlan Life Sciences Building Chicago IL USA
WWF Central African Republic Bangui Central African Republic
Citace poskytuje Crossref.org
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- $a Mapping gastrointestinal gene expression patterns in wild primates and humans via fecal RNA-seq / $c AK. Sharma, B. Pafčo, K. Vlčková, B. Červená, J. Kreisinger, S. Davison, K. Beeri, T. Fuh, SR. Leigh, MB. Burns, R. Blekhman, KJ. Petrželková, A. Gomez,
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- $a BACKGROUND: Limited accessibility to intestinal epithelial tissue in wild animals and humans makes it challenging to study patterns of intestinal gene regulation, and hence to monitor physiological status and health in field conditions. To explore solutions to this limitation, we have used a noninvasive approach via fecal RNA-seq, for the quantification of gene expression markers in gastrointestinal cells of free-range primates and a forager human population. Thus, a combination of poly(A) mRNA enrichment and rRNA depletion methods was used in tandem with RNA-seq to quantify and compare gastrointestinal gene expression patterns in fecal samples of wild Gorilla gorilla gorilla (n = 9) and BaAka hunter-gatherers (n = 10) from The Dzanga Sangha Protected Areas, Central African Republic. RESULTS: Although only a small fraction (< 4.9%) of intestinal mRNA signals was recovered, the data was sufficient to detect significant functional differences between gorillas and humans, at the gene and pathway levels. These intestinal gene expression differences were specifically associated with metabolic and immune functions. Additionally, non-host RNA-seq reads were used to gain preliminary insights on the subjects' dietary habits, intestinal microbiomes, and infection prevalence, via identification of fungi, nematode, arthropod and plant RNA. CONCLUSIONS: Overall, the results suggest that fecal RNA-seq, targeting gastrointestinal epithelial cells can be used to evaluate primate intestinal physiology and gut gene regulation, in samples obtained in challenging conditions in situ. The approach used herein may be useful to obtain information on primate intestinal health, while revealing preliminary insights into foraging ecology, microbiome, and diet.
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- $a Kreisinger, Jakub $u The Czech Academy of Sciences, Institute of Vertebrate Biology, Květná 8, 603 65, Brno, Czech Republic. Department of Zoology, Faculty of Science, Charles University, Viničná 7, 128 44, Praha, Czech Republic.
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- $a Petrželková, Klára J $u The Czech Academy of Sciences, Institute of Vertebrate Biology, Květná 8, 603 65, Brno, Czech Republic. petrzelkova@ivb.cz. The Czech Academy of Sciences, Biology Centre, Institute of Parasitology, Branišovská 31, 370 05, České Budějovice, Czech Republic. petrzelkova@ivb.cz. Liberec Zoo, Lidové sady 425/1, 460 01, Liberec, Czech Republic. petrzelkova@ivb.cz.
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