Cargando…
Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity
Bitter taste receptors (Tas2rs in mice) detect bitterness, a warning signal for toxins and poisons, and are expressed in enteroendocrine cells. We tested the hypothesis that Tas2r138 and Tas2r116 mRNAs are modulated by microbiota alterations induced by a long-term high-fat diet (HFD) and antibiotics...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574285/ https://www.ncbi.nlm.nih.gov/pubmed/37836428 http://dx.doi.org/10.3390/nu15194145 |
_version_ | 1785120658101895168 |
---|---|
author | Caremoli, Filippo Huynh, Jennifer Lagishetty, Venu Markovic, Daniela Braun, Jonathan Dong, Tien S. Jacobs, Jonathan P. Sternini, Catia |
author_facet | Caremoli, Filippo Huynh, Jennifer Lagishetty, Venu Markovic, Daniela Braun, Jonathan Dong, Tien S. Jacobs, Jonathan P. Sternini, Catia |
author_sort | Caremoli, Filippo |
collection | PubMed |
description | Bitter taste receptors (Tas2rs in mice) detect bitterness, a warning signal for toxins and poisons, and are expressed in enteroendocrine cells. We tested the hypothesis that Tas2r138 and Tas2r116 mRNAs are modulated by microbiota alterations induced by a long-term high-fat diet (HFD) and antibiotics (ABX) (ampicillin and neomycin) administered in drinking water. Cecum and colon specimens and luminal contents were collected from C57BL/6 female and male mice for qRT-PCR and microbial luminal 16S sequencing. HFD with/without ABX significantly increased body weight and fat mass at 4, 6, and 8 weeks. Tas2r138 and Tas2r116 mRNAs were significantly increased in mice fed HFD for 8 weeks vs. normal diet, and this increase was prevented by ABX. There was a distinct microbiota separation in each experimental group and significant changes in the composition and diversity of microbiome in mice fed a HFD with/without ABX. Tas2r mRNA expression in HFD was associated with several genera, particularly with Akkermansia, a Gram-negative mucus-resident bacterium. These studies indicate that luminal bacterial composition is affected by sex, diet, and ABX and support a microbial dependent upregulation of Tas2rs in HFD-induced obesity, suggesting an adaptive host response to specific diet-induced dysbiosis. |
format | Online Article Text |
id | pubmed-10574285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105742852023-10-14 Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity Caremoli, Filippo Huynh, Jennifer Lagishetty, Venu Markovic, Daniela Braun, Jonathan Dong, Tien S. Jacobs, Jonathan P. Sternini, Catia Nutrients Article Bitter taste receptors (Tas2rs in mice) detect bitterness, a warning signal for toxins and poisons, and are expressed in enteroendocrine cells. We tested the hypothesis that Tas2r138 and Tas2r116 mRNAs are modulated by microbiota alterations induced by a long-term high-fat diet (HFD) and antibiotics (ABX) (ampicillin and neomycin) administered in drinking water. Cecum and colon specimens and luminal contents were collected from C57BL/6 female and male mice for qRT-PCR and microbial luminal 16S sequencing. HFD with/without ABX significantly increased body weight and fat mass at 4, 6, and 8 weeks. Tas2r138 and Tas2r116 mRNAs were significantly increased in mice fed HFD for 8 weeks vs. normal diet, and this increase was prevented by ABX. There was a distinct microbiota separation in each experimental group and significant changes in the composition and diversity of microbiome in mice fed a HFD with/without ABX. Tas2r mRNA expression in HFD was associated with several genera, particularly with Akkermansia, a Gram-negative mucus-resident bacterium. These studies indicate that luminal bacterial composition is affected by sex, diet, and ABX and support a microbial dependent upregulation of Tas2rs in HFD-induced obesity, suggesting an adaptive host response to specific diet-induced dysbiosis. MDPI 2023-09-25 /pmc/articles/PMC10574285/ /pubmed/37836428 http://dx.doi.org/10.3390/nu15194145 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Caremoli, Filippo Huynh, Jennifer Lagishetty, Venu Markovic, Daniela Braun, Jonathan Dong, Tien S. Jacobs, Jonathan P. Sternini, Catia Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title | Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title_full | Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title_fullStr | Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title_full_unstemmed | Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title_short | Microbiota-Dependent Upregulation of Bitter Taste Receptor Subtypes in the Mouse Large Intestine in High-Fat Diet-Induced Obesity |
title_sort | microbiota-dependent upregulation of bitter taste receptor subtypes in the mouse large intestine in high-fat diet-induced obesity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10574285/ https://www.ncbi.nlm.nih.gov/pubmed/37836428 http://dx.doi.org/10.3390/nu15194145 |
work_keys_str_mv | AT caremolifilippo microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT huynhjennifer microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT lagishettyvenu microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT markovicdaniela microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT braunjonathan microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT dongtiens microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT jacobsjonathanp microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity AT sterninicatia microbiotadependentupregulationofbittertastereceptorsubtypesinthemouselargeintestineinhighfatdietinducedobesity |