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Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model

BACKGROUND: Host genetic background and sex, play central roles in defining the pathogenesis of type 2 diabetes (T2D), obesity and infectious diseases. Our previous studies demonstrated the utilization of genetically highly diverse inbred mouse lines, namely collaborative cross (CC), for dissecting...

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Autores principales: Karkar, Luna, Abu‐Toamih Atamni, Hanifa J., Milhem, Asal, Houri-Haddad, Yael, Iraqi, Fuad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323698/
https://www.ncbi.nlm.nih.gov/pubmed/32613174
http://dx.doi.org/10.1002/ame2.12117
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author Karkar, Luna
Abu‐Toamih Atamni, Hanifa J.
Milhem, Asal
Houri-Haddad, Yael
Iraqi, Fuad A.
author_facet Karkar, Luna
Abu‐Toamih Atamni, Hanifa J.
Milhem, Asal
Houri-Haddad, Yael
Iraqi, Fuad A.
author_sort Karkar, Luna
collection PubMed
description BACKGROUND: Host genetic background and sex, play central roles in defining the pathogenesis of type 2 diabetes (T2D), obesity and infectious diseases. Our previous studies demonstrated the utilization of genetically highly diverse inbred mouse lines, namely collaborative cross (CC), for dissecting host susceptibility for the development of T2D and obesity, showing significant variations following high‐fat (42% fat) diet (HFD). Here, we aimed to assessing the host genetic background and sex effects on T2D and obesity development in response to oral‐mixed bacterial infection and HFD using the CC lines. MATERIALS AND METHODS: Study cohort consists of 97 mice from 2 CC lines (both sexes), maintained on either HFD or Standard diet (CHD) for 12 weeks. At week 5 a group of mice from each diet were infected with Porphyromonas gingivalis (Pg) and Fusobacterium nucleatum (Fn) bacteria (control groups without infection). Body weight (BW) and glucose tolerance ability were assessed at the end time point of the experiment. RESULTS: The CC lines varied (P < .05) at their BW gain and glucose tolerance ability (with sex effect) in response to diets and/or infection, showing opposite responses despite sharing the same environmental conditions. The combination of diet and infection enhances BW accumulation for IL1912, while restraints it for IL72. As for glucose tolerance ability, only females (both lines) were deteriorated in response to infection. CONCLUSIONS: This study emphasizes the power of the CC mouse population for the characterization of host genetic makeup for defining the susceptibility of the individual to development of obesity and/or impaired glucose tolerance.
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spelling pubmed-73236982020-06-30 Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model Karkar, Luna Abu‐Toamih Atamni, Hanifa J. Milhem, Asal Houri-Haddad, Yael Iraqi, Fuad A. Animal Model Exp Med Original Articles BACKGROUND: Host genetic background and sex, play central roles in defining the pathogenesis of type 2 diabetes (T2D), obesity and infectious diseases. Our previous studies demonstrated the utilization of genetically highly diverse inbred mouse lines, namely collaborative cross (CC), for dissecting host susceptibility for the development of T2D and obesity, showing significant variations following high‐fat (42% fat) diet (HFD). Here, we aimed to assessing the host genetic background and sex effects on T2D and obesity development in response to oral‐mixed bacterial infection and HFD using the CC lines. MATERIALS AND METHODS: Study cohort consists of 97 mice from 2 CC lines (both sexes), maintained on either HFD or Standard diet (CHD) for 12 weeks. At week 5 a group of mice from each diet were infected with Porphyromonas gingivalis (Pg) and Fusobacterium nucleatum (Fn) bacteria (control groups without infection). Body weight (BW) and glucose tolerance ability were assessed at the end time point of the experiment. RESULTS: The CC lines varied (P < .05) at their BW gain and glucose tolerance ability (with sex effect) in response to diets and/or infection, showing opposite responses despite sharing the same environmental conditions. The combination of diet and infection enhances BW accumulation for IL1912, while restraints it for IL72. As for glucose tolerance ability, only females (both lines) were deteriorated in response to infection. CONCLUSIONS: This study emphasizes the power of the CC mouse population for the characterization of host genetic makeup for defining the susceptibility of the individual to development of obesity and/or impaired glucose tolerance. John Wiley and Sons Inc. 2020-05-17 /pmc/articles/PMC7323698/ /pubmed/32613174 http://dx.doi.org/10.1002/ame2.12117 Text en © 2020 Tel‐Aviv University (TAU). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Karkar, Luna
Abu‐Toamih Atamni, Hanifa J.
Milhem, Asal
Houri-Haddad, Yael
Iraqi, Fuad A.
Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title_full Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title_fullStr Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title_full_unstemmed Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title_short Assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
title_sort assessing the host genetic background effects on type 2 diabetes and obesity development in response to mixed–oral bacteria and high‐fat diet using the collaborative cross mouse model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7323698/
https://www.ncbi.nlm.nih.gov/pubmed/32613174
http://dx.doi.org/10.1002/ame2.12117
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