Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice

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Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice. / Kashani, Alireza; Brejnrod, Asker Daniel; Jin, Chunyu; Kern, Timo; Madsen, Andreas Nygaard; Holm, Louise Aas; Gerber, Georg K.; Holm, Jens Christian; Hansen, Torben; Holst, Birgitte; Arumugam, Manimozhiyan.

I: Animal Microbiome, Bind 1, Nr. 1, 11, 2019.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Kashani, A, Brejnrod, AD, Jin, C, Kern, T, Madsen, AN, Holm, LA, Gerber, GK, Holm, JC, Hansen, T, Holst, B & Arumugam, M 2019, 'Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice', Animal Microbiome, bind 1, nr. 1, 11. https://doi.org/10.1186/s42523-019-0007-1

APA

Kashani, A., Brejnrod, A. D., Jin, C., Kern, T., Madsen, A. N., Holm, L. A., Gerber, G. K., Holm, J. C., Hansen, T., Holst, B., & Arumugam, M. (2019). Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice. Animal Microbiome, 1(1), [11]. https://doi.org/10.1186/s42523-019-0007-1

Vancouver

Kashani A, Brejnrod AD, Jin C, Kern T, Madsen AN, Holm LA o.a. Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice. Animal Microbiome. 2019;1(1). 11. https://doi.org/10.1186/s42523-019-0007-1

Author

Kashani, Alireza ; Brejnrod, Asker Daniel ; Jin, Chunyu ; Kern, Timo ; Madsen, Andreas Nygaard ; Holm, Louise Aas ; Gerber, Georg K. ; Holm, Jens Christian ; Hansen, Torben ; Holst, Birgitte ; Arumugam, Manimozhiyan. / Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice. I: Animal Microbiome. 2019 ; Bind 1, Nr. 1.

Bibtex

@article{6ec9cef7c7514ed7adf4d0a1b5fb330e,
title = "Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice",
abstract = "Background: Growing evidence supports the role of gut microbiota in obesity and its related disorders including type 2 diabetes. Ob/ob mice, which are hyperphagic due to leptin deficiency, are commonly used models of obesity and were instrumental in suggesting links between gut microbiota and obesity. Specific changes in their gut microbiota such as decreased microbial diversity and increased Firmicutes to Bacteroidetes ratio have been suggested to contribute to obesity via increased microbiota capacity to harvest energy. However, the differential development of ob/ob mouse gut microbiota compared to wild type microbiota and the role of hyperphagia in their metabolic impairment have not been investigated thoroughly. Results: We performed a 10-week long study in ob/ob (n = 12) and wild type control (n = 12) mice fed ad libitum. To differentiate effects of leptin deficiency from hyperphagia, we pair-fed an additional group of ob/ob mice (n = 11) based on the food consumption of control mice. Compared to control mice, ob/ob mice fed ad libitum exhibited compromised glucose metabolism and increased body fat percentage. Pair-fed ob/ob mice exhibited even more compromised glucose metabolism and maintained strikingly similar high body fat percentage at the cost of lean body mass. Acclimatization of the microbiota to our facility took up to 5 weeks. Leptin deficiency impacted gut microbial composition, explaining 18.3% of the variance. Pair-feeding also altered several taxa, although the overall community composition at the end of the study was not significantly different. We found 24 microbial taxa associations with leptin deficiency, notably enrichment of members of Lactobacillus and depletion of Akkermansia muciniphila. Microbial metabolic functions related to energy harvest, including glycan degradation, phosphotransferase systems and ABC transporters, were enriched in the ob/ob mice. Taxa previously reported as relevant for obesity were associated with body weight, including Oscillibacter and Alistipes (both negatively correlated) and Prevotella (positively correlated). Conclusions: Leptin deficiency caused major changes in the mouse gut microbiota composition. Several microbial taxa were associated with body composition. Pair-fed mice maintained a pre-set high proportion of body fat despite reduced calorie intake, and exhibited more compromised glucose metabolism, with major implications for treatment options for genetically obese individuals.",
keywords = "16S rRNA gene amplicon sequencing, Calorie restriction, Leptin deficiency, Leptin-deficient mice, Mouse gut microbiota, Ob/Ob mice, Obesity",
author = "Alireza Kashani and Brejnrod, {Asker Daniel} and Chunyu Jin and Timo Kern and Madsen, {Andreas Nygaard} and Holm, {Louise Aas} and Gerber, {Georg K.} and Holm, {Jens Christian} and Torben Hansen and Birgitte Holst and Manimozhiyan Arumugam",
note = "Funding Information: We are thankful to members of Arumugam group for inspiring discussions. We thank members of Karsten Kristiansen lab at Department of Biology, University of Copenhagen, for assistance in sequencing. We thank Claus Thorn Ekstrom for helpful discussions on the statistical analysis. Publisher Copyright: {\textcopyright} 2019, The Author(s).",
year = "2019",
doi = "10.1186/s42523-019-0007-1",
language = "English",
volume = "1",
journal = "BMC Animal Microbiome",
issn = "2524-4671",
publisher = "BioMed Central",
number = "1",

}

RIS

TY - JOUR

T1 - Impaired glucose metabolism and altered gut microbiome despite calorie restriction of ob/ob mice

AU - Kashani, Alireza

AU - Brejnrod, Asker Daniel

AU - Jin, Chunyu

AU - Kern, Timo

AU - Madsen, Andreas Nygaard

AU - Holm, Louise Aas

AU - Gerber, Georg K.

AU - Holm, Jens Christian

AU - Hansen, Torben

AU - Holst, Birgitte

AU - Arumugam, Manimozhiyan

N1 - Funding Information: We are thankful to members of Arumugam group for inspiring discussions. We thank members of Karsten Kristiansen lab at Department of Biology, University of Copenhagen, for assistance in sequencing. We thank Claus Thorn Ekstrom for helpful discussions on the statistical analysis. Publisher Copyright: © 2019, The Author(s).

PY - 2019

Y1 - 2019

N2 - Background: Growing evidence supports the role of gut microbiota in obesity and its related disorders including type 2 diabetes. Ob/ob mice, which are hyperphagic due to leptin deficiency, are commonly used models of obesity and were instrumental in suggesting links between gut microbiota and obesity. Specific changes in their gut microbiota such as decreased microbial diversity and increased Firmicutes to Bacteroidetes ratio have been suggested to contribute to obesity via increased microbiota capacity to harvest energy. However, the differential development of ob/ob mouse gut microbiota compared to wild type microbiota and the role of hyperphagia in their metabolic impairment have not been investigated thoroughly. Results: We performed a 10-week long study in ob/ob (n = 12) and wild type control (n = 12) mice fed ad libitum. To differentiate effects of leptin deficiency from hyperphagia, we pair-fed an additional group of ob/ob mice (n = 11) based on the food consumption of control mice. Compared to control mice, ob/ob mice fed ad libitum exhibited compromised glucose metabolism and increased body fat percentage. Pair-fed ob/ob mice exhibited even more compromised glucose metabolism and maintained strikingly similar high body fat percentage at the cost of lean body mass. Acclimatization of the microbiota to our facility took up to 5 weeks. Leptin deficiency impacted gut microbial composition, explaining 18.3% of the variance. Pair-feeding also altered several taxa, although the overall community composition at the end of the study was not significantly different. We found 24 microbial taxa associations with leptin deficiency, notably enrichment of members of Lactobacillus and depletion of Akkermansia muciniphila. Microbial metabolic functions related to energy harvest, including glycan degradation, phosphotransferase systems and ABC transporters, were enriched in the ob/ob mice. Taxa previously reported as relevant for obesity were associated with body weight, including Oscillibacter and Alistipes (both negatively correlated) and Prevotella (positively correlated). Conclusions: Leptin deficiency caused major changes in the mouse gut microbiota composition. Several microbial taxa were associated with body composition. Pair-fed mice maintained a pre-set high proportion of body fat despite reduced calorie intake, and exhibited more compromised glucose metabolism, with major implications for treatment options for genetically obese individuals.

AB - Background: Growing evidence supports the role of gut microbiota in obesity and its related disorders including type 2 diabetes. Ob/ob mice, which are hyperphagic due to leptin deficiency, are commonly used models of obesity and were instrumental in suggesting links between gut microbiota and obesity. Specific changes in their gut microbiota such as decreased microbial diversity and increased Firmicutes to Bacteroidetes ratio have been suggested to contribute to obesity via increased microbiota capacity to harvest energy. However, the differential development of ob/ob mouse gut microbiota compared to wild type microbiota and the role of hyperphagia in their metabolic impairment have not been investigated thoroughly. Results: We performed a 10-week long study in ob/ob (n = 12) and wild type control (n = 12) mice fed ad libitum. To differentiate effects of leptin deficiency from hyperphagia, we pair-fed an additional group of ob/ob mice (n = 11) based on the food consumption of control mice. Compared to control mice, ob/ob mice fed ad libitum exhibited compromised glucose metabolism and increased body fat percentage. Pair-fed ob/ob mice exhibited even more compromised glucose metabolism and maintained strikingly similar high body fat percentage at the cost of lean body mass. Acclimatization of the microbiota to our facility took up to 5 weeks. Leptin deficiency impacted gut microbial composition, explaining 18.3% of the variance. Pair-feeding also altered several taxa, although the overall community composition at the end of the study was not significantly different. We found 24 microbial taxa associations with leptin deficiency, notably enrichment of members of Lactobacillus and depletion of Akkermansia muciniphila. Microbial metabolic functions related to energy harvest, including glycan degradation, phosphotransferase systems and ABC transporters, were enriched in the ob/ob mice. Taxa previously reported as relevant for obesity were associated with body weight, including Oscillibacter and Alistipes (both negatively correlated) and Prevotella (positively correlated). Conclusions: Leptin deficiency caused major changes in the mouse gut microbiota composition. Several microbial taxa were associated with body composition. Pair-fed mice maintained a pre-set high proportion of body fat despite reduced calorie intake, and exhibited more compromised glucose metabolism, with major implications for treatment options for genetically obese individuals.

KW - 16S rRNA gene amplicon sequencing

KW - Calorie restriction

KW - Leptin deficiency

KW - Leptin-deficient mice

KW - Mouse gut microbiota

KW - Ob/Ob mice

KW - Obesity

U2 - 10.1186/s42523-019-0007-1

DO - 10.1186/s42523-019-0007-1

M3 - Journal article

AN - SCOPUS:85097396663

VL - 1

JO - BMC Animal Microbiome

JF - BMC Animal Microbiome

SN - 2524-4671

IS - 1

M1 - 11

ER -

ID: 378315728