
f Bacterial communities in the small intestine respond differently to those in the caecum and colon in mice fed low- and high-fat diets
- Authors: Janet C. Onishi1 , Sara Campbell2 , Michael Moreau3 , Falshruti Patel3 , Andrew I. Brooks3 , Yin Xiu Zhou4 , Max M. Häggblom1 , Judith Storch4
-
- VIEW AFFILIATIONS
-
1 1Department of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ 08901, USA 2 2Department of Kinesiology and Health, Rutgers University, New Brunswick, NJ 08901, USA 3 3RUCDR Infinite Biologics, Piscataway, NJ 08854, USA 4 4Department of Nutritional Sciences, Rutgers University, New Brunswick, NJ 08901, USA
- *Correspondence: Janet C. Onishi, [email protected]
- First Published Online: 26 July 2017, Microbiology 163: 1189-1197, doi: 10.1099/mic.0.000496
- Subject: Host-microbe Interaction
- Received:
- Accepted:
- Cover date:




Bacterial communities in the small intestine respond differently to those in the caecum and colon in mice fed low- and high-fat diets, Page 1 of 1
< Previous page | Next page > /docserver/preview/fulltext/micro/163/8/1189_micro000496-1.gif
-
Bacterial communities in the mouse caecum and faeces are known to be altered by changes in dietary fat. The microbiota of the mouse small intestine, by contrast, has not been extensively profiled and it is unclear whether small intestinal bacterial communities shift with dietary fat levels. We compared the microbiota in the small intestine, caecum and colon in mice fed a low-fat (LF) or high-fat (HF) diet using 16S rRNA gene sequencing. The relative abundance of major phyla in the small intestine, Bacteriodetes, Firmicutes and Proteobacteria, was similar to that in the caecum and colon; the relative abundance of Verrucomicrobia was significantly reduced in the small intestine compared to the large intestine. Several genera were uniquely detected in the small intestine and included the aerotolerant anaerobe, Lactobacillus spp. The most abundant genera in the small intestine were accounted for by anaerobic bacteria and were identical to those identified in the large intestine. An HF diet was associated with significant weight gain and adiposity and with changes in the bacterial communities throughout the intestine, with changes in the small intestine differing from those in the caecum and colon. Prominent Gram-negative bacteria including genera of the phylum Bacteroidetes and a genus of Proteobacteria significantly changed in the large intestine. The mechanistic links between these changes and the development of obesity, perhaps involving metabolic endotoxemia, remain to be determined.
-
Sequence data have been uploaded to the NCBI Short Read Archive (SRA) database under accession number SRP066846.
-
Four supplementary tables and two supplementary figures are available with the online Supplementary Material.
- Keyword(s): 16S rRNA gene sequencing, high-fat diet, gut microbiome, metabolic endotoxaemia, mouse diet-induced obesity model
© 2017 The Authors
-
1. Lee JE, Lee S, Sung J, Ko G. Analysis of human and animal fecal microbiota for microbial source tracking. Isme J 2011;5:362–365 [CrossRef][PubMed]
-
2. Nguyen TL, Vieira-Silva S, Liston A, Raes J. How informative is the mouse for human gut microbiota research?. Dis Model Mech 2015;8:1–16 [CrossRef][PubMed]
-
3. Canny GO, McCormick BA. Bacteria in the intestine, helpful residents or enemies from within?. Infect Immun 2008;76:3360–3373 [CrossRef][PubMed]
-
4. Berg RD. The indigenous gastrointestinal microflora. Trends Microbiol 1996;4:430–435 [CrossRef][PubMed]
-
5. Breen DM, Rasmussen BA, Côté CD, Jackson VM, Lam TK. Nutrient-sensing mechanisms in the gut as therapeutic targets for diabetes. Diabetes 2013;62:3005–3013 [CrossRef][PubMed]
-
6. Angelakis E, Armougom F, Carrière F, Bachar D, Laugier R et al. A metagenomic investigation of the duodenal microbiota reveals links with obesity. PLoS One 2015;10:e0137784 [CrossRef][PubMed]
-
7. Turnbaugh PJ, Ridaura VK, Faith JJ, Rey FE, Knight R et al. The effect of diet on the human gut microbiome: a metagenomic analysis in humanized gnotobiotic mice. Sci Transl Med 2009;1:6ra14 [CrossRef][PubMed]
-
8. Zoetendal EG, Raes J, van den Bogert B, Arumugam M, Booijink CC et al. The human small intestinal microbiota is driven by rapid uptake and conversion of simple carbohydrates. Isme J 2012;6:1415–1426 [CrossRef][PubMed]
-
9. Kim YS, Kim J, Park SJ. High-throughput 16S rRNA gene sequencing reveals alterations of mouse intestinal microbiota after radiotherapy. Anaerobe 2015;33:1–7 [CrossRef][PubMed]
-
10. Hildebrandt MA, Hoffmann C, Sherrill-Mix SA, Keilbaugh SA, Hamady M et al. High-fat diet determines the composition of the murine gut microbiome independently of obesity. Gastroenterology 2009;137:1716–1724 [CrossRef][PubMed]
-
11. Zhang C, Zhang M, Pang X, Zhao Y, Wang L et al. Structural resilience of the gut microbiota in adult mice under high-fat dietary perturbations. Isme J 2012;6:1848–1857 [CrossRef][PubMed]
-
12. Cani PD, Amar J, Iglesias MA, Poggi M, Knauf C et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes 2007;56:1761–1772 [CrossRef][PubMed]
-
13. Van Heek M, Compton DS, France CF, Tedesco RP, Fawzi AB et al. Diet-induced obese mice develop peripheral, but not central, resistance to leptin. J Clin Invest 1997;99:385–390 [CrossRef][PubMed]
-
14. Douris N, Melman T, Pecherer JM, Pissios P, Flier JS et al. Adaptive changes in amino acid metabolism permit normal longevity in mice consuming a low-carbohydrate ketogenic diet. Biochim Biophys Acta 2015;1852:2056–2065 [CrossRef][PubMed]
-
15. Gajda AM, Zhou YX, Agellon LB, Fried SK, Kodukula S et al. Direct comparison of mice null for liver or intestinal fatty acid-binding proteins reveals highly divergent phenotypic responses to high fat feeding. J Biol Chem 2013;288:30330–30344 [CrossRef][PubMed]
-
16. Delmont TO, Simonet P, Vogel TM. Describing microbial communities and performing global comparisons in the 'omic era. Isme J 2012;6:1625–1628 [CrossRef][PubMed]
-
17. Moreau MM, Eades SC, Reinemeyer CR, Fugaro MN, Onishi JC. Illumina sequencing of the V4 hypervariable region 16S rRNA gene reveals extensive changes in bacterial communities in the cecum following carbohydrate oral infusion and development of early-stage acute laminitis in the horse. Vet Microbiol 2014;168:436–441 [CrossRef][PubMed]
-
19. Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C et al. Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res 2013;41:e1 [CrossRef][PubMed]
-
20. Milinovich GJ, Burrell PC, Pollitt CC, Klieve AV, Blackall LL et al. Microbial ecology of the equine hindgut during oligofructose-induced laminitis. Isme J 2008;2:1089–1100 [CrossRef][PubMed]
-
23. Dean-Ross D, Mills AL. Bacterial community structure and function along a heavy metal gradient. Appl Environ Microbiol 1989;55:2002–2009[PubMed]
-
24. Campbell SC, Wisniewski PJ, Noji M, Mcguinness LR, Häggblom MM et al. The effect of diet and exercise on intestinal integrity and microbial diversity in mice. PLoS One 2016;11:e0150502 [CrossRef][PubMed]
-
25. Yanke LJ, Cheng KJ. A method for the selective enumeration and isolation of ruminal Lactobacillus and Streptococcus. Lett Appl Microbiol 1998;26:248–252 [CrossRef][PubMed]
-
26. Ali N, Dashti N, Salamah S, Sorkhoh N, Al-Awadhi H et al. Dynamics of bacterial populations during bench-scale bioremediation of oily seawater and desert soil bioaugmented with coastal microbial mats. Microb Biotechnol 2016;9:157–171 [CrossRef][PubMed]
-
27. Zhang J, Cai X, Qi L, Shao C, Lin Y et al. Effects of aeration strategy on the evolution of dissolved organic matter (DOM) and microbial community structure during sludge bio-drying. Appl Microbiol Biotechnol 2015;99:7321–7331 [CrossRef][PubMed]
-
28. Wang Y, Gao L, Ming H, Zhang P, Zhu W. Polaribacter marinaquae sp. nov., isolated from seawater. Int J Syst Evol Microbiol 2016;66:4594–4599 [CrossRef][PubMed]
-
29. Gupta A, Logan J, Elhag N, Almond M. Sphingobacterium spiritivorum infection in a patient with end stage renal disease on haemodialysis. Ann Clin Microbiol Antimicrob 2016;15:25 [CrossRef][PubMed]
-
30. Deepnarain N, Kumari S, Ramjith J, Swalaha FM, Tandoi V et al. A logistic model for the remediation of filamentous bulking in a biological nutrient removal wastewater treatment plant. Water Sci Technol 2015;72:391–405 [CrossRef][PubMed]
-
31. Calabuig R, Weems WA, Moody FG. Ileo-cecal junction: a valve or a sphincter? An experimental study in the opossum. Rev Esp Enferm Dig 1996;88:828–839[PubMed]
-
32. Brannon P, Tso P, Jandacek RJ. Digestion and absorption of lipids. In Stipanuk M. (editor) Biochemical, Physiological, and Molecular Aspects of Human Nutrition, 3rd ed. St. Louis: Saunders Elsevier; 2012; pp.179–191
-
33. Dirusso CC, Black PN. Long-chain fatty acid transport in bacteria and yeast. Paradigms for defining the mechanism underlying this protein-mediated process. Mol Cell Biochem 1999;192:41–52 [CrossRef][PubMed]
-
34. Nunn WD. A molecular view of fatty acid catabolism in Escherichia coli. Microbiol Rev 1986;50:179–192[PubMed]
-
35. Kennedy AR, Pissios P, Otu H, Roberson R, Xue B et al. A high-fat, ketogenic diet induces a unique metabolic state in mice. Am J Physiol Endocrinol Metab 2007;292:E1724E1739 [CrossRef][PubMed]
-
36. Ghibaudi L, Cook J, Farley C, van Heek M, Hwa JJ. Fat intake affects adiposity, comorbidity factors, and energy metabolism of Sprague-Dawley rats. Obes Res 2002;10:956–963 [CrossRef][PubMed]
-
37. Tinsley FC, Taicher GZ, Heiman ML. Evaluation of a quantitative magnetic resonance method for mouse whole body composition analysis. Obes Res 2004;12:150–160 [CrossRef][PubMed]
-
38. Raetz CR, Whitfield C. Lipopolysaccharide endotoxins. Annu Rev Biochem 2002;71:635–700 [CrossRef][PubMed]
-
39. Munford RS. Sensing gram-negative bacterial lipopolysaccharides: a human disease determinant?. Infect Immun 2008;76:454–465 [CrossRef][PubMed]
-
40. Munford RS, Varley AW. Shield as signal: lipopolysaccharides and the evolution of immunity to gram-negative bacteria. PLoS Pathog 2006;2:e67 [CrossRef][PubMed]
-
41. Boutagy NE, Mcmillan RP, Frisard MI, Hulver MW. Metabolic endotoxemia with obesity: Is it real and is it relevant?. Biochimie 2016;124:11–20 [CrossRef][PubMed]
-
42. Munford RS. Endotoxemia-menace, marker, or mistake?. J Leukoc Biol 2016;100:687–698 [CrossRef][PubMed]
-
43. Turnbaugh PJ, Bäckhed F, Fulton L, Gordon JI. Diet-induced obesity is linked to marked but reversible alterations in the mouse distal gut microbiome. Cell Host Microbe 2008;3:213–223 [CrossRef][PubMed]
-
44. Turnbaugh PJ, Ley RE, Mahowald MA, Magrini V, Mardis ER et al. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature 2006;444:1027–1131 [CrossRef][PubMed]
-
45. Duncan SH, Lobley GE, Holtrop G, Ince J, Johnstone AM et al. Human colonic microbiota associated with diet, obesity and weight loss. Int J Obes 2008;32:1720–1724 [CrossRef][PubMed]
-
46. Ericsson AC, Davis JW, Spollen W, Bivens N, Givan S et al. Effects of vendor and genetic background on the composition of the fecal microbiota of inbred mice. PLoS One 2015;10:e0116704 [CrossRef][PubMed]

Supplementary Data
Data loading....

Article metrics loading...

Full text loading...
Author and Article Information
-
This Journal
/content/journal/micro/10.1099/mic.0.000496dcterms_title,dcterms_subject,pub_serialTitlepub_serialIdent:journal/micro AND -contentType:BlogPost104 -
Other Society Journals
/content/journal/micro/10.1099/mic.0.000496dcterms_title,dcterms_subject-pub_serialIdent:journal/micro AND -contentType:BlogPost104 -
PubMed
-
Google Scholar
Figure data loading....