Journal of Biological Chemistry
Volume 290, Issue 9, 27 February 2015, Pages 5647-5660
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Molecular Bases of Disease
Transmission of Atherosclerosis Susceptibility with Gut Microbial Transplantation*

https://doi.org/10.1074/jbc.M114.618249Get rights and content
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Recent studies indicate both clinical and mechanistic links between atherosclerotic heart disease and intestinal microbial metabolism of certain dietary nutrients producing trimethylamine N-oxide (TMAO). Here we test the hypothesis that gut microbial transplantation can transmit choline diet-induced TMAO production and atherosclerosis susceptibility. First, a strong association was noted between atherosclerotic plaque and plasma TMAO levels in a mouse diversity panel (n = 22 strains, r = 0.38; p = 0.0001). An atherosclerosis-prone and high TMAO-producing strain, C57BL/6J, and an atherosclerosis-resistant and low TMAO-producing strain, NZW/LacJ, were selected as donors for cecal microbial transplantation into apolipoprotein e null mice in which resident intestinal microbes were first suppressed with antibiotics. Trimethylamine (TMA) and TMAO levels were initially higher in recipients on choline diet that received cecal microbes from C57BL/6J inbred mice; however, durability of choline diet-dependent differences in TMA/TMAO levels was not maintained to the end of the study. Mice receiving C57BL/6J cecal microbes demonstrated choline diet-dependent enhancement in atherosclerotic plaque burden as compared with recipients of NZW/LacJ microbes. Microbial DNA analyses in feces and cecum revealed transplantation of donor microbial community features into recipients with differences in taxa proportions between donor strains that were transmissible to recipients and that tended to show coincident proportions with TMAO levels. Proportions of specific taxa were also identified that correlated with plasma TMAO levels in donors and recipients and with atherosclerotic lesion area in recipients. Atherosclerosis susceptibility may be transmitted via transplantation of gut microbiota. Gut microbes may thus represent a novel therapeutic target for modulating atherosclerosis susceptibility.

Background

Recent human and animal studies suggest that gut microbes can influence atherosclerosis via generation of trimethylamine N-oxide (TMAO).

Results

Cecal microbial transplantation from atherosclerosis-prone versus -resistant inbred strains of mice transmitted enhanced choline diet-dependent atherosclerosis and TMAO levels.

Conclusion

Atherosclerosis susceptibility can be transmitted with gut microbial transplantation.

Significance

Gut microbes participate in atherosclerosis susceptibility and are thus a potential therapeutic target.

Atherosclerosis
Dyslipidemia
Lipid
Nutrition
Phospholipid
Koch's Postulate
Choline
Gut Microbiota
Trimethylamine N-Oxide (TMAO)

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*

This work was supported, in whole or in part, by National Institutes of Health Grants R01 HL103866 (to S. L. H.), P20 HL113452 (to S. L. H.), and HL28481 and HL30568 (to A. J. L.) from the Office of Dietary Supplements. Drs. Hazen, Wang, and Levison are named as co-inventors on pending and issued patents held by the Cleveland Clinic relating to cardiovascular diagnostics and therapeutics. Dr. Hazen reports he has been paid as a consultant or speaker by the following companies: Cleveland Heart Lab, Inc., Esperion, Liposciences Inc., Merck & Co., Inc., Pfizer Inc., and Proctor & Gamble. Dr. Hazen reports he has received research funds from Abbott, Cleveland HeartLab, Liposciences, Inc., Proctor & Gamble, and Takeda. Drs. Hazen, Wang, and Levison have the right to receive royalty payments for inventions or discoveries related to cardiovascular diagnostics or therapeutics from Cleveland HeartLab, Inc., Esperion, and/or Frantz Biomarkers.

1

Supported in part by National Institutes of Health Training Grant T32 GM088088.

2

Supported in part by Postdoctoral Grants MJD252 (from MOBILITAS) and FP7-People-IOF (330381) (from the European Union).