Integrated metagenomics identifies a crucial role for trimethylamine-producing Lachnoclostridium in promoting atherosclerosis

This study discloses the significance and efficiency of the human gut bacterium L. saccharolyticum WM1 in transforming choline to TMA and consequently promoting the development of atherosclerosis.
Published in Microbiology
Integrated metagenomics identifies a crucial role for trimethylamine-producing Lachnoclostridium in promoting atherosclerosis

Numerous studies on intestinal microbiota over the past ten years have confirmed their pivotal roles in human health and diseases, including cardiovascular diseases1,2,3. Recently, the gut microbiota as a whole, has recently been found to be an important contributor to the progression of cardiovascular diseases1,4,5. Plasma trimethylamine-N-oxide (TMAO) has been confirmed as an independent risk factor for atherosclerosis, thrombus formation6, and myocardial infarction5,7Trimethylamine (TMA), a precursor of TMAO, is a small molecular weight byproduct of intestinal microbial metabolism of dietary choline, carnitine, and phosphatidylcholines8,9,10and converted to trimethylamine-N-oxide (TMAO) in the liver via flavin-containing monooxygenase 311,12. 

In our work, using an integrated metagenomic approach, we analyzed reference genomes from the three reference resources, 12 metagenomic datasets from public metagenomic databases and biologically validated our findings with an Apoe−/− mice model. We sought to investigate: (1) the bacteria in the human gut microbiota that encode TMA-lyase in their genomes (2) the abundances and activities of these TMA-producing bacteria in the gut and (3) whether or not the TMA-producing bacteria increase the risk of developing atherosclerosis.

The gut microbiota is known to convert carnitine, betaine, and choline to TMA by utilizing three TMA-lyase complexes, cntA/ByeaW/X, and cutC/D, respectively. We identified the TMA-lyase sequences of the TMA-producing bacteria based on the three reference genomic resources. The final 885 TMA-lyase reference sequences were identified from three resources, 451 from the Human Microbiome Project database, 216 from the Unified Human Gastrointestinal Genome, and 218 reference sequences from 4930 species-level genome bins by taking the initial 983 sequences as query. In order to achieve the representing TMA-producing bacteria, we applied an integrated reference metagenomic sequence dataset was acquired from several public cohorts (Fig. 2). 

Fig. 2: Relative abundance distribution and taxonomic identification of cntA and cutC.

After our taxonomic identification, we unexpectedly found cutC showed significantly increased relative abundance in the patients with atherosclerosis, and the genus Lachnoclostridium, the highest cutC containing genus, were significantly increased in patients with atherosclerosis. As a result, L. saccharolyticum WM1, a representative strain of Lachnoclostridium, effectively converted choline to TMA at a transformation rate near 100%, much higher than 63% for C. sporogenes. This strain was found to elevate serum TMAO and promote the formation of atherosclerosis in ApoE−/− mice when co-administered with choline.


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Live biotherapeutics and medicinal microbiome products

This Collection welcomes contributions on recent developments in the utilization of live biotherapeutics and medicinal microbiome products for the treatment or prevention of diseases. In many cases, suitable drug treatments are still lacking due to the ineffectiveness of existing standards or the presence of long-term side effects. We are particularly interested in difficult-to-treat non-communicable diseases whose pathogenesis is associated with microbiota.

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Deadline: Aug 02, 2024