# Deciphering the Arterial and Venous Blood Bacterial DNA Profile: Pioneering Insights into Coronary Heart Disease Etiology and Progression

**Authors:** Mengru Liu, Lin Zhao, Tianli Li, Xuelin Li, Hong Jiang, Peng Yang

PMC · DOI: 10.3390/microorganisms14020359 · Microorganisms · 2026-02-03

## TL;DR

This study explores bacterial DNA in arterial and venous blood to understand its role in coronary heart disease progression.

## Contribution

The study is the first to observe higher microbial diversity in plasma compared to serum in CHD patients.

## Key findings

- Higher microbial diversity was found in plasma than in serum.
- Significant differences in microbial richness were observed across various blood fractions.
- Detected bacteria were linked to intestinal, oral, or skin microbiota.

## Abstract

Background: Coronary heart disease (CHD) is the leading cause of death and disability worldwide. The human microbiota, particularly gut bacteria, plays a role in the development of CHD. However, determining the contribution of gut bacteria translocation to systemic circulation in the progression of atherosclerosis remains challenging. Methods and Results: In this exploratory study, we conducted 16S rRNA–based metagenomic analysis to characterize systemic bacterial profiles in a cohort of 27 patients with CHD (9 with severe coronary artery stenosis and 18 with mild to moderate stenosis). We compared microbial diversity between arterial and venous blood and across different blood fractions. For the first time, we observed higher microbial diversity in plasma than in serum. We also identified differences in microbial richness among arterial whole blood, venous whole blood, arterial plasma, venous plasma, arterial serum, and venous serum, with 15, 22, 43, 10, 4, and 3 genera showing significant differences, respectively. Many of the detected blood taxa belonged to genera typically found in intestinal, oral, or skin microbiota, although their precise source cannot be determined from this study. Conclusions: Our study provides preliminary evidence of distinct bacterial profiles between arterial and venous blood fractions in patients with CHD, as determined by 16S rRNA sequencing. These findings should be interpreted with caution given the small sample size and the absence of a healthy control group, and they warrant confirmation in larger, controlled studies.

## Linked entities

- **Diseases:** Coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** ischemic (MESH:D002545), diabetes (MESH:D003920), tumors (MESH:D009369), gut barrier failure (MESH:D051437), hepatitis B and C (MESH:D006509), liver cirrhosis (MESH:D008103), cirrhosis (MESH:D005355), hyperlipidemia (MESH:D006949), critically ill (MESH:D016638), syphilis (MESH:D013587), injury to (MESH:D014947), inflammation (MESH:D007249), liver disease (MESH:D008107), acute coronary syndromes (MESH:D054058), Parkinson's disease (MESH:D010300), CHD (MESH:D003327), stenosis (MESH:D003251), coronary artery stenosis (MESH:D023921), STEMI (MESH:D000072657), obese (MESH:D009765), compromised LV function (MESH:D018487), AIDS (MESH:D000163), bacteremia (MESH:D016470), MI (MESH:D009203), cardiovascular disease (MESH:D002318), arthritis (MESH:D001168), Atherosclerosis (MESH:D050197), hypertension (MESH:D006973), death (MESH:D003643), HIV (MESH:D015658), sepsis (MESH:D018805), infectious (MESH:D003141), infarct (MESH:D007238), heart failure (MESH:D006333), inflammatory bowel disease (MESH:D015212), mucosal injury (MESH:D052016), type 2 diabetes (MESH:D003924), systemic (MESH:D015619), Coronary Artery (MESH:D003324), cardiac dysfunction (MESH:D006331)
- **Chemicals:** choline (MESH:D002794), EDTA (MESH:D004492), oxygen (MESH:D010100), TMAO (MESH:C005855), essential amino acids (MESH:D000601), aspirin (MESH:D001241), amino acids (MESH:D000596), carbohydrates (MESH:D002241), BAs (MESH:D001647), antiplatelet (-), SCFAs (MESH:D005232), agarose (MESH:D012685), lipid (MESH:D008055)
- **Species:** Bifidobacteriales (order) [taxon 85004], Lactobacillus (genus) [taxon 1578], Catenibacterium (genus) [taxon 135858], Faecalibacterium (genus) [taxon 216851], Anaerobacillus (genus) [taxon 704093], Alterileibacterium (genus) [taxon 1980680], Caryophanales (order) [taxon 1385], Lachnoclostridium (genus) [taxon 1506553], [Clostridium] innocuum (species) [taxon 1522], Ruminococcus (genus) [taxon 1263], Neisseria (genus) [taxon 482], Veillonella (genus) [taxon 29465], Phascolarctobacterium (genus) [taxon 33024], Bacteroides (genus) [taxon 816], Cutibacterium (genus) [taxon 1912216], Helicobacter pylori (species) [taxon 210], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Mycobacterium (genus) [taxon 1763], Escherichia coli BL21 (strain) [taxon 511693], Streptococcus (genus) [taxon 1301], Anaerostipes (genus) [taxon 207244], Bacillus (genus) [taxon 55087], Bacteroidia (class) [taxon 200643], Bacilli (class) [taxon 91061], Bacillota (clostridial firmicutes, phylum) [taxon 1239]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943319/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943319/full.md

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Source: https://tomesphere.com/paper/PMC12943319