Morphomolecular Characterization of Serum Nanovesicles From Microbiomes Differentiates Stable and Infarcted Atherosclerotic Patients

Microbial communities are considered decisive for maintaining a healthy situation or for determining diseases. Acute myocardial infarction (AMI) is an important complication of atherosclerosis caused by the rupture of atheroma plaques containing proinflammatory cytokines, reactive oxygen species, ox...

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Veröffentlicht in:Frontiers in cardiovascular medicine 2021-08, Vol.8, p.694851-694851, Article 694851
Hauptverfasser: Moreno, Camila Rodrigues, Franchini Ramires, Jose Antonio, Lotufo, Paulo Andrade, Soeiro, Alexandre Matos, da Silva Oliveira, Luanda Mara, Ikegami, Renata Nishiyama, Kawakami, Joyce Tiyeko, Pereira, Jaqueline de Jesus, Reis, Marcia Martins, Higuchi, Maria de Lourdes
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Sprache:eng
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Zusammenfassung:Microbial communities are considered decisive for maintaining a healthy situation or for determining diseases. Acute myocardial infarction (AMI) is an important complication of atherosclerosis caused by the rupture of atheroma plaques containing proinflammatory cytokines, reactive oxygen species, oxidized low-density lipoproteins (oxLDL), damaged proteins, lipids, and DNA, a microenvironment compatible with a pathogenic microbial community. Previously, we found that archaeal DNA-positive infectious microvesicles (iMVs) were detected in vulnerable plaques and in the sera of Chagas disease patients with heart failure. Now, we characterize and quantify the levels of serum microbiome extracellular vesicles through their size and content using morphomolecular techniques to differentiate clinical outcomes in coronary artery disease (CAD). We detected increased numbers of large iMVs (0.8-1.34 nm) with highly negative surface charge that were positive for archaeal DNA, Mycoplasma pneumoniae antigens and MMP9 in the sera of severe AMI patients, strongly favoring our hypothesis that pathogenic archaea may play a role in the worst outcomes of atherosclerosis. The highest numbers of EVs
ISSN:2297-055X
2297-055X
DOI:10.3389/fcvm.2021.694851