What is it about?

This study explored changes (mutations) in mitochondrial genes (MT-CYB and MT-ATP6) in COVID-19 patients and healthy individuals. Certain gene mutations were more common in those with COVID-19. Among these, two specific mutations may negatively impact the structure and function of key mitochondrial proteins, potentially contributing to how COVID-19 affects the body and causes symptoms.

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Why is it important?

This study identified one novel mtDNA mutation, along with several relatively common mutations in the MT-CYB and MT-ATP6 genes among COVID-19 patients. As mtDNA mutations are commonly observed in COVID-19 patients, it indicates that SARS-CoV-2 may alter the host’s genetic material, particularly in mtDNA. Findings of this study indicate that there may be a correlation between the m.14942A > C mutation in the MT-CYB gene and the m.8744T > G mutation in the MT-ATP6 gene, with the clinical symptoms of COVID-19. The results of this study will help better understand the links among SARS-CoV-2 infection, mtDNA mutations in these two genes, and mitochondrial dysfunction.

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This page is a summary of: Evaluating the MT-CYB and MT-ATP6 variations in COVID-19 patients: A case-control study, PLOS One, August 2025, PLOS,
DOI: 10.1371/journal.pone.0329866.
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