Mitochondria and microbiota dysfunction in COVID-19 pathogenesis

Highlights

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  Mitochondria are the hub of cellular oxidative homeostasis.

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  Mitochondria are the major source of reactive oxygen species (ROS).

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  Extracellular mitochondria are found in blood, in circulating platelets and vesicles.

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  COVID-19 pathogenesis is aggravated by the hyper- inflammatory state.

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  Inflammation activates events leading to microbiota & mitochondrial oxidative damage.

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  Mitochondrial damage contributes to coagulopathy, ferroptosis & microbial dysbiosis.

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  Blood & platelet mitochondria dysfunction may accelerate systemic coagulopathy events.

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  Targeting mitochondria dysfunction may provide useful therapeutic strategies against COVID-19 pathogenesis.

Abstract

The COVID-19 pandemic caused by the coronavirus (SARS-CoV-2) has taken the world by surprise into a major crisis of overwhelming morbidity and mortality. This highly infectious disease is associated with respiratory failure unusual in other coronavirus infections. Mounting evidence link the accelerated progression of the disease in COVID-19 patients to the hyper-inflammatory state termed as the “cytokine storm” involving major systemic perturbations. These include iron dysregulation manifested as hyperferritinemia associated with disease severity. Iron dysregulation induces reactive oxygen species (ROS) production and promotes oxidative stress. The mitochondria are the hub of cellular oxidative homeostasis. In addition, the mitochondria may circulate “cell-free” in non-nucleated platelets, in extracellular vesicles and mitochondrial DNA is found in the extracellular space. The heightened inflammatory/oxidative state may lead to mitochondrial dysfunction leading to platelet damage and apoptosis. The interaction of dysfunctional platelets with coagulation cascades aggravates clotting events and thrombus formation. Furthermore, mitochondrial oxidative stress may contribute to microbiota dysbiosis, altering coagulation pathways and fueling the inflammatory/oxidative response leading to the vicious cycle of events.

Here, we discuss various cellular and systemic incidents caused by SARS-CoV-2 that may critically impact intra and extracellular mitochondrial function, and contribute to the progression and severity of the disease. It is crucial to understand how these key modulators impact COVID-19 pathogenesis in the quest to identify novel therapeutic targets that may reduce fatal outcomes of the disease.