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DOI 10.1016/j.micpath.2022.105704

Медицинская библиотека · Microbial pathogenesis · 2022

Gut bacteria, bacteriophages, and probiotics: Tripartite mutualism to quench the SARS-CoV2 storm.

Zeinali Tahereh, Faraji Niloofar, Joukar Farahnaz, Khan Mirzaei Mohammadali, Kafshdar Jalali Hossnieh, Shenagari Mohammad, Mansour-Ghanaei Fariborz

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Аннотация

Patients with SARS-CoV-2 infection, exhibit various clinical manifestations and severity including respiratory and enteric involvements. One of the main reasons for death among covid-19 patients is excessive immune responses directed toward cytokine storm with a low chance of recovery. Since the balanced gut microbiota could prepare health benefits by protecting against pathogens and regulating immune homeostasis, dysbiosis or disruption of gut microbiota could promote severe complications including autoimmune disorders; we surveyed the association between the imbalanced gut bacteria and the development of cytokine storm among COVID-19 patients, also the impact of probiotics and bacteriophages on the gut bacteria community to alleviate cytokine storm in COVID-19 patients. In present review, we will scrutinize the mechanism of immunological signaling pathways which may trigger a cytokine storm in SARS-CoV2 infections. Moreover, we are explaining in detail the possible immunological signaling pathway-directing by the gut bacterial community. Consequently, the specific manipulation of gut bacteria by using probiotics and bacteriophages for alleviation of the cytokine storm will be investigated. The tripartite mutualistic cooperation of gut bacteria, probiotics, and phages as a candidate prophylactic or therapeutic approach in SARS-CoV-2 cytokine storm episodes will be discussed at last.

Для цитирования: Zeinali Tahereh, Faraji Niloofar, Joukar Farahnaz, Khan Mirzaei Mohammadali, Kafshdar Jalali Hossnieh, Shenagari Mohammad, Mansour-Ghanaei Fariborz. Gut bacteria, bacteriophages, and probiotics: Tripartite mutualism to quench the SARS-CoV2 storm.. Microbial pathogenesis. 2022. DOI: 10.1016/j.micpath.2022.105704.

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