Possible Role for Bacteriophages in the Treatment of SARS-CoV-2 Infection

An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in Wuhan City, China, in December 2019. Since then, the outbreak has grown into a global pandemic, and neither a vaccine nor a treatment for the disease, termed coronavirus disease 2019 (COVID-19), is currently available. The slow translational progress in the field of research suggests that a large number of studies are urgently required. In this context, this review explores the impact of bacteriophages on SARS-CoV-2, especially concerning phage therapy (PT). Bacteriophages are viruses that infect and kill bacterial cells. Several studies have confirmed that in addition to their antibacterial abilities, bacteriophages also show antiviral and antifungal properties. It has also been shown that PT is effective for building immunity against viral pathogens by reducing the activation of NF kappa B; additionally, phages produce the antiviral protein phagicin. The Ganges river in India, which originates from the Himalayan range, is known to harbor a large number of bacteriophages, which are released into the river gradually by the melting permafrost. Water from this river has traditionally been considered a therapeutic agent for several diseases. In this review, we hypothesize that the Ganges river may play a therapeutic role in the treatment of COVID-19.

[1]  Claire Duvallet,et al.  SARS-CoV-2 Titers in Wastewater Are Higher than Expected from Clinically Confirmed Cases , 2020, mSystems.

[2]  S. Mallapaty How sewage could reveal true scale of coronavirus outbreak , 2020, Nature.

[3]  S. De Carlo,et al.  Phage capsid nanoparticles with defined ligand arrangement block influenza virus entry , 2020, Nature Nanotechnology.

[4]  G. Medema,et al.  Presence of SARS-Coronavirus-2 in sewage , 2020, medRxiv.

[5]  Hong Jiang,et al.  Coronavirus disease 2019 in elderly patients: Characteristics and prognostic factors based on 4-week follow-up , 2020, Journal of Infection.

[6]  A. Mishra,et al.  Self-cleansing properties of Ganga during mass ritualistic bathing on Maha-Kumbh , 2020, Environmental Monitoring and Assessment.

[7]  M. Oosting,et al.  The role of Toll‐like receptor 10 in modulation of trained immunity , 2019, Immunology.

[8]  J. Borysowski,et al.  The effects of bacteriophages on the expression of genes involved in antimicrobial immunity* , 2019, Postępy Higieny i Medycyny Doświadczalnej.

[9]  J. Borysowski,et al.  Perspectives of Phage Therapy in Non-bacterial Infections , 2019, Front. Microbiol..

[10]  W. Xie,et al.  Metformin action through the microbiome and bile acids , 2018, Nature Medicine.

[11]  S. Stick,et al.  Use of a Primary Epithelial Cell Screening Tool to Investigate Phage Therapy in Cystic Fibrosis , 2018, Front. Pharmacol..

[12]  J. Borysowski Bacteriophage preparations affect the expression of genes involved in antimicrobial immune responses , 2018 .

[13]  J. Chu,et al.  Drug repurposing of quinine as antiviral against dengue virus infection. , 2018, Virus research.

[14]  Maoda Pang,et al.  Staphylococcus aureus Bacteriophage Suppresses LPS-Induced Inflammation in MAC-T Bovine Mammary Epithelial Cells , 2018, Front. Microbiol..

[15]  J. Borysowski,et al.  Phage Therapy: What Have We Learned? , 2018, Viruses.

[16]  G. Guglielmi Do bacteriophage guests protect human health? , 2017, Science.

[17]  Barbara A. Bailey,et al.  Bacteriophage Transcytosis Provides a Mechanism To Cross Epithelial Cell Layers , 2017, mBio.

[18]  A. Rynda-Apple,et al.  Induction of Antiviral Immune Response through Recognition of the Repeating Subunit Pattern of Viral Capsids Is Toll-Like Receptor 2 Dependent , 2017, mBio.

[19]  M. Vaneechoutte,et al.  Pro- and anti-inflammatory responses of peripheral blood mononuclear cells induced by Staphylococcus aureus and Pseudomonas aeruginosa phages , 2017, Scientific Reports.

[20]  U. Sharma,et al.  Bacteriophage lysins as antibacterials , 2017, Critical Care.

[21]  J. Borysowski,et al.  Phages and immunomodulation. , 2017, Future microbiology.

[22]  Krishna Khairnar,et al.  Ganges: special at its origin , 2016, Journal of Biological Research-Thessaloniki.

[23]  M. Fort Permafrost in the Himalayas: specific characteristics, evolution vs. climate change and impacts on potential natural hazards , 2015 .

[24]  S. Perlman,et al.  Coronaviruses: An Overview of Their Replication and Pathogenesis , 2015, Methods in molecular biology.

[25]  C. Nautiyal Self-Purificatory Ganga Water Facilitates Death of Pathogenic Escherichia coli O157:H7 , 2008, Current Microbiology.

[26]  Dottore Emiliano Fruciano,et al.  Phage as an antimicrobial agent: d'Herelle's heretical theories and their role in the decline of phage prophylaxis in the West. , 2007, The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale.

[27]  Tsung-Han Hsieh,et al.  Severe acute respiratory syndrome coronavirus 3C‐like protease‐induced apoptosis , 2006, FEMS immunology and medical microbiology.

[28]  J. S. Pandey,et al.  Assessment of Environmental Water Demands (EWD) of Forests for Two Distinct Indian Ecosystems , 2006, Environmental management.

[29]  W. Gorczyca,et al.  Bacteriophages and transplantation tolerance. , 2006, Transplantation proceedings.

[30]  W. Fortuna,et al.  Bacterial viruses against viruses pathogenic for man? , 2005, Virus research.

[31]  Sankar Ghosh,et al.  Signaling to NF-kappaB. , 2004, Genes & development.

[32]  L. Staudt,et al.  Active NF-kappaB signalling is a prerequisite for influenza virus infection. , 2004, The Journal of general virology.

[33]  H. Pahl Activators and target genes of Rel/NF-κB transcription factors , 1999, Oncogene.

[34]  Miyoko Takahashi,et al.  Differential Inhibition by Phagicin of DNA Synthesis in Cells infected with Vaccinia , 1968, Nature.

[35]  Y. Centifanto Antiviral Agent from λ-infected Escherichia coli K-12: I. Isolation , 1968 .