scispace - formally typeset
Open AccessJournal ArticleDOI

Host Defence RNases as Antiviral Agents against Enveloped Single Stranded RNA Viruses.

Jiarui Li, +1 more
- 04 Mar 2021 - 
- Vol. 12, Iss: 1, pp 444-469
Reads0
Chats0
TLDR
In this article, the authors summarize the currently available information on human RNases that can target viral pathogens, with special focus on enveloped single-stranded RNA (ssRNA) viruses.
Abstract
Owing to the recent outbreak of Coronavirus Disease of 2019 (COVID-19), it is urgent to develop effective and safe drugs to treat the present pandemic and prevent other viral infections that might come in the future. Proteins from our own innate immune system can serve as ideal sources of novel drug candidates thanks to their safety and immune regulation versatility. Some host defense RNases equipped with antiviral activity have been reported over time. Here, we try to summarize the currently available information on human RNases that can target viral pathogens, with special focus on enveloped single-stranded RNA (ssRNA) viruses. Overall, host RNases can fight viruses by a combined multifaceted strategy, including the enzymatic target of the viral genome, recognition of virus unique patterns, immune modulation, control of stress granule formation, and induction of autophagy/apoptosis pathways. The review also includes a detailed description of representative enveloped ssRNA viruses and their strategies to interact with the host and evade immune recognition. For comparative purposes, we also provide an exhaustive revision of the currently approved or experimental antiviral drugs. Finally, we sum up the current perspectives of drug development to achieve successful eradication of viral infections.

read more

Citations
More filters
Journal ArticleDOI

Characterization of SARS2 Nsp15 nuclease activity reveals it's mad about U.

TL;DR: In this paper, the authors used cryo-EM to capture structures of Nsp15 bound to RNA in pre-and post-cleavage states, and determined how the sequence of the RNA substrate dictates cleavage and found that outside of polyU tracts, nsp15 has a strong preference for purines 3' of the cleaved uridine.
Journal ArticleDOI

Enzyme Therapy: Current Challenges and Future Perspectives.

TL;DR: In this article, the angiotensin-converting enzyme 2 (ACE2) is used to treat COVID-19, which can convert a wide range of target molecules to restore the correct physiological metabolism.
Journal ArticleDOI

Tea Polyphenols Prevent and Intervene in COVID-19 through Intestinal Microbiota

TL;DR: Preliminary reasoning and judgments have been made about the possible mechanism of the effect of tea polyphenols on the COVID-19 control and prevention mediated by the microbiota and may be of great significance to the future exploration of specialized research in this field.
Journal ArticleDOI

Selective cleavage of ncRNA and antiviral activity by RNase2/EDN in THP1-induced macrophages

TL;DR: In this article , the authors showed that RSV induced RNase2 expression, which significantly enhanced cell survival, and provided evidence of its cleavage selectivity on ncRNAs, which was confirmed in vitro using the recombinant protein.
Journal ArticleDOI

Effect of cannabidiol on apoptosis and cellular interferon and interferon-stimulated gene responses to the SARS-CoV-2 genes ORF8, ORF10 and M protein

TL;DR: In this paper , the effects of CBD on cellular innate immune responses to ORF8, ORF10, and Membrane protein (M protein) from the Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes COVID-19, in combination with cannabidiol (CBD).
References
More filters
Journal ArticleDOI

Severe Acute Respiratory Syndrome Coronavirus Nonstructural Proteins 3, 4, and 6 Induce Double-Membrane Vesicles

TL;DR: Transfection of plasmid constructs encoding full-length versions of the three transmembrane-containing nonstructural proteins of the severe acute respiratory syndrome (SARS) coronavirus are used to examine the ability of each to induce double- Membrane vesicles in tissue culture.
Journal ArticleDOI

SARS coronavirus pathogenesis: host innate immune responses and viral antagonism of interferon.

TL;DR: Gene transcription signatures unique to SARS-CoV disease states have been identified, but host factors that regulate exacerbated disease phenotypes still remain largely undetermined.
Journal ArticleDOI

Functional screen reveals SARS coronavirus nonstructural protein nsp14 as a novel cap N7 methyltransferase

TL;DR: Mutational analysis in a replicon system showed that the N7-MTase activity was important for SARS virus replication/transcription and can thus be used as an attractive drug target to develop antivirals for control of coronaviruses including the deadly Sars virus.
Journal ArticleDOI

Targeting the Endocytic Pathway and Autophagy Process as a Novel Therapeutic Strategy in COVID-19.

TL;DR: This mini-review will focus on the importance of the endocytic pathway as well as the autophagy process in viral infection of several pathogenic CoVs inclusive of SARS- coV, MERS-CoV and the new CoV named as severe acute respiratory syndrome coronavirus 2 (SARS- CoV-2), and discuss the development of therapeutic agents by targeting these processes.
Related Papers (5)