Double-Barreled CRISPR Technology as a Novel Treatment Strategy For COVID-19

Dhanusha A Nalawansha1, Kusal T G Samarasinghe1

  • 1Department of Molecular, Cellular & Developmental Biology, Yale University, New Haven, Connecticut 06511, United States.

Insights

This perspective discusses COVID-19 treatments, highlighting CRISPR technology as a potential pan-antiviral therapy. Novel delivery methods aim to target infected cells by utilizing SARS-CoV-2 surface proteins.

Area of Science:

  • Virology and Immunology
  • Molecular Biology
  • Infectious Diseases

Background:

  • Coronaviruses cause human respiratory illnesses, with a novel strain causing the COVID-19 pandemic.
  • The severe acute respiratory syndrome (SARS)-CoV-2 has led to a global health crisis, with significant impact in the United States.
  • Understanding coronavirus pathogenicity is crucial for developing effective treatments.

Purpose of the Study:

  • To review current knowledge on coronavirus pathogenicity, antiviral therapies, and prophylactic strategies for COVID-19.
  • To explore the potential of CRISPR technology as a novel pan-antiviral therapeutic approach.
  • To address challenges in CRISPR delivery and propose innovative solutions for targeted therapy.

Main Methods:

  • Review of existing literature on coronaviruses, COVID-19, and antiviral treatments.
  • Discussion of CRISPR technology's mechanism and its application in antiviral therapy.
  • Exploration of challenges and proposed strategies for efficient and selective *in vivo* delivery of CRISPR components.

Main Results:

  • CRISPR technology shows promise as a broad-spectrum antiviral therapy against coronaviruses.
  • Challenges exist in achieving efficient and specific delivery of CRISPR components into infected cells.
  • Hijacking SARS-CoV-2 surface proteins offers a potential strategy for targeted delivery.

Conclusions:

  • CRISPR-based therapies represent a promising avenue for combating COVID-19 and future viral threats.
  • Overcoming delivery challenges is key to realizing the therapeutic potential of CRISPR technology.
  • Targeted delivery systems utilizing viral surface proteins could enhance the efficacy and safety of CRISPR treatments.

Related Concept Videos

CRISPR01:59

CRISPR

Genome editing technologies allow scientists to modify an organism’s DNA via the addition, removal, or rearrangement of genetic material at specific genomic locations. These types of techniques could potentially be used to cure genetic disorders such as hemophilia and sickle cell anemia. One popular and widely used DNA-editing research tool that could lead to safe and effective cures for genetic disorders is the CRISPR-Cas9 system. CRISPR-Cas9 stands for Clustered Regularly Interspaced...
56.0K
CRISPR/Cas9 Genome Editing01:28

CRISPR/Cas9 Genome Editing

The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
1.2K
CRISPR and crRNAs02:53

CRISPR and crRNAs

Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
18.3K
The Antiviral System of Bacteria and Archaea: CRISPR01:23

The Antiviral System of Bacteria and Archaea: CRISPR

CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats is a adaptive immune system found in bacteria and archaea that protects against viral infections. This system enables prokaryotic cells to identify, remember, and neutralize foreign genetic elements, primarily bacteriophages, by storing fragments of the invader’s DNA as a genetic memory.The CRISPR immune response begins during an initial infection. Cas (CRISPR-associated) proteins play a central role in this...
476
Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
61.0K