The CRISPR Therapy of Viral Infections

A special issue of Pathogens (ISSN 2076-0817). This special issue belongs to the section "Viral Pathogens".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 7929

Special Issue Editors


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Guest Editor
Laboratory of Experimental Virology, Department of Medical Microbiology, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands
Interests: virology; antiviral approaches; HIV; gene therapy

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Guest Editor
Laboratory of Experimental Virology, Department of Medical Microbiology, University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands
Interests: virology; antiviral approaches; virus evolution; drug resistance
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Special Issue Information

Dear Colleagues,

In recent years, there has been an increasing demand for the development of new antiviral strategies due to the prevalence of viral infections such as those caused by the human immunodeficiency virus (HIV) or the hepatitis B and C viruses (HBV and HCV) and the emergence of a variety of “new” viruses, including SARS-CoV-2. The pharmaceutical industry and the scientific community work on the development of new antiviral drugs, including the repurposing of previously approved drugs. However, alternative strategies are also welcome, such as the development of novel RNA-based therapeutics based on the clustered regularly interspaced short palindromic repeats (CRISPR)-Cas system.

This Special Issue launched by Pathogens will be devoted to “The CRISPR Therapy of Viral Infections” and will accept both original research papers and review articles. This Special Issue will focus on how CRISPR-Cas can be used as a screening method and a therapeutic gene editing tool to treat or cure viral infections. Potential topics include but are not limited to the following:

  • Targeting RNA viruses;
  • Targeting DNA viruses;
  • Targeting host factors;
  • CRISPR screening methods to identify new therapeutic targets.

Dr. Elena Herrera-Carrillo
Prof. Dr. Ben Berkhout
Guest Editors

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Keywords


  • CRISPR-Cas
  • Cas13
  • Cas9
  • Cas12
  • dCas9 activators
  • dCas9 repressors
  • CRISPR Therapy
  • HIV
  • HCV
  • HBV

Published Papers (2 papers)

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Review

23 pages, 1377 KiB  
Review
A Landscape of CRISPR/Cas Technique for Emerging Viral Disease Diagnostics and Therapeutics: Progress and Prospects
by Shyam Tripathi, Purnima Khatri, Zeeshan Fatima, Ramendra Pati Pandey and Saif Hameed
Pathogens 2023, 12(1), 56; https://doi.org/10.3390/pathogens12010056 - 29 Dec 2022
Cited by 5 | Viewed by 4039
Abstract
Viral diseases have emerged as a serious threat to humanity and as a leading cause of morbidity worldwide. Many viral diagnostic methods and antiviral therapies have been developed over time, but we are still a long way from treating certain infections caused by [...] Read more.
Viral diseases have emerged as a serious threat to humanity and as a leading cause of morbidity worldwide. Many viral diagnostic methods and antiviral therapies have been developed over time, but we are still a long way from treating certain infections caused by viruses. Acquired immunodeficiency syndrome (AIDS) is one of the challenges where current medical science advancements fall short. As a result, new diagnostic and treatment options are desperately needed. The CRISPR/Cas9 system has recently been proposed as a potential therapeutic approach for viral disease treatment. CRISPR/Cas9 is a specialised, effective, and adaptive gene-editing technique that can be used to modify, delete, or correct specific DNA sequences. It has evolved into an advanced, configurable nuclease-based single or multiple gene-editing tool with a wide range of applications. It is widely preferred simply because its operational procedures are simple, inexpensive, and extremely efficient. Exploration of infectious virus genomes is required for a comprehensive study of infectious viruses. Herein, we have discussed the historical timeline-based advancement of CRISPR, CRISPR/Cas9 as a gene-editing technology, the structure of CRISPR, and CRISPR as a diagnostic tool for studying emerging viral infections. Additionally, utilizing CRISPR/Cas9 technology to fight viral infections in plants, CRISPR-based diagnostics of viruses, pros, and cons, and bioethical issues of CRISPR/Cas9-based genomic modification are discussed. Full article
(This article belongs to the Special Issue The CRISPR Therapy of Viral Infections)
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27 pages, 3003 KiB  
Review
Application of CRISPR-Cas9 Gene Editing for HIV Host Factor Discovery and Validation
by William J. Cisneros, Daphne Cornish and Judd F. Hultquist
Pathogens 2022, 11(8), 891; https://doi.org/10.3390/pathogens11080891 - 09 Aug 2022
Cited by 1 | Viewed by 2916
Abstract
Human Immunodeficiency Virus (HIV) interacts with a wide array of host factors at each stage of its lifecycle to facilitate replication and circumvent the immune response. Identification and characterization of these host factors is critical for elucidating the mechanism of viral replication and [...] Read more.
Human Immunodeficiency Virus (HIV) interacts with a wide array of host factors at each stage of its lifecycle to facilitate replication and circumvent the immune response. Identification and characterization of these host factors is critical for elucidating the mechanism of viral replication and for developing next-generation HIV-1 therapeutic and curative strategies. Recent advances in CRISPR-Cas9-based genome engineering approaches have provided researchers with an assortment of new, valuable tools for host factor discovery and interrogation. Genome-wide screening in a variety of in vitro cell models has helped define the critical host factors that play a role in various cellular and biological contexts. Targeted manipulation of specific host factors by CRISPR-Cas9-mediated gene knock-out, overexpression, and/or directed repair have furthermore allowed for target validation in primary cell models and mechanistic inquiry through hypothesis-based testing. In this review, we summarize several CRISPR-based screening strategies for the identification of HIV-1 host factors and highlight how CRISPR-Cas9 approaches have been used to elucidate the molecular mechanisms of viral replication and host response. Finally, we examine promising new technologies in the CRISPR field and how these may be applied to address critical questions in HIV-1 biology going forward. Full article
(This article belongs to the Special Issue The CRISPR Therapy of Viral Infections)
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