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Rescooped by Gilbert C FAURE from Genetic Engineering in the Press by GEG
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TSRI researchers reveal how viruses incapacitate bacterial defense system

TSRI researchers reveal how viruses incapacitate bacterial defense system | Immunology | Scoop.it
Picture bacteria and viruses locked in an arms race. For many bacteria, one line of defense against viral infection is a sophisticated RNA-guided "immune system" called CRISPR-Cas.

Via BigField GEG Tech
BigField GEG Tech's curator insight, November 23, 2022 7:20 AM

For many bacteria, one line of defense against viral infection is the CRISPR-Cas system. At the center of this system is a surveillance complex that recognizes viral DNA and triggers its destruction. However, viruses can fight back and disable this surveillance complex by using anti-CRISPR proteins. For the first time, researchers have solved, using a high-resolution imaging technique called cryo-electron microscopy, the structure of viral anti-CRISPR proteins attached to a bacterial CRISPR surveillance complex, revealing precisely how viruses neutralize the bacterial defense system. The research team found that the anti-CRISPR proteins act by locking down CRISPR's ability to identify and attack the viral genome. The proteins within the complex wrap around the CRISPR RNA exposing specific sections of bacterial RNA. One type of anti-CRISPR protein covers the exposed section of CRISPR RNA, preventing the CRISPR system from scanning the viral DNA. Based on its location and negative charge, an anti-CRISPR protein acts as a DNA mimic, fooling CRISPR into binding this immobilizing protein, rather than invading viral DNA. The researchers believe that this new understanding of anti-CRISPR proteins could eventually lead to more sophisticated and effective tools for gene editing.

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Antigen-specific naive CD8+ T cells produce a sing... [J Immunol. 2014] - PubMed - NCBI

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Gilbert C FAURE's insight:
... a single pulse of IFN-γ in vivo within hours of infection, but without antiviral effect.
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Editorial overview: Viral immunology: Dealing with bad news

Understanding immunity to viruses therefore encompasses many, if not nearly all aspects of cell biology and immunology. A positive trend of the past twenty years of viral research is that the connection between viruses and innate cellular anti-viral mechanisms has cemented virology as an important sub-discipline of cell biology, and converted many virologists into at least honorary immunologists. The inherent simplicity of viruses and their marked tendency towards robust expression of their proteome and flagrant manipulation of host cells and immunity, make them superb tools to make basic discoveries.

Pragmatically, basic research in viral immunology provides the foundation for improving and developing new anti-viral vaccines and therapies. Recent outbreaks of MERs, Ebola and Zika viruses provide a pointed reminder of the threat that rapidly evolving viruses pose to human health and even existence, and underscore the importance of having a sufficient understanding of virus host interactions to quickly develop vaccines.

This issue of Current Opinion in Virology features eight outstanding reviews that summarize current knowledge of a number of the immune hurdles to viral replication. The immune system can be broadly, if imprecisely divided into innate vs. adaptive elements. Innate immunity is generally immediate and agent non-specific. Adaptive immunity is based on the functions of B and T cells, which due to their high antigen specificity, exist in relatively small numbers at the start of infection of a naïve host, and need nearly a week of exceedingly rapid division to attain fighting strength (four to six doublings per day, for six days geometrically increases their numbers up to 16 million-fold).
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