New “decision aid” for CRISPR immune responses

HIRI scientists show that target RNA levels influence defense against invaders.

Friend or foe? Immune systems constantly face this question. They must recognize and clear foreign invaders without eliciting autoimmunity. Prokaryotic CRISPR-Cas systems recognize invaders based on genetic sequence. But what happens if the host genome shares the same sequences? A research team of the Helmholtz Institute in Würzburg in cooperation with the North Carolina State University (USA) has now discovered a control mechanism exhibited by CRISPR-Cas systems that use Cas13 nucleases: These systems only trigger an extensive immune response if the concentration of the target RNA exceeds a certain threshold. This discovery opens new opportunities for the use of CRISPR-Cas13 in the treatment of hereditary and infectious diseases. The scientists now published their findings in the journal “Cell Host & Microbe”.

Distinguishing self from non-self poses a major challenge for immune systems. Failure to recognize an attacker exposes the host to a potentially fatal infection, while erroneous recognition of the host itself can trigger an autoimmune response. “In order to treat infectious and autoimmune diseases, it is critical to understand how immune systems make these decisions,“ says Chase Beisel. Beisel heads the RNA Synthetic Biology Department at the Helmholtz Institute for RNA-based Infection Research (HIRI) in Würzburg, a site of the Helmholtz Centre for Infection Research (HZI) in Braunschweig in cooperation with the Julius-Maximilians-Universität (JMU) Würzburg, and is the corresponding author of the study.

Three golden rules

CRISPR-Cas defense systems, which are present in bacteria and protect them from viral attacks, regularly have to decide whether or not to trigger an immune response. In systems that rely on Cas13 nucleases, the immune response manifests through widespread ribonucleic acid (RNA) degradation, which causes the cell to go dormant. The invading virus cannot replicate in this environment, restricting viral spread to other bacteria. “Up to now, it was assumed that CRISPR-Cas13 systems are triggered when two criteria are met: a match between a target RNA and the system’s guide RNA and the presence of an additional flanking sequence,” Elena Vialetto, PhD student at the HIRI and first author of the study, explains. “The fact that the concentration of the target RNA also plays an important role was completely unexpected.” This additional “decision aid” allows the cells to differentiate between an acute and potentially lethal infection and a benign infection that can be ignored. “Cells can therefore decide if an infection poses a threat,” Vialetto summarizes. According to Beisel, this is important because some infections can actually be beneficial to a bacterium. Certain invaders, for example, contain antibiotic resistance genes and only integrate into the bacterial genome without killing the cell.

New possibilities for therapies and gene silencing

The nuclease Cas13 has the potential to be used in the future to fight viral diseases or to silence adverse genes. “It has always been a curiosity that Cas13 induces dormancy in bacteria through widespread RNA cleavage, yet only cleaves the target RNA in human cells. Our work indicates that RNA levels could help explain this difference,” Vialetto says. “This provides an extra factor to consider when applying Cas13 to gene silencing,” Beisel adds. The findings of the research team provide a better understanding of the nuclease, laying the groundwork for new innovative therapeutics.

As a next step, the researchers plan to investigate how this threshold extends to other CRISPR-Cas systems that recognize RNA. According to Beisel, this opens up future research opportunities: “There is a whole class of systems, called type III systems, that recognize RNA but rely on other proteins for collateral RNA or DNA cleavage. Here, RNA levels could also have a big impact on the induction of an immune response and on how these systems differentiate between benign and dangerous invaders.”

The study was supported by the Joint Programming Initiative on Antimicrobial Resistance (JPIAMR), the National Institutes of Health (NIH), a bayresq.net Bavarian research network grant, and the Safe Genes Program of the Defense Advanced Research Projects Agency (DARPA).

This press release is also available on our homepage: https://www.helmholtz-hzi.de/en/news-events/news/view/article/complete/neue-ents….

The Helmholtz Centre for Infection Research:
Scientists at the Helmholtz Centre for Infection Research (HZI) in Braunschweig and its other sites in Germany are engaged in the study of bacterial and viral infections and the body’s defence mechanisms. They have a profound expertise in natural compound research and its exploitation as a valuable source for novel anti-infectives. As member of the Helmholtz Association and the German Center for Infection Research (DZIF) the HZI performs translational research laying the ground for the development of new treatments and vaccines against infectious diseases. http://www.helmholtz-hzi.de/en

The Helmholtz Institute for RNA-based Infection Research:
The Helmholtz Institute for RNA-based Infection Research (HIRI) was founded in May 2017. It is a joint institution of the Helmholtz Centre for Infection Research (HZI) in Braunschweig and the Julius-Maximilians-Universität Würzburg (JMU). Based on the University hospital campus, the HIRI is the first federal institute to focus on the role of ribonucleic acids (RNAs) in infection processes. Its mission is to combine basic research with the development of new RNA-centric therapeutic approaches to treat infections. http://www.helmholtz-hiri.de

Contact:
Dr. Britta Grigull
Presse & Public Relations
+49 (0)931-31-81801
britta.grigull@helmholtz-hiri.de

Originalpublikation:

A target expression threshold dictates invader defense and prevents autoimmunity by CRISPR-Cas13. Vialetto E, Yu Y, Collins SP, Wandera KG, Barquist L, Beisel CL (2022). Cell Host & Microbe, DOI: https://doi.org/10.1016/j.chom.2022.05.013