Cell Host Microbe. 2019 Oct 9;26(4):515-526.e6. doi: 10.1016/j.chom.2019.09.002. | PubMed

Philip M Nussenzweig ¹ , Jon McGinn ¹ , Luciano A Marraffini ²

1. Laboratory of Bacteriology, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA.
2. Laboratory of Bacteriology, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA; Howard Hughes Medical Institute, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA. Electronic address: marraffini@rockefeller.edu.

Abstract

Type II CRISPR-Cas systems defend prokaryotes from bacteriophage infection through the acquisition of short viral DNA sequences known as spacers, which are transcribed into short RNA guides to specify the targets of the Cas9 nuclease. To counter the potentially devastating propagation of escaper phages with mutations in the target sequences, the host population acquires many different spacers. Whether and how pre-existing spacers in type II systems affect the acquisition of new ones is unknown. Here, we demonstrate that previously acquired spacers promote additional spacer acquisition from the vicinity of the target DNA site cleaved by Cas9. Therefore, CRISPR immune cells acquire additional spacers at the same time as they destroy the infecting virus. This anticipates the rise of escapers or related viruses that could escape targeting by the first spacer acquired. Our results thus reveal Cas9's role in the generation of immunological memories.

Presented by Philip Nussenzweig