Ectopic Spacer Acquisition in CRISPR3 Array.

Microorganisms

Département de Biochimie, De Microbiologie et de Bio-Informatique, Faculté des Sciences et de Génie, Université Laval, Québec, QC G1V 0A6, Canada.

Published: March 2021

relies heavily on two type II-A CRISPR-Cas systems, CRISPR1 and CRISPR3, to resist siphophage infections. One hallmark of these systems is the integration of a new spacer at the 5' end of the CRISPR arrays following phage infection. However, we have previously shown that ectopic acquisition of spacers can occur within the CRISPR1 array. Here, we present evidence of the acquisition of new spacers within the array of CRISPR3 of . The analysis of randomly selected bacteriophage-insensitive mutants of the strain Uy01 obtained after phage infection, as well as the comparison with other strains with similar CRISPR3 content, showed that a specific spacer within the array could be responsible for misguiding the adaptation complex. These results also indicate that while the vast majority of new spacers are added at the 5' end of the CRISPR array, ectopic spacer acquisition is a common feature of both CRISPR1 and CRISPR3 systems in , and it can still provide phage resistance. Ectopic spacer acquisition also appears to have occurred naturally in some strains of , suggesting that it is a general phenomenon, at least in type II-A systems.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999890PMC
http://dx.doi.org/10.3390/microorganisms9030512DOI Listing

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