Persistence of plasmids targeted by CRISPR interference in bacterial populations.
Viktor MamontovAlexander MartynovNatalia MorozovaAnton BukatinDmitry B StaroverovKonstantin A LukyanovIaroslav IspolatovEkaterina SemenovaKonstantin V SeverinovPublished in: Proceedings of the National Academy of Sciences of the United States of America (2022)
CRISPR-Cas systems provide prokaryotes with an RNA-guided defense against foreign mobile genetic elements (MGEs) such as plasmids and viruses. A common mechanism by which MGEs avoid interference by CRISPR consists of acquisition of escape mutations in regions targeted by CRISPR. Here, using microbiological, live microscopy and microfluidics analyses we demonstrate that plasmids can persist for multiple generations in some Escherichia coli cell lineages at conditions of continuous targeting by the type I-E CRISPR-Cas system. We used mathematical modeling to show how plasmid persistence in a subpopulation of cells mounting CRISPR interference is achieved due to the stochastic nature of CRISPR interference and plasmid replication events. We hypothesize that the observed complex dynamics provides bacterial populations with long-term benefits due to continuous maintenance of mobile genetic elements in some cells, which leads to diversification of phenotypes in the entire community and allows rapid changes in the population structure to meet the demands of a changing environment.
Keyphrases
- crispr cas
- genome editing
- escherichia coli
- induced apoptosis
- genome wide
- klebsiella pneumoniae
- cancer therapy
- cell cycle arrest
- healthcare
- high resolution
- mental health
- endoplasmic reticulum stress
- single cell
- stem cells
- cell death
- copy number
- single molecule
- dna methylation
- cell proliferation
- high throughput
- high speed
- pseudomonas aeruginosa
- mass spectrometry
- signaling pathway