Efficient CRISPR-mediated base editing in <i>Agrobacterium</i> spp.

Abstract

<i>Agrobacterium</i> spp. are important plant pathogens that are the causative agents of crown gall or hairy root disease. Their unique infection strategy depends on the delivery of part of their DNA to plant cells. Thanks to this capacity, these phytopathogens became a powerful and indispensable tool for plant genetic engineering and agricultural biotechnology. Although <i>Agrobacterium</i> spp. are standard tools for plant molecular biologists, current laboratory strains have remained unchanged for decades and functional gene analysis of <i>Agrobacterium</i> has been hampered by time-consuming mutation strategies. Here, we developed clustered regularly interspaced short palindromic repeats (CRISPR)-mediated base editing to enable the efficient introduction of targeted point mutations into the genomes of both <i>Agrobacterium tumefaciens</i> and <i>Agrobacterium rhizogenes</i> As an example, we generated EHA105 strains with loss-of-function mutations in <i>recA</i>, which were fully functional for maize (<i>Zea mays</i>) transformation and confirmed the importance of RolB and RolC for hairy root development by <i>A. rhizogenes</i> K599. Our method is highly effective in 9 of 10 colonies after transformation, with edits in at least 80% of the cells. The genomes of EHA105 and K599 were resequenced, and genome-wide off-target analysis was applied to investigate the edited strains after curing of the base editor plasmid. The off-targets present were characteristic of Cas9-independent off-targeting and point to TC motifs as activity hotspots of the cytidine deaminase used. We anticipate that CRISPR-mediated base editing is the start of "engineering the engineer," leading to improved <i>Agrobacterium</i> strains for more efficient plant transformation and gene editing.