Abstract

CRISPR-Cas systems provide immunity against phages and plasmids in bacteria and archaea. Despite the popularity of CRISPR-Cas9 based genome editing, few endogenous systems have been characterized to date. Here, we sampled 1,262 publically available lactobacilli genomes found them to be enriched with CRISPR-Cas adaptive immunity. While CRISPR-Cas is ubiquitous in some Lactobacillus species, CRISPR-Cas content varies at the strain level in most Lactobacillus species. We identified that Type II is the most abundant type across the genus, with II-A being the most dominant sub-type. We found that many Type II-A systems are actively transcribed, and encode spacers that efficiently provide resistance against plasmid uptake. Analysis of various CRISPR transcripts revealed that guide sequences are highly diverse in terms of crRNA and tracrRNA length and structure. Interference assays revealed highly diverse target PAM sequences. Lastly, we show that these systems can be readily repurposed for self-targeting by expressing an engineered single guide RNA. Our results reveal that Type II-A systems in lactobacilli are naturally active in their native host in terms of expression and efficiently targeting invasive and genomic DNA. Together, these systems increase the possible Cas9 targeting space and provide multiplexing potential in native hosts and heterologous genome editing purpose.

Highlights

  • CRISPR-Cas (Clustered regularly interspaced short palindromic repeats and CRISPR associated genes) systems have been shown to protect bacteria and archaea from invasive mobile genetic elements (MGEs)[1,2,3]

  • We set out to understand the native variability in occurrence and activity of CRISPR using endogenous systems occurring in lactobacilli, as it has been published that they are enriched in CRISPR-Cas systems 6-fold compared to the canonical rate of occurrence for bacteria (5% of all bacteria vs. 30% of all lactobacilli)[19,25]

  • We have set out to determine the diverse activities in several novel Type II CRISPR-Cas systems

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Summary

Introduction

CRISPR-Cas (Clustered regularly interspaced short palindromic repeats and CRISPR associated genes) systems have been shown to protect bacteria and archaea from invasive mobile genetic elements (MGEs)[1,2,3]. These systems are identified by a genetic locus with a CRISPR repeat-spacer array and cas genes[4,5]. The second stage of CRISPR immunity, expression, leads to the biogenesis of individual small crRNAs (CRISPR RNAs), that each contain a single partial spacer and partial repeat; these RNAs act as a guide molecule to direct the Cas proteins to a complementary foreign nucleic acid target[2,10,11]. We used one model system, Lactobacillus gasseri, to investigate a novel species of tracrRNA to develop biotechnological CRISPR-Cas[9] based genetic engineering tools using the native CRISPR components

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