Abstract
Summary Interactions between microbes and their mobile genetic elements (MGEs), including viruses and plasmids, are critical drivers of microbiome structures and processes. CRISPR-Cas systems are important regulators of these host-MGE interactions, but a global understanding of CRISPR loci diversity, activity, and roles across Earth’s biomes is still lacking. Here, we use an optimized computational approach to search short-read data and collect ∼800 million CRISPR spacers across ∼450,000 public metagenomes. From this extensive CRISPR spacer dataset, we identified 1.18 billion hits between 41 million spacers and 2.5 million viruses and plasmids. Focusing on the role of CRISPR as anti-phage defense, we observed an over-representation of prevalent and conserved spacers consistent with a positive selection pressure associated with phage targeting. Identification of sustained CRISPR targeting by microbes not expected to be viable hosts suggested that some phage genomes may frequently enter non-host microbial cells. Taken together, these results outline the extensive diversity of CRISPR loci across microbiomes, and highlight key parameters driving CRISPR targeting patterns likely to influence strain-level diversification and selection processes within microbial populations.
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Summary
Interactions between microbes and their mobile genetic elements (MGEs), including viruses and plasmids, are critical drivers of microbiome structures and processes. CRISPR-Cas systems are important regulators of these host-MGE interactions, but a global understanding of CRISPR loci diversity, activity, and roles across Earth’s biomes is still lacking. Here, we use an optimized computational approach to search short-read data and collect ∼800 million CRISPR spacers across ∼450,000 public metagenomes. From this extensive CRISPR spacer dataset, we identified 1.18 billion hits between 41 million spacers and 2.5 million viruses and plasmids. Focusing on the role of CRISPR as anti-phage defense, we observed an over-representation of prevalent and conserved spacers consistent with a positive selection pressure associated with phage targeting. Identification of sustained CRISPR targeting by microbes not expected to be viable hosts suggested that some phage genomes may frequently enter non-host microbial cells. Taken together, these results outline the extensive diversity of CRISPR loci across microbiomes, and highlight key parameters driving CRISPR targeting patterns likely to influence strain-level diversification and selection processes within microbial populations.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Main changes: Updated analyses and new simplified figures 4 and 5
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