PT  - JOURNAL ARTICLE
AU  - S. Meaden
AU  - A. Biswas
AU  - K. Arkhipova
AU  - S. E. Morales
AU  - B. E. Dutilh
AU  - E. R. Westra
AU  - P. C. Fineran
TI  - High viral abundance and low diversity are associated with increased CRISPR-Cas prevalence across microbial ecosystems
AID  - 10.1101/2021.06.24.449667
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.06.24.449667
4099  - http://biorxiv.org/content/early/2021/06/25/2021.06.24.449667.short
4100  - http://biorxiv.org/content/early/2021/06/25/2021.06.24.449667.full
AB  - CRISPR-Cas are adaptive immune systems that protect their hosts against viruses and other parasitic mobile genetic elements. Consequently, selection from viruses and other genetic parasites is often assumed to drive the acquisition and maintenance of these immune systems in nature, but this remains untested. Here, we analyse the abundance of CRISPR arrays in natural environments using metagenomic datasets from 332 terrestrial, aquatic and host-associated ecosystems. For each metagenome we quantified viral abundance and levels of viral community diversity to test whether these variables can explain variation in CRISPR-Cas abundance across ecosystems. We find a strong positive correlation between CRISPR-Cas abundance and viral abundance. In addition, when controlling for differences in viral abundance, we found that the CRISPR-Cas systems are more abundant when viral diversity is low. We also found differences in relative CRISPR-Cas abundance among environments, with environmental classification explaining ∼24% of variation in CRISPR-Cas abundance. However, the correlations with viral abundance and diversity are broadly consistent across diverse natural environments. These results indicate that viral abundance and diversity are major ecological factors that drive the selection and maintenance of CRISPR-Cas in microbial ecosystems.Significance statement Numerous studies demonstrate that CRISPR-Cas immune systems can provide defence against bacteriophage and archaeal viruses, yet little is known about the ecological conditions where CRISPR-Cas immunity is favoured. Moreover, our knowledge is largely confined to laboratory studies and it is unknown if viruses are a key selective driver of CRISPR-Cas in nature. Using metagenomic data from diverse environments we find that both viral abundance and the abundance of CRISPR-Cas immune systems correlate positively across most environments. Furthermore, CRISPR-Cas systems are more prevalent when viral diversity is low. These results extend previous theoretical work by demonstrating that viruses are a key driver of selection of CRISPR-Cas immune systems across many natural ecosystems.Competing Interest StatementThe authors have declared no competing interest.