Marine viral particles reveal an expansive repertoire of phage-parasitizing mobile elements.
John M EppleySteven J BillerElaine LuoAndrew BurgerEdward F DeLongPublished in: Proceedings of the National Academy of Sciences of the United States of America (2022)
Phage satellites are mobile genetic elements that propagate by parasitizing bacteriophage replication. We report here the discovery of abundant and diverse phage satellites that were packaged as concatemeric repeats within naturally occurring bacteriophage particles in seawater. These same phage-parasitizing mobile elements were found integrated in the genomes of dominant co-occurring bacterioplankton species. Like known phage satellites, many marine phage satellites encoded genes for integration, DNA replication, phage interference, and capsid assembly. Many also contained distinctive gene suites indicative of unique virus hijacking, phage immunity, and mobilization mechanisms. Marine phage satellite sequences were widespread in local and global oceanic virioplankton populations, reflecting their ubiquity, abundance, and temporal persistence in marine planktonic communities worldwide. Their gene content and putative life cycles suggest they may impact host-cell phage immunity and defense, lateral gene transfer, bacteriophage-induced cell mortality and cellular host and virus productivity. Given that marine phage satellites cannot be distinguished from bona fide viral particles via commonly used microscopic techniques, their predicted numbers (∼3.2 × 10 26 in the ocean) may influence current estimates of virus densities, production, and virus-induced mortality. In total, the data suggest that marine phage satellites have potential to significantly impact the ecology and evolution of bacteria and their viruses throughout the oceans. We predict that any habitat that harbors bacteriophage will also harbor similar phage satellites, making them a ubiquitous feature of most microbiomes on Earth.
Keyphrases
- pseudomonas aeruginosa
- genome wide
- climate change
- copy number
- sars cov
- gene expression
- type diabetes
- cell therapy
- risk assessment
- risk factors
- dna methylation
- coronary artery disease
- transcription factor
- high glucose
- genome wide identification
- artificial intelligence
- minimally invasive
- high throughput
- microbial community
- genetic diversity
- wastewater treatment
- molecularly imprinted
- antibiotic resistance genes
- stress induced
- anaerobic digestion