A mutant fitness assay identifies bacterial interactions in a model ocean hot spot.
Jeremy E SchreierChrista B SmithThomas R IoergerMary Ann MoranPublished in: Proceedings of the National Academy of Sciences of the United States of America (2023)
Bacteria that assemble in phycospheres surrounding living phytoplankton cells metabolize a substantial proportion of ocean primary productivity. Yet the type and extent of interactions occurring among species that colonize these micron-scale "hot spot" environments are challenging to study. We identified genes that mediate bacterial interactions in phycosphere communities by culturing a transposon mutant library of copiotrophic bacterium Ruegeria pomeroyi DSS-3 with the diatom Thalassiosira pseudonana CCMP1335 as the sole source of organic matter in the presence or absence of other heterotrophic bacterial species. The function of genes having significant effects on R. pomeroyi fitness indicated explicit cell-cell interactions initiated in the multibacterial phycospheres. We found that R. pomeroyi simultaneously competed for shared substrates while increasing reliance on substrates that did not support the other species' growth. Fitness outcomes also indicated that the bacterium competed for nitrogen in the forms of ammonium and amino acids; obtained purines, pyrimidines, and cofactors via crossfeeding; both initiated and defended antagonistic interactions; and sensed an environment with altered oxygen and superoxide levels. The large genomes characteristic of copiotrophic marine bacteria are hypothesized to enable responses to dynamic ecological challenges occurring at the scale of microns. Here, we discover >200 nonessential genes implicated in the management of fitness costs and benefits of membership in a globally significant bacterial community.
Keyphrases
- genome wide
- body composition
- physical activity
- single cell
- cell therapy
- organic matter
- induced apoptosis
- type diabetes
- adipose tissue
- bioinformatics analysis
- dna methylation
- mesenchymal stem cells
- metabolic syndrome
- risk assessment
- amino acid
- gene expression
- transcription factor
- cell cycle arrest
- bone marrow
- insulin resistance
- skeletal muscle
- wild type