Genomic mosaicism underlies the adaptation of marine Synechococcus ecotypes to distinct oceanic iron niches

Environ Microbiol. 2020 May;22(5):1801-1815. doi: 10.1111/1462-2920.14893. Epub 2019 Dec 27.

Abstract

Phytoplankton are limited by iron (Fe) in ~40% of the world's oceans including high-nutrient low-chlorophyll (HNLC) regions. While low-Fe adaptation has been well-studied in large eukaryotic diatoms, less is known for small, prokaryotic marine picocyanobacteria. This study reveals key physiological and genomic differences underlying Fe adaptation in marine picocyanobacteria. HNLC ecotype CRD1 strains have greater physiological tolerance to low Fe congruent with their expanded repertoire of Fe transporter, storage and regulatory genes compared to other ecotypes. From metagenomic analysis, genes encoding ferritin, flavodoxin, Fe transporters and siderophore uptake genes were more abundant in low-Fe waters, mirroring paradigms of low-Fe adaptation in diatoms. Distinct Fe-related gene repertories of HNLC ecotypes CRD1 and CRD2 also highlight how coexisting ecotypes have evolved independent approaches to life in low-Fe habitats. Synechococcus and Prochlorococcus HNLC ecotypes likewise exhibit independent, genome-wide reductions of predicted Fe-requiring genes. HNLC ecotype CRD1 interestingly was most similar to coastal ecotype I in Fe physiology and Fe-related gene content, suggesting populations from these different biomes experience similar Fe-selective conditions. This work supports an improved perspective that phytoplankton are shaped by more nuanced Fe niches in the oceans than previously implied from mostly binary comparisons of low- versus high-Fe habitats and populations.

MeSH terms

  • Acclimatization / genetics
  • Adaptation, Physiological / genetics
  • Diatoms / genetics
  • Ecosystem
  • Ecotype
  • Genome, Bacterial / genetics*
  • Iron / metabolism
  • Metagenomics
  • Mosaicism*
  • Oceans and Seas
  • Phytoplankton
  • Prochlorococcus / genetics*
  • Prochlorococcus / physiology*
  • Seawater / microbiology
  • Synechococcus / genetics*
  • Synechococcus / physiology*

Substances

  • Iron