Marine microbe contains multitudes
A deep dive into microbial genomics reveals one bacterial species is made of four ecologically distinct groups with different lifestyles.
The bacterium SAR324 is unusually cosmopolitan. In the ocean's North Pacific Subtropical Gyre, microbes tend to stay localized at different depths. But SAR324 can be found throughout the water column, from the warm, well-lit surface, to the blue-lit twilight zone, to the continuous pressure of the dark abyss, 4000 m (2.5 miles) deep. Scientists have wondered, how can SAR324 exist in so many varied environments? Now, a recent study published in Microbiome has uncovered that SAR324 encompasses four subgroups, adapted to different oceanic depths and relying on different ways of living.
Microbes help regulate the global carbon cycle—fixing, transforming, and respiring carbon. Understanding the metabolisms that SAR324 and other microbes use could inform scientists' understanding of carbon fluxes in the environment. Moreover, the deep ocean is the largest inorganic reservoir of carbon on earth; because SAR324—one of the most abundant organisms in the deep ocean—can fix carbon, SAR324 is able to influence this carbon pool.
To study the lifestyles of SAR324, lead author Dominique Boeuf and colleagues set sail on research cruises in 2015 and 2016. At Station ALOHA, site of the 30-years-long Hawaii Ocean Time-series (HOT), they collected samples of the ocean's microbial communities periodically at different depths. In order to determine the genome structure of SAR324 cells and their gene expression, the team then sequenced community genomes and expressed gene transcripts (metagenomes, metatranscriptomes), as well as the genomes of single cells of the uncultivated SAR324. The constellation of data gave the team unprecedented resolution to study the network of genes that contribute to the metabolisms that individual SAR324 cells can carry out. The work on single cells was done in collaboration with scientists Tanja Woyke and Rex Malmstrom at the U.S. Department of Energy Joint Genome Institute (JGI), a DOE Office of Science User Facility located at Lawrence Berkeley National Laboratory (Berkeley Lab), through the JGI Community Science Program. The metagenomes were also processed using the JGI-developed software suite, BBTools, and relying on the JGI Integrated Microbial Genomes & Microbiomes (IMG/M) system.
By analyzing the metagenomes, metatranscriptomes and single cell genomes, Boeuf—then a postdoctoral associate in Ed DeLong's group at the University of Hawaii at Manoa—and colleagues were able to see that SAR324 was made up of four ecologically distinct clusters, or ecotypes. These ecotypes fall into two main groups: two ecotypes dwell in the sunlit upper waters (above 200 m, or 656 ft), and have genes to support a photoheterotrophic lifestyle. In other words, they snack on fixed carbon if they can get it, rather than make it themselves, but use sunlight to help in the struggle to survive near the surface. The other two ecotypes, on the other hand, thrive in the dark, below 200 m (656 ft). They have genes supporting a chemolithoautotrophic way of life; they can fix carbon dioxide, but they drive that high-energy reaction using simple inorganic sulfur-containing chemicals instead of light.
Boeuf pointed out that, without the JGI, the discoveries made in this project wouldn't have been possible. Scientists hadn't known that SAR324 encompassed these different ecotypes because, historically, they have used the sequence of a "marker gene," namely the 16S ribosomal RNA (rRNA) gene, to mark or identify microbial species. All SAR324 have very closely related 16S rRNA genes, but these genes mask the striking diversity of their genomic capabilities. According to Boeuf, 16S rRNA genes are like stamps on packages: Focus only on the stamps, and you might miss the rich contents they're attached to.
More information: Dominique Boeuf et al, Metapangenomics reveals depth-dependent shifts in metabolic potential for the ubiquitous marine bacterial SAR324 lineage, Microbiome (2021). DOI: 10.1186/s40168-021-01119-5
Provided by DOE/Joint Genome Institute