Cold, salty and promiscuous: Gene-shuffling microbes dominate Antarctica's Deep Lake

Sep 30, 2013
This is Deep Lake in Antartica. The water in the 36-metre deep lake is so salty it remains in liquid form down to a temperature of minus 20 degrees Celsius. Credit: UNSW

Sequestered in Antarctica's Vestfold Hills, Deep Lake became isolated from the ocean 3,500 years ago by the Antarctic continent rising, resulting in a saltwater ecosystem that remains liquid in extreme cold, and providing researchers a unique niche for studying the evolution of the microbes that now thrive under such conditions. Deep Lake's microscopic inhabitants are dominated by haloarchaea, microbes that require high salt concentrations to grow and are naturally adapted to conditions – at minus 20C – that would prove lethally cold to other organisms. In a detailed analysis published online the week of September 30, 2013 in the journal Proceedings of the National Academy of Sciences (PNAS), researchers have, for the first time, been able to get a complete ecological picture of the Deep Lake microbial community.

A team led by Rick Cavicchioli of the University of New South Wales, Australia partnered with the U.S. Department of Energy Joint Genome Institute (DOE JGI) to generate sequence data from DNA isolated from individual microbes and compared them with metagenomic (microbial community) information sampled at various depths of Deep Lake.

"Understanding how haloarchaea can thrive in Deep Lake could be used to develop engineering concepts for reducing energy costs in a variety of situations, such as for cleaning up contaminated sites in permanently or seasonally cold regions," Cavicchioli said. Owing to the ability of salt-loving enzymes to function under extremes, he suggests they could also be used as catalysts for peptide synthesis and enhanced oil recovery, and can function in water-organic solvent mixtures. "These enzymes will be especially useful for transforming contaminated sites with particularly high levels of petroleum-based products," he added.

Deep Lake's extremes have rendered the microbial neighborhood rather homogeneous. Four isolates in the study represented about 72 percent of the cells in the community. Though gene exchange across species boundaries is considered infrequent, the researchers observed that haloarchaea living in the Lake's hypersaline environment practice it comparatively often, like neighbors "chewing the fat" in a small-town coffee klatch. "It's intriguing that while gene exchange is rampant, species lineages appear to be maintained by virtue of each species having a high level of specialization, enabling niche partitioning and peaceful coexistence," said Cavicchioli of their findings. "Haloarchaea are known for being 'promiscuous,' that is, prone to exchange DNA between themselves. Our study demonstrated that this exchange occurs at a much higher level than has previously been documented in nature. They communicate, share, specialize, and coexist."

What distinguishes this "conversation" is that the haloarchaea of Deep Lake exchange the information of DNA not just between species but among distinct genera, and moreover in huge tranches, some 35,000 letters of code, with not a letter out of place. While it may be slow, that give-and-take is chock full of essential information and the word gets around the community. "The long stretches of highly identical shared sequence between the different lake organisms spurred a strong suspicion of potential cross-contamination at first," said Tanja Woyke, Microbial Program Lead at the DOE JGI and co-author of the study. "By painstaking validation of the manually finished and curated genomes, however, we were able to exclude any process-introduced artifacts and confirm that this is true inter-genera gene exchange."

Cavicchioli noted that, "as the content being shifted around lack core genes, it speaks to these microbes' ability to be flexible and collaborative. This shuttled gene content could confer such benefits as resistance to viruses or bolster their ability to respond to specific environmental factors. Moreover, the markers that we analyzed indicated that a high level of gene exchange occurs throughout the Deep Lake community."

Longtime DOE Joint Genome Institute collaborator Rick Cavicchioli from the University of New South Wales, Australia is the senior author of the PNAS paper on the microbial community thriving in Deep Lake, Antarctica, which was published the week of September 30, 2013. In this image he is shown collecting water samples from the deepest point of Deep Lake. Credit: Rick Cavicchioli

One particular microbial player, dubbed tADL, represented about 44 percent of the cell content of the lake community, which is one of the least productive environments on the planet with respect to synthesis of organic compounds from carbon dioxide. Most life on earth is dependent on this process, but microbial life in Deep Lake has only six generations of cell division annually, so tADL's comparatively "high energy" metabolism makes it adept at degrading carbohydrates, with a particular taste for glycerol, a natural byproduct of the light-harvesting algae. "A key thing about what they eat is that by choosing different food sources they can coexist and continue to reproduce and eke out a living in relative harmony," said Cavicchioli.

Cavicchioli acknowledged that the PNAS paper represents the synthesis of the more striking findings that arose from merging and analyzing collective data sets that have been assembled over the last eight years. Along the way, a major milestone logged was the genome sequencing and analysis of the first member of the archaeal branch of the tree of life ever isolated from a polar environment.

"Every time we 'poke an omics stick' in there we find things we never expected," Cavicchioli said. "Each lake also has its own unique characteristics, so there is a lot more to be discovered. These Antarctic expeditions represent big logistical investments, with millions in funding from the Australian Antarctic Division and the Australian Antarctic Science Program leveraging the powerful resources of JGI. As a long-term investment strategy, this has proven to be an excellent model of how a flexible group of clever scientists can provide a sure path for enabling strong science to come to fruition."

Explore further: Life found in the sediments of an Antarctic subglacial lake for the first time

More information: High level of intergenera gene exchange shapes the evolution of haloarchaea in an isolated Antarctic lake , PNAS, www.pnas.org/cgi/doi/10.1073/pnas.1307090110

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JVK
1 / 5 (6) Sep 30, 2013
How much more experimental evidence of nutrient-dependent ecological niche construction and pheromone-controlled reproduction in species from microbes to man will be required to refute ridiculous ideas about mutation-driven evolution? With the requirements for the conserved molecular mechanisms of thermodynamics and organism-level thermoregulation in every other species that has adaptively involved via nutrient-dependent changes in intercellular signaling that enable stochastic gene expression at temperatures – of minus 20C – and higher, who would like to try to explain the role of mutations and natural selection for comparison to the scientific facts represented in this news article or in any other extant literature that accurately portrays what is currently known about nutrient-dependent pheromone-controlled adaptive evolution sans mutations?