Dr. Robert Bowers
Research Scientist, US Department of Energy Joint Genome Institute (JGI)
Dr. Robert Bowers, from the Department of Energy Joint Genome Institute (JGI), describes new technologies applied to investigate microbial function in extreme environments, at the Labcyte Genomics Symposium - Edinburgh 2016. View the video presentation to learn about the latest single-cell and metagenomics projects on diverse environmental samples such as deep ocean, sub-sea floor hydrothermal vents, geothermal hot springs and sub-glacial lakes.
Dr. Bowers introduces the concept of bacterial ‘dark matter’ in environmental microbial ecology, and how the JGI are modifying their single-cell genome production pipeline to expand what is known about the environmental microbial phylogenetic tree.
Dr. Robert Bowers, from the Department of Energy Joint Genome Institute (JGI), describes new technologies applied to investigate microbial function in extreme environments, at the Labcyte Genomics Symposium. Learn about the latest single-cell and metagenomics projects at JGI.
Dr. Bowers describes the sequencing and analysis services provided by the JGI, and provides an overview of its research areas: metagenomics, plants, fungi, microbes and DNA synthesis. The current JGI pipeline for production of single-cell genomics is well established, providing targeted sequencing of candidate phyla lineages to its users. For this, single-cell isolation is followed by genome amplification, 16s RNA gene identification and, finally, shotgun sequencing and assembly. However, many environmental microbes cannot be mapped using conventional culturing and sequencing techniques. Novel phyla are often missed by 16s primers used in traditional amplicon studies, most likely due to primer mutation mismatches or large insertions, that even high quality 16s universal primers cannot eliminate completely.
Dr. Bakal describes the workflows employed for high-content phenotypic studies at the Institute of Cancer Research. RNAi is used to produce gene knock downs, the cells are then imaged and the images segmented to obtain morphological signatures of up to 600 different features, that capture the ‘shape’ of each cell. A complex picture of the cells with thousands of different RNAi and conditions is built up, which generates large data sets.
Dr. Bowers describes how new technologies, in particular automated liquid handling, are improving shotgun metagenomics and single-cell genomic pipelines to help identify single-cell genomes from extreme environments. The group uses whole genome amplification of 16s PCR-negative single cells to permit sequencing and assembly. Going forwards, the JGI aims to use this more widely for remote environmental samples.
During the presentation, a test case from the Dewar Creek Hot Spring, British Columbia, in collaboration with the University of Calgary, is presented. The case demonstrates that the application of this technology to samples, has provided several new candidate phyla from single-cells.
Dr. Bowers uses the investigation into the composition and phylogeny of Dewar Creek Genomes, to illustrate how single-cell genomes that cannot be amplified with 16s primers, differ from the metagenome bins and 16s-positive genomes collected, and how genome level phylogeny uncovers potentially novel single-cell genomes, that may represent novel branches of phylogeny. Looking to the future, population level genomics, metabolic reconstructions and single nucleotide polymorphism (SNP) identification within single cell genomes is the planned approach for new candidate phylum.
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