SEP 11, 2019 9:00 AM PDT

Using metagenomics and bioinformatics to investigate bacterial-fungal interactions

Sponsored by: Illumina
C.E. Credits: P.A.C.E. CE Florida CE
Speaker
  • Scientist V, Bioinformatics and Applied Genomics, Bioscience Division, Los Alamos National Laboratory
    Biography
      Patrick Chain directs the Metagenomics Applications, and the Bioinformatics and Analytics Teams in the Bioscience Division at Los Alamos National Laboratory and co-manages the Division's Genomics Program. His research group both develops novel algorithms and methods in bioinformatics and metagenomics, and applies them to both applied organism detection and sample characterization and to more basic research questions in a range of 'biomes', from human and other eukaryotic microbiomes, to the study of environmental ecosystems. He was awarded a B.Sc. and M.Sc. at McMaster University and a Ph.D. at Michigan State University. He has previously led microbial genomics and microbial interactions groups at the Department of Energy's Joint Genome Institute and Lawrence Livermore National Laboratory, and at LANL focuses his research on metagenomic applications and data analysis.

    Abstract

    Fungi and bacteria form different types of associations that are central to numerous environmental processes. Similar to human dysbioses and microbiome manipulation via antibiotics and probiotic remediation, it may be possible to steer agricultural ecosystem function by altering soil environmental parameters to select for desired microbes and traits. As a first step, we wish to investigate and characterize bacterial interactions with fungi at a fundamental level, to establish the types of interactions, their breadth both phylogenetically and functionally, and later, to characterize these interactions at the molecular level. Prior work suggests that bacteria and fungi exploit each other both on the surfaces of fungal mycelial networks, as well as within mycelia. We begin by exploring the diverse nature of these associations by screening both genomic databases as well as culture collections. Available fungal genome projects are screened for the presence of bacterial genomic signatures that may have been inadvertently sequenced. Challenges in this field of taxonomy classification and bacterial identification will be discussed. In addition, we screen diverse fungal collections for bacterial signatures using an approach based on sequencing of the 16S rRNA gene combined with microscopic confirmation of the presence of endohyphal bacteria. For some isolates, we explore some of the interactions phenotypically, by monitoring growth during confrontation assays. We have used devices dubbed ‘fungal highway’ columns, to isolate bacteria capable of utilizing fungal mycelia as a dispersal mechanism, and are testing a 3D fabrication of this type of device for routine exploration of such interactions. Growth phenotypes of some of these bacterial and fungal isolates, as well as known interacting bacterial-fungal pairs, are being examined. Collectively, these studies begin to shed light into the diversity, and range of interactions that occur among these dominant microbial players.  

    https://github.com/LANL-Bioinformatics
    https://genomicscience.energy.gov/research/sfas/lanlbfi.shtml
    This study was supported by the U.S. Department of Energy, Office of Science, Biological and Environmental Research Division, under award numbers LANLF59T and LANLF59C.

    Learning objectives:
    1. Metagenomic analysis is already complex, and complicated further by incomplete and non-standardized databases of known organisms
    2. fungi may have their own 'microbiomes', as we discover signatures of bacteria both within and on the surface of fungal hyphae


    Show Resources
    You May Also Like
    DEC 02, 2020 8:00 AM PST
    C.E. CREDITS
    DEC 02, 2020 8:00 AM PST
    DATE: December 2nd, 2020 TIME: 08:00am PDT, 11:00pm EDT Bioreactors and shakers are used to cultivate microorganisms, plant, insect, and mammalian cells in different volumes. Upscaling of pr...
    OCT 08, 2020 7:00 AM PDT
    C.E. CREDITS
    OCT 08, 2020 7:00 AM PDT
    DATE: October 8, 2020 TIME: 7:00am PDT, 10:00am EDT, 4:00pm CEST How often do you pipette in your cell culture lab every day? Usually, we do it so often that we tend stop thinking about ho...
    SEP 10, 2020 9:00 AM PDT
    C.E. CREDITS
    SEP 10, 2020 9:00 AM PDT
    Date: September 10, 2020 Time: 9:00am (PDT), 12:00pm (EDT) Osmolality testing is relevant throughout the entire bioprocessing workflow. As customers look to refine mAb and gene therapy workf...
    AUG 25, 2020 8:00 AM PDT
    C.E. CREDITS
    AUG 25, 2020 8:00 AM PDT
    DATE: August 25, 2020 TIME: 8:00am PDT, 10:00am CDT, 11:00am EDT Recombinant lentivirus (LV) and adeno-associated virus (AAV) are critical components of cell and gene therapies, which show g...
    NOV 16, 2020 8:00 AM PST
    C.E. CREDITS
    NOV 16, 2020 8:00 AM PST
    Date: November 16, 2020 Time: 8:00am (PST), 11:00am (EST) CRISPR screening has become the prime discovery tool in modern biomedical research and drug discovery. At the same time, most screen...
    DEC 16, 2020 8:00 AM PST
    Add to Calendar Select one of the following: iCal Google Calendar Outlook Calendar Yahoo Calendar
    C.E. CREDITS
    DEC 16, 2020 8:00 AM PST
    Add to Calendar Select one of the following: iCal Google Calendar Outlook Calendar Yahoo Calendar
    Date: December 16, 2020 Time: 8:00am (PST), 11:00am (EST) Molecular imaging of living specimens offers a means to draw upon the growing body of high-throughput molecular data to better under...
    Loading Comments...
    Show Resources
    Attendees
    • See more