The Thrash lab is oriented around generating and testing hypotheses about the relationships among and between aquatic microorganisms and their environment. We combine cultivation independent methods (e.g., metagenomics, metatranscriptomics, and single-cell genomics) with high throughput culturing, physiology, and microbial genomics, as well as chemical and physical information from the environment. We seek to understand why microorganisms occur where they do and what they are doing there. See our Publications page to get a sense of our recent work.
High throughput culturing
We have systematically collected samples from across the Southern Louisiana coastline and collaborated with other researchers in marine and freshwater environments to conduct high throughput cultivation (HTC) experiments using tailored, defined media. We also collect water chemistry and microbial communities data from the source water to evaluate cultivation efficacy and refine our defined media recipes. To date, we have isolated over 400 microorganisms, 43% of which occur within the top 50 most abundant taxa in the sampled environments. Prominent examples include the first isolation of a freshwater SAR11 (a.k.a. LD12) representative, members of SAR11 subclade IIIa, OM43, OM182, SAR92, SAR116, Limnohabitans, Polynucleobacter, Actinobacter acIV, and many others. See our culture collection page for a comprehensive list.
“A Microbial High Throughput Culturing Laboratory at LSU.” Louisiana Board of Regents Research Competitiveness Subprogram
Henson, Michael W., V. Celeste Lanclos, Brant C. Faircloth, and J. Cameron Thrash. (2018) Cultivation and genomics of the first freshwater SAR11 (LD12) isolate.The ISME Journal 12:1846-1860. Supplementary Information.
Henson, Michael W., David M. Pitre, Jessica Lee Weckhorst, V. Celeste Lanclos, Austen T. Webber, and J. Cameron Thrash. (2016) Artificial seawater media facilitates cultivating members of the microbial majority from the Gulf of Mexico. mSphere 1(2). doi: 10.1128/mSphere.00028-16. Supplementary Information.
Lanclos, V. Celeste, Michael W. Henson, David M. Pitre, and J. Cameron Thrash. (2016) Draft Genome Sequence of strain LSUCC0135, an early diverging member of the Methylophilales in the Betaproteobacteria. Genome Announcements 4(6):e01231-16.
Thrash, J. Cameron, Jessica Lee Weckhorst, and David M. Pitre. (2015) Cultivating Fastidious Microbes. In Hydrocarbon and Lipid Microbiology Protocols, vol. 4 (Cultivation). Edited by Terry J. McGenity, Kenneth N. Timmis and Balbina Nogales. In Press.
Evolution of salinity tolerance in SAR11
During 2018-2019, in collaboration with Liz Kujawinski (WHOI) we will be quantifying the mechanistic differences between sister clades of SAR11 that have evolved to inhabit environments of with very different ionic strength regimes. Stay tuned for more!
“Collaborative Research: EAGER: Salinity-based selection between sister clades of abundant coastal bacterioplankton.” National Science Foundation OCE-1747681
Microbial ecology of the northern Gulf of Mexico “dead zone”
We collaborate with Nancy Rabalais (LSU/LUMCON), Olivia Mason (Florida State University), and Brett Baker (University of Texas) in deploying a wide range of cultivation-independent techniques to learn about the microbial communities and genetics associated with the generation and maintenance of seasonal bottom water hypoxia on the Northern Gulf of Mexico shelf region (see lab blog entries for 2013 and 2014 cruise information).
“Cultivation independent assessment of microbial communities in the Gulf of Mexico dead zone.” Ralph E. Powe Junior Faculty Enhancement Award, Oak Ridge Associated Universities.
Thrash, J. Cameron , Kiley W. Seitz, Brett J. Baker, Ben Temperton, Lauren E. Gillies, Nancy N. Rabalais, Bernard Henrissat, Olivia U. Mason. (2017) Metabolic roles of uncultivated bacterioplankton lineages in the northern Gulf of Mexico “Dead Zone.” mBio 8(5):e01017-17. Supplementary Information.
Gilles, Lauren E., J. Cameron Thrash, Sergio deRada, Nancy N. Rabalais, and Olivia U. Mason. (2015) Archaeal enrichment in the hypoxic zone in the northern Gulf of Mexico. Environmental Microbiology 17(10): 3847-3856
J. Cameron Thrash, Brett J. Baker, Kiley W. Seitz, Ben Temperton, Lauren Gillies Campbell, Nancy N. Rabalais, Bernard Henrissat, and Olivia U. Mason. (2018) Metagenomic assembly and prokaryotic MAGs from the northern Gulf of Mexico “Dead Zone”. Microbiology Resource Announcements 7:e01033-18 Table S1
Microbial ecology of the Mississippi River
We have been coordinating with OAR Northwest in a citizen science and education program to explore the microbial assemblages inhabiting the Mississippi River and begin quantifying their relationship to eutrophication. To date, we have completed two full-length Mississippi River transects using rowboats, and are in the process of publishing our results. You can read more about the science HERE and watch a promotional video from the 2014 season:
Henson, Michael W., Jordan Hanssen, Greg Spooner, Patrick Flemming, Markus Pukonen, Frederick Stahr, and J. Cameron Thrash. (2018) Nutrient dynamics and stream order influence microbial community patterns along a 2914 km transect of the Mississippi River. Limnology and Oceanography 63(5):1837-1855 Supplemental Material.