1 / 17

Biologic Ground Truth

Biologic Ground Truth. Life in the Atacama 2004 Science & Technology Workshop Ned Minkley Center for Biotechnology and Environmental Processes Carnegie Mellon University. Detecting Life in Extreme Environments. Photographs from the November, 2003 trip to the Atacama. Methods

dotty
Télécharger la présentation

Biologic Ground Truth

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Biologic Ground Truth Life in the Atacama 2004Science & Technology Workshop Ned MinkleyCenter for Biotechnology and Environmental Processes Carnegie Mellon University

  2. Detecting Life in Extreme Environments Photographs from the November, 2003 trip to the Atacama Carnegie Mellon

  3. Methods Macroscopic vs. Microscopic Microscopes Light TEM, SEM Cultivation Semi-solid surfaces (petri plates) Liquid media (tubes, flasks) Detection without Cultivation PCR amplification of 16S rDNA Molecular Phylogeny Endolithic Biota Atacama Desert Rocks Atacama Desert Soils Limitations Preparation artifacts Extraction (e.g. biofilm) Choice of Media Extraction; inhibitors Life Detection Methods for Microorganisms Carnegie Mellon

  4. Detecting Macroscopic Life Is Unambiguous? Carnegie Mellon

  5. Endolithic Microorganims • Friedmann & Ocampo (1976) report blue-green algae (cyanobacteria) in rocks from the Dry Valley area of the Ross Desert, Antarctica. • SEM and CLSM images of the communities in the fissure of a granite rock and 1-2 mm below the surface of sandstone. Ascaso & Wierzchos, Int. Microbiol. 5:215-222 (2002) Carnegie Mellon

  6. Detection and Enumeration via Cultivation Dilution and Plating Most Probable Number (MPN) Analysis Carnegie Mellon

  7. Cultivation of Microorganisms on Plates • Cultivation of bacteria from a field at a wood-treating plant • Left, an area contaminated with creosote and pentachlorophenol • Right, a nearby uncontaminated region Carnegie Mellon

  8. Detection without Cultivation • Estimates of culturability from various media • Seawater 0.001-0.1% • Freshwater 0.25% • Lake 0.1-1% • Estuary 0.1-3% • Activat. sludge 1-15% • Sediments 0.25% • Soil 0.3% Amann et al., Microbiol. Rev. 59:143-169 (1995) Carnegie Mellon

  9. The Polymerase Chain Reaction (PCR) • PCR can be used to selectively amplify a defined segment of a DNA molecule by one million-fold or more • Sensitivity can be increased by carrying out a total genomic pre-amplification using Phi29 DNA polymerase and random hexanucleotide primers • A homogeneous PCR product can be gel purified and sequenced directly • A PCR product mixture can be cloned into a vector plasmid, introduced into a bacterial host strain (transformation) and recombinant bacteria that contain unique PCR products obtained by dilution and plating onto selective media Carnegie Mellon

  10. Molecular Phylogeny Casamayor et al., Environ. Microbiol. 4:338-348 (2002) • Relatedness of microorganisms based on a comparison of the sequences of their small subunit (SSU) ribosomal RNA genes • Rationale: DNA › RNA › Protein • Genetic code is universal • Ribosome translates the code • Large and small subunits • 3 rRNAs + 75 proteins Carnegie Mellon

  11. Phylogenetic Trees Woese, Microbiol. Rev. 51:221-271 (1987) • Eubacteria and archaea are prokaryotes • Eubacterial branch includes chloroplasts and mitochondria • Diversity comes from microorganisms Carnegie Mellon

  12. Phylotypes in Clone Libraries de la Torre, Goebel, Friedmann & Pace, Appl. Environ. Microbiol. 69: 3858-3867 (2003) • Samples of beacon sandstone from McMurdo Dry Valleys • Microscopic examination to identify two community types • Extraction of total community genomic DNA • PCR amplification and construction of rDNA clone libraries • DNA sequence determination and phylogenetic analysis of 672 • lichen community clones and 480 cyanobacterial clones Carnegie Mellon

  13. Atacama Rocks from the Spring, 2003 Trip Carnegie Mellon

  14. Atacama Soil Samples: Sites and Profiles Navarro-Gonzalez et al. Science, 302:1018-1021 (2003) Carnegie Mellon

  15. Bacteria in Atacama Desert Soils • Results from Navarro-Gonzalez et al. • Six nearby samples (≈ 2m radius) collected with a sterile scoop from the upper 10-cm soil layer and composited in polyethylene bags (500 g total weight) • Total culturable heterotrophic bacteria by dilution and plating on Difco plate count agar at 3 strengths • 1st dilution contains 0.01 g soil (102 cfu/g is MDL) • Counts ranged from nd (≤102) to 2.2 x 106 CFU/g-soil) • Diversity from SSU rDNA PCR clones • 6 TU per 75 clones to 26 TU/75 clones • 35 TU per 75 clones in coastal sample • Yungay area (S 24º 4’ 9.6”) was the most arid studied and contained no detectable bacteria by dilution plating on PCA, no recoverable DNA and no PCR products • A few colonies were detected by MPN analysis with 1-10 g soil • Genotypes are those typically found in arid soils AT02-23 (S 27º 1’ 17.4”) AT02-22 (S 28º 7’ 4.5”) Carnegie Mellon

  16. Where Are the Bacteria in Atacama Soils? • Key finding was presence of bacteria in every soil sample tested • Need guidance on strategy for robotic search for soil bacteria • Spatial distribution of microbes in the near-surface soil layer can be distinguished by collecting core samples and sectioning • Multiple nearby samples can reveal extent of local heterogeneity Carnegie Mellon

  17. Biologic Ground Truth-Conclusions • Levels of analysis • Level 1. Visible analysis of macroscopic targets (field) • Level 2. Microscopic imaging of target rocks/soils (field) • Level 3. Laboratory analysis of target rocks/soils • Sample acquisition for lab analysis • Sample log (sample no., GPS coordinates, local environmental data) • Photodocumentation • Asceptic 10-cm sample cores (coincident with imaged area) • Rocks (actual field samples) • Laboratory analyses • Microscopic • Light • EM • Geochemistry (N, P, TOC, moisture content) • Culture-based • Chemoautotrophs (R2A, FA Min) • Photoautotrophs (B-G + nitrate) • Chemoautotrophs (ammonia oxidizers) • Direct PCR clone libraries • Decision--Do we pursue Level 3 analyses? • Level 3.1. Single cores. Yes/No. Spatial distribution. Limited diversity. • Level 3.2. Multiple nearby cores. Spatial distribution. Local heterogeneity. Diversity. • Level 3.3. West-to-East traverse following a precipitation gradient. Microbial Ecology. Carnegie Mellon

More Related