Visualizing in situ translational activity for identifying and sorting slow-growing archaeal-bacterial consortia

被引:136
作者
Hatzenpichler, Roland [1 ]
Connon, Stephanie A. [1 ]
Goudeau, Danielle [2 ]
Malmstrom, Rex R. [2 ]
Woyke, Tanja [2 ]
Orphan, Victoria J. [1 ]
机构
[1] CALTECH, Div Geol & Planetary Sci, Pasadena, CA 91125 USA
[2] Joint Genome Inst, Dept Energy, Walnut Creek, CA 94598 USA
基金
奥地利科学基金会; 美国国家科学基金会;
关键词
activity-based cell sorting; BONCAT; click chemistry; ecophysiology; single-cell microbiology; SULFATE-REDUCING BACTERIA; NEWLY SYNTHESIZED PROTEINS; TARGETED OLIGONUCLEOTIDE PROBES; METHANE-OXIDIZING ARCHAEA; SINGLE-CELL GENOMICS; ANAEROBIC OXIDATION; RIBOSOMAL-RNA; METHANOTROPHIC ARCHAEA; ELECTRON-TRANSFER; AMINO-ACIDS;
D O I
10.1073/pnas.1603757113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To understand the biogeochemical roles of microorganisms in the environment, it is important to determine when and under which conditions they are metabolically active. Bioorthogonal noncanonical amino acid tagging (BONCAT) can reveal active cells by tracking the incorporation of synthetic amino acids into newly synthesized proteins. The phylogenetic identity of translationally active cells can be determined by combining BONCAT with rRNA-targeted fluorescence in situ hybridization (BONCAT-FISH). In theory, BONCAT-labeled cells could be isolated with fluorescence-activated cell sorting (BONCAT-FACS) for subsequent genetic analyses. Here, in the first application, to our knowledge, of BONCAT-FISH and BONCAT-FACS within an environmental context, we probe the translational activity of microbial consortia catalyzing the anaerobic oxidation of methane (AOM), a dominant sink of methane in the ocean. These consortia, which typically are composed of anaerobic methane-oxidizing archaea (ANME) and sulfate-reducing bacteria, have been difficult to study due to their slow in situ growth rates, and fundamental questions remain about their ecology and diversity of interactions occurring between ANME and associated partners. Our activity-correlated analyses of >16,400 microbial aggregates provide the first evidence, to our knowledge, that AOM consortia affiliated with all five major ANME clades are concurrently active under controlled conditions. Surprisingly, sorting of individual BONCAT-labeled consortia followed by whole-genome amplification and 16S rRNA gene sequencing revealed previously unrecognized interactions of ANME with members of the poorly understood phylum Verrucomicrobia. This finding, together with our observation that ANME-associated Verrucomicrobia are found in a variety of geographically distinct methane seep environments, suggests a broader range of symbiotic relationships within AOM consortia than previously thought.
引用
收藏
页码:E4069 / E4078
页数:10
相关论文
共 96 条
[1]   COMBINATION OF 16S RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDE PROBES WITH FLOW-CYTOMETRY FOR ANALYZING MIXED MICROBIAL-POPULATIONS [J].
AMANN, RI ;
BINDER, BJ ;
OLSON, RJ ;
CHISHOLM, SW ;
DEVEREUX, R ;
STAHL, DA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (06) :1919-1925
[2]  
[Anonymous], 2005, Molecular Microbial Ecology
[3]   Development of a 16S rRNA-targeted probe set for Verrucomicrobia and its application for fluorescence in situ hybridization in a humic lake [J].
Arnds, Julia ;
Knittel, Katrin ;
Buck, Ulrike ;
Winkel, Matthias ;
Amann, Rudolf .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 2010, 33 (03) :139-148
[4]   Quantitative, Time-Resolved Proteomic Analysis by Combining Bioorthogonal Noncanonical Amino Acid Tagging and Pulsed Stable Isotope Labeling by Amino Acids in Cell Culture [J].
Bagert, John D. ;
Xie, Yushu J. ;
Sweredoski, Michael J. ;
Qi, Yutao ;
Hess, Sonja ;
Schuman, Erin M. ;
Tirrell, David A. .
MOLECULAR & CELLULAR PROTEOMICS, 2014, 13 (05) :1352-1358
[5]   Selective dye-labeling of newly synthesized proteins in bacterial cells [J].
Beatty, KE ;
Xie, F ;
Wang, Q ;
Tirrell, DA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (41) :14150-14151
[6]   Two-color labeling of temporally defined protein populations in mammalian cells [J].
Beatty, Kimberly E. ;
Tirrell, David A. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (22) :5995-5999
[7]   Fluorescence visualization of newly synthesized proteins in mammalian cells [J].
Beatty, Kimberly E. ;
Liu, Julie C. ;
Xie, Fang ;
Dieterich, Daniela C. ;
Schuman, Erin M. ;
Wang, Qian ;
Tirrell, David A. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (44) :7364-7367
[8]   In situ accessibility of small-subunit rRNA of members of the domains Bacteria, Archaea, and Eucarya to Cy3-labeled oligonucleotide probes [J].
Behrens, S ;
Rühland, C ;
Inácio, J ;
Huber, H ;
Fonseca, A ;
Spencer-Martins, I ;
Fuchs, BM ;
Amann, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (03) :1748-1758
[9]   Distribution of the verrucomicrobial clade Spartobacteria along a salinity gradient in the Baltic Sea [J].
Bergen, Benjamin ;
Herlemann, Daniel P. R. ;
Labrenz, Matthias ;
Juergens, Klaus .
ENVIRONMENTAL MICROBIOLOGY REPORTS, 2014, 6 (06) :625-630
[10]   Tracking heavy water (D2O) incorporation for identifying and sorting active microbial cells [J].
Berry, David ;
Mader, Esther ;
Lee, Tae Kwon ;
Woebken, Dagmar ;
Wang, Yun ;
Zhu, Di ;
Palatinszky, Marton ;
Schintimeister, Arno ;
Schmid, Markus C. ;
Hanson, Buck T. ;
Shterzer, Naama ;
Mizrahi, Itzhak ;
Rauch, Isabella ;
Decker, Thomas ;
Bocklitz, Thomas ;
Popp, Jurgen ;
Gibson, Christopher M. ;
Fowler, Patrick W. ;
Huang, Wei E. ;
Wagner, Michael .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (02) :E194-E203