Elevated temperature alters proteomic responses of individual organisms within a biofilm community

被引:44
作者
Mosier, Annika C. [1 ]
Li, Zhou [2 ,3 ]
Thomas, Brian C. [1 ]
Hettich, Robert L. [2 ]
Pan, Chongle [2 ]
Banfield, Jillian F. [1 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Earth & Planetary Sci, Berkeley, CA 94720 USA
[2] Oak Ridge Natl Lab, Oak Ridge, TN USA
[3] Univ Tennessee, Oak Ridge Natl Lab, Grad Sch Genome Sci & Technol, Knoxville, TN USA
[4] Univ Calif Berkeley, Dept Environm Sci Policy & Management, Berkeley, CA 94720 USA
关键词
IN-SITU DETECTION; TANDEM MASS TAGS; QUANTITATIVE PROTEOMICS; PHYLOGENETIC IDENTIFICATION; VIRAL LYSIS; PROTEIN; BACTERIAL; LEPTOSPIRILLUM; REVEALS; GROWTH;
D O I
10.1038/ismej.2014.113
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Microbial communities that underpin global biogeochemical cycles will likely be influenced by elevated temperature associated with environmental change. Here, we test an approach to measure how elevated temperature impacts the physiology of individual microbial groups in a community context, using a model microbial-based ecosystem. The study is the first application of tandem mass tag (TMT)-based proteomics to a microbial community. We accurately, precisely and reproducibly quantified thousands of proteins in biofilms growing at 40, 43 and 46 degrees C. Elevated temperature led to upregulation of proteins involved in amino-acid metabolism at the level of individual organisms and the entire community. Proteins from related organisms differed in their relative abundance and functional responses to temperature. Elevated temperature repressed carbon fixation proteins from two Leptospirillum genotypes, whereas carbon fixation proteins were significantly upregulated at higher temperature by a third member of this genus. Leptospirillum group III bacteria may have been subject to viral stress at elevated temperature, which could lead to greater carbon turnover in the microbial food web through the release of viral lysate. Overall, these findings highlight the utility of proteomics-enabled community-based physiology studies, and provide a methodological framework for possible extension to additional mixed culture and environmental sample analyses.
引用
收藏
页码:180 / 194
页数:15
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