Stewart Frank J, Dmytrenko Oleg, Delong Edward F, Cavanaugh Colleen M
School of Biology, Georgia Institute of Technology Atlanta, GA, USA.
Front Microbiol. 2011 Jun 20;2:134. doi: 10.3389/fmicb.2011.00134. eCollection 2011.
Thioautotrophic endosymbionts in the Domain Bacteria mediate key sulfur transformations in marine reducing environments. However, the molecular pathways underlying symbiont metabolism and the extent to which these pathways are expressed in situ are poorly characterized for almost all symbioses. This is largely due to the difficulty of culturing symbionts apart from their hosts. Here, we use pyrosequencing of community RNA transcripts (i.e., the metatranscriptome) to characterize enzymes of dissimilatory sulfur metabolism in the model symbiosis between the coastal bivalve Solemya velum and its intracellular thioautotrophic symbionts. High-throughput sequencing of total RNA from the symbiont-containing gill of a single host individual generated 1.6 million sequence reads (500 Mbp). Of these, 43,735 matched Bacteria protein-coding genes in BLASTX searches of the NCBI database. The taxonomic identities of the matched genes indicated relatedness to diverse species of sulfur-oxidizing Gammaproteobacteria, including other thioautotrophic symbionts and the purple sulfur bacterium Allochromatium vinosum. Manual querying of these data identified 28 genes from diverse pathways of sulfur energy metabolism, including the dissimilatory sulfite reductase (Dsr) pathway for sulfur oxidation to sulfite, the APS pathway for sulfite oxidation, and the Sox pathway for thiosulfate oxidation. In total, reads matching sulfur energy metabolism genes represented 7% of the Bacteria mRNA pool. Together, these data highlight the dominance of thioautotrophy in the context of symbiont community metabolism, identify the likely pathways mediating sulfur oxidation, and illustrate the utility of metatranscriptome sequencing for characterizing community gene transcription of uncultured symbionts.
细菌域中的硫自养型内共生体介导了海洋还原环境中的关键硫转化过程。然而,几乎对于所有的共生关系而言,共生体代谢的分子途径以及这些途径在原位的表达程度都鲜有确切描述。这主要是由于将共生体与其宿主分开培养存在困难。在此,我们利用群落RNA转录本的焦磷酸测序(即宏转录组)来表征沿海双壳贝类索氏泥蛤及其细胞内硫自养型共生体之间的典型共生关系中异化硫代谢的酶。对单个宿主个体含共生体的鳃中的总RNA进行高通量测序,产生了160万个序列读数(500兆碱基对)。其中,43,735个在NCBI数据库的BLASTX搜索中与细菌蛋白质编码基因匹配。匹配基因的分类身份表明它们与多种硫氧化γ-变形菌相关,包括其他硫自养型共生体和紫色硫细菌嗜酒嗜色菌。对这些数据进行人工查询,从硫能量代谢的不同途径中鉴定出28个基因,包括将硫氧化为亚硫酸盐的异化亚硫酸盐还原酶(Dsr)途径、亚硫酸盐氧化的APS途径以及硫代硫酸盐氧化的Sox途径。总体而言,与硫能量代谢基因匹配的读数占细菌mRNA库的7%。这些数据共同突显了硫自养在共生体群落代谢中的主导地位,确定了介导硫氧化的可能途径,并说明了宏转录组测序在表征未培养共生体的群落基因转录方面的效用。