Nakagawa Tatsunori, Ishibashi Jun-Ichiro, Maruyama Akihiko, Yamanaka Toshiro, Morimoto Yusuke, Kimura Hiroyuki, Urabe Tetsuro, Fukui Manabu
Department of Biological Science, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan.
Appl Environ Microbiol. 2004 Jan;70(1):393-403. doi: 10.1128/AEM.70.1.393-403.2004.
This study describes the occurrence of unique dissimilatory sulfite reductase (DSR) genes at a depth of 1,380 m from the deep-sea hydrothermal vent field at the Suiyo Seamount, Izu-Bonin Arc, Western Pacific, Japan. The DSR genes were obtained from microbes that grew in a catheter-type in situ growth chamber deployed for 3 days on a vent and from the effluent water of drilled holes at 5 degrees C and natural vent fluids at 7 degrees C. DSR clones SUIYOdsr-A and SUIYOdsr-B were not closely related to cultivated species or environmental clones. Moreover, samples of microbial communities were examined by PCR-denaturing gradient gel electrophoresis (DGGE) analysis of the 16S rRNA gene. The sequence analysis of 16S rRNA gene fragments obtained from the vent catheter after a 3-day incubation revealed the occurrence of bacterial DGGE bands affiliated with the Aquificae and gamma- and epsilon-Proteobacteria as well as the occurrence of archaeal phylotypes affiliated with the Thermococcales and of a unique archaeon sequence that clustered with "Nanoarchaeota." The DGGE bands obtained from drilled holes and natural vent fluids from 7 to 300 degrees C were affiliated with the delta-Proteobacteria, genus Thiomicrospira, and Pelodictyon. The dominant DGGE bands retrieved from the effluent water of casing pipes at 3 and 4 degrees C were closely related to phylotypes obtained from the Arctic Ocean. Our results suggest the presence of microorganisms corresponding to a unique DSR lineage not detected previously from other geothermal environments.
本研究描述了在日本西太平洋伊豆-小笠原弧的水妖海山深海热液喷口场1380米深处独特的异化亚硫酸盐还原酶(DSR)基因的出现情况。DSR基因是从在喷口处部署3天的导管型原位生长室中生长的微生物以及5℃钻孔的流出水和7℃天然喷口流体中获得的。DSR克隆SUIYOdsr-A和SUIYOdsr-B与已培养物种或环境克隆没有密切关系。此外,通过对16S rRNA基因进行PCR-变性梯度凝胶电泳(DGGE)分析来检测微生物群落样本。对在3天培养后从喷口导管获得的16S rRNA基因片段进行序列分析,结果显示出现了与水生栖热菌属、γ-和ε-变形菌纲相关的细菌DGGE条带,以及与热球菌目相关的古菌系统发育型和一个与“纳米古菌门”聚类的独特古菌序列。从7至300℃的钻孔和天然喷口流体中获得的DGGE条带与δ-变形菌纲、硫微螺菌属和板状绿菌属相关。从3℃和4℃套管流出水中回收的主要DGGE条带与从北冰洋获得的系统发育型密切相关。我们的结果表明存在与先前在其他地热环境中未检测到的独特DSR谱系相对应的微生物。