Baker Brett J, Lutz Michelle A, Dawson Scott C, Bond Philip L, Banfield Jillian F
Department of Earth and Planetary Sciences, 40 Hilgard Hall, University of California at Berkeley, Berkeley, CA 94720, USA.
Appl Environ Microbiol. 2004 Oct;70(10):6264-71. doi: 10.1128/AEM.70.10.6264-6271.2004.
Acid mine drainage (AMD) microbial communities contain microbial eukaryotes (both fungi and protists) that confer a biofilm structure and impact the abundance of bacteria and archaea and the community composition via grazing and other mechanisms. Since prokaryotes impact iron oxidation rates and thus regulate AMD generation rates, it is important to analyze the fungal and protistan populations. We utilized 18S rRNA and beta-tubulin gene phylogenies and fluorescent rRNA-specific probes to characterize the eukaryotic diversity and distribution in extremely acidic (pHs 0.8 to 1.38), warm (30 to 50 degrees C), metal-rich (up to 269 mM Fe(2+), 16.8 mM Zn, 8.5 mM As, and 4.1 mM Cu) AMD solutions from the Richmond Mine at Iron Mountain, Calif. A Rhodophyta (red algae) lineage and organisms from the Vahlkampfiidae family were identified. The fungal 18S rRNA and tubulin gene sequences formed two distinct phylogenetic groups associated with the classes Dothideomycetes and Eurotiomycetes. Three fungal isolates that were closely related to the Dothideomycetes clones were obtained. We suggest the name "Acidomyces richmondensis" for these isolates. Since these ascomycete fungi were morphologically indistinguishable, rRNA-specific oligonucleotide probes were designed to target the Dothideomycetes and Eurotiomycetes via fluorescent in situ hybridization (FISH). FISH analyses indicated that Eurotiomycetes are generally more abundant than Dothideomycetes in all of the seven locations studied within the Richmond Mine system. This is the first study to combine the culture-independent detection of fungi with in situ detection and a demonstration of activity in an acidic environment. The results expand our understanding of the subsurface AMD microbial community structure.
酸性矿山排水(AMD)微生物群落包含微生物真核生物(真菌和原生生物),它们赋予生物膜结构,并通过捕食和其他机制影响细菌和古菌的丰度以及群落组成。由于原核生物会影响铁氧化速率,进而调节AMD的产生速率,因此分析真菌和原生生物种群非常重要。我们利用18S rRNA和β-微管蛋白基因系统发育以及荧光rRNA特异性探针,对加利福尼亚州铁山里士满矿极端酸性(pH值0.8至1.38)、温暖(30至50摄氏度)、富含金属(铁离子浓度高达269 mM、锌离子浓度16.8 mM、砷离子浓度8.5 mM、铜离子浓度4.1 mM)的AMD溶液中的真核生物多样性和分布进行了表征。鉴定出了一个红藻门(红藻)谱系和来自瓦氏变形虫科的生物。真菌的18S rRNA和微管蛋白基因序列形成了与座囊菌纲和散囊菌纲相关的两个不同的系统发育组。获得了三个与座囊菌纲克隆密切相关的真菌分离株。我们建议将这些分离株命名为“里士满酸性菌”。由于这些子囊菌真菌在形态上无法区分,因此设计了rRNA特异性寡核苷酸探针,通过荧光原位杂交(FISH)靶向座囊菌纲和散囊菌纲。FISH分析表明,在里士满矿系统内研究的所有七个地点中,散囊菌纲通常比座囊菌纲更为丰富。这是第一项将不依赖培养的真菌检测与原位检测相结合,并证明其在酸性环境中活性的研究。这些结果扩展了我们对地下AMD微生物群落结构的理解。