Mincer Tracy J, Fenical William, Jensen Paul R
Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093-0204, USA.
Appl Environ Microbiol. 2005 Nov;71(11):7019-28. doi: 10.1128/AEM.71.11.7019-7028.2005.
Salinispora is the first obligate marine genus within the order Actinomycetales and a productive source of biologically active secondary metabolites. Despite a worldwide, tropical or subtropical distribution in marine sediments, only two Salinispora species have thus far been cultivated, suggesting limited species-level diversity. To further explore Salinispora diversity and distributions, the phylogenetic diversity of more than 350 strains isolated from sediments collected around the Bahamas was examined, including strains cultured using new enrichment methods. A culture-independent method, using a Salinispora-specific seminested PCR technique, was used to detect Salinispora from environmental DNA and estimate diversity. Overall, the 16S rRNA gene sequence diversity of cultured strains agreed well with that detected in the environmental clone libraries. Despite extensive effort, no new species level diversity was detected, and 97% of the 105 strains examined by restriction fragment length polymorphism belonged to one phylotype (S. arenicola). New intraspecific diversity was detected in the libraries, including an abundant new phylotype that has yet to be cultured, and a new depth record of 1,100 m was established for the genus. PCR-introduced error, primarily from Taq polymerase, significantly increased clone library sequence diversity and, if not masked from the analyses, would have led to an overestimation of total diversity. An environmental DNA extraction method specific for vegetative cells provided evidence for active actinomycete growth in marine sediments while indicating that a majority of sediment samples contained predominantly Salinispora spores at concentrations that could not be detected in environmental clone libraries. Challenges involved with the direct sequence-based detection of spore-forming microorganisms in environmental samples are discussed.
盐孢菌属是放线菌目首个专性海洋属,也是生物活性次生代谢产物的丰富来源。尽管该属在全球热带或亚热带海洋沉积物中均有分布,但迄今为止仅培养出两个盐孢菌物种,这表明其物种水平的多样性有限。为进一步探索盐孢菌属的多样性和分布情况,研究人员对从巴哈马群岛周边沉积物中分离出的350多个菌株进行了系统发育多样性分析,其中包括采用新富集方法培养的菌株。同时,还使用了一种不依赖培养的方法,即利用盐孢菌属特异性半巢式PCR技术,从环境DNA中检测盐孢菌属并估计其多样性。总体而言,培养菌株的16S rRNA基因序列多样性与环境克隆文库中检测到的结果高度一致。尽管付出了巨大努力,但未检测到新的物种水平多样性,在通过限制性片段长度多态性分析的105个菌株中,97%属于一个系统型(沙栖盐孢菌)。在文库中检测到了新的种内多样性,包括一个尚未培养的丰富新系统型,并且该属的新深度记录被刷新至1100米。PCR引入的错误(主要来自Taq聚合酶)显著增加了克隆文库序列的多样性,如果在分析中不加以掩盖,将会导致对总多样性的高估。一种针对营养细胞的环境DNA提取方法为海洋沉积物中放线菌的活跃生长提供了证据,同时表明大多数沉积物样本中主要含有盐孢菌属孢子,其浓度在环境克隆文库中无法检测到。文中还讨论了在环境样本中基于直接序列检测产孢微生物所面临的挑战。