Whitby C B, Saunders J R, Rodriguez J, Pickup R W, McCarthy A
School of Biological Sciences, University of Liverpool, Liverpool L69 7ZB, United Kingdom.
Appl Environ Microbiol. 1999 Nov;65(11):4855-62. doi: 10.1128/AEM.65.11.4855-4862.1999.
The population of ammonia-oxidizing bacteria in a temperate oligotrophic freshwater lake was analyzed by recovering 16S ribosomal DNA (rDNA) from lakewater and sediment samples taken throughout a seasonal cycle. Nitrosospira and Nitrosomonas 16S rRNA genes were amplified in a nested PCR, and the identity of the products was confirmed by oligonucleotide hybridization. Nitrosospira DNA was readily identified in all samples, and nitrosomonad DNA of the Nitrosomonas europaea-Nitrosomonas eutropha lineage was also directly detected, but during the summer months only. Phylogenetic delineation with partial (345 bp) 16S rRNA gene sequences of clones obtained from sediments confirmed the fidelity of the amplified nitrosomonad DNA and identified two sequence clusters closely related to either N. europaea or N. eutropha that were equated with the littoral and profundal sediment sites, respectively. Determination of 701-bp sequences for 16S rDNA clones representing each cluster confirmed this delineation. A PCR-restriction fragment length polymorphism (RFLP) system was developed that enabled identification of clones containing N. europaea and N. eutropha 16S rDNA sequences, including subclasses therein. It proved possible to analyze 16S rDNA amplified directly from sediment samples to determine the relative abundance of each species compared with that of the other. N. europaea and N. eutropha are very closely related, and direct evidence for their presence in lake systems is limited. The correlation of each species with a distinct spatial location in sediment is an unusual example of niche adaptation by two genotypically similar bacteria. Their occurrence and relative distribution can now be routinely monitored in relation to environmental variation by the application of PCR-RFLP analysis.
通过从一个季节性周期内采集的湖水和沉积物样本中回收16S核糖体DNA(rDNA),对一个温带贫营养淡水湖中的氨氧化细菌种群进行了分析。在巢式PCR中扩增亚硝化螺菌属和亚硝化单胞菌属的16S rRNA基因,并通过寡核苷酸杂交确认产物的身份。在所有样本中都很容易鉴定出亚硝化螺菌属DNA,并且也直接检测到了欧洲亚硝化单胞菌-嗜养亚硝化单胞菌谱系的亚硝化单胞菌属DNA,但仅在夏季月份检测到。对从沉积物中获得的克隆的部分(345 bp)16S rRNA基因序列进行系统发育分析,证实了扩增的亚硝化单胞菌属DNA的准确性,并鉴定出两个分别与欧洲亚硝化单胞菌或嗜养亚硝化单胞菌密切相关的序列簇,它们分别对应于沿岸和深水沉积物位点。对代表每个簇的16S rDNA克隆的701 bp序列进行测定,证实了这种划分。开发了一种PCR-限制性片段长度多态性(RFLP)系统,该系统能够鉴定含有欧洲亚硝化单胞菌和嗜养亚硝化单胞菌16S rDNA序列的克隆,包括其中的亚类。事实证明,可以分析直接从沉积物样本中扩增的16S rDNA,以确定每个物种相对于另一个物种的相对丰度。欧洲亚硝化单胞菌和嗜养亚硝化单胞菌密切相关,它们在湖泊系统中存在的直接证据有限。每个物种与沉积物中不同空间位置的相关性是两个基因型相似的细菌生态位适应的一个不寻常例子。现在可以通过应用PCR-RFLP分析,根据环境变化对它们的出现和相对分布进行常规监测。