Miteva V I, Sheridan P P, Brenchley J E
NASA Astrobiology Institute and Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Appl Environ Microbiol. 2004 Jan;70(1):202-13. doi: 10.1128/AEM.70.1.202-213.2004.
We studied a sample from the GISP 2 (Greenland Ice Sheet Project) ice core to determine the diversity and survival of microorganisms trapped in the ice at least 120,000 years ago. Previously, we examined the phylogenetic relationships among 16S ribosomal DNA (rDNA) sequences in a clone library obtained by PCR amplification from genomic DNA extracted from anaerobic enrichments. Here we report the isolation of nearly 800 aerobic organisms that were grouped by morphology and amplified rDNA restriction analysis patterns to select isolates for further study. The phylogenetic analyses of 56 representative rDNA sequences showed that the isolates belonged to four major phylogenetic groups: the high-G+C gram-positives, low-G+C gram-positives, Proteobacteria, and the Cytophaga-Flavobacterium-Bacteroides group. The most abundant and diverse isolates were within the high-G+C gram-positive cluster that had not been represented in the clone library. The Jukes-Cantor evolutionary distance matrix results suggested that at least 7 isolates represent new species within characterized genera and that 49 are different strains of known species. The isolates were further categorized based on the isolation conditions, temperature range for growth, enzyme activity, antibiotic resistance, presence of plasmids, and strain-specific genomic variations. A significant observation with implications for the development of novel and more effective cultivation methods was that preliminary incubation in anaerobic and aerobic liquid prior to plating on agar media greatly increased the recovery of CFU from the ice core sample.
我们研究了来自格陵兰冰盖项目2(GISP 2)冰芯的样本,以确定至少12万年前被困在冰中的微生物的多样性和生存情况。此前,我们通过PCR扩增从厌氧富集物中提取的基因组DNA,研究了克隆文库中16S核糖体DNA(rDNA)序列之间的系统发育关系。在此,我们报告分离出近800种需氧生物,这些生物通过形态学和扩增rDNA限制性分析模式进行分组,以选择分离株进行进一步研究。对56个代表性rDNA序列的系统发育分析表明,这些分离株属于四个主要的系统发育组:高G+C革兰氏阳性菌、低G+C革兰氏阳性菌、变形菌门和噬纤维菌-黄杆菌-拟杆菌群。最丰富和多样的分离株属于克隆文库中未出现的高G+C革兰氏阳性菌簇。朱克斯-坎托进化距离矩阵结果表明,至少有7个分离株代表已鉴定属内的新物种,49个是已知物种的不同菌株。根据分离条件、生长温度范围、酶活性、抗生素抗性、质粒的存在以及菌株特异性基因组变异,对分离株进行了进一步分类。一个对开发新的更有效的培养方法有重要意义的显著观察结果是,在琼脂培养基上平板接种之前,先在厌氧和需氧液体中进行初步培养,可大大提高冰芯样本中菌落形成单位(CFU)的回收率。