Pei Caixia, Mao Shengyong, Zhu Weiyun
Laboratory of Gastrointestinal Microbiology, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Wei Sheng Wu Xue Bao. 2008 Jan;48(1):8-14.
Molecular diversities of rumen archaea of Jinnan (South Shanxi Province, China) cattle was analyzed and compared by 16S rRNA gene sequencing from three clone libraries generated using three different archaea-specific primer sets, respectively. DNA from rumen of 4 Jinnan cattle was extracted, and methanogen 16S rRNA gene was amplified using archaea-specific primer sets. Three clone libraries were generated by using vector pGEM-T and cloning into E.coli JM109. One hundred clones were randomly picked up for each library and RFLP was analyzed for each clone to obtain OTUs. Sequences from each OTU were analyzed and compared with available sequences in GenBank. The first library, generated with primers Arch f364/1386, produced four groups of sequences, affiliated with 4 Methanobrevibacter strains, 1Y (61% of clones), SM9 (23% of clones), NT7 (14% of clones), and AK-87(2% of clones). The second library, generated with primers 1 Af/1100Ar, two groups of sequences, one affiliated with Methanobacterium aarhusense (72% of clones) and the other with Methanosphaera stadtmanae DSM 3091 (28% of clones). The third library, generated with primers Met86F/Met1340R, produced a high degree of diversity. It included the sequence groups found in the first and the second libraries, as well as sequences affiliated with the Methanomicrobium mobile (2% of clones) and uncultured euryarchaeote sequences (7% of clones). The phylogenetic analysis indicated that archaea found in the three libraries were clustered in Methanobrevibacter, Methanobacterium, Methanosphaera, Methanomicrobium, and unidentified euryarchaeote of the Euryarcharota. There were 25 unidentified sequences belonged to Euryarchaeota. This suggests the existence of novel methanogens in the rumen of Jinnan cattle.
分别使用三种不同的古菌特异性引物对,从构建的三个克隆文库中通过16S rRNA基因测序,对中国山西省南部的晋南牛瘤胃古菌的分子多样性进行了分析和比较。提取了4头晋南牛瘤胃的DNA,使用古菌特异性引物对扩增产甲烷菌16S rRNA基因。利用载体pGEM-T并克隆到大肠杆菌JM109中,构建了三个克隆文库。每个文库随机挑选100个克隆,对每个克隆进行RFLP分析以获得操作分类单元(OTU)。分析每个OTU的序列,并与GenBank中可用序列进行比较。用引物Arch f364/1386构建的第一个文库产生了四组序列,分别属于4株短柄产甲烷杆菌,即1Y(占克隆的61%)、SM9(占克隆的23%)、NT7(占克隆的14%)和AK-87(占克隆的2%)。用引物1 Af/1100Ar构建的第二个文库产生了两组序列,一组属于奥尔胡斯产甲烷杆菌(占克隆的72%),另一组属于史氏甲烷球形菌DSM 3091(占克隆的28%)。用引物Met86F/Met13,40R构建的第三个文库具有高度的多样性。它包括在第一个和第二个文库中发现的序列组,以及与运动甲烷微菌(占克隆的2%)和未培养的广古菌序列(占克隆的7%)相关的序列。系统发育分析表明,在三个文库中发现的古菌聚集在广古菌门的短柄产甲烷杆菌属、产甲烷杆菌属、甲烷球形菌属、甲烷微菌属和未鉴定的广古菌中。有25个未鉴定序列属于广古菌门。这表明晋南牛瘤胃中存在新型产甲烷菌。