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A comparative study of microbial diversity and community structure in marine sediments using poly(A) tailing and reverse transcription-PCR

机译:聚(A)拖尾和逆转录PCR技术对海洋沉积物中微生物多样性和群落结构的比较研究

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摘要

To obtain a better understanding of metabolically active microbial communities, we tested a molecular ecological approach using poly(A) tailing of environmental 16S rRNA, followed by full-length complementary DNA (cDNA) synthesis and sequencing to eliminate potential biases caused by mismatching of polymerase chain reaction (PCR) primer sequences. The RNA pool tested was extracted from marine sediments of the Yonaguni Knoll IV hydrothermal field in the southern Okinawa Trough. The sequences obtained using the poly(A) tailing method were compared statistically and phylogenetically with those obtained using conventional reverse transcription-PCR (RT-PCR) with published domain-specific primers. Both methods indicated that Deltaproteobacteria are predominant in sediment (>85% of the total sequence read). The poly(A) tailing method indicated that Desulfobacterales were the predominant Deltaproteobacteria, while most of the sequences in libraries constructed using RT-PCR were derived from Desulfuromonadales. This discrepancy may have been due to low coverage of Desulfobacterales by the primers used. A comparison of library diversity indices indicated that the poly(A) tailing method retrieves more phylogenetically diverse sequences from the environment. The four archaeal 16S rRNA sequences that were obtained using the poly(A) tailing method formed deeply branching lineages that were related to Candidatus “Parvarchaeum” and the ancient archaeal group. These results clearly demonstrate that poly(A) tailing followed by cDNA sequencing is a powerful and less biased molecular ecological approach for the study of metabolically active microbial communities.
机译:为了更好地了解代谢活跃的微生物群落,我们测试了一种分子生态学方法,该方法使用环境16S rRNA的poly(A)拖尾,然后进行全长互补DNA(cDNA)合成和测序,以消除聚合酶错配引起的潜在偏见链反应(PCR)引物序列。从冲绳海槽南部Yonaguni Knoll IV热液场的海洋沉积物中提取了测试的RNA库。使用poly(A)拖尾法获得的序列与使用常规逆转录PCR(RT-PCR)和已公开的域特异性引物获得的序列进行统计和系统分析。两种方法均表明,三角洲变形杆菌在沉积物中占主导地位(占读取的总序列的> 85%)。聚(A)拖尾法表明,脱硫细菌是主要的三角洲变形杆菌,而使用RT-PCR构建的文库中的大多数序列均来自脱硫呋喃类。这种差异可能是由于所用引物对脱硫细菌的覆盖率较低。库多样性指数的比较表明,poly(A)拖尾法从环境中检索到更多系统发育的序列。使用poly(A)拖尾法获得的四个古细菌16S rRNA序列形成了与Candidatus“ Parvarchaeum”和古代古细菌群体有关的深分支谱系。这些结果清楚地表明,poly(A)拖尾再进行cDNA测序是一种功能强大且偏差较小的分子生态学方法,可用于研究代谢活性微生物群落。

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