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Investigation of Unknown Genomes through Metagenomic Analysis of (+)ssRNA Viruses in Wastewater

机译:通过废水中的(+)ssRNA病毒的元基因组分析调查未知基因组。

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Most human viruses cannot be detected due to unknown genome information. The objective of this study was to investigate unknown genomes selected (+)ssRNA viruses in wastewater. Metagenomic analysis targeting (+)ssRNA viruses in wastewater has found huge number of unknown sequence fragments, which implies presence of unknown human enteric viruses. We assembled contigs using the unknown fragments obtained from the selective metagenomic analysis of wastewater samples (n = 6). We additionally carried out detection of the contigs in the wastewater samples using quantitative reverse-transcription PCR (RT-qPCR) to confirm presence of genomes with the sequences of constructed contigs. The number of contigs with unidentified sequences from each wastewater sample was 4-27, and a total of 7 contigs with 114-1585 bases were further assembled as common contigs among multiple samples. All the common contigs were not assigned to any nucleotide sequence by BLASTn, and 3 out of them were aligned to the protein sequence of Laverivirus UC1 with low identities (38-60%) by BLASTx. One of the common contigs was detected in all the wastewater samples with the concentration ranging up to 2.8 logio copies/mL by the RT-qPCR. These results suggested the presence of unknown (+)ssRNA viruses in the samples. (196/200 words)
机译:由于未知的基因组信息,无法检测到大多数人类病毒。这项研究的目的是调查废水中的未知基因组选择(+)ssRNA病毒。针对废水中的(+)ssRNA病毒进行的元基因组分析发现了大量未知序列片段,这意味着存在未知的人类肠道病毒。我们使用从废水样品的选择性宏基因组学分析中获得的未知片段组装了重叠群(n = 6)。我们还使用定量逆转录PCR(RT-qPCR)对废水样品中的重叠群进行了检测,以确认具有已构建重叠群序列的基因组的存在。每个废水样本中序列不确定的重叠群的数量为4-27,并且进一步将总共114个1585个碱基的7个重叠群作为多个样本中的常见重叠群进行了组装。 BLASTn未将所有常见重叠群分配给任何核苷酸序列,而BLASTx将其中的3个与紫薇病毒UC1的蛋白质序列进行了比对,具有较低的同一性(38-60%)。通过RT-qPCR在所有废水样品中检测到一种常见的重叠群,其浓度范围高达2.8 log 10个拷贝/ mL。这些结果表明样品中存在未知的(+)ssRNA病毒。 (196/200字)

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