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用于长读长宏基因组测序的土壤DNA提取试剂盒的比较评估

Comparative evaluation of soil DNA extraction kits for long read metagenomic sequencing.

作者信息

Child Harry T, Wierzbicki Lucy, Joslin Gabrielle R, Tennant Richard K

机构信息

Geography, Faculty of Environment, Science and Economy, University of Exeter, Amory Building, Rennes Drive, Exeter, Devon, EX4 4RJ, UK.

出版信息

Access Microbiol. 2024 Sep 27;6(9). doi: 10.1099/acmi.0.000868.v3. eCollection 2024.

Abstract

Metagenomics has been transformative in our understanding of the diversity and function of soil microbial communities. Applying long read sequencing to whole genome shotgun metagenomics has the potential to revolutionise soil microbial ecology through improved taxonomic classification, functional characterisation and metagenome assembly. However, optimisation of robust methods for long read metagenomics of environmental samples remains undeveloped. In this study, Oxford Nanopore sequencing using samples from five commercially available soil DNA extraction kits was compared across four soil types, in order to optimise read length and reproducibility for comparative long read soil metagenomics. Average extracted DNA lengths varied considerably between kits, but longer DNA fragments did not translate consistently into read lengths. Highly variable decreases in the length of resulting reads from some kits were associated with poor classification rate and low reproducibility in microbial communities identified between technical repeats. Replicate samples from other kits showed more consistent conversion of extracted DNA fragment size into read length and resulted in more congruous microbial community representation. Furthermore, extraction kits showed significant differences in the community representation and structure they identified across all soil types. Overall, the QIAGEN DNeasy PowerSoil Pro Kit displayed the best suitability for reproducible long-read WGS metagenomic sequencing, although further optimisation of DNA purification and library preparation may enable translation of higher molecular weight DNA from other kits into longer read lengths. These findings provide a novel insight into the importance of optimising DNA extraction for achieving replicable results from long read metagenomic sequencing of environmental samples.

摘要

宏基因组学在我们对土壤微生物群落多样性和功能的理解方面带来了变革。将长读长测序应用于全基因组鸟枪法宏基因组学,有潜力通过改进分类学分类、功能表征和宏基因组组装,彻底改变土壤微生物生态学。然而,针对环境样本长读长宏基因组学的稳健方法的优化仍未得到充分发展。在本研究中,我们比较了使用来自五种市售土壤DNA提取试剂盒的样本进行牛津纳米孔测序,跨越四种土壤类型,以优化比较长读长土壤宏基因组学的读长和可重复性。试剂盒之间平均提取的DNA长度差异很大,但较长的DNA片段并不能始终转化为读长。一些试剂盒产生的读长长度高度可变的减少与分类率低和技术重复之间鉴定的微生物群落中低可重复性相关。来自其他试剂盒的重复样本显示提取的DNA片段大小到读长的转化更一致,并导致更一致的微生物群落代表性。此外,提取试剂盒在它们所鉴定的所有土壤类型的群落代表性和结构上显示出显著差异。总体而言,QIAGEN DNeasy PowerSoil Pro试剂盒显示出最适合可重复的长读长全基因组鸟枪法宏基因组测序,尽管进一步优化DNA纯化和文库制备可能使其他试剂盒中更高分子量的DNA转化为更长的读长。这些发现为优化DNA提取对于从环境样本的长读长宏基因组测序获得可重复结果的重要性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a077/11432601/6efce4ee6237/acmi-6-00868-g001.jpg

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