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Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction
BACKGROUND: While genome-resolved metagenomics has revolutionized our understanding of microbial and genetic diversity in environmental samples, assemblies of short-reads often result in incomplete and/or highly fragmented metagenome-assembled genomes (MAGs), hampering in-depth genomics. Although Na...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693096/ https://www.ncbi.nlm.nih.gov/pubmed/38041056 http://dx.doi.org/10.1186/s12864-023-09853-w |
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author | Simon, Sophie A. Schmidt, Katharina Griesdorn, Lea Soares, André R. Bornemann, Till L. V. Probst, Alexander J. |
author_facet | Simon, Sophie A. Schmidt, Katharina Griesdorn, Lea Soares, André R. Bornemann, Till L. V. Probst, Alexander J. |
author_sort | Simon, Sophie A. |
collection | PubMed |
description | BACKGROUND: While genome-resolved metagenomics has revolutionized our understanding of microbial and genetic diversity in environmental samples, assemblies of short-reads often result in incomplete and/or highly fragmented metagenome-assembled genomes (MAGs), hampering in-depth genomics. Although Nanopore sequencing has increasingly been used in microbial metagenomics as long reads greatly improve the assembly quality of MAGs, the recommended DNA quantity usually exceeds the recoverable amount of DNA of environmental samples. Here, we evaluated lower-than-recommended DNA quantities for Nanopore library preparation by determining sequencing quality, community composition, assembly quality and recovery of MAGs. RESULTS: We generated 27 Nanopore metagenomes using the commercially available ZYMO mock community and varied the amount of input DNA from 1000 ng (the recommended minimum) down to 1 ng in eight steps. The quality of the generated reads remained stable across all input levels. The read mapping accuracy, which reflects how well the reads match a known reference genome, was consistently high across all libraries. The relative abundance of the species in the metagenomes was stable down to input levels of 50 ng. High-quality MAGs (> 95% completeness, ≤ 5% contamination) could be recovered from metagenomes down to 35 ng of input material. When combined with publicly available Illumina reads for the mock community, Nanopore reads from input quantities as low as 1 ng improved the quality of hybrid assemblies. CONCLUSION: Our results show that the recommended DNA amount for Nanopore library preparation can be substantially reduced without any adverse effects to genome recovery and still bolster hybrid assemblies when combined with short-read data. We posit that the results presented herein will enable studies to improve genome recovery from low-biomass environments, enhancing microbiome understanding. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09853-w. |
format | Online Article Text |
id | pubmed-10693096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106930962023-12-03 Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction Simon, Sophie A. Schmidt, Katharina Griesdorn, Lea Soares, André R. Bornemann, Till L. V. Probst, Alexander J. BMC Genomics Research BACKGROUND: While genome-resolved metagenomics has revolutionized our understanding of microbial and genetic diversity in environmental samples, assemblies of short-reads often result in incomplete and/or highly fragmented metagenome-assembled genomes (MAGs), hampering in-depth genomics. Although Nanopore sequencing has increasingly been used in microbial metagenomics as long reads greatly improve the assembly quality of MAGs, the recommended DNA quantity usually exceeds the recoverable amount of DNA of environmental samples. Here, we evaluated lower-than-recommended DNA quantities for Nanopore library preparation by determining sequencing quality, community composition, assembly quality and recovery of MAGs. RESULTS: We generated 27 Nanopore metagenomes using the commercially available ZYMO mock community and varied the amount of input DNA from 1000 ng (the recommended minimum) down to 1 ng in eight steps. The quality of the generated reads remained stable across all input levels. The read mapping accuracy, which reflects how well the reads match a known reference genome, was consistently high across all libraries. The relative abundance of the species in the metagenomes was stable down to input levels of 50 ng. High-quality MAGs (> 95% completeness, ≤ 5% contamination) could be recovered from metagenomes down to 35 ng of input material. When combined with publicly available Illumina reads for the mock community, Nanopore reads from input quantities as low as 1 ng improved the quality of hybrid assemblies. CONCLUSION: Our results show that the recommended DNA amount for Nanopore library preparation can be substantially reduced without any adverse effects to genome recovery and still bolster hybrid assemblies when combined with short-read data. We posit that the results presented herein will enable studies to improve genome recovery from low-biomass environments, enhancing microbiome understanding. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09853-w. BioMed Central 2023-12-01 /pmc/articles/PMC10693096/ /pubmed/38041056 http://dx.doi.org/10.1186/s12864-023-09853-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Simon, Sophie A. Schmidt, Katharina Griesdorn, Lea Soares, André R. Bornemann, Till L. V. Probst, Alexander J. Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title | Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title_full | Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title_fullStr | Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title_full_unstemmed | Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title_short | Dancing the Nanopore limbo – Nanopore metagenomics from small DNA quantities for bacterial genome reconstruction |
title_sort | dancing the nanopore limbo – nanopore metagenomics from small dna quantities for bacterial genome reconstruction |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693096/ https://www.ncbi.nlm.nih.gov/pubmed/38041056 http://dx.doi.org/10.1186/s12864-023-09853-w |
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