Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates

Marine invertebrate microbiomes have been a rich source of bioactive compounds and interesting genomic features. In cases where the achievable amounts of metagenomic DNA are too low for direct sequencing, multiple displacement amplification (MDA) can be used for whole genome amplification. However,...

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Published in:Marine Drugs
Main Authors: Andrea Iselin Elvheim, Chun Li, Bjarne Landfald
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2023
Subjects:
Online Access:https://doi.org/10.3390/md21030165
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spelling ftmdpi:oai:mdpi.com:/1660-3397/21/3/165/ 2023-08-20T04:04:17+02:00 Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates Andrea Iselin Elvheim Chun Li Bjarne Landfald agris 2023-03-02 application/pdf https://doi.org/10.3390/md21030165 EN eng Multidisciplinary Digital Publishing Institute https://dx.doi.org/10.3390/md21030165 https://creativecommons.org/licenses/by/4.0/ Marine Drugs; Volume 21; Issue 3; Pages: 165 marine invertebrates microbiomes multiple displacement amplification metagenomics biosynthetic gene clusters Text 2023 ftmdpi https://doi.org/10.3390/md21030165 2023-08-01T09:05:02Z Marine invertebrate microbiomes have been a rich source of bioactive compounds and interesting genomic features. In cases where the achievable amounts of metagenomic DNA are too low for direct sequencing, multiple displacement amplification (MDA) can be used for whole genome amplification. However, MDA has known limitations which can affect the quality of the resulting genomes and metagenomes. In this study, we evaluated the conservation of biosynthetic gene clusters (BGCs) and enzymes in MDA products from low numbers of prokaryotic cells (estimated 2–850). Marine invertebrate microbiomes collected from Arctic and sub-Arctic areas served as source material. The cells were separated from the host tissue, lysed, and directly subjected to MDA. The MDA products were sequenced by Illumina sequencing. Corresponding numbers of bacteria from a set of three reference strains were treated the same way. The study demonstrated that useful information on taxonomic, BGC, and enzyme diversities was obtainable from such marginal quantities of metagenomic material. Although high levels of assembly fragmentation resulted in most BGCs being incomplete, we conclude that this genome mining approach has the potential to reveal interesting BGCs and genes from hard-to-reach biological sources. Text Arctic MDPI Open Access Publishing Arctic Marine Drugs 21 3 165
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic marine invertebrates
microbiomes
multiple displacement amplification
metagenomics
biosynthetic gene clusters
spellingShingle marine invertebrates
microbiomes
multiple displacement amplification
metagenomics
biosynthetic gene clusters
Andrea Iselin Elvheim
Chun Li
Bjarne Landfald
Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
topic_facet marine invertebrates
microbiomes
multiple displacement amplification
metagenomics
biosynthetic gene clusters
description Marine invertebrate microbiomes have been a rich source of bioactive compounds and interesting genomic features. In cases where the achievable amounts of metagenomic DNA are too low for direct sequencing, multiple displacement amplification (MDA) can be used for whole genome amplification. However, MDA has known limitations which can affect the quality of the resulting genomes and metagenomes. In this study, we evaluated the conservation of biosynthetic gene clusters (BGCs) and enzymes in MDA products from low numbers of prokaryotic cells (estimated 2–850). Marine invertebrate microbiomes collected from Arctic and sub-Arctic areas served as source material. The cells were separated from the host tissue, lysed, and directly subjected to MDA. The MDA products were sequenced by Illumina sequencing. Corresponding numbers of bacteria from a set of three reference strains were treated the same way. The study demonstrated that useful information on taxonomic, BGC, and enzyme diversities was obtainable from such marginal quantities of metagenomic material. Although high levels of assembly fragmentation resulted in most BGCs being incomplete, we conclude that this genome mining approach has the potential to reveal interesting BGCs and genes from hard-to-reach biological sources.
format Text
author Andrea Iselin Elvheim
Chun Li
Bjarne Landfald
author_facet Andrea Iselin Elvheim
Chun Li
Bjarne Landfald
author_sort Andrea Iselin Elvheim
title Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
title_short Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
title_full Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
title_fullStr Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
title_full_unstemmed Conservation of Genomic Information in Multiple Displacement Amplified Low-Quantity Metagenomic Material from Marine Invertebrates
title_sort conservation of genomic information in multiple displacement amplified low-quantity metagenomic material from marine invertebrates
publisher Multidisciplinary Digital Publishing Institute
publishDate 2023
url https://doi.org/10.3390/md21030165
op_coverage agris
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source Marine Drugs; Volume 21; Issue 3; Pages: 165
op_relation https://dx.doi.org/10.3390/md21030165
op_rights https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.3390/md21030165
container_title Marine Drugs
container_volume 21
container_issue 3
container_start_page 165
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