Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias

Plankton metabarcoding is increasingly implemented in marine ecosystem assessments and is more cost-efficient and less time-consuming than monitoring based on microscopy (morphological). 18S rRNA gene is the most widely used marker for groups’ and species’ detection and classification within marine...

Full description

Bibliographic Details
Main Authors: Jon Lapeyra Martin, Ioulia Santi, Paraskevi Pitta, Uwe John, Nathalie Gypens
Format: Article
Language:English
Published: Pensoft Publishers 2022-08-01
Series:Metabarcoding and Metagenomics
Online Access:https://mbmg.pensoft.net/article/85794/download/pdf/
_version_ 1818483668464697344
author Jon Lapeyra Martin
Ioulia Santi
Paraskevi Pitta
Uwe John
Nathalie Gypens
author_facet Jon Lapeyra Martin
Ioulia Santi
Paraskevi Pitta
Uwe John
Nathalie Gypens
author_sort Jon Lapeyra Martin
collection DOAJ
description Plankton metabarcoding is increasingly implemented in marine ecosystem assessments and is more cost-efficient and less time-consuming than monitoring based on microscopy (morphological). 18S rRNA gene is the most widely used marker for groups’ and species’ detection and classification within marine eukaryotic microorganisms. These datasets have commonly relied on the acquisition of organismal abundances directly from the number of DNA sequences (i.e. reads). Besides the inherent technical biases in metabarcoding, the largely varying 18S rRNA gene copy numbers (GCN) among marine protists (ranging from tens to thousands) is one of the most important biological biases for species quantification. In this work, we present a gene copy number correction factor (CF) for four marine planktonic groups: Bacillariophyta, Dinoflagellata, Ciliophora miscellaneous and flagellated cells. On the basis of the theoretical assumption that ‘1 read’ is equivalent to ‘1 GCN’, we used the GCN median values per plankton group to calculate the corrected cell number and biomass relative abundances. The species-specific absolute GCN per cell were obtained from various studies published in the literature. We contributed to the development of a species-specific 18S rRNA GCN database proposed by previous authors. To assess the efficiency of the correction factor we compared the metabarcoding, morphological and corrected relative abundances (in cell number and biomass) of 15 surface water samples collected in the Belgian Coastal Zone. Results showed that the application of the correction factor over metabarcoding results enables us to significantly improve the estimates of cell abundances for Dinoflagellata, Ciliophora and flagellated cells, but not for Bacillariophyta. This is likely to due to large biovolume plasticity in diatoms not corresponding to genome size and gene copy numbers. C-biomass relative abundance estimations directly from amplicon reads were only improved for Dinoflagellata and Ciliophora. The method is still facing biases related to the low number of species GCN assessed. Nevertheless, the increase of species in the GCN database may lead to the refinement of the proposed correction factor.
first_indexed 2024-12-10T15:44:57Z
format Article
id doaj.art-7348a627bc6243dfaa02125cf89aabe7
institution Directory Open Access Journal
issn 2534-9708
language English
last_indexed 2024-12-10T15:44:57Z
publishDate 2022-08-01
publisher Pensoft Publishers
record_format Article
series Metabarcoding and Metagenomics
spelling doaj.art-7348a627bc6243dfaa02125cf89aabe72022-12-22T01:42:59ZengPensoft PublishersMetabarcoding and Metagenomics2534-97082022-08-01624525910.3897/mbmg.6.8579485794Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number biasJon Lapeyra Martin0Ioulia Santi1Paraskevi Pitta2Uwe John3Nathalie Gypens4Université Libre de BruxellesInstitute of Marine BiologyInstitute of OceanographyHelmholtz Institute for Functional Marine Biodiversity at the University of OldenburgUniversité Libre de BruxellesPlankton metabarcoding is increasingly implemented in marine ecosystem assessments and is more cost-efficient and less time-consuming than monitoring based on microscopy (morphological). 18S rRNA gene is the most widely used marker for groups’ and species’ detection and classification within marine eukaryotic microorganisms. These datasets have commonly relied on the acquisition of organismal abundances directly from the number of DNA sequences (i.e. reads). Besides the inherent technical biases in metabarcoding, the largely varying 18S rRNA gene copy numbers (GCN) among marine protists (ranging from tens to thousands) is one of the most important biological biases for species quantification. In this work, we present a gene copy number correction factor (CF) for four marine planktonic groups: Bacillariophyta, Dinoflagellata, Ciliophora miscellaneous and flagellated cells. On the basis of the theoretical assumption that ‘1 read’ is equivalent to ‘1 GCN’, we used the GCN median values per plankton group to calculate the corrected cell number and biomass relative abundances. The species-specific absolute GCN per cell were obtained from various studies published in the literature. We contributed to the development of a species-specific 18S rRNA GCN database proposed by previous authors. To assess the efficiency of the correction factor we compared the metabarcoding, morphological and corrected relative abundances (in cell number and biomass) of 15 surface water samples collected in the Belgian Coastal Zone. Results showed that the application of the correction factor over metabarcoding results enables us to significantly improve the estimates of cell abundances for Dinoflagellata, Ciliophora and flagellated cells, but not for Bacillariophyta. This is likely to due to large biovolume plasticity in diatoms not corresponding to genome size and gene copy numbers. C-biomass relative abundance estimations directly from amplicon reads were only improved for Dinoflagellata and Ciliophora. The method is still facing biases related to the low number of species GCN assessed. Nevertheless, the increase of species in the GCN database may lead to the refinement of the proposed correction factor.https://mbmg.pensoft.net/article/85794/download/pdf/
spellingShingle Jon Lapeyra Martin
Ioulia Santi
Paraskevi Pitta
Uwe John
Nathalie Gypens
Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
Metabarcoding and Metagenomics
title Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
title_full Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
title_fullStr Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
title_full_unstemmed Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
title_short Towards quantitative metabarcoding of eukaryotic plankton: an approach to improve 18S rRNA gene copy number bias
title_sort towards quantitative metabarcoding of eukaryotic plankton an approach to improve 18s rrna gene copy number bias
url https://mbmg.pensoft.net/article/85794/download/pdf/
work_keys_str_mv AT jonlapeyramartin towardsquantitativemetabarcodingofeukaryoticplanktonanapproachtoimprove18srrnagenecopynumberbias
AT iouliasanti towardsquantitativemetabarcodingofeukaryoticplanktonanapproachtoimprove18srrnagenecopynumberbias
AT paraskevipitta towardsquantitativemetabarcodingofeukaryoticplanktonanapproachtoimprove18srrnagenecopynumberbias
AT uwejohn towardsquantitativemetabarcodingofeukaryoticplanktonanapproachtoimprove18srrnagenecopynumberbias
AT nathaliegypens towardsquantitativemetabarcodingofeukaryoticplanktonanapproachtoimprove18srrnagenecopynumberbias