TY - JOUR
T1 - Towards harmonization of DNA metabarcoding for monitoring marine macrobenthos: The effect of technical replicates and pooled DNA extractions on species detection
AU - Van den Bulcke, Laure
AU - De Backer, Annelies
AU - Ampe, Bart
AU - Maes, Sara
AU - Wittoeck, Jan
AU - Waegeman, Willem
AU - Hostens, Kris
AU - Derycke, Sofie
PY - 2021/12/29
Y1 - 2021/12/29
N2 - DNA-based monitoring methods are potentially faster and cheaper compared to traditional morphological benthic identification. DNA metabarcoding involves various methodological choices which can introduce bias leading to a different outcome in biodiversity patterns. Therefore, it is important to harmonize DNA metabarcoding protocols to allow comparison across studies and this requires a good understanding of the effect of methodological choices on diversity estimates. This study investigated the impact of DNA and PCR replicates on the detection of macrobenthos species in locations with high, medium and low diversity. Our results show that two to three DNA replicates were needed in locations with a high and medium diversity to detect at least 80% of the species found in the six DNA replicates, while three to four replicates were needed in the location with low diversity. In contrast to general belief, larger body size or higher abundance of the species in a sample did not increase its detection prevalence among DNA replicates. However, rare species were less consistently detected across all DNA replicates of the location with high diversity compared to locations with less diversity. Our results further show that pooling of DNA replicates did not significantly alter diversity patterns, although a small number of rare species was lost. Finally, our results confirm high variation in species detection between PCR replicates, especially for the detection of rare species. These results contribute to create reliable, time and cost efficient metabarcoding protocols for the characterization of macrobenthos.
AB - DNA-based monitoring methods are potentially faster and cheaper compared to traditional morphological benthic identification. DNA metabarcoding involves various methodological choices which can introduce bias leading to a different outcome in biodiversity patterns. Therefore, it is important to harmonize DNA metabarcoding protocols to allow comparison across studies and this requires a good understanding of the effect of methodological choices on diversity estimates. This study investigated the impact of DNA and PCR replicates on the detection of macrobenthos species in locations with high, medium and low diversity. Our results show that two to three DNA replicates were needed in locations with a high and medium diversity to detect at least 80% of the species found in the six DNA replicates, while three to four replicates were needed in the location with low diversity. In contrast to general belief, larger body size or higher abundance of the species in a sample did not increase its detection prevalence among DNA replicates. However, rare species were less consistently detected across all DNA replicates of the location with high diversity compared to locations with less diversity. Our results further show that pooling of DNA replicates did not significantly alter diversity patterns, although a small number of rare species was lost. Finally, our results confirm high variation in species detection between PCR replicates, especially for the detection of rare species. These results contribute to create reliable, time and cost efficient metabarcoding protocols for the characterization of macrobenthos.
KW - Biological replicates
KW - Bulk DNA
KW - DNA replicates
KW - Diversity
KW - Macrobenthos
KW - Metabarcoding protocol
KW - North Sea
KW - PCR replicates
KW - Pooling
KW - Technical replicates
UR - https://www.mendeley.com/catalogue/b5e0a2dc-ab2c-34f4-b476-4e170e7c2d5a/
U2 - https://doi.org/10.3897/mbmg.5.71107
DO - https://doi.org/10.3897/mbmg.5.71107
M3 - A1: Web of Science-article
VL - 5
SP - 233
EP - 247
JO - Metabarcoding and Metagenomics
JF - Metabarcoding and Metagenomics
SN - 2534-9708
M1 - e71107
ER -