Abstract

Amplicon based metabarcoding promises rapid and cost-efficient analyses of species composition. However, it is disputed whether abundance estimates can be derived from metabarcoding due to taxon specific PCR amplification biases. PCR-free approaches have been suggested to mitigate this problem, but come with considerable increases in workload and cost. Here, we analyze multilocus datasets of diverse arthropod communities, to evaluate whether amplification bias can be countered by (1) targeting loci with highly degenerate primers or conserved priming sites, (2) increasing PCR template concentration, (3) reducing PCR cycle number or (4) avoiding locus specific amplification by directly sequencing genomic DNA. Amplification bias is reduced considerably by degenerate primers or targeting amplicons with conserved priming sites. Surprisingly, a reduction of PCR cycles did not have a strong effect on amplification bias. The association of taxon abundance and read count was actually less predictable with fewer cycles. Even a complete exclusion of locus specific amplification did not exclude bias. Copy number variation of the target loci may be another explanation for read abundance differences between taxa, which would affect amplicon based and PCR free methods alike. As read abundance biases are taxon specific and predictable, the application of correction factors allows abundance estimates.

Highlights

  • Generation sequencing technology has ushered in a revolution in evolutionary biology and ecology, enabling analyses at unprecedented throughput and detail[1]

  • The direct sequencing of genomic DNA or sequence capture of barcodes does not require a PCR amplification stage and is assumed to provide more accurate predictions of abundance[30,31,32]. Such PCR-free methods come with a considerable increase in workload and processing cost, and while they mitigate amplification bias, they are sensitive to copy number variation (CNV) in the target loci

  • The proportion of input DNA of a taxon in a community should be tightly correlated to the proportion of recovered reads of that taxon, and amplification bias or CNVs should only affect the slope of this correlation

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Summary

Introduction

Generation sequencing technology has ushered in a revolution in evolutionary biology and ecology, enabling analyses at unprecedented throughput and detail[1]. The direct sequencing of genomic DNA or sequence capture of barcodes does not require a PCR amplification stage and is assumed to provide more accurate predictions of abundance[30,31,32] Such PCR-free methods come with a considerable increase in workload and processing cost (for enrichment, library preparation, and required sequencing coverage), and while they mitigate amplification bias, they are sensitive to CNV in the target loci. Considering the afore-mentioned issues, the current study examines the hypotheses that PCR bias in amplicon based metabarcoding can be countered by: (1) Choosing appropriate barcode markers with high sequence conservation and/or high levels of primer degeneracy, (2) reducing the PCR cycle number and increasing the template concentration during library preparation, (3) completely avoiding locus specific amplification and (4) identifying and correcting for taxon-specific read abundance bias

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