AI Article Synopsis

  • The success of a metabarcoding study relies on taxonomic coverage and the quality of the DNA barcodes in the reference database.
  • This study focused on creating DNA barcode sequences (rbcL and trnL) for plant species that could be food sources for herbivores in eastern South Africa's semi-arid savannas, compiling a list of 765 species.
  • The final datasets included 1238 rbcL sequences and 921 trnL sequences, with high identification success rates of 85.86% and 73.72%, respectively, although both datasets are meant to be used together for accurate plant identification.

Article Abstract

Success of a metabarcoding study is determined by the extent of taxonomic coverage and the quality of records available in the DNA barcode reference database used. This study aimed to create an rbcL and a trnL (UAA) DNA barcode sequence reference database of plant species that are potential herbivore foraging targets and commonly found in semi-arid savannas of eastern South Africa. An area-specific species list of 765 species was compiled according to plant collection records available and areas comparable to an eastern semi-arid South African savanna. Thereafter, rbcL and trnL sequences of species from this list were mined from GenBank and BOLD sequence databases according to specific quality criteria to ensure accurate taxonomic coverage and resolution. These were supplemented with sequences of 24 species sequenced for this study. A phylogenetic approach, employing Neighbor-Joining, was used to verify the topology of the reference libraries to known angiosperm phylogeny. The taxonomic reliability of these reference libraries was evaluated by testing for the presence of a barcode gap, identifying a data-appropriate identification threshold, and determining the identification accuracy of reference sequences via primary distance-based criteria. The final rbcL reference dataset consisted of 1238 sequences representing 318 genera and 562 species. The final trnL dataset consisted of 921 sequences representing 270 genera and 461 species. Barcode gaps were found for 76% of the taxa in the rbcL barcode reference dataset and 68% of the taxa in the trnL barcode reference dataset. The identification success rate, calculated with the k-nn criterion was 85.86% for the rbcL dataset and 73.72% for the trnL dataset. The datasets for rbcL and trnL combined during this study are not presented as complete DNA reference libraries, but rather as two datasets that should be used in unison to identify plants present in the semi-arid eastern savannas of South Africa.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198553PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0286144PLOS

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