# Dye-based qPCR assays for the separate quantification of total bacterial, fungal, arthropod, and plant DNA

**Authors:** Teresa M. Tiedge, Kim R. Love, Kelly A. Meiklejohn

PMC · DOI: 10.1371/journal.pone.0343035 · 2026-03-06

## TL;DR

This paper introduces validated dye-based qPCR assays to separately quantify bacterial, fungal, arthropod, and plant DNA in environmental samples.

## Contribution

The study provides rigorously validated qPCR assays for quantifying total DNA from four major taxa in environmental samples.

## Key findings

- The four assays are specific, sensitive, and reproducible for quantifying DNA from single-source and mixed environmental samples.
- Melt curve temperatures were identified for each taxon to confirm assay specificity.
- Standard curves using synthetic DNA enabled accurate quantification of the target DNA molecules.

## Abstract

Characterization of bacterial, fungal, arthropod, and plant communities from bulk environmental samples can enhance our understanding of the biodiversity on Earth and aid in biomonitoring of various biomes. An important step in any molecular biology protocol is DNA quantification. While fast methods that determine the total amount of DNA in a sample are widely available, quantitative polymerase chain reaction (qPCR) is often preferred as it permits quantification of specific DNA molecules of interest. Currently, commercial qPCR assays are only available to quantify total bacterial and fungal DNA; limited studies describe the use of qPCR to quantify total arthropod and plant DNA. Here we describe the rigorous validation of four dye-based qPCR assays to separately quantify total bacterial, fungal, arthropod, and plant DNA following the MIQE guidelines. Validation experiments included primer annealing, primer concentration, specificity (in vitro and in silico), sensitivity, and reproducibility. Standard curves were created using synthetic double stranded DNA (gBlocks™) that were designed to quantify the DNA molecules of interest. Melt curve temperatures were identified for each taxon for specificity confirmation. These four assays were found to be specific, sensitive, and reproducible and can quantify DNA from single source specimens and mixed DNA samples, such as environmental DNA.

## Full-text entities

- **Chemicals:** SYBR  Green (MESH:C098022), melanin (MESH:D008543), agarose (MESH:D012685), SYBR (-), Humic acid (MESH:D006812), water (MESH:D014867), EDTA (MESH:D004492), agar (MESH:D000362)
- **Species:** Serratia marcescens (species) [taxon 615], Ruminobacter (genus) [taxon 866], Drosophila melanogaster (fruit fly, species) [taxon 7227], Verrucomicrobiota (phylum) [taxon 74201], Hexapoda (hexapods, subphylum) [taxon 6960], Fusobacteriota (phylum) [taxon 32066], Macaca mulatta (rhesus macaque, species) [taxon 9544], Cercopithecidae (monkey, family) [taxon 9527], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Selaginella braunii (species) [taxon 1353958], Armadillidium vulgare (common pillbug, species) [taxon 13347], Homo sapiens (human, species) [taxon 9606], Giraffa camelopardalis (giraffe, species) [taxon 9894], Arthropoda (arthropods, phylum) [taxon 6656], Ocimum basilicum (basil, species) [taxon 39350], Ovis aries (domestic sheep, species) [taxon 9940], Hyoscyamus niger (black henbane, species) [taxon 4079], Zenaida macroura (mourning dove, species) [taxon 47245], Fungi (kingdom) [taxon 4751], Corcyra cephalonica (rice moth, species) [taxon 139036], Coemansia nantahalensis (species) [taxon 2789366], Escherichia coli (E. coli, species) [taxon 562], Salmonella (genus) [taxon 590], Raiamas senegalensis (Senegal minnow, species) [taxon 516811], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Nephrolepis exaltata (Boston fern, species) [taxon 34165], Alligator (genus) [taxon 8495], Oxalis crassipes [taxon 53797], Croton (genus) [taxon 100370], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12965568/full.md

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Source: https://tomesphere.com/paper/PMC12965568