A PCR primer design method for identifying spider mite species using k-mer counting

Using PCR to distinguish closely related species can be difficult because they may have very similar genomes. Advances in bioinformatics make it possible to design PCR primers that are species-specific. In this study, we developed a bioinformatics method for extracting species-specific primer candidate sequences (i.e., unpaired primers that were specific to a single species) from RNA-Seq data sets of 19 species of spider mites (Acari, Tetranychidae). Using k-mer counting, we obtained between 257 and 48,621 species-specific unpaired primer candidates for the 19 species. We then manually obtained a second primer that was also species-specific. The primer pairs were then confirmed to work in the target species and not to work in the non-target species. Finally, species-specific primer pairs were obtained for 17 of the 19 species tested. Such species-specific primers may be used for practical species discrimination by optimizing multiplex PCR. Our primer design method is expected to be applicable to other taxa.

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Publication Details

Journal
PLoS ONE
Published
2025-06-09
DOI
https://doi.org/10.1371/journal.pone.0321199
Primary Topic
Insect-Plant Interactions and Control
Type
article
Field-Weighted Citation Impact
0.00
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article

A PCR primer design method for identifying spider mite species using k-mer counting

Tomoko Matsuda, Toshinori Kozaki, Tetsuo Gotoh, Hironori Sakamoto et al.
PLoS ONE
Insect-Plant Interactions and Control
article

A PCR primer design method for identifying spider mite species using k-mer counting

Tomoko Matsuda, Toshinori Kozaki, Tetsuo Gotoh, Hironori Sakamoto, Yasuki Kitashima, Takumi Kayukawa
article en

Abstract

Using PCR to distinguish closely related species can be difficult because they may have very similar genomes. Advances in bioinformatics make it possible to design PCR primers that are species-specific. In this study, we developed a bioinformatics method for extracting species-specific primer candidate sequences (i.e., unpaired primers that were specific to a single species) from RNA-Seq data sets of 19 species of spider mites (Acari, Tetranychidae). Using k-mer counting, we obtained between 257 and 48,621 species-specific unpaired primer candidates for the 19 species. We then manually obtained a second primer that was also species-specific. The primer pairs were then confirmed to work in the target species and not to work in the non-target species. Finally, species-specific primer pairs were obtained for 17 of the 19 species tested. Such species-specific primers may be used for practical species discrimination by optimizing multiplex PCR. Our primer design method is expected to be applicable to other taxa.

PLoS ONEVol. 20(6)
NEC (Japan) (JP), National Agriculture and Food Research Organization (JP), National Institute for Environmental Studies (JP), Institute of Agrobiological Sciences (JP), Ryutsu Keizai University (JP), Ibaraki University (JP)
Peace, Justice and strong institutions
Openalex Percentile: Top 88%
Insect-Plant Interactions and Control
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A PCR primer design method for identifying spider mite species using k-mer counting — Tomoko Matsuda, Toshinori Kozaki, et al. · PLoS ONE (2025) | TGRS Research Map | TGRS