# COI barcoding can distinguish bisexual and parthenogenetic populations of Haemaphysalis longicornis in Japan: Revisiting methods with SNP analysis as another possible method

**Authors:** Mizue Inumaru, Kentaro Itokawa, Ryo Matsumura, Kyoko Sawabe, Mamoru Watanabe, Haruhiko Isawa, Shinji Kasai, Yukiko Higa

PMC · DOI: 10.1016/j.ijppaw.2025.101083 · International Journal for Parasitology: Parasites and Wildlife · 2025-05-15

## TL;DR

This study shows that COI barcoding and SNP analysis can reliably distinguish between two reproductive forms of the Asian long-horned tick in Japan.

## Contribution

The study is the first to demonstrate the effectiveness of COI barcoding and SNP genotyping for identifying parthenogenetic and bisexual tick populations.

## Key findings

- COI haplotypes clustered into two distinct haplogroups representing different ploidy levels.
- SNP genotyping confirmed individuals from each haplogroup belonged to distinct reproductive populations.
- Morphological measurements showed overlaps and were insufficient for accurate identification.

## Abstract

Haemaphysalis longicornis, the Asian long-horned tick, is an important vector for various infectious diseases, such as severe fever with thrombocytopenia syndrome (SFTS) and Japanese spotted fever. In this species, a triploid parthenogenetic reproductive form occurs along with a diploid bisexual form. Several approaches have been used to distinguish these two groups, including the presence/absence of males in the population, karyotyping, flow cytometry, and most recently, mitochondrial phylogeny. Mitochondrial gene (COI) barcoding has also been casually used, although its validity has not been investigated. In the present study, the validity of COI barcoding, genotyping nuclear markers (SNPs), and morphometrics was evaluated for distinguishing the reproductive forms of H. longicornis in Japan. Ticks were collected using the flagging method at two locations in Hyogo, Japan. DNA was extracted from ticks after photography, which was used for morphometric measurements. The DNA was used for COI barcoding by direct sequencing and genotyping SNPs in the nuclear genome. The resulting COI haplotypes were clustered into two distinct haplogroups, which represented different ploidy levels, corresponding to the different reproductive groups. Genotypes of nuclear SNPs supported that the individuals from each mitochondrial haplogroup belonged to distinct reproductive populations with different ploidy levels. Meanwhile, although significant differences were observed in multiple morphometric characteristics between these reproductive groups, large overlaps were generally evident in the distribution, indicating that morphological identification is not sufficient to distinguish the reproductive groups. This study suggested for the first time that COI barcoding and SNP genotyping are both convenient and reliable methods to distinguish the two reproductive forms of H. longicornis in Japan.

Image 1

•Triploid (parthenogenetic) haplogroup formed monophyletic clade.•SNP genotyping and COI barcoding effective to distinguish reproductive forms.•COI region by itself well represents mitochondrial genome.•Morphometrics insufficient to accurately distinguish reproductive forms.

Triploid (parthenogenetic) haplogroup formed monophyletic clade.

SNP genotyping and COI barcoding effective to distinguish reproductive forms.

COI region by itself well represents mitochondrial genome.

Morphometrics insufficient to accurately distinguish reproductive forms.

## Linked entities

- **Genes:** COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512]
- **Diseases:** Japanese spotted fever (MONDO:0000233)
- **Species:** Haemaphysalis longicornis (taxon 44386)

## Full-text entities

- **Diseases:** SFTS (MESH:D000085142), Japanese spotted fever (MESH:D000073605), infectious diseases (MESH:D003141)
- **Species:** Haemaphysalis longicornis (longhorned tick, species) [taxon 44386]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12143733/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12143733/full.md

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Source: https://tomesphere.com/paper/PMC12143733