# First Genomic Evidence of California Hare Coltivirus from Natural Populations of Ixodes persulcatus Ticks in Northeast China

**Authors:** Zhenyu Hu, Jingtao Zhang, Yantao Liu, Liming Liu, Fang Tang, Guangqian Si, Meiqi Zhang, Shuang Li, Yunfa Zhang, Cong Peng, Lei Zhang, Xiaofang Ma, Xiaoai Zhang, Wei Liu

PMC · DOI: 10.3390/pathogens13080614 · 2024-07-25

## TL;DR

Scientists found California hare coltivirus in ticks in China, showing it's more widespread and genetically diverse than previously known.

## Contribution

First genomic evidence of CHCV in Ixodes persulcatus ticks in China, expanding its geographic and host range.

## Key findings

- CHCV RNA was detected in 1.56% of tick samples, all from Ixodes persulcatus.
- The virus showed high genetic similarity to previously reported CHCV strains except for segment seven.
- CHCV clustered with human pathogenic coltiviruses in phylogenetic analysis.

## Abstract

Background: California hare coltivirus (CHCV) was isolated in California in 1976 from a hare. Despite its long history, it remained unclear whether CHCV was exclusively distributed in California with limited host ranges. Main body: By next-generation sequencing (NGS), we obtained a complete sequence of CHCV from Ixodes persulcatus collected in 2019 in northeast China. An expanded epidemiological investigation was subsequently performed on ticks belonging to four species (Ix. persulcatus, Haemaphysalis concinna, Devmacentor silvarum, Haemaphysalis longicornis) collected in northeastern China by applying CHCV-specific RT-PCR and sequencing. CHCV RNA-positive results were found in 1.56% of the tick samples. Positive ticks were obtained in three of four sampled locations, with the highest rate observed in Inner Mongolia (2.69%), followed by Heilongjiang (1.94%) and Jilin provinces (0.55%). All positive results were derived from Ix. persulcatus ticks (2.33%), while no positive detection was found in the other tick species, even at the same location. Sequence analysis revealed that the current CHCV showed a high genetic identity (>80% amino acid identity) with the previously reported CHCV in all segments except segment seven (64.59% amino acid identity). Phylogenetic analysis based on RNA-dependent RNA polymerase (RdRp) amino acid sequences demonstrated that both the current and previously reported CHCV strains were grouped phylogenetically into the genus Coltivirus. Both CHCV strains formed a distinct clade, clustering with three human pathogenic coltiviruses (Colorado tick fever virus, Salmon River virus, and Eyach virus), and were distant from the other coltiviruses. Conclusions: We report the identification and characterization of CHCV for the first time in Ix. persulcatus ticks, expanding the currently known geographic scope, host, and genetic heterogeneity in CHCV.

## Linked entities

- **Proteins:** RNA-dependent RNA polymerase (RNA-dependent RNA polymerase)
- **Species:** Ixodes persulcatus (taxon 34615), Haemaphysalis concinna (taxon 523089), Dermacentor silvarum (taxon 543639), Haemaphysalis longicornis (taxon 44386)

## Full-text entities

- **Species:** Homo sapiens (human, species) [taxon 9606], Eyach virus (no rank) [taxon 62352], Haemaphysalis concinna (species) [taxon 523089], California hare coltivirus (species) [taxon 2936928], Coltivirus (genus) [taxon 10911], Salmon River virus (species) [taxon 2952130], Haemaphysalis longicornis (longhorned tick, species) [taxon 44386], Colorado tick fever virus (no rank) [taxon 46839], Ixodes persulcatus (taiga tick, species) [taxon 34615]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11357685/full.md

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Source: https://tomesphere.com/paper/PMC11357685