# Rapid and visual detection of Tacheng tick virus 1 using loop-mediated isothermal amplification technique

**Authors:** Qiqi Guo, Zheng Gui, Yuanning Ren, Ziyan Liu, Ning Liu, Liang Li, Zedong Wang, Jingfeng Yu

PMC · DOI: 10.3389/fcimb.2025.1660327 · Frontiers in Cellular and Infection Microbiology · 2026-01-07

## TL;DR

This study developed a fast and accurate test for detecting Tacheng tick virus 1, which causes fever in humans and can be used in field or low-resource settings.

## Contribution

A novel LAMP assay for the specific and sensitive detection of Tacheng tick virus 1 is developed and validated.

## Key findings

- The LAMP assay detected as few as 1×10-1 copies/μL of TcTV-1 within 60 minutes at 65 °C.
- The assay showed no cross-reactivity with other related viruses and had 100% sensitivity and specificity.
- Eight tick samples tested positive for TcTV-1 using both LAMP and RT-qPCR, confirming the method's accuracy.

## Abstract

Tacheng tick virus 1 (TcTV-1) is an emerging tick-borne nairovirus associated with human febrile illness. To date, no reliable detection method for TcTV-1 has been established. In this study, we developed and evaluated a rapid loop-mediated isothermal amplification (LAMP) assay for the detection of TcTV-1.

The primers were designed based on the nucleocapsid protein (NP) gene of TcTV-1. Sensitivity was assessed using ten-fold serial dilutions of recombinant plasmids containing the target sequence. Specificity was evaluated using cDNA from Songling virus (SGLV), Yezo virus (YEZV), Tick-borne encephalitis virus (TBEV), Severe fever with thrombocytopenia syndrome virus (SFTSV), and Beiji nairovirus (BJNV). The assay was validated using field-collected tick samples.

The TcTV-1-specific LAMP assay detected as few as 1×10-1 copies/μL within 60 minutes at 65 °C and specifically amplified TcTV-1, with no cross-reactivity to SGLV, YEZV, TBEV, SFTSV, or BJNV. Positive reactions exhibited a clear color change from purple to blue, indicating a robust colorimetric response. A total of eight tick specimens (16.0%; 95% CI: 7.2–29.1) tested positive for TcTV-1 using both the established LAMP assay and SYBR Green real time quantitative polymerase chain reaction (RT-qPCR), demonstrating 100% sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy for the LAMP assay.

We report a TcTV-1-specific LAMP assay with high sensitivity, specificity, and cost-effectiveness, making it a practical tool for use in field-based or resource-limited settings.

## Full-text entities

- **Diseases:** febrile illness (MESH:D005334)
- **Species:** Severe fever with thrombocytopenia syndrome virus (no rank) [taxon 1003835], Homo sapiens (human, species) [taxon 9606], Tick-borne encephalitis virus (no rank) [taxon 11084], Songling virus (no rank) [taxon 2795181], Beiji nairovirus (no rank) [taxon 2304647], Tacheng Tick Virus 1 (no rank) [taxon 1608083], Yezo virus (no rank) [taxon 2825847]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12819602/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12819602/full.md

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Source: https://tomesphere.com/paper/PMC12819602