Evidence map›Paper›PMID 39856717›Full record

ArticleParasites & vectors2025

Identification of fine antigenic epitopes of Tamdy virus glycoprotein Gn fragment and establishment of ELISA detection method.

Yujiao Fu, Liping Liu, Beibei Zhang, Xiaoshan Chao, Junxia Jin, Ying Wang, Juntao Ding

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Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yujiao FuCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China.
Liping LiuCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China.
Beibei ZhangCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China.
Xiaoshan ChaoCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China.
Junxia JinCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China.
Ying WangCollege of Textiles and Clothing, Xinjiang University, Urumqi, 830017, China.
Juntao DingCollege of Life Science and Technology, Xinjiang University, Urumqi, 830017, China. dingjuntao2004@126.com.

Funding

The epidemiological investigation of significant arbovirus pathogens carried by rodents and vector ticks in the Junggar Basin 81760365
6 · The paper itself

Abstract

backgroundTamdy virus (TAMV) was first isolated in Uzbekistan and Turkmenistan. In 2018, it was found in China, marking its entry into the molecular research era. TAMV is linked to febrile diseases, but its epidemiology and spillover risks are poorly understood, necessitating urgent molecular research and detection method development.

methodsThe secondary structure of TAMV glycoprotein Gn was predicted, and the results showed that it had rich antigenic epitopes. According to the predicted results, glycoprotein Gn was divided into 46 truncated 16-peptides by modified synthetic peptide method, and the antigenicity of 46 truncated 16-peptides was verified by western blotting analysis.

resultsThe results showed that P8, P9, P24, P25, P28, P29, and P39 had antigenicity. Subsequently, the seven positive 16-peptide sequences with antigenicity were truncated to form 8-peptide sequences with an overlap of seven amino acids. After analysis with the same method, eight fine antigenic epitopes E1 (

conclusionsEight precise epitopes were identified, and an indirect ELISA method based on fusion multiepitope peptide (r-Gn-MEPX

Indexed as

Antigens, ViralEpitopesGlycoproteinsViral Envelope ProteinsAmino Acid SequenceAnimalsChinaEnzyme-Linked Immunosorbent AssayAntigens, ViralEpitopesGlycoproteinsViral Envelope ProteinsAntigenic epitopesELISAGlycoprotein GnTamdy virusWestern blotting

Identifiers

PMID39856717
PMCPMC11762889

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