Cell surface Toll-like receptor polymorphisms influence Bartonella and ectoparasite infections in striped hamsters

This study explored how polymorphisms in cell surface Toll-like receptors (TLRs) influence susceptibility to <i>Bartonella</i> and ectoparasite infections in striped hamsters. Among six TLR genes, four sites in TLR1, TLR4, and TLR10 genes were associated with <i>Bartonella</i> susceptibility, while twelve sites across TLR4, TLR5, and TLR10 contributed to flea resistance. Similarly, eleven sites in TLR5, TLR6, and TLR10 were linked to gamasid mite parasitism. Genetic polymorphism analysis revealed that when heterozygous or rare genotypes protected the host from infections, the polymorphisms of these sites in uninfected individuals exceeded that of the infected group. The distribution of these sites on the three-dimensional structure of TLRs varied. All <i>Bartonella</i>-related sites were in the extracellular domain, whereas some of those related to fleas and gamasid mites were located in other domains. This research highlights the importance of cell surface TLRs in immune regulation and provides insights into evolutionary dynamics in natural environments.

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Publication Details

Journal
iScience
Published
2025-06-13
DOI
https://doi.org/10.1016/j.isci.2025.112883
Primary Topic
Bartonella species infections research
Type
article
Field-Weighted Citation Impact
0.00

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article

Cell surface Toll-like receptor polymorphisms influence Bartonella and ectoparasite infections in striped hamsters

Qiyong Liu, Yujuan Yue, Guichang Li, Yiguan Wang et al.
iScience
Bartonella species infections research
article

Cell surface Toll-like receptor polymorphisms influence Bartonella and ectoparasite infections in striped hamsters

Qiyong Liu, Yujuan Yue, Guichang Li, Yiguan Wang, Fengxia Meng, Xinchang Lun, Jun Wang, Zihao Wang, Ning Zhao, Xiuping Song, Liang Lu, Pengbo Liu, Ying Liang, Zhenxu Wang
article en

Abstract

This study explored how polymorphisms in cell surface Toll-like receptors (TLRs) influence susceptibility to <i>Bartonella</i> and ectoparasite infections in striped hamsters. Among six TLR genes, four sites in TLR1, TLR4, and TLR10 genes were associated with <i>Bartonella</i> susceptibility, while twelve sites across TLR4, TLR5, and TLR10 contributed to flea resistance. Similarly, eleven sites in TLR5, TLR6, and TLR10 were linked to gamasid mite parasitism. Genetic polymorphism analysis revealed that when heterozygous or rare genotypes protected the host from infections, the polymorphisms of these sites in uninfected individuals exceeded that of the infected group. The distribution of these sites on the three-dimensional structure of TLRs varied. All <i>Bartonella</i>-related sites were in the extracellular domain, whereas some of those related to fleas and gamasid mites were located in other domains. This research highlights the importance of cell surface TLRs in immune regulation and provides insights into evolutionary dynamics in natural environments.

iScienceVol. 28(7)
Center for Excellence in Molecular Plant Sciences (CN), National Institute for Communicable Disease Control and Prevention (CN), Nanjing Medical University (CN)
National Natural Science Foundation of China, Special Project for Research and Development in Key areas of Guangdong Province
Openalex Percentile: Top 86%
Bartonella species infections research
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