Multiorgan proteomic analysis of infected animal models predict potential host factors for chikungunya virus
2025

Understanding Chikungunya Virus Effects on Different Organs

Sample size: 12 publication 10 minutes Evidence: high

Author Information

Author(s): Lin Dongdong, Tang Cong, Wang Junbin, Yang Yun, Yang Hao, Zhou Yanan, Yu Wenhai, Li Bai, Huang Qing, Wang Haixuan, An Ran, Liang Xiaoming, Yan Yuhuan, Yuan Longhai, Du Xuena, Yuan Yuxia, Li Yanwen, Lu Shuaiyao

Primary Institution: Yunnan Key Laboratory of Cross‐Border Infectious Disease Prevention and New Drug Development, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College

Hypothesis

What are the host factors involved in the pathogenesis of chikungunya virus as revealed by proteomic analysis in infected animal models?

Conclusion

The study identifies key host factors and immune responses involved in chikungunya virus infection across various organs, highlighting potential therapeutic targets.

Supporting Evidence

  • Proteomic analysis revealed significant differences in immune responses between rhesus monkeys and mice.
  • Key proteins involved in the anti-CHIKV defense were identified, including ISG15 and RIG-I.
  • Host factors contributing to inflammation and hemorrhage were predicted through bioinformatic analyses.
  • Distinct metabolic responses were observed in CHIKV-infected rhesus monkeys compared to mice.
  • Activation of the RLR signaling pathway was noted in both animal models.
  • ISG15 was identified as a potential biomarker for distinguishing CHIKV infection.
  • Histopathological analysis confirmed organ damage due to CHIKV infection.
  • Correlation analysis linked specific proteins to hemorrhage in infected organs.

Takeaway

Researchers studied how chikungunya virus affects different organs in animals and found important proteins that help fight the virus, which could lead to new treatments.

Methodology

The study used proteomic analysis on tissues from infected rhesus monkeys and mice to identify differences in immune responses and metabolic regulation.

Potential Biases

Potential bias due to the reliance on animal models that may not fully replicate human disease.

Limitations

The study's findings may be limited by the single time point of sample collection and the lack of functional validation for identified host factors.

Participant Demographics

Rhesus monkeys and C57BL/6J mice, both male and female, aged 7-14 years and 6-8 weeks respectively.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1002/mco2.70013

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