Pathogenicity of tick-derived lymphocytic choriomeningitis virus in BALB/c mice

Ziyan Liu1,2,3, Xiaojie Liang1, Liang Li3

  • 1Laboratory of Pathogen Microbiology and Immunology, College of Life Science, Jilin Agricultural University, Changchun, Jilin Province, China.

BMC Veterinary Research
|January 6, 2025
PubMed
Abstract

Insights

Tick-borne lymphocytic choriomeningitis virus (LCMV) causes temporary illness in mice, with persistent viral RNA in the heart and genetic changes over time. This study offers a model for chronic viral infection research.

Area of Science:

  • Virology
  • Immunology
  • Infectious Diseases

Background:

  • Lymphocytic choriomeningitis virus (LCMV) is a zoonotic pathogen typically spread by rodents.
  • LCMV has recently been identified in ticks in northeastern China.
  • The pathogenicity of tick-derived LCMV strains in animal models requires further investigation.

Purpose of the Study:

  • To investigate the pathogenicity of a tick-derived LCMV strain (JX14) in a murine model.
  • To characterize the clinical, virological, and pathological outcomes of LCMV infection in BALB/c mice.
  • To explore the potential of this model for studying chronic viral infections.

Main Methods:

  • BALB/c mice were inoculated with the tick-derived LCMV strain JX14.
  • Clinical signs, viral shedding, viral RNA presence in blood and organs, and pathological lesions were monitored.
  • Amino acid substitutions in viral proteins and interferon-gamma levels were analyzed.

Main Results:

  • LCMV-infected mice showed transient clinical signs and survived infection.
  • Viral RNA persisted for up to six months in the heart, with detectable levels in blood and other organs early on.
  • Significant amino acid substitutions occurred in viral proteins, and elevated interferon-gamma levels were observed during early infection.

Conclusions:

  • The tick-derived LCMV strain JX14 exhibits distinct pathogenic traits in mice.
  • Persistent viral RNA and observed genetic mutations suggest chronic infection potential.
  • This study establishes a valuable in vivo model for researching immune responses to chronic viral infections.

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