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Published on: August 10, 2018
An enterovirus 71 strain causes skeletal muscle damage in infected mice
Peixin Lin1, Lulu Gao1, Yeen Huang1
1Department of Pathology, School of Basic Medical Sciences, Southern Medical University Tonghe, Guangzhou, China.
Objective:
To study the target organs for enterovirus 71 (EV71) in infected suckling mice.
Methods:
5-day-old BALB/c suckling mice were infected with an EV71 strain. Tissues of the infected mice were processed for histopathological examination, including immunohistochemistry, in situ hybridization, ultrastructural observation.
Results:
Some mice developed limb paralysis, trouble walking and loss of balance. Results of the histopathological study showed that a large amount of EV71 existed in the skeletal muscle tissues, accounting for the damage of the skeletal muscles.
Conclusion:
The EV71 clinical isolate used in this study presented evident myotropism. Skeletal muscles are important target organs for EV71 in the infected suckling mice. To clarify the relationship between EV71 infection and muscle diseases may contribute to a better understanding of the pathogenesis of EV71.
Insights
Enterovirus 71 (EV71) primarily targets skeletal muscles in young mice, leading to muscle damage and neurological symptoms like paralysis. This highlights the myotropic nature of EV71 infection.
Area of Science:
- Virology
- Pathology
- Neurology
Background:
- Enterovirus 71 (EV71) is a significant human pathogen causing a range of illnesses, from mild febrile disease to severe neurological complications.
- Understanding the tissue tropism of EV71 is crucial for elucidating its pathogenesis and developing effective therapeutic strategies.
Purpose of the Study:
- This study aimed to identify the primary target organs of EV71 in experimentally infected suckling mice.
- The research specifically investigated the tropism of a particular EV71 clinical isolate.
Main Methods:
- Suckling BALB/c mice (5 days old) were inoculated with an EV71 strain.
- Infected mice underwent comprehensive histopathological examination, including immunohistochemistry, in situ hybridization, and ultrastructural analysis.
Main Results:
- Mice exhibited clinical signs such as limb paralysis, ataxia, and loss of balance.
- Histopathological findings revealed a high viral load of EV71 within skeletal muscle tissues.
- Skeletal muscle damage correlated directly with the presence of the virus.
Conclusions:
- The EV71 clinical isolate demonstrated significant myotropism, indicating a preference for muscle tissue.
- Skeletal muscles were identified as key target organs for EV71 in this suckling mouse model.
- Further research into the EV71-muscle disease relationship is warranted to better understand EV71 pathogenesis.
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