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Causation of Acute Flaccid Paralysis by Myelitis and Myositis in Enterovirus-D68 Infected Mice Deficient in
John D Morrey1, Hong Wang2, Brett L Hurst3
1Institute for Antiviral Research, Department of Animal, Dairy, and Veterinary Sciences, 5600 Old Main Hill, Utah State University, Logan, UT 84322, USA. john.morrey@usu.edu.
Abstract:
Enterovirus D68 (EV-D68) caused a large outbreak in the summer and fall of 2014 in the United States. It causes serious respiratory disease, but causation of associated paralysis is controversial, because the virus is not routinely identified in cerebrospinal fluid. To establish clinical correlates with human disease, we evaluated EV-D68 infection in non-lethal paralysis mouse models. Ten-day-old mice lacking interferon responses were injected intraperitoneally with the virus. Paralysis developed in hindlimbs. After six weeks of paralysis, the motor neurons were depleted due to viral infection. Hindlimb muscles were also infected and degenerating. Even at the earliest stage of paralysis, muscles were still infected and were degenerating, in addition to presence of virus in the spinal cord. To model natural respiratory infection, five-day-old mice were infected intranasally with EV-D68. Two of the four infected mice developed forelimb paralysis. The affected limbs had muscle disease, but no spinal cord infection was detected. The unique contributions of this study are that EV-D68 causes paralysis in mice, and that causation by muscle disease, with or without spinal cord disease, may help to resolve the controversy that the virus can cause paralysis, even if it cannot be identified in cerebrospinal fluid.
Insights
Enterovirus D68 (EV-D68) causes paralysis in mice, impacting motor neurons and muscles. This study suggests muscle disease, not just spinal cord infection, explains EV-D68-associated paralysis.
Area of Science:
- Virology
- Neurology
- Immunology
Background:
- Enterovirus D68 (EV-D68) outbreaks cause respiratory illness.
- The link between EV-D68 and paralysis is debated due to low virus detection in cerebrospinal fluid.
Purpose of the Study:
- To investigate EV-D68 infection in mouse models to understand paralysis causation.
- To establish clinical and pathological correlates of EV-D68-induced disease.
Main Methods:
- EV-D68 was administered to immunocompromised young mice via intraperitoneal injection.
- A separate cohort of young mice was infected intranasally to model natural respiratory transmission.
- Neurological and muscular tissues were examined for viral presence, damage, and motor neuron loss.
Main Results:
- Intraperitoneal EV-D68 infection led to hindlimb paralysis, motor neuron depletion, and muscle degeneration.
- Intranasal infection caused forelimb paralysis in some mice, characterized by muscle disease but no spinal cord infection.
- Muscle infection and degeneration were observed early in paralysis, irrespective of spinal cord involvement.
Conclusions:
- EV-D68 can induce paralysis in mouse models.
- Muscle disease, with or without spinal cord involvement, is a potential mechanism for EV-D68-associated paralysis.
- Findings may help resolve controversy regarding EV-D68's role in paralysis, even without CSF detection.
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