Class

Article

College

College of Science

Department

Nursing and Health Professions

Faculty Mentor

Justin Julander

Presentation Type

Poster Presentation

Abstract

Chikungunya virus (CHIKV) is an infectious alphavirus spread by Aedes aegypti and Aedes albopictus mosquitoes. Recently, there have been various outbreaks in the Americas, the Caribbean, and across Asia and Africa (Bettis et al., 2022). Although mortality rates of Chikungunya disease are relatively low, the disease has been shown to have high morbidity and chronic effects. Currently, there are no approved antivirals for treatment of CHIKV infection. The goal of this study was to identify whether Compound X is an effective treatment in a mouse model of CHIKV infection. Compound X was active in cell culture models of CHIKV infection, therefore efficacy in vivo was anticipated. To test this hypothesis, Compound X was first tested for toxicity in C57BL/6 black mice. After the initial study, no gross toxicity was observed, and the infection study proceeded. Once the mice were infected with chikungunya via a subcutaneous injection in the right hind footpad, Compound X was administered twice a day for 7 days post-infection at two doses. Efficacy was determined by measuring footpad swelling and spleen weights and collecting samples to quantify infectious virus. Upon completion of the study, it was concluded that Compound X was not an effective treatment in this mouse model of CHIKV infection and diseases, and further evaluation toward clinical development is not warranted.

Location

Logan, UT

Start Date

4-12-2023 12:30 PM

End Date

4-12-2023 1:30 PM

Included in

Public Health Commons

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Apr 12th, 12:30 PM Apr 12th, 1:30 PM

Chikungunya: The Evaluation of Compound X in a Mouse Model of CHIKV Disease

Logan, UT

Chikungunya virus (CHIKV) is an infectious alphavirus spread by Aedes aegypti and Aedes albopictus mosquitoes. Recently, there have been various outbreaks in the Americas, the Caribbean, and across Asia and Africa (Bettis et al., 2022). Although mortality rates of Chikungunya disease are relatively low, the disease has been shown to have high morbidity and chronic effects. Currently, there are no approved antivirals for treatment of CHIKV infection. The goal of this study was to identify whether Compound X is an effective treatment in a mouse model of CHIKV infection. Compound X was active in cell culture models of CHIKV infection, therefore efficacy in vivo was anticipated. To test this hypothesis, Compound X was first tested for toxicity in C57BL/6 black mice. After the initial study, no gross toxicity was observed, and the infection study proceeded. Once the mice were infected with chikungunya via a subcutaneous injection in the right hind footpad, Compound X was administered twice a day for 7 days post-infection at two doses. Efficacy was determined by measuring footpad swelling and spleen weights and collecting samples to quantify infectious virus. Upon completion of the study, it was concluded that Compound X was not an effective treatment in this mouse model of CHIKV infection and diseases, and further evaluation toward clinical development is not warranted.