Cynomolgus Monkeys (Macaca fascicularis) as an Experimental Infection Model for Human Group A Rotavirus

Gentil Arthur Bentes1, Juliana Rodrigues Guimarães2, Eduardo de Mello Volotão3

  • 1Laboratório de Desenvolvimento Tecnológico em Virologia, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro/RJ 21.040-360, Brazil. gentilbentes@fiocruz.br.

Viruses
|July 6, 2018
PubMed

Insights

Group A rotavirus (RVA) causes severe gastroenteritis in children. Cynomolgus monkeys experimentally infected with human RVA showed viral shedding and mild symptoms, suggesting their utility as a model for antiviral research.

Area of Science:

  • Virology
  • Gastroenterology
  • Infectious Diseases

Background:

  • Group A rotaviruses (RVA) are a leading cause of severe acute gastroenteritis in infants globally.
  • Faecal-oral transmission is the primary route for rotavirus spread, affecting nearly all unvaccinated children within their first two years.
  • Developing a reliable experimental animal model for RVA is crucial for evaluating novel therapeutic strategies.

Purpose of the Study:

  • To establish and validate an experimental monkey model for human Group A rotavirus infection.
  • To assess viral shedding and viraemia in *Macaca fascicularis* following oral inoculation with the Wa RVA prototype.

Main Methods:

  • Nine juvenile-adult *Macaca fascicularis* monkeys were orally inoculated with human Wa RVA (seven animals) or saline (two controls).
  • Monkeys were clinically monitored, with faeces and blood samples collected and tested for RVA RNA.
  • Viral RNA detection in faecal and serum samples indicated successful infection and replication.

Main Results:

  • Oligosymptomatic infection was observed in inoculated monkeys, with two exhibiting self-limited diarrhoea for three days.
  • A reduction in plasmatic potassium content was noted in monkeys with diarrhoea.
  • Viral RNA was detected in faecal samples from seven animals and serum samples from five animals.

Conclusions:

  • Cynomolgus monkeys (*Macaca fascicularis*) are susceptible to human Wa RVA infection via oral inoculation.
  • The observed self-limited diarrhoea and viral shedding confirm the utility of this species as a potential animal model.
  • This model holds promise for evaluating the efficacy of new antiviral treatments against rotavirus infections.

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