Table 2.
Animal models | Advantages | Disadvantages |
---|---|---|
Mice | Low cost, easy to use Transgenic and knockout models are available |
Only i.p. infection is 100% lethal Mouse-adapted variants needed |
Guinea pigs | Low cost, larger animals to study disease progression and easy to use | Transgenic and knockout models are not available Lack of immunological tools and reagents to evaluate cell-mediated responses to vaccines and therapeutics Guinea pig-adapted variants needed |
Syrian Hamsters | An alternative to guinea pigs Elegant model to compare differences in immune responses to EBOV infection |
Mouse-adapted variants needed Lack of commercially available reagents and host genomic information Transgenic and knockout models are available |
Ferrets | Small body size, low cost Closely resembles to human filoviral disease Can use clinical isolates to study pathogenesis |
Limited availability of ferret-specific reagents Ferret immune responses are poorly understood Transgenic and knockout models are available |
NHPs | Gold standard model to evaluate filovirus infections and closely recapitulate human disease | Animals are expensive, ethical considerations and extensively husbandry requirements needed Transgenic and knockout models are not available |
NHPs: Non-human primates.