Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Feb 23:14:1340017.
doi: 10.3389/fcimb.2024.1340017. eCollection 2024.

Marmosets as models of infectious diseases

Affiliations
Review

Marmosets as models of infectious diseases

Ian C T Herron et al. Front Cell Infect Microbiol. .

Abstract

Animal models of infectious disease often serve a crucial purpose in obtaining licensure of therapeutics and medical countermeasures, particularly in situations where human trials are not feasible, i.e., for those diseases that occur infrequently in the human population. The common marmoset (Callithrix jacchus), a Neotropical new-world (platyrrhines) non-human primate, has gained increasing attention as an animal model for a number of diseases given its small size, availability and evolutionary proximity to humans. This review aims to (i) discuss the pros and cons of the common marmoset as an animal model by providing a brief snapshot of how marmosets are currently utilized in biomedical research, (ii) summarize and evaluate relevant aspects of the marmoset immune system to the study of infectious diseases, (iii) provide a historical backdrop, outlining the significance of infectious diseases and the importance of developing reliable animal models to test novel therapeutics, and (iv) provide a summary of infectious diseases for which a marmoset model exists, followed by an in-depth discussion of the marmoset models of two studied bacterial infectious diseases (tularemia and melioidosis) and one viral infectious disease (viral hepatitis C).

Keywords: Burkholderia pseudomallei; Francisella tularensis; animal models; common marmoset; hepatitis C virus; immunology; inflammation.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Similar articles

Cited by

References

    1. ‘T Hart B. A. (2019). Experimental autoimmune encephalomyelitis in the common marmoset: a translationally relevant model for the cause and course of multiple sclerosis. Primate. Biol. 6, 17–58. doi: 10.5194/pb-6-17-2019 - DOI - PMC - PubMed
    1. ‘T Hart B. A., Abbott D. H., Nakamura K., Fuchs E. (2012). The marmoset monkey: a multi-purpose preclinical and translational model of human biology and disease. Drug Discovery Today 17, 1160–1165. doi: 10.1016/j.drudis.2012.06.009 - DOI - PMC - PubMed
    1. Abbink F. C., Orendi J. M., De Beaufort A. J. (2001). Mother-to-child transmission of Burkholderia pseudomallei . N. Engl. J. Med. 344, 1171–1172. doi: 10.1056/NEJM200104123441516 - DOI - PubMed
    1. Abbott D. H., Barnett D. K., Colman R. J., Yamamoto M. E., Schultz-Darken N. J. (2003). Aspects of common marmoset basic biology and life history important for biomedical research. Comp. Med. 53, 339–350. - PubMed
    1. Adams A. P., Aronson J. F., Tardif S. D., Patterson J. L., Brasky K. M., Geiger R., et al. . (2008). Common marmosets (Callithrix jacchus) as a nonhuman primate model to assess the virulence of eastern equine encephalitis virus strains. J. Virol. 82, 9035–9042. doi: 10.1128/JVI.00674-08 - DOI - PMC - PubMed