Nonprimate models of congenital cytomegalovirus (CMV) infection: gaining insight into pathogenesis and prevention of disease in newborns
- PMID: 16391432
- DOI: 10.1093/ilar.47.1.65
Nonprimate models of congenital cytomegalovirus (CMV) infection: gaining insight into pathogenesis and prevention of disease in newborns
Abstract
Congenital and perinatal infections with cytomegalovirus (CMV) are responsible for considerable short- and long- term morbidity in infants. CMV is the most common congenital viral infection in the developed world, and is a common cause of neurodevelopmental injury, including mental retardation and sensorineural hearing loss (SNHL). Antiviral therapy has been shown to be valuable in ameliorating the severity of SNHL, but CMV disease control in newborns ultimately depends on successful development of a vaccine. Because CMVs are extremely species specific, preclinical evaluation of vaccines must be performed in animal models using the appropriate CMV of the animal being studied. Several small animal models available for CMV vaccine and pathogenesis research are described. The discussion focuses on the guinea pig model because guinea pig cytomegalovirus (GPCMV), which crosses the placenta and causes infection in utero, is uniquely useful. Examination of vaccines in the GPCMV and other nonprimate models should provide insights into the determinants of the host response that protect the fetus, and may help to prioritize potential vaccine strategies for use in human clinical trials related to this important public health problem.
Similar articles
-
Animal models of congenital cytomegalovirus infection: an overview of progress in the characterization of guinea pig cytomegalovirus (GPCMV).J Clin Virol. 2002 Aug;25 Suppl 2:S37-49. doi: 10.1016/s1386-6532(02)00100-2. J Clin Virol. 2002. PMID: 12361755 Review.
-
Inclusion of the Viral Pentamer Complex in a Vaccine Design Greatly Improves Protection against Congenital Cytomegalovirus in the Guinea Pig Model.J Virol. 2019 Oct 29;93(22):e01442-19. doi: 10.1128/JVI.01442-19. Print 2019 Nov 15. J Virol. 2019. PMID: 31484753 Free PMC article.
-
Comparison of vaccine strategies against congenital CMV infection in the guinea pig model.J Clin Virol. 2008 Mar;41(3):224-30. doi: 10.1016/j.jcv.2007.10.008. Epub 2007 Dec 3. J Clin Virol. 2008. PMID: 18060834 Review.
-
The guinea pig as a relevant preclinical model in the rat race for a vaccine against congenital cytomegalovirus infection.Virology. 2025 Sep;610:110560. doi: 10.1016/j.virol.2025.110560. Epub 2025 May 6. Virology. 2025. PMID: 40413831 Review.
-
Vaccination with a Live Attenuated Cytomegalovirus Devoid of a Protein Kinase R Inhibitory Gene Results in Reduced Maternal Viremia and Improved Pregnancy Outcome in a Guinea Pig Congenital Infection Model.J Virol. 2015 Oct;89(19):9727-38. doi: 10.1128/JVI.01419-15. Epub 2015 Jul 15. J Virol. 2015. PMID: 26178990 Free PMC article.
Cited by
-
Recent Approaches and Strategies in the Generation of Anti-human Cytomegalovirus Vaccines.Methods Mol Biol. 2021;2244:403-463. doi: 10.1007/978-1-0716-1111-1_19. Methods Mol Biol. 2021. PMID: 33555597
-
Human cytomegalovirus manipulation of latently infected cells.Viruses. 2013 Nov 21;5(11):2803-24. doi: 10.3390/v5112803. Viruses. 2013. PMID: 24284875 Free PMC article. Review.
-
An Attenuated CMV Vaccine with a Deletion in Tegument Protein GP83 (pp65 Homolog) Protects against Placental Infection and Improves Pregnancy Outcome in a Guinea Pig Challenge Model.Future Virol. 2013 Dec 1;8(12):1151-1160. doi: 10.2217/fvl.13.107. Future Virol. 2013. PMID: 24465269 Free PMC article.
-
Complete genome sequence of cell culture-attenuated Guinea pig cytomegalovirus cloned as an infectious bacterial artificial chromosome.Genome Announc. 2014 Oct 16;2(5):e00928-14. doi: 10.1128/genomeA.00928-14. Genome Announc. 2014. PMID: 25323707 Free PMC article.
-
Listeria monocytogenes traffics from maternal organs to the placenta and back.PLoS Pathog. 2006 Jun;2(6):e66. doi: 10.1371/journal.ppat.0020066. PLoS Pathog. 2006. PMID: 16846254 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical