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Published on: July 6, 2013
Intrauterine cytomegalovirus infection and glycoprotein B genotypes
J F Bale1, J R Murph, G J Demmler
1Division of Pediatric Neurology, Primary Children's Medical Center, Salt Lake City, UT 84113, USA. pcjbale@ihc.com
Abstract:
Cytomegalovirus (CMV) strains display polymorphisms for the gene encoding glycoprotein B (gB; gpUL55). Recent data suggest that the gB genotype may influence the outcome of acquired CMV infections. To determine whether the gB genotype also contributes to the outcome of intrauterine infection, CMV strains were studied from 56 infants with culture-confirmed intrauterine CMV infections who were born in Iowa or Texas. CMV gB genotypes were compared with the neonatal clinical features and neurodevelopmental outcomes. Fifty-three strains (95%) could be assigned a gB genotype. The overall distribution of genotypes was as follows: type 1, 50%; type 2, 18%; type 3, 23%; and type 4, 4%. Strains with the gB 3 genotype were more common among the Iowa infants (P=.082). The gB 3 genotype was more common among infants with asymptomatic infections (P=.004), but geographic location and ascertainment biases may have accounted for these differences. The gB genotypes did not correlate with the neurodevelopmental outcome of intrauterine infection.
Insights
Cytomegalovirus (CMV) glycoprotein B (gB) genotypes were analyzed in infants with intrauterine infections. The gB 3 genotype was more frequent in asymptomatic cases, but did not impact neurodevelopmental outcomes.
Area of Science:
- Virology
- Genetics
- Neonatal Medicine
Background:
- Cytomegalovirus (CMV) strains exhibit genetic variations in glycoprotein B (gB; gpUL55).
- Emerging evidence suggests a link between gB genotype and acquired CMV infection outcomes.
- The role of gB genotype in intrauterine CMV infection outcomes requires further investigation.
Purpose of the Study:
- To investigate the association between Cytomegalovirus (CMV) glycoprotein B (gB) genotypes and clinical/neurodevelopmental outcomes in infants with intrauterine CMV infections.
Main Methods:
- Analysis of CMV strains from 56 infants with culture-confirmed intrauterine CMV infections.
- Genotyping of the CMV gB gene (gpUL55) for 53 strains.
- Comparison of gB genotypes with neonatal clinical features and neurodevelopmental assessments.
Main Results:
- Fifty-three (95%) CMV strains were successfully genotyped.
- Prevalent gB genotypes included type 1 (50%), type 3 (23%), type 2 (18%), and type 4 (4%).
- The gB 3 genotype was more common in asymptomatic infants (P=.004), though geographic factors may play a role.
- No significant correlation was found between gB genotypes and neurodevelopmental outcomes.
Conclusions:
- CMV gB genotype distribution varies among infants with intrauterine infections.
- The gB 3 genotype may be associated with asymptomatic intrauterine CMV infections.
- CMV gB genotype does not appear to influence the neurodevelopmental outcome of intrauterine CMV infection.
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