Key result
Infection with a pentameric complex-deleted rhesus cytomegalovirus resulted in similar transplacental transmission rates compared to a PC-intact virus, indicating the complex is not required for congenital transmission.
Why the study?
Congenital cytomegalovirus is the leading infectious cause of neonatal neurological impairment, but the essential virological determinants of transplacental transmission, including the role of the pentameric complex, remain unclear.
Does deletion of the viral pentameric complex prevent transplacental CMV transmission in seronegative pregnant rhesus macaques?
Does deletion of the viral pentameric complex prevent transplacental CMV transmission in seronegative pregnant rhesus macaques?
The viral pentameric complex is not required for transplacental CMV transmission in a rhesus macaque model, suggesting that targeting the PC alone may be insufficient for vaccines aiming to prevent congenital CMV.
PC remains a candidate vaccine target in cCMV; leaves open key virological determinants of transplacental transmission.
Congenital cytomegalovirus (cCMV) infection is the leading infectious cause of neonatal neurological impairment but essential virological determinants of transplacental CMV transmission remain unclear. The pentameric complex (PC), composed of five subunits, glycoproteins H (gH), gL, UL128, UL130, and UL131A, is essential for efficient entry into non-fibroblast cells in vitro . Based on this role in cell tropism, the PC is considered a possible target for CMV vaccines and immunotherapies to prevent cCMV. To determine the role of the PC in transplacental CMV transmission in a non-human primate model of cCMV, we constructed a PC-deficient rhesus CMV (RhCMV) by deleting the homologues of the HCMV PC subunits UL128 and UL130 and compared congenital transmission to PC-intact RhCMV in CD4+ T cell-depleted or immunocompetent RhCMV-seronegative, pregnant rhesus macaques (RM). Surprisingly, we found that the transplacental transmission rate was similar for PC-intact and PC-deleted RhCMV based on viral genomic DNA detection in amniotic fluid. Moreover, PC-deleted and PC-intact RhCMV acute infection led to similar peak maternal plasma viremia. However, there was less viral shedding in maternal urine and saliva and less viral dissemination in fetal tissues in the PC-deleted group. As expected, dams inoculated with PC-deleted RhCMV demonstrated lower plasma IgG binding to PC-intact RhCMV virions and soluble PC, as well as reduced neutralization of PC-dependent entry of the PC-intact RhCMV isolate UCD52 into epithelial cells. In contrast, binding to gH expressed on the cell surface and neutralization of entry into fibroblasts by the PC-intact RhCMV was higher for dams infected with PC-deleted RhCMV compared to those infected with PC-intact RhCMV. Our data demonstrates that the PC is dispensable for transplacental CMV infection in our non-human primate model. One Sentence Summary Congenital CMV transmission frequency in seronegative rhesus macaques is not affected by the deletion of the viral pentameric complex.
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Wang et al. (2023) studied Congenital cytomegalovirus (cCMV) infection (n=18). PC-deleted rhesus cytomegalovirus (RhCMV) vs. PC-intact RhCMV was evaluated on Transplacental transmission rate (detection of viral genomic DNA in amniotic fluid or fetal tissues). Infection with a pentameric complex-deleted rhesus cytomegalovirus resulted in similar transplacental transmission rates compared to a PC-intact virus, indicating the complex is not required for congenital transmission.
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