Human Papillomavirus E6/E7 Expression in Preeclampsia-Affected Placentae.
Ashley L Reily-BellAmanda FisherBryony HarrisonSara BowieSankalita RayMary HawkesLyn M WiseRyuji FukuzawaErin C MacaulayCelia J DevenishNoelyn A HungTania L SlatterPublished in: Pathogens (Basel, Switzerland) (2020)
Whether HPV is causative of pregnancy complications is uncertain. E6 and E7 affect functions underling preeclampsia (PET) in cultured trophoblasts, but whether E6 and E7 is produced in the placenta is uncertain. Here, we investigated whether E6/E7 was expressed in the placentae from pregnancies with PET, other pregnancy complications (fetal growth restriction (FGR) and diabetes mellitus), and uncomplicated pregnancies. Placental tissues collected from two geographical locations were subjected to RNAscope analyses of high- and low- risk E6/E7, and individual HPV types identified using an HPV array. High-risk E6/E7 expression was increased in both PET cohorts, (81% and 86% of patients positive for high-risk HPV DNA compared to 13% of control patients). Various HPV types were identified. Although HPV 18 was the most frequent in all cohorts, the majority of individuals had multiple HPV types (55% of the PET compared to 25% of the control cohort). Further evidence that E6 and E7 is present early when placental pathology underlying preeclampsia is established, is provided with the finding of high-risk E6/E7 in the first-trimester placenta anchoring trophoblast. In conclusion, E6/E7 expression and multiple HPV types were frequent in placentae from preeclampsia-complicated pregnancies.
Keyphrases
- high grade
- pregnancy outcomes
- preterm birth
- end stage renal disease
- poor prognosis
- early onset
- cervical cancer screening
- computed tomography
- pet ct
- ejection fraction
- newly diagnosed
- positron emission tomography
- gene expression
- peritoneal dialysis
- pet imaging
- prognostic factors
- binding protein
- pregnant women
- endothelial cells
- patient reported outcomes
- single molecule
- high resolution
- weight loss
- circulating tumor cells