TY - JOUR
T1 - The human papillomavirus 16 E5 gene potentiates MmuPV1-Dependent pathogenesis
AU - Torres, Alexandra D.
AU - Spurgeon, Megan E.
AU - Bilger, Andrea
AU - Blaine-Sauer, Simon
AU - Uberoi, Aayushi
AU - Buehler, Darya
AU - McGregor, Stephanie M.
AU - Ward-Shaw, Ella
AU - Lambert, Paul F.
N1 - Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2020/2
Y1 - 2020/2
N2 - The papillomavirus E5 gene contributes to transformation and tumorigenesis; however, its exact function in these processes and viral pathogenesis is unclear. While E5 is present in high-risk mucosotropic HPVs that cause anogenital and head and neck cancers, it is absent in cutaneous HPVs and the recently discovered mouse papillomavirus (MmuPV1), which causes papillomas and squamous cell carcinomas of the skin and mucosal epithelia in laboratory mice. We infected K14E5 transgenic mice, which express the high-risk mucosotropic HPV16 E5 gene in stratified epithelia, with MmuPV1 to investigate the effects of E5 on papillomavirus-induced pathogenesis. Skin lesions in MmuPV1-infected K14E5 mice had earlier onset, higher incidence, and reduced frequency of spontaneous regression compared to those in non-transgenic mice. K14E5 mice were also more susceptible to cervicovaginal cancers when infected with MmuPV1 and treated with estrogen compared to non-transgenic mice. Our studies support the hypothesis that E5 contributes to papillomavirus-induced pathogenesis.
AB - The papillomavirus E5 gene contributes to transformation and tumorigenesis; however, its exact function in these processes and viral pathogenesis is unclear. While E5 is present in high-risk mucosotropic HPVs that cause anogenital and head and neck cancers, it is absent in cutaneous HPVs and the recently discovered mouse papillomavirus (MmuPV1), which causes papillomas and squamous cell carcinomas of the skin and mucosal epithelia in laboratory mice. We infected K14E5 transgenic mice, which express the high-risk mucosotropic HPV16 E5 gene in stratified epithelia, with MmuPV1 to investigate the effects of E5 on papillomavirus-induced pathogenesis. Skin lesions in MmuPV1-infected K14E5 mice had earlier onset, higher incidence, and reduced frequency of spontaneous regression compared to those in non-transgenic mice. K14E5 mice were also more susceptible to cervicovaginal cancers when infected with MmuPV1 and treated with estrogen compared to non-transgenic mice. Our studies support the hypothesis that E5 contributes to papillomavirus-induced pathogenesis.
KW - E5
KW - Human papillomavirus
KW - Mouse papillomavirus
KW - Oncogene
KW - Pathogenesis
UR - http://www.scopus.com/inward/record.url?scp=85075949716&partnerID=8YFLogxK
U2 - 10.1016/j.virol.2019.12.002
DO - 10.1016/j.virol.2019.12.002
M3 - Article
C2 - 31826841
AN - SCOPUS:85075949716
SN - 0042-6822
VL - 541
SP - 1
EP - 12
JO - Virology
JF - Virology
ER -