TY - JOUR T1 - Prediction of non-canonical routes for SARS-CoV-2 infection in human placenta cells JF - bioRxiv DO - 10.1101/2020.06.12.148411 SP - 2020.06.12.148411 AU - F. B. Constantino AU - S. S. Cury AU - C. R. Nogueira AU - R. F. Carvalho AU - L. A. Justulin Y1 - 2020/01/01 UR - http://biorxiv.org/content/early/2020/06/12/2020.06.12.148411.abstract N2 - The SARS-CoV-2 is the causative agent of the COVID-19 pandemic. The data available about COVID-19 during pregnancy have demonstrated placental infection; however, the intrauterine transmission of SARS-CoV-2 is still debated. Intriguingly, while canonical SARS-CoV-2 cell entry mediators are expressed at low levels in placental cells, the receptors for viruses that cause congenital infections such as the cytomegalovirus and Zika virus are highly expressed in these cells. Here we analyzed the transcriptional profile (microarray and single-cell RNA-Seq) of proteins potentially interacting with coronaviruses to identify non-canonical mediators of SARS-CoV-2 infection and replication in the placenta. We show that, despite low levels of the canonical cell entry mediators ACE2 and TMPRSS2, villous trophoblast cells co-express high levels of the potential non-canonical cell-entry mediators DPP4 and CTSL. We also found changes in the expression of DAAM1 and PAICS genes during pregnancy, which are translated into proteins also predicted to interact with coronaviruses proteins. These results provide new insight into the interaction between SARS-CoV-2 and host proteins that may act as non-canonical routes for SARS-CoV-2 infection and replication in the placenta cells.Competing Interest StatementThe authors have declared no competing interest. ER -