Title Genetic deficiency and polymorphisms of cyclophilin A reveal its essential role for Human Coronavirus 229E replication.
Author von Brunn, Albrecht; Ciesek, Sandra; von Brunn, Brigitte; Carbajo-Lozoya, Javier
Journal Curr Opin Virol Publication Year/Month 2015-Oct
PMID 26318518 PMCID PMC7102849
Affiliation + expend 1.Max-von-Pettenkofer Institute, Ludwig-Maximilians-Universitat, Munchen, Germany; German Center for Infection Research (DZIF), Germany. Electronic address: vonbrunn@mvp.uni-muenchen.de.

Replication of coronaviruses is inhibited in vitro by cyclosporin A, a well-known immunosuppressive drug which binds to cellular cyclophilins thus inactivating their enzymatic cis-trans peptidyl-prolyl isomerase function. Latter is required for proper folding of cellular proteins and of proteins of several viruses. Here, we summarize present knowledge on the role of cyclophilin A during coronavirus replication. We present data on the effect of cyclophilin A single nucleotide polymorphism mutants on the replication of human CoV-229E demonstrating the requirement of proper cyclophilin A function for virus propagation. Results define cellular cyclophilin A as a host target for inhibition of coronaviruses ranging from relatively mild common cold to highly pathogenic SARS-CoV and MERS-CoV viruses with the perspective of disclosing non-immunosuppressive cyclosporin A analogs to broadly inactivate the coronavirus family.

  • Copyright © 2023
    National Institute of Pathogen Biology, CAMS & PUMC, Bejing, China
    All rights reserved.