Middle East respiratory syndrome coronavirus (MERS-CoV) entry inhibitors targeting spike protein

Virus Res. 2014 Dec 19:194:200-10. doi: 10.1016/j.virusres.2014.10.007. Epub 2014 Oct 14.

Abstract

The recent outbreak of Middle East respiratory syndrome (MERS) coronavirus (MERS-CoV) infection has led to more than 800 laboratory-confirmed MERS cases with a high case fatality rate (∼35%), posing a serious threat to global public health and calling for the development of effective and safe therapeutic and prophylactic strategies to treat and prevent MERS-CoV infection. Here we discuss the most recent studies on the structure of the MERS-CoV spike protein and its role in virus binding and entry, and the development of MERS-CoV entry/fusion inhibitors targeting the S1 subunit, particularly the receptor-binding domain (RBD), and the S2 subunit, especially the HR1 region, of the MERS-CoV spike protein. We then look ahead to future applications of these viral entry/fusion inhibitors, either alone or in combination with specific and nonspecific MERS-CoV replication inhibitors, for the treatment and prevention of MERS-CoV infection.

Keywords: Entry inhibitor; Fusion inhibitor; MERS-CoV; Middle East respiratory syndrome coronavirus; Receptor-binding domain; Six-helix bundle.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use
  • Coronavirus Infections / drug therapy
  • Humans
  • Middle East Respiratory Syndrome Coronavirus / drug effects*
  • Middle East Respiratory Syndrome Coronavirus / physiology*
  • Spike Glycoprotein, Coronavirus / antagonists & inhibitors*
  • Virus Attachment / drug effects*
  • Virus Internalization / drug effects*

Substances

  • Antiviral Agents
  • Spike Glycoprotein, Coronavirus