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MERS-CoV

MERS-CoV

and

en

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Middle East respiratory syndrome coronavirus (MERS-CoV) is an emerging zoonotic coronavirus. First identified in 2012, MERS-CoV has caused over 2460 infections and a fatality rate of about 35% in humans. Similar to severe acute respiratory syndrome coronavirus (SARS-CoV), MERS-CoV likely originated from bats; however, different from SARS-CoV, which potentially utilized palm civets as its intermediate hosts, MERS-CoV likely transmits to humans through dromedary camels. Animal models, such as humanized mice and nonhuman primates, have been developed for studying MERS-CoV infection. Currently, there are no vaccines and therapeutics approved for the prevention and treatment of MERS-CoV infection, although a number of them have been developed preclinically or tested clinically. This book covers one editorial and 16 articles (including seven review articles and nine original research papers) written by researchers working in the field of MERS-CoV. It describes the following three main aspects: (1) MERS-CoV epidemiology, transmission, and pathogenesis; (2) current progress on MERS-CoV animal models, vaccines, and therapeutics; and (3) challenges and future prospects for MERS-CoV research. Overall, this book will help researchers in the MERS-CoV field to further advance their work on the virus. It also has important implications for other coronaviruses as well as viruses outside the coronavirus family with pandemic potentials.

This book is included in DOAB.

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Keywords

  • animal model
  • Animal Models
  • authentic virus
  • camels
  • cell–cell fusion
  • combination
  • complement
  • Coronavirus
  • coronavirus spike glycoprotein
  • Coronaviruses
  • correlates of immunity
  • cross-neutralization
  • DPP4
  • drivers
  • fusion inhibitor
  • HCoV-229E
  • hDPP4
  • HKU4
  • host factors
  • Inflammation
  • lipidomics
  • mechanism of action
  • MERS-coronavirus
  • MERS-CoV
  • MERS-CoV nucleocapsid protein
  • Middle East respiratory syndrome coronavirus
  • Middle East Respiratory Syndrome Virus
  • mouse model
  • murine CD8+ T cell epitope
  • Mutation
  • MVA vaccine
  • n/a
  • nanobodies
  • neutralizing antibody
  • neutralizing monoclonal antibodies
  • One Health
  • Pathogenesis
  • peptide
  • Prevention and treatment
  • pseudotyped virus
  • pyroptosis
  • Qatar
  • Rabbits
  • RBD
  • receptor-binding domain
  • SARS-CoV
  • severe acute respiratory syndrome coronavirus
  • small-molecule inhibitor
  • spike protein
  • spike proteins
  • therapeutic antibodies
  • Therapeutics
  • Transmission
  • UHPLC–MS
  • vaccine platforms
  • Vaccines

Links

DOI: 10.3390/books978-3-03921-851-6

Editions

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