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Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins

Middle East respiratory syndrome (MERS) is a viral respiratory disease caused by a de novo coronavirus—MERS-CoV—that is associated with high mortality. However, the mechanism by which MERS-CoV infects humans remains unclear. To date, there is no effective vaccine or antibody for human immunity and t...

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Autores principales: Li, Yan-Hua, Hu, Chen-Yu, Wu, Nan-Ping, Yao, Hang-Ping, Li, Lan-Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7104727/
https://www.ncbi.nlm.nih.gov/pubmed/32288963
http://dx.doi.org/10.1016/j.eng.2018.11.035
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author Li, Yan-Hua
Hu, Chen-Yu
Wu, Nan-Ping
Yao, Hang-Ping
Li, Lan-Juan
author_facet Li, Yan-Hua
Hu, Chen-Yu
Wu, Nan-Ping
Yao, Hang-Ping
Li, Lan-Juan
author_sort Li, Yan-Hua
collection PubMed
description Middle East respiratory syndrome (MERS) is a viral respiratory disease caused by a de novo coronavirus—MERS-CoV—that is associated with high mortality. However, the mechanism by which MERS-CoV infects humans remains unclear. To date, there is no effective vaccine or antibody for human immunity and treatment, other than the safety and tolerability of the fully human polyclonal Immunoglobulin G (IgG) antibody (SAB-301) as a putative therapeutic agent specific for MERS. Although rapid diagnostic and public health measures are currently being implemented, new cases of MERS-CoV infection are still being reported. Therefore, various effective measures should be taken to prevent the serious impact of similar epidemics in the future. Further investigation of the epidemiology and pathogenesis of the virus, as well as the development of effective therapeutic and prophylactic anti-MERS-CoV infections, is necessary. For this purpose, detailed information on MERS-CoV proteins is needed. In this review, we describe the major structural and nonstructural proteins of MERS-CoV and summarize different potential strategies for limiting the outbreak of MERS-CoV. The combination of computational biology and virology can accelerate the advanced design and development of effective peptide therapeutics against MERS-CoV. In summary, this review provides important information about the progress of the elimination of MERS, from prevention to treatment.
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spelling pubmed-71047272020-03-31 Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins Li, Yan-Hua Hu, Chen-Yu Wu, Nan-Ping Yao, Hang-Ping Li, Lan-Juan Engineering (Beijing) Research Medicine—Review Middle East respiratory syndrome (MERS) is a viral respiratory disease caused by a de novo coronavirus—MERS-CoV—that is associated with high mortality. However, the mechanism by which MERS-CoV infects humans remains unclear. To date, there is no effective vaccine or antibody for human immunity and treatment, other than the safety and tolerability of the fully human polyclonal Immunoglobulin G (IgG) antibody (SAB-301) as a putative therapeutic agent specific for MERS. Although rapid diagnostic and public health measures are currently being implemented, new cases of MERS-CoV infection are still being reported. Therefore, various effective measures should be taken to prevent the serious impact of similar epidemics in the future. Further investigation of the epidemiology and pathogenesis of the virus, as well as the development of effective therapeutic and prophylactic anti-MERS-CoV infections, is necessary. For this purpose, detailed information on MERS-CoV proteins is needed. In this review, we describe the major structural and nonstructural proteins of MERS-CoV and summarize different potential strategies for limiting the outbreak of MERS-CoV. The combination of computational biology and virology can accelerate the advanced design and development of effective peptide therapeutics against MERS-CoV. In summary, this review provides important information about the progress of the elimination of MERS, from prevention to treatment. THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company. 2019-10 2019-07-17 /pmc/articles/PMC7104727/ /pubmed/32288963 http://dx.doi.org/10.1016/j.eng.2018.11.035 Text en © 2019 THE AUTHORS Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Research Medicine—Review
Li, Yan-Hua
Hu, Chen-Yu
Wu, Nan-Ping
Yao, Hang-Ping
Li, Lan-Juan
Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title_full Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title_fullStr Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title_full_unstemmed Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title_short Molecular Characteristics, Functions, and Related Pathogenicity of MERS-CoV Proteins
title_sort molecular characteristics, functions, and related pathogenicity of mers-cov proteins
topic Research Medicine—Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7104727/
https://www.ncbi.nlm.nih.gov/pubmed/32288963
http://dx.doi.org/10.1016/j.eng.2018.11.035
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