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Evaluation of Serologic and Antigenic Relationships Between Middle Eastern Respiratory Syndrome Coronavirus and Other Coronaviruses to Develop Vaccine Platforms for the Rapid Response to Emerging Coronaviruses

Identifieur interne : 001F95 ( Main/Exploration ); précédent : 001F94; suivant : 001F96

Evaluation of Serologic and Antigenic Relationships Between Middle Eastern Respiratory Syndrome Coronavirus and Other Coronaviruses to Develop Vaccine Platforms for the Rapid Response to Emerging Coronaviruses

Auteurs : Sudhakar Agnihothram ; Robin Gopal [Royaume-Uni] ; Boyd L. Yount ; Eric F. Donaldson ; Vineet D. Menachery ; Rachel L. Graham ; Trevor D. Scobey ; Lisa E. Gralinski ; Mark R. Denison [États-Unis] ; Maria Zambon [Royaume-Uni] ; Ralph S. Baric

Source :

RBID : PMC:3952667

Descripteurs français

English descriptors

Abstract

Abstract

Background. Middle East respiratory syndrome coronavirus (MERS-CoV) emerged in 2012, causing severe acute respiratory disease and pneumonia, with 44% mortality among 136 cases to date. Design of vaccines to limit the virus spread or diagnostic tests to track newly emerging strains requires knowledge of antigenic and serologic relationships between MERS-CoV and other CoVs.

Methods. Using synthetic genomics and Venezuelan equine encephalitis virus replicons (VRPs) expressing spike and nucleocapsid proteins from MERS-CoV and other human and bat CoVs, we characterize the antigenic responses (using Western blot and enzyme-linked immunosorbent assay) and serologic responses (using neutralization assays) against 2 MERS-CoV isolates in comparison with those of other human and bat CoVs.

Results. Serologic and neutralization responses against the spike glycoprotein were primarily strain specific, with a very low level of cross-reactivity within or across subgroups. CoV N proteins within but not across subgroups share cross-reactive epitopes with MERS-CoV isolates. Our findings were validated using a convalescent-phase serum specimen from a patient infected with MERS-CoV (NA 01) and human antiserum against SARS-CoV, human CoV NL63, and human CoV OC43.

Conclusions. Vaccine design for emerging CoVs should involve chimeric spike protein containing neutralizing epitopes from multiple virus strains across subgroups to reduce immune pathology, and a diagnostic platform should include a panel of nucleocapsid and spike proteins from phylogenetically distinct CoVs.


Url:
DOI: 10.1093/infdis/jit609
PubMed: 24253287
PubMed Central: 3952667


Affiliations:


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Le document en format XML

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<name sortKey="Agnihothram, Sudhakar" sort="Agnihothram, Sudhakar" uniqKey="Agnihothram S" first="Sudhakar" last="Agnihothram">Sudhakar Agnihothram</name>
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<name sortKey="Gopal, Robin" sort="Gopal, Robin" uniqKey="Gopal R" first="Robin" last="Gopal">Robin Gopal</name>
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<nlm:aff id="af4">
<addr-line>Viral Zoonosis Unit</addr-line>
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,
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<name sortKey="Donaldson, Eric F" sort="Donaldson, Eric F" uniqKey="Donaldson E" first="Eric F." last="Donaldson">Eric F. Donaldson</name>
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<nlm:aff id="af2">
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,
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,
<addr-line>Chapel Hill</addr-line>
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<name sortKey="Menachery, Vineet D" sort="Menachery, Vineet D" uniqKey="Menachery V" first="Vineet D." last="Menachery">Vineet D. Menachery</name>
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<nlm:aff id="af1">
<addr-line>Department of Epidemiology</addr-line>
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<affiliation>
<nlm:aff id="af2">
<addr-line>Department of Microbiology and Immunology</addr-line>
,
<institution>University of North Carolina</institution>
,
<addr-line>Chapel Hill</addr-line>
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<name sortKey="Graham, Rachel L" sort="Graham, Rachel L" uniqKey="Graham R" first="Rachel L." last="Graham">Rachel L. Graham</name>
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<nlm:aff id="af1">
<addr-line>Department of Epidemiology</addr-line>
</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="af2">
<addr-line>Department of Microbiology and Immunology</addr-line>
,
<institution>University of North Carolina</institution>
,
<addr-line>Chapel Hill</addr-line>
</nlm:aff>
</affiliation>
</author>
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<name sortKey="Scobey, Trevor D" sort="Scobey, Trevor D" uniqKey="Scobey T" first="Trevor D." last="Scobey">Trevor D. Scobey</name>
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<nlm:aff id="af1">
<addr-line>Department of Epidemiology</addr-line>
</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="af2">
<addr-line>Department of Microbiology and Immunology</addr-line>
,
<institution>University of North Carolina</institution>
,
<addr-line>Chapel Hill</addr-line>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Gralinski, Lisa E" sort="Gralinski, Lisa E" uniqKey="Gralinski L" first="Lisa E." last="Gralinski">Lisa E. Gralinski</name>
<affiliation>
<nlm:aff id="af1">
<addr-line>Department of Epidemiology</addr-line>
</nlm:aff>
</affiliation>
<affiliation>
<nlm:aff id="af2">
<addr-line>Department of Microbiology and Immunology</addr-line>
,
<institution>University of North Carolina</institution>
,
<addr-line>Chapel Hill</addr-line>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Denison, Mark R" sort="Denison, Mark R" uniqKey="Denison M" first="Mark R." last="Denison">Mark R. Denison</name>
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<nlm:aff id="af3">
<addr-line>Departments of Pediatrics and Microbiology and Immunology</addr-line>
,
<institution>Vanderbilt University</institution>
,
<addr-line>Nashville, Tennessee</addr-line>
</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Tennessee</region>
</placeName>
<wicri:cityArea>Nashville</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Zambon, Maria" sort="Zambon, Maria" uniqKey="Zambon M" first="Maria" last="Zambon">Maria Zambon</name>
<affiliation wicri:level="1">
<nlm:aff id="af4">
<addr-line>Viral Zoonosis Unit</addr-line>
,
<institution>Public Health of England</institution>
,
<addr-line>London</addr-line>
,
<country>United Kingdom</country>
</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea># see nlm:aff country strict</wicri:regionArea>
</affiliation>
</author>
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<name sortKey="Baric, Ralph S" sort="Baric, Ralph S" uniqKey="Baric R" first="Ralph S." last="Baric">Ralph S. Baric</name>
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<nlm:aff id="af1">
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</nlm:aff>
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<nlm:aff id="af2">
<addr-line>Department of Microbiology and Immunology</addr-line>
,
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,
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<title level="j">The Journal of Infectious Diseases</title>
<idno type="ISSN">0022-1899</idno>
<idno type="eISSN">1537-6613</idno>
<imprint>
<date when="2013">2013</date>
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<term>Animals</term>
<term>Antibodies, Viral (blood)</term>
<term>Antigens, Viral (immunology)</term>
<term>Blotting, Western</term>
<term>Chiroptera</term>
<term>Coronaviridae (immunology)</term>
<term>Coronaviridae (isolation & purification)</term>
<term>Cross Reactions</term>
<term>Enzyme-Linked Immunosorbent Assay</term>
<term>Humans</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Middle Aged</term>
<term>Neutralization Tests</term>
<term>Nucleocapsid Proteins (immunology)</term>
<term>Spike Glycoprotein, Coronavirus (immunology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Animaux</term>
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<term>Antigènes viraux (immunologie)</term>
<term>Chiroptera</term>
<term>Coronaviridae (immunologie)</term>
<term>Coronaviridae (isolement et purification)</term>
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<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Technique de Western</term>
<term>Test ELISA</term>
<term>Tests de neutralisation</term>
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<term>Antibodies, Viral</term>
</keywords>
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<term>Antigens, Viral</term>
<term>Nucleocapsid Proteins</term>
<term>Spike Glycoprotein, Coronavirus</term>
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<term>Antigènes viraux</term>
<term>Coronaviridae</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Protéines nucléocapside</term>
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<term>Coronaviridae</term>
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<term>Coronaviridae</term>
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<term>Coronaviridae</term>
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<term>Anticorps antiviraux</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Blotting, Western</term>
<term>Chiroptera</term>
<term>Cross Reactions</term>
<term>Enzyme-Linked Immunosorbent Assay</term>
<term>Humans</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Middle Aged</term>
<term>Neutralization Tests</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Animaux</term>
<term>Chiroptera</term>
<term>Humains</term>
<term>Réactions croisées</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Technique de Western</term>
<term>Test ELISA</term>
<term>Tests de neutralisation</term>
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<front>
<div type="abstract" xml:lang="en">
<title>Abstract</title>
<p>
<bold>
<italic>Background.</italic>
</bold>
 Middle East respiratory syndrome coronavirus (MERS-CoV) emerged in 2012, causing severe acute respiratory disease and pneumonia, with 44% mortality among 136 cases to date. Design of vaccines to limit the virus spread or diagnostic tests to track newly emerging strains requires knowledge of antigenic and serologic relationships between MERS-CoV and other CoVs.</p>
<p>
<bold>
<italic>Methods.</italic>
</bold>
 Using synthetic genomics and Venezuelan equine encephalitis virus replicons (VRPs) expressing spike and nucleocapsid proteins from MERS-CoV and other human and bat CoVs, we characterize the antigenic responses (using Western blot and enzyme-linked immunosorbent assay) and serologic responses (using neutralization assays) against 2 MERS-CoV isolates in comparison with those of other human and bat CoVs.</p>
<p>
<bold>
<italic>Results.</italic>
</bold>
 Serologic and neutralization responses against the spike glycoprotein were primarily strain specific, with a very low level of cross-reactivity within or across subgroups. CoV N proteins within but not across subgroups share cross-reactive epitopes with MERS-CoV isolates. Our findings were validated using a convalescent-phase serum specimen from a patient infected with MERS-CoV (NA 01) and human antiserum against SARS-CoV, human CoV NL63, and human CoV OC43.</p>
<p>
<bold>
<italic>Conclusions.</italic>
</bold>
 Vaccine design for emerging CoVs should involve chimeric spike protein containing neutralizing epitopes from multiple virus strains across subgroups to reduce immune pathology, and a diagnostic platform should include a panel of nucleocapsid and spike proteins from phylogenetically distinct CoVs.</p>
</div>
</front>
<back>
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<name sortKey="Graham, Rl" uniqKey="Graham R">RL Graham</name>
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<name sortKey="Baric, Rs" uniqKey="Baric R">RS Baric</name>
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<name sortKey="Masters, Ps" uniqKey="Masters P">PS Masters</name>
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<author>
<name sortKey="Pyrc, K" uniqKey="Pyrc K">K Pyrc</name>
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<author>
<name sortKey="Sims, Ac" uniqKey="Sims A">AC Sims</name>
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<name sortKey="Dijkman, R" uniqKey="Dijkman R">R Dijkman</name>
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<name sortKey="Van Der Hoek, L" uniqKey="Van Der Hoek L">L van der Hoek</name>
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<name sortKey="Pyrc, K" uniqKey="Pyrc K">K Pyrc</name>
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