Serveur d'exploration MERS

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Detection of MERS-CoV antigen on formalin-fixed paraffin-embedded nasal tissue of alpacas by immunohistochemistry using human monoclonal antibodies directed against different epitopes of the spike protein

Identifieur interne : 000740 ( Pmc/Curation ); précédent : 000739; suivant : 000741

Detection of MERS-CoV antigen on formalin-fixed paraffin-embedded nasal tissue of alpacas by immunohistochemistry using human monoclonal antibodies directed against different epitopes of the spike protein

Auteurs : Ann-Kathrin Haverkamp [Allemagne] ; Berend J. Bosch [Pays-Bas] ; Ingo Spitzbarth [Allemagne] ; Annika Lehmbecker [Allemagne] ; Nigeer Te [Espagne] ; Albert Bensaid [Espagne] ; Joaquim Segalés [Espagne] ; Wolfgang Baumg Rtner [Allemagne]

Source :

RBID : PMC:7112921

Abstract

Middle East respiratory syndrome (MERS) represents an important respiratory disease accompanied by lethal outcome in one third of human patients. In recent years, several investigators developed protective antibodies which could be used as prophylaxis in prospective human epidemics. In the current study, eight human monoclonal antibodies (mAbs) with neutralizing and non-neutralizing capabilities, directed against different epitopes of the MERS-coronavirus (MERS-CoV) spike (MERS-S) protein, were investigated with regard to their ability to immunohistochemically detect respective epitopes on formalin-fixed paraffin-embedded (FFPE) nasal tissue sections of MERS-CoV experimentally infected alpacas. The most intense immunoreaction was detected using a neutralizing antibody directed against the receptor binding domain S1B of the MERS-S protein, which produced an immunosignal in the cytoplasm of ciliated respiratory epithelium and along the apical membranous region. A similar staining was obtained by two other mAbs which recognize the sialic acid-binding domain and the ectodomain of the membrane fusion subunit S2, respectively. Five mAbs lacked immunoreactivity for MERS-CoV antigen on FFPE tissue, even though they belong, at least in part, to the same epitope group. In summary, three tested human mAbs demonstrated capacity for detection of MERS-CoV antigen on FFPE samples and may be implemented in double or triple immunohistochemical methods.


Url:
DOI: 10.1016/j.vetimm.2019.109939
PubMed: 31526954
PubMed Central: 7112921

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PMC:7112921

Le document en format XML

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<p>Middle East respiratory syndrome (MERS) represents an important respiratory disease accompanied by lethal outcome in one third of human patients. In recent years, several investigators developed protective antibodies which could be used as prophylaxis in prospective human epidemics. In the current study, eight human monoclonal antibodies (mAbs) with neutralizing and non-neutralizing capabilities, directed against different epitopes of the MERS-coronavirus (MERS-CoV) spike (MERS-S) protein, were investigated with regard to their ability to immunohistochemically detect respective epitopes on formalin-fixed paraffin-embedded (FFPE) nasal tissue sections of MERS-CoV experimentally infected alpacas. The most intense immunoreaction was detected using a neutralizing antibody directed against the receptor binding domain S1B of the MERS-S protein, which produced an immunosignal in the cytoplasm of ciliated respiratory epithelium and along the apical membranous region. A similar staining was obtained by two other mAbs which recognize the sialic acid-binding domain and the ectodomain of the membrane fusion subunit S2, respectively. Five mAbs lacked immunoreactivity for MERS-CoV antigen on FFPE tissue, even though they belong, at least in part, to the same epitope group. In summary, three tested human mAbs demonstrated capacity for detection of MERS-CoV antigen on FFPE samples and may be implemented in double or triple immunohistochemical methods.</p>
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</TEI>
<pmc article-type="brief-report">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Vet Immunol Immunopathol</journal-id>
<journal-id journal-id-type="iso-abbrev">Vet. Immunol. Immunopathol</journal-id>
<journal-title-group>
<journal-title>Veterinary Immunology and Immunopathology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0165-2427</issn>
<issn pub-type="epub">1873-2534</issn>
<publisher>
<publisher-name>Elsevier B.V.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">31526954</article-id>
<article-id pub-id-type="pmc">7112921</article-id>
<article-id pub-id-type="publisher-id">S0165-2427(19)30171-0</article-id>
<article-id pub-id-type="doi">10.1016/j.vetimm.2019.109939</article-id>
<article-id pub-id-type="publisher-id">109939</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Detection of MERS-CoV antigen on formalin-fixed paraffin-embedded nasal tissue of alpacas by immunohistochemistry using human monoclonal antibodies directed against different epitopes of the spike protein</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" id="aut0005">
<name>
<surname>Haverkamp</surname>
<given-names>Ann-Kathrin</given-names>
</name>
<xref rid="aff0005" ref-type="aff">a</xref>
<xref rid="fn0005" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="aut0010">
<name>
<surname>Bosch</surname>
<given-names>Berend J.</given-names>
</name>
<xref rid="aff0010" ref-type="aff">b</xref>
<xref rid="fn0005" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="aut0015">
<name>
<surname>Spitzbarth</surname>
<given-names>Ingo</given-names>
</name>
<xref rid="aff0005" ref-type="aff">a</xref>
<xref rid="aff0015" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author" id="aut0020">
<name>
<surname>Lehmbecker</surname>
<given-names>Annika</given-names>
</name>
<xref rid="aff0005" ref-type="aff">a</xref>
<xref rid="aff0015" ref-type="aff">c</xref>
</contrib>
<contrib contrib-type="author" id="aut0025">
<name>
<surname>Te</surname>
<given-names>Nigeer</given-names>
</name>
<xref rid="aff0020" ref-type="aff">d</xref>
</contrib>
<contrib contrib-type="author" id="aut0030">
<name>
<surname>Bensaid</surname>
<given-names>Albert</given-names>
</name>
<xref rid="aff0020" ref-type="aff">d</xref>
</contrib>
<contrib contrib-type="author" id="aut0035">
<name>
<surname>Segalés</surname>
<given-names>Joaquim</given-names>
</name>
<xref rid="aff0025" ref-type="aff">e</xref>
<xref rid="aff0030" ref-type="aff">f</xref>
</contrib>
<contrib contrib-type="author" id="aut0040">
<name>
<surname>Baumgärtner</surname>
<given-names>Wolfgang</given-names>
</name>
<email>Wolfgang.Baumgaertner@tiho-hannover.de</email>
<xref rid="aff0005" ref-type="aff">a</xref>
<xref rid="aff0015" ref-type="aff">c</xref>
<xref rid="cor0005" ref-type="corresp"></xref>
</contrib>
</contrib-group>
<aff id="aff0005">
<label>a</label>
Department of Pathology, University of Veterinary Medicine Hannover Foundation, 30559 Hannover, Germany</aff>
<aff id="aff0010">
<label>b</label>
Virology Division, Department of Infectious Diseases & Immunology, Faculty of Veterinary Medicine, Utrecht University, 3584 CL Utrecht, the Netherlands</aff>
<aff id="aff0015">
<label>c</label>
Center for Systems Neuroscience, 30559 Hannover, Germany</aff>
<aff id="aff0020">
<label>d</label>
IRTA, Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain</aff>
<aff id="aff0025">
<label>e</label>
Departament de Sanitat i Anatomia Animals, Facultat de Veterinària, UAB, 08193 Bellaterra, Barcelona, Spain</aff>
<aff id="aff0030">
<label>f</label>
UAB, Centre de Recerca en Sanitat Animal (CReSA, IRTA-UAB), Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain</aff>
<author-notes>
<corresp id="cor0005">
<label></label>
Corresponding author at: Department of Pathology, University of Veterinary Medicine Hannover Foundation, Bünteweg 17, 30559 Hannover, Germany.
<email>Wolfgang.Baumgaertner@tiho-hannover.de</email>
</corresp>
<fn id="fn0005">
<label>1</label>
<p id="npar0005">both authors contributed equally.</p>
</fn>
</author-notes>
<pub-date pub-type="pmc-release">
<day>9</day>
<month>9</month>
<year>2019</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub">
<month>12</month>
<year>2019</year>
</pub-date>
<pub-date pub-type="epub">
<day>9</day>
<month>9</month>
<year>2019</year>
</pub-date>
<volume>218</volume>
<fpage>109939</fpage>
<lpage>109939</lpage>
<history>
<date date-type="received">
<day>10</day>
<month>5</month>
<year>2019</year>
</date>
<date date-type="rev-recd">
<day>2</day>
<month>9</month>
<year>2019</year>
</date>
<date date-type="accepted">
<day>8</day>
<month>9</month>
<year>2019</year>
</date>
</history>
<permissions>
<copyright-statement>© 2019 Elsevier B.V. All rights reserved.</copyright-statement>
<copyright-year>2019</copyright-year>
<copyright-holder>Elsevier B.V.</copyright-holder>
<license>
<license-p>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.</license-p>
</license>
</permissions>
<abstract id="abs0005">
<p>Middle East respiratory syndrome (MERS) represents an important respiratory disease accompanied by lethal outcome in one third of human patients. In recent years, several investigators developed protective antibodies which could be used as prophylaxis in prospective human epidemics. In the current study, eight human monoclonal antibodies (mAbs) with neutralizing and non-neutralizing capabilities, directed against different epitopes of the MERS-coronavirus (MERS-CoV) spike (MERS-S) protein, were investigated with regard to their ability to immunohistochemically detect respective epitopes on formalin-fixed paraffin-embedded (FFPE) nasal tissue sections of MERS-CoV experimentally infected alpacas. The most intense immunoreaction was detected using a neutralizing antibody directed against the receptor binding domain S1B of the MERS-S protein, which produced an immunosignal in the cytoplasm of ciliated respiratory epithelium and along the apical membranous region. A similar staining was obtained by two other mAbs which recognize the sialic acid-binding domain and the ectodomain of the membrane fusion subunit S2, respectively. Five mAbs lacked immunoreactivity for MERS-CoV antigen on FFPE tissue, even though they belong, at least in part, to the same epitope group. In summary, three tested human mAbs demonstrated capacity for detection of MERS-CoV antigen on FFPE samples and may be implemented in double or triple immunohistochemical methods.</p>
</abstract>
<kwd-group id="kwd0005">
<title>Keywords</title>
<kwd>Immunohistochemistry</kwd>
<kwd>Middle East respiratory syndrome coronavirus</kwd>
<kwd>Spike protein</kwd>
<kwd>Monoclonal human antibodies</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>

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