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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Active Replication of Middle East Respiratory Syndrome Coronavirus and Aberrant Induction of Inflammatory Cytokines and Chemokines in Human Macrophages: Implications for Pathogenesis</title><author><name sortKey="Zhou, Jie" sort="Zhou, Jie" uniqKey="Zhou J" first="Jie" last="Zhou">Jie Zhou</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chu, Hin" sort="Chu, Hin" uniqKey="Chu H" first="Hin" last="Chu">Hin Chu</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Li, Cun" sort="Li, Cun" uniqKey="Li C" first="Cun" last="Li">Cun Li</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wong, Bosco Ho Yin" sort="Wong, Bosco Ho Yin" uniqKey="Wong B" first="Bosco Ho-Yin" last="Wong">Bosco Ho-Yin Wong</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cheng, Zhong Shan" sort="Cheng, Zhong Shan" uniqKey="Cheng Z" first="Zhong-Shan" last="Cheng">Zhong-Shan Cheng</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Poon, Vincent Kwok Man" sort="Poon, Vincent Kwok Man" uniqKey="Poon V" first="Vincent Kwok-Man" last="Poon">Vincent Kwok-Man Poon</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Sun, Tianhao" sort="Sun, Tianhao" uniqKey="Sun T" first="Tianhao" last="Sun">Tianhao Sun</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Lau, Candy Choi Yi" sort="Lau, Candy Choi Yi" uniqKey="Lau C" first="Candy Choi-Yi" last="Lau">Candy Choi-Yi Lau</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wong, Kenneth Kak Yuen" sort="Wong, Kenneth Kak Yuen" uniqKey="Wong K" first="Kenneth Kak-Yuen" last="Wong">Kenneth Kak-Yuen Wong</name><affiliation><nlm:aff id="af5"><addr-line>Department of Surgery</addr-line>,<institution>University of Hong Kong, Hong Kong Special Administrative Region</institution>,<country>China</country></nlm:aff></affiliation></author><author><name sortKey="Chan, Jimmy Yu Wai" sort="Chan, Jimmy Yu Wai" uniqKey="Chan J" first="Jimmy Yu-Wai" last="Chan">Jimmy Yu-Wai Chan</name><affiliation><nlm:aff id="af5"><addr-line>Department of Surgery</addr-line>,<institution>University of Hong Kong, Hong Kong Special Administrative Region</institution>,<country>China</country></nlm:aff></affiliation></author><author><name sortKey="Chan, Jasper Fuk Woo" sort="Chan, Jasper Fuk Woo" uniqKey="Chan J" first="Jasper Fuk-Woo" last="Chan">Jasper Fuk-Woo Chan</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="To, Kelvin Kai Wang" sort="To, Kelvin Kai Wang" uniqKey="To K" first="Kelvin Kai-Wang" last="To">Kelvin Kai-Wang To</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chan, Kwok Hung" sort="Chan, Kwok Hung" uniqKey="Chan K" first="Kwok-Hung" last="Chan">Kwok-Hung Chan</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Zheng, Bo Jian" sort="Zheng, Bo Jian" uniqKey="Zheng B" first="Bo-Jian" last="Zheng">Bo-Jian Zheng</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="Yuen, Kwok Yung" sort="Yuen, Kwok Yung" uniqKey="Yuen K" first="Kwok-Yung" last="Yuen">Kwok-Yung Yuen</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">24065148</idno><idno type="pmc">7107356</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7107356</idno><idno type="RBID">PMC:7107356</idno><idno type="doi">10.1093/infdis/jit504</idno><date when="2013">2013</date><idno type="wicri:Area/Pmc/Corpus">001172</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001172</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Active Replication of Middle East Respiratory Syndrome Coronavirus and Aberrant Induction of Inflammatory Cytokines and Chemokines in Human Macrophages: Implications for Pathogenesis</title><author><name sortKey="Zhou, Jie" sort="Zhou, Jie" uniqKey="Zhou J" first="Jie" last="Zhou">Jie Zhou</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chu, Hin" sort="Chu, Hin" uniqKey="Chu H" first="Hin" last="Chu">Hin Chu</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Li, Cun" sort="Li, Cun" uniqKey="Li C" first="Cun" last="Li">Cun Li</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wong, Bosco Ho Yin" sort="Wong, Bosco Ho Yin" uniqKey="Wong B" first="Bosco Ho-Yin" last="Wong">Bosco Ho-Yin Wong</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Cheng, Zhong Shan" sort="Cheng, Zhong Shan" uniqKey="Cheng Z" first="Zhong-Shan" last="Cheng">Zhong-Shan Cheng</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Poon, Vincent Kwok Man" sort="Poon, Vincent Kwok Man" uniqKey="Poon V" first="Vincent Kwok-Man" last="Poon">Vincent Kwok-Man Poon</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Sun, Tianhao" sort="Sun, Tianhao" uniqKey="Sun T" first="Tianhao" last="Sun">Tianhao Sun</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Lau, Candy Choi Yi" sort="Lau, Candy Choi Yi" uniqKey="Lau C" first="Candy Choi-Yi" last="Lau">Candy Choi-Yi Lau</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wong, Kenneth Kak Yuen" sort="Wong, Kenneth Kak Yuen" uniqKey="Wong K" first="Kenneth Kak-Yuen" last="Wong">Kenneth Kak-Yuen Wong</name><affiliation><nlm:aff id="af5"><addr-line>Department of Surgery</addr-line>,<institution>University of Hong Kong, Hong Kong Special Administrative Region</institution>,<country>China</country></nlm:aff></affiliation></author><author><name sortKey="Chan, Jimmy Yu Wai" sort="Chan, Jimmy Yu Wai" uniqKey="Chan J" first="Jimmy Yu-Wai" last="Chan">Jimmy Yu-Wai Chan</name><affiliation><nlm:aff id="af5"><addr-line>Department of Surgery</addr-line>,<institution>University of Hong Kong, Hong Kong Special Administrative Region</institution>,<country>China</country></nlm:aff></affiliation></author><author><name sortKey="Chan, Jasper Fuk Woo" sort="Chan, Jasper Fuk Woo" uniqKey="Chan J" first="Jasper Fuk-Woo" last="Chan">Jasper Fuk-Woo Chan</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="To, Kelvin Kai Wang" sort="To, Kelvin Kai Wang" uniqKey="To K" first="Kelvin Kai-Wang" last="To">Kelvin Kai-Wang To</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="Chan, Kwok Hung" sort="Chan, Kwok Hung" uniqKey="Chan K" first="Kwok-Hung" last="Chan">Kwok-Hung Chan</name><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation></author><author><name sortKey="Zheng, Bo Jian" sort="Zheng, Bo Jian" uniqKey="Zheng B" first="Bo-Jian" last="Zheng">Bo-Jian Zheng</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author><author><name sortKey="Yuen, Kwok Yung" sort="Yuen, Kwok Yung" uniqKey="Yuen K" first="Kwok-Yung" last="Yuen">Kwok-Yung Yuen</name><affiliation><nlm:aff id="af1"><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af2"><addr-line>Department of Microbiology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af3"><addr-line>Research Centre of Infection and Immunology</addr-line></nlm:aff></affiliation><affiliation><nlm:aff id="af4"><addr-line>Carol Yu Centre for Infection</addr-line></nlm:aff></affiliation></author></analytic><series><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></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Abstract</title><p>Middle East respiratory syndrome coronavirus (MERS-CoV) infection caused severe pneumonia and multiorgan dysfunction and had a higher crude fatality rate (around 50% vs 10%) than SARS coronavirus (SARS-CoV) infection. To understand the pathogenesis, we studied viral replication, cytokine/chemokine response, and antigen presentation in MERS-CoV–infected human monocyte–derived macrophages (MDMs) versus SARS-CoV–infected MDMs. Only MERS-CoV can replicate in MDMs. Both viruses were unable to significantly stimulate the expression of antiviral cytokines (interferon α [IFN-α] and IFN-β) but induced comparable levels of tumor necrosis factor α and interleukin 6. Notably, MERS-CoV induced significantly higher expression levels of interleukin 12, IFN-γ, and chemokines (IP-10/CXCL-10, MCP-1/CCL-2, MIP-1α/CCL-3, RANTES/CCL-5, and interleukin 8) than SARS-CoV. The expression of major histocompatibility complex class I and costimulatory molecules were significantly higher in MERS-CoV–infected MDMs than in SARS-CoV–infected cells. MERS-CoV replication was validated by immunostaining of infected MDMs and ex vivo lung tissue. We conclusively showed that MERS-CoV can establish a productive infection in human macrophages. The aberrant induction of inflammatory cytokines/chemokines could be important in the disease pathogenesis.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Chan, Jf" uniqKey="Chan J">JF Chan</name></author><author><name sortKey="Li, Ks" uniqKey="Li K">KS Li</name></author><author><name sortKey="To, Kk" uniqKey="To K">KK To</name></author><author><name sortKey="Cheng, Vc" uniqKey="Cheng V">VC Cheng</name></author><author><name sortKey="Chen, H" uniqKey="Chen H">H Chen</name></author><author><name sortKey="Yuen, Ky" uniqKey="Yuen K">KY Yuen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zaki, Am" uniqKey="Zaki A">AM Zaki</name></author><author><name sortKey="Van Boheemen, S" uniqKey="Van Boheemen S">S van Boheemen</name></author><author><name sortKey="Bestebroer, Tm" uniqKey="Bestebroer T">TM Bestebroer</name></author><author><name sortKey="Osterhaus, Ad" uniqKey="Osterhaus A">AD 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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Infect Dis</journal-id><journal-id journal-id-type="iso-abbrev">J. Infect. Dis</journal-id><journal-id journal-id-type="publisher-id">jid</journal-id><journal-id journal-id-type="hwp">jinfdis</journal-id><journal-title-group><journal-title>The Journal of Infectious Diseases</journal-title></journal-title-group><issn pub-type="ppub">0022-1899</issn><issn pub-type="epub">1537-6613</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">24065148</article-id><article-id pub-id-type="pmc">7107356</article-id><article-id pub-id-type="doi">10.1093/infdis/jit504</article-id><article-id pub-id-type="publisher-id">jit504</article-id><article-categories><subj-group subj-group-type="heading"><subject>Major Articles and Brief Reports</subject><subj-group subj-group-type="category-toc-heading"><subject>Viruses</subject></subj-group></subj-group></article-categories><title-group><article-title>Active Replication of Middle East Respiratory Syndrome Coronavirus and Aberrant Induction of Inflammatory Cytokines and Chemokines in Human Macrophages: Implications for Pathogenesis</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Zhou</surname><given-names>Jie</given-names></name><author-comment><title>a</title><p>J. Z. and H. C. contributed equally to the study.</p></author-comment><xref ref-type="aff" rid="af1">1</xref><xref ref-type="aff" rid="af2">2</xref><xref ref-type="aff" rid="af3">3</xref><pmc-comment>kyyuen@hkucc.hku.hk </pmc-comment>
<xref ref-type="corresp" rid="d804669e334"></xref></contrib><contrib contrib-type="author"><name><surname>Chu</surname><given-names>Hin</given-names></name><author-comment><title>a</title><p>J. Z. and H. C. contributed equally to the study.</p></author-comment><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Li</surname><given-names>Cun</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Wong</surname><given-names>Bosco Ho-Yin</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Cheng</surname><given-names>Zhong-Shan</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Poon</surname><given-names>Vincent Kwok-Man</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Sun</surname><given-names>Tianhao</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Lau</surname><given-names>Candy Choi-Yi</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Wong</surname><given-names>Kenneth Kak-Yuen</given-names></name><xref ref-type="aff" rid="af5">5</xref></contrib><contrib contrib-type="author"><name><surname>Chan</surname><given-names>Jimmy Yu-Wai</given-names></name><xref ref-type="aff" rid="af5">5</xref></contrib><contrib contrib-type="author"><name><surname>Chan</surname><given-names>Jasper Fuk-Woo</given-names></name><xref ref-type="aff" rid="af1">1</xref><xref ref-type="aff" rid="af2">2</xref><xref ref-type="aff" rid="af3">3</xref><xref ref-type="aff" rid="af4">4</xref></contrib><contrib contrib-type="author"><name><surname>To</surname><given-names>Kelvin Kai-Wang</given-names></name><xref ref-type="aff" rid="af1">1</xref><xref ref-type="aff" rid="af2">2</xref><xref ref-type="aff" rid="af3">3</xref><xref ref-type="aff" rid="af4">4</xref></contrib><contrib contrib-type="author"><name><surname>Chan</surname><given-names>Kwok-Hung</given-names></name><xref ref-type="aff" rid="af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Zheng</surname><given-names>Bo-Jian</given-names></name><xref ref-type="aff" rid="af1">1</xref><xref ref-type="aff" rid="af2">2</xref><xref ref-type="aff" rid="af3">3</xref><xref ref-type="aff" rid="af4">4</xref></contrib><contrib contrib-type="author"><name><surname>Yuen</surname><given-names>Kwok-Yung</given-names></name><xref ref-type="aff" rid="af1">1</xref><xref ref-type="aff" rid="af2">2</xref><xref ref-type="aff" rid="af3">3</xref><xref ref-type="aff" rid="af4">4</xref></contrib></contrib-group><aff id="af1"><label>1</label><addr-line>State Key Laboratory of Emerging Infectious Diseases</addr-line></aff><aff id="af2"><label>2</label><addr-line>Department of Microbiology</addr-line></aff><aff id="af3"><label>3</label><addr-line>Research Centre of Infection and Immunology</addr-line></aff><aff id="af4"><label>4</label><addr-line>Carol Yu Centre for Infection</addr-line></aff><aff id="af5"><label>5</label><addr-line>Department of Surgery</addr-line>,<institution>University of Hong Kong, Hong Kong Special Administrative Region</institution>,<country>China</country></aff><author-notes><fn id="AN1" fn-type="con"><label>a</label><p>J. Z. and H. C. contributed equally to the study.</p></fn><corresp id="d804669e334">Correspondence: Kwok-Yung Yuen, MD, Carol Yu Centre for Infection, Department of Microbiology, University of Hong Kong, Queen Mary Hospital, 102 Pokfulam Rd, Pokfulam, Hong Kong Special Administrative Region, China (<email>kyyuen@hkucc.hku.hk</email>).</corresp></author-notes><pub-date pub-type="ppub"><day>1</day><month>5</month><year>2014</year></pub-date><pub-date pub-type="epub" iso-8601-date="2013-09-24"><day>24</day><month>9</month><year>2013</year></pub-date><volume>209</volume><issue>9</issue><fpage>1331</fpage><lpage>1342</lpage><history><date date-type="received"><day>17</day><month>7</month><year>2013</year></date><date date-type="accepted"><day>27</day><month>8</month><year>2013</year></date></history><permissions><copyright-statement>© The Author 2013. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: <email>journals.permissions@oup.com</email>.</copyright-statement><copyright-year>2013</copyright-year><license><license-p>This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.</license-p></license></permissions><self-uri xlink:href="jit504.pdf"></self-uri><abstract><title>Abstract</title><p>Middle East respiratory syndrome coronavirus (MERS-CoV) infection caused severe pneumonia and multiorgan dysfunction and had a higher crude fatality rate (around 50% vs 10%) than SARS coronavirus (SARS-CoV) infection. To understand the pathogenesis, we studied viral replication, cytokine/chemokine response, and antigen presentation in MERS-CoV–infected human monocyte–derived macrophages (MDMs) versus SARS-CoV–infected MDMs. Only MERS-CoV can replicate in MDMs. Both viruses were unable to significantly stimulate the expression of antiviral cytokines (interferon α [IFN-α] and IFN-β) but induced comparable levels of tumor necrosis factor α and interleukin 6. Notably, MERS-CoV induced significantly higher expression levels of interleukin 12, IFN-γ, and chemokines (IP-10/CXCL-10, MCP-1/CCL-2, MIP-1α/CCL-3, RANTES/CCL-5, and interleukin 8) than SARS-CoV. The expression of major histocompatibility complex class I and costimulatory molecules were significantly higher in MERS-CoV–infected MDMs than in SARS-CoV–infected cells. MERS-CoV replication was validated by immunostaining of infected MDMs and ex vivo lung tissue. We conclusively showed that MERS-CoV can establish a productive infection in human macrophages. The aberrant induction of inflammatory cytokines/chemokines could be important in the disease pathogenesis.</p></abstract><kwd-group><kwd>MERS-CoV</kwd><kwd>SARS-CoV</kwd><kwd>viral replication</kwd><kwd>pathogenesis</kwd><kwd>cytokine and chemokine response</kwd></kwd-group></article-meta></front><body><p>In September 2012, a novel human coronavirus, HCoV-EMC, later renamed Middle East respiratory syndrome coronavirus (MERS-CoV), was identified in 2 patients with severe pneumonia complicated with renal failure who once traveled to or resided in Saudi Arabia [<xref rid="JIT504C1" ref-type="bibr">1</xref>, <xref rid="JIT504C2" ref-type="bibr">2</xref>]. Retrospective analysis of archived specimens showed that the first virologically confirmed cases could be traced back to early April 2012 [<xref rid="JIT504C3" ref-type="bibr">3</xref>]. As of 1 August 2013, World Health Organization has confirmed 94 cases of infection with 46 deaths, and therefore an appalling fatality rate of around 50% [<xref rid="JIT504C4" ref-type="bibr">4</xref>]. Coronaviruses are the largest of all RNA viruses, with positive single-stranded RNA genomes of 26–32 kb. Many of them are globally distributed and detectable in a wide range of animals and humans [<xref rid="JIT504C5" ref-type="bibr">5</xref>]. They are classified into 4 genera: alphacoronavirus, betacoronavirus, gammacoronavirus, and deltacoronavirus [<xref rid="JIT504C6" ref-type="bibr">6</xref>, <xref rid="JIT504C7" ref-type="bibr">7</xref>]. HCoV-OC43 (lineage A betacoronavirus) and HCoV-229E (alphacoronavirus) are known causative agents of the common cold and rarely cause severe respiratory diseases [<xref rid="JIT504C8" ref-type="bibr">8</xref>, <xref rid="JIT504C9" ref-type="bibr">9</xref>]. In contrast, SARS coronavirus (SARS-CoV; lineage B betacoronavirus) caused the severe acute respiratory syndrome (SARS) outbreak during 2002–2003, affecting >8000 patients in >30 countries, with an overall fatality rate of 9.6% [<xref rid="JIT504C10" ref-type="bibr">10–13</xref>]. The discovery of SARS-CoV aroused a growing recognition that human coronaviruses are potentially highly pathogenic. The heightened awareness sparked an intense hunting for novel coronaviruses, which led to the subsequent identification of HCoV-NL63 (alphacoronavirus) and HCoV-HKU1 (lineage A betacoronavirus), that occasionally cause severe lower respiratory tract infections in young children, elderly individuals, and immunocompromised patients [<xref rid="JIT504C14" ref-type="bibr">14</xref>, <xref rid="JIT504C15" ref-type="bibr">15</xref>]. Ten years after the SARS outbreak, another novel betacoronavirus of lineage C, MERS-CoV, might have jumped species barriers from bats to humans and caused an ongoing epidemic of severe human infections in the Middle East [<xref rid="JIT504C6" ref-type="bibr">6</xref>, <xref rid="JIT504C16" ref-type="bibr">16–20</xref>]. Most patients with MERS presented with rapidly progressive pneumonia. Many of them developed multiorgan dysfunction, deranged coagulation profile, and hematological changes, including lymphopenia, neutrophilia, and thrombocytopenia [<xref rid="JIT504C3" ref-type="bibr">3</xref>]. Although the clinical syndromes of MERS resembled those described in severe SARS, MERS often had renal failure and substantially surpassed SARS in terms of crude fatality rate. Because of the increasing number of person-to-person transmission in both nosocomial and community settings [<xref rid="JIT504C21" ref-type="bibr">21</xref>, <xref rid="JIT504C22" ref-type="bibr">22</xref>], there is a growing concern for another SARS-like pandemic.</p><p>Among all coronaviruses that cause human infections, SARS-CoV is the most extensively characterized. Human airway epithelial cells are the primary targets of SARS-CoV [<xref rid="JIT504C23" ref-type="bibr">23</xref>]. However, virus-infected macrophages contributed significantly to disease pathogenesis [<xref rid="JIT504C23" ref-type="bibr">23</xref>, <xref rid="JIT504C24" ref-type="bibr">24</xref>]. Macrophages are the sentinel phagocytes of innate immune system, which functions to contain and eliminate pathogens, remove apoptotic cells, and present antigens to T cells. Macrophage-produced cytokines and chemokines modulate immune response, eradicate invading pathogens, and maintain tissue homeostasis [<xref rid="JIT504C25" ref-type="bibr">25</xref>]. Compared with other human primary macrophages, peripheral blood monocyte–derived macrophages (MDMs) are readily available and frequently used to recapitulate the initial innate immune responses in macrophages during viral infection.</p><p>Before the identification of MERS-CoV, SARS-CoV had been regarded as the most dangerous human coronavirus. However, a 5-fold higher fatality rate than that of SARS-CoV highlighted the possibly higher pathogenicity of MERS-CoV. Recent studies demonstrated that, similar to SARS-CoV, MERS-CoV was capable of infecting and productively replicating in primary human airway epithelial cells and ex vivo human lung tissues. Furthermore, MERS-CoV has a much broader tissue tropism than SARS-CoV and resembled SARS-CoV in its ability to suppress interferon production [<xref rid="JIT504C26" ref-type="bibr">26–29</xref>]. The high pathogenicity of MERS-CoV prompted us to explore the potential host-virus interaction in macrophages, the cells that were implicated in the pathogenesis of SARS [<xref rid="JIT504C24" ref-type="bibr">24</xref>]. Therefore, we studied viral infection/replication, cellular immune response, and antigen presentation in MERS-CoV–inoculated MDMs in comparison with SARS-CoV–inoculated MDMs. Further understanding of the pathogenesis of MERS will be important for optimizing treatment strategies for this highly fatal emerging infectious disease.</p><sec sec-type="methods" id="s2"><title>MATERIALS AND METHODS</title><sec id="s2a"><title>Virus Culture and Virus Titration by a 50% Tissue Culture Infective Dose (TCID<sub>50</sub>) Assay</title><p>A clinical isolate of MERS-CoV was kindly provided by Fouchier et al [<xref rid="JIT504C2" ref-type="bibr">2</xref>]. The isolate was cultured in Vero cells (ATCC) with serum-free minimum Dulbecco's modified Eagle's medium (DMEM; Life Technologies), supplemented with 100 U/mL penicillin and 100 μg/mL streptomycin, at 37°C with 5% CO<sub>2</sub>. SARS-CoV was cultured in FRhK-4 cells (ATCC) with the same medium. Two or 3 days after virus inoculation, culture supernatants were collected and stored in −80°C freezer in aliquots. For virus titration, aliquots of MERS-CoV and SARS-CoV were applied on confluent Vero cells in 96-well plates for TCID50 assay. Briefly, serial 10-fold dilutions of each virus were inoculated in a Vero cell monolayer in sextuplets and cultured in penicillin/streptomycin-supplemented DMEM. The plates were observed for cytopathic effect for 4–5 days. Viral titer was calculated with the Reed and Münch end point method. One TCID<sub>50</sub> is interpreted as the amount of virus that causes cytopathic effect in 50% of inoculated wells.</p></sec><sec id="s2b"><title>MDM Culture and Virus Infection</title><p>Healthy adult blood samples were collected from Hong Kong Red Cross Blood Transfusion Service according to a protocol approved by the Institutional Review Board of the University of Hong Kong. Monocyte preparation and differentiation were performed according to a well-established protocol described previously [<xref rid="JIT504C30" ref-type="bibr">30</xref>]. The purity of the macrophages assessed by flow cytometry analysis of CD14 and CD68 was >93% on average [<xref rid="JIT504C31" ref-type="bibr">31</xref>]. For viral infection, MDMs in 24-well plates were inoculated with MERS-CoV or SARS-CoV at 2 TCID<sub>50</sub>/cell or were mock inoculated for 1 hour at 37°C. Supernatants and cell lysates were harvested 0, 5, 10, 24, 48, and 72 hour(s) after infection. TCID<sub>50</sub> assay was performed on cell-free supernatants for viral titration. Cell lysates were extracted for RNA to detect viral RNA and cellular messenger RNA (mRNA). For immunostaining, MDMs were seeded in 24-well plates on glass coverslips. The cells were inoculated with MERS-CoV at 2 TCID<sub>50</sub>/cell. Twelve and 48 hours after infection, the cells were fixed with 4% paraformaldehyde and immunostained.</p></sec><sec id="s2c"><title>Quantification of Viral and Cellular RNA Transcript by Reverse-Transcription Quantitative Polymerase Chain Reaction (RT-qPCR)</title><p>Cellular RNA extraction and RT-qPCR were performed as described previously [<xref rid="JIT504C32" ref-type="bibr">32</xref>]. Viral RNA in the supernatant was extracted with the PureLink Viral RNA/DNA mini kit (Life Technologies). Virus-specific primer for MERS-CoV or SARS-CoV was used in reverse transcription to generate complementary DNAs (cDNAs) for the viruses and oligo(dT) for cellular cDNAs. Specific primers used in the qPCR analysis were listed in <xref ref-type="supplementary-material" rid="sup1">Supplementary Table 1</xref>. Cellular gene expression results were normalized to GAPDH and presented as the fold change in gene expression of virus-infected MDMs relative to that of mock-infected cells.</p></sec><sec id="s2d"><title>Ex Vivo Lung Tissue Culture and Virus Infection Experiment</title><p>The ex vivo lung tissue culture and virus infection experiment was approved by the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster. Fresh normal lung tissue was obtained from a patient undergoing resection of lung tumor. Lung tissue was cut into 2-mm<sup>3</sup> cubes and subsequently infected by a MERS-CoV inoculum of 1 × 10<sup>7</sup> TCID<sub>50</sub>/mL or were mock-infected for 1 hour at 37°C. After inoculation, tissue cubes were maintained in DMEM/F12 medium supplemented with 10% human serum and penicillin/streptomycin before fixation and cryosectioning as described previously [<xref rid="JIT504C32" ref-type="bibr">32</xref>].</p></sec><sec id="s2e"><title>Immunofluorescence Staining</title><p>MERS-CoV was detected using our previously described guinea pig anti–nucleocapsid protein (NP) antibody [<xref rid="JIT504C29" ref-type="bibr">29</xref>] for 1 hour at room temperature, followed by fluorescein isothiocyanate–conjugated rabbit–anti-guinea pig immunoglobulin G (IgG; Life Technologies) or Alexa 594 goat–anti-guinea pig IgG (Abcam) as the secondary antibody. In tissue slides, macrophages were labeled with mouse anti-CD68 antibody (KP1, Abcam) followed by Alexa 488 goat–anti-mouse IgG (Abcam). All primary and secondary antibodies were diluted at 1:200. Finally, slides were mounted with ProLong Gold antifade reagent (Life Technologies) and examined with a Carl Zeiss LSM 710 microscope.</p></sec><sec id="s2f"><title>Statistical Analysis</title><p>Experimental results represented mean and standard errors of the mean from at least 3 different donors. Statistical comparison between the groups was performed by the Student <italic>t</italic> test, using GraphPad Prism 6. Differences were considered statistically significant when the <italic>P</italic> value was <.05.</p></sec></sec><sec sec-type="results" id="s3"><title>RESULTS</title><sec id="s3a"><title>Viral Infectivity and Replication of MERS-CoV in MDMs</title><p>To understand the ability of MERS-CoV to infect human macrophages, we inoculated MDMs with MERS-CoV and SARS-CoV in parallel and observed the outcome of infection by examining levels of viral gene in the cell lysate and culture supernatant. As shown in Figure <xref ref-type="fig" rid="JIT504F1">1</xref>, the level of MERS-CoV RNA increased from 5 hours after infection in both cell lysate (Figure <xref ref-type="fig" rid="JIT504F1">1</xref><italic>A</italic>) and supernatant (Figure <xref ref-type="fig" rid="JIT504F1">1</xref><italic>B</italic>) of MDMs. Despite the variation among different donors, a 2–4-log increase in viral RNA level was consistently detected. MERS-CoV infection and replication in MDMs was confirmed with TCID<sub>50</sub> assays, in which increasing titers of infectious virus were observed after inoculation. On the contrary, when the same dose of SARS-CoV was inoculated onto MDMs, no sign of viral replication were observed because the viral RNA levels gradually decreased in the cell lysate and culture supernatant. Infectious viruses detected in the supernatants of SARS-CoV–infected MDMs remained at low levels, indicating an abortive infection.
</p><fig id="JIT504F1" orientation="portrait" position="float"><label>Figure 1.</label><caption><p>Middle East respiratory syndrome coronavirus (MERS-CoV) replication kinetics in human monocyte–derived macrophages (MDMs), compared with SARS coronavirus (SARS-CoV). MERS-CoV or SARS-CoV was inoculated onto MDMs at 2 tissue culture infective doses (TCID<sub>50</sub>) per cell. At the indicated hours after infection, cell lysate (<italic>A</italic>) and culture supernatant (<italic>B</italic>) were collected to detect the levels of positive-strand viral RNA by reverse-transcription quantitative polymerase chain reaction. Viral titration of the culture supernatants was performed with a TCID<sub>50</sub> assay (<italic>C</italic>). The results of 3 representative donors are demonstrated.</p></caption><graphic xlink:href="jit50401"></graphic></fig><p>Replication of MERS-CoV in MDMs was further verified by immunofluorescence study. As shown in Figure <xref ref-type="fig" rid="JIT504F2">2</xref>, strong fluorescence signals for MERS-CoV NP were observed in the cytoplasm of virus-inoculated MDMs. Twelve hours after infection most of the infected cells displayed puncta-like positivity in the cytoplasm, whereas 48 hours after infection there were more cells displaying homogeneous immunoreactivity to NP throughout the cytoplasm. Moreover, there were more NP-positive cells 48 hours after infection than 12 hours after infection (data not shown), compatible with a productive infection and replication. Mock-infected MDMs did not display any immunoreactivity to NP. Moreover, replacing anti-NP sera with preimmune sera did not yield any positive signal in infected MDMs (data not shown). Collectively, we demonstrated the infection and replication capability of MERS-CoV in MDMs.
</p><fig id="JIT504F2" orientation="portrait" position="float"><label>Figure 2.</label><caption><p>Immunofluorescence staining of Middle East respiratory syndrome coronavirus (MERS-CoV) nucleocapsid protein (NP) in MERS-CoV–inoculated human monocyte–derived macrophages (MDMs). MDMs seeded on glass coverslips were inoculated with MERS-CoV at 2 tissue culture infective doses per cell or subjected to mock infection. Twelve hours (<italic>A</italic>) and 48 hours (<italic>B</italic>) after inoculation, cells were fixed, blocked, and permeabilized; incubated with anti-NP primary antibody for 1 hour; and stained with fluorescein isothiocyanate–conjugated secondary antibody for 1 hour. The slides were mounted with DAPI-containing mounting buffer and examined with a Carl Zeiss LSM 710 microscope. <italic>C</italic>, Findings for mock-inoculated MDMs that underwent the same procedure as that described for MERS-CoV–infected MDMs.</p></caption><graphic xlink:href="jit50402"></graphic></fig><p>We next assessed the cell viability of MERS-CoV–infected, SARS-CoV–infected, and mock-infected MDMs by calculating the numbers of viable cells 48 hours after infection and comparing these data with values obtained right before infection. It was shown that approximately 87% of mock-infected MDMs remained viable 48 hours after infection, whereas the percentage of viable cells among MERS-CoV–infected MDMs was significantly reduced to 64% (Figure <xref ref-type="fig" rid="JIT504F3">3</xref>). In contrast, compared with mock infection, SARS-CoV appeared to have a protective effect from cell death. The difference, however, was not statistically significant. Our result suggested that MERS-CoV induced significantly higher cytotoxicity than SARS-CoV in infected MDMs.
</p><fig id="JIT504F3" orientation="portrait" position="float"><label>Figure 3.</label><caption><p>Cell viability of Middle East respiratory syndrome coronavirus (MERS-CoV)–infected and SARS coronavirus (SARS-CoV)–infected human monocyte–derived macrophages (MDMs). MDMs were seeded at 1.5 × 10<sup>5</sup>/well in a 24-well plate and inoculated with MERS-CoV or SARS-CoV at 2 median tissue culture infective doses per cell or subjected to mock infection. Before infection and 48 hours after infection, MDMs were trypsinized, stained with trypan blue, and counted in duplicate with disposable hemocytometers. Viability represents the ratio of viable cell number of inoculated MDMs 48 hours after infection, compared with that before infection. Results are the mean and standard error of the mean of at least 3 representative donors. *<italic>P</italic> < .05, by the Student <italic>t</italic> test.</p></caption><graphic xlink:href="jit50403"></graphic></fig></sec><sec id="s3b"><title>Innate Immune Response in MERS-CoV–Infected MDMs</title><p>To evaluate the response of MDMs to active MERS-CoV replication, we assessed the mRNA expression levels of a series of antiviral cytokines, proinflammatory cytokines, and chemokines in MERS-CoV–infected, SARS-CoV–infected, and mock-infected MDMs. The expression of antiviral cytokines—type I interferon (interferon α [IFN-α] and IFN-β), type II interferon (IFN-γ), proinflammatory cytokines (tumor necrosis factor α [TNF-α], interleukin 6 [IL-6], and interleukin 12 [IL-12]), and chemokines (IP-10/CXCL-10, MCP-1/CCL-2, MIP-1α/CCL-3, RANTES/CCL-5, and interleukin 8 [IL-8])—was examined by RT-qPCR. As shown in Figure <xref ref-type="fig" rid="JIT504F4">4</xref>, both MERS-CoV–infected and SARS-CoV–infected MDMs displayed fairly weak and comparable expression levels of IFN-α and IFN-β, whereas these IFNs were highly induced in influenza A(H5N1)–infected MDMs (data not shown). However, IFN-γ expression was highly induced by both viruses. IFN-γ induction was more prominent in MERS-CoV–inoculated MDMs than in SARS-CoV–inoculated cells. TNF-α and IL-6 were comparably induced in both MERS-CoV–infected and SARS-CoV–infected cells. IL-12 was more significantly induced by MERS-CoV than SARS-CoV. Consistent with the high induction of IFN-γ, IP-10 (IFN-γ–inducible protein 10), which is secreted by a variety of cells in response to INF-γ, was highly upregulated by both viruses and was more significantly induced in MERS-CoV–infected cells (Figure <xref ref-type="fig" rid="JIT504F5">5</xref>).
</p><fig id="JIT504F4" orientation="portrait" position="float"><label>Figure 4.</label><caption><p>Cytokine response in Middle East respiratory syndrome coronavirus (MERS-CoV)–infected and SARS coronavirus (SARS-CoV)–infected human monocyte–derived macrophages (MDMs). MDMs were inoculated with MERS-CoV or SARS-CoV at 2 median tissue culture infective doses per cell or subjected to mock infection. At the indicated hours after infection, cells were lysed for RNA extraction, and reverse-transcription quantitative polymerase chain reaction was performed to detect the messenger RNA expression levels for antiviral and proinflammatory cytokines. Results were normalized to those for GAPDH and are presented as the fold change in gene expression of virus-infected MDMs in relation to that of the mock-infected MDMs. Data displayed in this figure represent mean and standard error of the mean from at least 3 different donors. Statistical analyses between MERS-CoV– and SARS-CoV–inoculated MDMs at different time points were performed using the Student <italic>t</italic> test. *<italic>P</italic> < .05. Abbreviations: IFN-α, interferon α; IFN-β, interferon β; IFN-γ, interferon γ; IL-6, interleukin 6; IL-12, interleukin 12; TNF-α, tumor necrosis factor α.</p></caption><graphic xlink:href="jit50404"></graphic></fig><fig id="JIT504F5" orientation="portrait" position="float"><label>Figure 5.</label><caption><p>Chemokine response in Middle East respiratory syndrome coronavirus (MERS-CoV)–infected and SARS coronavirus (SARS-CoV)–infected human monocyte–derived macrophages (MDMs). MDMs were inoculated with MERS-CoV or SARS-CoV at 2 median tissue culture infective doses per cell or subjected to mock infection. At the indicated hours after infection, cells were lysed for RNA extraction, and reverse-transcription quantitative polymerase chain reaction was performed to detect the messenger RNA expression levels for immunoregulatory chemokines. Results were normalized to those for GAPDH and are presented as the fold change in gene expression of virus-infected MDMs relative to that of the mock-infected MDMs. Statistical analyses between MERS-CoV– and SARS-CoV–infected MDMs at different time points were performed using the Student <italic>t</italic> test. *<italic>P</italic> < .05. Abbreviation: IL-8, interleukin 8.</p></caption><graphic xlink:href="jit50405"></graphic></fig><p>Chemokines were extensively studied and implicated in the immunopathogenicity of SARS-CoV [<xref rid="JIT504C33" ref-type="bibr">33</xref>, <xref rid="JIT504C34" ref-type="bibr">34</xref>]. Our data demonstrated that MERS-CoV induced significantly higher levels of MCP-1, MIP-1α, and IL-8 when compared with SARS-CoV (Figure <xref ref-type="fig" rid="JIT504F5">5</xref>). A trend of higher RANTES expression was documented in MERS-CoV–inoculated MDMs. Notably, all of these chemokines, as well as IP-10, exhibited a sustained induction curve from an early time point (5 hours after infection) to a late time point (72 hours after infection) in MERS-CoV–inoculated cells. The expression patterns of many of these cytokines/chemokines in SARS-CoV–infected MDMs in this study were in agreement with those in a previous report [<xref rid="JIT504C35" ref-type="bibr">35</xref>]. Collectively, we found that, similar to SARS-CoV, MERS-CoV was unable to induce effective antiviral IFN response (IFN-α and IFN-β). Both viruses similarly upregulated the expression of TNF-α and IL-6, but MERS-CoV induced more IFN-γ expression. Remarkably, MERS-CoV profoundly and sustainably induced immune cell–recruiting chemokines and cytokines, such as IP-10/CXCL-10, MCP-1/CCL-2, MIP-1α/CCL-3, RANTES/CCL-5, IL-8, and IL-12, in MDMs.</p></sec><sec id="s3c"><title>Antigen-Presenting Function of MERS-CoV–Infected MDMs</title><p>Apart from dendritic cells, macrophages are the foremost antigen-presenting cells in the host immune system. Viral antigens displayed on infected cells, via major histocompatibility complex (MHC) class I molecules, can be recognized by specific cytotoxic T cells that trigger the elimination of infected cells and thereby abrogate further viral replication and dissemination. On the other hand, macrophages present viral antigens, coupled with MHC class II molecules, to helper T cells and B cells to elicit the cellular and humoral immune responses. The effective host immune response is an important determinant for disease presentation and outcome of viral infection. A number of molecules for antigen processing (PSMB8 and CD74), antigen expression and stability in MHC class I complex (B2M), and costimulation and activation (CD40, CD80, and CD86), together with MHC class I (HLA-A and HLA-B) and MHC class II (HLA-DMB and HLA-DPB1) molecules, were examined upon inoculation with MERS-CoV, SARS-CoV, or mock control. We demonstrated that SARS-CoV largely failed to stimulate the expression of MHC class I and MHC class II molecules in inoculated MDMs. However, MERS-CoV modestly upregulated the expression of MHC class I–related molecules, HLA-A, HLA-B, B2M, and PSMB8. As for MHC class II–related genes, MERS-CoV failed to induce the expression of HLA-DMB but upregulated the expression of HLA-DPB1 and CD74. Additionally, MERS-CoV significantly induced higher levels of CD40, CD80, and CD86 expression than SARS-CoV (Figure <xref ref-type="fig" rid="JIT504F6">6</xref>). In summary, our data suggested that MERS-CoV triggered the higher expression of MHC class I–, MHC class II–, and costimulation-related genes in MDMs than SARS-CoV.</p></sec><sec id="s3d"><title>MERS-CoV Infected Lung Macrophages in Ex Vivo Culture of Human Lung Tissues</title><p>Although MDMs can be productively infected in vitro, they cannot fully represent the scenario of a real MERS-CoV infection. To this end, we performed the MERS-CoV inoculation in ex vivo culture of human lung tissue, where macrophages are abundant. We found that airway epithelial cells, predominantly pneumocytes and epithelial cells of terminal bronchioles, were infected, based on the cell and tissue morphology (Figure <xref ref-type="fig" rid="JIT504F7">7</xref><italic>A</italic>). Moreover, intense immunoreactivity to MERS-CoV NP was observed in the endothelial cells of blood vessels in the interstitia (Figure <xref ref-type="fig" rid="JIT504F7">7</xref><italic>B</italic>). We did not specifically define these NP-positive cells by costaining with epithelial cell– and endothelial cell–specific markers, because they were not the focus of this study. In stark contrast to a recent study [<xref rid="JIT504C26" ref-type="bibr">26</xref>], we found that lung macrophages can be infected by MERS-CoV, as shown by the colocalization of MERS-CoV NP with CD68 (Figure <xref ref-type="fig" rid="JIT504F7">7</xref><italic>C</italic> and <xref ref-type="fig" rid="JIT504F7">7</xref><italic>D</italic>), although the fluorescence intensity of NP was stronger in respiratory epithelial cells than in macrophages. There was no colocalization of NP and CD68 in mock-infected tissues (Figure <xref ref-type="fig" rid="JIT504F7">7</xref><italic>E</italic>). On the basis of these observations, we demonstrated that human lung macrophages were susceptible to MERS-CoV infection ex vivo.<xref ref-type="fig" rid="JIT504F6"></xref></p><fig id="JIT504F6" orientation="portrait" position="float"><label>Figure 6.</label><caption><p>Antigen presentation function of human monocyte–derived macrophages (MDMs) upon Middle East respiratory syndrome coronavirus (MERS-CoV) versus SARS coronavirus (SARS-CoV) infection. MDMs were inoculated with MERS-CoV or SARS-CoV at 2 median tissue culture infective doses per cell or subjected to mock infection. At the indicated hours after infection, cells lysates were collected for RNA extraction, and reverse-transcription quantitative polymerase chain reaction was performed to detect the messenger RNA expression levels for major histocompatibility complex (MHC) class I– and MHC class II–related molecules and costimulation molecules involved in antigen presentation. Results were normalized to those for GAPDH and are presented as the fold change in gene expression of virus-infected MDMs relative to that of the mock-infected MDMs.</p></caption><graphic xlink:href="jit50406"></graphic></fig><fig id="JIT504F7" orientation="portrait" position="float"><label>Figure 7.</label><caption><p>Immunofluorescence double staining of Middle East respiratory syndrome coronavirus (MERS-CoV)–infected ex vivo lung tissue for MERS-CoV nucleocapsid protein (NP; red) and CD68 (green). Normal lung tissues were infected with MERS-CoV at 1 × 10<sup>7</sup> tissue culture infective doses per milliliter or subjected to mock infection for 1 hour at 37°C. A total of 48 hours after infection, tissues were fixed, cryoprotected, and cryosectioned. Slides were sequentially stained with guinea pig anti-NP sera, Alexa 694 goat–anti-guinea pig immunoglobulin G (IgG), mouse anti-CD68 antibody and Alexa 488 goat–anti-mouse IgG. Cell nuclei were counterstained by DAPI in the mounting buffer. Images were captured with a Carl Zeiss LSM 710 microscope. Immunoreactivity to NP was detected in epithelial cells of terminal bronchiole (<italic>A</italic>) and vascular endothelial (<italic>B</italic>) cells. <italic>C</italic> and <italic>D</italic>, Colocalization of MERS-CoV NP and CD68. <italic>E</italic>, A representative image of mock-infected lung tissue.</p></caption><graphic xlink:href="jit50407"></graphic></fig></sec></sec><sec sec-type="discussion" id="s4"><title>DISCUSSION</title><p>This study aimed to elucidate the pathogenesis of MERS-CoV. First, we found that the vascular endothelial cells in pulmonary interstitium and macrophages could be infected by MERS-CoV (Figure <xref ref-type="fig" rid="JIT504F7">7</xref>). This corroborated with the clinical observation that the virus was systemically disseminated in patients with MERS. A recent study described a patient with MERS who developed rapidly progressive pneumonia with respiratory failure, acute renal failure and septic shock, and eventually died [<xref rid="JIT504C36" ref-type="bibr">36</xref>]. The patient had high levels of viral RNA transcripts in bronchoalveolar lavage fluid. The patient's urine and stool samples also were positive for viral RNA. Despite a negative result for MERS-CoV in the blood sample of this patient, another study verified the presence of viral RNA transcripts in whole blood of a patient with MERS [<xref rid="JIT504C21" ref-type="bibr">21</xref>]. According to the gene expression profile in normal human tissue from public databases, DPP4, the MERS-CoV receptor [<xref rid="JIT504C37" ref-type="bibr">37</xref>], is abundantly expressed in a variety of human cells and tissues, which may facilitate the viral dissemination. Our previous study also provided strong evidence that cells derived from many human tissues can support MERS-CoV infection and replication [<xref rid="JIT504C29" ref-type="bibr">29</xref>]. Our present findings may provide the direct pathological basis for the systemic virus dissemination in MERS.</p><p>Second, immune cell–recruiting cytokines/chemokines were highly and endurably induced in MDMs upon MERS-CoV infection (Figures <xref ref-type="fig" rid="JIT504F4">4</xref> and <xref ref-type="fig" rid="JIT504F5">5</xref>). Additionally, other proinflammatory cytokines also contributed to this chemoattractant cascade. This might lead to large number of immune cells infiltrating a patient's lower respiratory tract, causing severe inflammation and tissue damage. Clinically, most patients with MERS presented with rapidly progressive pneumonia with multilobar consolidations in radiographs and computed tomography scans. Cytological examination of bronchoalveolar lavage fluid often showed high number of neutrophils and macrophages [<xref rid="JIT504C2" ref-type="bibr">2</xref>, <xref rid="JIT504C21" ref-type="bibr">21</xref>]. MERS-CoV–inoculated rhesus macaques displayed milder respiratory symptoms than patients with MERS. But histopathological examination of lung tissue showed acute pneumonia with infiltrating neutrophils and macrophages [<xref rid="JIT504C38" ref-type="bibr">38</xref>]. We believe cytokine/chemokine induction may have been responsible for the infiltration by immune cells and substantially contributed to the severe pneumonia and respiratory dysfunction in patients with MERS. Furthermore, most patients with MERS developed lymphopenia in the course of infection [<xref rid="JIT504C2" ref-type="bibr">2</xref>, <xref rid="JIT504C21" ref-type="bibr">21</xref>, <xref rid="JIT504C22" ref-type="bibr">22</xref>, <xref rid="JIT504C36" ref-type="bibr">36</xref>]. This clinical manifestation was attributed to the immune cell recruitment and sequestration in the lower respiratory tract that was triggered by cytokine/chemokine induction. Additionally, we found that IP-10 and MCP-1, which can suppress proliferation of human myeloid progenitor cells [<xref rid="JIT504C39" ref-type="bibr">39</xref>], were highly induced upon MERS-CoV infection. The induction of these chemokines may inevitably aggravate the lymphopenia in patients with MERS. Taken together, our experimental findings are compatible with patient's clinical presentations and also elucidate the pathogenic mechanism of this life-threatening disease.</p><p>We compared MERS-CoV with SARS-CoV in 3 aspects: viral replication, cytokine/chemokine production, and antigen presentation in MDMs. It has been well recognized that SARS-CoV infection in MDMs was abortive [<xref rid="JIT504C35" ref-type="bibr">35</xref>, <xref rid="JIT504C40" ref-type="bibr">40</xref>]. Unlike the abortive infection of SARS-CoV in MDMs, MERS-CoV can establish a productive infection in MDMs (Figures <xref ref-type="fig" rid="JIT504F1">1</xref> and <xref ref-type="fig" rid="JIT504F2">2</xref>). The decreased viral titer in donors 1 and 3 at 72 hours after virus inoculation may have been due to excessive cell death over time. The infectivity of MERS-CoV to human macrophages was substantiated by the presence of viral NP in the macrophages of virus-inoculated ex vivo lung tissue (Figure <xref ref-type="fig" rid="JIT504F7">7</xref>). Macrophages are among the first line of host defense against viral invasion. Efficient viral replication in these cells implicates that the virus can overcome the host defense and is highly virulent. The productive viral replication in macrophages may turn these phagocytes into viral reservoirs and vehicles for further replication and dissemination, as shown for human immunodeficiency virus [<xref rid="JIT504C41" ref-type="bibr">41</xref>].</p><p>In response to viral infection, macrophages secrete proinflammatory cytokines/chemokines to activate various antiviral mechanisms. However, direct infection of these immune cells by virus may cause dysregulated induction of these inflammatory mediators, which could be damaging to neighboring tissues. Among these proinflammatory mediators, aberrant induction of IL-6 and TNF-α is almost a hallmark of severe respiratory viral infection, such as SARS and human infection by avian influenza viruses [<xref rid="JIT504C34" ref-type="bibr">34</xref>, <xref rid="JIT504C42" ref-type="bibr">42</xref>]. The immunostimulatory effects of IFN-γ outweighed its antiviral effects in SARS [<xref rid="JIT504C33" ref-type="bibr">33</xref>]. IL-12 functions to stimulate the growth and activity of T cells and natural killer (NK) cells and induce the production of proinflammatory cytokines in these cells. MIP-1α, MCP-1, and IP-10 are notable for their strong chemoattraction of monocytes/macrophages, T cells, NK cells, and acute inflammatory cells to the site of infection. Apart from its chemotactic effect for granulocytes and T cells, RANTES can also promote T-cell and NK-cell activation. IL-8 shows strong chemotaxis for neutrophils and other granulocytes. It is also a potent inducer for other chemokines. A number of studies indicated that antiviral IFNs and cytokines were not induced in SARS-CoV–infected macrophages and dendritic cells [<xref rid="JIT504C35" ref-type="bibr">35</xref>, <xref rid="JIT504C43" ref-type="bibr">43</xref>, <xref rid="JIT504C44" ref-type="bibr">44</xref>], possibly because SARS-CoV evolved strategies to antagonize the innate responses [<xref rid="JIT504C45" ref-type="bibr">45</xref>]. In contrast, proinflammatory cytokines (IL-6 and TNF-α) and chemokines (IP-10, MIP-1α, and MCP-1) were upregulated [<xref rid="JIT504C35" ref-type="bibr">35</xref>, <xref rid="JIT504C43" ref-type="bibr">43</xref>]. A plethora of clinical studies reported that levels of proinflammatory cytokines/chemokines, including IL-6, IL-8, IFN-γ, MCP-1, and IP-10, were highly elevated in patients with SARS, some of which were correlated with disease severity or mortality [<xref rid="JIT504C33" ref-type="bibr">33</xref>, <xref rid="JIT504C34" ref-type="bibr">34</xref>]. Additionally, macrophages in the patient's lung tissue were believed to be the producer of cytokine storm and underlie the pathogenesis of SARS [<xref rid="JIT504C24" ref-type="bibr">24</xref>]. We compared and found that many of the cytokines/chemokines in MERS-CoV–infected MDMs shared a similar expression profile to SARS-CoV–infected cells. Notably, immune cell–recruiting chemokines and immunostimulating cytokines were induced at a significantly higher magnitude and prolonged interval by MERS-CoV, compared with SARS-CoV. Therefore, it is conceivable that immunopathogenesis, which is operative in SARS [<xref rid="JIT504C46" ref-type="bibr">46</xref>], may be aggravated in MERS, causing more severe disease and higher fatality. The detailed expression profile of the cytokine/chemokine responses in MERS-CoV–infected and SARS-CoV–infected MDMs should be investigated with microarray analysis.</p><p>The expression of MHC class I–, MHC class II–, and costimulation-related genes were modestly induced in MERS-CoV–infected MDMs and were marginally stronger than that in SARS-CoV–infected cells (Figure <xref ref-type="fig" rid="JIT504F6">6</xref>). This contrasts with a recent report showing a decreased antigen-presentation profile in a MERS-CoV–infected lung cancer cell line [<xref rid="JIT504C47" ref-type="bibr">47</xref>]. The disagreement is possibly attributable to differences in the properties of MDMs and the lung cancer cell line. The full scenario of antigen presentation in MERS definitely warrants further investigation. Nevertheless, based on our results, the increase in antigen presentation in MERS-CoV–infected MDMs may potentially contribute to exaggerate the immunopathology.</p><p>Taken together, we demonstrate that MERS-CoV can infect and effectively replicate in MDMs. MERS-CoV replication in MDMs causes extensive cytotoxicity and induces the expression of a number of proinflammatory cytokines/chemokines. The mixture of high viral replication and immune-mediated pathology could be important factors in the pathogenesis of MERS.</p></sec><sec sec-type="supplementary-material"><title>Supplementary Material</title><supplementary-material content-type="local-data" id="sup1"><label>Supplementary Data</label><media xlink:href="jit504_Supplementary_Data.zip"><caption><p>Click here for additional data file.</p></caption></media></supplementary-material></sec></body><back><ack><title>Notes</title><p><bold><italic>Acknowledgments.</italic></bold> We thank the Core Imaging Facility, Li Ka Shing Faculty of Medicine, University of Hong Kong, for facilitation of the study.</p><p><bold><italic>Financial support.</italic></bold> This work was supported by the Providence Foundation Limited in memory of the late Dr Lui Hac Minh and by the HKSAR Health and Medical Research Fund.</p><p><bold><italic>Potential conflicts of interest.</italic></bold> All authors: No reported conflicts.</p><p>All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed. 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