Molecular pathology of emerging coronavirus infections
Identifieur interne : 001847 ( Pmc/Corpus ); précédent : 001846; suivant : 001848Molecular pathology of emerging coronavirus infections
Auteurs : Lisa E. Gralinski ; Ralph S. BaricSource :
- The Journal of Pathology [ 0022-3417 ] ; 2014.
Abstract
Respiratory viruses can cause a wide spectrum of pulmonary diseases, ranging from mild, upper respiratory tract infections to severe and life‐threatening lower respiratory tract infections, including the development of acute lung injury (
Url:
DOI: 10.1002/path.4454
PubMed: 25270030
PubMed Central: 4267971
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PMC:4267971Le document en format XML
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<front><div type="abstract" xml:lang="en"><title>Abstract</title>
<p id="path4454-para-0001">Respiratory viruses can cause a wide spectrum of pulmonary diseases, ranging from mild, upper respiratory tract infections to severe and life‐threatening lower respiratory tract infections, including the development of acute lung injury (<styled-content style="fixed-case" toggle="no">ALI</styled-content>
) and acute respiratory distress syndrome (<styled-content style="fixed-case" toggle="no">ARDS</styled-content>
). Viral clearance and subsequent recovery from infection require activation of an effective host immune response; however, many immune effector cells may also cause injury to host tissues. Severe acute respiratory syndrome (<styled-content style="fixed-case" toggle="no">SARS</styled-content>
) coronavirus and Middle East respiratory syndrome (<styled-content style="fixed-case" toggle="no">MERS</styled-content>
) coronavirus cause severe infection of the lower respiratory tract, with 10% and 35% overall mortality rates, respectively; however, >50% mortality rates are seen in the aged and immunosuppressed populations. While these viruses are susceptible to interferon treatment <italic>in vitro</italic>
, they both encode numerous genes that allow for successful evasion of the host immune system until after high virus titres have been achieved. In this review, we discuss the importance of the innate immune response and the development of lung pathology following human coronavirus infection. © 2014 The Authors. <italic>The Journal of Pathology</italic>
published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.</p>
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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Pathol</journal-id>
<journal-id journal-id-type="iso-abbrev">J. Pathol</journal-id>
<journal-id journal-id-type="doi">10.1002/(ISSN)1096-9896</journal-id>
<journal-id journal-id-type="publisher-id">PATH</journal-id>
<journal-title-group><journal-title>The Journal of Pathology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0022-3417</issn>
<issn pub-type="epub">1096-9896</issn>
<publisher><publisher-name>John Wiley & Sons, Ltd</publisher-name>
<publisher-loc>Chichester, UK</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">25270030</article-id>
<article-id pub-id-type="pmc">4267971</article-id>
<article-id pub-id-type="doi">10.1002/path.4454</article-id>
<article-id pub-id-type="publisher-id">PATH4454</article-id>
<article-categories><subj-group subj-group-type="overline"><subject>Invited Review</subject>
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<subj-group subj-group-type="heading"><subject>Invited Reviews</subject>
</subj-group>
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<title-group><article-title>Molecular pathology of emerging coronavirus infections</article-title>
<alt-title alt-title-type="right-running-head">Molecular pathology of emerging coronavirus infections</alt-title>
<alt-title alt-title-type="left-running-head"><styled-content style="fixed-case" toggle="no">LE</styled-content>
Gralinski and <styled-content style="fixed-case" toggle="no">RS</styled-content>
Baric</alt-title>
</title-group>
<contrib-group><contrib id="path4454-cr-0001" contrib-type="author"><name><surname>Gralinski</surname>
<given-names>Lisa E</given-names>
</name>
<xref ref-type="aff" rid="path4454-aff-0001"><sup>1</sup>
</xref>
</contrib>
<contrib id="path4454-cr-0002" contrib-type="author" corresp="yes"><name><surname>Baric</surname>
<given-names>Ralph S</given-names>
</name>
<xref ref-type="aff" rid="path4454-aff-0001"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="path4454-aff-0002"><sup>2</sup>
</xref>
</contrib>
</contrib-group>
<aff id="path4454-aff-0001"><label><sup>1</sup>
</label>
<named-content content-type="organisation-division">Department of Epidemiology</named-content>
<institution>University of North Carolina</institution>
<city>Chapel Hill</city>
<named-content content-type="country-part">NC</named-content>
<country country="US">USA</country>
</aff>
<aff id="path4454-aff-0002"><label><sup>2</sup>
</label>
<named-content content-type="organisation-division">Department of Microbiology and Immunology</named-content>
<institution>University of North Carolina</institution>
<city>Chapel Hill</city>
<named-content content-type="country-part">NC</named-content>
<country country="US">USA</country>
</aff>
<author-notes><corresp id="correspondenceTo"><label>*</label>
Correspondence to: RS Baric, Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599–7435, USA. E‐mail: <email>rbaric@email.unc.ed</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub"><month>1</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub"><day>11</day>
<month>12</month>
<year>2014</year>
</pub-date>
<volume>235</volume>
<issue>2</issue>
<issue-id pub-id-type="doi">10.1002/path.2015.235.issue-2</issue-id>
<issue-title content-type="special-issue-title">Viruses and Disease</issue-title>
<fpage>185</fpage>
<lpage>195</lpage>
<history><date date-type="received"><day>18</day>
<month>9</month>
<year>2014</year>
</date>
<date date-type="accepted"><day>25</day>
<month>9</month>
<year>2014</year>
</date>
</history>
<permissions><pmc-comment> Copyright © 2015 Pathological Society of Great Britain and Ireland </pmc-comment>
<copyright-statement content-type="article-copyright">© 2014 The Authors. <italic>The Journal of Pathology</italic>
published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.</copyright-statement>
<license license-type="creativeCommonsBy-nc-nd"><license-p>This is an open access article under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc-nd/3.0/">http://creativecommons.org/licenses/by-nc-nd/3.0/</ext-link>
License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="file:PATH-235-185.pdf"></self-uri>
<abstract id="path4454-abs-0001"><title>Abstract</title>
<p id="path4454-para-0001">Respiratory viruses can cause a wide spectrum of pulmonary diseases, ranging from mild, upper respiratory tract infections to severe and life‐threatening lower respiratory tract infections, including the development of acute lung injury (<styled-content style="fixed-case" toggle="no">ALI</styled-content>
) and acute respiratory distress syndrome (<styled-content style="fixed-case" toggle="no">ARDS</styled-content>
). Viral clearance and subsequent recovery from infection require activation of an effective host immune response; however, many immune effector cells may also cause injury to host tissues. Severe acute respiratory syndrome (<styled-content style="fixed-case" toggle="no">SARS</styled-content>
) coronavirus and Middle East respiratory syndrome (<styled-content style="fixed-case" toggle="no">MERS</styled-content>
) coronavirus cause severe infection of the lower respiratory tract, with 10% and 35% overall mortality rates, respectively; however, >50% mortality rates are seen in the aged and immunosuppressed populations. While these viruses are susceptible to interferon treatment <italic>in vitro</italic>
, they both encode numerous genes that allow for successful evasion of the host immune system until after high virus titres have been achieved. In this review, we discuss the importance of the innate immune response and the development of lung pathology following human coronavirus infection. © 2014 The Authors. <italic>The Journal of Pathology</italic>
published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.</p>
</abstract>
<kwd-group kwd-group-type="author-generated"><kwd id="path4454-kwd-0001"><styled-content style="fixed-case" toggle="no">SARS‐CoV</styled-content>
</kwd>
<kwd id="path4454-kwd-0002"><styled-content style="fixed-case" toggle="no">MERS‐CoV</styled-content>
</kwd>
<kwd id="path4454-kwd-0003">coronavirus</kwd>
<kwd id="path4454-kwd-0004">acute respiratory distress syndrome</kwd>
<kwd id="path4454-kwd-0005"><styled-content style="fixed-case" toggle="no">ARDS</styled-content>
</kwd>
<kwd id="path4454-kwd-0006">acute lung injury</kwd>
<kwd id="path4454-kwd-0007">type <styled-content style="fixed-case" toggle="no">II</styled-content>
pneumocytes</kwd>
</kwd-group>
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<meta-value>January 2015</meta-value>
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<notes><fn-group id="path4454-ntgp-0001"><fn id="path4454-note-0001"><p>No conflicts of interest were declared.</p>
</fn>
</fn-group>
</notes>
</front>
<body id="path4454-body-0001"><sec id="path4454-sec-0001"><title>Introduction</title>
<p id="path4454-para-0003">Acute lung injury (ALI) and its more severe form, acute respiratory distress syndrome (ARDS), can arise after many types of injury to the lung, including sepsis, mechanical and chemical injury and bacterial and viral infections <xref rid="path4454-bib-0001" ref-type="ref">1</xref>
. In ALI, the mortality rate is in the range 20–30%, with about 55% of the cases progressing to ARDS within a few days. ARDS causes significant morbidity and approximately 40% mortality, resulting in ∼75 000 deaths/year in the USA alone <xref rid="path4454-bib-0002" ref-type="ref">2</xref>
. In the past two decades, five emerging viruses have been known to cause significant ARDS‐related mortality, including influenza H1N1 2009 and, in particular, the highly pathogenic avian influenza H5N1 and H7N9 viruses and the SARS and MERS coronaviruses. In this review we focus on mechanisms of coronavirus‐induced lung pathogenesis and ARDS.</p>
<p id="path4454-para-0004">Human coronavirus (CoV) infections have traditionally caused a low percentage of annual upper and lower respiratory infections <xref rid="path4454-bib-0003" ref-type="ref">3</xref>
, including severe disease outcomes in the elderly, immunocompromised patients and infants. HCoV‐OC43 (OC43) and HCoV‐229E (229E) were the first documented human CoVs but, more recently, HCoV‐NL63 (NL63) <xref rid="path4454-bib-0004" ref-type="ref">4</xref>
and HCoV‐HKU1 (HKU1) <xref rid="path4454-bib-0005" ref-type="ref">5</xref>
were identified as a consequence of increased viral surveillance efforts in the early twenty‐first century (Table <xref rid="path4454-tbl-0001" ref-type="table">1</xref>
). These four viruses usually cause acute infection of the upper respiratory tract and less frequently are associated with lower respiratory tract <xref rid="path4454-bib-0006" ref-type="ref">6</xref>
, <xref rid="path4454-bib-0007" ref-type="ref">7</xref>
diseases as well. Severe disease is both rare and typically associated with co‐morbidities and/or immunosenescence. The past 15 years have also seen the emergence of two new human coronaviruses that cause significant disease and mortality. SARS‐CoV was identified in 2003 and caused an acute, atypical pneumonia and diffuse alveolar damage (DAD) in roughly 8000 patients <xref rid="path4454-bib-0008" ref-type="ref">8</xref>
, <xref rid="path4454-bib-0009" ref-type="ref">9</xref>
. Those over 65 years of age often developed ARDS, resulting in mortality rates that exceeded 50%. Overall, SARS‐CoV infection caused nearly 800 fatalities, representing a nearly 10% mortality rate. More recently, in 2012, a new human coronavirus, designated MERS‐CoV, was identified. MERS‐CoV continues to circulate in camels and humans, with over 857 official cases and 334 deaths, representing an approximately 35% case fatality rate to date in humans <xref rid="path4454-bib-0010" ref-type="ref">10</xref>
, <xref rid="path4454-bib-0011" ref-type="ref">11</xref>
. MERS‐CoV‐induced disease is particularly severe in aged patients and those with pre‐existing co‐morbidities. MERS‐CoV does not appear to be highly pathogenic or virulent in camels.</p>
<table-wrap id="path4454-tbl-0001" xml:lang="en" orientation="portrait" position="float"><label>Table 1</label>
<caption><p>Human coronaviruses, their receptors, emergence, disease and infection data</p>
</caption>
<table frame="hsides" rules="groups"><col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<thead valign="bottom"><tr style="border-bottom:solid 1px #000000"><th id="path4454-ent-0001" align="left" valign="bottom" rowspan="1" colspan="1">Virus</th>
<th id="path4454-ent-0002" align="left" valign="bottom" rowspan="1" colspan="1">Receptor</th>
<th id="path4454-ent-0003" align="left" valign="bottom" rowspan="1" colspan="1">Discovery and estimated date of divergence</th>
<th id="path4454-ent-0004" align="left" valign="bottom" rowspan="1" colspan="1">Cell types infected</th>
<th id="path4454-ent-0005" align="left" valign="bottom" rowspan="1" colspan="1">Disease types caused</th>
</tr>
</thead>
<tbody valign="top"><tr><td id="path4454-ent-0006" align="left" valign="top" rowspan="1" colspan="1">OC43</td>
<td id="path4454-ent-0007" align="left" valign="top" rowspan="1" colspan="1">Receptor unknown, sialic acid and HLA class 1 involvement <xref rid="path4454-bib-0113" ref-type="ref">113</xref>
, <xref rid="path4454-bib-0114" ref-type="ref">114</xref>
</td>
<td id="path4454-ent-0008" align="left" valign="top" rowspan="1" colspan="1">Divergence from BCoV in 1890 <xref rid="path4454-bib-0115" ref-type="ref">115</xref>
</td>
<td id="path4454-ent-0009" align="left" valign="top" rowspan="1" colspan="1">Ciliated airway epithelial cells <xref rid="path4454-bib-0116" ref-type="ref">116</xref>
, macrophages in culture <xref rid="path4454-bib-0117" ref-type="ref">117</xref>
, neuronal cells <xref rid="path4454-bib-0118" ref-type="ref">118</xref>
</td>
<td id="path4454-ent-0010" align="left" valign="top" rowspan="1" colspan="1">Upper respiratory infection, GI infection, pneumonia <xref rid="path4454-bib-0119" ref-type="ref">119</xref>
</td>
</tr>
<tr><td id="path4454-ent-0011" align="left" valign="top" rowspan="1" colspan="1">229E</td>
<td id="path4454-ent-0012" align="left" valign="top" rowspan="1" colspan="1">Aminopeptidase N <xref rid="path4454-bib-0120" ref-type="ref">120</xref>
</td>
<td id="path4454-ent-0013" align="left" valign="top" rowspan="1" colspan="1">Divergence in 1700–1800 <xref rid="path4454-bib-0121" ref-type="ref">121</xref>
, divergence from NL63 in the eleventh century <xref rid="path4454-bib-0122" ref-type="ref">122</xref>
</td>
<td id="path4454-ent-0014" align="left" valign="top" rowspan="1" colspan="1">Non‐ciliated airway epithelial cells <xref rid="path4454-bib-0116" ref-type="ref">116</xref>
, human monocytes <xref rid="path4454-bib-0123" ref-type="ref">123</xref>
, neuronal cells <xref rid="path4454-bib-0118" ref-type="ref">118</xref>
</td>
<td id="path4454-ent-0015" align="left" valign="top" rowspan="1" colspan="1">Upper respiratory infection <xref rid="path4454-bib-0124" ref-type="ref">124</xref>
, GI infection, pneumonia <xref rid="path4454-bib-0125" ref-type="ref">125</xref>
</td>
</tr>
<tr><td id="path4454-ent-0016" align="left" valign="top" rowspan="1" colspan="1">NL63</td>
<td id="path4454-ent-0017" align="left" valign="top" rowspan="1" colspan="1">Ace2 <xref rid="path4454-bib-0126" ref-type="ref">126</xref>
</td>
<td id="path4454-ent-0018" align="left" valign="top" rowspan="1" colspan="1">Discovered in 2004 <xref rid="path4454-bib-0004" ref-type="ref">4</xref>
, divergence between 1200 and 1500 <xref rid="path4454-bib-0127" ref-type="ref">127</xref>
</td>
<td id="path4454-ent-0019" align="left" valign="top" rowspan="1" colspan="1">Ciliated airway epithelial cells <xref rid="path4454-bib-0116" ref-type="ref">116</xref>
</td>
<td id="path4454-ent-0020" align="left" valign="top" rowspan="1" colspan="1">Upper and lower respiratory infection <xref rid="path4454-bib-0006" ref-type="ref">6</xref>
, <xref rid="path4454-bib-0128" ref-type="ref">128</xref>
, associated with croup in children <xref rid="path4454-bib-0129" ref-type="ref">129</xref>
</td>
</tr>
<tr><td id="path4454-ent-0021" align="left" valign="top" rowspan="1" colspan="1">HKU1</td>
<td id="path4454-ent-0022" align="left" valign="top" rowspan="1" colspan="1">Unknown</td>
<td id="path4454-ent-0023" align="left" valign="top" rowspan="1" colspan="1">Discovered in 2005 <xref rid="path4454-bib-0005" ref-type="ref">5</xref>
</td>
<td id="path4454-ent-0024" align="left" valign="top" rowspan="1" colspan="1">Ciliated airway epithelial cells <xref rid="path4454-bib-0116" ref-type="ref">116</xref>
</td>
<td id="path4454-ent-0025" align="left" valign="top" rowspan="1" colspan="1">Upper respiratory infection and pneumonia <xref rid="path4454-bib-0130" ref-type="ref">130</xref>
, enteric symptoms <xref rid="path4454-bib-0131" ref-type="ref">131</xref>
</td>
</tr>
<tr><td id="path4454-ent-0026" align="left" valign="top" rowspan="1" colspan="1">SARS</td>
<td id="path4454-ent-0027" align="left" valign="top" rowspan="1" colspan="1">Ace2 <xref rid="path4454-bib-0130" ref-type="ref">130</xref>
, role for DC‐sign <xref rid="path4454-bib-0132" ref-type="ref">132</xref>
</td>
<td id="path4454-ent-0028" align="left" valign="top" rowspan="1" colspan="1">Emerged in 2002 <xref rid="path4454-bib-0133" ref-type="ref">133</xref>
, divergence estimates from 1986–2002 <xref rid="path4454-bib-0134" ref-type="ref">134</xref>
, <xref rid="path4454-bib-0135" ref-type="ref">135</xref>
</td>
<td id="path4454-ent-0029" align="left" valign="top" rowspan="1" colspan="1">Epithelial cells <xref rid="path4454-bib-0136" ref-type="ref">136</xref>
, ciliated cells, type II pneumocytes <xref rid="path4454-bib-0137" ref-type="ref">137</xref>
</td>
<td id="path4454-ent-0030" align="left" valign="top" rowspan="1" colspan="1">Lower respiratory infection <xref rid="path4454-bib-0099" ref-type="ref">99</xref>
, <xref rid="path4454-bib-0138" ref-type="ref">138</xref>
, pneumonia, DAD, ARDS</td>
</tr>
<tr><td id="path4454-ent-0031" align="left" valign="top" rowspan="1" colspan="1">MERS</td>
<td id="path4454-ent-0032" align="left" valign="top" rowspan="1" colspan="1">DPP4 <xref rid="path4454-bib-0139" ref-type="ref">139</xref>
</td>
<td id="path4454-ent-0033" align="left" valign="top" rowspan="1" colspan="1">Emerged in 2012 <xref rid="path4454-bib-0025" ref-type="ref">25</xref>
, common ancestor from 2011–2012 <xref rid="path4454-bib-0140" ref-type="ref">140</xref>
</td>
<td id="path4454-ent-0034" align="left" valign="top" rowspan="1" colspan="1">Airway epithelial cells <xref rid="path4454-bib-0141" ref-type="ref">141</xref>
, renal epithelial cells <xref rid="path4454-bib-0142" ref-type="ref">142</xref>
, dendritic cells <xref rid="path4454-bib-0143" ref-type="ref">143</xref>
</td>
<td id="path4454-ent-0035" align="left" valign="top" rowspan="1" colspan="1">Lower respiratory infection <xref rid="path4454-bib-0025" ref-type="ref">25</xref>
, <xref rid="path4454-bib-0144" ref-type="ref">144</xref>
, pneumonia, renal failure</td>
</tr>
</tbody>
</table>
</table-wrap>
<p id="path4454-para-0005">SARS‐CoV and MERS‐CoV have clear zoonotic origins, although their exact paths from animal reservoir to human infection are not yet clear. Viruses with high nucleotide identity to SARS‐CoV were found in key amplifying hosts such as palm civets and raccoon dogs in Guangdong Province China during the 2002–2003 SARS epidemic <xref rid="path4454-bib-0012" ref-type="ref">12</xref>
. Later studies identified highly conserved viruses circulating in horseshoe bats, including some strains that are able to bind to, and infect, human cells <xref rid="path4454-bib-0013" ref-type="ref">13</xref>
, <xref rid="path4454-bib-0014" ref-type="ref">14</xref>
, <xref rid="path4454-bib-0015" ref-type="ref">15</xref>
, <xref rid="path4454-bib-0016" ref-type="ref">16</xref>
. The existence of novel bat SARS‐like coronaviruses that also use bat, civet and human angiotensin 1 converting enzyme 2 (ACE2) receptors for entry, such as SARS‐CoV, strongly suggests an opportunity for further zoonotic disease outbreaks in human and animal populations.</p>
<p id="path4454-para-0006">SARS causes an atypical pneumonia characterized by cough, fever and infiltrates with a ground‐glass appearance on X‐ray <xref rid="path4454-bib-0017" ref-type="ref">17</xref>
, <xref rid="path4454-bib-0018" ref-type="ref">18</xref>
. Early‐stage disease was characterized by acute DAD, with oedema, fibrin and hyaline membranes in the alveolar spaces, typical of ALI <xref rid="path4454-bib-0019" ref-type="ref">19</xref>
. Other patients predominantly showed an acute fibrinous and organizing pneumonia pattern or a mixture of the two patterns <xref rid="path4454-bib-0020" ref-type="ref">20</xref>
, <xref rid="path4454-bib-0021" ref-type="ref">21</xref>
. Longer‐term disease courses typically progressed to organizing phase DAD and eventual deposition of fibrous tissue. Autopsy of fatal SARS‐CoV cases also revealed denuded airways, haemorrhage and increased macrophage populations in the lung <xref rid="path4454-bib-0022" ref-type="ref">22</xref>
, <xref rid="path4454-bib-0023" ref-type="ref">23</xref>
. During the SARS epidemic, researchers noted that late‐term disease progression was unrelated to viraemia but was more likely to be associated with immunopathological damage <xref rid="path4454-bib-0024" ref-type="ref">24</xref>
.</p>
<p id="path4454-para-0007">MERS‐CoV has caused sporadic infections, along with several local outbreaks throughout the Middle East since its discovery in 2012 <xref rid="path4454-bib-0025" ref-type="ref">25</xref>
, <xref rid="path4454-bib-0026" ref-type="ref">26</xref>
. Although much remains unknown, closely related viruses have been isolated from camels <xref rid="path4454-bib-0027" ref-type="ref">27</xref>
and highly homologous MERS‐like bat CoVs have been identified in African <italic>Neoromicia capensis</italic>
bats <xref rid="path4454-bib-0028" ref-type="ref">28</xref>
. Local surveillance efforts have detected high levels of antibodies that recognize MERS‐CoV in dromedary camels <xref rid="path4454-bib-0029" ref-type="ref">29</xref>
; furthermore, sampling of archived camel serum samples has revealed MERS antibodies from as early as 1992 <xref rid="path4454-bib-0030" ref-type="ref">30</xref>
. These data suggest that bat to camel to human transmission routes may have seeded the 2012 outbreak in human populations, perhaps associated with the expanding camel trade that has emerged between equatorial Africa and Saudi Arabia over the past 20 years.</p>
<p id="path4454-para-0008">Animal models of human disease should recapitulate many of the pathological and immune outcomes seen in human infections. Numerous models have been established to better enable our understanding of the mechanics of SARS‐CoV infection and pathogenesis, although few recapitulate the human disease phenotypes (Table <xref rid="path4454-tbl-0002" ref-type="table">2</xref>
). Initial studies utilized late epidemic strains in non‐human primates <xref rid="path4454-bib-0031" ref-type="ref">31</xref>
, <xref rid="path4454-bib-0032" ref-type="ref">32</xref>
, <xref rid="path4454-bib-0033" ref-type="ref">33</xref>
, where mild to severe disease was observed, depending on the study location and animal age. To date, the differences in disease severity noted in primates have not been reconciled, but may reflect differences in virus strains or infection conditions. Although still under development, MERS‐CoV replication and disease have been reported in both rhesus macaques and common marmosets <xref rid="path4454-bib-0034" ref-type="ref">34</xref>
, <xref rid="path4454-bib-0035" ref-type="ref">35</xref>
. SARS‐CoV replication resulted in limited disease in young models of immunocompetent mice <xref rid="path4454-bib-0036" ref-type="ref">36</xref>
, <xref rid="path4454-bib-0037" ref-type="ref">37</xref>
, <xref rid="path4454-bib-0038" ref-type="ref">38</xref>
; however, mild clinical disease was noted in 1 year‐old mice <xref rid="path4454-bib-0039" ref-type="ref">39</xref>
. A mouse‐adapted SARS (MA‐SARS) strain was also developed that provides a model for moderate to lethal disease, depending on infectious dose, animal age and genetic background of the host <xref rid="path4454-bib-0040" ref-type="ref">40</xref>
, <xref rid="path4454-bib-0041" ref-type="ref">41</xref>
, <xref rid="path4454-bib-0042" ref-type="ref">42</xref>
(Table <xref rid="path4454-tbl-0002" ref-type="table">2</xref>
). The MA‐SARS model faithfully replicates the age‐dependent susceptibility observed in human patients, as well as key features of human lung pathology, including virus tropism to airway epithelial cells and type II pneumocytes, pneumonia, hyaline membrane formation, development of DAD and denudation of airway epithelial cells <xref rid="path4454-bib-0040" ref-type="ref">40</xref>
, <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
. A limitation may be the rapid clearance of virus titres that is seen in younger and, to a much lesser extent, in aged animals. Development of the MA‐SARS model has allowed for in‐depth studies of viral pathogenesis and the host immune response, taking advantage of immunological tools and reagents for the mouse as well as the existence of knockout mouse strains. Use of these tools has greatly added to our understanding of SARS‐CoV pathogenesis, far beyond what could be learned in <italic>in vitro</italic>
experiments or observational studies of human cases. Because of receptor incompatibilities, MERS‐CoV does not replicate in mice unless the animals are first transduced with adenovirus vectors encoding the receptor for entry, human dipeptidyl peptidase‐4 (DPP4) <xref rid="path4454-bib-0044" ref-type="ref">44</xref>
.</p>
<table-wrap id="path4454-tbl-0002" xml:lang="en" orientation="portrait" position="float"><label>Table 2</label>
<caption><p>Non‐human primate and mouse models of SARS‐CoV and MERS‐CoV infection; less common models include hamster <xref rid="path4454-bib-0145" ref-type="ref">145</xref>
, ferret <xref rid="path4454-bib-0146" ref-type="ref">146</xref>
and cat</p>
</caption>
<table frame="hsides" rules="groups"><col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="left" span="1"></col>
<col align="center" span="1"></col>
<thead valign="bottom"><tr style="border-bottom:solid 1px #000000"><th id="path4454-ent-0036" align="left" valign="bottom" rowspan="1" colspan="1">Virus</th>
<th id="path4454-ent-0037" align="left" valign="bottom" rowspan="1" colspan="1">Animal model</th>
<th id="path4454-ent-0038" align="left" valign="bottom" rowspan="1" colspan="1">Virus modifications?</th>
<th id="path4454-ent-0039" align="left" valign="bottom" rowspan="1" colspan="1">Disease types caused</th>
<th id="path4454-ent-0040" align="left" valign="bottom" rowspan="1" colspan="1">Drawbacks</th>
<th id="path4454-ent-0041" align="center" valign="bottom" rowspan="1" colspan="1">Aged model?</th>
</tr>
</thead>
<tbody valign="top"><tr><td id="path4454-ent-0042" align="left" valign="top" rowspan="1" colspan="1">SARS‐CoV</td>
<td id="path4454-ent-0043" align="left" valign="top" rowspan="1" colspan="1">Rhesus macaque</td>
<td id="path4454-ent-0044" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0045" align="left" valign="top" rowspan="1" colspan="1">Viral replication, mild pneumonia <xref rid="path4454-bib-0147" ref-type="ref">147</xref>
</td>
<td id="path4454-ent-0046" align="left" valign="top" rowspan="1" colspan="1">Expense, ethical considerations, no severe disease</td>
<td id="path4454-ent-0047" align="center" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td id="path4454-ent-0048" align="left" valign="top" rowspan="1" colspan="1"></td>
<td id="path4454-ent-0049" align="left" valign="top" rowspan="1" colspan="1">African green monkey</td>
<td id="path4454-ent-0050" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0051" align="left" valign="top" rowspan="1" colspan="1">Viral replication, pneumonitis <xref rid="path4454-bib-0033" ref-type="ref">33</xref>
, hyaline membrane formation <xref rid="path4454-bib-0102" ref-type="ref">102</xref>
</td>
<td id="path4454-ent-0052" align="left" valign="top" rowspan="1" colspan="1">Expense, ethical considerations, no severe disease</td>
<td id="path4454-ent-0053" align="center" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td id="path4454-ent-0054" align="left" valign="top" rowspan="1" colspan="1"></td>
<td id="path4454-ent-0055" align="left" valign="top" rowspan="1" colspan="1">Cynomolgus macaque</td>
<td id="path4454-ent-0056" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0057" align="left" valign="top" rowspan="1" colspan="1">Viral replication, upper respiratory symptoms, pneumonia <xref rid="path4454-bib-0031" ref-type="ref">31</xref>
, <xref rid="path4454-bib-0148" ref-type="ref">148</xref>
</td>
<td id="path4454-ent-0058" align="left" valign="top" rowspan="1" colspan="1">Expense, ethical considerations</td>
<td id="path4454-ent-0059" align="center" valign="top" rowspan="1" colspan="1">Yes <xref rid="path4454-bib-0149" ref-type="ref">149</xref>
</td>
</tr>
<tr><td id="path4454-ent-0060" align="left" valign="top" rowspan="1" colspan="1"></td>
<td id="path4454-ent-0061" align="left" valign="top" rowspan="1" colspan="1">Ace2 transgenic mice</td>
<td id="path4454-ent-0062" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0063" align="left" valign="top" rowspan="1" colspan="1">Viral replication, weight loss, inflammatory cell infiltrates <xref rid="path4454-bib-0150" ref-type="ref">150</xref>
</td>
<td id="path4454-ent-0064" align="left" valign="top" rowspan="1" colspan="1">Virus causes encephalitis <xref rid="path4454-bib-0150" ref-type="ref">150</xref>
, use of knockout mice requires extensive breeding</td>
<td id="path4454-ent-0065" align="center" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td id="path4454-ent-0066" align="left" valign="top" rowspan="1" colspan="1"></td>
<td id="path4454-ent-0067" align="left" valign="top" rowspan="1" colspan="1">Mouse</td>
<td id="path4454-ent-0068" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0069" align="left" valign="top" rowspan="1" colspan="1">Virus replication, mild pneumonia in aged mice <xref rid="path4454-bib-0039" ref-type="ref">39</xref>
</td>
<td id="path4454-ent-0070" align="left" valign="top" rowspan="1" colspan="1">Minimal pathogenesis, especially in young mice <xref rid="path4454-bib-0036" ref-type="ref">36</xref>
</td>
<td id="path4454-ent-0071" align="center" valign="top" rowspan="1" colspan="1">Yes <xref rid="path4454-bib-0039" ref-type="ref">39</xref>
</td>
</tr>
<tr><td id="path4454-ent-0072" align="left" valign="top" rowspan="1" colspan="1">SARS‐MA15</td>
<td id="path4454-ent-0073" align="left" valign="top" rowspan="1" colspan="1">Mouse</td>
<td id="path4454-ent-0074" align="left" valign="top" rowspan="1" colspan="1">Six point mutations from serial mouse passage <xref rid="path4454-bib-0040" ref-type="ref">40</xref>
</td>
<td id="path4454-ent-0075" align="left" valign="top" rowspan="1" colspan="1">Viral replication, weight loss <xref rid="path4454-bib-0040" ref-type="ref">40</xref>
, pneumonia, DAD <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
, pulmonary fibrosis <xref rid="path4454-bib-0056" ref-type="ref">56</xref>
</td>
<td id="path4454-ent-0076" align="left" valign="top" rowspan="1" colspan="1">Virus has been adapted from human strains</td>
<td id="path4454-ent-0077" align="center" valign="top" rowspan="1" colspan="1">Yes <xref rid="path4454-bib-0041" ref-type="ref">41</xref>
</td>
</tr>
<tr><td id="path4454-ent-0078" align="left" valign="top" rowspan="1" colspan="1">MERS‐CoV</td>
<td id="path4454-ent-0079" align="left" valign="top" rowspan="1" colspan="1">Rhesus macaque</td>
<td id="path4454-ent-0080" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0081" align="left" valign="top" rowspan="1" colspan="1">Viral replication <xref rid="path4454-bib-0035" ref-type="ref">35</xref>
, transient pneumonia</td>
<td id="path4454-ent-0082" align="left" valign="top" rowspan="1" colspan="1">Expense, ethical considerations, no severe disease</td>
<td id="path4454-ent-0083" align="center" valign="top" rowspan="1" colspan="1"></td>
</tr>
<tr><td id="path4454-ent-0084" align="left" valign="top" rowspan="1" colspan="1"></td>
<td id="path4454-ent-0085" align="left" valign="top" rowspan="1" colspan="1">hAd5‐DPP4 mouse</td>
<td id="path4454-ent-0086" align="left" valign="top" rowspan="1" colspan="1">None</td>
<td id="path4454-ent-0087" align="left" valign="top" rowspan="1" colspan="1">Viral replication <xref rid="path4454-bib-0044" ref-type="ref">44</xref>
, weight loss in immune knockouts</td>
<td id="path4454-ent-0088" align="left" valign="top" rowspan="1" colspan="1">Requires infection with hAd5 to express human DPP4</td>
<td id="path4454-ent-0089" align="center" valign="top" rowspan="1" colspan="1">Yes <xref rid="path4454-bib-0044" ref-type="ref">44</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<p id="path4454-para-0009">In this review we focus solely on hCoV interactions within the context of the respiratory system and infection of relevant cell types. More specifically, we review some CoV–host interactions that alter cell‐intrinsic antiviral defence programmes and other host pathways that contribute to pathological findings of ARDS, with its associated exudative and organizing phase diffuse alveolar damage and pulmonary fibrosis.</p>
</sec>
<sec id="path4454-sec-0002"><title>Innate immune response</title>
<p id="path4454-para-0010">NF‐<italic>κ</italic>
B signalling is an important component of numerous cellular responses, including stress, cytokine signalling, response to bacterial or viral infection and apoptosis <xref rid="path4454-bib-0045" ref-type="ref">45</xref>
, <xref rid="path4454-bib-0046" ref-type="ref">46</xref>
. The SARS‐CoV envelope (E) protein stimulates NF‐<italic>κ</italic>
B signalling <xref rid="path4454-bib-0047" ref-type="ref">47</xref>
, leading to lung cytokine signalling and inflammatory cell recruitment. The SARS‐CoV papain‐like protease (PLP) has also been shown to antagonize NF‐<italic>κ</italic>
B signalling <xref rid="path4454-bib-0048" ref-type="ref">48</xref>
<italic>in vitro</italic>
. Chemical inhibitors of NF‐<italic>κ</italic>
B signalling reduce lung pathology and inflammation following MA‐SARS infection, demonstrating the importance of this pathway <xref rid="path4454-bib-0047" ref-type="ref">47</xref>
in pathogenesis. While the SARS‐CoV E protein is not required for viral replication, it is important for inhibition of the host cellular stress response, apoptosis and unfolded protein response <xref rid="path4454-bib-0049" ref-type="ref">49</xref>
, <xref rid="path4454-bib-0050" ref-type="ref">50</xref>
. The E protein, along with the SARS‐CoV ORF3a and ORF8a proteins, has ion channel activity <xref rid="path4454-bib-0050" ref-type="ref">50</xref>
and may contribute to vascular permeability and fluid accumulation in the lung following SARS‐CoV infection. SARS‐CoV lacking E has been shown to be an effective vaccine <xref rid="path4454-bib-0051" ref-type="ref">51</xref>
, <xref rid="path4454-bib-0052" ref-type="ref">52</xref>
and a MERS‐CoV clone lacking E has been generated <xref rid="path4454-bib-0053" ref-type="ref">53</xref>
, although replication requires expression of E in <italic>trans</italic>
.</p>
<p id="path4454-para-0011">SARS‐CoV, and to a greater extent MERS‐CoV, are highly sensitive to interferon treatment in cell culture. Interestingly, SARS‐CoV pathogenesis does not significantly change in various type I interferon (IFN) knockout mouse models, except for a slight increase in overall virus titres <xref rid="path4454-bib-0054" ref-type="ref">54</xref>
, <xref rid="path4454-bib-0055" ref-type="ref">55</xref>
, <xref rid="path4454-bib-0056" ref-type="ref">56</xref>
. Despite this, STAT1‐ and Myd88‐deficient mice are significantly more vulnerable to lethal outcomes following infection <xref rid="path4454-bib-0056" ref-type="ref">56</xref>
, <xref rid="path4454-bib-0057" ref-type="ref">57</xref>
. Like many viruses, CoVs encode a suite of genes that antagonize cell‐intrinsic innate immune defence programmes in the infected host cell (reviewed in <xref rid="path4454-bib-0058" ref-type="ref">58</xref>
). Numerous <italic>in vitro</italic>
studies have demonstrated the IFN antagonist activity of both SARS‐CoV and MERS‐CoV proteins <xref rid="path4454-bib-0059" ref-type="ref">59</xref>
, <xref rid="path4454-bib-0060" ref-type="ref">60</xref>
, <xref rid="path4454-bib-0061" ref-type="ref">61</xref>
, and a detailed review of SARS‐CoV evasion of the innate immune response was recently published by Totura and Baric <xref rid="path4454-bib-0062" ref-type="ref">62</xref>
.</p>
<p id="path4454-para-0012">Analysis of IFN‐stimulated gene (ISG) expression in Calu‐3 human airway epithelial cells highlighted the ability of SARS‐CoV and MERS‐CoV to avoid detection by the host <xref rid="path4454-bib-0063" ref-type="ref">63</xref>
. As compared with influenza A viruses, ISG transcripts and proteins are not induced until late after SARS‐CoV and MERS‐CoV infection, when peak titres have already occurred in culture (∼18–24 h). Late in infection, ISGs showed nearly universally increased expression following SARS‐CoV infection, except for <italic>ACE2</italic>
and <italic>Serping1</italic>
. However, a much larger subset of ISGs had significantly decreased expression following MERS‐CoV infection. Like MERS‐CoV, H5N1 VN1203 infection also resulted in significant down‐regulation of subsets of ISGs. No consistent pattern in up‐regulation or down‐regulation of gene expression correlated with transcription factor usage, suggesting that a novel mechanism may be responsible for expression of the ISG subsets. Cells infected with MERS‐CoV and H5N1 avian influenza were shown to have specifically altered open and closed chromatin structures, potentially limiting the ability of transcription factors to access and bind certain ISG promoter regions. The mechanism by which MERS‐CoV induces this chromatin structural alteration is as yet unknown. In contrast, the NS1 protein of H5N1 was responsible for the chromatin changes in influenza‐infected cells. Although speculative, it seems likely that many RNA viruses may encode strategies to epigenetically alter host chromatin structure, influencing host gene expression. This newly identified method of ISG control requires additional study.</p>
<p id="path4454-para-0013">SARS‐CoV further evades the host immune response by masking its RNA genome. This mechanism may be partially mediated by the production of double‐membrane vesicles, which could sequester RNA replication intermediates away from the host‐sensing machinery <xref rid="path4454-bib-0064" ref-type="ref">64</xref>
, <xref rid="path4454-bib-0065" ref-type="ref">65</xref>
. <italic>MDA5</italic>
and <italic>IFIT1</italic>
are important host antiviral sensor or antiviral defence ISGs that detect viral RNAs. IFIT1 recognizes unmethylated 2′‐O RNA <xref rid="path4454-bib-0066" ref-type="ref">66</xref>
and alters efficient translation/stability of uncapped viral mRNAs <xref rid="path4454-bib-0067" ref-type="ref">67</xref>
. SARS‐CoV and other coronavirus RNAs are protected from IFIT recognition because they encode a 2′‐<italic>O</italic>
‐methyltransferase (2‐OMT) activity in the viral replicase protein, nsp16 <xref rid="path4454-bib-0068" ref-type="ref">68</xref>
, <xref rid="path4454-bib-0069" ref-type="ref">69</xref>
. SARS‐CoV is much more sensitive to interferon treatment in the absence of functional nsp16 methyltransferase activity, and mutant viral titres drop rapidly in both infected epithelial cells and mice. Deletion or knockdown of either <italic>MDA5</italic>
or <italic>IFIT1</italic>
restored mutant SARS‐CoV viral loads demonstrated the essential role of these host proteins in detecting pathogen‐associated molecular patterns. Ablation of the 2‐OMT activity may provide a universal strategy to rationally design live attenuated mutants of contemporary and newly emerging CoV.</p>
<p id="path4454-para-0014">Both <italic>in vivo</italic>
and <italic>in vitro</italic>
studies have addressed the role of specific proteins in the innate immune system, often ISGs, in SARS‐CoV pathogenesis. Transcriptional analysis on autopsy tissue from SARS‐CoV‐infected patients revealed increased expression of <italic>STAT1</italic>
along with other IFN‐induced cytokines <xref rid="path4454-bib-0070" ref-type="ref">70</xref>
. The SARS‐CoV accessory protein ORF6 was identified as an interferon antagonist important for viral replication in low multiplicity of infection (MOI) <italic>in vitro</italic>
infections <xref rid="path4454-bib-0071" ref-type="ref">71</xref>
, <xref rid="path4454-bib-0072" ref-type="ref">72</xref>
. ORF6 was subsequently found to sequester Karyopherin 2<italic>α</italic>
, a nuclear import factor, and block the nuclear translocation of STAT1 after SARS‐CoV infection. Interestingly, STAT1 translocation to the nucleus is not blocked in MERS‐CoV‐infected cells, so it remains uncertain whether antagonists of nuclear import are encoded in the viral genome <xref rid="path4454-bib-0073" ref-type="ref">73</xref>
. Transcriptional profiling of SARS‐CoV‐infected macaques revealed robust IFN signalling, including STAT1 translocation to the nucleus, in the lung but not in the cells that stained positive for viral antigen <xref rid="path4454-bib-0074" ref-type="ref">74</xref>
. These data highlight the importance of <italic>in vivo</italic>
studies versus high MOI <italic>in vitro</italic>
studies. Significantly, they also highlight the need to examine, or at least consider, expressing and signalling differences in specific cell types instead of global transcriptomic studies in those <italic>in vivo</italic>
experiments.</p>
<p id="path4454-para-0015"><italic>STAT1</italic>
knockout mice have been studied extensively in the context of viral infection, typically showing a heightened susceptibility to disease, due to the lack of a type I IFN response <xref rid="path4454-bib-0075" ref-type="ref">75</xref>
. These knockouts were first tested for SARS‐CoV susceptibility using the Tor2 strain in a sublethal model; animals deficient in <italic>STAT1</italic>
were unable to clear virus from the lung and developed a more severe and longer‐lasting pneumonia than the control mice <xref rid="path4454-bib-0076" ref-type="ref">76</xref>
. Frieman <italic>et al</italic>
showed that <italic>STAT1</italic>
knockout mice are highly susceptible to infection with MA‐SARS in a novel, IFN‐independent mechanism <xref rid="path4454-bib-0056" ref-type="ref">56</xref>
. MA‐SARS‐infection causes massive inflammatory cell influx in the lungs of <italic>STAT1</italic>
knockout mice, including large numbers of macrophages, neutrophils and eosinophils. <italic>STAT1</italic>
knockout mice have gross pathological changes in their lungs, including massive haemorrhage as well as increased lung size and stiffness. As seen in some humans, these mice develop severe pulmonary fibrosis and succumb to disease at late time points after infection. Stained lung sections revealed the presence of collagen protein in alveolar exudates in <italic>STAT1</italic>
knockouts, indicating development of early‐stage pulmonary fibrosis. Subsequent studies demonstrated that <italic>STAT1</italic>
knockout animals developed a Th2‐skewed immune response and had significant numbers of alternatively activated or M2 macrophages in their lungs <xref rid="path4454-bib-0077" ref-type="ref">77</xref>
. These macrophages were characterized by positive CD11c, arginase and mannose receptor staining. <italic>STAT6</italic>
is required for the development of alternatively activated macrophages, and <italic>STAT1</italic>
/<italic>STAT6</italic>
double knockout mice do not develop the severe lung disease and pro‐fibrotic lesions observed in the <italic>STAT1</italic>
single knockout <xref rid="path4454-bib-0078" ref-type="ref">78</xref>
, thus demonstrating that these macrophages are essential for development of the pulmonary fibrosis phenotype. Further elegant experiments showed that it is the <italic>STAT1</italic>
deficiency in monocyte/macrophage cells, not the infected epithelial cells, that drives alternatively activated macrophage production and induction of fibrotic lung disease following SARS‐CoV infection. Alternatively activated macrophages are typically induced by the Th2 cytokines IL‐4 and IL‐13; they have an anti‐inflammatory role and play an important role in wound‐healing processes <xref rid="path4454-bib-0151" ref-type="ref">151</xref>
.</p>
<p id="path4454-para-0016">ACE2 is expressed on well‐differentiated airway epithelial cells <xref rid="path4454-bib-0079" ref-type="ref">79</xref>
and its expression increases following type I interferon treatment <xref rid="path4454-bib-0063" ref-type="ref">63</xref>
. Both ACE2 protein levels and RNA expression are down‐regulated after either <italic>in vitro</italic>
or <italic>in vivo</italic>
SARS‐CoV infection <xref rid="path4454-bib-0063" ref-type="ref">63</xref>
, <xref rid="path4454-bib-0080" ref-type="ref">80</xref>
and NL63 also down‐regulates <italic>ACE2</italic>
expression following <italic>in vitro</italic>
infection <xref rid="path4454-bib-0081" ref-type="ref">81</xref>
. It has previously been reported that ACE2 and angiotensin‐2 protect mice from sepsis‐ and acid aspiration‐induced ALI <xref rid="path4454-bib-0082" ref-type="ref">82</xref>
. Additionally, histopathological lung disease worsens when spike‐Fc is inoculated into mice with ALI <xref rid="path4454-bib-0080" ref-type="ref">80</xref>
. The normal function of ACE2 is to inactivate angiotensin‐2, a negative regulator of the renin–angiotensin system <xref rid="path4454-bib-0083" ref-type="ref">83</xref>
, <xref rid="path4454-bib-0084" ref-type="ref">84</xref>
. This system controls blood pressure and is involved in the development of pulmonary hypertension and pulmonary fibrosis. The renin–angiotensin system is involved in lipopolysaccharide (LPS)‐induced neutrophil recruitment to the lung <xref rid="path4454-bib-0085" ref-type="ref">85</xref>
. Multiple genome‐wide association studies have investigated an association between genetic variation in ACE and susceptibility to ARDS, with mixed results <xref rid="path4454-bib-0086" ref-type="ref">86</xref>
. The role of DPP4 in MERS‐CoV infection is discussed in detail by Haagmans <italic>et al</italic>
in a separate review in this issue <xref rid="path4454-bib-0152" ref-type="ref">152</xref>
.</p>
<p id="path4454-para-0017">High ISG expression has been linked to development of ARDS <xref rid="path4454-bib-0087" ref-type="ref">87</xref>
. Furthermore, it has been suggested that unregulated IFN responses contributed to development of immunopathology and severe disease following SARS‐CoV infection <xref rid="path4454-bib-0088" ref-type="ref">88</xref>
. The data discussed above support this hypothesis and suggest that early control of ISG signalling may be a means of preventing or controlling the development of severe lung disease. Expression of the ISG <italic>Serping1</italic>
is also decreased following SARS‐CoV infection of epithelial cells; it functions by inhibiting the complement system as well as several proteases in the coagulation pathway. The role of the coagulation, fibrinolysis and wound healing in ARDS development are discussed below.</p>
</sec>
<sec id="path4454-sec-0003"><title>Acute respiratory distress syndrome (<styled-content style="fixed-case" toggle="no">ARDS</styled-content>
), coagulation, fibrinolysis and respiratory function</title>
<p id="path4454-para-0018">The alveoli of the lung are where gas exchange occurs, providing oxygen to blood flowing through capillaries in the alveolar membrane. The alveolar walls are composed of type I and type II pneumocytes, along with alveolar macrophages <xref rid="path4454-bib-0089" ref-type="ref">89</xref>
. Type I pneumocytes cover 95% of the alveolar surface area and allow for gas exchange with blood in the capillaries of the lung. Type II pneumocytes are the progenitors of type I pneumocytes and are also responsible for generating pulmonary surfactant <xref rid="path4454-bib-0090" ref-type="ref">90</xref>
, a mixture of lipids and surfactant proteins that is crucial in reducing surface tension in the lung. SARS‐CoV infection causes desquamation of pneumocytes in humans and mice, contributing to alveolar dysfunction, oedema and haemorrhage. Alveolar macrophages play an essential role in surveillance of the local environment and inhibit an excessive immune response, although this inhibition can also block an effective response to SARS‐CoV infection <xref rid="path4454-bib-0091" ref-type="ref">91</xref>
. The functions of these cell types are critical in maintaining balance between inflammation, coagulation and wound repair, especially following lung injuries such as viral infection <xref rid="path4454-bib-0092" ref-type="ref">92</xref>
.</p>
<p id="path4454-para-0019">In ARDS patients, uncontrolled inflammation, fluid accumulation and developing fibrosis severely compromise gas exchange and lead to respiratory failure. SARS‐CoV and influenza infect type I and type II pneumocytes in the lung <xref rid="path4454-bib-0093" ref-type="ref">93</xref>
, <xref rid="path4454-bib-0094" ref-type="ref">94</xref>
. ARDS patients exhibit decreased surfactant levels <xref rid="path4454-bib-0095" ref-type="ref">95</xref>
and MA‐SARS infection results in decreased surfactant transcript and protein levels <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
. Decreased surfactant, and the consequent increase in surface tension, reduces the ability of the lung to expand and contract during normal respiration; it also heightens the risk of lung collapse during expiration. Respiratory dysfunction occurs when the alveolar membranes are obstructed, or when the ability of the lung to expand and contract, circulating oxygenated air, is compromised. Lethal SARS‐CoV infection in the mouse and human is characterized by a breakdown of alveolar membrane integrity, resulting in accumulation of fluid exudates in the alveolar spaces. Virus infection also results in an overwhelming cytokine response, severe lung tissue damage and respiratory failure <xref rid="path4454-bib-0096" ref-type="ref">96</xref>
, <xref rid="path4454-bib-0097" ref-type="ref">97</xref>
, <xref rid="path4454-bib-0098" ref-type="ref">98</xref>
, <xref rid="path4454-bib-0099" ref-type="ref">99</xref>
. The progression from initial disease to diffuse alveolar damage and the exudative and organizing stage of DAD is often independent of high‐titre viral replication <xref rid="path4454-bib-0024" ref-type="ref">24</xref>
, indicating that this severe disease outcome is primarily driven by an immunopathological response, including inflammatory cell recruitment and viral damage to type II pneumocytes. This conclusion is further supported by non‐human primate and mouse models of SARS‐CoV infection, where lethal disease is more often associated with severe pulmonary lesions, alveolar exudates and respiratory dysfunction than with high viral load <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
, <xref rid="path4454-bib-0100" ref-type="ref">100</xref>
. MA‐SARS infection results in peak viral titres at 1–2 days post‐infection, along with airway denudation and resulting debris, which can occlude the small airways. Severe lung disease, including inflammatory cell infiltrates, haemorrhage, alveolar oedema and hyaline membrane formation typical of the exudative stage of DAD (Figure <xref rid="path4454-fig-0001" ref-type="fig">1</xref>
), occurs at days 4–7 post‐infection, when virus loads in the lung are dropping rapidly and/or are below the limit of detection. Many ISGs stimulated by SARS‐CoV infection are involved in wound‐healing responses and thus may contribute to SARS‐induced ALI and ARDS.</p>
<fig fig-type="Figure" xml:lang="en" id="path4454-fig-0001" orientation="portrait" position="float"><label>Figure 1</label>
<caption><p>MA‐SARS lung immunopathology. (A) Mock‐infected lung stained with haematoxylin and eosin. (B) Large airway of a C57BL/6 J (B6) mouse, 7 days post‐infection, with 10<sup>5</sup>
plaque‐forming units (PFU) MA‐SARS, shows denudation of the epithelial cells. (C, D) Immunohistochemical staining of the SARS‐CoV N protein at 2 days post‐infection shows staining consistent with infection of airway epithelial cells and type II pneumocytes, respectively. (E) MSB staining highlights fibrin in the parenchyma of the lung (red staining) in B6 mice, 7 days post‐infection with 10<sup>5</sup>
PFU MA‐SARS. (F) Perivascular cuffing in a B6 mouse, 4 days post‐infection with 10<sup>5</sup>
PFU MA‐SARS. (G) Hyaline membranes in the parenchyma of the lung of a B6 mouse, 7 days post‐infection with 10<sup>5</sup>
PFU MA‐SARS. (H) Inflammation in the lung of a B6 mouse, 7 days post‐infection with 10<sup>4</sup>
PFU MA‐SARS. (I) Haemorrhage in the lung of a <italic>Serpine1</italic>
mouse, 7 days post‐infection with 10<sup>4</sup>
PFU MA‐SARS.</p>
</caption>
<graphic id="nlm-graphic-1" xlink:href="PATH-235-185-g001"><alt-text>PATH-4454-FIG-0001-c</alt-text>
</graphic>
</fig>
<fig fig-type="Figure" xml:lang="en" id="path4454-fig-0002" orientation="portrait" position="float"><label>Figure 2</label>
<caption><p>Model of an infected alveolus in the lung. Type I and type II pneumocytes make up the alveolar walls and resident alveolar macrophages and pulmonary surfactant exist in the airspace (A). In the acute phase of SARS‐CoV infection (B), type I and type II pneumocytes are infected and secrete inflammatory cytokines, while surfactant levels decrease. During the late stage/tissue damage portion of viral infection, viral titres decrease, while airway debris, pulmonary oedema and hyaline membrane formation all impede respiration (C).</p>
</caption>
<graphic id="nlm-graphic-3" xlink:href="PATH-235-185-g002"><alt-text>PATH-4454-FIG-0002-c</alt-text>
</graphic>
</fig>
<p id="path4454-para-0020">While SARS‐CoV evades detection by the host immune system and causes minimal changes in transcript and protein levels for the first 24 h of infection <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
, it ultimately induces a massive signalling response in infected lungs. Pro‐inflammatory cytokines and chemokines, including IL‐6, TNF<italic>α</italic>
, IL‐1<italic>β</italic>
and CCL2 <xref rid="path4454-bib-0057" ref-type="ref">57</xref>
, recruit inflammatory cells to the site of infection. Neutrophils and cytotoxic T cells, along with these cytokines, can induce tissue damage, including vascular leakage, and stimulate pulmonary fibrosis <xref rid="path4454-bib-0101" ref-type="ref">101</xref>
. Pro‐fibrotic genes, including <italic>Tgfβ1</italic>
, <italic>Ctgf</italic>
and <italic>Pdgfa</italic>
and numerous collagen transcripts, have increased expression following MA‐SARS infection. Fluid exudates, haemorrhage and fibrin are all observed in the alveolar spaces of SARS patients, as well as in animal models of disease <xref rid="path4454-bib-0017" ref-type="ref">17</xref>
, <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
, <xref rid="path4454-bib-0102" ref-type="ref">102</xref>
, increasing in severity as a function of age. In response, the coagulation cascade is activated, including increased <italic>factor 10</italic>
(<italic>FX</italic>
), <italic>F2</italic>
, <italic>F3</italic>
(<italic>tissue factor</italic>
), <italic>F11</italic>
, <italic>F12</italic>
and <italic>F7</italic>
transcript levels. Activation of the coagulation cascade results in F10 cleavage of prothrombin into thrombin and subsequent thrombin cleavage of fibrinogen into fibrin <xref rid="path4454-bib-0103" ref-type="ref">103</xref>
. Fibrin clots in the alveoli are a prominent feature of SARS‐CoV infection in humans and mice. The goal of this coagulation response is likely to protect the host by sealing the alveoli, preventing alveolar flooding and haemorrhage, which limit oxygen exchange and endanger patient survival. Collagen expression is also increased following SARS‐CoV infection <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
. Collagen accumulation, fibrin and fibrin clots all contribute to a developing fibrotic lung state, while at the same time stimulating the infected host to up‐regulate fibrinolytic pathways <xref rid="path4454-bib-0092" ref-type="ref">92</xref>
.</p>
<p id="path4454-para-0021">Profibrinolytic genes include members of the urokinase pathway, such as <italic>urokinase</italic>
(<italic>plau</italic>
), <italic>tPA</italic>
and <italic>plasmin</italic>
(<italic>plg</italic>
) <xref rid="path4454-bib-0104" ref-type="ref">104</xref>
. The urokinase signalling pathway leads to cleavage and activation of plasmin into plasminogen; this protease then cleaves fibrin clots. Serpine1 and Serpine2 are negative regulators of urokinase pathway and inhibit urokinase and tissue plasminogen activator (tPA) activity. Urokinase signalling is highly active in the absence of Serpine1, and this imbalance often results in haemorrhage in knockout mice. Serpine1 is highly expressed in SARS patients, non‐human primates and small animal models <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
, <xref rid="path4454-bib-0074" ref-type="ref">74</xref>
, <xref rid="path4454-bib-0105" ref-type="ref">105</xref>
. ARDS studies, independent of coronavirus infection, have attributed this Serpine1 expression to alveolar macrophages and type II pneumocytes <xref rid="path4454-bib-0106" ref-type="ref">106</xref>
, <xref rid="path4454-bib-0107" ref-type="ref">107</xref>
. MA‐SARS infection in a <italic>Serpine1</italic>
knockout mouse model results in lethal disease with extreme lung pathology <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
. Conversely, MA‐SARS‐infected mice with a genetic deficiency in <italic>tPA</italic>
have increased exudates in the lung. The dysregulation of these coagulation/anti‐coagulation cascades can result in worsening end‐stage lung disease conditions, resulting in death.</p>
<p id="path4454-para-0022">Profibrotic and profibrinolytic signalling are part of the wound‐healing response, along with other extracellular matrix (ECM) remodelling pathways <xref rid="path4454-bib-0101" ref-type="ref">101</xref>
. SARS‐CoV infection causes massive tissue remodelling through urokinase and coagulation pathways activity, as discussed above. Other important wound‐healing pathways and ECM proteins with altered signalling following SARS‐CoV infection include matrix metalloproteinases, EGFR and collagens <xref rid="path4454-bib-0043" ref-type="ref">43</xref>
. Successful recovery from ALI requires a delicate balance of pro‐inflammatory, profibrotic and profibrinolytic responses. By altering ISG expression, including <italic>ACE2</italic>
, <italic>STAT1</italic>
and <italic>Serpine1</italic>
, SARS‐CoV infection of alveolar epithelial cells sets the stage for the development of severe lung disease, including ARDS.</p>
<p id="path4454-para-0023">SARS and MERS patients with severe lung disease exhibited lung consolidation, decreased blood oxygen saturation and often required intubation and ventilation <xref rid="path4454-bib-0099" ref-type="ref">99</xref>
, <xref rid="path4454-bib-0108" ref-type="ref">108</xref>
, <xref rid="path4454-bib-0109" ref-type="ref">109</xref>
. Small animal models of severe lung disease typically lack physiological readouts of respiratory function that can be directly correlated back to human signs of disease. Whole‐body plethysmography captures respiratory data in unrestrained animals, allowing for longitudinal measurement of pulmonary function; these data can also be directly related to some human respiratory metrics <xref rid="path4454-bib-0110" ref-type="ref">110</xref>
, <xref rid="path4454-bib-0111" ref-type="ref">111</xref>
. SARS‐CoV infection causes increased Penh, a calculated measure of airway resistance and increased EF50 (mid‐breath exhalation force), indicating that respiratory function is compromised and animals must do more work to breathe <xref rid="path4454-bib-0069" ref-type="ref">69</xref>
. Unpublished data (Gralinski and Menachery) indicate that it is the exhalation portion of each breath that is impacted by SARS‐CoV infection, likely due to extensive debris clogging the conducting airways. Further experiments have shown that <italic>Stat1</italic>
knockout mice have increased Penh levels early after infection, and that at late timepoints they have reduced lung capacity, corresponding with the profibrotic histopathological changes observed in the lung (Gralinski, unpublished data).</p>
</sec>
<sec id="path4454-sec-0004"><title>Concluding thoughts</title>
<p id="path4454-para-0024">ARDS is a devastating end‐stage lung disease with no cure. Despite numerous clinical trials, improved clinical outcomes have remained marginal at best <xref rid="path4454-bib-0112" ref-type="ref">112</xref>
. Several highly pathogenic emerging virus infections cause ARDS with high frequency, underscoring the critical public health importance of understanding the virological components and molecular mechanisms that drive this devastating end‐stage lung disease. Furthermore, a portion of ARDS cases may progress to pulmonary fibrosis, another clinically devastating end‐stage lung disease with few treatment options. Consequently, understanding the development of ARDS following viral infection remains a high‐priority research topic that is germane to global health and pandemic disease control. The twenty‐first century has demonstrated that zoonotic events will continue to introduce coronaviruses and other viruses into the human population, and that these viruses have the potential to spread rapidly, cause significant disease in communities and disrupt the global economy. An emerging theme is the connectivity between virus infection, complement and coagulation cascade activation, pro‐inflammatory and profibrotic cytokine responses and disease severity. More studies are needed to unravel the complex interactions between these pathways that can interact to promote or dysregulate wound recovery after life‐threatening respiratory virus infection. In particular there is a need for including well‐articulated animal models that faithfully recapitulate disease processes across species. Only through a better understanding of the interplay between a dysregulated host immune response and ALI and ARDS can more effective treatments and therapeutics be developed.</p>
</sec>
<sec id="path4454-sec-0006"><title>Author contributions</title>
<p id="path4454-para-0026">LEG and RSB wrote the paper.</p>
</sec>
</body>
<back><ack id="path4454-sec-0005"><title>Acknowledgements</title>
<p id="path4454-para-0025">This study was supported by funds from the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services, contract number HHSN272200800060C, U19 AI109761 and U19 AI100625.</p>
</ack>
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</back>
</pmc>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/SrasV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001847 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 001847 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= SrasV1 |flux= Pmc |étape= Corpus |type= RBID |clé= PMC:4267971 |texte= Molecular pathology of emerging coronavirus infections }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i -Sk "pubmed:25270030" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd \ | NlmPubMed2Wicri -a SrasV1
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