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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Experimental Human Metapneumovirus Infection of Cynomolgus Macaques (<italic>Macaca fascicularis</italic>) Results in Virus Replication in Ciliated Epithelial Cells and Pneumocytes with Associated Lesions throughout the Respiratory Tract</title><author><name sortKey="Kuiken, Thijs" sort="Kuiken, Thijs" uniqKey="Kuiken T" first="Thijs" last="Kuiken">Thijs Kuiken</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Den Hoogen, Bernadette G" sort="Van Den Hoogen, Bernadette G" uniqKey="Van Den Hoogen B" first="Bernadette G." last="Van Den Hoogen">Bernadette G. Van Den Hoogen</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Riel, Debby A J" sort="Van Riel, Debby A J" uniqKey="Van Riel D" first="Debby A. J." last="Van Riel">Debby A. J. Van Riel</name><affiliation><nlm:aff id="aff2">Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Laman, Jon D" sort="Laman, Jon D" uniqKey="Laman J" first="Jon D." last="Laman">Jon D. Laman</name><affiliation><nlm:aff id="aff2">Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Amerongen, Geert" sort="Van Amerongen, Geert" uniqKey="Van Amerongen G" first="Geert" last="Van Amerongen">Geert Van Amerongen</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Sprong, Leo" sort="Sprong, Leo" uniqKey="Sprong L" first="Leo" last="Sprong">Leo Sprong</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Fouchier, Ron A M" sort="Fouchier, Ron A M" uniqKey="Fouchier R" first="Ron A. M." last="Fouchier">Ron A. M. Fouchier</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Osterhaus, Albert D M E" sort="Osterhaus, Albert D M E" uniqKey="Osterhaus A" first="Albert D. M. E." last="Osterhaus">Albert D. M. E. Osterhaus</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">15161626</idno><idno type="pmc">1615765</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1615765</idno><idno type="RBID">PMC:1615765</idno><idno type="doi">10.1016/S0002-9440(10)63750-9</idno><date when="2004">2004</date><idno type="wicri:Area/Pmc/Corpus">000822</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000822</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Experimental Human Metapneumovirus Infection of Cynomolgus Macaques (<italic>Macaca fascicularis</italic>) Results in Virus Replication in Ciliated Epithelial Cells and Pneumocytes with Associated Lesions throughout the Respiratory Tract</title><author><name sortKey="Kuiken, Thijs" sort="Kuiken, Thijs" uniqKey="Kuiken T" first="Thijs" last="Kuiken">Thijs Kuiken</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Den Hoogen, Bernadette G" sort="Van Den Hoogen, Bernadette G" uniqKey="Van Den Hoogen B" first="Bernadette G." last="Van Den Hoogen">Bernadette G. Van Den Hoogen</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Riel, Debby A J" sort="Van Riel, Debby A J" uniqKey="Van Riel D" first="Debby A. J." last="Van Riel">Debby A. J. Van Riel</name><affiliation><nlm:aff id="aff2">Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Laman, Jon D" sort="Laman, Jon D" uniqKey="Laman J" first="Jon D." last="Laman">Jon D. Laman</name><affiliation><nlm:aff id="aff2">Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Van Amerongen, Geert" sort="Van Amerongen, Geert" uniqKey="Van Amerongen G" first="Geert" last="Van Amerongen">Geert Van Amerongen</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Sprong, Leo" sort="Sprong, Leo" uniqKey="Sprong L" first="Leo" last="Sprong">Leo Sprong</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Fouchier, Ron A M" sort="Fouchier, Ron A M" uniqKey="Fouchier R" first="Ron A. M." last="Fouchier">Ron A. M. Fouchier</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author><author><name sortKey="Osterhaus, Albert D M E" sort="Osterhaus, Albert D M E" uniqKey="Osterhaus A" first="Albert D. M. E." last="Osterhaus">Albert D. M. E. Osterhaus</name><affiliation><nlm:aff id="aff1">Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</nlm:aff></affiliation></author></analytic><series><title level="j">The American Journal of Pathology</title><idno type="ISSN">0002-9440</idno><idno type="eISSN">1525-2191</idno><imprint><date when="2004">2004</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A substantial proportion of hitherto unexplained respiratory tract illnesses is associated with human metapneumovirus (hMPV) infection. This virus also was found in patients with severe acute respiratory syndrome (SARS). To determine the dynamics and associated lesions of hMPV infection, six cynomolgus macaques (<bold><italic>Macaca fascicularis</italic></bold>) were inoculated with hMPV and examined by pathological and virological assays. They were euthanized at 5 (<bold><italic>n</italic></bold> = 2) or 9 (<bold><italic>n</italic></bold> = 2) days post-infection (dpi), or monitored until 14 dpi (<bold><italic>n</italic></bold> = 2). Viral excretion peaked at 4 dpi and decreased to zero by 10 dpi. Viral replication was restricted to the respiratory tract and associated with minimal to mild, multi-focal erosive and inflammatory changes in conducting airways, and increased numbers of macrophages in alveoli. Viral expression was seen mainly at the apical surface of ciliated epithelial cells throughout the respiratory tract, and less frequently in type 1 pneumocytes and alveolar macrophages. Both cell tropism and respiratory lesions were distinct from those of SARS-associated coronavirus infection, excluding hMPV as the primary cause of SARS. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Am J Pathol</journal-id><journal-id journal-id-type="iso-abbrev">Am. J. Pathol</journal-id><journal-title-group><journal-title>The American Journal of Pathology</journal-title></journal-title-group><issn pub-type="ppub">0002-9440</issn><issn pub-type="epub">1525-2191</issn><publisher><publisher-name>American Society for Investigative Pathology. Published by Elsevier Inc.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">15161626</article-id><article-id pub-id-type="pmc">1615765</article-id><article-id pub-id-type="publisher-id">S0002-9440(10)63750-9</article-id><article-id pub-id-type="doi">10.1016/S0002-9440(10)63750-9</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Experimental Human Metapneumovirus Infection of Cynomolgus Macaques (<italic>Macaca fascicularis</italic>) Results in Virus Replication in Ciliated Epithelial Cells and Pneumocytes with Associated Lesions throughout the Respiratory Tract</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Kuiken</surname><given-names>Thijs</given-names></name><email>t.kuiken@erasmusmc.nl</email><xref rid="cor1" ref-type="corresp">*</xref><xref rid="aff1" ref-type="aff">*</xref></contrib><contrib contrib-type="author"><name><surname>van den Hoogen</surname><given-names>Bernadette G.</given-names></name><xref rid="aff1" ref-type="aff">*</xref></contrib><contrib contrib-type="author"><name><surname>van Riel</surname><given-names>Debby A.J.</given-names></name><xref rid="aff2" ref-type="aff">†</xref></contrib><contrib contrib-type="author"><name><surname>Laman</surname><given-names>Jon D.</given-names></name><xref rid="aff2" ref-type="aff">†</xref></contrib><contrib contrib-type="author"><name><surname>van Amerongen</surname><given-names>Geert</given-names></name><xref rid="aff1" ref-type="aff">*</xref></contrib><contrib contrib-type="author"><name><surname>Sprong</surname><given-names>Leo</given-names></name><xref rid="aff1" ref-type="aff">*</xref></contrib><contrib contrib-type="author"><name><surname>Fouchier</surname><given-names>Ron A.M.</given-names></name><xref rid="aff1" ref-type="aff">*</xref></contrib><contrib contrib-type="author"><name><surname>Osterhaus</surname><given-names>Albert D.M.E.</given-names></name><xref rid="aff1" ref-type="aff">*</xref></contrib></contrib-group><aff id="aff1"><label>*</label>Department of Virology, Erasmus Medical Center, Rotterdam, the Netherlands</aff><aff id="aff2"><label>†</label>Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands</aff><author-notes><corresp id="cor1"><label>*</label>Address reprint requests to Thijs Kuiken, Department of Virology, Erasmus Medical Center, P.O. Box 1738, 3000 DR Rotterdam, the Netherlands <email>t.kuiken@erasmusmc.nl</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>16</day><month>12</month><year>2010</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>6</month><year>2004</year></pub-date><pub-date pub-type="epub"><day>16</day><month>12</month><year>2010</year></pub-date><volume>164</volume><issue>6</issue><fpage>1893</fpage><lpage>1900</lpage><history><date date-type="accepted"><day>2</day><month>3</month><year>2004</year></date></history><permissions><copyright-statement>Copyright © 2004 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.</copyright-statement><copyright-year>2004</copyright-year><copyright-holder>American Society for Investigative Pathology</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><abstract><p>A substantial proportion of hitherto unexplained respiratory tract illnesses is associated with human metapneumovirus (hMPV) infection. This virus also was found in patients with severe acute respiratory syndrome (SARS). To determine the dynamics and associated lesions of hMPV infection, six cynomolgus macaques (<bold><italic>Macaca fascicularis</italic></bold>) were inoculated with hMPV and examined by pathological and virological assays. They were euthanized at 5 (<bold><italic>n</italic></bold> = 2) or 9 (<bold><italic>n</italic></bold> = 2) days post-infection (dpi), or monitored until 14 dpi (<bold><italic>n</italic></bold> = 2). Viral excretion peaked at 4 dpi and decreased to zero by 10 dpi. Viral replication was restricted to the respiratory tract and associated with minimal to mild, multi-focal erosive and inflammatory changes in conducting airways, and increased numbers of macrophages in alveoli. Viral expression was seen mainly at the apical surface of ciliated epithelial cells throughout the respiratory tract, and less frequently in type 1 pneumocytes and alveolar macrophages. Both cell tropism and respiratory lesions were distinct from those of SARS-associated coronavirus infection, excluding hMPV as the primary cause of SARS. This study demonstrates that hMPV is a respiratory pathogen and indicates that viral replication is short-lived, polarized to the apical surface, and occurs primarily in ciliated respiratory epithelial cells.</p></abstract></article-meta></front><body><p id="para10">A substantial proportion of hitherto unexplained respiratory tract illnesses in human beings is associated with infection by a recently discovered paramyxovirus, provisionally named human metapneumovirus (hMPV).<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> It is most closely related to avian pneumovirus type C (APV), the etiological agent of rhinitis and sinusitis in turkeys.<xref rid="bib1" ref-type="bibr">1</xref>, <xref rid="bib2" ref-type="bibr">2</xref> Human metapneumovirus was first identified in the Netherlands, where serological studies indicate that it has been circulating in the human population since at least 1958 and that most children are infected by 5 years of age.<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> Since its discovery in the Netherlands, hMPV infection also has been reported elsewhere in Europe,<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib4" ref-type="bibr">4</xref>, <xref rid="bib5" ref-type="bibr">5</xref>, <xref rid="bib6" ref-type="bibr">6</xref>, <xref rid="bib7" ref-type="bibr">7</xref> North America,<xref rid="bib8" ref-type="bibr">8</xref>, <xref rid="bib9" ref-type="bibr">9</xref> Asia,<xref rid="bib10" ref-type="bibr">10</xref>, <xref rid="bib11" ref-type="bibr">11</xref> and Australia.<xref rid="bib12" ref-type="bibr"><sup>12</sup></xref> Respiratory tract disease associated with hMPV infection occurs both in children and adults, suggesting that hMPV is capable of causing clinically important re-infection of individuals later in life.<xref rid="bib3" ref-type="bibr">3</xref>, <xref rid="bib8" ref-type="bibr">8</xref> Clinically, hMPV-associated disease includes rhinitis, pharyngitis, bronchitis, bronchiolitis, and pneumonia, and resembles that of human respiratory syncytial virus (RSV) infection.<xref rid="bib13" ref-type="bibr"><sup>13</sup></xref> Severity of disease varies from common cold to death, with very young children, the elderly, and immunocompromised patients being predisposed to severe lower respiratory tract disease.<xref rid="bib13" ref-type="bibr"><sup>13</sup></xref></p><p id="para20">In the recent epidemic of severe acute respiratory syndrome (SARS), the role of hMPV as a primary pathogen or co-pathogen was considered.<xref rid="bib14" ref-type="bibr"><sup>14</sup></xref> Although a newly discovered virus, SARS-associated coronavirus (SCV), proved to be the primary cause of the disease,<xref rid="bib15" ref-type="bibr">15</xref>, <xref rid="bib16" ref-type="bibr">16</xref> 12% (41 of 335) of SARS patients also were infected with hMPV,<xref rid="bib17" ref-type="bibr"><sup>17</sup></xref> so that the role of hMPV as a co-pathogen cannot be ruled out at this time.</p><p id="para30">Until now, pathological confirmation that hMPV is a primary respiratory pathogen is lacking.<xref rid="bib18" ref-type="bibr"><sup>18</sup></xref> Diagnosis of hMPV as the etiological agent of respiratory illness in the above studies was based on virus isolation, reverse transcription-polymerase chain reaction (RT-PCR), seroconversion to hMPV, or a combination of these methods, combined with the failure to detect other known respiratory pathogens. To characterize the virus excretion, virus distribution, and associated lesions of hMPV infection, and to determine whether they differ from those of SCV infection, we experimentally inoculated six cynomolgus macaques (<italic>Macaca fascicularis</italic>) with the prototype hMPV isolate NL/1/00<sup>2</sup>. They were euthanized at 5 (<italic>n</italic> = 2) or 9 (<italic>n</italic> = 2) days post-infection (dpi), or monitored until 14 dpi (<italic>n</italic> = 2). Here, we report the pathological, immunohistochemical, virological, serological, and molecular biological findings of this experiment.</p><sec id="cesec10"><title>Materials and Methods</title><sec id="cesec20"><title>Virus Preparation</title><p id="para40">The prototype hMPV isolate NL/1/00<sup>2</sup> was propagated three times on tertiary monkey kidney (tMK) cells and used to make a virus stock on tMK cells as previously described.<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> Virus was harvested 7 dpi and frozen in 25% sucrose at −70°C. The infectious virus titer of this stock was 10<sup>4.5</sup> median tissue culture infective dose (TCID<sub>50</sub>) per ml by titration on tMK cells.</p></sec><sec id="cesec30"><title>Experimental Protocol</title><p id="para50">Five days before infection, six juvenile cynomolgus macaques were placed in a negatively pressurized glove box in pairs of one male and one female. They were provided with commercial food pellets and water <italic>ad libitum</italic>. These macaques were colony-bred and had been maintained in group housing, where they were screened annually, and tested negative, for the following infections: simian virus 40, polyomavirus, tuberculosis, measles virus, mumps, simian immunodeficiency virus, simian retrovirus type D, and simian T-cell leukemia virus. Before infection, they were examined clinically and determined as healthy by a registered veterinarian. The macaques were infected with 5.0 × 10<sup>4</sup> TCID<sub>50</sub> of hMPV, which was suspended in 5 ml of phosphate-buffered saline (PBS). Approximately 4 ml was applied intratracheally by use of a catheter, 0.5 ml on the tonsils, and 0.25 ml on each of the conjunctivae.</p><p id="para60">The macaques were observed daily for the occurrence of malaise, coughing, exudate from the eyes or nose, forced respiration, and any other signs of illness. Macaques No. 1 and No. 2 were euthanized at 5 dpi and macaques No. 3 and No. 4 at 9 dpi by exsanguination under ketamine anesthesia, while macaques No. 5 and No. 6 were monitored until 14 dpi. Macaques No. 5 and No. 6 were subsequently used for a follow-up experiment, not described here. The body temperatures of macaques No. 5 and No. 6 were measured by telemetry (IMAG, Wageningen, the Netherlands) every 3 minutes. To this end, a transponder was placed in their abdomens 30 days before inoculation.</p><p id="para70">Just before infection and daily from 2 dpi until euthanasia or 10 dpi, the macaques were anesthetized with ketamine and pharyngeal swabs were collected in 1 ml transport medium<xref rid="bib19" ref-type="bibr"><sup>19</sup></xref> and stored at −70°C until RT-PCR and/or virus isolation. In addition, blood was collected from an inguinal vein just before infection in all macaques and at 14 dpi in macaques No. 5 and No. 6. Blood samples were collected in EDTA tubes and centrifuged at 2500 × <italic>g</italic> for 15 minutes, the plasma was collected and stored at −70°C until immunofluorescence assay. All animal procedures were approved by our institutional Animal Care and Use Committee.</p></sec><sec id="cesec40"><title>Pathological Examination</title><p id="para80">Necropsies were carried out according to a standard protocol. Samples for histological examination were stored in 10% neutral-buffered formalin (lungs after inflation with formalin), embedded in paraffin, sectioned at 4 μm, and stained with hematoxylin and eosin (H & E) for examination by light microscopy. The following tissues were examined by light microscopy: adrenal gland, brain stem, cerebellum, cerebrum, heart (left and right ventricle), kidney, larynx, lung (left and right, cranial, medial, and caudal lobes), liver, nasal septum (posterior section covered by respiratory epithelium), pancreas, primary bronchus (left and right), small intestine, spleen, stomach, tonsil, trachea, tracheo-bronchial lymph node, upper eyelid (left and right), and urinary bladder. Tissue sections of a clinically healthy juvenile male cynomolgus macaque that had not been infected with hMPV were used as a negative control.</p></sec><sec id="cesec50"><title>Immunohistochemistry</title><p id="para90">Formalin-fixed, paraffin-embedded, 4-μm thick sections of the same tissues examined by light microscopy were stained using an immunoperoxidase method. Tissue sections were mounted on coated slides (Klinipath, Duiven, the Netherlands), deparaffinized, rehydrated, and boiled for 15 minutes in citric acid buffer (10 mmol/L, pH 6.0) using a microwave oven. Endogenous peroxidase was revealed with 4-chloro-1-naphthol (Sigma Chemical Co., St. Louis, MO), yielding a blue-black precipitate. Sections were subsequently washed with PBS containing 0.05% Tween 20 (Fluka, Chemie AG, Buchs, Switzerland) and incubated with a polyclonal guinea pig antiserum (dilution 1:200) to hMPV prepared as described previously<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> or with a negative control guinea pig serum for 1 hour at room temperature. After washing, sections were incubated with a horseradish peroxidase (HRP)-labeled rabbit-anti-guinea pig Ig (DAKO, Glostrup, Denmark) for 1 hour at room temperature. HRP activity was revealed by incubating the sections in 3-amino-9-ethylcarbazole (Sigma Chemical Co.) solution for 10 minutes, resulting in a red precipitate. Sections were counterstained with hematoxylin. Formalin-fixed, paraffin-embedded tMK cells infected with hMPV were included as a positive control. Tissue sections of a clinically healthy juvenile male cynomolgus macaque that had not been infected with hMPV were used as a negative control. Selected lung sections were stained with monoclonal antibody AE1/AE3 (Neomarkers, Fremont, CA) for the identification of epithelial cells according to standard immunohistochemical procedures.</p></sec><sec id="cesec60"><title>RT-PCR</title><p id="para100">Tissue samples of brain, heart, kidney, lung (cranial and caudal lobes), liver, nasal septum, primary bronchus, spleen, tonsil, trachea, and tracheo-bronchial lymph node were weighed and homogenized in minimal essential medium (10 ml per g tissue; Biowhittaker, Verviers, Belgium) by use of Potter tissue grinders (Fisher Scientific, 's-Hertogenbosch, the Netherlands). The homogenates were incubated with lysis buffer (2 ml per ml homogenate; Roche Diagnostics, Almere, the Netherlands) containing proteinase K for 1 hour at room temperature, and RNA was isolated by use of a High Pure RNA Isolating kit (Roche Diagnostics) according to the manufacturer's instructions, resulting in 50 μl RNA. RNA was isolated from 200 μl of transport medium from the pharyngeal swabs according to the same method. A Taqman real-time PCR developed in-house<xref rid="bib20" ref-type="bibr"><sup>20</sup></xref> was performed in triplicate on 5 μl of isolated RNA from each sample, using serial dilutions of a titrated stock of the same virus as the calibration curve. The virus titer was expressed as TCID<sub>50</sub> per mg tissue or ml transport medium from pharyngeal swabs.</p></sec><sec id="cesec70"><title>Virus Isolation</title><p id="para110">Virus isolation on pharyngeal swabs was performed on Vero cells, clone 118, in the absence of fetal calf serum in the presence of 0.02% trypsin and 0.3% bovine albumin Fraction V (Invitrogen, Groningen, the Netherlands). The Vero-118 cell line, developed in-house, has equal susceptibility and sensitivity to all known genetic lineages of hMPV. The Vero-118 cells had been grown in Iscove's Modified Dulbecco's medium (Biowhittaker) supplemented with 10% fetal calf serum (Biowhittaker) and 2 mmol/L glutamine (Biowhittaker). The identity of the virus was confirmed by RT-PCR and automatic sequencing.<xref rid="bib21" ref-type="bibr"><sup>21</sup></xref></p></sec><sec id="cesec80"><title>Immunofluorescence Assay</title><p id="para120">Ninety-six-well plates coated with Vero-118 cells and infected with hMPV NL/1/00 were incubated with serial dilutions (up to 1:64) of plasma samples for 1 hour at 37°C. After washing with PBS, plates were incubated with fluorescein isothiocyanate-labeled anti-human IgG (DAKO, 1:60) for 1 hour at 37°C. After washing with PBS and background staining with eriochrome black (Sigma Chemical Co.) for 1 minute, plates were read under an ultraviolet microscope. Non-infected Vero-118 cells were used as a negative control. Titers were expressed as the reciprocal of the last positive dilution.</p></sec></sec><sec id="cesec90"><title>Results</title><sec id="cesec100"><title>Clinical Findings</title><p id="para130">Rhinorrhea was seen in macaque No. 4 and No. 5 at 8 dpi. No clinical signs, including increased body temperatures in macaques No. 5 and No. 6, were seen in the other macaques.</p></sec><sec id="cesec110"><title>Gross Pathology</title><p id="para140">Inspissated purulent exudate was present in the nasal cavity of macaques No. 2 and No. 4. In the former, the lining mucosa was reddened. Macaque No. 4 had aspirated food remains immediately before euthanasia and was excluded from further laboratory examination because histological lesions of hMPV infection were masked and aspirated debris reacted non-specifically by immunohistochemistry. No other gross lesions were seen in these two macaques or in the other macaques.</p></sec><sec id="cesec120"><title>Histopathology</title><p id="para150">Macaques No. 1 to No. 3 had a mild rhinitis, characterized in the epithelium by loss of ciliation, architectural disruption, intra- and intercellular edema, and transmigration of a few neutrophils (<xref rid="fig1" ref-type="fig">Figure 1B</xref>). There was edema and infiltration with a few neutrophils in the underlying submucosa.<fig id="fig1"><label>Figure 1</label><caption><p>Histopathology of experimental human metapneumovirus infection in cynomolgus macaques. <bold>A:</bold> Section of respiratory mucosa from nasal septum of negative control macaque. The pseudo-stratified epithelium consists of ciliated cells with cilia on apical surface, goblet cells with clear cytoplasm, and basal cells lying on the basement membrane. (H&E, original magnification, ×100). <bold>B:</bold> Section of respiratory mucosa from nasal septum of macaque No. 1. Suppurative rhinitis. There is loss of cilia, intercellular edema, architectural disruption, erosion, and infiltration with many neutrophils in the epithelium and submucosa. (H&E, original magnification, ×100). <bold>C:</bold> Section of tracheal mucosa of negative control macaque. The pseudo-stratified epithelium has the same constituent cells as in panel <bold>A</bold>. (H&E, original magnification, ×250). <bold>D:</bold> Tracheal section of macaque No. 1. Suppurative tracheitis. There is multi-focal loss of cilia, intercellular edema, architectural disruption, and infiltration with a few neutrophils in the epithelium and submucosa. (H&E, original magnification, ×250). <bold>E:</bold> Pulmonary section of macaque No. 3. Bronchiolitis. The bronchiolar lumen (<bold>arrowhead</bold>) is partly filled with macrophages. An increased number of macrophages also is present in alveolar lumina (<bold>arrows</bold>) adjacent to the bronchiole. (H&E, original magnification ×25). <bold>F:</bold> Pulmonary section of macaque No. 3. Erosive bronchiolitis. There is loss of bronchiolar epithelium, and the bronchiolar lumen is filled with macrophages. (H&E, original magnification, ×100). <bold>G:</bold> Pulmonary section of macaque No. 3. Erosive bronchiolitis. Detail of panel <bold>F</bold>. Cuboidal cells (<bold>arrowheads</bold>) line the bronchiolar wall. The bronchiolar wall in between the arrowheads is denuded. (H&E, original magnification, ×250).</p></caption><graphic xlink:href="gr1_lrg"></graphic></fig></p><p id="para160">All three macaques had minimal multi-focal lesions in the conducting airways, variable in extension from larynx to bronchioles (<xref rid="tbl1" ref-type="table">Table 1</xref>; <xref rid="fig1" ref-type="fig">Figure 1, D to G</xref>). Epithelial lesions consisted of loss of ciliation, architectural disruption, erosion, intercellular edema, and transmigration of neutrophils. There was infiltration with a few neutrophils in the underlying submucosa. The lumen of some bronchi contained a few sloughed ciliated epithelial cells admixed with scant cellular debris and mucus. The lumen of some bronchioles contained a few alveolar macrophages, rare multinucleated giant cells and neutrophils, admixed with scant cellular debris and fibrin. Similar material was present in the alveoli around affected bronchioles. No significant histological changes were seen in sections of other tissues examined. Above lesions were not seen in the tissues of the negative control macaque.<table-wrap position="float" id="tbl1"><label>Table 1</label><caption><p>Microscopic Lesions and Presence of hMPV Antigen in Various Tissues of the Respiratory Tract of Cynomolgus Macaques Experimentally Infected with hMPV</p></caption><table frame="hsides" rules="groups"><thead><tr><th></th><th></th><th colspan="15" align="center">Evidence of lesions by histology (HI) or of hMPV by immunohistochemistry (IHC) or RT-PCR in the respiratory tract<hr></hr></th></tr><tr><th></th><th></th><th colspan="3" align="center">Nasal septum<hr></hr></th><th colspan="3" align="center">Trachea<hr></hr></th><th colspan="3" align="center">Bronchus<hr></hr></th><th colspan="3" align="center">Cranial lung<hr></hr></th><th colspan="3" align="center">Caudal lung<hr></hr></th></tr><tr><th align="center">Macaque no.</th><th align="center">Days post-infection</th><th align="center">HI</th><th align="center">IHC</th><th align="center">PCR</th><th align="center">HI</th><th align="center">IHC</th><th align="center">PCR</th><th align="center">HI</th><th align="center">IHC</th><th align="center">PCR</th><th align="center">HI</th><th align="center">IHC</th><th align="center">PCR</th><th align="center">HI</th><th align="center">IHC</th><th align="center">PCR</th></tr></thead><tbody><tr><td align="char">1</td><td align="char">5</td><td align="center">+<xref rid="tbl1fn1" ref-type="table-fn">*</xref></td><td align="center">+</td><td align="char">73 ± 9.5<xref rid="tbl1fn2" ref-type="table-fn">†</xref></td><td align="center">+</td><td align="center">+</td><td align="char">377 ± 41</td><td align="center">+</td><td align="center">+</td><td align="char">1675 ± 32</td><td align="center">+</td><td align="center">+</td><td align="char">32 ± 9.3</td><td align="center">+</td><td align="center">+</td><td align="char">73 ± 18</td></tr><tr><td align="char">2</td><td align="char">5</td><td align="center">+</td><td align="center">+</td><td align="char">47 ± 5.8</td><td align="center">−<xref rid="tbl1fn3" ref-type="table-fn">‡</xref></td><td align="center">−</td><td align="char">4 ± 1.7</td><td align="center">−</td><td align="center">+</td><td align="char">98 ± 16</td><td align="center">+</td><td align="center">+</td><td align="char">115 ± 30</td><td align="center">+</td><td align="center">+</td><td align="char">68 ± 7.4</td></tr><tr><td align="char">3</td><td align="char">9</td><td align="center">+</td><td align="char">−</td><td align="char">5 ± 2.3</td><td align="center">+</td><td align="center">−</td><td align="char">0 ± 0.2</td><td align="center">−</td><td align="center">−</td><td align="char">25 ± 7.8</td><td align="center">+</td><td align="center">+</td><td align="char">45 ± 5.9</td><td align="center">+</td><td align="center">+</td><td align="char">15 ± 7.5</td></tr></tbody></table><table-wrap-foot><fn id="tbl1fn1"><label>*</label><p>Positive.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tbl1fn2"><label>†</label><p>Mean ± standard deviation TCID<sub>50</sub>/mg tissue.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tbl1fn3"><label>‡</label><p>Negative.</p></fn></table-wrap-foot></table-wrap></p></sec><sec id="cesec130"><title>Immunohistochemistry</title><p id="para170">Expression of hMPV occurred mainly in ciliated respiratory epithelium from the nasal cavity to the bronchioles in both macaques euthanized at 5 dpi, but not in the macaque euthanized at 9 dpi (<xref rid="tbl1" ref-type="table">Table 1</xref>; <xref rid="fig2" ref-type="fig">Figure 2, A to C</xref>). It occurred multi-focally in individual or groups of adjacent ciliated epithelial cells, and was seen both in morphologically normal (<xref rid="fig2" ref-type="fig">Figure 2B</xref>) and in degenerate or sloughed ciliated cells (<xref rid="fig2" ref-type="fig">Figure 2A</xref>). Expression of hMPV was visible as dark red staining of the cilia and apical plasma membrane, and diffuse lighter red staining of the cytoplasm. Neither goblet cells nor basal cells stained positively, even where they were located immediately adjacent to positively staining ciliated cells.<fig id="fig2"><label>Figure 2</label><caption><p>Immunohistochemistry of experimental human metapneumovirus (hMPV) infection in cynomolgus macaques. <bold>A:</bold> Section of respiratory mucosa from nasal septum of macaque No. 2. Expression of hMPV occurs in the cytoplasm of degenerate epithelial cells and in cell debris. (Immunoperoxidase stain for hMPV, original magnification, ×100). <bold>B:</bold> Bronchial section of macaque No. 1. Expression of hMPV occurs in the cytoplasm of morphologically normal ciliated epithelial cells. (Immunoperoxidase stain for hMPV, original magnification, ×100). <bold>C:</bold> Bronchial section of macaque No. 1. Detail of panel <bold>B</bold>. Expression of hMPV is most pronounced in the cilia and apical plasma membrane of ciliated epithelial cells. Mucus cells and basal cells stain negative. (Immunoperoxidase stain for hMPV, original magnification, ×250). <bold>D</bold> and <bold>E:</bold> Pulmonary section of macaque No. 1. Expression of hMPV occurs diffusely in the cytoplasm of type 1 pneumocytes lining the alveolar walls. (Immunoperoxidase stain for hMPV, original magnification, ×250). <bold>F:</bold> Pulmonary section of macaque No. 1. Expression of hMPV occurs in the cytoplasm of alveolar macrophages and in intraluminal cell debris. Staining of alveolar macrophages is multi-focal and granular. (Immunoperoxidase stain for hMPV, original magnification, ×250). <bold>G:</bold> Bronchial section of negative control macaque. There is no expression of hMPV. (Immunoperoxidase stain for hMPV; original magnification, ×250). <bold>H:</bold> Pulmonary section of negative control macaque. There is no expression of hMPV. (Immunoperoxidase stain for hMPV, original magnification, ×250).</p></caption><graphic xlink:href="gr2_lrg"></graphic></fig></p><p id="para180">Expression of hMPV occurred occasionally in alveoli of all three macaques (<xref rid="fig2" ref-type="fig">Figure 2, D to F</xref>). It occurred multi-focally in type 1 pneumocytes, individual or small clusters of adjacent alveolar macrophages, and in intraluminal cellular debris. Expression in type 1 pneumocytes was visible as diffuse cytoplasmic staining (<xref rid="fig2" ref-type="fig">Figure 2, D and E</xref>). These cells were identified as type 1 pneumocytes because they lined the alveolar walls, were squamous, and expressed keratin in serial sections. In alveolar macrophages, it consisted of multiple distinct dark red granules in the cytoplasm (<xref rid="fig2" ref-type="fig">Figure 2F</xref>). Multinucleated giant cells did not stain positively. No positive staining was observed in any of the other tissues examined, nor in tissues of the negative control macaque (<xref rid="fig2" ref-type="fig">Figure 2, G and H</xref>).</p></sec><sec id="cesec140"><title>RT-PCR and Virus Isolation</title><p id="para190">After an incubation period of 2 days at most, excretion of hMPV increased rapidly to a peak of 1.3 × 10<sup>6</sup> TCID<sub>50</sub>/ml at 4 dpi, and then decreased gradually to zero at 10 dpi (<xref rid="fig3" ref-type="fig">Figure 3</xref>). The results of RT-PCR were confirmed by virus isolation: hMPV was re-isolated from pharyngeal swabs collected at the peak of virus excretion of all six macaques.<fig id="fig3"><label>Figure 3</label><caption><p>Pharyngeal excretion of human metapneumovirus by experimentally infected macaques. The numbers in the bars indicate the number of macaques sampled on each day.</p></caption><graphic xlink:href="gr3_lrg"></graphic></fig></p><p id="para200">At necropsy, hMPV was detected by RT-PCR throughout the respiratory tract, from the nasal cavity to the lungs, and virus titers were generally higher at 5 dpi than at 9 dpi (<xref rid="tbl1" ref-type="table">Table 1</xref>). The virus titers (mean ± SD TCID<sub>50</sub> per mg tissue) in the tonsil (26 ± 6.4 in macaque No. 1, 14 ± 3.2 in macaque No. 2, and 0 in macaque No. 3) and tracheo-bronchial lymph node (192 ± 42 in macaque No. 1, 2.1 ± 0.7 in macaque No. 2, and 3.2 ± 2.5 in macaque No. 3) corresponded to this temporal pattern. Human metapneumovirus was not detected by RT-PCR in brain, heart, kidney, liver, or spleen of any of the macaques.</p></sec><sec id="cesec150"><title>Immunofluorescence Assay</title><p id="para210">Before inoculation, anti-hMPV antibodies were not detected in plasma samples of any of the six macaques. At 14 dpi, both macaques No. 5 and No. 6 had seroconverted with an anti-hMPV antibody titer of ≥64.</p></sec></sec><sec id="cesec160"><title>Discussion</title><p id="para220">This experimental infection confirms that hMPV is a primary pathogen of the upper and lower respiratory tract in cynomolgus macaques. Clinical signs in hMPV-infected macaques were limited to rhinorrhea, and corresponded with a suppurative rhinitis at pathological examination. Additional histological lesions in the respiratory tract were minimal to mild erosive and inflammatory changes in mucosa and submucosa of conducting airways, and an increased number of alveolar macrophages in bronchioles and pulmonary alveoli. The close association between the respiratory lesions and the specific expression of hMPV antigen by immunohistochemistry, together with the absence of these lesions in the negative control tissues, support our conclusion that hMPV infection was the cause of these lesions.</p><p id="para230">Based on expression of hMPV by immunohistochemistry, viral replication in ciliated epithelial cells was widespread throughout the respiratory tract and more sporadic in type 1 pneumocytes. Viral antigen also was detected in alveolar macrophages, but the distinct granular character of cytoplasmic staining suggests phagocytosis of viral material rather than viral replication. The strong reduction in the distribution of hMPV-infected cells in the respiratory tract between 5 and 9 dpi (<xref rid="tbl1" ref-type="table">Table 1</xref>) corresponds with the reduction in viral excretion, as measured by RT-PCR, from the peak at 4 dpi to zero by 10 dpi (<xref rid="fig3" ref-type="fig">Figure 3</xref>). If possible, these immunohistochemical results should be substantiated with a larger number of animals. The absence of hMPV expression by immunohistochemistry in other tissues indicates that hMPV replication is restricted to the respiratory tract. The above conclusions were corroborated by the results of virus isolation and RT-PCR.</p><p id="para240">These findings substantiate the claim of van den Hoogen et al<xref rid="bib1" ref-type="bibr"><sup>1</sup></xref> that hMPV infection causes respiratory tract illness in human beings. The subclinical or mild character of the disease associated with hMPV infection in these macaques corresponds to that in immunocompetent middle-age adults.<xref rid="bib13" ref-type="bibr"><sup>13</sup></xref> Based on the ability of hMPV to replicate in the bronchioles and alveoli of cynomolgus macaques, one may expect more extensive viral replication and an associated increased severity of lesions in the lower respiratory tract of immunocompromised human beings, resulting in the severe bronchiolitis and pneumonia diagnosed clinically in such patients.<xref rid="bib22" ref-type="bibr">22</xref>, <xref rid="bib23" ref-type="bibr">23</xref></p><p id="para250">The predominant tropism of hMPV for ciliated epithelial cells in the conducting airways and the mildness of the associated lesions, as seen in this study, contrasts with the predilection of SCV for alveolar epithelial cells and the severity of the associated pneumonia in SARS patients<xref rid="bib15" ref-type="bibr">15</xref>, <xref rid="bib24" ref-type="bibr">24</xref>, <xref rid="bib25" ref-type="bibr">25</xref>, <xref rid="bib26" ref-type="bibr">26</xref> and experimentally infected macaques.<xref rid="bib16" ref-type="bibr">16</xref>, <xref rid="bib17" ref-type="bibr">17</xref> These differences confirm that SCV and not hMPV is the primary etiological agent of SARS.</p><p id="para260">The pathogenesis of hMPV infection in macaques is similar in many ways to that of RSV in human beings, as far as it has been studied. As in hMPV, incubation period and excretion period are short, although RSV excretion may be prolonged in infants and immunocompromised individuals.<xref rid="bib27" ref-type="bibr"><sup>27</sup></xref> Both initial infection and subsequent shedding of RSV are restricted to ciliated epithelial cells, based on an <italic>in vitro</italic> study using recombinant RSV expressing green fluorescent protein.<xref rid="bib28" ref-type="bibr"><sup>28</sup></xref> Similar to the localization of RSV in that study, the results of immunohistochemistry in these macaques show that hMPV infection is polarized to the apical surface of ciliated respiratory epithelium. In immunocompetent individuals, the most common clinical manifestation of RSV infection is mild upper respiratory tract disease.<xref rid="bib29" ref-type="bibr"><sup>29</sup></xref> However, viral distribution and associated lesions of this mild disease have not been reported. In very young or immunocompromised individuals, RSV replication occurs in epithelial cells of bronchus, bronchiole, and in alveolar macrophages,<xref rid="bib30" ref-type="bibr">30</xref>, <xref rid="bib31" ref-type="bibr">31</xref> and is associated with severe bronchiolitis, interstitial pneumonia, or giant cell pneumonia.<xref rid="bib32" ref-type="bibr"><sup>32</sup></xref> Although clinical studies indicate that hMPV infection may cause similar lesions in this category of patients, confirmation of fatal bronchiolitis or pneumonia from hMPV infection awaits pathological assessment of biopsy or autopsy samples.<xref rid="bib18" ref-type="bibr"><sup>18</sup></xref></p><p id="para270">The pathogenesis of hMPV infection also is similar to that of APV, its closest known relative.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> As for hMPV infection in cynomolgus macaques, APV infection in turkeys has a short incubation and excretion period (2 and 8 days, respectively), occurs primarily in ciliated respiratory epithelial cells, and is associated with superficial erosive and inflammatory changes. In contrast to hMPV infection, APV antigen is not present in alveolar macrophages or alveolar walls. However, this difference may be explained, at least in part, by the intratracheal application of hMPV in macaques (this study) compared to the conjunctival and intranasal application of APV in experimentally infected turkeys.<xref rid="bib33" ref-type="bibr"><sup>33</sup></xref></p><p id="para280">The results of this study provide the first characterization of the viral excretion, viral distribution and associated lesions of hMPV infection in cynomolgus macaques, and help to understand the pathology of this infection in human beings. 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R.F. is a fellow of the Royal Dutch Academy of Arts and Sciences.</p></fn><fn id="d32e828"><p>T.K. and B.G.V.D.H. contributed equally to this work.</p></fn></fn-group></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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