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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Replication of MERS and SARS coronaviruses in bat cells offers insights to their ancestral origins</title><author><name sortKey="Lau, Susanna K P" sort="Lau, Susanna K P" uniqKey="Lau S" first="Susanna K. P." last="Lau">Susanna K. P. Lau</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Fan, Rachel Y Y" sort="Fan, Rachel Y Y" uniqKey="Fan R" first="Rachel Y. Y." last="Fan">Rachel Y. Y. Fan</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Luk, Hayes K H" sort="Luk, Hayes K H" uniqKey="Luk H" first="Hayes K. H." last="Luk">Hayes K. H. Luk</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Zhu, Longchao" sort="Zhu, Longchao" uniqKey="Zhu L" first="Longchao" last="Zhu">Longchao Zhu</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Fung, Joshua" sort="Fung, Joshua" uniqKey="Fung J" first="Joshua" last="Fung">Joshua Fung</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Li, Kenneth S M" sort="Li, Kenneth S M" uniqKey="Li K" first="Kenneth S. M." last="Li">Kenneth S. M. Li</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Wong, Emily Y M" sort="Wong, Emily Y M" uniqKey="Wong E" first="Emily Y. M." last="Wong">Emily Y. M. Wong</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Ahmed, Syed Shakeel" sort="Ahmed, Syed Shakeel" uniqKey="Ahmed S" first="Syed Shakeel" last="Ahmed">Syed Shakeel Ahmed</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Chan, Jasper F W" sort="Chan, Jasper F W" uniqKey="Chan J" first="Jasper F. W." last="Chan">Jasper F. W. Chan</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Kok, Raven K H" sort="Kok, Raven K H" uniqKey="Kok R" first="Raven K. H." last="Kok">Raven K. H. Kok</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Chan, Kwok Hung" sort="Chan, Kwok Hung" uniqKey="Chan K" first="Kwok-Hung" last="Chan">Kwok-Hung Chan</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Wernery, Ulrich" sort="Wernery, Ulrich" uniqKey="Wernery U" first="Ulrich" last="Wernery">Ulrich Wernery</name><affiliation><nlm:aff id="Aff5"><institution-wrap><institution-id institution-id-type="ISNI">0000 0004 1796 4199</institution-id><institution-id institution-id-type="GRID">grid.417775.7</institution-id><institution>Central Veterinary Research Laboratory,</institution></institution-wrap>Dubai, United Arab Emirates</nlm:aff></affiliation></author><author><name sortKey="Yuen, Kwok Yung" sort="Yuen, Kwok Yung" uniqKey="Yuen K" first="Kwok-Yung" last="Yuen">Kwok-Yung Yuen</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Woo, Patrick C Y" sort="Woo, Patrick C Y" uniqKey="Woo P" first="Patrick C. Y." last="Woo">Patrick C. Y. Woo</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">30531999</idno><idno type="pmc">6286955</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286955</idno><idno type="RBID">PMC:6286955</idno><idno type="doi">10.1038/s41426-018-0208-9</idno><date when="2018">2018</date><idno type="wicri:Area/Pmc/Corpus">000360</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000360</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Replication of MERS and SARS coronaviruses in bat cells offers insights to their ancestral origins</title><author><name sortKey="Lau, Susanna K P" sort="Lau, Susanna K P" uniqKey="Lau S" first="Susanna K. P." last="Lau">Susanna K. P. Lau</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Fan, Rachel Y Y" sort="Fan, Rachel Y Y" uniqKey="Fan R" first="Rachel Y. Y." last="Fan">Rachel Y. Y. Fan</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Luk, Hayes K H" sort="Luk, Hayes K H" uniqKey="Luk H" first="Hayes K. H." last="Luk">Hayes K. H. Luk</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Zhu, Longchao" sort="Zhu, Longchao" uniqKey="Zhu L" first="Longchao" last="Zhu">Longchao Zhu</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Fung, Joshua" sort="Fung, Joshua" uniqKey="Fung J" first="Joshua" last="Fung">Joshua Fung</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Li, Kenneth S M" sort="Li, Kenneth S M" uniqKey="Li K" first="Kenneth S. M." last="Li">Kenneth S. M. Li</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Wong, Emily Y M" sort="Wong, Emily Y M" uniqKey="Wong E" first="Emily Y. M." last="Wong">Emily Y. M. Wong</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Ahmed, Syed Shakeel" sort="Ahmed, Syed Shakeel" uniqKey="Ahmed S" first="Syed Shakeel" last="Ahmed">Syed Shakeel Ahmed</name><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Chan, Jasper F W" sort="Chan, Jasper F W" uniqKey="Chan J" first="Jasper F. W." last="Chan">Jasper F. W. Chan</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Kok, Raven K H" sort="Kok, Raven K H" uniqKey="Kok R" first="Raven K. H." last="Kok">Raven K. H. Kok</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Chan, Kwok Hung" sort="Chan, Kwok Hung" uniqKey="Chan K" first="Kwok-Hung" last="Chan">Kwok-Hung Chan</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Wernery, Ulrich" sort="Wernery, Ulrich" uniqKey="Wernery U" first="Ulrich" last="Wernery">Ulrich Wernery</name><affiliation><nlm:aff id="Aff5"><institution-wrap><institution-id institution-id-type="ISNI">0000 0004 1796 4199</institution-id><institution-id institution-id-type="GRID">grid.417775.7</institution-id><institution>Central Veterinary Research Laboratory,</institution></institution-wrap>Dubai, United Arab Emirates</nlm:aff></affiliation></author><author><name sortKey="Yuen, Kwok Yung" sort="Yuen, Kwok Yung" uniqKey="Yuen K" first="Kwok-Yung" last="Yuen">Kwok-Yung Yuen</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author><author><name sortKey="Woo, Patrick C Y" sort="Woo, Patrick C Y" uniqKey="Woo P" first="Patrick C. Y." last="Woo">Patrick C. Y. Woo</name><affiliation><nlm:aff id="Aff1"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff2"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff3"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation><affiliation><nlm:aff id="Aff4"><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</nlm:aff></affiliation></author></analytic><series><title level="j">Emerging Microbes & Infections</title><idno type="eISSN">2222-1751</idno><imprint><date when="2018">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p id="Par1">Previous findings of Middle East Respiratory Syndrome coronavirus (MERS-CoV)-related viruses in bats, and the ability of <italic>Tylonycteris</italic>-BatCoV HKU4 spike protein to utilize MERS-CoV receptor, human dipeptidyl peptidase 4 hDPP4, suggest a bat ancestral origin of MERS-CoV. We developed 12 primary bat cell lines from seven bat species, including <italic>Tylonycteris pachypus</italic>, <italic>Pipistrellus abramus</italic> and <italic>Rhinolophus sinicus</italic> (hosts of <italic>Tylonycteris</italic>-BatCoV HKU4, <italic>Pipistrellus</italic>-BatCoV HKU5, and SARS-related-CoV respectively), and tested their susceptibilities to MERS-CoVs, SARS-CoV, and human coronavirus 229E (HCoV-229E). Five cell lines, including <italic>P. abramus</italic> and <italic>R. sinicus</italic> but not <italic>T. pachypus</italic> cells, were susceptible to human MERS-CoV EMC/2012. However, three tested camel MERS-CoV strains showed different infectivities, with only two strains capable of infecting three and one cell lines respectively. SARS-CoV can only replicate in <italic>R. sinicus</italic> cells, while HCoV-229E cannot replicate in any bat cells. Bat dipeptidyl peptidase 4 (DPP4) sequences were closely related to those of human and non-human primates but distinct from dromedary DPP4 sequence. Critical residues for binding to MERS-CoV spike protein were mostly conserved in bat DPP4. DPP4 was expressed in the five bat cells susceptible to MERS-CoV, with significantly higher mRNA expression levels than those in non-susceptible cells (<italic>P</italic> = 0.0174), supporting that DPP4 expression is critical for MERS-CoV infection in bats. However, overexpression of <italic>T. pachypus</italic> DPP4 failed to confer MERS-CoV susceptibility in <italic>T. pachypus</italic> cells, suggesting other cellular factors in determining viral replication. The broad cellular tropism of MERS-CoV should prompt further exploration of host diversity of related viruses to identify its ancestral origin.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Woo, Pc" uniqKey="Woo P">PC Woo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Woo, Pc" uniqKey="Woo P">PC Woo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gorbalenya, Ae" uniqKey="Gorbalenya A">AE Gorbalenya</name></author><author><name sortKey="Snijder, Ej" uniqKey="Snijder E">EJ Snijder</name></author><author><name sortKey="Spaan, Wjm" uniqKey="Spaan W">WJM Spaan</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Drosten, C" uniqKey="Drosten C">C Drosten</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fouchier, Ram" uniqKey="Fouchier R">RAM 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uniqKey="Lau S">SKP Lau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lau, Skp" uniqKey="Lau S">SKP Lau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Guan, Y" uniqKey="Guan Y">Y Guan</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lau, Sk" uniqKey="Lau S">SK Lau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Li, W" uniqKey="Li W">W Li</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lau, Sk" uniqKey="Lau S">SK Lau</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Song, Hd" uniqKey="Song H">HD Song</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Chinese, Smec" uniqKey="Chinese S">SMEC Chinese</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lau, Skp" uniqKey="Lau S">SKP 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Emerg Microbes Infect</journal-id><journal-id journal-id-type="iso-abbrev">Emerg Microbes Infect</journal-id><journal-title-group><journal-title>Emerging Microbes & Infections</journal-title></journal-title-group><issn pub-type="epub">2222-1751</issn><publisher><publisher-name>Nature Publishing Group UK</publisher-name><publisher-loc>London</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">30531999</article-id><article-id pub-id-type="pmc">6286955</article-id><article-id pub-id-type="publisher-id">208</article-id><article-id pub-id-type="doi">10.1038/s41426-018-0208-9</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Replication of MERS and SARS coronaviruses in bat cells offers insights to their ancestral origins</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes" equal-contrib="yes"><name><surname>Lau</surname><given-names>Susanna K. P.</given-names></name><address><email>skplau@hku.hk</email></address><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name><surname>Fan</surname><given-names>Rachel Y. Y.</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author" equal-contrib="yes"><name><surname>Luk</surname><given-names>Hayes K. H.</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Zhu</surname><given-names>Longchao</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Fung</surname><given-names>Joshua</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Li</surname><given-names>Kenneth S. M.</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Wong</surname><given-names>Emily Y. M.</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Ahmed</surname><given-names>Syed Shakeel</given-names></name><xref ref-type="aff" rid="Aff2">2</xref></contrib><contrib contrib-type="author"><name><surname>Chan</surname><given-names>Jasper F. W.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">http://orcid.org/0000-0003-3426-332X</contrib-id><name><surname>Kok</surname><given-names>Raven K. H.</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Chan</surname><given-names>Kwok-Hung</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Wernery</surname><given-names>Ulrich</given-names></name><xref ref-type="aff" rid="Aff5">5</xref></contrib><contrib contrib-type="author"><name><surname>Yuen</surname><given-names>Kwok-Yung</given-names></name><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Woo</surname><given-names>Patrick C. Y.</given-names></name><address><email>pcywoo@hku.hk</email></address><xref ref-type="aff" rid="Aff1">1</xref><xref ref-type="aff" rid="Aff2">2</xref><xref ref-type="aff" rid="Aff3">3</xref><xref ref-type="aff" rid="Aff4">4</xref></contrib><aff id="Aff1"><label>1</label><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>State Key Laboratory of Emerging Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</aff><aff id="Aff2"><label>2</label><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Department of Microbiology, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</aff><aff id="Aff3"><label>3</label><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Carol Yu Centre for Infection, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</aff><aff id="Aff4"><label>4</label><institution-wrap><institution-id institution-id-type="ISNI">0000000121742757</institution-id><institution-id institution-id-type="GRID">grid.194645.b</institution-id><institution>Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine,</institution><institution>The University of Hong Kong,</institution></institution-wrap>Hong Kong, China</aff><aff id="Aff5"><label>5</label><institution-wrap><institution-id institution-id-type="ISNI">0000 0004 1796 4199</institution-id><institution-id institution-id-type="GRID">grid.417775.7</institution-id><institution>Central Veterinary Research Laboratory,</institution></institution-wrap>Dubai, United Arab Emirates</aff></contrib-group><pub-date pub-type="epub"><day>10</day><month>12</month><year>2018</year></pub-date><pub-date pub-type="pmc-release"><day>10</day><month>12</month><year>2018</year></pub-date><pub-date pub-type="collection"><year>2018</year></pub-date><volume>7</volume><elocation-id>209</elocation-id><history><date date-type="received"><day>24</day><month>8</month><year>2018</year></date><date date-type="rev-recd"><day>8</day><month>11</month><year>2018</year></date><date date-type="accepted"><day>11</day><month>11</month><year>2018</year></date></history><permissions><copyright-statement>© The Author(s) 2018</copyright-statement><license license-type="OpenAccess"><license-p><bold>Open Access</bold> This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>.</license-p></license></permissions><abstract id="Abs1"><p id="Par1">Previous findings of Middle East Respiratory Syndrome coronavirus (MERS-CoV)-related viruses in bats, and the ability of <italic>Tylonycteris</italic>-BatCoV HKU4 spike protein to utilize MERS-CoV receptor, human dipeptidyl peptidase 4 hDPP4, suggest a bat ancestral origin of MERS-CoV. We developed 12 primary bat cell lines from seven bat species, including <italic>Tylonycteris pachypus</italic>, <italic>Pipistrellus abramus</italic> and <italic>Rhinolophus sinicus</italic> (hosts of <italic>Tylonycteris</italic>-BatCoV HKU4, <italic>Pipistrellus</italic>-BatCoV HKU5, and SARS-related-CoV respectively), and tested their susceptibilities to MERS-CoVs, SARS-CoV, and human coronavirus 229E (HCoV-229E). Five cell lines, including <italic>P. abramus</italic> and <italic>R. sinicus</italic> but not <italic>T. pachypus</italic> cells, were susceptible to human MERS-CoV EMC/2012. However, three tested camel MERS-CoV strains showed different infectivities, with only two strains capable of infecting three and one cell lines respectively. SARS-CoV can only replicate in <italic>R. sinicus</italic> cells, while HCoV-229E cannot replicate in any bat cells. Bat dipeptidyl peptidase 4 (DPP4) sequences were closely related to those of human and non-human primates but distinct from dromedary DPP4 sequence. Critical residues for binding to MERS-CoV spike protein were mostly conserved in bat DPP4. DPP4 was expressed in the five bat cells susceptible to MERS-CoV, with significantly higher mRNA expression levels than those in non-susceptible cells (<italic>P</italic> = 0.0174), supporting that DPP4 expression is critical for MERS-CoV infection in bats. However, overexpression of <italic>T. pachypus</italic> DPP4 failed to confer MERS-CoV susceptibility in <italic>T. pachypus</italic> cells, suggesting other cellular factors in determining viral replication. The broad cellular tropism of MERS-CoV should prompt further exploration of host diversity of related viruses to identify its ancestral origin.</p></abstract><custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name><meta-value>© The Author(s) 2018</meta-value></custom-meta></custom-meta-group></article-meta></front><body><sec id="Sec1" sec-type="introduction"><title>Introduction</title><p id="Par2">Coronaviruses (CoVs) are important pathogens in animals and humans, responsible for a variety of respiratory, enteric, hepatic, and neurological diseases. They are now classified into four genera, <italic>Alphacoronavirus</italic>, <italic>Betacoronavirus</italic>, <italic>Gammacoronavirus</italic>, and <italic>Deltacoronavirus</italic>, with <italic>Betacoronavirus</italic> further divided into lineages A to D<sup><xref ref-type="bibr" rid="CR1">1</xref>–<xref ref-type="bibr" rid="CR4">4</xref></sup>. Humans are infected by six CoVs, including <italic>human CoV 229E</italic> (HCoV-229E) and <italic>human CoV NL63</italic> (HCoV-NL63) belonging to <italic>Alphacoronavirus</italic>; human CoV OC43 (HCoV-OC43) and <italic>human CoV HKU1</italic> (HCoV HKU1) belonging to <italic>Betacoronavirus</italic> lineage A; <italic>Severe Acute Respiratory Syndrome-related CoV</italic> (SARSr-CoV) belonging to <italic>Betacoronavirus</italic> lineage B; and <italic>Middle East Respiratory Syndrome CoV</italic> (MERS-CoV) belonging to <italic>Betacoronavirus</italic> lineage C<sup><xref ref-type="bibr" rid="CR5">5</xref>–<xref ref-type="bibr" rid="CR12">12</xref></sup>. The emergence potential of CoVs is believed to be related to their tendency for mutation and recombination, allowing the generation of new viruses being able to adapt to new hosts<sup><xref ref-type="bibr" rid="CR3">3</xref>,<xref ref-type="bibr" rid="CR13">13</xref>–<xref ref-type="bibr" rid="CR18">18</xref></sup>.</p><p id="Par3">Bats are an important reservoir of alphacoronaviruses and betacoronaviruses, which may jump to other animals or humans to cause new epidemics<sup><xref ref-type="bibr" rid="CR2">2</xref>,<xref ref-type="bibr" rid="CR19">19</xref></sup>. For example, SARS-CoV is likely a recombinant virus originated from horseshoe bats as the primary reservoir and palm civet as the intermediate host<sup><xref ref-type="bibr" rid="CR16">16</xref>,<xref ref-type="bibr" rid="CR20">20</xref>–<xref ref-type="bibr" rid="CR25">25</xref></sup>. Since the SARS epidemic, numerous other novel CoVs from humans or animals have been discovered<sup><xref ref-type="bibr" rid="CR2">2</xref>,<xref ref-type="bibr" rid="CR26">26</xref>–<xref ref-type="bibr" rid="CR30">30</xref></sup>, allowing a better understanding of the evolutionary origin of emerging CoVs.</p><p id="Par4">Although dromedary camels are now known to be the immediate animal source of the recent MERS epidemic, the evolutionary origin of MERS-CoV remains obscure<sup><xref ref-type="bibr" rid="CR31">31</xref>,<xref ref-type="bibr" rid="CR32">32</xref></sup>. When the virus was first discovered, it was found to be closely related to <italic>Tylonycteris</italic> bat CoV HKU4 (Ty-BatCoV HKU4) and <italic>Pipistrellus</italic> bat CoV HKU5 (Pi-BatCoV HKU5) previously discovered in lesser bamboo bat (<italic>Tylonycteris pachypus</italic>) and Japanese pipistrelle (<italic>Pipistrellus abramus</italic>) respectively in Hong Kong<sup><xref ref-type="bibr" rid="CR3">3</xref>,<xref ref-type="bibr" rid="CR11">11</xref>,<xref ref-type="bibr" rid="CR33">33</xref>,<xref ref-type="bibr" rid="CR34">34</xref></sup>. Five other lineage C betacoronaviruses closely related to MERS-CoV were subsequently detected in bats, including BtVs-BetaCoV/SC2013, <italic>Hypsugo</italic> BatCoV HKU25 from China bats, and coronavirus Neoromicia/PML-PHE1/RSA/2011 (NeoCoV), BtCoVNeo5038/KZN/RSA/2015, and BatCoV PREDICT/PDF-2180 from African bats<sup><xref ref-type="bibr" rid="CR35">35</xref>–<xref ref-type="bibr" rid="CR39">39</xref></sup>. Besides bats, a lineage C betacoronavirus, Erinaceus CoV VMC/DEU, subsequently defined as a novel species, Hedgehog coronavirus 1, has also been discovered in European hedgehogs, a group of animals being phylogenetically closely related to bats<sup><xref ref-type="bibr" rid="CR40">40</xref></sup>. While none of these animal viruses represent the immediate ancestor of MERS-CoV, the spike protein of Ty-BatCoV HKU4 was most closely related to that of MERS-CoV, and was shown to utilize the MERS-CoV receptor, human dipeptidyl peptidase 4 (hDPP4) or CD26, for cell entry<sup><xref ref-type="bibr" rid="CR41">41</xref>,<xref ref-type="bibr" rid="CR42">42</xref></sup>. Previous studies have also shown that MERS-CoV was able to infect bat cell lines and Jamaican fruit bats<sup><xref ref-type="bibr" rid="CR43">43</xref>,<xref ref-type="bibr" rid="CR44">44</xref></sup>. These findings suggest that bats may be the primary host of the ancestor of MERS-CoV.</p><p id="Par5">Although MERS-CoV has been shown to replicate in various animal cell lines including bat cells<sup><xref ref-type="bibr" rid="CR43">43</xref>–<xref ref-type="bibr" rid="CR48">48</xref></sup>, the broad tissue tropism was mainly demonstrated using type strain EMC/2012, and no comparison was made between different MERS-CoV strains. Moreover, cells from the bat hosts of MERS-CoV-related viruses, such as <italic>T. pachypus</italic> and <italic>P. abramus</italic> which harbor Ty-BatCoV HKU4 and Pi-BatCoV HKU5, respectively, were not included in previous studies, which may be due to the geographical limitation of these bat species. To better understand the replicative ability of MERS-CoV in bat cells, which may provide clues on the origin of MERS-CoV, we developed diverse primary bat cell lines from different bat species, including <italic>Rhinolophus sinicus</italic> (the host of SARSr-BatCoV) and <italic>T. pachypus</italic> (the host of Ty-BatCoV HKU4), and tested their susceptibilities to infection by different strains of MERS-CoV, SARS-CoV, and HCoV-229E. The DPP4 mRNA sequences of six bat species and their expression in bat cells were determined to correlate with viral replication results. Our findings showed differential cell tropism between different strains of MERS-CoV, SARS-CoV, and HCoV-229E, which offers insights to the origin of MERS-CoV.</p></sec><sec id="Sec2" sec-type="results"><title>Results</title><sec id="Sec3"><title>Five of 12 tested bat cell lines are susceptible to MERS-CoV EMC/2012 infection</title><p id="Par6">Since lineage C betacoronaviruses closely related to MERS-CoV were detected in bats, we developed 12 diverse primary bat cell lines from seven different bat species, including <italic>Hipposideros pomona</italic>, <italic>Miniopterus pusillus</italic>, <italic>Myotis ricketti</italic>, <italic>Pipistrellus abramus</italic> (the host of Pi-BatCoV HKU5), <italic>Rhinolophus sinicus</italic> (the host of SARSr-BatCoV and Rs-BatCoV HKU2), <italic>Tylonycteris pachypus</italic> (the host of Ty-BatCoV HKU4), <italic>Rousettus leschenaultii</italic> (the host of many viruses including Ro-BatCoV HKU9), which were subjected to infection with MERS-CoV at multiplicity of infection (MOI) of 1. Viral titers were determined by RT-qPCR on day 5 p.i. Five of the 12 cell lines (<italic>M. ricketti</italic> lung, <italic>P. abramus</italic> kidney, <italic>R. sinicus</italic> kidney and lung, and <italic>R. leschenaulti</italic> kidney cells) and Vero cells propagated MERS-CoV with at least one log<sub>10</sub> increase in viral load. The highest increase in viral load was observed in <italic>R. sinicus</italic> kidney and lung cells, which was comparable with that observed in Vero cells (Fig. <xref rid="Fig1" ref-type="fig">1</xref>). Cytopathic effects (CPEs) were observed in infected <italic>M. ricketti</italic> lung and <italic>R. sinicus</italic> lung cells with rounding of cells (Fig. <xref rid="Fig2" ref-type="fig">2</xref>). The infectivities of the viruses from culture supernatants were confirmed by passage in Vero cells with CPE. <italic>H. pomona</italic> kidney, <italic>M. pusillus</italic> kidney, <italic>M. ricketti</italic> kidney, <italic>P. abramus</italic> lung, <italic>R. leschenaulti</italic> lung, and <italic>T. pachypus</italic> kidney and lung cells did not support MERS-CoV infection.<fig id="Fig1"><label>Fig. 1</label><caption><title>The twelve bat cell lines and Vero cells were subject to infection by MERS-CoV in clade A and clade B.</title><p>The 12 bat cell lines (PAK: Pipistrellus abramus kidney, PAL Pipistrellus abramus lung, RSK: Rhinolophus sinicus kidney, RSL: Rhinolophus sinicus lung, MRK: Myotis ricketti kidney, MRL: Myotis ricketti lung, TPK: Tylonycteris pachypus kidney, TPL: Tylonycteris pachypus lung, HPK: Hipposideros pomona kidney, RLK: Rousettus leschenaultii kidney, RLL: Rousettus leschenaultii lung, MPK: Miniopterus pusillus kidney) and Vero cells were subject to infection by MERS-CoV EMC/2012 (belonging to clade A1) with MOI of 1 (<bold>a</bold>). Culture supernatants were harvested at day 0 and 5 postinfection. Viral titers were determined by real-time quantitative RT-PCR. Viral load was expressed as log<sub>10</sub> copies/mL. Error bars indicate the standard deviation of triplicate samples. The five bat cell lines susceptible to MERS-CoV EMC/2012 infection with ≥ 1 log<sub>10</sub> increase in viral load at day 5 were marked with red triangles. They were subject to infection by three other MERS-CoV strains isolated from camels in Dubai, D998/15 (belonging to clade A2) (<bold>b</bold>), D1189.1/15 (<bold>c</bold>) and D1271.1/15 (<bold>d</bold>) (belonging to clade B3) (<bold>b</bold>). Different MERS-CoV strains displayed different infectivities in these five bat cells. (*<italic>P</italic> < 0.05; **<italic>P</italic> < 0.01; ***<italic>P</italic> < 0.001)</p></caption><graphic xlink:href="41426_2018_208_Fig1_HTML" id="d29e699"></graphic></fig><fig id="Fig2"><label>Fig. 2</label><caption><title>Cytopathic effects (CPE) were observed in infected <italic>M. ricketti</italic> lung, <italic>R. sinicus</italic> lung and Vero cells on 5 days postinfection.</title><p>CPE was compared between <italic>Myotis ricketti</italic> lung (immortalized) cells that were uninfected (control) (<bold>a</bold>), and infected with Dubai camel MERS strains D998/15 (<bold>b</bold>), D1189.1/15 (<bold>c</bold>) & D1271.1/15 (<bold>d</bold>). CPE was compared between <italic>Rhinolophus sinicus</italic> lung (immortalized) cells that were uninfected (control) (<bold>e</bold>), and infected with Dubai camel MERS strains D998/15 (<bold>f</bold>), D1189.1/15 (<bold>g</bold>), and D1271.1/15 (<bold>h</bold>). CPE was compared between Vero cells that were uninfected (control) (<bold>i</bold>), and infected with Dubai camel MERS strains D998/15 (<bold>g</bold>), D1189.1/15 (<bold>k</bold>), and D1271.1/15 (<bold>l</bold>)</p></caption><graphic xlink:href="41426_2018_208_Fig2_HTML" id="d29e760"></graphic></fig></p></sec><sec id="Sec4"><title>Different MERS-CoV strains displayed different infectivities on bat cells</title><p id="Par7">MERS-CoVs are currently classified into three major clades, clade A, B, and C, which were further divided into subclades A1-A2, B1-B6, C1, and non-C1<sup><xref ref-type="bibr" rid="CR49">49</xref>–<xref ref-type="bibr" rid="CR52">52</xref></sup>. To test if different MERS-CoV strains may show similar infectivities on bat cells, the five bat cells (<italic>M. ricketti</italic> lung, <italic>P. abramus</italic> kidney, <italic>R. sinicus</italic> kidney and lung, and <italic>R. leschenaulti</italic> kidney cells), which were susceptible to MERS-CoV EMC/2012 (belonging to clade A1), were subjected to infection by three other MERS-CoV strains isolated from camels in Dubai, D998/15 (belonging to clade A2, but with spike gene belonging to clade C), and D1189.1/15 and D1271.1/15 (both belonging to clade B3)<sup><xref ref-type="bibr" rid="CR51">51</xref></sup>. Among the five challenged bat cells, <italic>M. ricketti</italic> lung supported infection by both D1189.1/15 and D1271.1/15; while <italic>R. sinicus</italic> lung and <italic>R. leschenaulti</italic> kidney supported infection by D1189.1/15, with at least one log<sub>10</sub> increase in viral load. None of the cells supported infection by D998/15 (Fig. <xref rid="Fig1" ref-type="fig">1</xref>).</p></sec><sec id="Sec5"><title>SARS-CoV can replicate in <italic>R. sinicus</italic> cells</title><p id="Par8">Since Chinese horseshoe bats are the major reservoir of SARS-related-CoVs, we also tested the 12 bat cell lines, including <italic>R. sinicus</italic> cells, for susceptibility to a clinical strain of SARS-CoV. SARS-CoV strain HKU-39849 can replicate in <italic>R. sinicus</italic> kidney but not lung cells, with at least one log<sub>10</sub> increase in viral load (Fig. <xref rid="Fig3" ref-type="fig">3a</xref>). The other bat cells did not support SARS-CoV infection.<fig id="Fig3"><label>Fig. 3</label><caption><title>The twelve bat cell lines and Vero/HFL cells were subject to infection by SARS-CoV and HCoV-229E.</title><p>The 12 bat cell lines (PAK: Pipistrellus abramus kidney, PAL Pipistrellus abramus lung, RSK: Rhinolophus sinicus kidney, RSL: Rhinolophus sinicus lung, MRK: Myotis ricketti kidney, MRL: Myotis ricketti lung, TPK: Tylonycteris pachypus kidney, TPL: Tylonycteris pachypus lung, HPK: Hipposideros pomona kidney, RLK: Rousettus leschenaultii kidney, RLL: Rousettus leschenaultii lung, MPK: Miniopterus pusillus kidney) and Vero/HFL cells were subject to infection by SARS-CoV with MOI of 1 (<bold>a</bold>) and HCoV-229E with MOI of 0.01(<bold>b</bold>). Culture supernatants were harvested at day 0 and 5 postinfection. Viral titers were determined by real-time quantitative RT-PCR. Viral load was expressed as log<sub>10</sub> copies/mL. Error bars indicate the standard deviation of triplicate samples. Only RSK cells can support SARS-CoV infection with ≥ 1 log<sub>10</sub> increase in viral load at day 5 (blue triangle) and none of the 12 bat cell lines support HCoV-229E infection. (*<italic>P</italic> < 0.05; **<italic>P</italic> < 0.01; ***<italic>P</italic> < 0.001)</p></caption><graphic xlink:href="41426_2018_208_Fig3_HTML" id="d29e857"></graphic></fig></p></sec><sec id="Sec6"><title>HCoV-229E cannot replicate in bat cells</title><p id="Par9">The 12 bat cells were also tested for susceptible to HCoV-229E infection. HCoV-229E strain ATCC VR-740, previously isolated from a man with upper respiratory illness, cannot replicate in any of the tested bat cells (Fig. <xref rid="Fig3" ref-type="fig">3b</xref>).</p></sec><sec id="Sec7"><title>mRNA transcript sequence analysis and expression of DPP4 in bat cells</title><p id="Par10">Partial DPP4 mRNA transcript sequences (corresponding to nt 688–1040 of hDPP4 which includes residue 229–346, where the critical residues for MERS-CoV spike protein binding are present) were determined for six of the seven bat species from which the 12 tested bat cells were developed. The sequence of <italic>M. pusillus</italic> was not determined, as RT-PCR for the DPP4 mRNA from bat cells was negative. Phylogenetic analysis showed that the bat DPP4 mRNA sequences formed a distinct cluster being closely related to sequences from human and non-human primates; while the dromedary camel DPP4 sequence was most closely related to that of wild boar (Fig. <xref rid="Fig4" ref-type="fig">4a</xref>). Previous studies have identified 14 critical residues in hDPP4 for binding of MERS-CoV spike protein<sup><xref ref-type="bibr" rid="CR53">53</xref>,<xref ref-type="bibr" rid="CR54">54</xref></sup>. Upon multiple sequence alignment of the corresponding regions that contain these critical residues, most of the residues are conserved in the six bat DPP4 sequences in this study (Fig. <xref rid="Fig3" ref-type="fig">3b</xref>). Notably, <italic>T. pachypus</italic> DPP4 (Tp-DPP4) contains an I → K substitution at position 295 compared with hDPP4. On the other hand, residue R336 of hDPP4 was only conserved in <italic>T. pachypus</italic> and <italic>H. pomona</italic>, both not susceptible to MERS-CoV infection.<fig id="Fig4"><label>Fig. 4</label><caption><title>Phylogenetic analyses of partial DPP4 mRNA sequences and comparison of critical amino acid residues of human, camels, bats and other animals.</title><p>(<bold>a</bold>) The trees were constructed by Neighbor-Joining method using JTT substitution models and bootstrap values calculated from 1000 trees. Only bootstrap values >70% are shown. One hundred and twelve aa positions were included in the analyses. The scale bars represent 20 substitutions per site. Bat DPP4s that are sequenced in this study are labeled with black circles. Comparison of critical amino acid residues in DPP4 from different animal host for receptor binding in the region of residues 229–346 with respect to human DPP4 (<bold>b</bold>)</p></caption><graphic xlink:href="41426_2018_208_Fig4_HTML" id="d29e913"></graphic></fig></p><p id="Par11">RT-qPCR of bat DPP4 mRNA in the corresponding bat cells was performed to determine the mRNA expression levels. Results showed that DPP4 mRNA was expressed in all the five bat cells that were susceptible to MERS-CoV infection, while it was also expressed in <italic>H. pomona</italic> kidney and <italic>R. leschenaulti</italic> lung cells which were not susceptible to MERS-CoV infection. The mRNA expression level in <italic>P. abramus</italic> kidney (susceptible to MERS-CoV) was significantly higher than that in its lung (non-susceptible) cells (<italic>P</italic> = 0.0185 by Student’s <italic>t</italic> test). Similarly, the mRNA expression level in <italic>R. leschenaulti</italic> kidney (susceptible to MERS-CoV) was significantly higher than that in its lung (non-susceptible) cells (<italic>P</italic> = 0.0009 by Student’s <italic>t</italic> test). Compared with bat cells that are non-susceptible, bat cells that are susceptible to MERS-CoV showed a significantly higher mRNA expression level (<italic>P</italic> = 0.0174 by Student’s <italic>t</italic> test) (Fig. <xref rid="Fig5" ref-type="fig">5</xref>).<fig id="Fig5"><label>Fig. 5</label><caption><title>DPP4 expression analysis of bat cell lines.</title><p>(<bold>a</bold>) mRNA levels of DPP4 were measured in various bat cells extracts by RT-qPCR and plotted relative to Vero cells, normalized by β-actin mRNA levels. The mRNA levels of DPP4 were compared between susceptible and non-susceptible bat cell lines (<bold>b</bold>). Statistical significance was assessed by Student’s <italic>t</italic> test <italic>P</italic> < 0.05</p></caption><graphic xlink:href="41426_2018_208_Fig5_HTML" id="d29e973"></graphic></fig></p></sec><sec id="Sec8"><title>Overexpression of Tp-DPP4 does not confer MERS-CoV EMC/2012 susceptibility to <italic>T. pachypus</italic> cells</title><p id="Par12">Since DPP4 was not expressed in <italic>T. pachypus</italic> cells while this bat species hosts Ty-BatCoV HKU4, a close relative of MERS-CoV which can utilize hDPP4 for cell entry<sup><xref ref-type="bibr" rid="CR41">41</xref>,<xref ref-type="bibr" rid="CR42">42</xref></sup>, we overexpressed Tp-DPP4 in <italic>T. pachypus</italic> lung and kidney cells for infection by MERS-CoV. While a slight increase (less than one log<sub>10</sub>) in viral replication was noted in both mock and Tp-DPP4-overexpressed cells on day 5 p.i., no significant difference was noted between mock and Tp-DPP4-overexpressed cells (Fig. <xref rid="Fig6" ref-type="fig">6</xref>), suggesting that overexpression of Tp-DPP4 does not confer MERS-CoV susceptibility to <italic>T. pachypus</italic> cells.<fig id="Fig6"><label>Fig. 6</label><caption><title>Infection assay of <italic>T. pachypus</italic> lung and kidney cells with tpDPP4 overexpression.</title><p>Cells were infected with MERS-CoV at a multiplicity of infection (MOI) of 1 for 5 days. Determination of MERS-CoV viral load in supernatant (<italic>n</italic> = 3) by RT-qPCR with normalization to β-actin (represented by bar). Determination of tpDPP4 expression in cell lysates (<italic>n</italic> = 3) by RT-qPCR with normalization to beta-actin (represented by dot). (*<italic>P</italic> < 0.05, **<italic>P</italic> < 0.01, ***<italic>P</italic> < 0.001)</p></caption><graphic xlink:href="41426_2018_208_Fig6_HTML" id="d29e1033"></graphic></fig></p></sec></sec><sec id="Sec9" sec-type="discussion"><title>Discussion</title><p id="Par13">The present study provides further support to the bat origin of MERS-CoV. Previous studies have shown that MERS-CoV can infect cell lines from different animals, including cells from various bat species<sup><xref ref-type="bibr" rid="CR43">43</xref>–<xref ref-type="bibr" rid="CR47">47</xref></sup>. However, bat cells from host species of MERS-CoV-related viruses, such as <italic>T. pachypus</italic> and <italic>P. abramus</italic> which harbor Ty-BatCoV HKU4 and Pi-BatCoV HKU5, respectively, were not included in these studies. In this study, MERS-CoV EMC/2012 was able to replicate in cells from four different bat genera/species belonging to three different bat families including <italic>Pteropodidae</italic>, <italic>Rhinolophidae</italic>, and <italic>Vespertilionidae</italic>. None of these bat cells were previously reported to support MERS-CoV replication. While lineage C betacoronaviruses have not been detected in bats outside the <italic>Vespertilionidae</italic> family, such diverse cellular tropism should prompt further studies to explore the host diversity of this group of CoVs and hence the possible evolutionary origin of MERS-CoV. In particular, the ability of MERS-CoV to replicate in cells from <italic>P. abramus</italic>, the host of Pi-BatCoV HKU5, may suggest that the ancestor of MERS-CoV could have originated from <italic>Pipistrellus</italic>-related bats. Interestingly, MERS-CoV showed the highest replicative ability in cells from <italic>R. sinicus</italic>. This suggests that MERS-CoV may potentially infect this bat species which is also the natural reservoir of SARSr-CoVs and animal origin of SARS-CoV<sup><xref ref-type="bibr" rid="CR21">21</xref></sup>. Nevertheless, three other MERS-CoV strains belonging to either clade A2 or B3 showed differential replicative abilities in the five bat cell lines that were susceptible to EMC/2012 strain (clade A1), with strain D998/15 (clade A2) unable to replicate in all five tested cell lines. Interestingly, it has been shown in a recent study that some clade C MERS-CoV strains from Nigeria and Burkina Faso replicated at a lower titre in Calu-3 cells<sup><xref ref-type="bibr" rid="CR52">52</xref></sup>. This is in line with the present study that our clade A2 strain D998/15 (with its spike gene belonging to clade C), conferred less broad cellular tropism. Our findings suggest that different clades or strains of MERS-CoV may possess different cellular tropism and host range, while all MERS-CoVs can replicate well in the immune-deficient Vero cells.</p><p id="Par14">The broader cellular tropism of MERS-CoV than SARS-CoV and HCoV-229E in bat cells may reflect the host diversity of lineage C betacoronaviruses in bats. Bats are now known to be the recent origin of at least two human CoVs, including SARS-CoV and HCoV-229E. SARS-CoV is likely a recombinant virus arising from horseshoe bats before it jumped to civet as the intermediate host and then human<sup><xref ref-type="bibr" rid="CR16">16</xref>,<xref ref-type="bibr" rid="CR24">24</xref></sup>. SARSr-CoVs in bats were shown to utilize the SARS-CoV receptor, human angiotensin-converting enzyme 2 (hACE2), for cell entry<sup><xref ref-type="bibr" rid="CR55">55</xref></sup>. Similar to SARS-CoV, HCoV-229E is likely to have originated from bats. CoVs closely related to HCoV-229E have been detected in bats of the genus <italic>Hipposideros</italic> in Africa<sup><xref ref-type="bibr" rid="CR56">56</xref></sup>. More recently, CoVs even closer to HCoV-229E were identified in dromedary camels in the Middle East, which were able to utilize the receptor of HCoV-229E, human aminopeptidase N (hAPN) for cell entry<sup><xref ref-type="bibr" rid="CR57">57</xref></sup>. This suggests that dromedary camels may have served as intermediate hosts for bat-to-human transmission of HCoV-229E, which may be analogous to the evolution of MERS-CoV. Recently, a CoV, closely related to HCoV-NL63 in most genome regions except the spike protein, was detected from a bat of the genus <italic>Triaenops</italic> in Kenya<sup><xref ref-type="bibr" rid="CR58">58</xref></sup>. However, further studies are required to identify even closer relatives of HCoV-NL63 to ascertain its possible bat origin. In contrast to SARSr-CoVs and HCoV-229E which were mainly found in horseshoe and roundleaf bats, respectively, a more diverse host range was observed in lineage C betacoronaviruses. Yet, the different bat species harboring lineage C betacoronaviruses all belonged to the family <italic>Vespertilionidae</italic>. Specifically, Ty-BatCoV HKU4, Pi-BatCoV HKU5, Hp-BatCoV HKU25, and BtVs-BetaCoV/SC2013 were detected in bats belonging to the genera, <italic>Tylonycteris</italic>, <italic>Pipistrellus</italic>, <italic>Hypsugo,</italic> and <italic>Verspetilio</italic>, respectively, in China, whereas NeoCoV and BatCoV PREDICT/PDF-2180 were detected in bats belonging to <italic>Neoromicia</italic> and <italic>Pipistrellus</italic> in Africa<sup><xref ref-type="bibr" rid="CR36">36</xref>,<xref ref-type="bibr" rid="CR37">37</xref></sup>. In this study, SARS-CoV could only replicate in <italic>R. sinicus</italic> kidney cells but not other bat cells, which reflects its evolutionary origin from horseshoe bats. On the other hand, HCoV-229E was unable to replicate in any tested bat cells including cells from <italic>Hipposideros</italic>. This may suggest a relatively narrow host range of SARS-CoV and HCoV-229E in bats compared with lineage C betacoronaviruses including MERS-CoV.</p><p id="Par15">The close phylogenetic relationship between bat and primate DPP4 sequences may reflect the replicative ability of MERS-CoV in bat cells. Moreover, cells that supported MERS-CoV replication showed significantly higher DPP4 mRNA expression than those that were non-susceptible to MERS-CoV, suggesting that cellular DPP4 expression is critical for viral infection. Since Ty-BatCoV HKU4 from <italic>T. pachypus</italic> was previously shown to be able to utilize hDPP4 for cell entry<sup><xref ref-type="bibr" rid="CR41">41</xref>,<xref ref-type="bibr" rid="CR42">42</xref></sup>, we expected MERS-CoV to be able to utilize Tp-DPP4 for receptor binding and infect <italic>T. pachypus</italic> cells. While the inability of MERS-CoV to replicate in <italic>T. pachypus</italic> cells may be partly explained by the lack of DPP4 expression, overexpression of Tp-DPP4 was unable to confer viral susceptibility. Since mRNA expression may not always correlate with cell surface expression of the receptor, further studies are required to study the receptor-binding interphase between MERS-CoV and Tp-DPP4 and whether other cellular factors may play a role in determining viral replicative abilities in <italic>T. pachypus</italic> cells, which may offer further insights into the evolutionary origin and mechanisms of interspecies transmission of MERS-CoV. Interestingly, one of the critical residues for binding to MERS-CoV spike protein, R336, was only conserved in <italic>T. pachypus</italic> and <italic>H. pomona</italic> DPP4 (cells from these two species did not support MERS-CoV replication), but not in the other four sequenced bat DPP4 (cells from these four species supported MERS-CoV replication). This suggests that this residue may not be critical for receptor binding. Binding and mutagenesis studies may help better understand the role of receptor-binding-interphase during viral evolution and interspecies jumping.</p></sec><sec id="Sec10" sec-type="materials|methods"><title>Materials and methods</title><sec id="Sec11"><title>Ethics statement</title><p id="Par16">The collection of bat samples for developing bat cell lines was approved by the Committee on the Use of Live Animals for Teaching and Research, the University of Hong Kong, Hong Kong, China.</p></sec><sec id="Sec12"><title>Cell lines</title><p id="Par17">The bat cells, Vero (African green monkey kidney) cells, and HFL (human embryonic lung fibroblast) cells used in this study are described in Table <xref rid="Tab1" ref-type="table">1</xref>. For development of primary bat cell lines, bats were captured in Hong Kong and euthanized before dissection for recovery of cells from organs aseptically. Briefly, the kidney and lung tissue were rinsed with cold PBS and cut into small pieces. Cold 0.25% trypsin-EDTA was added to the tissues and incubated at 4 °C overnight. Tissues were then incubated at 37 °C on shaking platform for 30 min. Supernatants were filtered through cell strainers to remove large pieces of tissues<sup><xref ref-type="bibr" rid="CR59">59</xref></sup>. Bat cells were harvested by spinning down the supernatant at 1200 rpm for 8 min and were grown in DMEM/F12 supplemented with 15% FBS. Vero and HFL cells were grown in MEM supplemented with 10% FBS. All cells were incubated at 37 °C with 5% CO<sub>2</sub>.<table-wrap id="Tab1"><label>Table 1</label><caption><p>Cell lines used in the present study</p></caption><table frame="hsides" rules="groups"><thead><tr><th colspan="2">Organism</th><th>Site of origin</th><th>Source</th></tr></thead><tbody><tr><td rowspan="12">Bat</td><td><italic>Hipposideros pomona</italic> (Pomona roundleaf bat)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Miniopterus pusillus</italic> (Lesser bent-winged bat)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Myotis ricketti</italic> (Rickett’s big-footed bat)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Myotis ricketti</italic> (Rickett’s big-footed bat)</td><td>Lung</td><td>In-house development</td></tr><tr><td><italic>Pipistrellus abramus</italic> (Japanese pipistrelle)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Pipistrellus abramus</italic> (Japanese pipistrelle)</td><td>Lung</td><td>In-house development</td></tr><tr><td><italic>Rhinolophus sinicus</italic> (Chinese horseshoe bat)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Rhinolophus sinicus</italic> (Chinese horseshoe bat)</td><td>Lung</td><td>In-house development</td></tr><tr><td><italic>Tylonycteris pachypus</italic> (Lesser bamboo bat)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Tylonycteris pachypus</italic> (Lesser bamboo bat)</td><td>Lung</td><td>In-house development</td></tr><tr><td><italic>Rousettus leschenaultii</italic> (Leschenault’s rousette)</td><td>Kidney</td><td>In-house development</td></tr><tr><td><italic>Rousettus leschenaultii</italic> (Leschenault’s rousette)</td><td>Lung</td><td>In-house development</td></tr><tr><td>Human</td><td><italic>Homo sapiens</italic></td><td>Embryonic Lung</td><td>HFL (In-house development)</td></tr><tr><td>Monkey</td><td><italic>Cercopithecus aethiops</italic> (African green monkey)</td><td>Kidney</td><td>Vero (ATCC CCL-81)</td></tr></tbody></table></table-wrap></p></sec><sec id="Sec13"><title>Virus isolates</title><p id="Par18">MERS-CoV strain EMC/2012 was provided by Fouchier and Zaki et al.<sup><xref ref-type="bibr" rid="CR11">11</xref></sup>. MERS-CoV strains D998/15, D1189.1/15, and D1271.1/15 were isolated from dromedary camels in Dubai<sup><xref ref-type="bibr" rid="CR51">51</xref></sup>. SARS-CoV strain HKU-39849 was isolated from the brother-in-law of the index patient in Hong Kong during the SARS epidemic<sup><xref ref-type="bibr" rid="CR8">8</xref></sup>. The HCoV-229E strain ATCC VR-740 was used. MERS-CoV isolates and SARS-CoV were propagated in Vero cells at MOI of 0.01 in MEM supplemented with 1% FBS. HCoV-229E was propagated in HFL.</p></sec><sec id="Sec14"><title>Infection of bat cell lines</title><p id="Par19">Viral titers were determined as median tissue culture infective dose (TCID<sub>50</sub>) per ml in confluent cells in 96-well microtiter plates. Cells were seeded onto 24-well tissue culture plates, at 2 × 10<sup>5</sup> cells per well with the respective medium and incubated at 37 °C and 5% CO<sub>2</sub> for 24 h prior to experiment. Cells were washed once with PBS and inoculated with 1 MOI of MERS-CoV or SARS-CoV, or 0.01 MOI of 229E for 1 h. After 1 h of viral adsorption, the supernatant was removed and cells were washed twice with PBS. The cells were maintained in MEM supplemented with 1% FBS for Vero and HFL cells and DMEM/F12 supplemented with 1% FBS for bat cells, before further incubation for 5 days.</p></sec><sec id="Sec15"><title>Viral replication studies</title><p id="Par20">To study viral replication efficiency, progeny viruses from cell culture supernatants collected at 5 days postinfection (p.i.) were subjected to reverse transcription-quantitative PCR (RT-qPCR) according to our previous protocols<sup><xref ref-type="bibr" rid="CR60">60</xref></sup>. Briefly, total RNA extracted from cell culture supernatants with QIAsymphony DSP Virus/Pathogen Mini Kit (Qiagen, Hilden, Germany) was reverse transcribed and amplified with MERS-CoV primers (forward primer 5′-CAAAACCTTCCCTAAGAAGGAAAAG-3′ reverse primer 5′-GCTCCTTTGGAGGTTCAGACAT-3′), SARS-CoV primers (forward 5′- ACCAGAATGGAGGACGCAATG-3′ reverse 5′-GCTGTGAACCAAGACGCAGTATTAT-3′) and HCoV-229E primers (forward 5’-CAGTCAAATGGGCTGATGCA-3′ reverse 5′-AAAGGGCTATAAAGAGAATAAGGTATTCT-3′) using real-time one-step quantitative RT-PCR assay as described previously with modifications<sup><xref ref-type="bibr" rid="CR45">45</xref>,<xref ref-type="bibr" rid="CR60">60</xref></sup>. Probes for MERS-CoV [5′-(FAM)ACAAAAGGCACCAAAAGAAGAATCAACAGACC(BHQ1)-3′], SARS-CoV [5′-(FAM)ACCCCAAGGTTTACCC(NFQ)-3′] and HCoV-229E [5′-(FAM)CCCTGACGACCACGTTGTGGTTCA(BHQ1)-3′] were used (Table <xref rid="Tab2" ref-type="table">2</xref>). Reactions were first incubated at 50 °C for 30 min, followed by 95 °C for 2 min, and were then thermal cycled for 50 cycles (95 °C for 15 s, 55 °C for 30 s). A series of 10 log<sub>10</sub> dilutions equivalent to 1 × 10<sup>1</sup> to 1 × 10<sup>10</sup> copies per reaction mixture were prepared to generate calibration curves and were run in parallel with the test samples. All experiments were performed in triplicate.<table-wrap id="Tab2"><label>Table 2</label><caption><p>Primers used for RT-qPCR in this study</p></caption><table frame="hsides" rules="groups"><thead><tr><th rowspan="2">Target</th><th colspan="3">Primers</th></tr><tr><th>Forward</th><th>Reverse</th><th>Probe</th></tr></thead><tbody><tr><td>MERS-CoV N gene</td><td>5′-CAAAACCTTCCCTAAGAAGGAAAAG -3′</td><td>5′-GCTCCTTTGGAGGTTCAGACAT-3′</td><td>(5′-(FAM)ACAAAAGGCACCAAAAGAAGAATCAACAGACC(BHQ1)-3′</td></tr><tr><td>SARS-CoV N gene</td><td>5′- ACCAGAATGGAGGACGCAATG-3′</td><td>5’-GCTGTGAACCAAGACGCAGTATTAT-3′</td><td>5′-(FAM)ACCCCAAGGTTTACCC(NFQ)-3′</td></tr><tr><td>HCoV-229E N gene</td><td>5′-CAGTCAAATGGGCTGATGCA-3′</td><td>5’-AAAGGGCTATAAAGAGAATAAGGTATTCT-3’</td><td>5’-(FAM)CCCTGACGACCACGTTGTGGTTCA(BHQ1)-3′</td></tr><tr><td>DPP4</td><td>5′-TGATCTTGCCTCCTCATTTTGATAA-3′</td><td>5’-GTAACCACTTCCTCTGCCATCAA-3’ or 5’-GTAACCACTTCCTCTGCCGTCAA-3’ (for Rousettus cell lines)</td><td>5’-(FAM)CCACMTTCAMACTCARYTGGGCTACTTACC(BHQ1)-3′</td></tr><tr><td>β-actin</td><td>5′-CTCTTCCAGCCCTCCTTCCT-3′</td><td>5′-TTCATCGTGCTGGGAGCC-3′ or 5′-TTCATTGTGCTGGGAGCC-3’ (for <italic>Rousettus</italic> cell lines) or 5′-TTCATGGTGCTGGGGGCC-3′ (for <italic>Rhinolophus</italic> cell lines)</td><td>5’-(FAM)CATGAAGTGYGACGTBGACATCCG(BHQ1)-3′</td></tr></tbody></table></table-wrap></p></sec><sec id="Sec16"><title>Amplification and sequencing of partial bat DPP4 mRNA transcripts</title><p id="Par21">Total RNA was extracted from bat cell lysates using RNeasy Mini Spin Column (QIAgen). cDNA was PCR amplified with primers, 5′-GTCACCAGAGGGTCATAAA-3′ and 5′-CCACTTCCTCTGCCATCAAA-3′. The PCR mixture (25 μl) contained cDNA, PCR buffer, 200 μM (each) dNTPs, and 1.0 U Iproof Polymerase (Bio-Rad, Hercules, CA, USA). The mixtures were amplified for 40 cycles of 98 °C for 10 s, 55 °C for 30 s, and 72 °C for 72 s and a final extension at 72 °C for 10 min in an automated thermal cycler (Applied Biosystems, Foster City, CA, USA). RT-PCR products were gel purified using QIAquick gel extraction kit (Qiagen), and sequenced with an ABI Prism 3700 DNA Analyzer (Applied Biosystems). The sequences obtained were compared with sequences of DPP4 genes in GenBank database. Phylogenetic tree construction was performed based on an amino acid alignment of partial DPP4 sequences (corresponding to residue 229–346 of hDPP4) using the Neighbor-Joining method with JTT model by MEGA 6.0, with bootstrap values calculated from 1000 trees.</p></sec><sec id="Sec17"><title>DPP4 expression analysis</title><p id="Par22">To study DPP4 expression profiles in different bat cell lines, cell lysates were collected for total RNA extraction using RNeasy Mini Spin Column (QIAgen). RNA was eluted in 50 μl of RNase-free water and was used as a template for one-step RT-qPCR with SuperScript III platinum One-step qRT-PCR system (Invitrogen, Carlsbad, CA, USA). RT-qPCR assays were performed using conserved primers designed by multiple alignment of available bat DPP4 gene sequences (Table <xref rid="Tab2" ref-type="table">2</xref>), using <italic>β</italic>-<italic>actin</italic> for normalization. cDNA was amplified in a LightCycler 480 (Roche, Basel, Switzerland) with 25 μl reaction mixtures containing 2 × reaction mix, 5 μl RNA, 25 μM ROX reference dye, 50 μM primers, and 10 μM probe at 50 °C for 30 min, then 95 °C for 2 min followed by 50 cycles of denaturation, annealing and extension. Experiments were performed in triplicates, and results were expressed as the mean expression level of DPP4<italic>/β-actin</italic>. The relative expression between different bat cells was then calculated by the ΔΔCt method.</p></sec><sec id="Sec18"><title>tpDPP4 overexpression in <italic>T. pachypus</italic> cells</title><p id="Par23"><italic>T. pachypus</italic> DPP4 (tpDPP4) sequence was cloned into pLenti7.3/V5-TOPO vector (Invitrogen). The construct was transfected into 293FT cells together with ViraPower Packaging Mix (Invitrogen) using Lipofectamine 2000 (Life Technologies, Carlsbad, CA, USA). Lentivirus was harvested from the supernatant and concentrated using PEG-it (System Biosciences, Palo Alto, USA). <italic>T. pachypus</italic> cells resistant to MERS-CoV were transduced using the concentrated lentivirus for tpDPP4 overexpression and were subsequently subjected to inoculation with 1 MOI of MERS-CoV.</p></sec><sec id="Sec19"><title>Nucleotide sequence accession numbers</title><p id="Par24">The nucleotide sequences of bat DPP4 obtained from this study have been deposited in the GenBank sequence database under accession numbers MH345671-MH345676.</p></sec></sec></body><back><fn-group><fn><p><bold>Publisher’s note:</bold> Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p></fn><fn><p>These authors contributed equally: Susanna K. P. Lau, Rachel Y. Y. Fan, Hayes K. H. Luk</p></fn></fn-group><ack><title>Acknowledgements</title><p>We thank C.T. Shek, Agriculture, Fisheries, and Conservation Department, the Government of the HKSAR, for capture of bats for bat cell development and expert opinion. This work is partly supported by Theme-Based Research Scheme (T11-707/15-R) and Research Grant Council Grant, University Grant Council; Health and Medical Research Fund of the Food and Health Bureau of HKSAR; University Development Fund and Special Research Achievement Award, The University of Hong Kong; Consultancy Service for Enhancing Laboratory Surveillance of Emerging Infectious Disease for the HKSAR Department of Health; The Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, the Ministry of Education of China; National Science and Technology Major Project of China (grant number 2012ZX10004213). Views expressed in this paper are those of the authors only, and may not represent the opinion of the AFCD or the Government of the HKSAR.</p></ack><notes notes-type="author-contribution"><title>Author contributions</title><p>S.K.P.L. and P.C.Y.W. conceived the study and designed the experiments. R.Y.Y.F., H.K.H.L., L.C., J.F., K.S.M.L., E.Y.M.W. and S.S.A. performed the experiments. S.K.P.L., R.F.F.Y., H.K.H.L., J.F., K.S.M.L., J.F.W.C., R.K.H.K., K.H.C., U.W., K.Y.Y. and P.C.Y.W. analyzed the data. S.K.P.L., R.F.F.Y., H.K.H.L., K.S.M.L., L.C. and P.C.Y.W. wrote the paper.</p></notes><notes notes-type="COI-statement"><title>Conflict of interest</title><p id="Par25">The authors declare that they have no conflict of interest.</p></notes><ref-list id="Bib1"><title>References</title><ref id="CR1"><label>1.</label><mixed-citation publication-type="other">de Groot R. J. et al. Coronaviridae. In: Virus Taxonomy, Classification and Nomenclature of Viruses. 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