A humanized MDCK cell line for the efficient isolation and propagation of human influenza viruses
Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human viru...
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Published in | Nature microbiology Vol. 4; no. 8; pp. 1268 - 1273 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
01.08.2019
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Abstract | Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells.
The authors report the development of a Madin-Darby canine kidney (MDCK) cell line that is more suitable than conventional MDCK or human virus receptor-overexpressing cells for the isolation and propagation of human influenza viruses without cell culture-adaptive mutations. |
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AbstractList | Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells.
The authors report the development of a Madin-Darby canine kidney (MDCK) cell line that is more suitable than conventional MDCK or human virus receptor-overexpressing cells for the isolation and propagation of human influenza viruses without cell culture-adaptive mutations. Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells.Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells. Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells.The authors report the development of a Madin-Darby canine kidney (MDCK) cell line that is more suitable than conventional MDCK or human virus receptor-overexpressing cells for the isolation and propagation of human influenza viruses without cell culture-adaptive mutations. Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian virus receptors. hCK cells supported human A/H3N2 influenza virus isolation and growth much more effectively than conventional MDCK or human virus receptor-overexpressing (AX4) cells. A/H3N2 viruses propagated in hCK cells also maintained higher genetic stability than those propagated in MDCK and AX4 cells. |
Author | Kawakami, Chiharu Lopes, Tiago J. S. Takasaki, Sara Watanabe, Tokiko Takada, Kosuke Shimizu, Kohei Khan, Zenab Kriti, Divya Kawaoka, Yoshihiro Zhong, Gongxun Sakai-Tagawa, Yuko Dutta, Jayeeta van Bakel, Harm Imai, Masaki Fan, Shufang Gu, Chunyang Yamada, Shinya Chiba, Shiho |
Author_xml | – sequence: 1 givenname: Kosuke surname: Takada fullname: Takada, Kosuke organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 2 givenname: Chiharu surname: Kawakami fullname: Kawakami, Chiharu organization: Yokohama City Institute of Public Health – sequence: 3 givenname: Shufang surname: Fan fullname: Fan, Shufang organization: Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison – sequence: 4 givenname: Shiho surname: Chiba fullname: Chiba, Shiho organization: Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison – sequence: 5 givenname: Gongxun surname: Zhong fullname: Zhong, Gongxun organization: Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison – sequence: 6 givenname: Chunyang surname: Gu fullname: Gu, Chunyang organization: Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison – sequence: 7 givenname: Kohei surname: Shimizu fullname: Shimizu, Kohei organization: Yokohama City Institute of Public Health – sequence: 8 givenname: Sara surname: Takasaki fullname: Takasaki, Sara organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 9 givenname: Yuko surname: Sakai-Tagawa fullname: Sakai-Tagawa, Yuko organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 10 givenname: Tiago J. S. surname: Lopes fullname: Lopes, Tiago J. S. organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison – sequence: 11 givenname: Jayeeta surname: Dutta fullname: Dutta, Jayeeta organization: Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai – sequence: 12 givenname: Zenab surname: Khan fullname: Khan, Zenab organization: Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai – sequence: 13 givenname: Divya orcidid: 0000-0002-9357-5588 surname: Kriti fullname: Kriti, Divya organization: Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai – sequence: 14 givenname: Harm orcidid: 0000-0002-1376-6916 surname: van Bakel fullname: van Bakel, Harm organization: Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai – sequence: 15 givenname: Shinya surname: Yamada fullname: Yamada, Shinya organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 16 givenname: Tokiko surname: Watanabe fullname: Watanabe, Tokiko organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 17 givenname: Masaki orcidid: 0000-0001-6988-1975 surname: Imai fullname: Imai, Masaki email: mimai@ims.u-tokyo.ac.jp organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo – sequence: 18 givenname: Yoshihiro orcidid: 0000-0001-5061-8296 surname: Kawaoka fullname: Kawaoka, Yoshihiro email: yoshihiro.kawaoka@wisc.edu organization: Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Department of Special Pathogens, International Research Center for Infectious Diseases, Institute of Medical Science, University of Tokyo |
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Snippet | Here, we developed hCK, a Madin-Darby canine kidney (MDCK) cell line that expresses high levels of human influenza virus receptors and low levels of avian... |
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SubjectTerms | 631/326/596/1578 692/699/255/1578 Animals Antigens, CD - metabolism Biomedical and Life Sciences Brief Communication Cell Line Dogs Humans Infectious Diseases Influenza Influenza A Virus, H3N2 Subtype - genetics Influenza A Virus, H3N2 Subtype - growth & development Influenza A Virus, H3N2 Subtype - isolation & purification Influenza, Human Life Sciences Madin Darby Canine Kidney Cells - virology Medical Microbiology Microbiology Mutation Orthomyxoviridae Orthomyxoviridae - genetics Orthomyxoviridae - isolation & purification Parasitology Receptors, Virus - genetics Receptors, Virus - metabolism Sialyltransferases - genetics Sialyltransferases - metabolism Virology Viruses |
Title | A humanized MDCK cell line for the efficient isolation and propagation of human influenza viruses |
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