Isolation and Characterization of Current Human Coronavirus Strains in Primary Human Epithelial Cell Cultures Reveal Differences in Target Cell Tropism

被引:112
作者
Dijkman, Ronald [1 ,2 ]
Jebbink, Maarten F. [2 ]
Koekkoek, Sylvie M. [3 ]
Deijs, Martin [2 ]
Jonsdottir, Hulda R. [1 ]
Molenkamp, Richard [3 ]
Ieven, Margareta [4 ]
Goossens, Herman [4 ]
Thiel, Volker [5 ]
van der Hoek, Lia [2 ]
机构
[1] Kantonal Hosp, Inst Immunobiol, St Gallen, Switzerland
[2] Univ Amsterdam, Acad Med Ctr, Ctr Infect & Immun Amsterdam CINIMA, Lab Expt Virol,Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Ctr Infect & Immun Amsterdam CINIMA, Lab Clin Virol,Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Antwerp Hosp, Vaccine & Infect Dis Inst, Dept Med Microbiol, Antwerp, Belgium
[5] Univ Zurich, Vetsuisse Fac, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
CILIATED CELLS; AIRWAY EPITHELIA; GENOME SEQUENCE; VIRUS-INFECTION; COMMON-COLD; REAL-TIME; IN-VITRO; IDENTIFICATION; OC43; VOLUNTEERS;
D O I
10.1128/JVI.03368-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human airway epithelium (HAE) represents the entry port of many human respiratory viruses, including human coronaviruses (HCoVs). Nowadays, four HCoVs, HCoV-229E, HCoV-OC43, HCoV-HKU1, and HCoV-NL63, are known to be circulating worldwide, causing upper and lower respiratory tract infections in nonhospitalized and hospitalized children. Studies of the fundamental aspects of these HCoV infections at the primary entry port, such as cell tropism, are seriously hampered by the lack of a universal culture system or suitable animal models. To expand the knowledge on fundamental virus-host interactions for all four HCoVs at the site of primary infection, we used pseudostratified HAE cell cultures to isolate and characterize representative clinical HCoV strains directly from nasopharyngeal material. Ten contemporary isolates were obtained, representing HCoV-229E (n = 1), HCoV-NL63 (n = 1), HCoV-HKU1 (n = 4), and HCoV-OC43 (n = 4). For each strain, we analyzed the replication kinetics and progeny virus release on HAE cell cultures derived from different donors. Surprisingly, by visualizing HCoV infection by confocal microscopy, we observed that HCoV-229E employs a target cell tropism for nonciliated cells, whereas HCoVOC43, HCoV-HKU1, and HCoV-NL63 all infect ciliated cells. Collectively, the data demonstrate that HAE cell cultures, which morphologically and functionally resemble human airways in vivo, represent a robust universal culture system for isolating and comparing all contemporary HCoV strains.
引用
收藏
页码:6081 / 6090
页数:10
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