Journal of Clinical Microbiology, July 2004, p. 3196-3206, Vol. 42, No. 7
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.7.3196-3206.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Discovery of Novel Human and Animal Cells Infected by the Severe Acute Respiratory Syndrome Coronavirus by Replication-Specific Multiplex Reverse Transcription-PCR
Laura Gillim-Ross,1 Jill Taylor,1 David R. Scholl,2 Jared Ridenour,2 Paul S. Masters,1,3 and David E. Wentworth1,3*
Wadsworth Center, New York State Department of Health,1
Department of Biomedical Sciences, State University of New York, Albany, New York 12002,3
Diagnostic Hybrids, Inc., Athens, Ohio 457012
Received 20 November 2003/
Returned for modification 27 January 2004/
Accepted 4 April 2004
The severe acute respiratory syndrome coronavirus (SARS-CoV) is the causative agent of the recent outbreak of severe acute respiratory syndrome. VeroE6 cells, fetal rhesus monkey kidney cells, and human peripheral blood mononuclear cells were the only cells known to be susceptible to SARS-CoV. We developed a multiplex reverse transcription-PCR assay to analyze the susceptibility of cells derived from a variety of tissues and species to SARS-CoV. Additionally, productive infection was determined by titration of cellular supernatants. Cells derived from three species of monkey were susceptible to SARS-CoV. However, the levels of SARS-CoV produced differed by 4 log10. Mink lung epithelial cells (Mv1Lu) and R-Mix, a mixed monolayer of human lung-derived cells (A549) and mink lung-derived cells (Mv1Lu), are used by diagnostic laboratories to detect respiratory viruses (e.g., influenza virus); they were also infected with SARS-CoV, indicating that the practices of diagnostic laboratories should be examined to ensure appropriate biosafety precautions. Mv1Lu cells produce little SARS-CoV compared to that produced by VeroE6 cells, which indicates that they are a safer alternative for SARS-CoV diagnostics. Evaluation of cells permissive to other coronaviruses indicated that these cell types are not infected by SARS-CoV, providing additional evidence that SARS-CoV binds an alternative receptor. Analysis of human cells derived from lung, kidney, liver, and intestine led to the discovery that human cell lines were productively infected by SARS-CoV. This study identifies new cell lines that may be used for SARS-CoV diagnostics and/or basic research. Our data and other in vivo studies indicate that SARS-CoV has a wide host range, suggesting that the cellular receptor(s) utilized by SARS-CoV is highly conserved and is expressed by a variety of tissues.
* Corresponding author. Mailing address: Wadsworth Center, NYSDOH, 120 New Scotland Ave., Albany, NY 12208. Phone: (518) 408-2396. Fax: (518) 473-1326. E-mail: dwentwor{at}wadsworth.org.
Journal of Clinical Microbiology, July 2004, p. 3196-3206, Vol. 42, No. 7
0095-1137/04/$08.00+0 DOI: 10.1128/JCM.42.7.3196-3206.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Cheng, V. C. C., Lau, S. K. P., Woo, P. C. Y., Yuen, K. Y.
(2007). Severe Acute Respiratory Syndrome Coronavirus as an Agent of Emerging and Reemerging Infection. Clin. Microbiol. Rev.
20: 660-694
[Abstract]
[Full Text]
-
DeDiego, M. L., Alvarez, E., Almazan, F., Rejas, M. T., Lamirande, E., Roberts, A., Shieh, W.-J., Zaki, S. R., Subbarao, K., Enjuanes, L.
(2007). A Severe Acute Respiratory Syndrome Coronavirus That Lacks the E Gene Is Attenuated In Vitro and In Vivo. J. Virol.
81: 1701-1713
[Abstract]
[Full Text]
-
Leland, D. S., Ginocchio, C. C.
(2007). Role of Cell Culture for Virus Detection in the Age of Technology. Clin. Microbiol. Rev.
20: 49-78
[Abstract]
[Full Text]
-
Ling, T.-Y., Kuo, M.-D., Li, C.-L., Yu, A. L., Huang, Y.-H., Wu, T.-J., Lin, Y.-C., Chen, S.-H., Yu, J.
(2006). Identification of pulmonary Oct-4+ stem/progenitor cells and demonstration of their susceptibility to SARS coronavirus (SARS-CoV) infection in vitro. Proc. Natl. Acad. Sci. USA
103: 9530-9535
[Abstract]
[Full Text]
-
Yen, Y.-T., Liao, F., Hsiao, C.-H., Kao, C.-L., Chen, Y.-C., Wu-Hsieh, B. A.
(2006). Modeling the Early Events of Severe Acute Respiratory Syndrome Coronavirus Infection In Vitro. J. Virol.
80: 2684-2693
[Abstract]
[Full Text]
-
Sims, A. C., Baric, R. S., Yount, B., Burkett, S. E., Collins, P. L., Pickles, R. J.
(2005). Severe Acute Respiratory Syndrome Coronavirus Infection of Human Ciliated Airway Epithelia: Role of Ciliated Cells in Viral Spread in the Conducting Airways of the Lungs. J. Virol.
79: 15511-15524
[Abstract]
[Full Text]
-
Surjit, M., Kumar, R., Mishra, R. N., Reddy, M. K., Chow, V. T. K., Lal, S. K.
(2005). The Severe Acute Respiratory Syndrome Coronavirus Nucleocapsid Protein Is Phosphorylated and Localizes in the Cytoplasm by 14-3-3-Mediated Translocation. J. Virol.
79: 11476-11486
[Abstract]
[Full Text]
-
Lambert, D. W., Yarski, M., Warner, F. J., Thornhill, P., Parkin, E. T., Smith, A. I., Hooper, N. M., Turner, A. J.
(2005). Tumor Necrosis Factor-{alpha} Convertase (ADAM17) Mediates Regulated Ectodomain Shedding of the Severe-acute Respiratory Syndrome-Coronavirus (SARS-CoV) Receptor, Angiotensin-converting Enzyme-2 (ACE2). J. Biol. Chem.
280: 30113-30119
[Abstract]
[Full Text]
-
Tan, Y.-J., Tham, P.-Y., Chan, D. Z. L., Chou, C.-F., Shen, S., Fielding, B. C., Tan, T. H. P., Lim, S. G., Hong, W.
(2005). The Severe Acute Respiratory Syndrome Coronavirus 3a Protein Up-Regulates Expression of Fibrinogen in Lung Epithelial Cells. J. Virol.
79: 10083-10087
[Abstract]
[Full Text]
-
Mossel, E. C., Huang, C., Narayanan, K., Makino, S., Tesh, R. B., Peters, C. J.
(2005). Exogenous ACE2 Expression Allows Refractory Cell Lines To Support Severe Acute Respiratory Syndrome Coronavirus Replication. J. Virol.
79: 3846-3850
[Abstract]
[Full Text]
-
Jeffers, S. A., Tusell, S. M., Gillim-Ross, L., Hemmila, E. M., Achenbach, J. E., Babcock, G. J., Thomas, W. D. Jr., Thackray, L. B., Young, M. D., Mason, R. J., Ambrosino, D. M., Wentworth, D. E., DeMartini, J. C., Holmes, K. V.
(2004). CD209L (L-SIGN) is a receptor for severe acute respiratory syndrome coronavirus. Proc. Natl. Acad. Sci. USA
101: 15748-15753
[Abstract]
[Full Text]
Copyright © 2004 by the American Society for Microbiology. All rights reserved.