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Journal of Virology, December 2000, p. 11983-11987, Vol. 74, No. 24
Department of Microbiology and Immunology,
University of California, San Francisco, California
Received 7 July 2000/Accepted 14 September 2000
We have previously shown that Xenopus oocytes require
coinjection of both poliovirus RNA and HeLa cell extracts to support a
complete cycle of viral replication yielding high levels of infectious
viral particles. This novel system provides a tool for identifying host
factors and for biochemically dissect individual steps that lead to
virus production. Here we demonstrate that Xenopus oocytes
are able to support replication of other picornaviruses such as human
rhinovirus 14 and mengovirus. Unlike poliovirus, microinjection of
mengovirus RNA yields high viral titers (about 107
PFU/oocyte) without the need for coinjection of additional cell extracts. In contrast, formation of infectious rhinovirus particles requires coinjection of human cell extracts. We found that one of these
human factors is required for efficient rhinovirus translation. Our
findings uncover differences in the host factor requirements among
members of the picornavirus family and provide the means to identify
the human protein(s) involved in rhinovirus production.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Translation and Replication of Human Rhinovirus
Type 14 and Mengovirus in Xenopus Oocytes
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Box 0414, University of California, San Francisco, CA 94143-0414. Phone: (415) 502-6358. Fax: (415) 476-0939. E-mail: andino{at}itsa.ucsf.edu.
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