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J Gen Virol 72 (1991), 573-578; DOI 10.1099/0022-1317-72-3-573
© 1991 Society for General Microbiology

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Persistent infection of Vero cells by the flavivirus Murray Valley encephalitis virus

Michael Poidinger, Robert J. Coelen and John S. Mackenzie

Department of Microbiology, Queen Elizabeth II Medical Centre, University of Western Australia, Nedlands, Western Australia 6009

Murray Valley encephalitis (MVE) virus strain OR2 was serially passaged on Vero cells to establish a persistent infection which was maintained for over 300 days. Supernatants from infected cells protected Vero cells from c.p.e. and caused up to a 95% reduction of wild-type virus yield. These protective and interfering effects suggest that defective interfering (DI) particles are responsible for the establishment and maintenance of the MVE virus persistent infection. The persistently infected cell supernatant preparations shared several features with DI particle preparations from other viral systems, such as their amplification to detectable levels after two to four passages of virus. However, results from this study suggest that DI particles of MVE virus differ from other studied systems in that they are able to affect only moderately the yield of infectious wild-type virus. The genetic drift of the parental virus during the course of a long term persistent infection in vitro appears to be minimal.

Received 13 July 1990; accepted 4 December 1990.


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