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Journal of Virology, December 2001, p. 11464-11473, Vol. 75, No. 23
Division of Comparative Medicine, The Johns
Hopkins University School of Medicine, Baltimore, Maryland 21287
Received 20 March 2001/Accepted 18 August 2001
Pseudotype virus vectors serve as a powerful tool for the study of
virus receptor usage and entry. We describe the development of murine
leukemia virus (MuLV) particles pseudotyped with the visna virus
envelope glycoprotein and encoding a green fluorescent protein reporter
as a tool to study the expression of the visna virus receptor.
Functional MuLV/visna virus pseudotypes were obtained when the
cytoplasmic tail of the visna virus envelope TM protein was truncated
to 3, 7, or 11 amino acids in length. MuLV/visna virus particles were
used to transduce a panel of cell types from various organisms,
including sheep, goat, human, hamster, mouse, monkey, and quail. The
majority of the cells examined were susceptible to MuLV/visna
pseudotype viruses, supporting the notion that the visna virus cellular
receptor is a widely expressed protein found in many species. Of 16 different cell types tested, only mouse embryo fibroblast NIH 3T3
cells, hamster ovary CHO cells, and the human promonocyte cell line
U937 cells were not susceptible to transduction by the pseudotyped
virus. The production of functional MuLV/visna virus pseudotypes has
provided a sensitive, biologically relevant system to study visna virus
cell entry and envelope-receptor interactions.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.23.11464-11473.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Functional Murine Leukemia Virus Vectors
Pseudotyped with the Visna Virus Envelope Show Expanded Visna Virus
Cell Tropism
*
Corresponding author. Mailing address: 600 N. Wolfe
St., Jefferson St. Bldg. 3-127, Baltimore, MD 21287. Phone: (410)
955-9770. Fax: (410) 955-9823. E-mail: jclement{at}jhmi.edu.
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