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Journal of Virology, October 2009, p. 10406-10416, Vol. 83, No. 20
0022-538X/09/$08.00+0 doi:10.1128/JVI.00990-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, California 92037
Received 15 May 2009/ Accepted 24 July 2009
Borna disease virus (BDV), the prototypic member of the Bornaviridae family within the order Mononegavirales, exhibits high neurotropism and provides an important and unique experimental model system for studying virus-cell interactions within the central nervous system. BDV surface glycoprotein (G) plays a critical role in virus cell entry via receptor-mediated endocytosis, and therefore, G is a critical determinant of virus tissue and cell tropism. However, the specific cell pathways involved in BDV cell entry have not been determined. Here, we provide evidence that BDV uses a clathrin-mediated, caveola-independent cell entry pathway. We also show that BDV G-mediated fusion takes place at an optimal pH of 6.0 to 6.2, corresponding to an early-endosome compartment. Consistent with this finding, BDV cell entry was Rab5 dependent but Rab7 independent and exhibited rapid fusion kinetics. Our results also uncovered a key role for microtubules in BDV cell entry, whereas the integrity and dynamics of actin cytoskeleton were not required for efficient cell entry of BDV.
Published ahead of print on 5 August 2009.
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