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Journal of Virology, April 2003, p. 4858-4866, Vol. 77, No. 8
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.8.4858-4866.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Binding of Adenovirus Capsid to Dipalmitoyl Phosphatidylcholine Provides a Novel Pathway for Virus Entry

Larissa Balakireva,1,{dagger}* Guy Schoehn,2 Eric Thouvenin,1 and Jadwiga Chroboczek1

Institut de Biologie Structurale Jean-Pierre Ebel, 38027 Grenoble Cedex 1,1 EMBL Grenoble Outstation, 156X, 38042 Grenoble Cedex 9, France2

Received 28 October 2002/ Accepted 23 January 2003

Adenovirus (Ad) is an airborne, nonenveloped virus infecting respiratory epithelium. To study the mechanism of Ad entry, we used alveolar adenocarcinoma A549 cells, which have retained the ability of alveolar epithelial type II cells to synthesize the major component of pulmonary surfactant, disaturated phosphatidylcholine. Stimulation of phosphatidylcholine secretion by calcium ionophore or phorbol ester augmented the susceptibility of these cells to Ad. Both Ad infection and recombinant-Ad-mediated transfection increased in the presence of dipalmitoyl phosphatidylcholine (DPPC) liposomes in culture medium. Importantly, in the presence of DPPC liposomes, virus penetrates the cells independently of virus-specific protein receptors. DPPC vesicles bind Ad and are efficiently incorporated by A549 lung cells, serving as a virus vehicle during Ad penetration. To identify the viral protein(s) mediating Ad binding, a flotation of liposomes preincubated with structural viral proteins was employed, showing that the only Ad protein bound to DPPC vesicles was a hexon. The hexon preserved its phospholipid-binding properties upon purification, confirming its involvement in virus binding to the phospholipid. Given that disaturated phosphatidylcholine not only covers the inner surface of alveoli in the lungs but also reenters alveolar epithelium during lung surfactant turnover, Ad binding to this phospholipid may provide a pathway for virus entry into alveolar epithelium in vivo.


* Corresponding author. Mailing address: Université Joseph Fourier, Domaine de la Merci, 38706 La Tronche, France. Phone: (33) 4 76 63 74 17. Fax: (33) 4 76 54 80 74. E-mail: Larissa.Balakireva{at}ujf-grenoble.fr.

{dagger} Permanent address: Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.


Journal of Virology, April 2003, p. 4858-4866, Vol. 77, No. 8
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.8.4858-4866.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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