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Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity

BACKGROUND: The presence of cholesterol in the Human Immunodeficiency Virus (HIV) lipid envelop is important for viral function as cholesterol depleted viral particles show reduced infectivity. However, it is less well established whether other viral membrane lipids are also important for HIV infect...

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Autores principales: van Til, Niek P, Heutinck, Kirstin M, van der Rijt, Roos, Paulusma, Coen C, van Wijland, Michel, Markusic, David M, Elferink, Ronald PJ Oude, Seppen, Jurgen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265746/
https://www.ncbi.nlm.nih.gov/pubmed/18241333
http://dx.doi.org/10.1186/1742-4690-5-14
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author van Til, Niek P
Heutinck, Kirstin M
van der Rijt, Roos
Paulusma, Coen C
van Wijland, Michel
Markusic, David M
Elferink, Ronald PJ Oude
Seppen, Jurgen
author_facet van Til, Niek P
Heutinck, Kirstin M
van der Rijt, Roos
Paulusma, Coen C
van Wijland, Michel
Markusic, David M
Elferink, Ronald PJ Oude
Seppen, Jurgen
author_sort van Til, Niek P
collection PubMed
description BACKGROUND: The presence of cholesterol in the Human Immunodeficiency Virus (HIV) lipid envelop is important for viral function as cholesterol depleted viral particles show reduced infectivity. However, it is less well established whether other viral membrane lipids are also important for HIV infection. The ABCB4 protein is a phosphatidyl choline (PC) floppase that mediates transport of PC from the inner to the outer membrane leaflet. This property enabled us to modulate the lipid composition of HIV vectors and study the effects on membrane composition and infection efficiency. RESULTS: Virus generated in the presence of ABCB4 was enriched in PC and cholesterol but contained less sphingomyelin (SM). Viral titers were reduced 5.9 fold. These effects were not observed with an inactive ABCB4 mutant. The presence of the ABC transport inhibitor verapamil abolished the effect of ABCB4 expression on viral titers. The ABCB4 mediated reduction in infectivity was caused by changes in the viral particles and not by components co purified with the virus because virus made in the presence of ABCB4 did not inhibit virus made without ABCB4 in a competition assay. Incorporation of the envelope protein was not affected by the expression of ABCB4. The inhibitory effect of ABCB4 was independent of the viral envelope as the effect was observed with two different envelope proteins. CONCLUSION: Our data indicate that increasing the PC content of HIV particles reduces infectivity.
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spelling pubmed-22657462008-03-08 Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity van Til, Niek P Heutinck, Kirstin M van der Rijt, Roos Paulusma, Coen C van Wijland, Michel Markusic, David M Elferink, Ronald PJ Oude Seppen, Jurgen Retrovirology Research BACKGROUND: The presence of cholesterol in the Human Immunodeficiency Virus (HIV) lipid envelop is important for viral function as cholesterol depleted viral particles show reduced infectivity. However, it is less well established whether other viral membrane lipids are also important for HIV infection. The ABCB4 protein is a phosphatidyl choline (PC) floppase that mediates transport of PC from the inner to the outer membrane leaflet. This property enabled us to modulate the lipid composition of HIV vectors and study the effects on membrane composition and infection efficiency. RESULTS: Virus generated in the presence of ABCB4 was enriched in PC and cholesterol but contained less sphingomyelin (SM). Viral titers were reduced 5.9 fold. These effects were not observed with an inactive ABCB4 mutant. The presence of the ABC transport inhibitor verapamil abolished the effect of ABCB4 expression on viral titers. The ABCB4 mediated reduction in infectivity was caused by changes in the viral particles and not by components co purified with the virus because virus made in the presence of ABCB4 did not inhibit virus made without ABCB4 in a competition assay. Incorporation of the envelope protein was not affected by the expression of ABCB4. The inhibitory effect of ABCB4 was independent of the viral envelope as the effect was observed with two different envelope proteins. CONCLUSION: Our data indicate that increasing the PC content of HIV particles reduces infectivity. BioMed Central 2008-02-01 /pmc/articles/PMC2265746/ /pubmed/18241333 http://dx.doi.org/10.1186/1742-4690-5-14 Text en Copyright © 2008 van Til et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
van Til, Niek P
Heutinck, Kirstin M
van der Rijt, Roos
Paulusma, Coen C
van Wijland, Michel
Markusic, David M
Elferink, Ronald PJ Oude
Seppen, Jurgen
Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title_full Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title_fullStr Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title_full_unstemmed Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title_short Alteration of viral lipid composition by expression of the phospholipid floppase ABCB4 reduces HIV vector infectivity
title_sort alteration of viral lipid composition by expression of the phospholipid floppase abcb4 reduces hiv vector infectivity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265746/
https://www.ncbi.nlm.nih.gov/pubmed/18241333
http://dx.doi.org/10.1186/1742-4690-5-14
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