HIV-1 Buds Predominantly at the Plasma Membrane of Primary Human Macrophages
Author(s) -
Sonja Welsch,
Oliver T. Keppler,
Anja Habermann,
Ina Allespach,
Jacomine KrijnseLocker,
HansGeorg Kräusslich
Publication year - 2007
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.0030036
Subject(s) - endosome , budding , membrane , microbiology and biotechnology , ruthenium red , intracellular , staining , biology , chemistry , viral envelope , biophysics , human immunodeficiency virus (hiv) , virology , biochemistry , genetics , organic chemistry , calcium
HIV-1 assembly and release are believed to occur at the plasma membrane in most host cells with the exception of primary macrophages, for which exclusive budding at late endosomes has been reported. Here, we applied a novel ultrastructural approach to assess HIV-1 budding in primary macrophages in an immunomarker-independent manner. Infected macrophages were fed with BSA-gold and stained with the membrane-impermeant dye ruthenium red to identify endosomes and the plasma membrane, respectively. Virus-filled vacuolar structures with a seemingly intracellular localization displayed intense staining with ruthenium red, but lacked endocytosed BSA-gold, defining them as plasma membrane. Moreover, HIV budding profiles were virtually excluded from gold-filled endosomes while frequently being detected on ruthenium red–positive membranes. The composition of cellular marker proteins incorporated into HIV-1 supported a plasma membrane–derived origin of the viral envelope. Thus, contrary to current opinion, the plasma membrane is the primary site of HIV-1 budding also in infected macrophages.
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