» Articles » PMID: 39334915

Secondary Envelopment of Human Cytomegalovirus Is a Fast Process Utilizing the Endocytic Compartment As a Major Membrane Source

Overview
Journal Biomolecules
Publisher MDPI
Date 2024 Sep 28
PMID 39334915
Authors
Affiliations
Soon will be listed here.
Abstract

Secondary envelopment of the human cytomegalovirus (HCMV) is a critical but not well-understood process that takes place at the cytoplasmic viral assembly complex (cVAC) where nucleocapsids acquire their envelope by budding into cellular membranes containing viral glycoproteins. Previous studies presented controversial results regarding the composition of the viral envelope, suggesting trans-Golgi and endosomal origins, as well as intersections with the exosomal and endocytic pathways. Here, we investigated the role of endocytic membranes for the secondary envelopment of HCMV by using wheat germ agglutinin (WGA) pulse labeling to label glycoproteins at the plasma membrane and to follow their trafficking during HCMV infection by light microscopy and transmission electron microscopy (TEM). WGA labeled different membrane compartments within the cVAC, including early endosomes, multivesicular bodies, trans-Golgi, and recycling endosomes. Furthermore, TEM analysis showed that almost 90% of capsids undergoing secondary envelopment and 50% of enveloped capsids were WGA-positive within 90 min. Our data reveal extensive remodeling of the endocytic compartment in the late stage of HCMV infection, where the endocytic compartment provides an optimized environment for virion morphogenesis and serves as the primary membrane source for secondary envelopment. Furthermore, we show that secondary envelopment is a rapid process in which endocytosed membranes are transported from the plasma membrane to the cVAC within minutes to be utilized by capsids for envelopment.

Citing Articles

Rab10-associated tubulation as an early marker for biogenesis of the assembly compartment in cytomegalovirus-infected cells.

Mahmutefendic Lucin H, Stimac I, Marcelic M, Skocaj M, Lisnic B, Omerovic A Front Cell Dev Biol. 2025; 12:1517236.

PMID: 39866842 PMC: 11760598. DOI: 10.3389/fcell.2024.1517236.

References
1.
Radsak K, Eickmann M, Mockenhaupt T, Bogner E, Kern H, Eis-Hubinger A . Retrieval of human cytomegalovirus glycoprotein B from the infected cell surface for virus envelopment. Arch Virol. 1996; 141(3-4):557-72. DOI: 10.1007/BF01718317. View

2.
Jean Beltran P, Mathias R, Cristea I . A Portrait of the Human Organelle Proteome In Space and Time during Cytomegalovirus Infection. Cell Syst. 2016; 3(4):361-373.e6. PMC: 5083158. DOI: 10.1016/j.cels.2016.08.012. View

3.
White S, Roller R . Herpes simplex virus type-1 cVAC formation in neuronal cells is mediated by dynein motor function and glycoprotein retrieval from the plasma membrane. J Virol. 2024; 98(7):e0071324. PMC: 11265375. DOI: 10.1128/jvi.00713-24. View

4.
Granzow H, Weiland F, Jons A, Klupp B, Karger A, Mettenleiter T . Ultrastructural analysis of the replication cycle of pseudorabies virus in cell culture: a reassessment. J Virol. 1997; 71(3):2072-82. PMC: 191296. DOI: 10.1128/JVI.71.3.2072-2082.1997. View

5.
Tugizov S, Maidji E, Xiao J, Pereira L . An acidic cluster in the cytosolic domain of human cytomegalovirus glycoprotein B is a signal for endocytosis from the plasma membrane. J Virol. 1999; 73(10):8677-88. PMC: 112888. DOI: 10.1128/JVI.73.10.8677-8688.1999. View