Herpesvirus Entry: an Update
Top Cited Papers
Open Access
- 1 October 2003
- journal article
- review article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 77 (19) , 10179-10185
- https://doi.org/10.1128/jvi.77.19.10179-10185.2003
Abstract
Members of the Herpesviridae form a large and diverse fam- ily comprised of three subfamilies designated alpha-, beta-, and gammaherpesviruses. Virions are composed of a large DNA genome encased in an icosahedral capsid, which is in turn coated with a layer of proteins called the tegument and an envelope composed of about a dozen viral proteins and glyco- proteins in a lipid bilayer. At least three, sometimes four, of these envelope glycoproteins are absolutely essential for viral entry. The three glycoproteins thought to be essential for the entry of all herpesviruses are designated gB, gH, and gL. The genes for these glycoproteins are conserved, with gB exhibiting the highest degree of sequence similarity. For at least some herpesviruses, gB is a homodimer or homotrimer displayed as a prominent spike. Heterodimerization of gH and gL is a conserved feature, with the addition of another viral protein subunit for some viruses. Common features of herpesvirus biology include a high in- cidence of asymptomatic infections and the establishment of latent infections which can be reactivated to cause recurrent or new episodes of disease. The human herpesviruses exhibit these common features as well as diversity in biology and pathogenesis. They include the alphaherpesviruses, herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) and varicella- zoster virus (VZV); the betaherpesviruses, cytomegalovirus (CMV) and human herpesviruses 6 and 7; and the gammaher- pesviruses, Epstein-Barr virus (EBV) and human herpesvirus 8 (HHV-8). HSV-1 and HSV-2 are responsible for localized mucocutaneous lesions, most commonly, but can also cause meningitis and encephalitis. VZV causes systemic disease with skin lesions during primary infection (chicken pox) and zoster. All three viruses establish latent infections in neurons and can be reactivated from neurons. The betaherpesviruses cause mostly asymptomatic infections in immunocompetent individ- uals and can establish latent infections in several cell types, including leukocytes of various lineages. EBV is the major cause of infectious mononucleosis and is causally associated with various malignancies, including Burkitt's lymphoma, Hodgkin's disease, other lymphomas, and nasopharyngeal car- cinoma. HHV-8 is associated with Kaposi's sarcoma, multicen- tric Castleman's disease, and primary effusion lymphoma.Keywords
This publication has 60 references indexed in Scilit:
- Differences in the N Termini of Herpes Simplex Virus Type 1 and 2 gDs That Influence Functional Interactions with the Human Entry Receptor Nectin-2 and an Entry Receptor Expressed in Chinese Hamster Ovary CellsJournal of Virology, 2003
- Human Herpesvirus 6 Variant A Glycoprotein H-Glycoprotein L-Glycoprotein Q Complex Associates with Human CD46Journal of Virology, 2003
- Human Herpesvirus 8 Envelope Glycoprotein B Mediates Cell Adhesion via Its RGD SequenceJournal of Virology, 2003
- Involvement of tumor necrosis factor receptor superfamily (TNFRSF) members in the pathogenesis of inflammatory diseasesExperimental & Molecular Medicine, 2003
- Amino Acid Substitutions in the V Domain of Nectin-1 (HveC) That Impair Entry Activity for Herpes Simplex Virus Types 1 and 2 but Not for Pseudorabies Virus or Bovine Herpesvirus 1Journal of Virology, 2002
- Cell Surface Heparan Sulfate Is a Receptor for Human Herpesvirus 8 and Interacts with Envelope Glycoprotein K8.1Journal of Virology, 2001
- Structural Features of Nectin-2 (HveB) Required for Herpes Simplex Virus EntryJournal of Virology, 2001
- Human Herpesvirus 8 Envelope Glycoprotein K8.1A Interaction with the Target Cells Involves Heparan SulfateJournal of Virology, 2001
- Herpes simplex virus glycoprotein D bound to the human receptor HveA.Published by Elsevier ,2001
- Penetration of cells by herpes simplex virus does not require a low pH-dependent endocytic pathwayVirus Research, 1991