Published July 2014 | Version v1
Journal article

Sequestration of human cytomegalovirus by human renal and mammary epithelial cells

  • 1. Institute for Medical Immunology, Université Libre de Bruxelles, Rue A. Bolland 8, B-6041 Charleroi (Belgium)
  • 2. Laboratory of Virology and Chemotherapy, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven (Belgium)
  • 3. ImmuneHealth, Rue A. Bolland 8, B-6041 Charleroi (Belgium)
  • 4. Department of Obstetrics and Gynecology, Erasme Hospital, Route de Lennik 808, 1070 Brussels (Belgium)
  • 5. Laboratory of Molecular Parasitology, Institut de Biologie et Médecine Moléculaires, Université Libre de Bruxelles, Gosselies (Belgium)
  • 6. Pathology Department, U.Z. Leuven, Minderbroedersstraat 12, Leuven (Belgium)

Description

Urine and breast milk represent the main routes of human cytomegalovirus (HCMV) transmission but the contribution of renal and mammary epithelial cells to viral excretion remains unclear. We observed that kidney and mammary epithelial cells were permissive to HCMV infection and expressed immediate early, early and late antigens within 72 h of infection. During the first 24 h after infection, high titers of infectious virus were measured associated to the cells and in culture supernatants, independently of de novo synthesis of virus progeny. This phenomenon was not observed in HCMV-infected fibroblasts and suggested the sequestration and the release of HCMV by epithelial cells. This hypothesis was supported by confocal and electron microscopy analyses. The sequestration and progressive release of HCMV by kidney and mammary epithelial cells may play an important role in the excretion of the virus in urine and breast milk and may thereby contribute to HCMV transmission. - Highlights: • Primary renal and mammary epithelial cells are permissive to HCMV infection. • HCMV is sequestered by epithelial cells and this phenomenon does not require viral replication. • HCMV sequestration by epithelial cells is reduced by antibodies and IFN-γ

Availability note (English)

Available from http://dx.doi.org/10.1016/j.virol.2014.04.032

Additional details

Identifiers

DOI
10.1016/j.virol.2014.04.032;
PII
S0042-6822(14)00155-X;

Publishing Information

Journal Title
Virology
Journal Volume
460-461
Journal Page Range
p. 55-65
ISSN
0042-6822
CODEN
VIRLAX

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.