The nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia

Brajesh K. Singh, Andrew L. Hornick, Sateesh Krishnamurthy, Anna C. Locke, Crystal A. Mendoz, Mathieu Mateo, Catherine L. Miller-Hunt, Roberto Cattaneo, Patrick L. Sinn

Research output: Contribution to journalArticle

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Abstract

The discovery that measles virus (MV) uses the adherens junction protein nectin-4 as its epithelial receptor provides a new vantage point from which to characterize its rapid spread in the airway epithelium. We show here that in well-differentiated primary cultures of airway epithelial cells from human donors (HAE), MV infectious centers form rapidly and become larger than those of other respiratory pathogens: human respiratory syncytial virus, parainfluenza virus 5, and Sendai virus. While visible syncytia do not form after MV infection of HAE, the cytoplasm of an infected cell suddenly flows into an adjacent cell, as visualized through wild-type MV-expressed cytoplasmic green fluorescent protein (GFP). High-resolution video microscopy documents that GFP flows through openings that form on the lateral surfaces between columnar epithelial cells. To assess the relevance of the protein afadin, which connects nectin-4 to the actin cytoskeleton, we knocked down its mRNA. This resulted in more-limited infectious-center formation. We also generated a nectin-4 mutant without the afadin-binding site in its cytoplasmic tail. This mutant was less effective than wild-type human nectin-4 at promoting MV infection in primary cultures of porcine airway epithelia. Thus, in airway epithelial cells, MV spread requires the nectin-4/afadin complex and is based on cytoplasm transfer between columnar cells. Since the viral membrane fusion apparatus may open the passages that allow cytoplasm transfer, we refer to them as intercellular membrane pores. Virus-induced intercellular pores may contribute to extremely efficient measles contagion by promoting the rapid spread of the virus through the upper respiratory epithelium.

Original languageEnglish (US)
Pages (from-to)7089-7096
Number of pages8
JournalJournal of Virology
Volume89
Issue number14
DOIs
StatePublished - 2015

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Measles virus
epithelium
Epithelium
Membranes
Cytoplasm
Proteins
epithelial cells
cytoplasm
proteins
Epithelial Cells
Virus Diseases
Green Fluorescent Proteins
green fluorescent protein
Parainfluenza virus 5
Parainfluenza Virus 5
Human respiratory syncytial virus
Sendai virus
Viruses
respiratory mucosa
Adherens Junctions

ASJC Scopus subject areas

  • Immunology
  • Virology

Cite this

Singh, B. K., Hornick, A. L., Krishnamurthy, S., Locke, A. C., Mendoz, C. A., Mateo, M., ... Sinn, P. L. (2015). The nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia. Journal of Virology, 89(14), 7089-7096. https://doi.org/10.1128/JVI.00821-15

The nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia. / Singh, Brajesh K.; Hornick, Andrew L.; Krishnamurthy, Sateesh; Locke, Anna C.; Mendoz, Crystal A.; Mateo, Mathieu; Miller-Hunt, Catherine L.; Cattaneo, Roberto; Sinn, Patrick L.

In: Journal of Virology, Vol. 89, No. 14, 2015, p. 7089-7096.

Research output: Contribution to journalArticle

Singh, BK, Hornick, AL, Krishnamurthy, S, Locke, AC, Mendoz, CA, Mateo, M, Miller-Hunt, CL, Cattaneo, R & Sinn, PL 2015, 'The nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia', Journal of Virology, vol. 89, no. 14, pp. 7089-7096. https://doi.org/10.1128/JVI.00821-15
Singh, Brajesh K. ; Hornick, Andrew L. ; Krishnamurthy, Sateesh ; Locke, Anna C. ; Mendoz, Crystal A. ; Mateo, Mathieu ; Miller-Hunt, Catherine L. ; Cattaneo, Roberto ; Sinn, Patrick L. / The nectin-4/afadin protein complex and intercellular membrane pores contribute to rapid spread of measles virus in primary human airway epithelia. In: Journal of Virology. 2015 ; Vol. 89, No. 14. pp. 7089-7096.
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