Herpes simplex virus type 1 modifies the protein composition of extracellular vesicles to promote neurite outgrowth and neuroinfection

Author:

Sun Guorong1ORCID,Kropp Kai Alexander1ORCID,Kirchner Marieluise2ORCID,Plückebaum Nina1ORCID,Selich Anton3,Serrero Manutea1,Dhingra Akshay1,Cabrera Jorge Rubén4,Ritter Birgit1,Bauerfeind Rudolf5,Wyler Emanuel6,Landthaler Markus67ORCID,Schambach Axel3,Sodeik Beate18ORCID,Mertins Philipp2,Viejo-Borbolla Abel18ORCID

Affiliation:

1. Institute of Virology, Hannover Medical School, Hannover, Germany

2. Proteomics platform, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC) and Berlin Institute of Health (BIH), Berlin, Germany

3. Institute of Experimental Hematology, Hannover Medical School, Hannover, Germany

4. Centro de Biología Molecular Severo Ochoa, Consejo Superior de Investigaciones Científicas—Universidad Autónoma de Madrid, Madrid, Spain

5. Research Core Unit for Laser Microscopy, Hannover Medical School, Hannover, Germany

6. Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany

7. Institute for Biology, Humboldt University of Berlin, Berlin, Germany

8. Cluster of Excellence-Resolving Infection Susceptibility (RESIST, EXC 2155), Hannover Medical School, Hannover, Germany

Abstract

Herpes simplex virus type 1 (HSV-1) must infect neurites (or nerve endings) to establish a chronic infection in neurons. Neurites are highly dynamic structures that retract or grow in the presence of repulsive or attractive proteins. Some of these proteins are released by epithelial cells in extracellular vesicles and act upon interaction with their receptor present on neurites. We show here that HSV-1 infection of epithelial cells modulated their effect on neurites, increasing neurite growth. Mechanistically, HSV-1 glycoprotein G (gG) modifies the protein composition of extracellular vesicles released by epithelial cells, increasing the amount of attractive proteins that enhance neurite outgrowth and facilitate neuronal infection. These results could inform of therapeutic strategies to block HSV-1 induction of neurite outgrowth and, thereby, neuronal infection.

Funder

Deutsche Forschungsgemeinschaft

CSC | China Scholarship Council

Publisher

American Society for Microbiology

Reference106 articles.

1. Herpes simplex virus: global infection prevalence and incidence estimates, 2016

2. Pathogenesis and virulence of herpes simplex virus

3. Herpes Simplex Viruses

4. Whitley R, Johnston C. 2021. Herpes simplex viruses: pathogenesis and clinical insights, p 297–323. In Howley PM, Knipe DM, Cohen JL, Damania BA (ed), Fields Virol DNA viruses

5. Isolation of Latent Herpes Simplex Virus from the Superior Cervical and Vagus Ganglions of Human Beings

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