Molecular Features of the Measles Virus Viral Fusion Complex That Favor Infection and Spread in the Brain

Cyrille Mathieu(Université Claude Bernard Lyon 1), Francesca T. Bovier(University of Campania "Luigi Vanvitelli"), Marion Ferren(Université Claude Bernard Lyon 1), Nicole A. P. Lieberman(University of Washington Medical Center), Camilla Predella(Columbia University), Alexandre Lalande(Université Claude Bernard Lyon 1), Vikas Peddu(University of Washington Medical Center), Michelle J. Lin(University of Washington Medical Center), Amin Addetia(University of Washington Medical Center), Achchhe Patel(Columbia University), Victor K. Outlaw(University of Wisconsin–Madison), Barbara Corneo(Columbia University), N. Valerio Dorrello(Columbia University), Thomas Briese(Columbia University), Diana Hardie(National Health Laboratory Service), Branka Horvat(Université Claude Bernard Lyon 1), Anne Moscona(Columbia University), Alexander L. Greninger(University of Washington Medical Center), Matteo Porotto(University of Campania "Luigi Vanvitelli")
mBio
June 11, 2021
Cited by 40Open Access
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Abstract

Measles virus (MeV) infection can cause serious complications in immunocompromised individuals, including measles inclusion body encephalitis (MIBE). In some cases, MeV persistence and subacute sclerosing panencephalitis (SSPE), another severe central nervous system (CNS) complication, develop even in the face of a systemic immune response. Both MIBE and SSPE are relatively rare but lethal. It is unclear how MeV causes CNS infection. We introduced specific mutations that are found in MIBE or SSPE cases into the MeV fusion protein to test the hypothesis that dysregulation of the viral fusion complex-comprising F and the receptor binding protein, H-allows virus to spread in the CNS. Using metagenomic, structural, and biochemical approaches, we demonstrate that altered fusion properties of the MeV H-F fusion complex permit MeV to spread in brain tissue.


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