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Atomic structure of a rhinovirus C, a virus species linked to severe childhood asthma.


ABSTRACT: Isolates of rhinovirus C (RV-C), a recently identified Enterovirus (EV) species, are the causative agents of severe respiratory infections among children and are linked to childhood asthma exacerbations. The RV-C have been refractory to structure determination because they are difficult to propagate in vitro. Here, we report the cryo-EM atomic structures of the full virion and native empty particle (NEP) of RV-C15a. The virus has 60 "fingers" on the virus outer surface that probably function as dominant immunogens. Because the NEPs also display these fingers, they may have utility as vaccine candidates. A sequence-conserved surface depression adjacent to each finger forms a likely binding site for the sialic acid on its receptor. The RV-C, unlike other EVs, are resistant to capsid-binding antiviral compounds because the hydrophobic pocket in VP1 is filled with multiple bulky residues. These results define potential molecular determinants for designing antiviral therapeutics and vaccines.

SUBMITTER: Liu Y 

PROVIDER: S-EPMC4987780 | biostudies-literature | 2016 Aug

REPOSITORIES: biostudies-literature

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Atomic structure of a rhinovirus C, a virus species linked to severe childhood asthma.

Liu Yue Y   Hill Marchel G MG   Klose Thomas T   Chen Zhenguo Z   Watters Kelly K   Bochkov Yury A YA   Jiang Wen W   Palmenberg Ann C AC   Rossmann Michael G MG  

Proceedings of the National Academy of Sciences of the United States of America 20160711 32


Isolates of rhinovirus C (RV-C), a recently identified Enterovirus (EV) species, are the causative agents of severe respiratory infections among children and are linked to childhood asthma exacerbations. The RV-C have been refractory to structure determination because they are difficult to propagate in vitro. Here, we report the cryo-EM atomic structures of the full virion and native empty particle (NEP) of RV-C15a. The virus has 60 "fingers" on the virus outer surface that probably function as  ...[more]

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