Key result
Cryo-EM of enteric adenovirus HAdV-F41 reveals vertex reinforcement and unique protein IX organization.
Why the study?
Enteric adenoviruses must withstand harsh gut conditions to cause gastroenteritis, suggesting capsid stability differs from other adenoviruses.
The structural determination of enteric adenovirus HAdV-F41 reveals unique capsid stabilization features that could inform the design of viral vectors for oral delivery.
These capsid features may guide enteric vector engineering for oral delivery; leaves open clinical translation pending validation studies.
Enteric adenoviruses are one of the main causes of viral gastroenteritis in the world. To carry out a successful infection, the virions must withstand the harsh conditions found in the gut. This requirement suggests that capsid stability must be different from that of other adenoviruses. We have determined the structure of a human enteric adenovirus, HAdV-F41, at 4.0 Å resolution by single particle averaging cryo-electron microscopy, and compared it with that of other adenoviruses with respiratory (HAdV-C5) and ocular (HAdV-D26) tropisms. While the overall structures of hexon, penton base and internal minor coat proteins IIIa and VIII are conserved, we observe partially ordered elements reinforcing the vertex region, which suggests their role in enhancing the physicochemical capsid stability of HAdV-F41. Unexpectedly, we find an organization of the external minor coat protein IX different from all previously characterized human and non-human mastadenoviruses. Knowledge of the structure of enteric adenoviruses can provide a starting point for the design of vectors suitable for oral delivery or intestinal targeting.
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Pérez-Illana et al. (2020) studied Enteric adenovirus infection. Cryo-EM structural analysis vs. HAdV-C5 and HAdV-D26 structures was evaluated on Capsid structure and stability. Cryo-EM structure of enteric adenovirus HAdV-F41 at 4.0 Å resolution reveals elements reinforcing the vertex region and a unique organization of the external minor coat protein IX.
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