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. 2023 Apr;1522(1):60-73.
doi: 10.1111/nyas.14958. Epub 2023 Feb 1.

Respiratory viruses: New frontiers-a Keystone Symposia report

Affiliations

Respiratory viruses: New frontiers-a Keystone Symposia report

Jennifer Cable et al. Ann N Y Acad Sci. 2023 Apr.

Abstract

Respiratory viruses are a common cause of morbidity and mortality around the world. Viruses like influenza, RSV, and most recently SARS-CoV-2 can rapidly spread through a population, causing acute infection and, in vulnerable populations, severe or chronic disease. Developing effective treatment and prevention strategies often becomes a race against ever-evolving viruses that develop resistance, leaving therapy efficacy either short-lived or relevant for specific viral strains. On June 29 to July 2, 2022, researchers met for the Keystone symposium "Respiratory Viruses: New Frontiers." Researchers presented new insights into viral biology and virus-host interactions to understand the mechanisms of disease and identify novel treatment and prevention approaches that are effective, durable, and broad.

Keywords: COVID-19; RSV; adaptive immunity; influenza virus; innate immunity; respiratory virus.

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Conflict of interest statement

Competing Interests

J. Sun is a consultant for the Teneofour company.

Figures

Figure 1.
Figure 1.
The delay that occurred in setting up the MOSAIC consortium in 2009 following the traditional path of applying for a grant and getting it funded. This occurred despite all parties recognising that speed was essential.
Figure 2.
Figure 2.
Expanding the translatable regions of viral genomes. (A) Segmented negative strand RNA viruses (sNSVs) such as the influenza viruses transcribe their genes by ‘cap snatching’ from host mRNAs. (B) Cap snatching results in a hybrid mRNA containing host and viral sequences. If the host mRNA contains upstream start codons (uAUGs) this can provide additional opportunities to translate viral proteins through ‘start snatching.’ (C) Start snatching expands the accessory proteome of sNSVs by allowing the translation of proteins with N-terminal extensions (from in-frame uAUGs) or novel upstream frameshifted open reading frames (from out-of-frame uAUGs).

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