AI Article Synopsis

  • The foot-and-mouth disease virus (FMDV) Leader proteinase L prevents host cell mRNA translation and interferon responses, aiding the virus's survival.
  • A variant of FMDV lacking most of the L coding region (ΔLb) was created to study its effect on cattle after infection.
  • The study found that this leaderless variant could replicate in lab conditions but failed to cause acute infection or persistently infect the upper respiratory tract of cattle.

Article Abstract

The foot-and-mouth disease virus (FMDV) Leader proteinase L inhibits host mRNA translation and blocks the interferon response which promotes viral survival. L is not required for viral replication in vitro but serotype A FMDV lacking L has been shown to be attenuated in cattle and pigs. However, it is not known, whether leaderless viruses can cause persistent infection in vivo after simulated natural infection and whether the attenuated phenotype is the same in other serotypes. We have generated an FMDV O/FRA/1/2001 variant lacking most of the L coding region (ΔLb). Cattle were inoculated intranasopharyngeally and observed for 35 days to determine if O FRA/1/2001 ΔLb is attenuated during the acute phase of infection and whether it can maintain a persistent infection in the upper respiratory tract. We found that although this leaderless virus can replicate in vitro in different cell lines, it is unable to establish an acute infection with vesicular lesions and viral shedding nor is it able to persistently infect bovine pharyngeal tissues.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11100440PMC
http://dx.doi.org/10.1080/22221751.2024.2348526DOI Listing

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