ETIDIOH - NEW

{Excerpt} Highly pathogenic H5N1 avian influenza (HPAI) viruses started circulating in lactating dairy cattle in the USA at the end of 2023 (ref. 1) and these viruses are now rapidly spreading between cows2. Eisfeld et al.3 found that a clade 2.3.4.4b H5N1 virus from this cattle outbreak can bind to α2,6-linked sialyl-glycopolymers on microtitre plates . Here we show that the haemagglutinin from a clade 2.3.4.4b H5N1 virus binds poorly to glycans that terminate with α2-6 sialic acids. This is an important finding, as α2,6 sialic acid is abundant in the upper respiratory tract of humans , and acquisition of α2,6 sialic acid receptor specificity is believed to be required for efficient transmission of influenza virus in humans and is considered a risk factor for the emergence of a new pandemic virus4. (...) Source: Nature,  https://www.nature.com/articles/s41586-025-08821-6 ____

Abstract In 2023, an outbreak of highly pathogenic avian influenza occurred among critically endangered California condors (Gymnogyps californianus), and >21 died. We evaluated safety, immunogenicity, vaccination strategies, and correlates of antibody response of an influenza vaccine for poultry in black vultures (Coragyps atratus) and then California condors. We noted differences in antibody titers between vaccinated and unvaccinated birds (vultures p<0.004; condors p­<0.02) but no adverse effects of vaccination. All vaccinated vultures and 80% of vaccinated condors showed maximum measured antibody response within the published range associated with survival of vaccinated and virally challenged chickens. We noted weak evidence of higher antibody responses for birds given two 0.5-mL vaccines versus those given one 1-mL vaccine but no correlation between antibody titers and sex for either species or between antibody titers and bone lead concentrations in vultures. Our results p...

Significance We explored how H5Nx influenza viruses , which can infect many different birds and mammals, could adapt to infect humans by altering the hemagglutinin (HA). HA must change to bind human-type receptors for transmission between people. We compared two strains from viruses isolated in 2016 and found that one ( 2.3.4.4e ) can switch to human receptor binding with a single mutation , while another ( 2.3.4.4b ) might require more complex changes to bind simple human-type receptors. These findings highlight the potential for specific strains to evolve and become a pandemic threat, underscoring the importance of monitoring mutations that could lead to human-type receptor adaptation. Abstract H5Nx viruses continue to wreak havoc in avian and mammalian species worldwide . The virus distinguishes itself by the ability to replicate to high titers and transmit efficiently in a wide variety of hosts in diverse climatic environments. Fortunately, transmission to and between humans is sca...

Abstract SARS-like betacoronaviruses (sarbecoviruses) endemic in bats pose a significant zoonotic threat to humans . Genetic pathways associated with spillover of bat sarbecoviruses into humans are incompletely understood. We previously showed that the WT spike of the rhinolophid bat coronavirus SHC014 -CoV has poor entry activity and uncovered two distinct genetic pathways outside the receptor-binding domain (RBD) that increased spike opening, ACE2 binding , and cell entry. Herein, we show that the widely studied bat sarbecovirus WIV1-CoV is likely a cell culture-adapted variant of Rs3367-CoV, which was sequenced from the same population of rhinolophid bats as SHC014-CoV. We demonstrate that the acquisition of a single amino-acid substitution in the ‘630-loop’ of the S1 subunit was the key spike adaptation event during the successful isolation of WIV1-CoV, and that it enhances spike opening, virus-receptor recognition, and cell entry in much the same manner as the substitutions we pre...