tetano
Editor, Senior Moderator
J Virol. 2017 Apr 26. pii: JVI.00624-17. doi: 10.1128/JVI.00624-17. [Epub ahead of print]
[h=1]Salivary blockade protects the lower respiratory tract of mice from lethal influenza.[/h] Ivinson K[SUP]1[/SUP], Deliyannis G[SUP]1[/SUP], McNabb L[SUP]1[/SUP], Grollo L[SUP]1[/SUP], Gilbertson B[SUP]1[/SUP], Jackson D[SUP]1[/SUP], Brown LE[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] It is possible to model progression of influenza virus from the upper respiratory tract to the lower respiratory tract in the mouse using viral inoculum delivered in a restricted manner to the nose. In this model, infection with the A/Udorn/307/72 (Udorn) strain of virus results ultimately in high viral titres in both the trachea and lungs. In contrast, the A/Puerto Rico/8/34 (PR8) strain causes an infection that is almost entirely limited to the nasal passages. The factors that govern the progression of virus down the respiratory tract are not well understood. Here we show that, while PR8 virus grows to high titres in the nose, an inhibitor present in the saliva, blocks further progression of infection to the trachea and lungs, and renders an otherwise lethal dose of virus completely asymptomatic. In vitro, the salivary inhibitor was capable of potent neutralisation of PR8 virus and an additional twenty strains of Type A virus and two Type B strains that were tested. Exceptions were Udorn virus and the closely related H3N2 strains A/Port Chalmers/1/73 and A/Victoria/3/75. Characterisation of the salivary inhibitor showed it to be independent of sialic acid and other carbohydrates for its function. This and other biochemical properties, together with its virus-strain specificity and in vivo function indicate that the mouse salivary inhibitor is a previously undescribed innate inhibitory molecule that may have evolved to provide pulmonary protection of this species from fatal influenza infection.IMPORTANCE Influenza A virus occasionally jumps from aquatic birds, its natural host, into mammals to cause outbreaks of varying severity, including pandemics in humans. Despite the laboratory mouse being used as a model to study influenza pathogenesis, natural outbreaks of influenza have not been reported in this species. Here we shed light on one mechanism that might allow mice to be protected from influenza in the wild. We show that virus deposited in the mouse upper-respiratory tract will not progress to the lower-respiratory tract due to the presence of a potent inhibitor of the virus in saliva. Containing inhibitor-sensitive virus to the upper-respiratory tract renders an otherwise lethal infection subclinical. This knowledge sheds light on how natural inhibitors may have evolved to improve survival in this species.
Copyright ? 2017 American Society for Microbiology.
PMID: 28446669 DOI: 10.1128/JVI.00624-17
[h=1]Salivary blockade protects the lower respiratory tract of mice from lethal influenza.[/h] Ivinson K[SUP]1[/SUP], Deliyannis G[SUP]1[/SUP], McNabb L[SUP]1[/SUP], Grollo L[SUP]1[/SUP], Gilbertson B[SUP]1[/SUP], Jackson D[SUP]1[/SUP], Brown LE[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] It is possible to model progression of influenza virus from the upper respiratory tract to the lower respiratory tract in the mouse using viral inoculum delivered in a restricted manner to the nose. In this model, infection with the A/Udorn/307/72 (Udorn) strain of virus results ultimately in high viral titres in both the trachea and lungs. In contrast, the A/Puerto Rico/8/34 (PR8) strain causes an infection that is almost entirely limited to the nasal passages. The factors that govern the progression of virus down the respiratory tract are not well understood. Here we show that, while PR8 virus grows to high titres in the nose, an inhibitor present in the saliva, blocks further progression of infection to the trachea and lungs, and renders an otherwise lethal dose of virus completely asymptomatic. In vitro, the salivary inhibitor was capable of potent neutralisation of PR8 virus and an additional twenty strains of Type A virus and two Type B strains that were tested. Exceptions were Udorn virus and the closely related H3N2 strains A/Port Chalmers/1/73 and A/Victoria/3/75. Characterisation of the salivary inhibitor showed it to be independent of sialic acid and other carbohydrates for its function. This and other biochemical properties, together with its virus-strain specificity and in vivo function indicate that the mouse salivary inhibitor is a previously undescribed innate inhibitory molecule that may have evolved to provide pulmonary protection of this species from fatal influenza infection.IMPORTANCE Influenza A virus occasionally jumps from aquatic birds, its natural host, into mammals to cause outbreaks of varying severity, including pandemics in humans. Despite the laboratory mouse being used as a model to study influenza pathogenesis, natural outbreaks of influenza have not been reported in this species. Here we shed light on one mechanism that might allow mice to be protected from influenza in the wild. We show that virus deposited in the mouse upper-respiratory tract will not progress to the lower-respiratory tract due to the presence of a potent inhibitor of the virus in saliva. Containing inhibitor-sensitive virus to the upper-respiratory tract renders an otherwise lethal infection subclinical. This knowledge sheds light on how natural inhibitors may have evolved to improve survival in this species.
Copyright ? 2017 American Society for Microbiology.
PMID: 28446669 DOI: 10.1128/JVI.00624-17