tetano
Editor, Senior Moderator
Antimicrob Agents Chemother
. 2020 Dec 7;AAC.01732-20.
doi: 10.1128/AAC.01732-20. Online ahead of print.
In Vitro Characterization of the Carbohydrate-Binding Agents HHA, GNA and UDA as Inhibitors of Influenza a and B Virus Replication
Evelien Vanderlinden[SUP] 1 [/SUP], Nathalie Van Winkel[SUP] 2 [/SUP], Lieve Naesens[SUP] 2 [/SUP], Els J M Van Damme[SUP] 3 [/SUP], Leentje Persoons[SUP] 2 [/SUP], Dominique Schols[SUP] 2 [/SUP]
Affiliations
Abstract
Here, we report on the anti-influenza virus activity of the mannose-binding agents, Hippeastrum hybrid agglutinin (HHA) and Galanthus nivalis agglutinin (GNA), and the (N-acetylglucosamine)[SUB]n[/SUB]-specific Urtica dioica agglutinin (UDA). These carbohydrate-binding agents (CBA) strongly inhibited various influenza A(H1N1), A(H3N2) and B viruses in vitro, with EC[SUB]50[/SUB] values ranging from 0.016 to 83 nM, generating selectivity indexes up to 125,000. Somewhat less activity was observed against the A/PR/8/34 and an A(H1N1)pdm09 strain. In time-of-addition experiments, these CBA lost their inhibitory activity when added 30 min p.i. Interference with virus entry processes was also evident from strong inhibition of virus-induced hemolysis at low pH. However, a direct effect on acid-induced refolding of the viral hemagglutinin (HA) was excluded by the tryptic digestion assay. Instead, HHA treatment of HA-expressing cells led to a significant reduction of plasma membrane mobility. Crosslinking of membrane glycoproteins, through interaction with HA, could also explain the inhibitory effect on the release of newly formed virions when HHA was added at 6 h p.i. These CBA presumably interact with one or more N-glycans on the globular head of HA, since their absence led to reduced activity against mutant influenza B viruses and HHA-resistant A(H1N1) viruses. The latter condition only emerged after 33 cell culture passages in the continuous presence of HHA, and the A(H3N2) virus even retained full sensitivity after 50 passages. Thus, these CBA qualify as potent inhibitors of influenza A and B viruses in vitro with a pleiotropic mechanism of action and a high barrier for viral resistance.
. 2020 Dec 7;AAC.01732-20.
doi: 10.1128/AAC.01732-20. Online ahead of print.
In Vitro Characterization of the Carbohydrate-Binding Agents HHA, GNA and UDA as Inhibitors of Influenza a and B Virus Replication
Evelien Vanderlinden[SUP] 1 [/SUP], Nathalie Van Winkel[SUP] 2 [/SUP], Lieve Naesens[SUP] 2 [/SUP], Els J M Van Damme[SUP] 3 [/SUP], Leentje Persoons[SUP] 2 [/SUP], Dominique Schols[SUP] 2 [/SUP]
Affiliations
- PMID: 33288640
- DOI: 10.1128/AAC.01732-20
Abstract
Here, we report on the anti-influenza virus activity of the mannose-binding agents, Hippeastrum hybrid agglutinin (HHA) and Galanthus nivalis agglutinin (GNA), and the (N-acetylglucosamine)[SUB]n[/SUB]-specific Urtica dioica agglutinin (UDA). These carbohydrate-binding agents (CBA) strongly inhibited various influenza A(H1N1), A(H3N2) and B viruses in vitro, with EC[SUB]50[/SUB] values ranging from 0.016 to 83 nM, generating selectivity indexes up to 125,000. Somewhat less activity was observed against the A/PR/8/34 and an A(H1N1)pdm09 strain. In time-of-addition experiments, these CBA lost their inhibitory activity when added 30 min p.i. Interference with virus entry processes was also evident from strong inhibition of virus-induced hemolysis at low pH. However, a direct effect on acid-induced refolding of the viral hemagglutinin (HA) was excluded by the tryptic digestion assay. Instead, HHA treatment of HA-expressing cells led to a significant reduction of plasma membrane mobility. Crosslinking of membrane glycoproteins, through interaction with HA, could also explain the inhibitory effect on the release of newly formed virions when HHA was added at 6 h p.i. These CBA presumably interact with one or more N-glycans on the globular head of HA, since their absence led to reduced activity against mutant influenza B viruses and HHA-resistant A(H1N1) viruses. The latter condition only emerged after 33 cell culture passages in the continuous presence of HHA, and the A(H3N2) virus even retained full sensitivity after 50 passages. Thus, these CBA qualify as potent inhibitors of influenza A and B viruses in vitro with a pleiotropic mechanism of action and a high barrier for viral resistance.