The inhibition effects and mechanisms of sulfated chitooligosaccharides on influenza A virus in vitro and in vivo

Abstract

Sulfated chitooligosaccharide was reported to possess inhibition effect on human immunodeficiency virus (HIV) entry into host cells. Herein, we prepared chitooligosaccharide COS and its sulfate derivative SCOS and explored whether the sulfation modification can enhance the anti-influenza A virus (IAV) activity of COS. Interestingly, we discovered that SCOS possessed broad-spectrum anti-IAV effects with low toxicity, while the non-sulfated chitooligosaccharide COS had very low inhibition on IAV, verifying that the sulfation modification is essential for the anti-IAV actions of chitooligosaccharide. SCOS may target virus hemagglutinin (HA) protein to block both virus adsorption and membrane fusion processes. Oral administration of SCOS significantly decreased pulmonary viral titers and improved survival rate in IAV infected mice, comparable to the effects of Oseltamivir. Therefore, our findings support further studies on the use of SCOS as a novel entry inhibitor for IAV and as a supplement to current therapeutics for influenza.

Keywords: 3′-SL (CID: 123914); Acetone (CID: 180); Adsorption; Dimethylformamide (CID: 6228); Eosin (CID: 11048); Glutaraldehyde (CID: 3485); HA protein; Hematoxylin (CID: 442514); Influenza A virus; MUNANA (CID: 122174046); Membrane fusion; Oseltamivir (CID: 65028); Paraformaldehyde (CID: 712); Sulfated chitooligosaccharide; l-Glutamine (CID: 5961).