scholarly journals Antiviral activity of diallyl trisulfide against H9N2 avian influenza virus infection in vitro and in vivo

2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Le Ming ◽  
Zhihui Li ◽  
Xiaofang Li ◽  
Ling Tang ◽  
Guimei He

Abstract Background Diallyl trisulfide (DATS) is a garlic-derived organosulfur compound. As it has been shown to have anti-viral activity, we hypothesized that it may alleviate infections caused by H9N2 avian influenza virus (AIV), which is prevalent in poultry with pandemic potential. Methods Human lung A549 epithelial cells were treated with three different concentrations of DATS 24 h before (pre-treatment) or one hour after (post-treatment) H9N2 AIV infection. Culture supernatants were collected 24 h and 48 h post-infection and analyzed for viral titers and levels of inflammatory and anti-viral immune responses. For in vivo experiments, BABL/c mice were administered daily by intraperitoneal injection with DATS (30 mg/kg) for 2 weeks starting 1 day after H9N2 AIV infection. Clinical signs, lung pathology, and inflammatory and anti-viral immune responses were assessed 2, 4, and 6 days after infection. Results Both pre-treatment and post-treatment of A549 cells with DATS resulted in reduced viral loads, increased expression of anti-viral genes (RIG-I, IRF-3, and interferon-β), and decreased expression of inflammatory cytokines (TNF-α and IL-6). These effects were also observed in H9N2 AIV-infected mice treated with DATS. Such treatment also reduced lung edema and inflammation in mice. Conclusions Results suggest that DATS has anti-viral activity against H9N2 AIV and may be used as an alternative treatment for influenza virus infection.

2021 ◽  
Author(s):  
Le Ming ◽  
Zhihui Li ◽  
Xiaofang Li ◽  
Ling Tang ◽  
Guimei He

Abstract BackgroundDiallyl trisulfide is a component of garlic. It has been shown to have anti-fungus, anti-cancer, and anti-virus activities. We hypothesized that diallyl trisulfide can enhance host defense mechanisms against the infection by influenza virus A subtype H9N2, which is the most prevalent subtype of influenza viruses in poultry in many countries in Asia.MethodsIn this study, the effects of diallyl trisulfide on influenza virus will be investigated in vivo and in vitro respectively. The expression levels of IL-6, TNF-α, RIG-I, IRF-3, IFN-β, and H9N2 avian influenza virus M gene were detected using Quantitative real-time RT-PCR.ResultsIn vitro, we found that treatment of A549 cells before or after H9N2 virus infection resulted in reduced viral loads, increased expression of antiviral genes (RIG-I, IRF-3 and interferon-β), and decreased expression of inflammatory cytokines (TNF-α and IL-6). These effects were also observed in H9N2 virus infected mice. ConclusionsThese results suggest that diallyl trisulfide inhibits H9N2 virus replication and down regulate the expression of inflammatory cytokines. Also this research indicates that diallyl trisulfide might be a kind of effective drug against influenza virus infection.


2021 ◽  
Author(s):  
Jingyun Li ◽  
Hongyan Wang ◽  
Pengjing Lian ◽  
Yu Bai ◽  
Zihui Zhang ◽  
...  

H9N2 avian influenza virus has been continuously circulating among poultry and could infect mammals, indicating that this virus is a potential pandemic strain. During influenza pandemics, secondary bacterial (particularly pneumococcal) pneumonia usually contributes to excess mortality. In the present study, we observed the dynamic effect of H9N2 virus infection on host defense against secondary pneumococcal infection in mice. BALB/c mice were intranasally inoculated with 1.2 × 105 plaque forming units (PFU) of H9N2 virus followed by 1 × 106 colony forming units of Streptococcus pneumoniae on 7, 14 or 28 days post-H9N2 infection (D.P.I.). The bacterial load, histopathology, body weight and survival were assessed after pneumococcal infection. Our results showed that H9N2 virus infection had no significant impact on host resistance to secondary pneumococcal infection on 7 D.P.I. However, H9N2 virus infection increased pulmonary pneumococcal clearance and reduced pneumococcal pneumonia-induced morbidity after secondary pneumococcal infection on 14 or 28 D.P.I., as reflected by significantly decreased bacterial loads, markedly alleviated pulmonary histopathological changes and significantly reduced weight loss in mice infected with H9N2 virus followed by S. pneumoniae compared with mice infected only with S. pneumoniae. Further, the significantly decreased bacterial loads were observed when mice were previously infected with a higher dose (1.2 × 106 PFU) of H9N2 virus. Besides, similar to the results obtained in BALB/c mice, improvement in pulmonary pneumococcal clearance was also observed in C57BL/6 mice. Overall, our results showed that pulmonary pneumococcal clearance is improved after resolution of H9N2 virus infection in mice.


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