Flos populi (Male Inflorescence of Populus tomentosa Carrière) Aqueous Extract Suppresses Salmonella Pullorum Infection by Affecting T3SS-1.
Wenting ZhangGuixing LiangZhengyu ChengYunqing GuoBoda JiangTingjiang LiuWeidong LiaoQin LuGuoyuan WenTengfei ZhangQingping LuoPublished in: Pathogens (Basel, Switzerland) (2023)
Pullorum disease, caused by Salmonella Pullorum ( S . Pullorum), is one of the most serious infectious diseases in the poultry industry. Flos populi is traditionally used in Eastern Asian countries to treat various intestinal diseases. However, the anti-infection mechanism of Flos populi is not very clear. In this study, we evaluated the anti-infective effects on S. Pullorum of Flos populi aqueous extract (FPAE) in chickens. FPAE significantly reduced S. Pullorum growth in vitro. At the cellular level, FPAE reduced S. Pullorum adhesion and invasion on DF-1 cells but did not affect its intracellular survival or replication in macrophages. Further investigation revealed that FPAE inhibited the transcription of T3SS-1 genes, which is the main virulence factor that mediates S. Pullorum adhesion and invasion in host cells. The results suggest that the anti-infective effect of FPAE likely occurs through the inhibition of S. Pullorum T3SS-1, thereby impairing its ability to adhere to and invade cells. Further, we evaluated its therapeutic effect on animal models (Jianghan domestic chickens) and found that FPAE reduced the bacterial loads in organs and decreased the mortality and weight loss of infected chickens. Our findings provide novel insights into the potential development of FPAE against S. Pullorum as an effective anti-virulence therapeutic substitute for antibiotics.
Keyphrases
- induced apoptosis
- escherichia coli
- cell cycle arrest
- weight loss
- biofilm formation
- pseudomonas aeruginosa
- oxidative stress
- staphylococcus aureus
- cell migration
- endoplasmic reticulum stress
- antimicrobial resistance
- bariatric surgery
- type diabetes
- cell proliferation
- south africa
- gene expression
- cell death
- ionic liquid
- cardiovascular events
- single cell
- cystic fibrosis
- pi k akt
- glycemic control