Bactericidal effect of AgNPs in vitro. (A) Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) of AgNPs and originated derivative AgNO3. (B) Agar well diffusion assay for bacterial inhibition. (C) Long‐term bacterial inhibition and bactericidal efficacy of the AgNPs. The antibacterial effect of the AgNPs against S. aureus and S. Typhimurium under five different preservation conditions (aerobic at 37°C, aerobic at 4°C, aerobic at room temperature, aerobic at −20°C, and anaerobic at room temperature) at different time intervals (0, 0.25, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12 months). (D) Visualization of AgNPs and AgNO3‐treated S. Typhimurium at 8 and 24 h using transmission electron microscopy analysis. The absence of AgNPs or AgNO3 was used as a control. Scale bars: 200 nm. (E) Contents of lactate dehydrogenase (LDH) and the efflux (protein and sugar) of bacterial contents after exposure to AgNPs and AgNO3. (F) ATPase activities after exposure to AgNPs and AgNO3. (G) Bacterial antioxidant enzyme activities after exposure to AgNPs and AgNO3, including glutathione peroxidase (GPX) and catalase (CAT). Red: bacteria treated with AgNPs. Gray: bacteria treated with AgNO3. Gray with points: control. Data were from at least three independent assays: *p < 0.05; **p < 0.01; ***p < 0.001. Sa, Staphylococcus aureus; Lm: Listeria monocytogenes; Es, Enterococcus faecalis; Em, Enterococcus faecium; ST, S. Typhimurium; Ec, Escherichia coli; Kp, Klebsiella pneumoniae; Ye, Yersinia enterocolitica. S. aureus, L. monocytogenes, E. faecalis, and E. faecium are Gam‐positive (G+) bacteria. S. Typhimurium, E. coli, K. pneumoniae, and Y. enterocolitica are Gram‐negative (G–) bacteria.