Department of Animal Science, University of Connecticut, Storrs, CT 06269, USA.
Food Microbiol. 2013 Oct;36(1):79-89. doi: 10.1016/j.fm.2013.04.010. Epub 2013 May 1.
The present study investigated the efficacy of sub-inhibitory concentrations (SICs, concentrations not inhibiting bacterial growth) and bactericidal concentrations (MBCs) of four, generally recognized as safe (GRAS), plant-derived antimicrobials (PDAs) in inhibiting Listeria monocytogenes (LM) biofilm formation and inactivating mature LM biofilms, at 37, 25 and 4 °C on polystyrene plates and stainless-steel coupons. In addition, the effect of SICs of PDAs on the expression of LM genes critical for biofilm synthesis was determined by real-time quantitative PCR. The PDAs and their SICs used for inhibition of biofilm were trans-cinnamaldehyde (TC 0.50, 0.75 mM), carvacrol (CR 0.50, 0.65 mM), thymol (TY 0.33, 0.50 mM), and eugenol (EG 1.8, 2.5 mM), whereas the PDA concentrations used for inactivating mature biofilms were 5.0 and 10.0 mM (TC, CR), 3.3 and 5.0 mM (TY), 18.5 and 25.0 mM (EG). All PDAs inhibited biofilm synthesis and inactivated fully formed LM biofilms on both matrices at three temperatures tested (P < 0.05). Real-time quantitative PCR data revealed that all PDAs down-regulated critical LM biofilm-associated genes (P < 0.05). Results suggest that TC, CR, TY, and EG could potentially be used to control LM biofilms in food processing environments, although further studies under commercial settings are necessary.
本研究调查了四种通常被认为是安全的(GRAS)植物源抗菌剂(PDAs)的亚抑菌浓度(SICs,不抑制细菌生长的浓度)和杀菌浓度(MBCs)在抑制李斯特菌(LM)生物膜形成和在聚苯乙烯板和不锈钢试片上 37、25 和 4°C 下失活成熟 LM 生物膜的效果。此外,通过实时定量 PCR 确定了 PDAs 的 SICs 对生物膜合成关键 LM 基因表达的影响。用于抑制生物膜的 PDAs 及其 SICs 为反式肉桂醛(TC 0.50、0.75 mM)、香芹酚(CR 0.50、0.65 mM)、麝香草酚(TY 0.33、0.50 mM)和丁香酚(EG 1.8、2.5 mM),而用于失活成熟生物膜的 PDA 浓度为 5.0 和 10.0 mM(TC、CR)、3.3 和 5.0 mM(TY)、18.5 和 25.0 mM(EG)。所有 PDAs 均在三种测试温度下抑制生物膜合成并失活两种基质上完全形成的 LM 生物膜(P<0.05)。实时定量 PCR 数据显示,所有 PDAs 均下调了关键的 LM 生物膜相关基因(P<0.05)。结果表明,TC、CR、TY 和 EG 可能有潜力用于控制食品加工环境中的 LM 生物膜,尽管需要在商业环境下进行进一步研究。