Wang Li-Wa, Zhang Sha, Wang Lin-Yang, Gong Hai-Yan, Tian Shu-Ge
College of Traditional Chinese Medicine, Xinjiang Medical University, Urumqi 830017, China.
The Fifth Affiliated Hospital of Xinjiang Medical University, Urumqi 830011, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2023 May;54(3):539-544. doi: 10.12182/20230560211.
To examine the inhibitory effect of flower extracts from Schang (SFE) on ( ).
The inhibitory effect of SFE on planktonic and the effect of SFE on the growth process of planktonic were determined by the agar drilling method and the microdilution method. Crystal violet staining and MTT reduction assay were conducted to determine the effect of SFE on biofilm formation. The effect of SFE on the production of exopolysaccharides (EPS) in biofilm was determined by anthrone-sulfuric acid method. The intracellular lactate dehydrogenase (LDH) activity in was determined by LDH colorimetric assay. The effects of SFE on the acid-producing capacity of was determined by pH meter.
The minimum inhibitory concentration (MIC) of SFE against was 14 μg/μL. SFE of the the concentration between 1/8 MIC and MIC could inhibit the growth rate of within 30 h and it could significantly inhibit the LDH activity compared with the control group ( <0.0001). SFE of the concentration between 4 MIC and 1/4 MIC had an inhibitory effect on the acid production of ( <0.001). Moreover, it could effectively restrain the formation of biofilm and significantly reduce the amount of EPS produced by biofilm ( <0.01).
SFE can effectively inhibit the activity of and its biofilm. The mechanism of inhibiting by SFE was preliminarily discussed as follows, it interferes with microbial adhesion and aggregation by reducing the production of bacterial EPS, thus inhibiting the formation of bacterial biofilms. In addition, it interferes with glycolysis of by reducing the LDH activity of bacteria, thus inhibiting the acid production of .
研究尚氏花提取物(SFE)对( )的抑制作用。
采用琼脂打孔法和微量稀释法测定SFE对浮游菌的抑制作用以及对浮游菌生长过程的影响。通过结晶紫染色和MTT还原试验测定SFE对生物膜形成的影响。采用蒽酮 - 硫酸法测定SFE对生物膜中胞外多糖(EPS)产生的影响。通过LDH比色法测定细菌内乳酸脱氢酶(LDH)活性。用pH计测定SFE对细菌产酸能力的影响。
SFE对该菌的最低抑菌浓度(MIC)为14μg/μL。浓度在1/8 MIC至MIC之间的SFE可在30小时内抑制该菌的生长速率,且与对照组相比能显著抑制LDH活性(<0.0001)。浓度在4 MIC至1/4 MIC之间的SFE对该菌的产酸有抑制作用(<0.001)。此外,它能有效抑制该菌生物膜的形成,并显著减少生物膜产生的EPS量(<0.01)。
SFE能有效抑制该菌及其生物膜的活性。初步探讨SFE抑制该菌的机制如下,它通过减少细菌EPS的产生干扰微生物的黏附和聚集,从而抑制细菌生物膜的形成。此外,它通过降低细菌的LDH活性干扰该菌的糖酵解,从而抑制该菌的产酸。