肉桂醛
抗菌剂
大肠杆菌
微生物学
致病性大肠杆菌
最小抑制浓度
殖民地化
细菌
最低杀菌浓度
生物
化学
生物化学
基因
遗传学
催化作用
作者
Wellison Amorim Pereira,Carlos Drielson S. Pereira,Raissa Guará Assunção,Iandeyara Savanna carneiro da Silva,Fabrícia S. Rego,Leylane S. R. Alves,Juliana Santos,Francisco Jonathas Rodrigues Nogueira,Adrielle Zagmignan,Thomas T. Thomsen,Anders Løbner‐Olesen,Karen A. Krogfelt,Luís Cláudio Nascimento da Silva,Afonso Gomes Abreu
出处
期刊:Biomolecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-02-18
卷期号:11 (2): 302-302
被引量:52
摘要
Escherichia coli is responsible for cases of diarrhea around the world, and some studies have shown the benefits of cinnamaldehyde in the treatment of bacterial disease. Therefore, the objective of this study was to evaluate the effects of cinnamaldehyde in mice colonized by pathogenic E. coli, as well as to provide more insights into its antimicrobial action mechanism. After determination of minimum inhibitory (MIC) and minimum bactericidal (MBC) concentrations, the interference of cinnamaldehyde in macromolecular pathways (synthesis of DNA, RNA, protein, and cell wall) was measured by incorporation of radioisotopes. The anti-adhesive properties of cinnamaldehyde towards E. coli 042 were evaluated using human epithelial type 2 (HEp-2) cells. Intestinal colonization was tested on mice, and the effect of cinnamaldehyde on Tenebrio molitor larvae. Cinnamaldehyde showed MIC and MBC values of 780 μg/mL and 1560 μg/mL, respectively; reduced the adhesion of E. coli 042 on HEp-2 cells; and affected all the synthetic pathways evaluated, suggesting that compost impairs the membrane/cell wall structure leading bacteria to total collapse. No effect on the expression of genes related to the SOS pathway (sulA and dinB1) was observed. The compound did not interfere with cell viability and was not toxic against T. molitor larvae. In addition, cinnamaldehyde-treated mice exhibited lower levels of colonization by E. coli 042 than the untreated group. Therefore, the results show that cinnamaldehyde is effective in treating the pathogenic E. coli strain 042 and confirm it as a promising lead molecule for the development of antimicrobial agents.
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