Anti-quorum sensing and antibacterial activities of Satureja sahendica hydroalcoholic extract against avian isolate of Salmonella Typhimurium

Q4 Veterinary
Razieh Sharchi, J. Shayegh, S. Hosseinzadeh
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引用次数: 1

Abstract

Quorum sensing (QS) is a cell density dependent mechanism used by many pathogenic bacteria for regulating virulence gene expression. Inhibition or interruption of QS by herbal remedies has been suggested as a new strategy for fighting against antibiotic resistant bacteria. The aim of this study was to evaluate the antibacterial activity of Satureja sahendica hydroalcoholic extract (SSHE) against Salmonella Typhimurium (S. Typhimurium) isolates, and to assess the impact of sub-inhibitory concentrations of this extract on the QS-associated gene (sdiA) expression. Using the Soxhlet method, hydroalcoholic extract of S. sahendica leaves was prepared and antimicrobial effects of the SSHE were determined by minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methodS. The reverse transcription quantitative PCR (RT-qPCR) assay was used to analyze the expression of sdiA in 20 S. Typhimurium isolates from poultry flocks in response to the treatment of sub-inhibitory concentrations of SSHE at 60-min time point. The MIC values of SSHE against S. Typhimurium isolates were ranged from 0.29-4.68 mg/ml-1 and MBC values were ranging from 75-150 mg/ml-1. The results also indicated that the expression of sdiA gene was reduced in S. Typhimurium isolates triggered by the treatment of SSHE comparatively with those from the control cultureS. Findings suggest that SSHE possess the antibacterial and anti-QS activity and can be used to control the expression of virulence genes in pathogenic bacteria, such as S. Typhimurium.
红花水醇提取物对鼠伤寒沙门菌禽分离物的抗群体感应及抑菌活性
群体感应(QS)是许多病原菌用来调节毒力基因表达的一种细胞密度依赖性机制。草药抑制或阻断QS已被认为是对抗抗生素耐药性细菌的一种新策略。本研究的目的是评估沙参水醇提取物(SSHE)对鼠伤寒沙门氏菌(S.Typhimurium)分离株的抗菌活性,并评估该提取物的亚抑制浓度对QS相关基因(sdiA)表达的影响。采用Soxhlet法,制备了沙参叶的水醇提取物,并用最小抑菌浓度(MIC)和最小杀菌浓度(MBC)法测定了SSHE的抗菌效果。使用逆转录定量PCR(RT-qPCR)分析来自家禽群的20个鼠伤寒沙门氏菌分离株中sdiA的表达,以响应在60分钟时间点亚抑制浓度的SSHE的处理。SSHE对鼠伤寒沙门氏菌分离株的MIC值范围为0.29-4.68 mg/ml-1,MBC值范围为75-150 mg/ml-1。结果还表明,与对照培养物相比,由SSHE处理引发的鼠伤寒沙门氏菌分离物中sdiA基因的表达降低。研究结果表明,SSHE具有抗菌和抗QS活性,可用于控制致病菌(如鼠伤寒杆菌)毒力基因的表达。
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CiteScore
0.40
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30 weeks
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