Quorum quenching strategies of endophytic Bacillus thuringiensis KMCL07 against soft rot pathogen Pectobacterium carotovorum subsp. carotovorum

IF 3.5 3区 医学 Q3 IMMUNOLOGY Microbial pathogenesis Pub Date : 2025-03-01 Epub Date: 2025-02-05 DOI:10.1016/j.micpath.2025.107356
Kanmani Anandan, Ravishankar Rai Vittal
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Abstract

Phytopathogens are global threats to agriculture, causing substantial economic losses and decreased crop productivity. Developing a control strategy without emerging resistance or creating environmental and health hazards is necessary. The majority of potential pathogens of crops are gram-negative and they communicate through Acyl homoserine lactones (AHLs)-mediated quorum sensing (QS) systems to establish their pathogenicity. By synthesizing small signal molecules, they collectively respond, regulate the expression of virulence factors, biofilm development, secondary metabolite production, and interactions with the host and other microbes in a population-density-dependent manner. Targeting QS mechanisms has been put forward as an attractive approach for conventional infection control.
The quorum quenching endophytic Bacillus thuringiensis strain KMCL07 cell free lysate (CFL) was used to attenuate the virulence of the soft-rot Pectobacterium carotovorum subsp. carotovorum (Pcc) by targeting its QS system. The CFL inhibition ability of Pcc on the AHL signal molecules were tested using a biosensor strain (Chromobacterium subtsugae), which showed a significant (p < 0.001) reduction in the production of AHL signalling molecules without inhibiting Pcc growth. Pcc pathogenicity is related to the expression of various virulence traits like the secretion of extracellular enzymes, motility, and biofilm. The test results showed a significant degree (p < 0.0001) of inhibition in the production of virulence-causing extracellular enzymes (Pel, Cel, and Prt) when Pcc was treated with CFL. Soft rot in-vitro assays revealed that CFL, irrespective of different families, showed a significant level (p ≤ 0.0001) of reduction in disease severity and effectively reduced tissue maceration under different temperature ranges (25°, 30°, and 40 °C). LC-MS analysis confirmed the hydrolytic degradation of QS signalling molecules (3-oxo-C6-HSL and 3-oxo-C8-HSL) by CFL indicating the presence of lactonase enzyme activity. These results suggest that CFL can degrade a wide range of AHL molecules, and control soft rot in a wide variety of hosts and temperatures without affecting the host. Applying cell free lysates (CFLs) from endophytic bacteria to control soft rot pathogens can be an environmentally friendly way to improve plant health. CFLs protect plants by preventing the establishment of pathogenic organisms.
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苏云金芽孢杆菌KMCL07对软腐病病原菌胡萝卜乳杆菌的群体猝灭策略。carotovorum
植物病原体是对农业的全球性威胁,造成重大经济损失并降低作物生产力。必须制定一项不产生抗药性或不造成环境和健康危害的控制战略。作物潜在病原菌多数为革兰氏阴性,它们通过酰基高丝氨酸内酯(AHLs)介导的群体感应(QS)系统进行交流,从而确定其致病性。它们通过合成小信号分子,以种群密度依赖的方式共同响应、调节毒力因子的表达、生物膜的发育、次生代谢物的产生以及与宿主和其他微生物的相互作用。靶向QS机制已被提出作为传统感染控制的一种有吸引力的途径。采用群体猝灭内生苏云金芽孢杆菌(Bacillus thuringiensis)菌株KMCL07细胞游离裂解物(cell free lysate, CFL)对软腐菌cartovorum subsp的毒力进行了减毒试验。通过对其QS系统进行定位。利用生物传感器菌株(subtsugae Chromobacterium)检测了Pcc对AHL信号分子的CFL抑制能力,结果表明(p <;0.001)在不抑制Pcc生长的情况下,AHL信号分子的产生减少。Pcc的致病性与多种毒力性状的表达有关,如胞外酶的分泌、运动性和生物膜。测试结果显示显著程度(p <;0.0001),当Pcc用CFL处理时,对致毒细胞外酶(Pel、Cel和Prt)的产生有抑制作用。软腐病体外试验显示,CFL在不同温度范围(25°,30°和40°C)下,无论不同家族,都能显著降低疾病严重程度(p≤0.0001),并有效降低组织浸渍。LC-MS分析证实了CFL对QS信号分子(3-oxo-C6-HSL和3-oxo-C8-HSL)的水解降解,表明存在内酯酶活性。这些结果表明,CFL可以降解多种AHL分子,并在多种寄主和温度下控制软腐病,而不影响寄主。利用内生细菌的游离细胞裂解物(cfl)控制软腐病病原体是一种环保的改善植物健康的方法。节能灯通过防止致病菌的形成来保护植物。
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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