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Pseudomonas brassicacearum Strain DF41 Kills Caenorhabditis elegans through Biofilm-Dependent and Biofilm-Independent Mechanisms

机译:Pseudomonas Brassicacearum菌株DF41通过依赖生物膜依赖和生物膜独立机制杀死Caenorhabditis elegiss

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Pseudomonas brassicacearum DF41 is a biocontrol agent that suppresses disease caused by the fungal pathogen Sclerotinia sclerotiorum . A number of exometabolites are produced by DF41, including the lipopeptide sclerosin, hydrogen cyanide (HCN), and degradative enzymes. The production of these compounds is controlled at both the transcriptional and posttranscriptional levels by quorum sensing (QS) and the Gac two-component regulatory system. In order to be successful, a biocontrol agent must persist in the environment at levels sufficient for pathogen control. Bacterivorous predators, including nematodes, represent a challenge to the establishment of introduced microorganisms. In the current study, DF41 was investigated for its ability to resist predation by Caenorhabditis elegans . We discovered that this bacterium is capable of killing C. elegans through two different mechanisms: the first involves exposure to toxic metabolites, and the second entails biofilm formation on the nematode head blocking the buccal cavity. Biofilm formation on nematodes, which has been reported only for Yersinia spp. and Xenorhabdus nematophila , is dependent upon the Gac system. Biofilms were not observed when bacteria were grown on NaCl-containing medium or on C. elegans biofilm-resistant mutants. Coculturing with nematodes led to the increased expression of the pdfRI-rfiA QS genes and hcnA , which is under QS control. HCN was the most nematicidal of the exometabolites, suggesting that this bacterium can respond to predator cues and upregulate expression of toxins accordingly. In , DF41 is able to respond to the presence of C. elegans , and through two distinct mechanisms, it can escape predation.IMPORTANCE Pseudomonas brassicacearum DF41 can suppress fungal pathogens through a process known as biocontrol. To be successful, a biocontrol agent must be able to persist in the environment at levels sufficient for pathogen control. Predators, including the nematode Caenorhabditis elegans , represent a threat to persistence. The aim of the current study was to investigate the DF41- C. elegans interaction. We discovered that DF41 is able to escape predation through two distinct mechanisms. The first involves exposure to toxic bacterial metabolites, and the second entails the formation of a sticky coating on the nematode head, called a biofilm, which blocks feeding and causes starvation. We report here a pseudomonad forming biofilms on the C. elegans surface. When grown with C. elegans , DF41 exhibits altered gene expression and metabolite production, indicating that this bacterium can sense the presence of these predators and adjust its physiology accordingly.
机译:Pseudomonas Brassicacearum DF41是一种抑制由真菌病原体Sclerotinia Sclerotiorum造成的疾病的生物抑制剂。 DF41产生了许多exometabolites,包括脂肽硬质素,氰化氢(HCN)和降解酶。通过仲裁感测(QS)和GAC双组分调节系统,在转录和后幕前水平中控制这些化合物的生产。为了成功,生物防治剂必须在足以进行病原体控制的水平的环境中持续存在。包括线虫在内的噬菌体捕食者代表了建立引入的微生物的挑战。在目前的研究中,研究了DF41,以抵御Caenorhabdise秀丽隐杆线虫的抗蚀性能力。我们发现这种细菌能够通过两种不同的机制杀死C.杆状杆菌:第一个涉及暴露于有毒代谢物,第二种涉及暴露于线虫头部的生物膜形成阻挡颊腔。对线虫的生物膜形成,仅针对Yersinia SPP报告。和Xenorhabdus nematophila取决于GAC系统。当细菌生长在含NaCl的培养基中或秀丽光圈生物膜抗突变体上时,未观察到生物膜。与线虫的共蜂化导致pdfri-rfia Qs基因和HCNA的表达增加,这是QS控制的。 HCN是exometabolites最象征的,这表明这种细菌可以对捕食者提示响应并相应地上调毒素的表达。在,DF41能够响应C.杆杆线虫的存在,并通过两个不同的机制,它可以逃避捕食。分析Pseudomonas Brassicacearum DF41可以通过称为生物控制的过程来抑制真菌病原体。为了成功,生物控制剂必须能够在足以进行病原体控制的水平的环境中持续存在。捕食者,包括线虫Caenorhabditis的秀丽隐塞,代表了持久性的威胁。目前研究的目的是调查DF41-C. Elegans互动。我们发现DF41能够通过两个独特的机制来逃避捕食。第一种涉及暴露于有毒的细菌代谢物,第二个涉及形成粘性涂层的粘性涂层,称为生物膜,嵌入饲喂并导致饥饿。我们在此报道了一种在C.杆状杆菌表面上形成生物膜的假单胞菌。当用C. Elegans生长时,DF41表现出改变的基因表达和代谢物生产,表明该细菌可以感测这些捕食者的存在并相应地调节其生理学。

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