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暴露于细菌素Lcn972后选择的突变激活了中的一个类似Bce的杆菌肽抗性模块。

Mutations Selected After Exposure to Bacteriocin Lcn972 Activate a Bce-Like Bacitracin Resistance Module in .

作者信息

Campelo Ana Belén, López-González María Jesús, Escobedo Susana, Janzen Thomas, Neves Ana Rute, Rodríguez Ana, Martínez Beatriz

机构信息

DairySafe group, Department of Technology and Biotechnology of Dairy Products, Instituto de Productos Lácteos de Asturias (IPLA), Consejo Superior de Investigaciones Científicas (CSIC), Villaviciosa, Spain.

Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

出版信息

Front Microbiol. 2020 Aug 13;11:1805. doi: 10.3389/fmicb.2020.01805. eCollection 2020.

Abstract

Resistance against antimicrobial peptides (AMPs) is often mediated by detoxification modules that rely on sensing the AMP through a BceAB-like ATP-binding cassette (ABC) transporter that subsequently activates a cognate two-component system (TCS) to mount the cell response. Here, the ABC transporter YsaDCB is shown to constitute, together with TCS-G, a detoxification module that protects against bacitracin and the bacteriocin Lcn972, both AMPs that inhibit cell wall biosynthesis. Initially, increased expression of was detected by RT-qPCR in three resistant to Lcn972, two of which were also resistant to bacitracin. These mutants shared, among others, single-point mutations in coding for the putative Bce-like permease. These results led us to investigate the function of YsaDCB ABC-transporter and study the impact of these mutations. Expression of in NZ9000, a strain that lacks a functional detoxification module, enhanced resistance to both AMPs, demonstrating its role as a resistance factor in . When the three different alleles from the mutants were expressed, all of them outperformed the wild-type transporter in resistance against Lcn972 but not against bacitracin, suggesting a distinct mode of protection against each AMP. Moreover, P promoter fusions, designed to measure the activation of the detoxification module, revealed that the mutations unlock transcriptional control by TCS-G, resulting in constitutive expression of the operon. Finally, deletion of was also performed to get an insight into the function of this gene. encodes a secreted peptide and is part of the operon. YsaD appears to modulate signal relay between the ABC transporter and TCS-G, based on the different response of the P promoter fusions when it is not present. Altogether, the results underscore the unique features of this lactococcal detoxification module that warrant further research to advance in our overall understanding of these important resistance factors in bacteria.

摘要

对抗菌肽(AMPs)的抗性通常由解毒模块介导,这些模块依赖于通过类似BceAB的ATP结合盒(ABC)转运蛋白感知AMP,随后激活同源双组分系统(TCS)以引发细胞反应。在此,ABC转运蛋白YsaDCB与TCS-G一起构成一个解毒模块,可抵御杆菌肽和细菌素Lcn972,这两种AMPs均抑制细胞壁生物合成。最初,通过RT-qPCR在三株对Lcn972耐药的菌株中检测到YsaDCB表达增加,其中两株也对杆菌肽耐药。这些突变体除其他外,在编码假定的Bce样通透酶的YsaD中存在单点突变。这些结果促使我们研究YsaDCB ABC转运蛋白的功能,并研究这些突变的影响。在缺乏功能性解毒模块的NZ9000菌株中表达YsaDCB可增强对两种AMPs的抗性,证明其作为乳酸乳球菌中抗性因子的作用。当表达来自突变体的三种不同YsaD等位基因时,它们在对Lcn972的抗性方面均优于野生型转运蛋白,但对杆菌肽则不然,这表明对每种AMP的保护模式不同。此外,旨在测量解毒模块激活的P YsaDCB启动子融合显示,YsaD突变解除了TCS-G的转录控制,导致YsaDCB操纵子的组成型表达。最后,还进行了YsaD的缺失以深入了解该基因的功能。YsaD编码一种分泌肽,是YsaDCB操纵子的一部分。基于P YsaDCB启动子融合在不存在YsaD时的不同反应,YsaD似乎调节ABC转运蛋白和TCS-G之间的信号传递。总之,这些结果强调了这种乳球菌解毒模块的独特特征,值得进一步研究以推进我们对细菌中这些重要抗性因子的全面理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb8b/7438565/0ddcf2dcf5b6/fmicb-11-01805-g001.jpg

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