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GadR4 通过负调控 gadT2/gadD2 簇介导单核细胞增生李斯特菌 10403S 的耐酸性和致病性。

GadR4 mediates the acid resistance and pathogenicity of Listeria monocytogenes 10403S by negatively regulating the gadT2/gadD2 cluster.

机构信息

College of Animal Science, Yangtze University, No.88, Jingmi Road, Jingzhou, 434025, China; College of Agriculture, Yangtze University, No.88, Jingmi Road, Jingzhou, 434025, China.

College of Animal Science, Yangtze University, No.88, Jingmi Road, Jingzhou, 434025, China.

出版信息

Food Microbiol. 2023 Jun;112:104248. doi: 10.1016/j.fm.2023.104248. Epub 2023 Feb 24.

Abstract

Listeria monocytogenes is an important foodborne pathogen that can survive under acidic conditions. The glutamate decarboxylase (GAD) system is one of the acid resistance systems of L. monocytogenes. It usually comprises two glutamate transporters (GadT1/T2) and three glutamate decarboxylases (GadD1/D2/D3). Among them, gadT2/gadD2 contributes most significantly to the acid resistance of L. monocytogenes. However, the regulation mechanisms of gadT2/gadD2 still remain unclear. The results of this study indicated that gadT2/gadD2 deletion significantly decreases the survival rate of L. monocytogenes under different acidic conditions, including brain and heart infusion (BHI) broth, with a pH of 2.5, 2% citric acid, 2% acetic acid and 2% lactic acid. Further, gadT2/gadD2 cluster was expressed in the representative strains in response to alkaline stress rather than acid stress. To explore the regulation of gadT2/gadD2, we knocked out the five transcriptional factors belonging to the Rgg family in L. monocytogenes 10403S. We found that the deletion of gadR4, which exhibits the highest homology with the gadR of Lactococcus lactis, resulted in a significant increase in the survival rate of L. monocytogenes upon acid stress. Western blot analysis showed that gadR4 deletion significantly increased the gadD2 expression of L. monocytogenes under alkaline and neutral conditions. Furthermore, the gfp reporter gene showed that gadR4 deletion significantly increased the expression of the gadT2/gadD2 cluster. Adhesion and invasion assays indicated that gadR4 deletion significantly increased the rates of adhesion and invasion of L. monocytogenes to epithelial Caco-2 cells. Virulence assays showed that gadR4 knockout significantly improved the colonization ability of L. monocytogenes in the livers and spleens of the infected mice. Taken together, our results showed that GadR4, a transcription factor belonging to the Rgg family, negatively regulates the gadT2/gadD2 cluster, thus, reducing the acid stress tolerance and pathogenicity of L. monocytogens 10403S. Our results provide a better understanding of the regulation of the GAD system of L. monocytogenes and a novel approach to potentially prevent and control listeriosis.

摘要

单增李斯特菌是一种重要的食源性病原体,能够在酸性条件下存活。谷氨酸脱羧酶(GAD)系统是单增李斯特菌的一种酸抗性系统。它通常由两个谷氨酸转运体(GadT1/T2)和三个谷氨酸脱羧酶(GadD1/D2/D3)组成。其中,gadT2/gadD2 对单增李斯特菌的酸抗性贡献最大。然而,gadT2/gadD2 的调控机制仍不清楚。本研究结果表明,gadT2/gadD2 缺失显著降低了单增李斯特菌在不同酸性条件下的存活率,包括脑心浸液(BHI)肉汤、pH 值为 2.5、2%柠檬酸、2%乙酸和 2%乳酸。此外,gadT2/gadD2 簇在代表性菌株中响应碱性应激而不是酸性应激表达。为了探索 gadT2/gadD2 的调控机制,我们敲除了单增李斯特菌 10403S 中属于 Rgg 家族的五个转录因子。我们发现,与乳球菌 gadR 同源性最高的 gadR4 的缺失导致单增李斯特菌在酸应激下的存活率显著增加。Western blot 分析表明,gadR4 缺失显著增加了单增李斯特菌在碱性和中性条件下的 gadD2 表达。此外,gfp 报告基因显示 gadR4 缺失显著增加了 gadT2/gadD2 簇的表达。黏附和侵袭实验表明,gadR4 缺失显著增加了单增李斯特菌黏附和侵袭上皮细胞 Caco-2 的比率。毒力实验表明,gadR4 敲除显著提高了单增李斯特菌在感染小鼠肝脏和脾脏中的定植能力。综上所述,我们的结果表明,属于 Rgg 家族的转录因子 GadR4 负调控 gadT2/gadD2 簇,从而降低单增李斯特菌 10403S 的酸应激耐受性和致病性。我们的研究结果为深入了解单增李斯特菌 GAD 系统的调控机制提供了依据,并为潜在的李斯特菌病预防和控制提供了新的思路。

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