新发现的c-二gmp途径推测的EAL结构域基因STM0343调控肠沙门氏菌血清型鼠伤寒菌的抗病性和毒力。

IF 3.7 1区 农林科学 Q1 VETERINARY SCIENCES
Kaifeng Chen, Lili Li, Nanwei Wang, Zhouping Zhou, Peng Pan, Chenggang Xu, Dage Sun, Jiayi Li, Changzhi Dai, Dai Kuang, Ming Liao, Jianmin Zhang
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引用次数: 0

摘要

鼠伤寒沙门氏菌是一种重要的人畜共患病原体,其生存和传播依赖于抗逆性和毒力因子。因此,确定鼠伤寒沙门氏菌的关键调控因子对于预防和控制鼠伤寒沙门氏菌至关重要。我们进行了转录组学分析并筛选了c-di-GMP通路关键基因STM0343,这是一个假定的EAL结构域蛋白,功能未知。我们的研究结果显示,该基因(269ΔSTM0343)的缺失导致c-di-GMP增加29.85%。在抗逆性方面,菌株269ΔSTM0343较野生菌株WT269有显著提高。通过上调相关基因的表达,细胞外蛋白和胞外多糖的产量分别增加了95.74%和35.96%。结果表明,269ΔSTM0343的生物成膜能力提高了21.54%,菌落形态呈现更明显的红色、干燥和粗糙。269ΔSTM0343也因flhD表达下调而表现出19.03%的运动性下降。结果,269ΔSTM0343增加了对各种抗生素以及酸性条件,氧化应激和消毒剂的抵抗力。在毒力方面,与WT269相比,269ΔSTM0343对HeLa细胞的粘附能力和侵袭能力分别提高了1倍和25.67%。在体内实验中,269ΔSTM0343刺激小鼠的体重下降幅度更大,脾脏、肝脏和肠道的细菌负荷分别增加了5倍、30倍和21倍,并伴有更严重的病理损伤。机理研究表明,269ΔSTM0343ΔCsgB的粘附能力和侵袭能力分别比269ΔSTM0343降低了29.41%和68.58%。此外,LacZ基因报告表明STM0343抑制CsgB的表达。这表明STM0343通过下调CsgB表达抑制毒力。本研究揭示了STM0343降低鼠伤寒沙门氏菌抗逆性和致病性的调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Newly identified c-di-GMP pathway putative EAL domain gene STM0343 regulates stress resistance and virulence in Salmonella enterica serovar Typhimurium.

S. Typhimurium is a significant zoonotic pathogen, and its survival and transmission rely on stress resistance and virulence factors. Therefore, identifying key regulatory elements is crucial for preventing and controlling S. Typhimurium. We performed transcriptomic analysis and screened for a c-di-GMP pathway key gene STM0343, a putative EAL domain protein with an unknown function. Our findings revealed that the deletion of this gene (269ΔSTM0343) led to a 29.85% increase in c-di-GMP. In terms of stress resistance, the strain 269ΔSTM0343 showed significant improvements compared to the wild strain WT269. Specifically, it exhibited increases of 95.74% in extracellular protein and 35.96% in exopolysaccharide production by upregulating the expression of relevant genes. As a result, the biofilm formation ability of 269ΔSTM0343 was enhanced by 21.54%, accompanied by a more pronounced red, dry, and rough colony morphology. 269ΔSTM0343 also showed a 19.03% decrease in motility due to the downregulation of flhD expression. As a result, 269ΔSTM0343 increased resistance to various antibiotics, as well as to acidic conditions, oxidative stress, and disinfectants. In terms of virulence, compared to WT269, the adhesion and invasive ability of 269ΔSTM0343 to HeLa cells was enhanced by onefold and 25.67%, respectively. In in vivo experiments, mice challenged with 269ΔSTM0343 experienced greater weight loss, and the bacterial loads in the spleen, liver, and intestines were elevated by fivefold, 30-fold, and 21-fold, respectively, accompanied by more severe pathological damage. Mechanistic studies revealed that the adhesion and invasion capacities of 269ΔSTM0343ΔCsgB decreased by 29.41% and 68.58%, respectively, compared to 269ΔSTM0343. Additionally, LacZ gene reporting indicated that STM0343 inhibited the expression of CsgB. This suggests that STM0343 suppresses virulence by downregulating CsgB expression. This study provides insights into the regulatory mechanisms by which STM0343 reduces the stress resistance and pathogenicity of S. Typhimurium.

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来源期刊
Veterinary Research
Veterinary Research 农林科学-兽医学
CiteScore
7.00
自引率
4.50%
发文量
92
审稿时长
3 months
期刊介绍: Veterinary Research is an open access journal that publishes high quality and novel research and review articles focusing on all aspects of infectious diseases and host-pathogen interaction in animals.
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