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铁载体毒力基因 entB 和 ybtS 对耐碳青霉烯类肺炎克雷伯菌毒力的影响。

The effect of siderophore virulence genes entB and ybtS on the virulence of Carbapenem-resistant Klebsiella pneumoniae.

机构信息

Yunnan Key Laboratory of Laboratory Medicine, Kunming, 650032, China; Yunnan Province Clinical Research Center for Laboratory Medicine, Kunming, 650032, China; Department of Clinical Laboratory, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, China; Department of Laboratory Medicine, Chuxiong Yi Autonomous Prefecture People's Hospital, Chuxiong, 675099, China.

Yunnan Key Laboratory of Laboratory Medicine, Kunming, 650032, China; Yunnan Province Clinical Research Center for Laboratory Medicine, Kunming, 650032, China; Department of Clinical Laboratory, The First Affiliated Hospital of Kunming Medical University, Kunming, 650032, China.

出版信息

Microb Pathog. 2022 Oct;171:105746. doi: 10.1016/j.micpath.2022.105746. Epub 2022 Sep 3.

Abstract

OBJECTIVE

With the detection rate increasing each year, highly resistant and virulent CRKP has been a serious challenge to clinical treatment because of the high morbidity and mortality. Considering the virulence of CRKP is closely related to over-expression of siderophore, the high detection rate of entB and ybtS genes in highly virulent CRKP may be an important reason for the high virulence phenotype of CRKP. Therefore, in this study, single/double knockout and complemented strains of siderophore virulence genes entB and ybtS were constructed to clarify the effect of siderophore virulence genes on the virulence of CRKP.

METHODS

1.The wire drawing experiment, mucus phenotype screening experiment, and PCR amplification were used to screen the target strain WT. the entB gene deletion strain △entB and the complementation strain C-△entB, ybtS gene deletion strain ΔybtS and complementation strain C-ΔybtS, entB and ybtS double gene deletion strain ΔentB + ybtS and complementation strain C-ΔentB + ybtS, were constructed by CrispR-Cas9 gene editing technology. PCR method was used to test whether the knockout and complementation were successful. 2. The colony morphology and mucus phenotype of the experimental strains were observed and the siderophore ability of the experimental strains was tested. Then the growth curves, biofilm-forming ability, and anti-serum killing ability of the strains were determined. 3. In order to understand the virulence of the experimental strain, the mouse intraperitoneal infection model was established to draw the survival curves and determine LD50 of experiment strains. Then to clarify the colonization ability of the experimental strains in the lung and liver of mice, the pathological biopsies were used to observe histopathological changes and ELISA method was used to determine the inflammatory factors IL-1β, LI-3 and TNF-α.

RESULTS

1 CRKP-27 was screened as the target strain WT, which is characterized by positive wire drawing test, strong mucus, strong virulence and carrying both entB and ybtS genes. The single/double knockout and complemented strains of siderophore virulence genes entB and ybtS were successfully constructed. 2 Siderophore virulence genes entB and ybtS had no significant effect on the colony morphology, mucus phenotype (drawing test) and biofilm formation ability of CRKP strains. The CRKP strains with entB and ybtS genes could significantly increase siderophore production. Although both the entB and ybtS genes could impair the growth rate of the CRKP strain, the role of ybtS gene was relatively slow. entB and ybtS genes enhanced the antiserum killing ability of CRKP strains. 3 The presence of entB and ybtS genes reduced the survival rate of mice infected with CRKP strains. Histopathological changes and inflammatory factor levels in the lungs and livers of infected mice were enhanced by the presence of entB and ybtS genes. Mice infected with the same strain had higher histopathological changes and levels of inflammatory factors in the lungs than in the livers.

CONCLUSIONS

1.The siderophore virulence genes entB and ybtS have no significant effect on the colony morphology, mucus phenotype and biofilm formation ability of CRKP strains.2.The siderophore virulence genes entB and ybtS can significantly enhance the virulence of the CRKP strain, but weaken its growth ability.

摘要

目的

由于高耐药性和高毒力的 CRKP 的检出率逐年增加,其发病率和死亡率很高,因此对临床治疗构成了严重挑战。由于 CRKP 的毒力与其对铁载体的过度表达密切相关,高毒力 CRKP 中 entB 和 ybtS 基因的高检出率可能是 CRKP 高毒力表型的重要原因。因此,本研究通过构建铁载体毒力基因 entB 和 ybtS 的单/双基因缺失和互补菌株,阐明铁载体毒力基因对 CRKP 毒力的影响。

方法

  1. 通过拉丝试验、黏液表型筛选试验和 PCR 扩增筛选目标菌株 WT。使用 CrispR-Cas9 基因编辑技术构建 entB 基因缺失菌株△entB 和互补菌株 C-△entB、ybtS 基因缺失菌株ΔybtS 和互补菌株 C-ΔybtS、entB 和 ybtS 双基因缺失菌株ΔentB+ybtS 和互补菌株 C-ΔentB+ybtS。PCR 方法用于检测敲除和互补是否成功。2. 观察实验菌株的菌落形态和黏液表型,检测实验菌株的铁载体能力。然后测定菌株的生长曲线、生物膜形成能力和抗血清杀伤能力。3. 为了了解实验菌株的毒力,建立了小鼠腹腔感染模型,绘制了生存曲线并确定了实验菌株的 LD50。然后,为了阐明实验菌株在小鼠肺和肝中的定植能力,使用病理活检观察组织病理学变化,ELISA 法测定炎症因子 IL-1β、LI-3 和 TNF-α。

结果

  1. 筛选出 CRKP-27 作为目标菌株 WT,其特征为拉丝试验阳性、黏液强、毒力强,且携带 entB 和 ybtS 基因。成功构建了铁载体毒力基因 entB 和 ybtS 的单/双基因缺失和互补菌株。2. 铁载体毒力基因 entB 和 ybtS 对 CRKP 菌株的菌落形态、黏液表型(拉丝试验)和生物膜形成能力无明显影响。携带 entB 和 ybtS 基因的 CRKP 菌株可显著增加铁载体的产生。虽然 entB 和 ybtS 基因都能削弱 CRKP 菌株的生长速度,但 ybtS 基因的作用相对较慢。entB 和 ybtS 基因增强了 CRKP 菌株对血清的杀伤能力。3. 携带 entB 和 ybtS 基因降低了感染 CRKP 菌株的小鼠的存活率。携带 entB 和 ybtS 基因增强了感染小鼠肺部和肝脏的组织病理学变化和炎症因子水平。相同菌株感染的小鼠肺部的组织病理学变化和炎症因子水平高于肝脏。

结论

  1. 铁载体毒力基因 entB 和 ybtS 对 CRKP 菌株的菌落形态、黏液表型和生物膜形成能力无明显影响。2. 铁载体毒力基因 entB 和 ybtS 可显著增强 CRKP 菌株的毒力,但削弱其生长能力。

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