Klebsiella pneumoniae increases invasion in intestinal epithelial cells by disrupting the cytoskeleton.

IF 1.3 4区 医学 Q4 IMMUNOLOGY
Acta microbiologica et immunologica Hungarica Pub Date : 2024-07-30 Print Date: 2024-09-18 DOI:10.1556/030.2024.02326
Xu Wang, Xiao-Hong Yin, Jin-Long Yang, Fan Tu, Xiao-Hong Rui, Jun Liu, Ping Xu
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引用次数: 0

Abstract

Klebsiella pneumoniae is an opportunistic pathogen and it can cause human mucosal lesions through the intestine, leading to bacteremia and abscess formation in liver and spleen. Previous studies have shown that K. pneumoniae can enter or cross cells through the intestinal epithelium, but the mechanism is unknown. In this study, we treated the intestinal epithelial cell line Caco-2 with KP1195, a clinically isolated strain with high adhesion and invasion of intestinal epithelial cells. The results showed that the treatment of K. pneumoniae could increase the expression of integrin gene and further disrupt the changes of cytoskeleton. Treating Caco-2 with cytoskeletal inhibitor cytorelaxin D can significantly increase the efficiency of K. pneumoniae invading Caco-2 cells. These data suggest that disruption of the cytoskeleton through integrins may be one of the mechanisms by which K. pneumoniae increases intracellular invasion. This study provides a theoretical basis for further understanding of the mechanism of K. pneumoniae entering intestinal epithelial cells.

肺炎克雷伯氏菌通过破坏细胞骨架来增加对肠上皮细胞的侵袭。
肺炎克雷伯菌是一种机会性病原体,可通过肠道引起人体粘膜病变,导致菌血症和肝脾脓肿的形成。以往的研究表明,肺炎克雷伯菌可通过肠上皮细胞进入或穿过细胞,但其机制尚不清楚。在本研究中,我们用 KP1195 处理肠上皮细胞系 Caco-2,KP1195 是一种临床分离的菌株,对肠上皮细胞具有高粘附性和高侵袭性。结果表明,肺炎克氏菌处理可增加整合素基因的表达,并进一步破坏细胞骨架的变化。用细胞骨架抑制剂 cytorelaxin D 处理 Caco-2 可显著提高肺炎克氏菌入侵 Caco-2 细胞的效率。这些数据表明,通过整合素破坏细胞骨架可能是肺炎克菌增加细胞内侵袭的机制之一。这项研究为进一步了解肺炎克氏菌进入肠上皮细胞的机制提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.30
自引率
13.30%
发文量
36
审稿时长
>12 weeks
期刊介绍: AMIH is devoted to the publication of research in all fields of medical microbiology (bacteriology, virology, parasitology, mycology); immunology of infectious diseases and study of the microbiome related to human diseases.
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