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Growth phase-dependent invasion of Pseudomonas aeruginosa and its survival within HeLa cells.铜绿假单胞菌生长阶段依赖性侵袭及其在HeLa细胞内的存活
Infect Immun. 2001 Jul;69(7):4398-406. doi: 10.1128/IAI.69.7.4398-4406.2001.
2
The Impact of ExoS on Internalization by Epithelial Cells Is Independent of and Correlates with Bistability of Type Three Secretion System Gene Expression.ExoS 对上皮细胞内化的影响不依赖于 III 型分泌系统基因表达的二态性,且与该影响相关。
mBio. 2018 May 1;9(3):e00668-18. doi: 10.1128/mBio.00668-18.
3
The arginine finger domain of ExoT contributes to actin cytoskeleton disruption and inhibition of internalization of Pseudomonas aeruginosa by epithelial cells and macrophages.外毒素T的精氨酸指结构域有助于破坏肌动蛋白细胞骨架,并抑制铜绿假单胞菌被上皮细胞和巨噬细胞内化。
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Polarisation of type III translocation by Pseudomonas aeruginosa requires PcrG, PcrV and PopN.铜绿假单胞菌III型转位的极化需要PcrG、PcrV和PopN。
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Activities of Pseudomonas aeruginosa effectors secreted by the Type III secretion system in vitro and during infection.铜绿假单胞菌III型分泌系统分泌的效应蛋白在体外及感染过程中的活性
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Mol Microbiol. 2004 Nov;54(4):1090-103. doi: 10.1111/j.1365-2958.2004.04331.x.
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Regulation of ExoS production and secretion by Pseudomonas aeruginosa in response to tissue culture conditions.铜绿假单胞菌响应组织培养条件对外毒素S产生和分泌的调控
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Mutation of csk, encoding the C-terminal Src kinase, reduces Pseudomonas aeruginosa internalization by mammalian cells and enhances bacterial cytotoxicity.编码C端Src激酶的csk发生突变,会减少哺乳动物细胞对铜绿假单胞菌的摄取,并增强细菌的细胞毒性。
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Comparison of the exoS gene and protein expression in soil and clinical isolates of Pseudomonas aeruginosa.铜绿假单胞菌土壤分离株与临床分离株中外毒素S基因及蛋白表达的比较。
Infect Immun. 2001 Apr;69(4):2198-210. doi: 10.1128/IAI.69.4.2198-2210.2001.
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FlhA, a component of the flagellum assembly apparatus of Pseudomonas aeruginosa, plays a role in internalization by corneal epithelial cells.鞭毛蛋白A是铜绿假单胞菌鞭毛组装装置的一个组成部分,在角膜上皮细胞的内化过程中发挥作用。
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Pseudomonas aeruginosa GroEL Stimulates Production of PTX3 by Activating the NF-κB Pathway and Simultaneously Downregulating MicroRNA-9.铜绿假单胞菌GroEL通过激活NF-κB途径并同时下调微小RNA-9来刺激PTX3的产生。
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本文引用的文献

1
Pseudomonas aeruginosa mediated apoptosis requires the ADP-ribosylating activity of exoS.铜绿假单胞菌介导的细胞凋亡需要外毒素S的ADP核糖基化活性。
Microbiology (Reading). 2000 Oct;146 ( Pt 10):2531-2541. doi: 10.1099/00221287-146-10-2531.
2
Pseudomonas aeruginosa ExoT is a Rho GTPase-activating protein.铜绿假单胞菌外毒素T是一种Rho GTP酶激活蛋白。
Infect Immun. 2000 Oct;68(10):6066-8. doi: 10.1128/IAI.68.10.6066-6068.2000.
3
Pseudomonas aeruginosa cystic fibrosis isolates induce rapid, type III secretion-dependent, but ExoU-independent, oncosis of macrophages and polymorphonuclear neutrophils.铜绿假单胞菌囊性纤维化分离株可诱导巨噬细胞和多形核中性粒细胞快速发生Ⅲ型分泌依赖性但ExoU非依赖性的胀亡。
Infect Immun. 2000 May;68(5):2916-24. doi: 10.1128/IAI.68.5.2916-2924.2000.
4
ExoT of cytotoxic Pseudomonas aeruginosa prevents uptake by corneal epithelial cells.细胞毒性铜绿假单胞菌的外毒素T可阻止角膜上皮细胞摄取。
Infect Immun. 2000 Jan;68(1):403-6. doi: 10.1128/IAI.68.1.403-406.2000.
5
Invasion and intracellular survival of Burkholderia cepacia.洋葱伯克霍尔德菌的侵袭与细胞内存活
Infect Immun. 2000 Jan;68(1):24-9. doi: 10.1128/IAI.68.1.24-29.2000.
6
The N-terminal domain of Pseudomonas aeruginosa exoenzyme S is a GTPase-activating protein for Rho GTPases.铜绿假单胞菌外毒素S的N端结构域是一种针对Rho GTP酶的GTP酶激活蛋白。
J Biol Chem. 1999 Dec 17;274(51):36369-72. doi: 10.1074/jbc.274.51.36369.
7
Bacterial biofilms: a common cause of persistent infections.细菌生物膜:持续性感染的常见原因。
Science. 1999 May 21;284(5418):1318-22. doi: 10.1126/science.284.5418.1318.
8
The amino-terminal domain of Pseudomonas aeruginosa ExoS disrupts actin filaments via small-molecular-weight GTP-binding proteins.铜绿假单胞菌外毒素S的氨基末端结构域通过小分子GTP结合蛋白破坏肌动蛋白丝。
Mol Microbiol. 1999 Apr;32(2):393-401. doi: 10.1046/j.1365-2958.1999.01359.x.
9
Biological effects of Pseudomonas aeruginosa type III-secreted proteins on CHO cells.铜绿假单胞菌III型分泌蛋白对CHO细胞的生物学效应。
Infect Immun. 1999 Apr;67(4):2040-4. doi: 10.1128/IAI.67.4.2040-2044.1999.
10
Regulation of ExoS production and secretion by Pseudomonas aeruginosa in response to tissue culture conditions.铜绿假单胞菌响应组织培养条件对外毒素S产生和分泌的调控
Infect Immun. 1999 Feb;67(2):914-20. doi: 10.1128/IAI.67.2.914-920.1999.

铜绿假单胞菌生长阶段依赖性侵袭及其在HeLa细胞内的存活

Growth phase-dependent invasion of Pseudomonas aeruginosa and its survival within HeLa cells.

作者信息

Ha U, Jin S

机构信息

Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida 32610, USA.

出版信息

Infect Immun. 2001 Jul;69(7):4398-406. doi: 10.1128/IAI.69.7.4398-4406.2001.

DOI:10.1128/IAI.69.7.4398-4406.2001
PMID:11401979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC98512/
Abstract

Clinical isolates of Pseudomonas aeruginosa are classified into invasive and noninvasive (cytolytic) strains. In a noninvasive PA103 background, ExoS and ExoT have recently been shown to function as anti-internalization factors. However, these two factors seemed not to have such a function in an invasive strain PAK background. In this study, using HeLa tissue culture cells, we observed that the internalization of invasive strain PAK is dependent on its growth phases, with the stationary-phase cells internalized about 100-fold more efficiently than the exponential-phase cells. This growth phase-dependent internalization was not observed in the noninvasive PA103 strain. Further analysis of various mutant derivatives of the invasive PAK and the noninvasive PA103 strains demonstrated that ExoS or ExoT that is injected into host cells by a type III secretion machinery functions as an anti-internalization factor in both types of strains. In correlation with the growth phase-dependent internalization, the invasive strain PAK translocates much higher amount of ExoS and ExoT into HeLa cells when it is in an exponential-growth phase than when it is in a stationary-growth phase, whereas the translocation of ExoT by the noninvasive strain PA103 is consistently high regardless of the growth phases, suggesting a difference in the regulatory mechanism of type III secretion between the two types of strains. Consistent with the invasive phenotype of the parent strain, an internalized PAK derivative survived well within the HeLa cells, whereas the viability of internalized PA103 derivative was dramatically decreased and completely cleared within 48 h. These results indicate that the invasive strains of P. aeruginosa have evolved the mechanism of intracellular survival, whereas the noninvasive P. aeruginosa strains have lost or not acquired the ability to survive within the epithelial cells.

摘要

铜绿假单胞菌的临床分离株可分为侵袭性和非侵袭性(细胞溶解性)菌株。在非侵袭性PA103背景下,最近研究表明外毒素S(ExoS)和外毒素T(ExoT)可作为抗内化因子发挥作用。然而,在侵袭性菌株PAK背景下,这两种因子似乎没有这种功能。在本研究中,我们使用HeLa组织培养细胞观察到,侵袭性菌株PAK的内化作用取决于其生长阶段,稳定期细胞的内化效率比指数期细胞高约100倍。在非侵袭性PA103菌株中未观察到这种生长阶段依赖性内化现象。对侵袭性PAK和非侵袭性PA103菌株的各种突变衍生物进行进一步分析表明,通过III型分泌机制注入宿主细胞的ExoS或ExoT在这两种菌株中均作为抗内化因子发挥作用。与生长阶段依赖性内化相关的是,侵袭性菌株PAK在指数生长期比稳定生长期向HeLa细胞转运的ExoS和ExoT量要高得多,而非侵袭性菌株PA103的ExoT转运量无论生长阶段如何都始终很高,这表明两种菌株在III型分泌调节机制上存在差异。与亲本菌株的侵袭表型一致,内化的PAK衍生物在HeLa细胞内存活良好,而内化的PA103衍生物的活力则显著下降,并在48小时内完全清除。这些结果表明,铜绿假单胞菌的侵袭性菌株已经进化出细胞内存活机制,而非侵袭性铜绿假单胞菌菌株已经丧失或未获得在上皮细胞内存活的能力。