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奇异变形杆菌被人肾上皮细胞内化

Internalization of Proteus mirabilis by human renal epithelial cells.

作者信息

Chippendale G R, Warren J W, Trifillis A L, Mobley H L

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore 21201.

出版信息

Infect Immun. 1994 Aug;62(8):3115-21. doi: 10.1128/iai.62.8.3115-3121.1994.

Abstract

Proteus mirabilis, a common agent of bacteriuria in humans, causes acute pyelonephritis and bacteremia. Renal epithelium provides a barrier between luminal organisms and the renal interstitium. We have hypothesized that P. mirabilis may be internalized into renal epithelium. To test this hypothesis, we added suspensions of three P. mirabilis strains (10(8) CFU) to confluent monolayers of primary cultures of human renal proximal tubular epithelial cells (HRPTEC) and, after 3 h, found the bacteria internalized within membrane-bound vacuoles by light and electron microscopy. Internalization of bacteria by HRPTEC was corroborated by using the gentamicin protection assay. Cytolysis of HRPTEC by the HpmA hemolysin, however, was a confounding factor in this assay, and therefore a hemolysin-negative hpmA mutant was used in subsequent experiments. The nonhemolytic mutant WPM111 did not disrupt the monolayer and was recovered in numbers that were 10- to 100-fold higher than those of the hemolytic parent BA6163. Cytochalasin D (20 micrograms/ml) inhibited internalization of Salmonella typhimurium but not that of P. mirabilis, suggesting that the latter species enters HRPTEC by a mechanism that is not dependent on actin polymerization. We suggest that HpmA hemolysin-mediated cytotoxicity and internalization of bacteria by HRPTEC may play a role in the development of Proteus pyelonephritis.

摘要

奇异变形杆菌是人类菌尿的常见病原体,可引起急性肾盂肾炎和菌血症。肾上皮在管腔微生物与肾间质之间形成一道屏障。我们推测奇异变形杆菌可能会被肾上皮细胞内化。为验证这一假设,我们将三种奇异变形杆菌菌株的悬液(10⁸CFU)加入人肾近端小管上皮细胞(HRPTEC)原代培养的汇合单层细胞中,3小时后,通过光学显微镜和电子显微镜发现细菌被内化于膜结合的液泡中。利用庆大霉素保护试验证实了HRPTEC对细菌的内化作用。然而,HpmA溶血素对HRPTEC的细胞溶解作用是该试验中的一个混杂因素,因此在后续实验中使用了溶血素阴性的hpmA突变体。非溶血突变体WPM111不会破坏单层细胞,其回收数量比溶血亲本BA6163高10至100倍。细胞松弛素D(20微克/毫升)可抑制鼠伤寒沙门氏菌的内化,但不能抑制奇异变形杆菌的内化,这表明奇异变形杆菌通过一种不依赖于肌动蛋白聚合的机制进入HRPTEC。我们认为HpmA溶血素介导的细胞毒性以及HRPTEC对细菌的内化作用可能在奇异变形杆菌肾盂肾炎的发展中起作用。

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