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粘质沙雷氏菌磷脂酶 A(PhlA)的溶血和细胞溶解活性依赖于 PhlA 产生的溶血磷脂。

The hemolytic and cytolytic activities of Serratia marcescens phospholipase A (PhlA) depend on lysophospholipid production by PhlA.

机构信息

Department of Bacteriology I, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, Tokyo 162-8640, Japan.

出版信息

BMC Microbiol. 2009 Dec 16;9:261. doi: 10.1186/1471-2180-9-261.

Abstract

BACKGROUND

Serratia marcescens is a gram-negative bacterium and often causes nosocomial infections. There have been few studies of the virulence factors of this bacterium. The only S. marcescens hemolytic and cytotoxic factor reported, thus far, is the hemolysin ShlA.

RESULTS

An S. marcescens shlAB deletion mutant was constructed and shown to have no contact hemolytic activity. However, the deletion mutant retained hemolytic activity on human blood agar plates, indicating the presence of another S. marcescens hemolytic factor. Functional cloning of S. marcescens identified a phospholipase A (PhlA) with hemolytic activity on human blood agar plates. A phlAB deletion mutant lost hemolytic activity on human blood agar plates. Purified recombinant PhlA hydrolyzed several types of phospholipids and exhibited phospholipase A1 (PLA1), but not phospholipase A2 (PLA2), activity. The cytotoxic and hemolytic activities of PhlA both required phospholipids as substrates.

CONCLUSION

We have shown that the S. marcescens phlA gene produces hemolysis on human blood agar plates. PhlA induces destabilization of target cell membranes in the presence of phospholipids. Our results indicated that the lysophospholipids produced by PhlA affected cell membranes resulting in hemolysis and cell death.

摘要

背景

粘质沙雷氏菌是一种革兰氏阴性细菌,常引起医院感染。目前对该菌毒力因子的研究较少。迄今为止,报道的唯一沙雷氏菌溶血和细胞毒性因子是溶血素 ShlA。

结果

构建了粘质沙雷氏菌 shlAB 缺失突变体,显示无接触溶血活性。然而,该缺失突变体在人血琼脂平板上仍保留溶血活性,表明存在另一种粘质沙雷氏菌溶血因子。粘质沙雷氏菌的功能克隆鉴定出一种在人血琼脂平板上具有溶血活性的磷脂酶 A(PhlA)。phlAB 缺失突变体在人血琼脂平板上丧失溶血活性。纯化的重组 PhlA 水解多种类型的磷脂,并表现出磷脂酶 A1(PLA1)活性,但没有磷脂酶 A2(PLA2)活性。PhlA 的细胞毒性和溶血活性均需要磷脂作为底物。

结论

我们已经表明,粘质沙雷氏菌的 phlA 基因在人血琼脂平板上产生溶血。PhlA 在存在磷脂的情况下导致靶细胞膜的不稳定。我们的结果表明,PhlA 产生的溶血磷脂影响细胞膜,导致溶血和细胞死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6546/2800117/23983bbda360/1471-2180-9-261-1.jpg

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