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利用差异显示聚合酶链反应分离并鉴定巨噬细胞胞内感染期间诱导产生的嗜肺军团菌基因座。

The use of differential display-PCR to isolate and characterize a Legionella pneumophila locus induced during the intracellular infection of macrophages.

作者信息

Abu Kwaik Y, Pederson L L

机构信息

Department of Microbiology and immunology, University of Kentucky Chandler Medical Center, Lexington 40536-0084, USA.

出版信息

Mol Microbiol. 1996 Aug;21(3):543-56. doi: 10.1111/j.1365-2958.1996.tb02563.x.

Abstract

The differential display (DD)-PCR technique has been modified to identify prokaryotic cDNA fragments that are differentially induced by facultative intracellular bacteria in response to the intracellular environment of eukaryotic cells. Several DD-PCR fragments identified from the intracellular bacterium Legionella pneumophila were induced at 4 h post-infection of the U937 macrophage-like cells. From these, a 700 bp fragment was cloned and sequenced. Neither the DNA sequence nor the predicted protein sequence from the open reading frame has similarity to other sequences in genetic databases. Transcription of the chromosomal locus containing the 700 bp fragment (eml, for early stage macrophage-induced locus) was induced by intracellular bacteria during the first few hours post-infection of macrophages but the expression was downregulated by 12 h post-infection. Transcription of eml was not growth phase-related in vitro, and was not affected by in vitro stress stimuli. A 3.7 kb EcoRI genomic fragment containing the 700 bp DD-PCR product was cloned. Six mini-Tn 10 insertions in the 3.7 kb EcoRI fragment were recombined into the L. pneumophila chromosome. Compared to the wild-type strain, five of the eml isogenic mutants had a similar phenotype of reduced cytopathicity to the U937 cells, showed a 100-fold increase in killing by macrophages during the first 5 h of the intracellular infection, and showed a 100-fold increase in killing during the first 24h of infection of the amoeba Hartmanella vermiformis. The 6th mutant had a phenotype indistinguishable from the wild-type strain. The cytopathicity defect of the mutants to the U937 cells was restored to wild-type levels by complementation of the mutants with a plasmid containing the 3.7 kb EcoRI fragment. These data showed that the 3.7 kb fragment containing eml is a novel L. pneumophila locus whose expression is uniquely induced by non-stress stimuli during early stages of the intracellular infection of phagocytic cells. Expression of this locus is required for survival of L. pneumophila within macrophages and within amoebae during early stages of the infection.

摘要

差异显示(DD)-PCR技术已被改进,用于鉴定真核细胞内环境中兼性胞内细菌差异诱导的原核cDNA片段。从细胞内细菌嗜肺军团菌中鉴定出的几个DD-PCR片段在U937巨噬细胞样细胞感染后4小时被诱导。从中克隆并测序了一个700 bp的片段。该开放阅读框的DNA序列和预测的蛋白质序列与遗传数据库中的其他序列均无相似性。包含700 bp片段(eml,早期巨噬细胞诱导基因座)的染色体位点的转录在巨噬细胞感染后的最初几个小时内被细胞内细菌诱导,但在感染后12小时表达下调。eml的转录在体外与生长阶段无关,且不受体外应激刺激的影响。克隆了一个包含700 bp DD-PCR产物的3.7 kb EcoRI基因组片段。该3.7 kb EcoRI片段中的六个mini-Tn10插入片段被重组到嗜肺军团菌染色体中。与野生型菌株相比,五个eml同基因突变体对U937细胞的细胞病变效应降低,在细胞内感染的前5小时巨噬细胞杀伤率增加100倍,在感染变形虫哈氏阿米巴的前24小时杀伤率增加100倍。第六个突变体的表型与野生型菌株无明显差异。通过用含有3.7 kb EcoRI片段的质粒对突变体进行互补,突变体对U937细胞的细胞病变效应缺陷恢复到野生型水平。这些数据表明,包含eml的3.7 kb片段是嗜肺军团菌的一个新基因座,其表达在吞噬细胞内感染早期由非应激刺激独特诱导。该基因座的表达是嗜肺军团菌在感染早期在巨噬细胞和阿米巴内生存所必需的。

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