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首页> 外文期刊>Infection and immunity >Expression of Listeriolysin O and ActA by Intracellular and Extracellular Listeria monocytogenes
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Expression of Listeriolysin O and ActA by Intracellular and Extracellular Listeria monocytogenes

机译:胞内和胞外李斯特菌引起李斯特菌溶血素O和ActA的表达

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Listeria monocytogenes requires listeriolysin O (LLO) and ActA, the products of hly and actA, respectively, to establish a productive intracellular infection. LLO is essential for vacuolar lysis and entry into the cytosol, while ActA is required for bacterial spread to adjacent cells. We have used a transcriptional reporter gene system to compare the expression ofactA and hly during intracellular growth to that during growth in broth cultures. The hly andactA genes were transcriptionally fused toEscherichia coli lacZ and Bacillus pumilus cat-86 (cat), and the fusions were integrated in single copies into the L. monocytogenes chromosome. A chloramphenicol resistance assay indicated that the hlyfusion but not the actA fusion was significantly activated in Luria-Bertani (LB) broth, and this finding correlated with LLO and ActA levels detectable in broth cultures. Quantitation of promoter activity on the basis of β-galactosidase activity revealed up to 10-fold-higher level of expression of the hly fusion relative to the actA fusion in LB broth. In contrast, both fusions were active in the cytosol of J774 cells, and the activity of the actA fusion was approximately 3-fold higher than that of the hly fusion under these conditions. However, quantitative immunoprecipitation of ActA and LLO from infected J774 cells demonstrated approximately 70-fold more cytosolic ActA than cytosolic LLO. Finally, in comparison to induction in broth cultures,actA was highly induced (226-fold) and hly was moderately induced (20-fold) in J774 cells. Collectively, these results indicate that actA and hly are differentially regulated in response to the growth environment and that both genes are preferentially expressed during intracellular growth. Further, while the lower level of production of ActA than of LLO in broth can be accounted for by transcriptional regulation, the relative abundance of intracellular ActA compared to that of intracellular LLO is a function of additional, possibly host-mediated, factors.
机译:单核细胞增生性李斯特菌需要分别由 hly actA 产生的李斯特菌溶血素O(LLO)和ActA。 LLO对于液泡裂解和进入细胞质是必不可少的,而ActA是细菌扩散到相邻细胞所必需的。我们已经使用了一种转录报告基因系统来比较细胞培养中 actA hly 在肉汤培养中的表达。将 hly actA 基因转录融合至大肠杆菌lacZ 短小芽孢杆菌cat- 86( cat ),然后将融合体以单份形式整合到 L中。单核细胞增生染色体氯霉素抗性试验表明,Luria-Bertani(LB)肉汤中的 hly 融合而不是 actA 融合被显着激活,这一发现与可检测到的LLO和ActA水平相关在肉汤文化中。基于β-半乳糖苷酶活性的启动子活性定量显示,相对于LB肉汤中的 actA 融合体, hly 融合体的表达水平高10倍。相反,两种融合在J774细胞的胞浆中均具有活性,在这种条件下, actA 融合的活性比 hly 融合的活性高约3倍。 。但是,从感染的J774细胞中对ActA和LLO进行定量免疫沉淀表明,胞质ActA比胞质LLO多约70倍。最后,与肉汤培养中的诱导相比,在J774细胞中, actA 被高度诱导(226倍),而 hly 被中等诱导(20倍)。总的来说,这些结果表明 actA hly 受生长环境的影响而受到差异调节,并且两个基因在细胞内生长过程中均优先表达。此外,尽管可以通过转录调节来解释培养液中ActA的产量低于LLO的水平,但是与胞内LLO相比,胞内ActA的相对丰度是附加的,可能是宿主介导的因子的函数。

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