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Francisella tularensis Genes Required for Inhibition of the Neutrophil Respiratory Burst and Intramacrophage Growth Identified by Random Transposon Mutagenesis of Strain LVS

机译:土霉素弗朗西斯菌抑制嗜中性粒细胞呼吸爆发和巨噬细胞内生长所必需的基因由菌株LVS的随机转座子诱变确定

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摘要

Francisella tularensis is a facultative intracellular pathogen and the causative agent of tularemia. We have shown that F. tularensis subspecies holarctica strain LVS prevents NADPH oxidase assembly and activation in human neutrophils, but how this is achieved is unclear. Herein, we used random transposon mutagenesis to identify LVS genes that affect neutrophil activation. Our initial screen identified carA, carB, and pyrB, which encode the small and large subunits of carbamoylphosphate synthase and aspartate carbamoyl transferase, respectively. These strains are uracil auxotrophs, and their growth was attenuated on cysteine heart agar augmented with sheep blood (CHAB) or in modified Mueller-Hinton broth. Phagocytosis of the uracil auxotrophic mutants triggered a respiratory burst in neutrophils, and ingested bacteria were killed and fragmented in phagosomes that contained superoxide. Conversely, phagocytosis did not trigger a respiratory burst in blood monocytes or monocyte-derived macrophages (MDM), and phagosomes containing wild-type or mutant bacteria lacked NADPH oxidase subunits. Nevertheless, the viability of mutant bacteria declined in MDM, and ultrastructural analysis revealed that phagosome egress was significantly inhibited despite synthesis of the virulence factor IglC. Other aspects of infection, such as interleukin-1β (IL-1β) and IL-8 secretion, were unaffected. The cultivation of carA, carB, or pyrB on uracil-supplemented CHAB was sufficient to prevent neutrophil activation and intramacrophage killing and supported escape from MDM phagosomes, but intracellular growth was not restored unless uracil was added to the tissue culture medium. Finally, all mutants tested grew normally in both HepG2 and J774A.1 cells. Collectively, our data demonstrate that uracil auxotrophy has cell type-specific effects on the fate of Francisella bacteria.
机译:图拉弗朗西斯菌是兼性的细胞内病原体,是图拉菌血症的病原体。我们已经表明,土拉弗朗西斯菌亚种holarctica菌株LVS阻止了NADPH氧化酶的组装和在人类嗜中性粒细胞中的活化,但是如何实现尚不清楚。本文中,我们使用随机转座子诱变来鉴定影响嗜中性粒细胞活化的LVS基因。我们的初步筛选确定了carA,carB和pyrB,它们分别编码氨基甲酰磷酸合酶和天冬氨酸氨基甲酰转移酶的小亚基和大亚基。这些菌株是尿嘧啶营养缺陷型,在生长有绵羊血(CHAB)的半胱氨酸心琼脂或改良的Mueller-Hinton肉汤中,它们的生长减弱。尿嘧啶营养缺陷型突变体的吞噬作用触发了嗜中性粒细胞的呼吸爆发,摄入的细菌被杀死并破碎成含有超氧化物的吞噬体。相反,吞噬作用不会在血液单核细胞或单核细胞衍生的巨噬细胞(MDM)中触发呼吸爆发,并且含有野生型或突变细菌的吞噬体缺少NADPH氧化酶亚基。然而,突变细菌的活力在MDM中下降,超微结构分析表明,尽管合成了毒力因子IglC,吞噬体的出口仍被显着抑制。感染的其他方面,例如白介素-1β(IL-1β)和IL-8分泌均未受影响。在尿嘧啶补充的CHAB上培养carA,carB或pyrB足以防止中性粒细胞活化和巨噬细胞杀伤,并支持从MDM吞噬体逃逸,但是除非将尿嘧啶添加到组织培养基中,否则细胞内的生长将无法恢复。最后,所有测试的突变体均在HepG2和J774A.1细胞中正常生长。总的来说,我们的数据表明尿嘧啶营养缺陷型对弗朗西斯菌细菌的命运具有细胞类型特异性的影响。

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