首页> 美国卫生研究院文献>PLoS Pathogens >Discrete Cyclic di-GMP-Dependent Control of Bacterial Predation versus Axenic Growth in Bdellovibrio bacteriovorus
【2h】

Discrete Cyclic di-GMP-Dependent Control of Bacterial Predation versus Axenic Growth in Bdellovibrio bacteriovorus

机译:Bdellovibrio细菌细菌的捕食与轴生生长的离散循环双GMP依赖控制。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Bdellovibrio bacteriovorus is a Delta-proteobacterium that oscillates between free-living growth and predation on Gram-negative bacteria including important pathogens of man, animals and plants. After entering the prey periplasm, killing the prey and replicating inside the prey bdelloplast, several motile B. bacteriovorus progeny cells emerge. The B. bacteriovorus HD100 genome encodes numerous proteins predicted to be involved in signalling via the secondary messenger cyclic di-GMP (c-di-GMP), which is known to affect bacterial lifestyle choices. We investigated the role of c-di-GMP signalling in B. bacteriovorus, focussing on the five GGDEF domain proteins that are predicted to function as diguanylyl cyclases initiating c-di-GMP signalling cascades. Inactivation of individual GGDEF domain genes resulted in remarkably distinct phenotypes. Deletion of dgcB (Bd0742) resulted in a predation impaired, obligately axenic mutant, while deletion of dgcC (Bd1434) resulted in the opposite, obligately predatory mutant. Deletion of dgcA (Bd0367) abolished gliding motility, producing bacteria capable of predatory invasion but unable to leave the exhausted prey. Complementation was achieved with wild type dgc genes, but not with GGAAF versions. Deletion of cdgA (Bd3125) substantially slowed predation; this was restored by wild type complementation. Deletion of dgcD (Bd3766) had no observable phenotype. In vitro assays showed that DgcA, DgcB, and DgcC were diguanylyl cyclases. CdgA lacks enzymatic activity but functions as a c-di-GMP receptor apparently in the DgcB pathway. Activity of DgcD was not detected. Deletion of DgcA strongly decreased the extractable c-di-GMP content of axenic Bdellovibrio cells. We show that c-di-GMP signalling pathways are essential for both the free-living and predatory lifestyles of B. bacteriovorus and that obligately predatory dgcC- can be made lacking a propensity to survive without predation of bacterial pathogens and thus possibly useful in anti-pathogen applications. In contrast to many studies in other bacteria, Bdellovibrio shows specificity and lack of overlap in c-di-GMP signalling pathways.
机译:Bdellovibrio bacteriovorus是一种Delta变形杆菌,可在自由生长和捕食革兰氏阴性细菌(包括人,动物和植物的重要病原体)之间振荡。进入猎物周质后,杀死猎物并在猎物浆膜内复制,出现了几个能动的芽孢杆菌子代细胞。细菌噬菌芽孢杆菌HD100基因组编码许多蛋白质,这些蛋白质预计会通过次级信使环di-GMP(c-di-GMP)参与信号传导,已知会影响细菌的生活方式选择。我们调查了C-di-GMP信号在细菌杆菌中的作用,重点研究了五个GGDEF域蛋白,这些蛋白预计起启动c-di-GMP信号级联反应的双胍基环化酶的作用。单个GGDEF结构域基因的失活导致明显不同的表型。删除dgcB(Bd0742)会导致捕食受损,专一的先天性突变体,而删除dgcC(Bd1434)会导致相反的专一掠食性突变。 dgcA(Bd0367)的删除消除了滑行运动,产生了能够掠夺性入侵但无法离开疲惫的猎物的细菌。与野生型dgc基因互补,但与GGAAF版本不互补。 cdgA(Bd3125)的删除大大减缓了捕食;通过野生型互补恢复。 dgcD(Bd3766)的删除没有可观察到的表型。体外测定显示DgcA,DgcB和DgcC是双胍基环化酶。 CdgA缺乏酶活性,但显然在DgcB途径中起c-di-GMP受体的作用。未检测到DgcD的活性。 DgcA的删除大大降低了轴突性Bdellovibrio细胞的可提取c-di-GMP含量。我们表明,c-di-GMP信号通路对于B. bacteriovorus的自由生活和掠食性生活方式都是必不可少的,并且可以使专性掠食性dgcC-缺乏缺乏细菌病原体的生存能力,因此可能在抗细菌中有用-病原体应用。与其他细菌的许多研究相比,Bdellovibrio显示出特异性,并且在c-di-GMP信号通路中没有重叠。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号