CRP improves the survival and competitive fitness of Salmonella Typhimurium under starvation by controlling the cellular maintenance rate.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2024-08-22 Epub Date: 2024-07-24 DOI:10.1128/jb.00010-24
L K Mishra, R Shashidhar
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引用次数: 0

Abstract

Catabolite repression is a mechanism of selectively utilizing preferred nutrient sources by redirecting the metabolic pathways. Therefore, it prevents non-essential energy expenditure by repressing the genes and proteins involved in the metabolism of other less favored nutrient sources. Catabolite repressor protein (CRP) is a chief mediator of catabolite repression in microorganisms. In this context, we investigated the role of CRP in starvation tolerance, at both cell physiology and molecular level, by comparing the growth, survival, competitive fitness, maintenance rate, and gene and protein expression of wild type (WT) and ∆crp of Salmonella Typhimurium, under nutrient-rich and minimal medium condition. The ∆crp shows slow growth upon the arrival of nutrient-limiting conditions, poor survival under prolong-starvation, and inability to compete with its counterpart WT strain in nutrient-rich [Luria broth (LB)] and glucose-supplemented M9 minimal medium. Surprisingly, we observed that the survival and competitive fitness of ∆crp are influenced by the composition of the growth medium. Consequently, compared to the glucose-supplemented M9 medium, ∆crp shows faster death and a higher maintenance rate in the LB medium. The comparative gene and protein expression studies of WT and ∆crp in LB medium show that ∆crp has partial or complete loss of repression from CRP-controlled genes, resulting in a high abundance of hundreds of proteins in ∆crp compared to WT. Subsequently, the addition of metabolizable sugar or fresh nutrients to the competing culture showed extended survival of ∆crp. Therefore, our results suggest that CRP-mediated gene repression improves starvation tolerance and competitive fitness of Salmonella Typhimurium by adapting its cellular maintenance rate to environmental conditions.IMPORTANCESalmonella Typhimurium is a master at adapting to chronic starvation conditions. However, the molecular mechanisms to adapt to such conditions are still unknown. In this context, we have evaluated the role of catabolite repressor protein (CRP), a dual transcriptional regulator, in providing survival and competitive fitness under starvation conditions. Also, it showed an association between CRP and nutrient composition. We observed that Δcrp growing on alternate carbon sources has lower survival and competitive fitness than Δcrp growing on glucose as a carbon source. We observed that this is due to the loss of repression from the glucose and CRP-controlled genes, resulting in elevated cellular metabolism (a high maintenance rate) of the Δcrp during growth in a medium having a carbon source other than glucose (e.g., Luria broth medium).

CRP 可通过控制细胞维持率提高饥饿状态下鼠伤寒沙门氏菌的存活率和竞争适应性。
代谢抑制是一种通过改变代谢途径来选择性利用首选营养源的机制。因此,它通过抑制参与其他不那么受青睐的营养源代谢的基因和蛋白质来防止非必要的能量消耗。代谢物抑制蛋白(CRP)是微生物中代谢物抑制的主要介质。在此背景下,我们通过比较野生型(WT)和Δcrp Typhimurium 沙门氏菌在营养丰富和极少培养基条件下的生长、存活、竞争能力、维持率以及基因和蛋白质表达,从细胞生理和分子水平研究了 CRP 在耐饥饿方面的作用。Δcrp在营养限制条件下生长缓慢,在长时间饥饿条件下存活率低,在营养丰富的[卢里亚肉汤(LB)]和葡萄糖补充的 M9 最小培养基中无法与其对应的 WT 菌株竞争。令人惊讶的是,我们观察到 ∆crp 的存活率和竞争力受生长培养基成分的影响。因此,与添加葡萄糖的 M9 培养基相比,∆crp 在 LB 培养基中的死亡速度更快,维持率更高。在 LB 培养基中对 WT 和 ∆crp 的基因和蛋白质表达进行的比较研究表明,∆crp 部分或完全失去了 CRP 控制基因的抑制,导致与 WT 相比,∆crp 中数百种蛋白质的丰度较高。随后,在竞争培养物中加入可代谢的糖或新鲜营养物质,∆crp 的存活时间延长。因此,我们的研究结果表明,CRP 介导的基因抑制可使鼠伤寒沙门氏菌的细胞维持率适应环境条件,从而提高鼠伤寒沙门氏菌的耐饥饿性和竞争适应性。然而,适应这种条件的分子机制仍然未知。在这种情况下,我们评估了代谢物抑制蛋白(CRP)--一种双重转录调节因子--在饥饿条件下提供生存和竞争能力的作用。同时,我们还发现了 CRP 与营养成分之间的联系。我们观察到,与以葡萄糖为碳源的Δcrp相比,以交替碳源生长的Δcrp存活率和竞争适应性更低。我们观察到,这是由于葡萄糖和 CRP 控制基因失去了抑制作用,导致 Δcrp 在葡萄糖以外的碳源培养基(如 Luria 肉汤培养基)中生长时细胞代谢升高(维持率高)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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