CemR atypical response regulator impacts energy conversion in Campylobacteria.

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2024-08-20 Epub Date: 2024-07-09 DOI:10.1128/msystems.00784-24
Mateusz Noszka, Agnieszka Strzałka, Jakub Muraszko, Dirk Hofreuter, Miriam Abele, Christina Ludwig, Kerstin Stingl, Anna Zawilak-Pawlik
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引用次数: 0

Abstract

Campylobacter jejuni and Arcobacter butzleri are microaerobic food-borne human gastrointestinal pathogens that mainly cause diarrheal disease. These related species of the Campylobacteria class face variable atmospheric environments during infection and transmission, ranging from nearly anaerobic to aerobic conditions. Consequently, their lifestyles require that both pathogens need to adjust their metabolism and respiration to the changing oxygen concentrations of the colonization sites. Our transcriptomic and proteomic studies revealed that C. jejuni and A. butzleri, lacking a Campylobacteria-specific regulatory protein, C. jejuni Cj1608, or a homolog, A. butzleri Abu0127, are unable to reprogram tricarboxylic acid cycle or respiration pathways, respectively, to produce ATP efficiently and, in consequence, adjust growth to changing oxygen supply. We propose that these Campylobacteria energy and metabolism regulators (CemRs) are long-sought transcription factors controlling the metabolic shift related to oxygen availability, essential for these bacteria's survival and adaptation to the niches they inhabit. Besides their significant universal role in Campylobacteria, CemRs, as pleiotropic regulators, control the transcription of many genes, often specific to the species, under microaerophilic conditions and in response to oxidative stress.

Importance: C. jejuni and A. butzleri are closely related pathogens that infect the human gastrointestinal tract. In order to infect humans successfully, they need to change their metabolism as nutrient and respiratory conditions change. A regulator called CemR has been identified, which helps them adapt their metabolism to changing conditions, particularly oxygen availability in the gastrointestinal tract so that they can produce enough energy for survival and spread. Without CemR, these bacteria, as well as a related species, Helicobacter pylori, produce less energy, grow more slowly, or, in the case of C. jejuni, do not grow at all. Furthermore, CemR is a global regulator that controls the synthesis of many genes in each species, potentially allowing them to adapt to their ecological niches as well as establish infection. Therefore, the identification of CemR opens new possibilities for studying the pathogenicity of C. jejuni and A. butzleri.

CemR 非典型反应调节器影响弯曲杆菌的能量转换。
空肠弯曲杆菌和丁兹勒弧杆菌是微需氧食源性人类胃肠道病原体,主要引起腹泻疾病。在感染和传播过程中,弯曲杆菌中的这些相关菌种面临着不同的大气环境,从几乎厌氧到需氧条件不等。因此,它们的生活方式要求这两种病原体都需要根据定植地点氧气浓度的变化调整其新陈代谢和呼吸。我们的转录组学和蛋白质组学研究发现,空肠弯曲杆菌和丁兹勒氏菌在缺乏弯曲杆菌特异性调控蛋白空肠弯曲杆菌 Cj1608 或同源物丁兹勒氏菌 Abu0127 的情况下,无法分别对三羧酸循环或呼吸途径进行重编程,以有效产生 ATP,从而使生长适应不断变化的氧气供应。我们认为,这些弯曲杆菌能量和代谢调节因子(CemRs)是人们长期寻找的转录因子,它们控制着与氧气供应相关的代谢转变,这对这些细菌的生存和适应其栖息的环境至关重要。除了在弯曲杆菌中发挥重要的普遍作用外,CemRs 作为多效调节因子,还能在微嗜氧条件下和应对氧化应激时控制许多基因的转录,这些基因往往是物种特有的:空肠大肠杆菌和丁兹勒氏菌是感染人类胃肠道的密切相关的病原体。为了成功感染人类,它们需要随着营养和呼吸条件的变化而改变新陈代谢。目前已发现一种名为 CemR 的调节因子,它能帮助细菌使新陈代谢适应不断变化的条件,特别是胃肠道中的氧气供应情况,从而使细菌能够产生足够的能量来生存和传播。如果没有 CemR,这些细菌以及相关的幽门螺旋杆菌产生的能量就会减少,生长速度就会减慢,空肠丙酸杆菌则根本不会生长。此外,CemR 是一种全局调控因子,可控制每个物种中许多基因的合成,从而使它们能够适应其生态位以及建立感染。因此,CemR 的鉴定为研究空肠大肠杆菌和丁兹勒氏菌的致病性提供了新的可能性。
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
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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