细菌病原体如何协调食欲和毒力。

IF 8 1区 生物学 Q1 MICROBIOLOGY
Microbiology and Molecular Biology Reviews Pub Date : 2023-09-26 Epub Date: 2023-06-26 DOI:10.1128/mmbr.00198-22
Nick D Pokorzynski, Eduardo A Groisman
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引用次数: 0

摘要

细胞调节生长和新陈代谢以获得营养。在感染动物宿主期间,兼性细胞内病原体能够获得各种碳源,必须有效地优先利用碳。在这里,我们讨论了碳源如何控制细菌毒力,重点是伤寒沙门氏菌,它会导致免疫能力强的人类肠胃炎和小鼠伤寒样疾病,并提出毒力因子可以通过改变细胞生理来调节碳源的优先顺序。一方面,碳代谢的细菌调节因子控制毒力程序,表明致病性状的出现是对碳源可用性的反应。另一方面,控制毒力调节剂的信号可能会影响碳源的利用,这表明细菌病原体在宿主体内经历的刺激可能会直接影响碳源优先顺序。此外,病原体引发的肠道炎症会破坏肠道微生物群,从而破坏碳源的可用性。通过将毒力因子与碳利用决定因素相协调,病原体采用的代谢途径可能不是最节能的,因为这些途径会促进对抗菌剂的耐药性,也因为宿主对特定营养素的剥夺可能会阻碍某些途径的运作。我们提出,细菌的代谢优先级是感染致病结果的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How Bacterial Pathogens Coordinate Appetite with Virulence.

Cells adjust growth and metabolism to nutrient availability. Having access to a variety of carbon sources during infection of their animal hosts, facultative intracellular pathogens must efficiently prioritize carbon utilization. Here, we discuss how carbon source controls bacterial virulence, with an emphasis on Salmonella enterica serovar Typhimurium, which causes gastroenteritis in immunocompetent humans and a typhoid-like disease in mice, and propose that virulence factors can regulate carbon source prioritization by modifying cellular physiology. On the one hand, bacterial regulators of carbon metabolism control virulence programs, indicating that pathogenic traits appear in response to carbon source availability. On the other hand, signals controlling virulence regulators may impact carbon source utilization, suggesting that stimuli that bacterial pathogens experience within the host can directly impinge on carbon source prioritization. In addition, pathogen-triggered intestinal inflammation can disrupt the gut microbiota and thus the availability of carbon sources. By coordinating virulence factors with carbon utilization determinants, pathogens adopt metabolic pathways that may not be the most energy efficient because such pathways promote resistance to antimicrobial agents and also because host-imposed deprivation of specific nutrients may hinder the operation of certain pathways. We propose that metabolic prioritization by bacteria underlies the pathogenic outcome of an infection.

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来源期刊
CiteScore
18.80
自引率
0.80%
发文量
27
期刊介绍: Microbiology and Molecular Biology Reviews (MMBR), a journal that explores the significance and interrelationships of recent discoveries in various microbiology fields, publishes review articles that help both specialists and nonspecialists understand and apply the latest findings in their own research. MMBR covers a wide range of topics in microbiology, including microbial ecology, evolution, parasitology, biotechnology, and immunology. The journal caters to scientists with diverse interests in all areas of microbial science and encompasses viruses, bacteria, archaea, fungi, unicellular eukaryotes, and microbial parasites. MMBR primarily publishes authoritative and critical reviews that push the boundaries of knowledge, appealing to both specialists and generalists. The journal often includes descriptive figures and tables to enhance understanding. Indexed/Abstracted in various databases such as Agricola, BIOSIS Previews, CAB Abstracts, Cambridge Scientific Abstracts, Chemical Abstracts Service, Current Contents- Life Sciences, EMBASE, Food Science and Technology Abstracts, Illustrata, MEDLINE, Science Citation Index Expanded (Web of Science), Summon, and Scopus, among others.
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