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CcpA在高血糖环境中影响(某种物质,原文未明确)的感染性。

CcpA Affects Infectivity of in a Hyperglycemic Environment.

作者信息

Bischoff Markus, Wonnenberg Bodo, Nippe Nadine, Nyffenegger-Jann Naja J, Voss Meike, Beisswenger Christoph, Sunderkötter Cord, Molle Virginie, Dinh Quoc Thai, Lammert Frank, Bals Robert, Herrmann Mathias, Somerville Greg A, Tschernig Thomas, Gaupp Rosmarie

机构信息

Institute for Medical Microbiology and Hygiene, Saarland UniversityHomburg, Germany.

Institute of Anatomy and Cell Biology, Saarland UniversityHomburg, Germany.

出版信息

Front Cell Infect Microbiol. 2017 May 9;7:172. doi: 10.3389/fcimb.2017.00172. eCollection 2017.

Abstract

Many bacteria regulate the expression of virulence factors via carbon catabolite responsive elements. In Gram-positive bacteria, the predominant mediator of carbon catabolite repression is the catabolite control protein A (CcpA). Hyperglycemia is a widespread disorder that predisposes individuals to an array of symptoms and an increased risk of infections. In hyperglycemic individuals, the bacterium causes serious, life-threatening infections. The importance of CcpA in regulating carbon catabolite repression in suggests it may be important for infections in hyperglycemic individuals. To test this suggestion, hyperglycemic non-obese diabetic (NOD; blood glucose level ≥20 mM) mice were challenged with the mouse pathogenic strain Newman and the isogenic deletion mutant (MST14), and the effects on infectivity were determined. Diabetic NOD mice challenged with the deletion mutant enhanced the symptoms of infection in an acute murine pneumonia model relative to the parental strain. Interestingly, when diabetic NOD mice were used in footpad or catheter infection models, infectivity of the mutant decreased relative to the parental strain. These differences greatly diminished when normoglycemic NOD mice (blood glucose level ≤ 10 mM) were used. These data suggest that CcpA is important for infectivity of in hyperglycemic individuals.

摘要

许多细菌通过碳分解代谢物反应元件来调节毒力因子的表达。在革兰氏阳性菌中,碳分解代谢物阻遏的主要介导因子是碳分解代谢物控制蛋白A(CcpA)。高血糖是一种普遍存在的病症,使个体易出现一系列症状并增加感染风险。在高血糖个体中,这种细菌会引发严重的、危及生命的感染。CcpA在调节[细菌名称未给出]的碳分解代谢物阻遏中的重要性表明,它可能对高血糖个体的感染具有重要意义。为了验证这一推测,用小鼠致病性[细菌名称未给出]菌株纽曼及其同基因[细菌名称未给出]缺失突变体(MST14)对高血糖非肥胖糖尿病(NOD;血糖水平≥20 mM)小鼠进行攻毒,并测定其对感染性的影响。相对于亲本菌株,在急性小鼠肺炎模型中,用[细菌名称未给出]缺失突变体攻毒的糖尿病NOD小鼠感染症状加重。有趣的是,当在足垫或导管感染模型中使用糖尿病NOD小鼠时,[细菌名称未给出]突变体的感染性相对于亲本菌株降低。当使用血糖正常的NOD小鼠(血糖水平≤10 mM)时,这些差异大大减小。这些数据表明,CcpA对高血糖个体中[细菌名称未给出]的感染性很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba9b/5422431/18c3934e6003/fcimb-07-00172-g0001.jpg

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