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对致乳腺炎大肠杆菌转录反应的荟萃分析

Meta-Analysis of Transcriptional Responses to Mastitis-Causing Escherichia coli.

作者信息

Younis Sidra, Javed Qamar, Blumenberg Miroslav

机构信息

The R. O. Perelman Department of Dermatology, Department of Biochemistry and Molecular Pharmacology, NYU Langone Medical Center, New York, United States of America.

Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.

出版信息

PLoS One. 2016 Mar 2;11(3):e0148562. doi: 10.1371/journal.pone.0148562. eCollection 2016.

Abstract

Bovine mastitis is a widespread disease in dairy cows, and is often caused by bacterial mammary gland infection. Mastitis causes reduced milk production and leads to excessive use of antibiotics. We present meta-analysis of transcriptional profiles of bovine mastitis from 10 studies and 307 microarrays, allowing identification of much larger sets of affected genes than any individual study. Combining multiple studies provides insight into the molecular effects of Escherichia coli infection in vivo and uncovers differences between the consequences of E. coli vs. Staphylococcus aureus infection of primary mammary epithelial cells (PMECs). In udders, live E. coli elicits inflammatory and immune defenses through numerous cytokines and chemokines. Importantly, E. coli infection causes downregulation of genes encoding lipid biosynthesis enzymes that are involved in milk production. Additionally, host metabolism is generally suppressed. Finally, defensins and bacteria-recognition genes are upregulated, while the expression of the extracellular matrix protein transcripts is silenced. In PMECs, heat-inactivated E. coli elicits expression of ribosomal, cytoskeletal and angiogenic signaling genes, and causes suppression of the cell cycle and energy production genes. We hypothesize that heat-inactivated E. coli may have prophylactic effects against mastitis. Heat-inactivated S. aureus promotes stronger inflammatory and immune defenses than E. coli. Lipopolysaccharide by itself induces MHC antigen presentation components, an effect not seen in response to E. coli bacteria. These results provide the basis for strategies to prevent and treat mastitis and may lead to the reduction in the use of antibiotics.

摘要

牛乳腺炎是奶牛中一种广泛存在的疾病,通常由细菌感染乳腺引起。乳腺炎会导致产奶量下降,并导致抗生素的过度使用。我们对来自10项研究和307个微阵列的牛乳腺炎转录谱进行了荟萃分析,从而能够鉴定出比任何单个研究中受影响基因数量多得多的基因集。整合多项研究有助于深入了解大肠杆菌体内感染的分子效应,并揭示大肠杆菌与金黄色葡萄球菌感染原代乳腺上皮细胞(PMECs)后果之间的差异。在乳房中,活的大肠杆菌通过多种细胞因子和趋化因子引发炎症和免疫防御。重要的是,大肠杆菌感染会导致参与产奶的脂质生物合成酶编码基因的下调。此外,宿主代谢通常会受到抑制。最后,防御素和细菌识别基因上调,而细胞外基质蛋白转录本的表达则沉默。在PMECs中,热灭活的大肠杆菌会引发核糖体、细胞骨架和血管生成信号基因的表达,并导致细胞周期和能量产生基因的抑制。我们假设热灭活的大肠杆菌可能对乳腺炎具有预防作用。热灭活的金黄色葡萄球菌比大肠杆菌能引发更强的炎症和免疫防御。脂多糖本身会诱导MHC抗原呈递成分,而对大肠杆菌的反应中未观察到这种效应。这些结果为预防和治疗乳腺炎的策略提供了依据,并可能导致抗生素使用的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b14/4775050/082603824e89/pone.0148562.g001.jpg

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