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艰难梭菌在猪回肠结扎模型中的时间差异蛋白质组学。

Temporal differential proteomes of Clostridium difficile in the pig ileal-ligated loop model.

机构信息

Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.

出版信息

PLoS One. 2012;7(9):e45608. doi: 10.1371/journal.pone.0045608. Epub 2012 Sep 18.

Abstract

The impact of Clostridium difficile infection (CDI) on healthcare is becoming increasingly recognized as it represents a major cause of nosocomial diarrhea. A rising number of CDI cases and outbreaks have been reported worldwide. Here, we developed the pig ileal-ligated loop model for semi-quantitative analysis comparing temporal differential proteomes in C. difficile following in vivo incubation with in vitro growth using isobaric tags for relative and absolute quantification (iTRAQ). Proteins retrieved from the in vitro cultures and the loop contents after 4, 8, and 12 h in vivo incubation were subjected to in-solution digestion, iTRAQ labeling, two-dimensional liquid chromatography/tandem mass spectrometry and statistical analyses. From a total of 1152 distinct proteins identified in this study, 705 proteins were available for quantitative measures at all time points in both biological and technical replicates; 109 proteins were found to be differentially expressed. With analysis of clusters of orthologous group and protein-protein network interactions, we identified the proteins that might play roles in adaptive responses to the host environment, hence enhancing pathogenicity during CDI. This report represents the quantitative proteomic analysis of C. difficile that demonstrates time-dependent protein expression changes under conditions that mimic in vivo infection and identifies potential candidates for diagnostic or therapeutic measures.

摘要

艰难梭菌感染(CDI)对医疗保健的影响正日益受到关注,因为它是医院获得性腹泻的主要原因之一。世界各地报告的 CDI 病例和疫情不断增加。在这里,我们使用相对和绝对定量同位素标记(iTRAQ),为体内孵育与体外生长的比较,开发了猪回肠结扎环模型,用于半定量分析艰难梭菌的时间差异蛋白质组。从体外培养物和体内孵育 4、8 和 12 小时后的环内容物中提取的蛋白质进行溶液消化、iTRAQ 标记、二维液相色谱/串联质谱和统计分析。在本研究中鉴定的 1152 种不同蛋白质中,有 705 种蛋白质在所有时间点的生物学和技术重复中均可进行定量测量;发现 109 种蛋白质表达差异。通过同源基因簇和蛋白质-蛋白质网络相互作用分析,我们鉴定了可能在适应宿主环境中发挥作用的蛋白质,从而增强了 CDI 期间的致病性。本报告代表了艰难梭菌的定量蛋白质组学分析,证明了在模拟体内感染的条件下,蛋白质表达随时间的变化,并确定了用于诊断或治疗措施的潜在候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea26/3445491/38e33f9f3b97/pone.0045608.g001.jpg

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