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荷斯坦弗里森奶牛不同病理形式副结核病的蛋白质组学血清分析揭示了急性期反应和脂代谢的变化。

Proteomic Serum Profiling of Holstein Friesian Cows with Different Pathological Forms of Bovine Paratuberculosis Reveals Changes in the Acute-Phase Response and Lipid Metabolism.

机构信息

Center for Animal Biotechnology, Servicio Regional de Investigación y Desarrollo Agroalimentario [SERIDA], 33394 Deva, Asturias, Spain.

Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad de León, 24071 León, Spain.

出版信息

J Proteome Res. 2024 Aug 2;23(8):2762-2779. doi: 10.1021/acs.jproteome.3c00244. Epub 2023 Oct 20.

DOI:10.1021/acs.jproteome.3c00244
PMID:37863471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11301775/
Abstract

The lack of sensitive diagnostic methods to detect subsp. (Map) subclinical infections has hindered the control of paratuberculosis (PTB). The serum proteomic profiles of naturally infected cows presenting focal and diffuse pathological forms of PTB and negative controls ( = 4 per group) were analyzed using TMT-6plex quantitative proteomics. Focal and diffuse are the most frequent pathological forms in subclinical and clinical stages of PTB, respectively. One (focal versus (vs.) control), eight (diffuse vs. control), and four (focal vs. diffuse) differentially abundant (DA) proteins (-value < 0.05) were identified. Ingenuity pathway analysis of the DA proteins revealed changes in the acute-phase response and lipid metabolism. Six candidate biomarkers were selected for further validation by specific ELISA using serum from animals with focal, multifocal, and diffuse PTB-associated lesions ( = 108) and controls ( = 56). Overall, the trends of the serum expression levels of the selected proteins were consistent with the proteomic results. Alpha-1-acid glycoprotein (ORM1)-based ELISA, insulin-like growth factor-binding protein 2 (IGFBP2)-based ELISA, and the anti-Map ELISA had the best diagnostic performance for detection of animals with focal, multifocal, and diffuse lesions, respectively. Our findings identify potential biomarkers that improve diagnostic sensitivity of PTB and help to elucidate the mechanisms involved in PTB pathogenesis.

摘要

缺乏敏感的诊断方法来检测(Map)亚临床感染,这阻碍了副结核病(PTB)的控制。使用 TMT-6plex 定量蛋白质组学分析了表现为局灶性和弥漫性 PTB 以及阴性对照(每组 4 个)的自然感染奶牛的血清蛋白质组图谱。局灶性和弥漫性是 PTB 亚临床和临床阶段最常见的病理形式。鉴定出一个(局灶性与(vs.)对照)、八个(弥漫性与对照)和四个(局灶性与弥漫性)差异丰度(DA)蛋白(-值<0.05)。DA 蛋白的 IPA 分析显示急性期反应和脂质代谢发生变化。使用来自具有局灶性、多灶性和弥漫性 PTB 相关病变的动物(=108)和对照(=56)的血清通过特异性 ELISA 选择了 6 种候选生物标志物进行进一步验证。总体而言,选定蛋白质的血清表达水平趋势与蛋白质组学结果一致。基于α-1-酸性糖蛋白(ORM1)的 ELISA、基于胰岛素样生长因子结合蛋白 2(IGFBP2)的 ELISA 和抗 Map ELISA 分别对检测具有局灶性、多灶性和弥漫性病变的动物具有最佳的诊断性能。我们的发现确定了潜在的生物标志物,可提高 PTB 的诊断敏感性,并有助于阐明 PTB 发病机制中涉及的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/ff4cab1224e6/pr3c00244_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/8f6682bee20e/pr3c00244_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/33004cf160e5/pr3c00244_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/cea0c0d4c06a/pr3c00244_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/a3a86d092dca/pr3c00244_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/2516d703fc47/pr3c00244_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/ff4cab1224e6/pr3c00244_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/8f6682bee20e/pr3c00244_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/33004cf160e5/pr3c00244_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/cea0c0d4c06a/pr3c00244_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/a3a86d092dca/pr3c00244_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/2516d703fc47/pr3c00244_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5551/11301775/ff4cab1224e6/pr3c00244_0006.jpg

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