应用结核分枝杆菌蛋白阵列技术鉴定牛约翰氏病血清反应性抗原。

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-07-05 Print Date: 2017-07-01 DOI:10.1128/CVI.00081-17
John P Bannantine, Joseph J Campo, Lingling Li, Arlo Randall, Jozelyn Pablo, Craig A Praul, Juan Antonio Raygoza Garay, Judith R Stabel, Vivek Kapur
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引用次数: 9

摘要

约翰氏病是一种由鸟分枝杆菌亚种副结核引起的慢性胃肠道炎症性疾病,在全世界的奶牛和其他反刍动物中流行,使用传统的血清学方法诊断仍然是一个挑战。鉴于禽支原体亚种之间密切的系统发育关系。在这里,我们应用全蛋白质组结核分枝杆菌蛋白阵列来鉴定血清反应性和诊断性禽分枝杆菌亚种。副结核抗原。禽分枝杆菌亚种同源蛋白氨基酸鉴定水平的基因组尺度两两分析。副结核和结核分枝杆菌的同源性平均为62%,超过一半的同源蛋白的同源性大于75%。禽分枝杆菌亚种血清检测结核分枝杆菌蛋白阵列分析。副结核感染的牛显示出与729个结核分枝杆菌蛋白结合的抗体,其中58%与鸟分枝杆菌亚种具有≥70%的同源性。副结核直接同源。结果显示,前40个血清反应性结核分枝杆菌抗原中,仅有4个与先前报道的禽分枝杆菌亚型同源。副结核抗原,揭示了大量以前未被识别的候选诊断抗原的存在。酶联免疫吸附试验(ELISA)检测20株鸟分枝杆菌亚群。副结核重组蛋白,代表反应性和非反应性结核分枝杆菌同源物,进一步证实结核分枝杆菌阵列作为筛选约翰氏病诊断候选抗原的工具具有实用价值。另外,对美国各地奶牛的现场血清样本进行ELISA检测发现,MAP2942c对约翰氏病阳性样本具有最强的血清反应性。总的来说,我们的研究大大增加了候选鸟分枝杆菌亚种的数量。副结核蛋白在下一代合理设计的约翰氏病诊断分析中具有潜在的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.

Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.

Identification of Novel Seroreactive Antigens in Johne's Disease Cattle by Using the Mycobacterium tuberculosis Protein Array.

Johne's disease, a chronic gastrointestinal inflammatory disease caused by Mycobacterium avium subspecies paratuberculosis, is endemic in dairy cattle and other ruminants worldwide and remains a challenge to diagnose using traditional serological methods. Given the close phylogenetic relationship between M. avium subsp. paratuberculosis and the human pathogen Mycobacterium tuberculosis, here, we applied a whole-proteome M. tuberculosis protein array to identify seroreactive and diagnostic M. avium subsp. paratuberculosis antigens. A genome-scale pairwise analysis of amino acid identity levels between orthologous proteins in M. avium subsp. paratuberculosis and M. tuberculosis showed an average of 62% identity, with more than half the orthologous proteins sharing >75% identity. Analysis of the M. tuberculosis protein array probed with sera from M. avium subsp. paratuberculosis-infected cattle showed antibody binding to 729 M. tuberculosis proteins, with 58% of them having ≥70% identity to M. avium subsp. paratuberculosis orthologs. The results showed that only 4 of the top 40 seroreactive M. tuberculosis antigens were orthologs of previously reported M. avium subsp. paratuberculosis antigens, revealing the existence of a large number of previously unrecognized candidate diagnostic antigens. Enzyme-linked immunosorbent assay (ELISA) testing of 20 M. avium subsp. paratuberculosis recombinant proteins, representing reactive and nonreactive M. tuberculosis orthologs, further confirmed that the M. tuberculosis array has utility as a screening tool for identifying candidate antigens for Johne's disease diagnostics. Additional ELISA testing of field serum samples collected from dairy herds around the United States revealed that MAP2942c had the strongest seroreactivity with Johne's disease-positive samples. Collectively, our studies have considerably expanded the number of candidate M. avium subsp. paratuberculosis proteins with potential utility in the next generation of rationally designed Johne's disease diagnostic assays.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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