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副结核分枝杆菌(约翰氏病的病原体)的发病机制、分子遗传学和基因组学

Pathogenesis, Molecular Genetics, and Genomics of subsp. , the Etiologic Agent of Johne's Disease.

作者信息

Rathnaiah Govardhan, Zinniel Denise K, Bannantine John P, Stabel Judith R, Gröhn Yrjö T, Collins Michael T, Barletta Raúl G

机构信息

School of Veterinary Medicine and Biomedical Sciences, University of Nebraska, Lincoln, NE, United States.

Infectious Bacterial Diseases, National Animal Disease Center, USDA-ARS, Ames, IA, United States.

出版信息

Front Vet Sci. 2017 Nov 6;4:187. doi: 10.3389/fvets.2017.00187. eCollection 2017.

Abstract

subsp. (MAP) is the etiologic agent of Johne's disease in ruminants causing chronic diarrhea, malnutrition, and muscular wasting. Neonates and young animals are infected primarily by the fecal-oral route. MAP attaches to, translocates the intestinal mucosa, and is phagocytosed by macrophages. The ensuing host cellular immune response leads to granulomatous enteritis characterized by a thick and corrugated intestinal wall. We review various tissue culture systems, ileal loops, and mice, goats, and cattle used to study MAP pathogenesis. MAP can be detected in clinical samples by microscopy, culturing, PCR, and an enzyme-linked immunosorbent assay. There are commercial vaccines that reduce clinical disease and shedding, unfortunately, their efficacies are limited and may not engender long-term protective immunity. Moreover, the potential linkage with Crohn's disease and other human diseases makes MAP a concern as a zoonotic pathogen. Potential therapies with anti-mycobacterial agents are also discussed. The completion of the MAP K-10 genome sequence has greatly improved our understanding of MAP pathogenesis. The analysis of this sequence has identified a wide range of gene functions involved in virulence, lipid metabolism, transcriptional regulation, and main metabolic pathways. We also review the transposons utilized to generate random transposon mutant libraries and the recent advances in the post-genomic era. This includes the generation and characterization of allelic exchange mutants, transcriptomic analysis, transposon mutant banks analysis, new efforts to generate comprehensive mutant libraries, and the application of transposon site hybridization mutagenesis and transposon sequencing for global analysis of the MAP genome. Further analysis of candidate vaccine strains development is also provided with critical discussions on their benefits and shortcomings, and strategies to develop a highly efficacious live-attenuated vaccine capable of differentiating infected from vaccinated animals.

摘要

亚种(MAP)是反刍动物约翰氏病的病原体,可导致慢性腹泻、营养不良和肌肉萎缩。新生动物和幼龄动物主要通过粪-口途径感染。MAP附着于肠黏膜,穿过肠黏膜,并被巨噬细胞吞噬。随后的宿主细胞免疫反应导致肉芽肿性肠炎,其特征为肠壁增厚且呈波纹状。我们综述了用于研究MAP致病机制的各种组织培养系统、回肠袢以及小鼠、山羊和牛。可通过显微镜检查、培养、聚合酶链反应(PCR)和酶联免疫吸附测定在临床样本中检测到MAP。有商业疫苗可减少临床疾病和病原体排出,遗憾的是,其效果有限,可能无法产生长期保护性免疫。此外,MAP与克罗恩病和其他人类疾病的潜在关联使其成为一种令人担忧的人畜共患病原体。还讨论了抗分枝杆菌药物的潜在治疗方法。MAP K-10基因组序列的完成极大地增进了我们对MAP致病机制的理解。对该序列的分析确定了一系列参与毒力、脂质代谢、转录调控和主要代谢途径的基因功能。我们还综述了用于生成随机转座子突变文库的转座子以及后基因组时代的最新进展。这包括等位基因交换突变体的产生和表征、转录组分析、转座子突变库分析、生成全面突变文库的新努力,以及转座子位点杂交诱变和转座子测序在MAP基因组全局分析中的应用。还对候选疫苗株的开发进行了进一步分析,对其优缺点进行了批判性讨论,并探讨了开发一种能够区分感染动物和接种动物的高效减毒活疫苗的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7381/5681481/baa8329d62cf/fvets-04-00187-g001.jpg

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