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用溶源化大肠杆菌中的肺炎支原体免疫原保护小鼠免受实验性鼠支原体病感染。

Protection of mice against experimental murine mycoplasmosis by a Mycoplasma pulmonis immunogen in lysogenized Escherichia coli.

作者信息

Lai W C, Bennett M, Gordon B E, Pakes S P

机构信息

Department of Pathology, University of Texas Southwestern Medical Center, Dallas 75235-9037.

出版信息

Vaccine. 1994 Mar;12(4):291-8. doi: 10.1016/0264-410x(94)90091-4.

Abstract

A construct of the Mycoplasma pulmonis (MP) genomic library, using randomly sheared DNA, was cloned in lambda gt11 and transfected into C600 Escherichia coli organisms. Clones of E. coli expressing a fusion protein reactive with anti-MP and monospecific serum were transferred orally or intravenously into Balb/c mice. Expression of the fusion protein was induced by adding isopropyl-beta-D-thiogalactopyranoside to the drinking water. This vaccination protocol led to local and systemic antibody formation, to generation of immune lymphocytes and to protection against large numbers of virulent MP organisms. This approach might be generally successful in preventing infectious disease.

摘要

利用随机剪切的 DNA 构建的肺炎支原体(MP)基因组文库,被克隆到 λgt11 中,并转染到 C600 大肠杆菌中。将表达与抗 MP 及单特异性血清反应的融合蛋白的大肠杆菌克隆,经口服或静脉注射到 Balb/c 小鼠体内。通过在饮用水中添加异丙基-β-D-硫代半乳糖苷来诱导融合蛋白的表达。这种疫苗接种方案导致了局部和全身抗体的形成、免疫淋巴细胞的产生以及对大量有毒力的 MP 生物体的保护作用。这种方法在预防传染病方面可能普遍成功。

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