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BBB07 有助于但并非是小鼠感染所必需的。

BBB07 contributes to, but is not essential for, infection in mice.

机构信息

Department of Medicine, Division of Infectious Diseases, Medical College of Wisconsin, Milwaukee, WI, USA.

Present address: Cardiovascular Research Foundation, New York, NY, USA.

出版信息

Microbiology (Reading). 2020 Oct;166(10):988-994. doi: 10.1099/mic.0.000972.

Abstract

a causative agent of Lyme disease, encodes a protein BBB07 on the genomic plasmid cp26. BBB07 was identified as a candidate integrin ligand based on the presence of an RGD tripeptide motif, which is present in a number of mammalian ligands for β and β integrins . Previous work demonstrated that BBB07 in recombinant form binds to β integrins and induces inflammatory responses in synovial cells in culture. Several transposon mutants in were attenuated in an screen of the transposon library in mice. We therefore tested individual transposon mutant clones in single-strain infections in mice and found that they were attenuated in terms of ID but did not have significantly reduced tissue burdens in mice. Based on data presented here we conclude that BBB07 is not essential for, but does contribute to, infectivity in mice.

摘要

伯氏疏螺旋体病的病原体,在基因组质粒 cp26 上编码 BBB07 蛋白。基于 RGD 三肽基序的存在,BBB07 被鉴定为候选整合素配体,该基序存在于许多哺乳动物的β和β整合素配体中。先前的工作表明,重组形式的 BBB07 与β整合素结合,并在体外培养的滑膜细胞中诱导炎症反应。在小鼠中转座子文库的 筛选中, 中的几种转座子突变体失活。因此,我们在小鼠的单菌株感染中测试了单个转座子突变克隆,发现它们在 ID 方面失活,但在小鼠中的组织负担没有明显降低。基于这里呈现的数据,我们得出结论,BBB07 对于 在小鼠中的感染不是必需的,但确实有助于其感染性。

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