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自转运蛋白BpaB在气溶胶感染模型中对鼻疽伯克霍尔德菌的毒力有贡献。

The Autotransporter BpaB Contributes to the Virulence of Burkholderia mallei in an Aerosol Model of Infection.

作者信息

Zimmerman Shawn M, Michel Frank, Hogan Robert J, Lafontaine Eric R

机构信息

Department of Infectious Diseases, University of Georgia College of Veterinary Medicine, Athens, Georgia, United States of America.

Department of Veterinary Biosciences and Diagnostic Imaging, University of Georgia College of Veterinary Medicine, Athens, GA, United States of America.

出版信息

PLoS One. 2015 May 20;10(5):e0126437. doi: 10.1371/journal.pone.0126437. eCollection 2015.

Abstract

Burkholderia mallei is a highly pathogenic bacterium that causes the zoonosis glanders. Previous studies indicated that the genome of the organism contains eight genes specifying autotransporter proteins, which are important virulence factors of Gram-negative bacteria. In the present study, we report the characterization of one of these autotransporters, BpaB. Database searches identified the bpaB gene in ten B. mallei isolates and the predicted proteins were 99-100% identical. Comparative sequence analyses indicate that the gene product is a trimeric autotransporter of 1,090 amino acids with a predicted molecular weight of 105-kDa. Consistent with this finding, we discovered that recombinant bacteria expressing bpaB produce a protein of ≥ 300-kDa on their surface that is reactive with a BpaB-specific monoclonal antibody. Analysis of sera from mice infected with B. mallei indicated that animals produce antibodies against BpaB during the course of disease, thus establishing production of the autotransporter in vivo. To gain insight on its role in virulence, we inactivated the bpaB gene of B. mallei strain ATCC 23344 and determined the median lethal dose of the mutant in a mouse model of aerosol infection. These experiments revealed that the bpaB mutation attenuates virulence 8-14 fold. Using a crystal violet-based assay, we also discovered that constitutive production of BpaB on the surface of B. mallei promotes biofilm formation. To our knowledge, this is the first report of a biofilm factor for this organism.

摘要

鼻疽伯克霍尔德菌是一种引起人畜共患病鼻疽的高致病性细菌。先前的研究表明,该生物体的基因组包含八个指定自转运蛋白的基因,这些蛋白是革兰氏阴性菌的重要毒力因子。在本研究中,我们报告了其中一种自转运蛋白BpaB的特性。数据库搜索在十种鼻疽伯克霍尔德菌分离株中鉴定出bpaB基因,预测的蛋白质具有99%-100%的同一性。比较序列分析表明,该基因产物是一种三聚体自转运蛋白,含有1090个氨基酸,预测分子量为105 kDa。与此发现一致,我们发现表达bpaB的重组细菌在其表面产生一种分子量≥300 kDa的蛋白质,该蛋白质可与BpaB特异性单克隆抗体发生反应。对感染鼻疽伯克霍尔德菌的小鼠血清分析表明,动物在疾病过程中产生针对BpaB的抗体,从而证实了该自转运蛋白在体内的产生。为了深入了解其在毒力中的作用,我们使鼻疽伯克霍尔德菌菌株ATCC 23344的bpaB基因失活,并在气溶胶感染小鼠模型中测定突变体的半数致死剂量。这些实验表明,bpaB突变使毒力减弱了8-14倍。使用基于结晶紫的检测方法,我们还发现鼻疽伯克霍尔德菌表面组成型产生的BpaB促进生物膜形成。据我们所知,这是关于该生物体生物膜因子的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6530/4438868/25801230f3cc/pone.0126437.g001.jpg

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