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与模型中[具体对象]生存相关的遗传决定因素。 (原文中“in the Model”部分缺失关键信息)

Genetic Determinants Associated With Survival of in the Model.

作者信息

Wong Yee-Chin, Abd El Ghany Moataz, Ghazzali Raeece N M, Yap Soon-Joo, Hoh Chee-Choong, Pain Arnab, Nathan Sheila

机构信息

School of Biosciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Malaysia.

Biological and Environmental Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia.

出版信息

Front Microbiol. 2018 May 29;9:1118. doi: 10.3389/fmicb.2018.01118. eCollection 2018.

Abstract

A infection usually leads to reduced survival and fatal syndrome in cystic fibrosis patients. The identification of essential genes for survival is key to designing new anti-infectives therapies. We used the Transposon-Directed Insertion Sequencing (TraDIS) approach to identify genes required for survival in the model infection host, . A J2315 transposon pool of ∼500,000 mutants was used to infect . We identified 178 genes as crucial for survival in the infected nematode. The majority of these genes code for proteins of unknown function, many of which are encoded by the genomic island BcenGI13, while other gene products are involved in nutrient acquisition, general stress responses and LPS -antigen biosynthesis. Deletion of the glycosyltransferase gene and a histone-like nucleoid structuring (H-NS) protein-encoding gene (BCAL0154) reduced bacterial accumulation and attenuated virulence in . Further analysis using quantitative RT-PCR indicated that BCAL0154 modulates pathogenesis via transcriptional regulation of motility-associated genes including , and . This screen has successfully identified genes required for survival within the host-associated environment, many of which are potential targets for developing new antimicrobials.

摘要

A感染通常会导致囊性纤维化患者的存活率降低和出现致命综合征。确定生存必需基因是设计新型抗感染疗法的关键。我们使用转座子定向插入测序(TraDIS)方法来确定在模型感染宿主[具体宿主未给出]中生存所需的基因。一个约有50万个突变体的J2315转座子文库被用于感染[具体宿主未给出]。我们确定了178个基因对于受感染线虫的生存至关重要。这些基因中的大多数编码功能未知的蛋白质,其中许多由基因组岛BcenGI13编码,而其他基因产物则参与营养获取、一般应激反应和LPS -抗原生物合成。糖基转移酶基因[具体基因未给出]和一个编码类组蛋白核oid结构蛋白(H-NS)的基因(BCAL0154)的缺失减少了细菌积累并减弱了在[具体宿主未给出]中的毒力。使用定量RT-PCR的进一步分析表明,BCAL0154通过对包括[具体基因未给出]、[具体基因未给出]和[具体基因未给出]在内的运动相关基因的转录调控来调节[具体病原体未给出]的致病性。该筛选成功地确定了在宿主相关环境中生存所需的基因,其中许多是开发新型抗菌药物的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f677/5987112/603a3047bcbb/fmicb-09-01118-g001.jpg

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