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使用定制的转录激活样效应物核酸酶敲除线虫致病芽孢杆菌B16中与定殖相关的adp基因。

Knockout of the adp gene related with colonization in Bacillus nematocida B16 using customized transcription activator-like effectors nucleases.

作者信息

Niu Qiuhong, Zheng Haoying, Zhang Lin, Qin Fujun, Facemire Loryn, Zhang Guo, Cao Feng, Zhang Ke-Qin, Huang Xiaowei, Yang Jianwei, He Lei, Liu Chanjuan

机构信息

Department of Life Science and Biotechnology, Nanyang Normal University, Nanyang, Henan, 473061, China.

Laboratory for Conservation and Utilization of Bio-Resources, Key Laboratory for Microbial Resources of the Ministry of Education, Yunnan University, Kunming, 650091, China.

出版信息

Microb Biotechnol. 2015 Jul;8(4):681-92. doi: 10.1111/1751-7915.12282. Epub 2015 Apr 24.

Abstract

Bacillus nematocida B16 is able to dominate in the intestines of the worm Caenorhabditis elegans in 'Trojan horse' pathogenic mechanism. The adp is one candidate gene which potentially play a vital role in the colonization from our previous random mutagenesis screening results. To analyse the functional role of this gene, we constructed the adp knockout mutant through customized transcription activator-like effectors nucleases (TALEN), which has been successfully used in yeasts, nematodes, zebrafish and human pluripotent cells. Here, we first time report this knockout method in bacteria on this paper. Bioassay experiments demonstrated that the adp knockout mutant of B16 showed considerably lower colonization activity, reduced numbers of intestines and less than 80% nematocidal activity compared with the wild-type strain when infected for 48 h. However, no obvious change on proteolytic activity was observed in the mutant. Conversely, the complementation of adp gene restored most of the above deficient phenotypes. These results indicated that the adp gene was involved in surface adhesion and played a comparatively important role in colonizing host nematodes. Moreover, TALENs successfully disrupt target genes in bacteria.

摘要

杀线虫芽孢杆菌B16能够通过“特洛伊木马”致病机制在秀丽隐杆线虫肠道中占据主导地位。根据我们之前的随机诱变筛选结果,adp是一个可能在定殖过程中发挥关键作用的候选基因。为了分析该基因的功能作用,我们通过定制的转录激活样效应核酸酶(TALEN)构建了adp基因敲除突变体,TALEN已成功应用于酵母、线虫、斑马鱼和人类多能细胞。在此,我们首次在本文中报道了在细菌中的这种敲除方法。生物测定实验表明,与野生型菌株相比,B16的adp基因敲除突变体在感染48小时后,定殖活性显著降低,肠道数量减少,杀线虫活性降低至80%以下。然而,在该突变体中未观察到明显的蛋白水解活性变化。相反,adp基因的互补恢复了上述大部分缺陷表型。这些结果表明,adp基因参与表面黏附,并且在定殖宿主线虫中发挥了相对重要的作用。此外,TALEN成功地在细菌中破坏了靶基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f826/4476823/2685bb9a6aff/mbt20008-0681-f1.jpg

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