4.7 Article

Coupling CRISPR/Cas9 and Lambda Red Recombineering System for Genome Editing of Salmonella Gallinarum and the Effect of ssaU Knock-Out Mutant on the Virulence of Bacteria

期刊

BIOMEDICINES
卷 10, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines10123028

关键词

CRISPR/Cas9; lambda recombineering; genome editing; type three secretion system; virulent genes; Salmonella Gallinarum; poultry experimental model

资金

  1. International Development Research Centre (IDRC) [109051-002]

向作者/读者索取更多资源

In this study, the ssaU gene encoding type III secretion system was successfully deleted from the genome of poultry-derived Salmonella Gallinarum using CRISPR/Cas9 and lambda recombination systems. This is the first report of CRISPR/Cas9-based genome editing of poultry-derived Salmonella Gallinarum. The mutant strain showed a loss of virulence and potential for live vaccine development against this resistant and pathogenic bacteria.
The poultry industry in developing countries still faces a significant threat from fowl typhoid, a disease caused by Salmonella Gallinarum that has been well contained in more economically developed countries. In addition to the virulence exhibited by large virulence plasmid (85 kb), Salmonella Pathogenicity Island 2 in S. Gallinarum plays a key role in mediating disease through its type III secretion systems (TTSS). The TTSS secrete effector protein across the Salmonella containing vacuoles and mediate the internalization of bacteria by modulating vesicular passage. In this study, candidate virulent ssaU gene (similar to 1 kb) encoding type III secretion system was successfully deleted from indigenously isolated S. Gallinarum genome through homology-directed repair using CRISPR/Cas9 and lambda recombination systems. CRISPR/Cas9-based genome editing of poultry-derived Salmonella Gallinarum has not been previously reported, which might be linked to a lack of efficiency in its genetic tools. This is the first study which demonstrates a complete CRISPR /Cas9-based gene deletion from this bacterial genome. More importantly, a poultry experimental model was employed to assess the virulence potential of this mutant strain (Delta ssaU_SG18) which was unable to produce any mortality in the experimentally challenged birds as compared to the wild type strain. No effect on weight gain was observed whereas bacteria were unable to colonize the intestine and liver in our challenge model. This in vivo loss of virulence in mutant strain provides an excellent functionality of this system to be useful in live vaccine development against this resistant and patho genic bacteria.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据