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Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis

Helicobacter pylori is a Gram-negative, microaerophilic bacterium associated with human gastric diseases. Further investigations on virulence genes are still required to clarify the pathogenic mechanism of H. pylori and the heterogeneous problem of infection. In order to develop an efficient and acc...

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Autores principales: Ji, Xiaofei, Wang, Ying, Li, Jiaojiao, Rong, Qianyu, Chen, Xingxing, Zhang, Ying, Liu, Xiaoning, Li, Boqing, Zhao, Huilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712585/
https://www.ncbi.nlm.nih.gov/pubmed/29238332
http://dx.doi.org/10.3389/fmicb.2017.02357
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author Ji, Xiaofei
Wang, Ying
Li, Jiaojiao
Rong, Qianyu
Chen, Xingxing
Zhang, Ying
Liu, Xiaoning
Li, Boqing
Zhao, Huilin
author_facet Ji, Xiaofei
Wang, Ying
Li, Jiaojiao
Rong, Qianyu
Chen, Xingxing
Zhang, Ying
Liu, Xiaoning
Li, Boqing
Zhao, Huilin
author_sort Ji, Xiaofei
collection PubMed
description Helicobacter pylori is a Gram-negative, microaerophilic bacterium associated with human gastric diseases. Further investigations on virulence genes are still required to clarify the pathogenic mechanism of H. pylori and the heterogeneous problem of infection. In order to develop an efficient and accurate method to study gene functions in H. pylori pathogenesis, an unmarked deletion method for both a single gene and a large fragment was established based on the FLP-FRT recombination system. Using this method, the gene hp0788, encoding an outer membrane protein (HofF), was deleted. Deletion of hp0788 did not affect growth or motility of H. pylori, but reduced the adherence of the bacteria to gastric epithelial cells. The apoptosis of GES-1 cells caused by H. pylori infection was also reduced by the defection of hp0788. These suggest that hp0788 takes part in the bacterium-host interaction and plays an important role in H. pylori infection. Furthermore, a large genomic fragment deletion from hp0541 to hp0547 in cag pathogenicity island was also successfully achieved using FLP-FRT method. The innovative application of the FLP-FRT recombination system in H. pylori to construct unmarked deletion would provide a helpful tool for further function research of putative pathogenic genes and contribute to the understanding of H. pylori pathogenesis.
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spelling pubmed-57125852017-12-13 Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis Ji, Xiaofei Wang, Ying Li, Jiaojiao Rong, Qianyu Chen, Xingxing Zhang, Ying Liu, Xiaoning Li, Boqing Zhao, Huilin Front Microbiol Microbiology Helicobacter pylori is a Gram-negative, microaerophilic bacterium associated with human gastric diseases. Further investigations on virulence genes are still required to clarify the pathogenic mechanism of H. pylori and the heterogeneous problem of infection. In order to develop an efficient and accurate method to study gene functions in H. pylori pathogenesis, an unmarked deletion method for both a single gene and a large fragment was established based on the FLP-FRT recombination system. Using this method, the gene hp0788, encoding an outer membrane protein (HofF), was deleted. Deletion of hp0788 did not affect growth or motility of H. pylori, but reduced the adherence of the bacteria to gastric epithelial cells. The apoptosis of GES-1 cells caused by H. pylori infection was also reduced by the defection of hp0788. These suggest that hp0788 takes part in the bacterium-host interaction and plays an important role in H. pylori infection. Furthermore, a large genomic fragment deletion from hp0541 to hp0547 in cag pathogenicity island was also successfully achieved using FLP-FRT method. The innovative application of the FLP-FRT recombination system in H. pylori to construct unmarked deletion would provide a helpful tool for further function research of putative pathogenic genes and contribute to the understanding of H. pylori pathogenesis. Frontiers Media S.A. 2017-11-29 /pmc/articles/PMC5712585/ /pubmed/29238332 http://dx.doi.org/10.3389/fmicb.2017.02357 Text en Copyright © 2017 Ji, Wang, Li, Rong, Chen, Zhang, Liu, Li and Zhao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ji, Xiaofei
Wang, Ying
Li, Jiaojiao
Rong, Qianyu
Chen, Xingxing
Zhang, Ying
Liu, Xiaoning
Li, Boqing
Zhao, Huilin
Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title_full Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title_fullStr Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title_full_unstemmed Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title_short Application of FLP-FRT System to Construct Unmarked Deletion in Helicobacter pylori and Functional Study of Gene hp0788 in Pathogenesis
title_sort application of flp-frt system to construct unmarked deletion in helicobacter pylori and functional study of gene hp0788 in pathogenesis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712585/
https://www.ncbi.nlm.nih.gov/pubmed/29238332
http://dx.doi.org/10.3389/fmicb.2017.02357
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