Comparison of three methods for preparation of bacterial ghosts from avian pathogenic Escherichia coli.

Jian'gang HU; Hongliang Dong; Lixia FU; Jiakun Zuo; Xiaoka WU; Rongsheng MI; Yan Huang; Ke LU; Zhaoguo Chen; Xian'gan Han; Shijun HU

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Comparison of three methods for preparation of bacterial ghosts from avian pathogenic Escherichia coli.

Author: Jian'gang HU ¹ ; Hongliang DONG ² ; Lixia FU ³ ; Jiakun ZUO ² ; Xiaoka WU ² ; Rongsheng MI ² ; Yan HUANG ² ; Ke LU ² ; Zhaoguo CHEN ² ; Xian'gan HAN ² ; Shijun HU ¹
Author Information

1. College of Animal Science, Southwest University, Chongqing 402460, China.
2. Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China.
3. Jiangsu Key Laboratory of Zoonosis, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, Jiangsu, China.
Publication Type:Journal Article
Keywords: avian pathogenic Escherichia coli; bacterial ghost; cell-penetrating peptide; lysis gene E
From: Chinese Journal of Biotechnology 2017;33(12):2009-2016
CountryChina
Language:Chinese
Abstract: Bacterial ghosts are bacterial cell envelopes devoid of cytoplasmic contents while maintaining their cellular morphology, which can be used as a new vaccine and delivery vector. In this study, a clinical isolate of avian pathogenic Escherichia coli (APEC) strain DE17 was used to prepare bacterial ghost through three different ways. The results showed that the cleavage efficiency of DE17 bacterial ghost was 99.9% with the lysis plasmid containing the PhiX174 lysis gene E. Scanning electron microscopy showed that transmembrane tunnels were formed in the middle or both ends of the cell envelope of DE17. Furthermore, the DE17 bacterial ghost was prepared with one of cell penetrating peptides (CPPs) named MAP (KLALKLALKALKAALKLA), which will completely inactivate DE17 (OD₆₀₀=0.1) by 10 μmol/L MAP. The cell envelope showed a gully-like structure and obvious transmembrane tunnels were not found through the SEM. However, the DE17 could not be lysed by importing the lysis plasmid (pBV220-MAP), which was used to express MAP. The present study will benefit for research on bacterial ghost preparation methods and provide a reference for biosafety of bacterial ghost vaccines.