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http://dx.doi.org/10.4014/jmb.1503.03083

Curing Both Virulent Mega-Plasmids from Bacillus anthracis Wild-Type Strain A16 Simultaneously Using Plasmid Incompatibility  

Wang, Dongshu (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Gao, Zhiqi (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Wang, Huagui (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Feng, Erling (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Zhu, Li (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Liu, Xiankai (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Wang, Hengliang (State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Biotechnology)
Publication Information
Journal of Microbiology and Biotechnology / v.25, no.10, 2015 , pp. 1614-1620 More about this Journal
Abstract
Plasmid-cured derivative strains of Bacillus anthracis are frequently used in laboratory studies. Plasmid incompatibility, which does not increase the risk of chromosomal mutation, is a useful method for plasmid curing. However, in bacteria containing multiple plasmids, it often requires the sequential introduction of multiple, specific incompatibility plasmids. This lengthy process renders the traditional plasmid incompatibility method inefficient and mutation-prone. In this study, we successfully cured plasmids pXO1 and pXO2 from B. anthracis A16 simultaneously using only one recombinant incompatible plasmid, pKORT, to obtain a plasmid-free strain, designated A16DD. This method may also be useful for the simultaneous, one-step curing of multiple plasmids from other bacteria, including Bacillus thuringiensis and Yersinia pestis.
Keywords
Bacillus anthracis; pXO1; pXO2; plasmid curing; plasmid incompatibility;
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1 Liu X, Wang D, Wang H, Feng E, Zhu L, Wang H. 2012. Curing of plasmid pXO1 from Bacillus anthracis using plasmid incompatibility. PLoS ONE 7: 230-230.
2 Novick RP. 1987. Plasmid incompatibility. Microbiol. Rev. 51: 381-395.
3 Park SH. 2007. Differential analysis of Bacillus anthracis after pX01 plasmid curing and comprehensive data on Bacillus anthracis infection in macrophages and glial cells. Proteomics 7: 3743-3758.   DOI
4 Pomerantsev AP, Camp A, Leppla SH. 2009. A new minimal replicon of Bacillus anthracis plasmid pXO1. J. Bacteriol. 19: 6192.   DOI
5 Shatalin KY, Neyfakh AA. 2005. Efficient gene inactivation in Bacillus anthracis. FEMS Microbiol. Lett. 245: 315-319.   DOI
6 Tinsley E, Naqvi A, Bourgogne A, Koehler TM, Khan SA. 2004. Isolation of a minireplicon of the virulence plasmid pXO2 of Bacillus anthracis and characterization of the plasmid-encoded RepS replication protein. J. Bacteriol. 186: 2717-2723.   DOI
7 Wang H, Liu X, Feng E, Zhu L, Wang D, Liao X, Wang H. 2011. Curing the plasmid pXO2 from Bacillus anthracis A16 using plasmid incompatibility. Curr. Microbiol. 62: 703-709.   DOI
8 Smith K, Youngman P. 1992. Use of a new integrational vector to investigate compartment-specific expression of the Bacillus subtilis spoIIM gene. Biochimie 74: 705-711.   DOI
9 Spengler G, Molnár A, Schelz Z, Amaral L, Sharples D, Molnár J. 2006. The mechanism of plasmid curing in bacteria. Curr. Drug Targets 7: 823-841.   DOI
10 Green BD. 1984. Demonstration of a capsule plasmid in Bacillus anthracis. Infect. Immun. 49: 291-297.
11 Kittell BL, Helinski DR. 1993. Plasmid incompatibility and replication control, pp. 223-242. Bacterial Conjugation. Springer.