Bacteriophage therapy: a novel method of lytic phage delivery

作者: Ratree Platt

DOI: 10.31274/RTD-180813-15276

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摘要: The widespread emergence of muki-antibiotic resistant bacteria has increased the need for alternatives to conventional antibiotic therapy. Accordingly, a significant amount effort been made investigate potential use bacteriophages as prophylactic and therapeutic agents bacterial infections. In this study, molecular biological techniques were applied construct iysogen lytic bacteriophage X in an attempt combat with multi-antibiotic by novel method phage delivery. To accomplish goal, two plasmid-based site-specific recombination (SSR) systems integration recovery DNA constructs from Escherichia coli Salnumella typhimurium chromosomes developed. are mediated SSR machineries X. £1 P22 S. typhimurium. These utilize plasmid vectors conditional replicating origin replication provide stable chromosomal genes at specific attachment sites without disruption any host gene or selection. E. contains both bacteriophages. When consecutively, different can be integrated locations. plasmids also completely excised recovered fi'om observe genetic changes, e.g. sequencing. Both very applicable construction strains well live recombinant vaccines expressing foreign interest. Iysogen X, applied. A mutant {ct) was marked cassette

参考文章(47)
M Dabrowski, B Weber-Dabrowska, M Cisło, A Woytoń, Bacteriophage treatment of suppurative skin infections. Archivum Immunologiae Et Therapiae Experimentalis. ,vol. 35, pp. 175- 183 ,(1987)
B Weber-Dabrowska, A Kucharewicz-Krukowska, M Dabrowski, S Slopek, Results of bacteriophage treatment of suppurative bacterial infections in the years 1981-1986. Archivum Immunologiae Et Therapiae Experimentalis. ,vol. 35, pp. 569- 583 ,(1987)
B Weber-Dabrowska, A Kucharewicz-Krukowska, R Bisikiewicz, M Dabrowski, I Durlakowa, S Slopek, Results of bacteriophage treatment of suppurative bacterial infections. II. Detailed evaluation of the results. Archivum Immunologiae Et Therapiae Experimentalis. ,vol. 31, pp. 293- 327 ,(1983)
Noreen E. Murray, [12] Special uses of γ phage for molecular cloning Methods in Enzymology. ,vol. 204, pp. 280- 301 ,(1991) , 10.1016/0076-6879(91)04014-F
L. W. Enquist, Thomas J. Silhavy, Michael L. Berman, Experiments With Gene Fusions ,(1984)
Eun Hee Cho, Chan-Eun Nam, Renato Alcaraz, Jeffrey F. Gardner, Site-Specific Recombination of Bacteriophage P22 Does Not Require Integration Host Factor Journal of Bacteriology. ,vol. 181, pp. 4245- 4249 ,(1999) , 10.1128/JB.181.14.4245-4249.1999
D F Lindsey, C Martínez, J R Walker, Physical map location of the Escherichia coli attachment site for the P22 prophage (attP22). Journal of Bacteriology. ,vol. 174, pp. 3834- 3835 ,(1992) , 10.1128/JB.174.11.3834-3835.1992
K Abremski, S Gottesman, Purification of the bacteriophage lambda xis gene product required for lambda excisive recombination. Journal of Biological Chemistry. ,vol. 257, pp. 9658- 9662 ,(1982) , 10.1016/S0021-9258(18)34123-1
Jeffrey H. Miller, A short course in bacterial genetics : a laboratory manual and handbook for Escherichia coli and related bacteria Published in <b>1992</b> in New York NY) by Cold Spring Harbor laboratory press. ,(1992)