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Applied and Environmental Microbiology, September 2006, p. 5908-5914, Vol. 72, No. 9
0099-2240/06/$08.00+0 doi:10.1128/AEM.01135-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Departments of Molecular Microbiology, Genetics, and Medicine, School of Medicine, Washington University, St. Louis, Missouri 63110
Received 16 May 2006/ Accepted 25 June 2006
Many Helicobacter pylori genetic studies would benefit from an ability to move DNA sequences easily between strains by transformation and homologous recombination, without needing to leave a conventional drug resistance determinant at the targeted locus. Presented here is a two-gene cassette that can be selected both (i) against, due to a Campylobacter jejuni rpsL gene (dominant streptomycin susceptibility in cells also carrying an rpsL-strr allele), and (ii) for, due to an erm gene (erythromycin resistance). This rpsL,erm cassette's utility was assessed by using it to replace four gene loci (mdaB, frxA, fur, and nikR) in four streptomycin-resistant [Strr] strain backgrounds (derivatives of 26695, SS1, X47, and G27MA). The resultant 16 strains (phenotypically erythromycin resistant [Ermr] and Strs) were each transformed with wild-type genomic DNAs, and Strr derivatives were selected. The desired Erms Strr isolates were obtained at frequencies that ranged from 17 to 96% among Strr transformants, with the Erms yield apparently depending on the strain background and genome location of the targeted locus. The ease of isolating unmarked transformants described here should be valuable for many H. pylori molecular genetic and evolutionary analyses.
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