Enhanced antibiotic multi-resistance in nasal and faecal bacteria after agricultural use of streptomycin
Article first published online: 15 NOV 2012
© 2012 Society for Applied Microbiology and Blackwell Publishing Ltd
Special Issue: Baeza
Volume 15, Issue 1, pages 297–304, January 2013
How to Cite
Scherer, A., Vogt, H.-R., Vilei, E. M., Frey, J. and Perreten, V. (2013), Enhanced antibiotic multi-resistance in nasal and faecal bacteria after agricultural use of streptomycin. Environmental Microbiology, 15: 297–304. doi: 10.1111/1462-2920.12028
- Issue published online: 3 JAN 2013
- Article first published online: 15 NOV 2012
- Accepted manuscript online: 22 OCT 2012 06:02AM EST
- Manuscript Accepted: 12 OCT 2012
- Manuscript Revised: 5 OCT 2012
- Manuscript Received: 12 JUN 2012
- Federal Office for the Environment (FOEN). Grant Number: 09.0012.PJ/I093-0183
- Swiss Expert Committee for Biosafety (SECB/EFBS)
- Federal Veterinary Office (FVO)
Fig. S1. Homology tree of aadA genes with subgroups used as common targets for real-time PCR. Subgroups were generated with sequences with > 85% similarities. The tree was generated using UPGMA [Pairwise (OG: 100%, UG: 0%) Gapcost: 0%] using Bionumerics 5.10 (Applied Maths, Sint-Martens-Latem, Belgium). The number designations of the different aadA genes correspond to their respective entries in GenBank. The letter designations of the different aadA genes were proposed by the present study.
Table S1. Streptomycin resistance and integrase genes used to design primers and probes for the TaqMan real-time PCR.
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