Zihler, A; Le Blay, G; de Wouters, T; Lacroix, C; Braegger, C; Lehner, A; Tischler, P; Rattei, T; Haechler, H; Stephan, R (2009). In vitro inhibition activity of different bacteriocin-producing E. coli against Salmonella strains isolated from clinical cases. Letters in Applied Microbiology, 49(1):31-38.
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Abstract
Aims: To compare in vitro the inhibitory activity of four bacteriocin producing E. coli to a well-characterized panel of Salmonella strains, recently isolated from clinical cases in Switzerland.
Methods and Results: A panel of 68 non-typhoidal Salmonella strains was characterized by PFGE analysis and susceptibility to antibiotics. The majority of tested strains were genetically different, with 40% resistant to at least one antibiotic. E. coli Mcc24 showed highest in vitro activity against Salmonella (100%, microcin 24), followed by E. coli L1000 (94%, microcin B17), E. coli 53 (49%, colicin H) and E. coli 52 (21%, colicin G) as revealed using a cross-streak activity assay.
Conclusion: E. coli Mcc24, a genetically modified organism producing microcin 24, and E. coli L1000, a natural strain isolated from human feces carrying the mcb-operon for microcin B17-production, were the most effective strains in inhibiting in vitro both antibiotic resistant and sensitive Salmonella isolates.
Significance and Impact of the Study: Due to an increasing prevalence of antibiotic resistant Salmonella strains, alternative strategies to fight these foodborne pathogens are needed. E. coli L1000 appears to be a promising candidate in view of developing biotechnological alternatives to antibiotics against Salmonella infections.
| Item Type: | Journal Article, refereed, original work |
|---|---|
| Communities & Collections: | 05 Vetsuisse Faculty > Institute of Food Safety and Hygiene |
| DDC: | 570 Life sciences; biology 610 Medicine & health |
| Language: | English |
| Date: | 2009 |
| Deposited On: | 15 Jan 2010 17:12 |
| Last Modified: | 23 Nov 2012 17:23 |
| Publisher: | Wiley-Blackwell |
| ISSN: | 0266-8254 |
| Publisher DOI: | 10.1111/j.1472-765X.2009.02614.x |
| PubMed ID: | 19413755 |
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