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The O-Antigen Epitope Governs Susceptibility to Colistin in Salmonella enterica
Vito Ricci1, Dexian Zhang1,2, Christopher Teale3
1Antimicrobials Research Group, Institute of Microbiology and Infection, College of Medical and Dental Science, University of Birmingham, Birmingham, United Kingdom.
Abstract:
Group D and group B Salmonella enterica serovars differ in their susceptibility to colistin with the former frequently intrinsically resistant (MIC > 2 μg/ml); however, the mechanism has not been described. Here, we show that the O-antigen epitope in group D Salmonella governs the levels of colistin susceptibility. Substitution of the rfbJ gene in a group B Salmonella with the rfbSE genes from a group D Salmonella conferred a decrease in susceptibility to colistin. The presence of dideoxyhexose, abequose, and the deoxymannose, tyvelose, differentiate the Salmonella group B and group D O antigens, respectively. We hypothesize that the subtle difference between abequose and tyvelose hinders the colistin molecule from reaching its target. Whole-genome sequencing also revealed that increased colistin susceptibility in a group D Salmonella veterinary isolate was due to a defect in the O-antigen polymerase protein, Rfc. This study shows that two different mechanisms that influence the presence and composition of O antigens affect colistin susceptibility in Salmonella entericaIMPORTANCE Some serovars of Salmonella, namely, those belonging to group D, appear to show a degree of intrinsic resistance to colistin. This observed intrinsic colistin resistance is of concern since this last-resort drug might no longer be effective for treating severe human infections with the most common Salmonella serovar, Salmonella enterica serovar Enteritidis. Here, we show that the O-antigen epitope in group D Salmonella governs the levels of colistin susceptibility. Using whole-genome sequencing, we also revealed that increased colistin susceptibility in a group D Salmonella veterinary isolate was due to a defect in the O-antigen polymerase protein, Rfc. In summary, we show that two different mechanisms that influence the presence and composition of O antigens affect colistin susceptibility in Salmonella enterica.
Insights
Group D Salmonella enterica shows intrinsic colistin resistance due to O-antigen differences. Alterations in O-antigen composition or polymerase function significantly impact Salmonella
Area of Science:
- Microbiology
- Genetics
- Drug Resistance
Background:
- Salmonella enterica serovars exhibit varying colistin susceptibility.
- Group D Salmonella are often intrinsically resistant to colistin, a critical last-resort antibiotic.
- The mechanisms underlying this resistance are not fully understood.
Purpose of the Study:
- To elucidate the mechanisms of colistin resistance in Group D Salmonella enterica.
- To investigate the role of O-antigen structure in colistin susceptibility.
- To identify genetic factors contributing to altered colistin resistance.
Main Methods:
- Comparative analysis of O-antigen biosynthesis genes (rfbJ, rfbSE) between Group B and D Salmonella.
- Gene substitution experiments to assess the impact on colistin susceptibility.
- Whole-genome sequencing of a colistin-susceptible Group D isolate.
- Identification of mutations in O-antigen polymerase (Rfc).
Main Results:
- The O-antigen epitope in Group D Salmonella dictates colistin susceptibility levels.
- Substitution of Group B rfbJ with Group D rfbSE genes decreased colistin susceptibility.
- The presence of tyvelose (Group D) versus abequose (Group B) in O-antigens influences colistin interaction.
- A defect in the Rfc protein in a Group D isolate led to increased colistin susceptibility.
- Two distinct mechanisms affecting O-antigen presence and composition influence Salmonella colistin resistance.
Conclusions:
- O-antigen composition and integrity are key determinants of colistin susceptibility in Salmonella enterica.
- Genetic variations in O-antigen biosynthesis and modification pathways can confer or alter colistin resistance.
- Understanding these mechanisms is crucial for effective treatment of Salmonella infections, especially with rising antibiotic resistance.
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