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Generating Transposon Insertion Libraries in Gram-Negative Bacteria for High-Throughput Sequencing
Published on: July 7, 2020
Mutations in Genes with a Role in Cell Envelope Biosynthesis Render Gram-Negative Bacteria Highly Susceptible to the
Samual C Allgood1, Calvin A Ewing1, Weiping Chu2
1Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, CO 80309, USA.
Abstract:
Anti-infectives include molecules that target microbes in the context of infection but lack antimicrobial activity under conventional growth conditions. We previously described D66, a small molecule that kills the Gram-negative pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) within cultured macrophages and murine tissues, with low host toxicity. While D66 fails to inhibit bacterial growth in standard media, the compound is bacteriostatic and disrupts the cell membrane voltage gradient without lysis under growth conditions that permeabilize the outer membrane or reduce efflux pump activity. To gain insights into specific bacterial targets of D66, we pursued two genetic approaches. Selection for resistance to D66 revealed spontaneous point mutations that mapped within the gmhB gene, which encodes a protein involved in the biosynthesis of the lipopolysaccharide core molecule. E. coli and S. Typhimurium gmhB mutants exhibited increased resistance to antibiotics, indicating a more robust barrier to entry. Conversely, S. Typhimurium transposon insertions in genes involved in outer membrane permeability or efflux pump activity reduced fitness in the presence of D66. Together, these observations underscore the significance of the bacterial cell envelope in safeguarding Gram-negative bacteria from small molecules.
Insights
The anti-infective D66 targets Salmonella Typhimurium by disrupting its cell membrane potential. Resistance mutations in gmhB reveal the importance of the bacterial cell envelope in D66
Area of Science:
- Microbiology
- Molecular Biology
- Drug Discovery
Background:
- Anti-infectives can target microbes during infection without inhibiting growth in standard conditions.
- D66 is a novel small molecule effective against Salmonella Typhimurium in host tissues with low toxicity.
Purpose of the Study:
- To identify specific bacterial targets of the anti-infective D66.
- To understand the mechanisms by which D66 exerts its anti-infective properties.
Main Methods:
- Genetic screens were employed to select for D66 resistance in Salmonella Typhimurium.
- Analysis of mutations in gmhB and transposon insertions in genes related to cell envelope function.
Main Results:
- Spontaneous D66 resistance mutations mapped to the gmhB gene, crucial for lipopolysaccharide core biosynthesis.
- gmhB mutants showed increased resistance to antibiotics, suggesting a strengthened cell barrier.
- Disruptions in outer membrane permeability or efflux pump genes decreased bacterial fitness in the presence of D66.
Conclusions:
- The bacterial cell envelope plays a critical role in protecting Gram-negative bacteria from small molecule anti-infectives like D66.
- Targeting cell envelope biosynthesis or function could be a strategy for developing new anti-infectives.
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