A smart antibiotic can kill germs while sparing the environment

Lolamicin, a compound that selectively kills Gram-negative bacteria, and leads to susceptibility to Clostridium difficile-induced colitis

Gram-negative bacteria include public-health villains such as Escherichia coli and Klebsiella pneumoniae. They cause diseases ranging from salmonella to cholera, and can trigger sepsis, a potentially lethal immune-system response to infection.

The study’s authors started with compounds that aren’t harmful to the bacterium but can affect theLol system, which is exclusive to Gram-negativebacteria. Tinkering with those compounds produced one that the researchers called lolamicin, which “selectively kills pathogenic bacteria over non-pathogenic bacteria based on differences in Lol proteins between these bacteria”, says study co-author Paul Hergenrother, a chemist at the University of Illinois at Urbana-Champaign.

C. G. et al. were both authors of Buffie. Profound alterations of intestinal microbiota following a single dose of clindamycin results in sustained susceptibility to Clostridium difficile-induced colitis. Infect. Immun. 80, 62- 73.

Gitai says that the study “proves the viability” of targeting the Lol system, but adds, “There is a long road from showing efficacy in mice to developing a drug for human use.”

Gram-negative-selective antibiotic that spares the gut microbiome: Comment on a cautionary note on recent discoveries of fabimycin

Hiller makes a cautious note. He says there is not much money to be made with a novel antibiotic that has been approved for clinical use. “Around ten to twenty new Gram-negative antibiotics have been discovered in the last ten years”, he adds, but none has gained approval from the US Food and Drug Administration.

Lesniak, N. A., Schubert, A. M., Sinani, H. & Schloss, P. D. Clearance of Clostridioides difficile colonization is associated with antibiotic-specific bacterial changes. mSphere 6, e01238-20 (2021).

Parker, E. N. et al. The late-stage antibiotic candidate fabimycin, which is an antibiotic called FabI, was discovered through an iterative approach. ACS Cent. Sci. 8, 1145–1158 (2022).

McMurdie, P.J. and the rest of the team have created R package for interactive analysis and graphics of census data. A journal, pplone 8, e61217

Lan, Y., Wang, Q., Cole, J. R. & Rosen, G. L. Using the RDP classifier to predict taxonomic novelty and reduce the search space for finding novel organisms. PLoS ONE 7, e 32491 was published.

Source: A Gram-negative-selective antibiotic that spares the gut microbiome

Molecular-dynamics simulation of lipids: CHARMM’s additive force field update and the toolkit for efficient lipid shuffling

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Klauda, J. B. et al. The CHARMM’s all-atom additive force field for lipids has been updated. J. Phys. Chem. B 114 was written in 2010; read here.

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The toolkit for efficient shuffling of the lipids in the biological membranes was developed by Licari, Dehghani-Ghahnaviran, S. and Tajkhorshid. There is a J. Chem. Inform. Model. 62, 986–996 (2022).

Source: A Gram-negative-selective antibiotic that spares the gut microbiome

Cell wall reporter assay for Gram-negative pathogens: A novel approach to countering resistance in E. coli by disrupting the outer portion of the cell

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Countering Gram-negative antibiotic resistance can be accomplished through disrupting the outer portion of the cell. Antibiotics 8, 163 (2019).

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Source: A Gram-negative-selective antibiotic that spares the gut microbiome

R. Pathania and his co-authors identify an inhibitors of bacterial lipoprotein targeting in Escherichia coli

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Source: A Gram-negative-selective antibiotic that spares the gut microbiome

Studies of the interaction of thiourea compounds with a lipoprotein targeting chaperone in the gut microbiota: repertoire and variations

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The long-term persistence of resistant Bacteroides spp. and resistance genes were studied. Antimicrob. The Chemother was published in 2006

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