Cilagicin was particularly active once morest Gram-positive bacteria such as Streptococcus pyogenes.
The synthetic antibiotic cilagicin was particularly active once morest Gram-positive bacteria such as Streptococcus pyogenes, shown in the image. Photo: Shutterstock.
Despite its importance in modern medicineantibiotics are under constant threat as pathogens adapt, acquire or develop resistance with frightening regularity, researchers say. researchers of a new study developed by the rockefeller university.
It is a new antibiotic, synthesized and derived from computer models of bacterial gene products, it seems to neutralize even the bacteria drug resistant. The compound, called the troubleworks well in mice and employs a novel mechanism to attack MRSAC. diff and several other deadly pathogens.
“This is not just an interesting new molecule, it is a validation of a novel approach for drug discovery. This study is an example of computational biology, genetic sequencing, and synthetic chemistry coming together to discover the secrets of bacterial evolution“, so indicated Sean F. Brady de Rockefeller, Associate professor, Tri-Institutional Associate Professor of the Genetically Encoded Small Molecule Laboratory.
In the statement published on the university website, they point out that Cilagicin reliably eliminated bacteria Gram positive in the lab, it did not harm human cells, and once it was chemically optimized for use in animals, it successfully treated bacterial infections in mice.
Of particular interest, cilagicin was potent once morest a number of drug-resistant bacteria, and even when pitted once morest bacteria cultured specifically to resist cilagicin, the synthetic compound prevailed.
In the details provided by the authors, cilagicin works by binding two molecules, C55-P and C55-PP, which help maintain bacterial cell walls. Existing antibiotics, such as bacitracin, bind to one of those two molecules, but never both, and bacteria can often resist such drugs by bonding a wall cell with remaining molecule.
Even the team suspects that cilagicin’s ability to switch the two molecules off may present an insurmountable barrier that prevents resistance.
“Cilagicin is still a long way from human trials. In follow-up studies, the laboratory of Brady will perform further synthesis to optimize the compound and test it in animal models once morest more diverse pathogens to determine which diseases it may be most effective in treating.”
However, beyond the clinical implications of cilagicin, the study demonstrates a scalable method that researchers might use to discover and develop new antibiotics.
“This work is an excellent example of what might be hidden within a cluster of genes,” says Brady. “We believe we can now unlock a large number of novel natural compounds with this strategy, which we hope will provide an exciting new group of drug candidates.”
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