Project description:tet(X)-positive isolates from clinical settings in China
| PRJNA595705 | ENA
Project description:tet(X)-positive isolates from a cow farm in China
| PRJNA624019 | ENA
Project description:Prevalence and risk factors of tet(X4)-positive Enterobacteriaceae in human gut microbiota
| PRJNA822927 | ENA
Project description:Low prevalence of mobilized resistance genes mcr-1and tet(X4) in blaNDM-positive Escherichia coli from a tertiary hospital in China
| PRJNA1110721 | ENA
Project description:tet(X4)-positive Escherichia coli from food animals in China, 2018
| PRJNA625924 | ENA
Project description:tet(x4)-positive plasmids
| PRJNA760806 | ENA
Project description:Genome sequence of clinical tet(X4)-positive Escherichia coli strains in China
Project description:Guanidine DNA quadruplex (G4-DNA) structures convey a distinctive layer of epigenetic information that is critical for the regulation of key biological activities and processes as genome transcription regulation, replication and repair. Despite several works that have been published recently, the information regarding their role and possible use as therapeutic drug targets in bacteria is still scarce. Here, we tested the biological activity of a small G4-DNA ligand library based on the naphthalene diimide (NDI) pharmacophore, against both Gram-positive and Gram-negative bacteria. For the best compound identified, NDI-10, the action mechanism was further characterized. Gram-negative bacteria were more resistant altogether due to the presence of the outer membrane, although the activity of the G4-Ligand was generally bactericidal, while it was bacteriostatic for Gram-positive bacteria. This asymmetric activity could be related to the different prevalence of putative G4-DNA structures in each group, the influence that they can exert on the gene expression (which was found more severe for the Gram-negative bacteria) and the role of the G4 structures in these bacteria, that seems to be more related to promote transcription in Gram-positive bacteria and repress transcription in Gram-negative.