AI Article Synopsis

  • The study investigates how Bifidobacterium adolescentis resists first-line anti-tubercular drugs like isoniazid, pyrazinamide, and streptomycin, finding that even at high drug concentrations, the bacteria continue to grow unaffected.
  • Some bacteria exhibited strong aggregation, which may help protect them from drug toxicity, and further microscopic analysis revealed that certain bacteria became elongated and protruded.
  • Whole genome sequencing showed few antibiotic resistance genes or bacteriocins present, but some hypothetical proteins were observed, with 3D structure analyses suggesting possible interactions with specific ligands.

Article Abstract

The current study aims to understand the resistance of Bifidobacterium adolescentis to different anti-tubercular drugs (first-line oral tuberculosis drugs). The bacteria were grown with anti-tubercular drugs such as isoniazid, pyrazinamide, and streptomycin to better understand the resistance phenomena. It was found that even at tenfold higher concentrations, growth rates remained unchanged. In addition, a small number of bacteria were found to aggregate strongly, a property that protects against the toxicity of the drug. Further FE-SEM (Field Emission Scanning Electron Microscopy) analysis revealed that some bacteria became excessively long, elongated, and protruded on the surface. Size scattering analysis confirmed the presence of bifidobacteria in the size range of 1.0-100 μm. After whole genome sequence analysis, certain mutations were found in the relevant gene. In vitro, foam formation and growth in the presence of HO and HPLC (High Performance Liquid Chromatography) studies provide additional evidence for the presence of catalase. According to RAST (Rapid Annotation Using Subsystems Technology) annotation and CARD (Comprehensive Antibiotic Resistance Database analysis), there were not many components in the genome that were resistant to antibiotics. Whole genome sequence (WGS) analysis does not show the presence of bacteriocins and antibiotic resistance genes, but few hypothetical proteins were observed. 3D structure and docking studies suggest their interaction with specific ligands.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11605034PMC
http://dx.doi.org/10.1038/s41598-024-78095-xDOI Listing

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