Article Synopsis

  • * Researchers discovered a new compound called COE-PNH, derived from conjugated oligoelectrolytes, which effectively kills the bacterium and shows low chances of resistance.
  • * COE-PNH works by damaging the bacteria's protective structures and has demonstrated safety and effectiveness in animal models, indicating its potential as a new treatment option for these infections.

Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Infections caused by nontuberculous mycobacteria have increased more than 50% in the past two decades and more than doubled in the elderly population. (Mab), one of the most prevalent of these rapidly growing species, is intrinsically resistant to numerous antibiotics. Current standard-of-care treatments are not satisfactory, with high failure rate and notable adverse effects. We report here a potent anti-Mab compound from the flexible molecular framework afforded by conjugated oligoelectrolytes (COEs). A screen of structurally diverse, noncytotoxic COEs identified a lead compound, COE-PNH, which was bactericidal against replicating, nonreplicating persisters and intracellular Mab.COE-PNH had low propensity for resistance development, with a frequency of resistance below 1.25 × 10 and showed no detectable resistance upon serial passaging. Mechanism of action studies were in line with COE-PNH affecting the physical and functional integrity of the bacterial envelope and disrupting the mycomembrane and associated essential bioenergetic pathways. Moreover, COE-PNH was well-tolerated and efficacious in a mouse model of Mab lung infection. This study highlights desirable in vitro and in vivo potency and safety index of this COE structure, which represents a promising anti-mycobacterial to tackle an unmet medical need.

Download full-text PDF

Source
http://dx.doi.org/10.1126/scitranslmed.adi7558DOI Listing

Publication Analysis

Top Keywords

anti-mycobacterial conjugated
4
conjugated oligoelectrolyte
4
oligoelectrolyte effective
4
effective infections
4
infections caused
4
caused nontuberculous
4
nontuberculous mycobacteria
4
mycobacteria increased
4
increased 50%
4
50% decades
4

Similar Publications

Disrupting Mycobacterium smegmatis biofilm using enzyme-immobilized rifampicin loaded silk fibroin nanoparticles for dual anti-bacterial and anti-biofilm action.

Microb Pathog

November 2024

Theevanam Additives Nutraceuts Pvt Ltd, IITM Bioincubator, Department of Biotechnology, IIT Madras, Chennai, 600036, India; Saveetha Dental College and Hospitals, SIMATS, Chennai, 600077, India. Electronic address:

Article Synopsis
  • Biofilm formation in tuberculosis complicates treatment by protecting bacteria from antibiotics, leading to persistent infections.
  • This study shows that rifampicin-encapsulated silk fibroin nanoparticles, combined with antibiofilm enzymes, can effectively disrupt Mycobacterium smegmatis biofilms, enhancing the antibiotic's effectiveness.
  • The research identifies specific hydrolytic enzymes that reduce biofilm thickness significantly and emphasizes the potential of combining these enzymes with antibiotics to improve tuberculosis treatment outcomes.
View Article and Find Full Text PDF
Article Synopsis
  • * Researchers discovered a new compound called COE-PNH, derived from conjugated oligoelectrolytes, which effectively kills the bacterium and shows low chances of resistance.
  • * COE-PNH works by damaging the bacteria's protective structures and has demonstrated safety and effectiveness in animal models, indicating its potential as a new treatment option for these infections.
View Article and Find Full Text PDF

We describe the design and synthesis of two isatin-tethered quinolines series (- and -), in connection with our research interest in developing novel isatin-bearing anti-tubercular candidates. In a previous study, a series of small molecules bearing a quinoline-3-carbohydrazone moiety was developed as anti-tubercular agents, and compound disclosed the highest potency with MIC value equal to 6.24 µg/mL.

View Article and Find Full Text PDF
Article Synopsis
  • - A series of 12 PEG-alkynyl C2-adenosine conjugates were created using a Sonogashira coupling method and characterized by NMR and mass spectrometry.
  • - The conjugates mostly showed low to moderate toxicity in mouse immune cells and had variable effectiveness against different bacteria, with 12c inhibiting Mycobacterium aurum but not Mycobacterium bovis BCG.
  • - Two conjugates, 10b and 11b, exhibited high water solubility and increased cAMP levels in cells, and docking studies indicated they had strong binding to specific adenosine receptors, maintaining good binding properties despite the PEG attachments.
View Article and Find Full Text PDF

Herein, we identified a potent lead compound RRA2, within a series of 54 derivatives of 1,2,4-triazolethiols (exhibit good potency as an anti-mycobacterial agents) against intracellular Mycobacterium tuberculosis (Mtb). Compound RRA2 showed significant mycobactericidal activity against active stage Mycobacterium bovis BCG and Mtb with minimum inhibitory concentration (MIC) values of 2.3 and 2.

View Article and Find Full Text PDF