4.7 Article

Eradication of Intracellular Salmonella Typhimurium by Polyplexes of Acid-Transforming Chitosan and Fragment DNA

期刊

MACROMOLECULAR BIOSCIENCE
卷 21, 期 7, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.202000408

关键词

antibacterial treatments; antimicrobial polymers; nanoparticles; Salmonella Typhimurium infections; stimuli‐ responsive transformations

资金

  1. California Institute of Regenerative Medicine Training Grant [TG2-01152]
  2. National Science Foundation Graduate Research Fellowship [DGE-1321846]
  3. USDA [2015-67017-23360, 2017-67015-26085]
  4. NIFA Hatch grant [CA-D-PLS-2327-H]
  5. NIFA-BARD award [2017-67017-26180]
  6. [R03 AI139557]

向作者/读者索取更多资源

This study investigates a novel form of nanomaterial-based antimicrobial agent, ATC, which efficiently treats intracellular Salmonella enterica sv Typhimurium infections, demonstrating effective and safe antimicrobial activity without affecting host cells. The findings show the utility of molecularly engineered nanomaterials as efficient antimicrobial agents against intracellular pathogens.
Antibiotics are highly successful against microbial infections. However, current challenges include rising antibiotic resistance rates and limited efficacy against intracellular pathogens. A novel form of a nanomaterial-based antimicrobial agent is investigated for efficient treatment of an intracellular Salmonella enterica sv Typhimurium infection. A known antimicrobial polysaccharide, chitosan, is engineered to be readily soluble under neutral aqueous conditions for systemic administration. The modified biologic, named acid-transforming chitosan (ATC), transforms into an insoluble, antimicrobial compound in the mildly acidic intracellular compartment. In cell culture experiments, ATC is confirmed to have antimicrobial activity against intracellular S. Typhimurium in a concentration- and pH-dependent manner, without affecting the host cells, RAW264.7 macrophages. For improved cellular uptake and pharmacokinetic/pharmacodynamic properties, ATC is further complexed with fragment DNA (fDNA), to form nano-sized spherical polyplexes. The resulting ATC/fDNA polyplexes efficiently eradicated S. Typhimurium from RAW264.7 macrophages. ATC/fDNA polyplexes may bind with microbial wall and membrane components. Consistent with this expectation, transposon insertion sequencing of a complex random mutant S. Typhimurium library incubated with ATC does not reveal specific genomic target regions of the antimicrobial. This study demonstrates the utility of a molecularly engineered nanomaterial as an efficient and safe antimicrobial agent, particularly against an intracellular pathogen.

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