Antimicrobial and Antiviral Nanofibers Halt Co-Infection Spread via Nuclease-Mimicry and Photocatalysis.
Jieran YaoZhenhong LuoJiaying LinNa MengJiangna GuoHui XuRongwei ShiLinhui ZhaoJiateng ZhouFeng YanBin WangHailei MaoPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
The escalating spread of drug-resistant bacteria and viruses is a grave concern for global health. Nucleic acids dominate the drug-resistance and transmission of pathogenic microbes. Here, imidazolium-type poly(ionic liquid)/porphyrin (PIL-P) based electrospun nanofibrous membrane and its cerium (IV) ion complex (PIL-P-Ce) are developed. The obtained PIL-P-Ce membrane exhibits high and stable efficiency in eradicating various microorganisms (bacteria, fungi, and viruses) and decomposing microbial antibiotic resistance genes and viral nucleic acids under light. The nuclease-mimetic and photocatalytic mechanisms of the PIL-P-Ce are elucidated. Co-infection wound models in mice with methicillin-resistant S. aureus and hepatitis B virus demonstrate that PIL-P-Ce integrate the triple effects of cationic polymer, photocatalysis, and nuclease-mimetic activities. As revealed by proteomic analysis, PIL-P-Ce shows minimal phototoxicity to normal tissues. Hence, PIL-P-Ce has potential as a "green" wound dressing to curb the spread of drug-resistant bacteria and viruses in clinical settings.
Keyphrases
- drug resistant
- ionic liquid
- hepatitis b virus
- multidrug resistant
- energy transfer
- acinetobacter baumannii
- global health
- antibiotic resistance genes
- staphylococcus aureus
- microbial community
- dna binding
- sars cov
- wound healing
- public health
- gene expression
- photodynamic therapy
- room temperature
- quantum dots
- anaerobic digestion
- liver failure
- transcription factor
- tissue engineering
- climate change
- human health
- insulin resistance