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March 3, 2026ACS Omega0 citationsOpen Access

Nanowire-Mediated Eradication of Polymicrobial Biofilms

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XMXiaojing MaCMC. MarloweLWLeli Wang

Key Points

  • Polymicrobial biofilms comprising S. pneumoniae and NTHi were effectively eradicated using vanadium pentoxide nanowires.
  • Combination treatment with nanowires and conventional antibiotics demonstrated synergistic effects against monocultured pathogens.
  • Isobologram analysis indicated additive effects against S. pneumoniae in mono- or cocultured conditions, except for one antibiotic pair.
  • Strategies presented may reduce antibiotic exposure and address antimicrobial resistance in biofilm-related infections.

Abstract

Streptococcus pneumoniae (S. pneumoniae) and Nontypeable Hemophiles influenzae (NTHi) are two of the most common pathogens causing otitis media (OM), which is the primary reason for pediatric antibiotic prescriptions. They have been shown to coexist and, in some cases, form biofilms that are resistant to antibiotics, causing recurrent or chronic OM. The current treatment regimen requires a rigorous course of multidose antibiotics over 5-10 days, which is nevertheless found insufficient to eradicate the polymicrobial biofilms. To tackle this challenge, we utilized a nanozyme, i.e., vanadium pentoxide nanowires (V2O5 NWs), to convert a metabolic product (H2O2) of S. pneumoniae into a potent antiseptic (HOBr), thus eradicating polymicrobial biofilms comprising S. pneumoniae and NTHi. Interestingly, when V2O5 NWs were combined with conventional antibiotics (i.e., ciprofloxacin and moxifloxacin), they exhibited synergistic effects against monocultured pathogens, as demonstrated using isobologram analysis. Against S. pneumoniae, regardless of mono- or coculture, additive effects were observed, with the exception of the levofloxacin-ciprofloxacin pair, which resulted in antagonistic effects in cocultured conditions. The strategies developed in this study, therefore, have the potential to tackle polymicrobial OM, biofilm-induced infections and associated antimicrobial resistance while reducing the overall antibiotic exposure incurred by OM.

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Cite This Study

Ma et al. (2026) studied this question.

synapsesocial.com/papers/69a76728badf0bb9e87dfd2bhttps://doi.org/10.1021/acsomega.5c12071
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