Nwankwo Chukwuemeka E, Osho Adeleke, Adewuy Adewale, Otuechere Chiagoziem, Olawoye Idowu B, Fayemi Scott O, Oguzie Judith U, Uwanibe Jessica, Adesina Adedotun F, Durugbo Ernest U, Adedokun Oluwatobi, Ajisegiri Damilola, Akinlawon Ladimeji, Eromon Philomena, Folarin Onikepe, Happi Christian
Department of Biological Sciences, Redeemer's University, Ede, Nigeria.
African Centre of Excellence for Genomics of Infectious Diseases (ACEGID), Redeemer's University, Ede, Nigeria.
GMS Hyg Infect Control. 2025 May 20;20:Doc22. doi: 10.3205/dgkh000551. eCollection 2025.
The burden of infectious and non-infectious debilitating diseases of oral etiology is common in developing countries. The pathogenicity of oral infectious diseases is believed to be exacerbated by the uncontrolled progression of biofilm-producing bacteria. In contemporary research endeavours, there is a proposition to utilize anti-infective compounds in the control of biofilm-induced infections. This research was carried out to isolate and control biofilm-producing bacteria using anti-infective nanoparticles and a plant extract.
Biofilm-producing bacteria were isolated and characterized using microbiological techniques and next-generation sequencing. Antimicrobial susceptibility testing and minimum inhibitory concentration were determined using titanium ferrite (TF) coupled with plant extracts. Bioactive antimicrobials were analyzed by Fourier-transform Infrared (FTIR) spectroscopy. The surface morphology was determined using a scanning electron microscope (SEM), and toxicological properties were characterized on adult Wistar rats.
Biofilm-producing bacteria isolated and sequenced in this study are and . The plant extracts coupled with nanoparticles were found to be more bioactive against the biofilm producers than either the plant extracts or the nanoparticles alone. The MICs observed here showed these complexes to be more bioactive against the pathogens in lower concentrations compared to that observed in similar studies. FTIR revealed that the bands at around 3,000-2,800 cm correspond to C-H stretching vibrations. The bands at around 1,700-1,600 cm corresponded to C=O stretching vibrations. The bands at around 1,500-1,400 cm corresponded to N-H bending vibrations. The presence of these functional groups suggests that doped with TF nanoparticles (MSLNP) is a complex compound that contains a variety of different chemical groups. Histology revealed no significant derangements observed in the histoarchitecture of experimental groups. This suggests that the compound shows potential as antimicrobial therapy in battling bacterial oral biofilms. It is recommended that the compound undergo further testing in the drug design process.
在发展中国家,由口腔病因引起的传染性和非传染性衰弱性疾病负担普遍存在。人们认为,产生生物膜的细菌不受控制的增殖会加剧口腔传染病的致病性。在当代研究中,有人提议使用抗感染化合物来控制生物膜引起的感染。本研究旨在使用抗感染纳米颗粒和一种植物提取物分离并控制产生生物膜的细菌。
使用微生物技术和下一代测序对产生生物膜的细菌进行分离和表征。使用钛铁氧体(TF)与植物提取物测定抗菌药敏试验和最低抑菌浓度。通过傅里叶变换红外(FTIR)光谱分析生物活性抗菌剂。使用扫描电子显微镜(SEM)确定表面形态,并在成年Wistar大鼠上表征毒理学特性。
本研究中分离和测序的产生生物膜的细菌为[具体细菌名称缺失]和[具体细菌名称缺失]。发现植物提取物与纳米颗粒结合对生物膜产生菌的生物活性比单独的植物提取物或纳米颗粒更高。此处观察到的最低抑菌浓度表明,与类似研究中观察到的情况相比,这些复合物在较低浓度下对病原体具有更高的生物活性。FTIR显示,在3000 - 2800 cm附近的波段对应于C - H伸缩振动。在1700 - 1600 cm附近的波段对应于C = O伸缩振动。在1500 - 1400 cm附近的波段对应于N - H弯曲振动。这些官能团的存在表明,掺杂TF纳米颗粒的[具体物质名称缺失](MSLNP)是一种含有多种不同化学基团的复合化合物。组织学显示,实验组的组织结构未观察到明显紊乱。这表明该化合物在对抗细菌性口腔生物膜方面显示出作为抗菌疗法的潜力。建议该化合物在药物设计过程中进行进一步测试。