利用苏丹假丝酵母菌的绿色合成纳米银颗粒:一种对抗抗菌素耐药性的可持续方法。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Nesreen A A Ibrahim, Humodi A Saeed, Samar M Saeed, Osama Mohamed, Omnia H Suliman, Sabah A E Ibrahim, Sofia B Mohamed
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引用次数: 0

摘要

背景:抗菌素耐药性(AMR)是一项重大的全球卫生挑战,特别是在苏丹,抗生素的过度使用和滥用导致了耐多药病原体的增加。由于耐药性的快速发展和有限的疗效,传统的抗微生物策略往往不足,这突出了对新方法的需求。纳米技术提供了有希望的替代方案,纳米银粒子(AgNPs)显示出强大的广谱抗菌活性。本研究旨在利用一种从苏丹土壤中分离的未开发酵母菌——假丝酵母菌(C. parapsilosis),开发一种生态友好的AgNPs合成方法,以对抗AMR。结果:通过紫外可见光谱(UV-Vis)、x射线衍射(XRD)和高分辨率透射电镜(HRTEM),成功证实了C. parapsilosis生物合成AgNPs,揭示了定义良好的纳米颗粒。生物合成的AgNPs对ATCC参考菌株和革兰氏阳性和革兰氏阴性细菌的MDR临床分离株均表现出较强的抗菌活性,且抑制区呈浓度依赖性增加。在最佳浓度下,铜绿假单胞菌(p.a uluginosa) (ATCC 27853)的抑菌带可达29 mm,而临床分离的伤寒沙门氏菌(S. typhi)(24.5±0.58 mm)和大肠杆菌(E. coli)(23.8±0.79 mm)表现出显著的敏感性。最小抑菌浓度(MIC)和最小杀菌浓度(MBC)测定表明,在0.3125 mg/mL时,对大肠杆菌和肺炎克雷伯菌(克雷伯菌)具有有效的杀菌活性。此外,AgNPs以物种依赖和抗生素依赖的方式协同增强了常规抗生素的疗效。粪肠球菌(E. faecalis)与鲍曼不动杆菌(A. baumannii)的协同作用最强(与粘菌素的协同作用高达9.84倍),与头孢他啶的协同作用高达5.11倍),这表明agnp增强的抗生素效果因细菌种类、纳米颗粒合成方法和抗生素类型而异。结论:本研究提出了一种利用苏丹酵母菌株绿色合成AgNPs的新型可持续方法来解决AMR问题。这些发现强调了AgNPs作为一种有效的抗菌剂的潜力,无论是单独使用还是与传统抗生素联合使用,都可以对抗耐多药病原体。通过整合微生物学和纳米技术,这项研究为减少抗菌素耐药性提供了一种具有成本效益和环境友好的解决方案。这些发现为未来的临床应用和公共卫生干预提供了坚实的基础,特别是在资源有限的环境中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green synthesis of silver nanoparticles using Sudanese Candida parapsilosis: a sustainable approach to combat antimicrobial resistance.

Background: Antimicrobial resistance (AMR) is a critical global health challenge, particularly in Sudan, where the overuse and misuse of antibiotics have driven the rise of multidrug-resistant (MDR) pathogens. Conventional antimicrobial strategies often fall short due to rapid resistance development and limited efficacy, highlighting the need for novel approaches. Nanotechnology offers promising alternatives, with silver nanoparticles (AgNPs) demonstrating potent broad-spectrum antimicrobial activity. This study aims to develop an eco-friendly synthesis of AgNPs using Candida parapsilosis (C. parapsilosis), an untapped yeast strain isolated from Sudanese soil, to combat AMR.

Results: Biosynthesis of AgNPs using C. parapsilosis was successfully confirmed through UV-Vis spectroscopy, X-ray diffraction (XRD), and high-resolution transmission electron microscopy (HRTEM), revealing well-defined nanoparticles. The biosynthesized AgNPs exhibited strong antibacterial activity against both ATCC reference strains and MDR clinical isolates of Gram-positive and Gram-negative bacteria, with inhibition zones increasing in a concentration-dependent manner. At optimal concentrations, inhibition zones reached 29 mm for Pseudomonas aeruginosa (P.aeruginosa) (ATCC 27853), while clinical isolates of Salmonella typhi (S. typhi) (24.5 ± 0.58 mm) and Escherichia coli (E. coli) (23.8 ± 0.79 mm) exhibited significant susceptibility. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) assays demonstrated potent bactericidal activity, particularly against E. coli and Klebsiella pneumoniae (K. pneumoniae) at 0.3125 mg/mL. Furthermore, AgNPs synergistically enhanced the efficacy of conventional antibiotics in a species- and antibiotic-dependent manner. The strongest synergy was observed in Enterococcus faecalis (E. faecalis) (up to 9.84-fold with Colistin) and Acinetobacter baumannii (A. baumannii) (up to 5.11-fold with Ceftazidime), suggesting that AgNP-enhanced antibiotic efficacy varies depending on bacterial species, nanoparticle synthesis method, and antibiotic type.

Conclusions: This study presents a novel and sustainable approach to tackling AMR by leveraging Sudanese yeast strains for the green synthesis of AgNPs. The findings underscore the potential of AgNPs as an effective antibacterial agent, both independently and in combination with conventional antibiotics, to combat MDR pathogens. By integrating microbiology and nanotechnology, this research offers a cost-effective and environmentally friendly solution for AMR mitigation. These findings provide a strong foundation for future clinical applications and public health interventions, particularly in resource-limited settings.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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