冷大气等离子体能在体外灭活黄曲霉和角斑镰刀菌的生物膜和分生孢子。

Darby Roberts, Jonathan Thomas, Jacklyn Salmon, Marc A Cubeta, Katharina Stapelmann, Brian C Gilger
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引用次数: 0

摘要

导言。黄曲霉菌(Aspergillus flavus)和角膜塑形镰刀菌(Fusarium keratoplasticum)是真菌性角膜炎(FK)的常见致病菌。现有抗真菌药物的抗真菌耐药性不断增加,给 FK 的治疗带来了重大挑战。冷大气等离子体(CAP)是一种开创性的非药物抗菌干预方法,已被证明具有广谱抗真菌治疗的潜力。以往的研究强调,生物膜相关耐药性是有效治疗 FK 的关键障碍。尽管 CAP 在治疗各种真菌感染方面前景看好,但其对 FK 病原体的生物膜和分生孢子形式的疗效仍未得到充分探索。本研究旨在体外研究 CAP 对临床真菌性角膜炎分离物黄曲霉和角膜塑形菌的抗真菌功效。对介质阻挡放电 CAP 设备的功率参数(22-27 kVpp、300-400 Hz 和 20-80 mA)进行了优化,以灭活黄曲霉生物膜。对角叉菜菌生物膜以及黄曲霉和角叉菜菌的分生孢子悬浮液施加了最佳应用电压和总电流。通过代谢活性、c.f.u.计数(c.f.u. ml-1)和生物膜形成来评估真菌活力,从而研究 CAP 处理的抗真菌效果。对于这两种真菌,CAP 都表现出了强烈的时间依赖性灭活作用,在 300 秒或更短时间内,代谢活性和 c.f.u. ml-1 降低了 80% 以上,在处理 600 秒后完全抑制。我们的研究结果表明,CAP 是一种前景广阔的广谱抗真菌干预措施。我们的研究结果表明,CAP 是一种很有前途的广谱抗真菌干预措施。CAP 处理可有效降低黄曲霉和角膜塑形菌的生物膜和分生孢子悬浮培养物中的真菌活力,这表明它有可能成为真菌性角膜炎的一种替代治疗策略。
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Cold atmospheric plasma inactivates Aspergillus flavus and Fusarium keratoplasticum biofilms and conidia in vitro.

Introduction. Aspergillus flavus and Fusarium keratoplasticum are common causative pathogens of fungal keratitis (FK), a severe corneal disease associated with significant morbidity and vision loss. Escalating incidence of antifungal resistance to available antifungal drugs poses a major challenge to FK treatment. Cold atmospheric plasma (CAP) is a pioneering nonpharmacologic antimicrobial intervention that has demonstrated potential as a broad-spectrum antifungal treatment.Gap statement. Previous research highlights biofilm-associated resistance as a critical barrier to effective FK treatment. Although CAP has shown promise against various fungal infections, its efficacy against biofilm and conidial forms of FK pathogens remains inadequately explored.Aim. This study aims to investigate the antifungal efficacy of CAP against clinical fungal keratitis isolates of A. flavus and F. keratoplasticum in vitro.Methodology. Power parameters (22-27 kVpp, 300-400 Hz and 20-80 mA) of a dielectric barrier discharge CAP device were optimized for inactivation of A. flavus biofilms. Optimal applied voltage and total current were applied to F. keratoplasticum biofilms and conidial suspensions of A. flavus and F. keratoplasticum. The antifungal effect of CAP treatment was investigated by evaluating fungal viability through means of metabolic activity, c.f.u. enumeration (c.f.u. ml-1) and biofilm formation.Results. For both fungal species, CAP exhibited strong time-dependent inactivation, achieving greater than 80 % reduction in metabolic activity and c.f.u. ml-1 within 300 s or less, and complete inhibition after 600 s of treatment.Conclusion. Our findings indicate that CAP is a promising broad-spectrum antifungal intervention. CAP treatment effectively reduces fungal viability in both biofilm and conidial suspension cultures of A. flavus and F. keratoplasticum, suggesting its potential as an alternative treatment strategy for fungal keratitis.

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