The Study of Antistaphylococcal Potential of Omiganan and Retro-Omiganan Under Flow Conditions.

IF 4.4 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Probiotics and Antimicrobial Proteins Pub Date : 2025-06-01 Epub Date: 2024-01-15 DOI:10.1007/s12602-023-10197-w
Maciej Jaśkiewicz, Damian Neubauer, Karol Sikora, Marta Bauer, Sylwia Bartoszewska, Izabela Błażewicz, Dariusz Marek, Wioletta Barańska-Rybak, Wojciech Kamysz
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Abstract

Staphylococcus aureus is considered one of the leading pathogens responsible for infections in humans and animals. The heterogeneous nature of diseases caused by these bacteria is due to the occurrence of multiple strains, differentiated by several mechanisms of antibiotic resistance and virulence factors. One of these is the ability to form biofilm. Biofilm-associated bacteria exhibit a different phenotype that protects them from external factors such as the activity of immune system or antimicrobial substances. Moreover, it has been shown that the majority of persistent and recurrent infections are associated with the presence of the biofilm. Omiganan, an analog of indolicidin - antimicrobial peptide (AMP) derived from bovine neutrophil granules, was found to exhibit high antistaphylococcal and antibiofilm potential. Furthermore, its analog with a reversed sequence (retro-omiganan) was found to display enhanced activity against a variety of pathogens. Based on experience of our group, we found out that counterion exchange can improve the antistaphylococcal activity of AMPs. The aim of this study was to investigate the activity of both compounds against S. aureus biofilm under flow conditions. The advantage of this approach was that it offered the opportunity to form and characterize the biofilm under more controlled conditions. To do this, unique flow cells made of polydimethylsiloxane (PDMS) were developed. The activity against pre-formed biofilm as well as AMPs-treated bacteria was measured. Also, the incorporation of omiganan and retro-omiganan into the channels was conducted to learn whether or not it would inhibit the development of biofilm. The results of the microbiological tests ultimately confirmed the high potential of the omiganan and its retro-analog as well as the importance of counterion exchange in terms of antimicrobial examination. We found out that retro-omiganan trifluoroacetate had the highest biofilm inhibitory properties, however, acetates of both compounds exhibited the highest activity against planktonic and biofilm cultures. Moreover, the developed methodology of investigation under flow conditions allows the implementation of the studies under flow conditions to other compounds.

Abstract Image

流动条件下奥美甘南和逆奥美甘南抗葡萄球菌潜力的研究
金黄色葡萄球菌被认为是导致人类和动物感染的主要病原体之一。由这些细菌引起的疾病性质各异,其原因是存在多种菌株,这些菌株因多种抗生素耐药性机制和毒力因子而各不相同。其中之一就是形成生物膜的能力。与生物膜相关的细菌表现出一种不同的表型,这种表型可以保护它们免受免疫系统或抗菌物质等外部因素的影响。此外,研究表明,大多数持续性和复发性感染都与生物膜的存在有关。研究发现,从牛中性粒细胞颗粒中提取的吲哚苷类似物--抗菌肽(AMP)--Omiganan 具有很高的抗葡萄球菌和抗生物膜潜力。此外,还发现其具有反向序列的类似物(retro-omiganan)对多种病原体具有更强的活性。根据我们小组的经验,我们发现反离子交换可以提高 AMP 的抗葡萄球菌活性。本研究的目的是研究这两种化合物在流动条件下对金黄色葡萄球菌生物膜的活性。这种方法的优势在于它提供了在更可控的条件下形成生物膜并确定其特征的机会。为此,我们开发了由聚二甲基硅氧烷(PDMS)制成的独特流动细胞。对预先形成的生物膜以及经 AMPs 处理的细菌的活性进行了测量。此外,还在通道中加入了奥米加南和后奥米加南,以了解其是否会抑制生物膜的形成。微生物测试结果最终证实了奥米加南及其逆奥米加南的巨大潜力,以及反离子交换在抗菌检查方面的重要性。我们发现,三氟乙酸后奥米加南具有最高的生物膜抑制特性,但这两种化合物的乙酸盐对浮游生物和生物膜培养物的活性最高。此外,所开发的流动条件下的研究方法还可用于其他化合物的流动条件下的研究。
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来源期刊
Probiotics and Antimicrobial Proteins
Probiotics and Antimicrobial Proteins BIOTECHNOLOGY & APPLIED MICROBIOLOGYMICROB-MICROBIOLOGY
CiteScore
11.30
自引率
6.10%
发文量
140
期刊介绍: Probiotics and Antimicrobial Proteins publishes reviews, original articles, letters and short notes and technical/methodological communications aimed at advancing fundamental knowledge and exploration of the applications of probiotics, natural antimicrobial proteins and their derivatives in biomedical, agricultural, veterinary, food, and cosmetic products. The Journal welcomes fundamental research articles and reports on applications of these microorganisms and substances, and encourages structural studies and studies that correlate the structure and functional properties of antimicrobial proteins.
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