The genome-wide de novo mutations and icaA gene expression levels in Staphylococcus aureus under long-term subinhibitory and semisubinhibitory nisin exposure.

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Hüseyin Özgür Özdemirel, Sibel Kucukyildirim
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引用次数: 0

Abstract

The emergence and rapid spread of multidrug-resistant pathogens have caused a need for alternative antimicrobials, and bacteriocins are considered promising alternatives due to their lower risk of resistance development. Regarding this, we aimed to investigate the long-term subinhibitory and semisubinhibitory concentrations of a commonly used bacteriocin (nisin) in Staphylococcus aureus using an experimental evolution approach followed by genome sequencing. We then performed RT-qPCR to examine changes in the expression level of the biofilm-related icaA gene in evolved lines. We found that while nisin treatment did not significantly elevate the base-substitution rates, there was a significant decrease in the insertion/deletion rate in the lines exposed to the subinhibitory concentration of nisin. We also revealed an increase in nonsynonymous mutations in specific genes (e.g. sarS and cap8) associated with resistance and virulence mechanisms. Importantly, we observed a transition bias in the nisin-treated lines for the first time, and it may be related to the resistance development to nisin. RT-qPCR analysis of the icaA gene showed a reduced expression levels in nisin-treated groups, although the results were not statistically significant. These findings show the potential outcomes of nisin exposure in S. aureus and emphasize the need for careful consideration of bacteriocins in clinical practice.

Abstract Image

Abstract Image

长期亚抑制性和半抑制性nisin暴露下金黄色葡萄球菌全基因组新生突变和icaA基因表达水平
耐多药病原体的出现和迅速传播导致需要替代抗菌素,细菌素被认为是有希望的替代品,因为它们产生耐药性的风险较低。为此,我们旨在通过实验进化方法和基因组测序来研究金黄色葡萄球菌中常用的细菌素(nisin)的长期亚抑制和半亚抑制浓度。然后,我们使用RT-qPCR检测进化系中与生物膜相关的icaA基因表达水平的变化。我们发现,虽然nisin处理没有显著提高碱基取代率,但在暴露于nisin亚抑制浓度的品系中,插入/删除率显著降低。我们还揭示了与抗性和毒力机制相关的特定基因(如sarS和cap8)的非同义突变的增加。重要的是,我们首次在nisin处理的品系中观察到过渡偏倚,这可能与对nisin的抗性发展有关。RT-qPCR分析显示,icaA基因在nisin处理组中表达水平降低,但结果无统计学意义。这些发现显示了金黄色葡萄球菌暴露于nisin的潜在结果,并强调了在临床实践中仔细考虑细菌素的必要性。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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