Enhanced Biofilm Formation by Tetracycline in a Staphylococcus aureus Naturally Lacking ica Operon and atl.

IF 2.3 4区 医学 Q3 INFECTIOUS DISEASES Microbial drug resistance Pub Date : 2024-02-01 Epub Date: 2024-01-22 DOI:10.1089/mdr.2023.0186
Yimin Zou, Xuejie Li, Yanxiong Mao, Wenjuan Song, Qing Liu
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Abstract

Staphylococcus aureus is a major, widespread pathogen, and its biofilm-forming characteristics make it even more difficult to eliminate by biocides. Tetracycline (TCY) is a major broad-spectrum antibiotic, the residues of which can cause deleterious health impacts, and subinhibitory concentrations of TCY have the potential to increase biofilm formation in S. aureus. In this study, we showed how the biofilm formation of S. aureus 123786 is enhanced in the presence of TCY at specific subinhibitory concentrations. S. aureus 123786 used in this study was identified as Staphylococcal Cassette Chromosome mec III, sequence type239 and naturally lacking ica operon and atl gene. Two assays were performed to quantify the formation of S. aureus biofilm. In the crystal violet (CV) assay, the absorbance values of biofilm stained with CV at optical density (OD)540 nm increased after 8 and 16 hr of incubation when the concentration of TCY was 1/2 minimum inhibitory concentration (MIC), whereas at the concentration of 1/16 MIC, the absorbance values increased after 16 and 24 hr of incubation. In tetrazolium salt reduction assay, the absorbance value at OD490 nm of S. aureus 123786 biofilms mixed with 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium solution increased after 8 hr when the concentration of TCY was 1/4 MIC, which may be correlated with the higher proliferation and maturation of biofilm. In conclusion, the biofilm formation of S. aureus 123786 could be enhanced in the presence of TCY at specific subinhibitory concentrations.

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在天然缺乏 ica 操作子和 atl 的金黄色葡萄球菌中,四环素增强了生物膜的形成。
金黄色葡萄球菌是一种广泛存在的主要病原体,其形成生物膜的特性使其更难被杀菌剂消灭。四环素(TCY)是一种主要的广谱抗生素,其残留物会对健康造成有害影响,而亚抑制浓度的四环素有可能增加金黄色葡萄球菌生物膜的形成。在这项研究中,我们展示了在特定亚抑制浓度的 TCY 存在下,金黄色葡萄球菌 123786 的生物膜形成是如何增强的。本研究中使用的金黄色葡萄球菌 123786 被鉴定为葡萄球菌盒式染色体 mec III,序列类型 239,天然缺乏 ica 操作子和 atl 基因。为量化金黄色葡萄球菌生物膜的形成进行了两种检测。在水晶紫(CV)检测中,当 TCY 浓度为最低抑菌浓度(MIC)的 1/2 时,培养 8 小时和 16 小时后,用水晶紫染色的生物膜在光密度(OD)540 nm 处的吸光度值增加;而当 TCY 浓度为最低抑菌浓度(MIC)的 1/16 时,培养 16 小时和 24 小时后,吸光度值增加。在四唑盐还原试验中,当 TCY 的浓度为 1/4 MIC 时,金黄色葡萄球菌 123786 生物膜与 3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺酸苯基)-2H-四唑溶液混合后的 OD490 纳米吸光度值在 8 小时后增加,这可能与生物膜的增殖和成熟程度较高有关。总之,在特定亚抑制浓度的 TCY 存在下,金黄色葡萄球菌 123786 的生物膜形成会增强。
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来源期刊
Microbial drug resistance
Microbial drug resistance 医学-传染病学
CiteScore
6.00
自引率
3.80%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Microbial Drug Resistance (MDR) is an international, peer-reviewed journal that covers the global spread and threat of multi-drug resistant clones of major pathogens that are widely documented in hospitals and the scientific community. The Journal addresses the serious challenges of trying to decipher the molecular mechanisms of drug resistance. MDR provides a multidisciplinary forum for peer-reviewed original publications as well as topical reviews and special reports. MDR coverage includes: Molecular biology of resistance mechanisms Virulence genes and disease Molecular epidemiology Drug design Infection control.
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