Bal Halil, Altanlar Nurten, Yıldız Sulhiye
Sivas Cumhuriyet University Faculty of Pharmacy, Department of Pharmaceutical Microbiology, Sivas, Türkiye.
Ankara University Faculty of Pharmacy, Department of Pharmaceutical Microbiology, Ankara, Türkiye.
Turk J Pharm Sci. 2025 May 14;22(2):131-139. doi: 10.4274/tjps.galenos.2025.26723.
The aim of this study was to determine the development of resistance and changes in biofilm forming abilities in methicillin-resistant (MRSA) isolates exposed to sub-minimal inhibitory concentrations (sub-MICs) of daptomycin and linezolid; and to investigate the presence of the methicillin resistance gene () and the biofilm-associated genes () by polymerase chain reaction.
This study was carried out with thirty-two MRSA isolates. The susceptibility of the isolates to daptomycin and linezolid was investigated by the broth microdilution method, and MIC values were determined (1 MIC). After serial passages, the 2 MIC and the 3 MIC values were similarly detected. Before and after serial passages, the biofilm-forming abilities of MRSA isolates were examined using the microtiter plate (MTP) method.
When the daptomycin and linezolid 1 MIC and 3 MIC values of the isolates were compared, there was a 2-8 fold increase in linezolid (<0.05) and a 4-32 fold increase in daptomycin (<0.05). According to the MTP method, 20 (62.5%) of the 32 isolates formed biofilm at various levels, while 12 (37.5%) did not form biofilm. After the second series of passages, biofilm formation was observed in 19 (59.4%) isolates with daptomycin (p>0.05) and in 16 (50%) isolates with linezolid (p>0.05). The gene was found in all isolates. Also, and genes were detected in 31 (96.9%) of 32 MRSA isolates.
MRSA isolates exposed to sub-MICs of the antibiotics daptomycin and linezolid were observed to form biofilms at varying levels or to lose their ability to form biofilms. The induction, reduction or eradication of biofilm depended on the type of antibiotic and the MRSA isolate.
本研究旨在确定耐甲氧西林金黄色葡萄球菌(MRSA)分离株在接触达托霉素和利奈唑胺的亚最小抑菌浓度(sub-MICs)后耐药性的发展及生物膜形成能力的变化;并通过聚合酶链反应研究甲氧西林耐药基因()和生物膜相关基因()的存在情况。
本研究使用了32株MRSA分离株。采用肉汤微量稀释法研究分离株对达托霉素和利奈唑胺的敏感性,并确定MIC值(1倍MIC)。连续传代后,同样检测2倍MIC和3倍MIC值。在连续传代前后,使用微量滴定板(MTP)法检测MRSA分离株的生物膜形成能力。
当比较分离株的达托霉素和利奈唑胺1倍MIC和3倍MIC值时,利奈唑胺增加了2 - 8倍(<0.05),达托霉素增加了4 - 32倍(<0.05)。根据MTP法,32株分离株中有20株(62.5%)在不同水平形成生物膜,而12株(37.5%)未形成生物膜。在第二轮传代后,使用达托霉素时,19株(59.4%)分离株观察到生物膜形成(p>0.05),使用利奈唑胺时,16株(50%)分离株观察到生物膜形成(p>0.05)。在所有分离株中均发现了基因。此外,在32株MRSA分离株中的31株(96.9%)中检测到和基因。
观察到接触抗生素达托霉素和利奈唑胺亚MICs的MRSA分离株在不同水平形成生物膜或失去其形成生物膜的能力。生物膜的诱导、减少或消除取决于抗生素的类型和MRSA分离株。