Priyanto Jepri Agung, Prastya Muhammad Eka, Hening Egiyanti Nur Widhia, Suryanti Erma, Kristiana Rhesi
Division of Microbiology, Department of Biology, Faculty of Mathematics and Natural Sciences, IPB University, Agatis Street, IPB Dramaga Campus, Bogor, West Java 16680 Indonesia.
Research Center for Pharmaceutical Ingredients and Traditional Medicine, National Research and Innovation Agency (BRIN), Kawasan Sains Dan Teknologi (KST) B.J Habibie (PUSPIPTEK), Serpong, South Tangerang, Banten Indonesia.
Indian J Microbiol. 2024 Dec;64(4):1884-1893. doi: 10.1007/s12088-024-01262-1. Epub 2024 Apr 2.
Methicillin-resistant (MRSA) is considered a priority pathogen causing high mortality that requires effective control measures. This study aimed to detect the presence of antibiotic-biosynthetic genes and to evaluate the anti-MRSA activity of two strains of endophytic isolated from . PCR-based screening showed that strains, such as DJ4 and DJ9 possessed six antibiotic-biosynthetic genes, namely , and According to the preliminary test conducted using disc-diffusion assay, metabolite extracts from these strains have anti-MRSA activity with clear zone diameters of 13.00 ± 0.82 mm, and 17.33 ± 0.47 mm, respectively. Extract from DJ9 strain was more active to MRSA, with minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of 62.50 µg/mL and 250 µg/mL, respectively. Furthermore, a bactericidal effect was observed, as evidenced by MBC/MIC ratio of four. Both DJ9 and DJ4 extracts showed a dose-dependent inhibitory effect on MRSA biofilm formation. Furthermore, a maximum inhibition percentage of 60.12 ± 2.5% was shown by DJ9 extract in two-fold MIC. The corresponding extract disrupted MRSA mature biofilms most effectively at 55.74 ± 1.4%. In conclusion, crude extract, particularly the DJ9 strain had significant potential in inhibiting MRSA cell growth, MRSA biofilm formation, and disrupting MRSA mature biofilm in vitro.
The online version contains supplementary material available at 10.1007/s12088-024-01262-1.
耐甲氧西林金黄色葡萄球菌(MRSA)被视为导致高死亡率的重点病原体,需要采取有效控制措施。本研究旨在检测抗生素生物合成基因的存在,并评估从……分离出的两株内生菌的抗MRSA活性。基于PCR的筛选表明,DJ4和DJ9等菌株拥有六个抗生素生物合成基因,即……。根据使用纸片扩散法进行的初步试验,这些菌株的代谢物提取物具有抗MRSA活性,透明圈直径分别为13.00±0.82毫米和17.33±0.47毫米。DJ9菌株的提取物对MRSA更具活性,其最低抑菌浓度(MIC)和最低杀菌浓度(MBC)值分别为62.50微克/毫升和250微克/毫升。此外,观察到杀菌效果,MBC/MIC比值为4证明了这一点。DJ9和DJ4提取物对MRSA生物膜形成均表现出剂量依赖性抑制作用。此外,DJ9提取物在两倍MIC时显示出最大抑制率为60.12±2.5%。相应提取物在55.74±1.4%时最有效地破坏了MRSA成熟生物膜。总之,粗提取物,特别是DJ9菌株在体外抑制MRSA细胞生长、MRSA生物膜形成和破坏MRSA成熟生物膜方面具有显著潜力。
在线版本包含可在10.1007/s12088-024-01262-1获取的补充材料。