Enzyme and Microbial Technology Research Center, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
PLoS One. 2021 May 11;16(5):e0251514. doi: 10.1371/journal.pone.0251514. eCollection 2021.
Infections caused by methicillin-resistant Staphylococcus aureus (MRSA) have reached epidemic proportions globally. Therefore, there is an urgent need for a continuous supply of antibiotics to combat the problem. In this study, bacteria initially identified as species belonging to the Bacillus amyloliquefaciens operational group were re-identified based on the housekeeping gene, gyrB. Cell-free supernatants (CFS) from the strains were used for antimicrobial tests using the agar well diffusion assay against MRSA and various types of pathogenic bacteria. The minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and physicochemical characteristics of the CFS were determined. Based on gyrB sequence analysis, five strains (PD9, B7, PU1, BP1 and L9) were identified as Bacillus velezensis. The CFS of all B. velezensis strains showed broad inhibitory activities against Gram-negative and -positive as well as MRSA strains. Strain PD9 against MRSA ATCC 33742 was chosen for further analysis as it showed the biggest zone of inhibition (21.0 ± 0.4 mm). The MIC and MBC values obtained were 125 μl/ml. The crude antimicrobial extract showed bactericidal activity and was stable at various temperatures (40-80°C), pH (4-12), surfactants (Tween 20, Tween 80, SDS and Triton X-100) and metal ions (MgCI2, NaCI2, ZnNO3 and CuSO4) when tested. However, the crude extract was not stable when treated with proteinase K. All these properties resembled the characteristics of peptides. The antimicrobial compound from the selected strain was purified by using solvent extraction method and silica gel column chromatography. The purified compound was subjected to High Performance Liquid Chromatography which resulted in a single peak of the anti-MRSA compound being detected. The molecular weight of the anti-MRSA compound was determined by using SDS-PAGE and zymogram. The size of the purified antimicrobial peptide was approximately ~ 5 kDa. The antimicrobial peptide produced from B. velezensis strain PD9 is a promising alternative to combat the spread of MRSA infections in the future.
耐甲氧西林金黄色葡萄球菌 (MRSA) 引起的感染在全球范围内已经达到流行程度。因此,迫切需要持续供应抗生素来解决这个问题。在这项研究中,根据管家基因 gyrB,最初鉴定为属于解淀粉芽孢杆菌操作群的细菌被重新鉴定。使用琼脂孔扩散法对抗 MRSA 和各种类型的致病菌对菌株的无细胞上清液 (CFS) 进行了抗菌测试。测定了最小抑菌浓度 (MIC)、最小杀菌浓度 (MBC) 和 CFS 的理化特性。根据 gyrB 序列分析,将 5 株 (PD9、B7、PU1、BP1 和 L9) 鉴定为解淀粉芽孢杆菌。所有解淀粉芽孢杆菌菌株的 CFS 对革兰氏阴性和阳性以及 MRSA 菌株均显示出广泛的抑制活性。选择 PD9 菌株对抗 ATCC 33742 的 MRSA 进行进一步分析,因为它显示出最大的抑制区 (21.0±0.4mm)。获得的 MIC 和 MBC 值分别为 125μl/ml。粗抗菌提取物具有杀菌活性,在各种温度 (40-80°C)、pH 值 (4-12)、表面活性剂 (吐温 20、吐温 80、SDS 和 Triton X-100) 和金属离子 (MgCI2、NaCI2、ZnNO3 和 CuSO4) 下稳定。然而,当用蛋白酶 K 处理时,粗提取物不稳定。所有这些特性都与肽的特性相似。从选定的菌株中通过使用溶剂萃取法和硅胶柱色谱法纯化抗菌化合物。对纯化的化合物进行高效液相色谱分析,结果检测到抗-MRSA 化合物的单个峰。通过 SDS-PAGE 和同工酶分析确定抗-MRSA 化合物的分子量。纯化的抗菌肽的大小约为~5kDa。来自解淀粉芽孢杆菌 PD9 菌株的抗菌肽是未来对抗 MRSA 感染传播的有前途的替代品。