Microbiology department, Faculty of Medicine, Hamadan University of Medical Sciences, Pajoohesh junction, Hamadan, Iran.
Department of Virology, School of Medicine, University of Hamadan, Pajoohesh junction, Hamadan, Iran.
Eur J Med Res. 2022 Sep 8;27(1):173. doi: 10.1186/s40001-022-00804-x.
Staphylococcus aureus and Pseudomonas aeruginosa were the most common bacteria in nosocomial infections. Different bacteriocins are currently being studied as antibiotics or in conjunction with antibiotics as potential strategies to treat resistant infectious agents. The study aimed to determine nisin's effect on the biofilm production, antimicrobial susceptibility, and biofilm formation of S. aureus and P. aeruginosa.
The experimental research tested two antibiotic-resistant isolates of S. aureus and P. aeruginosa strains. The experimental study tested two antibiotic-resistant isolates of S. aureus and P. aeruginosa strains. The MIC of bacteriocin nisin was determined using the micro broth dilution method, and crystal violet was used to assess the effect of bacteriocin on the biofilm. In addition, L929 cell culture was used to determine the effectiveness of bacteriocin on the isolate under similar cell conditions. Moreover, the MTT assay was used to and evaluate bacteriocin toxicity. In this study, the software Prism version 9 and Graph pad software were utilized.
The results of this study reveal that the nisin has different activities at different doses and is considered dose-dependent. At various times and doses, nisin inhibits biofilm formation in S. aureus, and P. aeruginosa isolates. Nisin also showed a decreasing survival of the isolates. Antibiotic-resistant bacteria can be made more vulnerable by nisin. Furthermore, nisin treatment affected the production of virulence factors such as hemolysins in S. aureus and had little or a negative effect on P. aeruginosa virulence factors. This medication stops S. aureus and P. aeruginosa from growing and causes bacterial cell damage.
Antibacterial properties of nicin against S. aureus and P. aeruginosa were successfully studied. This bacteriocin stops S. aureus and P. aeruginosa from growing and causes bacterial cell damage or death. Damage to the membrane among the fundamental causes is reduced membrane potential and enzyme inactivation.
金黄色葡萄球菌和铜绿假单胞菌是医院感染中最常见的细菌。目前正在研究不同的细菌素作为抗生素或与抗生素联合使用,作为治疗耐药感染因子的潜在策略。本研究旨在确定乳链菌肽对金黄色葡萄球菌和铜绿假单胞菌生物膜形成、抗菌药物敏感性和生物膜形成的影响。
实验研究检测了两种耐抗生素的金黄色葡萄球菌和铜绿假单胞菌分离株。使用微量肉汤稀释法测定细菌素乳链菌肽的 MIC,并用结晶紫评估细菌素对生物膜的影响。此外,使用 L929 细胞培养在类似细胞条件下测定细菌素对分离物的有效性。此外,使用 MTT 测定法评估细菌素的毒性。在这项研究中,使用了 Prism 版本 9 和 Graph pad 软件。
本研究结果表明,乳链菌肽在不同剂量下具有不同的活性,且被认为是剂量依赖性的。在不同的时间和剂量下,乳链菌肽抑制金黄色葡萄球菌和铜绿假单胞菌分离株的生物膜形成。乳链菌肽还显示出分离物存活率降低。耐抗生素细菌可以通过乳链菌肽变得更加脆弱。此外,乳链菌肽处理影响金黄色葡萄球菌的毒力因子如溶血素的产生,并且对铜绿假单胞菌的毒力因子几乎没有影响或产生负面影响。这种药物阻止金黄色葡萄球菌和铜绿假单胞菌生长并导致细菌细胞损伤。
成功研究了乳链菌肽对金黄色葡萄球菌和铜绿假单胞菌的抗菌特性。这种细菌素阻止金黄色葡萄球菌和铜绿假单胞菌生长并导致细菌细胞损伤或死亡。膜损伤是由于膜电位降低和酶失活等基本原因造成的。