Banerjee Satarupa, Vishakha Kumari, Das Shatabdi, Dutta Moumita, Mukherjee Debolina, Mondal Jyotsna, Mondal Sandhimita, Ganguli Arnab
Department of Microbiology, Techno India University, EM - 4 Sector -V, Saltlake City, Kolkata, West Bengal, 700091, India.
Division of Electron Microscopy, ICMR-National Institute of Cholera and Enteric Diseases, P- C.I.T. Scheme XM, Beleghata, 33, CIT Rd, Subhas Sarobar Park, Phool Bagan, Beleghata, Kolkata, West Bengal, 700010, India.
Colloids Surf B Biointerfaces. 2020 Jun;190:110921. doi: 10.1016/j.colsurfb.2020.110921. Epub 2020 Mar 4.
Staphylococcus aureus are known to cause diseases from normal skin wound to life intimidating infections. Among the drug resistant strain, management of methicillin resistant Staphylococcus aureus (MRSA) is very difficult by using conventional antibiotic treatment. Both Zinc oxide nanoparticles (ZnONPs) and pancreatin (PK) are known to have antibacterial activity. Our main objective is to dope PK on ZnONPs to reduced zinc-oxide toxicity but increased anti-bacterial and anti-biofilms activity. In present study, we showed that, functions of zinc oxide nanoparticles with pancreatin enzyme (ZnONPs-PK) have anti-bacterial, anti-biofilms, anti-motility and anti-virulence properties against MRSA. Moreover, ZnONPs-PK were more potent to eradicate MRSA than only ZnONPs and PK. Application of the produced nano-composites as treatment on infected swine dermis predominantly reflects the potential treatment property of it. The vancomycin sensitivity of MRSA was significantly increased on application with ZnONPs-PK. Further study revealed cell membrane was the target of the ZnONPs-PK and that leads to oxidative damage of the cells. The produced nanoparticles were found completely non-toxic to human's keratinocytes and lung epithelial cell lines at its bactericidal concentration. Overall, this study emphasizes the potential mechanisms underlying the selective bactericidal properties of ZnONPs-PK against MRSA. This novel nanoparticle strategy may provide the ideal solution for comprehensive management of MRSA and its associated diseases with minimising the use of antibiotics.
金黄色葡萄球菌已知可引发从普通皮肤伤口到危及生命的感染等各种疾病。在耐药菌株中,使用传统抗生素治疗耐甲氧西林金黄色葡萄球菌(MRSA)非常困难。氧化锌纳米颗粒(ZnONPs)和胰酶(PK)都已知具有抗菌活性。我们的主要目标是将PK掺杂在ZnONPs上,以降低氧化锌的毒性,但增强抗菌和抗生物膜活性。在本研究中,我们表明,含有胰酶的氧化锌纳米颗粒(ZnONPs-PK)对MRSA具有抗菌、抗生物膜、抗运动性和抗毒力特性。此外,ZnONPs-PK比单独的ZnONPs和PK更有效地根除MRSA。将制备的纳米复合材料应用于感染猪真皮的治疗,主要体现了其潜在的治疗特性。在应用ZnONPs-PK时,MRSA对万古霉素的敏感性显著增加。进一步研究表明,细胞膜是ZnONPs-PK的作用靶点,这会导致细胞的氧化损伤。所制备的纳米颗粒在其杀菌浓度下对人角质形成细胞和肺上皮细胞系完全无毒。总体而言,本研究强调了ZnONPs-PK对MRSA选择性杀菌特性的潜在机制。这种新型纳米颗粒策略可能为全面管理MRSA及其相关疾病提供理想解决方案,同时尽量减少抗生素的使用。