Kaur Gurmeet, Balamurugan P, Vasudevan Sahana, Jadav Saikiran, Princy S A
Quorum Sensing Laboratory, Centre for Research in Infectious Diseases, School of Chemical and Biotechnology, SASTRA UniversityThanjavur, India.
Front Microbiol. 2017 Sep 15;8:1767. doi: 10.3389/fmicb.2017.01767. eCollection 2017.
Multi-drug resistant (MDRSA) remains a great challenge despite a decade of research on antimicrobial compounds against their infections. In the present study, various acyclic amines and diamines were chemically synthesized and tested for their antimicrobial as well as antibiofilm activity against MDRSA. Among all the synthesized compounds, an acyclic diamine, (2,2'-((butane-1,4-diylbis(azanediyl)bis(methylene))diphenol) designated as ADM 3, showed better antimicrobial activity (minimum inhibitory concentration at 50 μg/mL) and antibiofilm activity (MBIC at 5 μg/mL). In addition, ADM 3 was capable of reducing the virulence factors expression (anti-virulence). Confocal laser scanning microscope analysis of the tested urinary catheters showed biofilm reduction as well as bacterial killing by ADM 3. On the whole, our data suggest that acyclic diamines, especially ADM 3 can be a potent lead for the further studies in alternative therapeutic approaches.
尽管针对耐多药金黄色葡萄球菌(MDRSA)感染的抗菌化合物已经进行了十年的研究,但它仍然是一个巨大的挑战。在本研究中,化学合成了各种无环胺和二胺,并测试了它们对MDRSA的抗菌和抗生物膜活性。在所有合成的化合物中,一种无环二胺,即(2,2'-((丁烷-1,4-二基双(氮杂二基)双(亚甲基))二酚),命名为ADM 3,表现出更好的抗菌活性(最低抑菌浓度为50μg/mL)和抗生物膜活性(最低生物膜抑制浓度为5μg/mL)。此外,ADM 3能够降低毒力因子的表达(抗毒力)。对测试的导尿管进行共聚焦激光扫描显微镜分析表明,ADM 3可减少生物膜并杀死细菌。总体而言,我们的数据表明,无环二胺,尤其是ADM 3可能是替代治疗方法进一步研究的有力先导。