Drug Applied Research Center, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran; Student Research Committee, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Veterinary Biosciences, Ohio State University, Columbus, OH, 43210, United States.
Microb Pathog. 2020 Feb;139:103907. doi: 10.1016/j.micpath.2019.103907. Epub 2019 Dec 5.
Enterococcus faecalis is one of the important causes of nosocomial infections. Nowadays, increasing prevalence of antibiotic-resistant bacteria and slow progress in recognizing new antimicrobial agents has limited the efficiency of conventional antibiotics, which cause to find novel strategies to overcome bacteria. Therefore, in this study, we aimed to assess the role of efaA gene in the biofilm formation and the role of ftsZ gene in the controlling of bacterial growth by the anti-sense PNAs(Peptide Nucleic Acid).E. faecalis ATCC® 29212™was used for the study of PNAs designed to targeting the start codon section of the ftsZ andefaA genes. PNA attachment to RNA was confirmed by blotting. Electroporation technique was used for the intracellular transfer of anti-ftsZ PNAs. The spot-plating method was used to the assessment of alteration in bacterial growth. Biofilm formation assay and real-time PCR were used for detection of biofilm inhibitory effect of cell penetrating peptide (CPP) conjugated to anti-efaA PNAs.ByftsZ PNAs treatment, no growth was seen from the strain in agar by a spot plating method and the inhibition zone of anti-ftsZ PNAs was not seen. PNAs against the efaA gene decreased by 95% the expression of the efaA gene and biofilm formation. In addition, the(3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide) MTT assay showed no toxicity on MCF7 cells for both of anti-ftsZand anti-efaA PNAs.This study used new genetic and molecular tools to inhibit pathogenicity and infection by E. faecalis. In this study, we suggested that efaA gene plays a critical role in the biofilm formation and anti-efaA PNAs could decrease the formation of biofilm, as well as, anti-ftsZ PNAs could eliminate bacterial growth.
粪肠球菌是医院感染的重要原因之一。如今,抗生素耐药菌的不断增加和新抗菌药物的识别进展缓慢,限制了常规抗生素的效率,因此需要寻找新的策略来克服细菌。因此,在这项研究中,我们旨在评估 efaA 基因在生物膜形成中的作用和 ftsZ 基因在通过反义 PNAs(肽核酸)控制细菌生长中的作用。使用粪肠球菌 ATCC®29212™来研究设计用于靶向 ftsZ 和 efaA 基因起始密码子区的 PNAs。通过印迹法证实 PNA 与 RNA 的结合。电穿孔技术用于细胞内反 ftsZ PNA 的转移。点平板法用于评估细菌生长的变化。生物膜形成测定和实时 PCR 用于检测细胞穿透肽(CPP)缀合的抗 efaA PNAs 的生物膜抑制作用。通过 ftsZ PNAs 处理,通过点平板法从琼脂中看不到菌株的生长,也看不到抗 ftsZ PNAs 的抑制带。针对 efaA 基因的 PNAs 使 efaA 基因的表达和生物膜形成降低了 95%。此外,MTT 法(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐)对 MCF7 细胞均显示出对两种抗 ftsZ 和抗 efaA PNAs 的无毒性。本研究使用新的遗传和分子工具来抑制粪肠球菌的致病性和感染。在这项研究中,我们认为 efaA 基因在生物膜形成中起关键作用,抗 efaA PNAs 可以减少生物膜的形成,而抗 ftsZ PNAs 可以消除细菌的生长。