Maryam Lubna, Khan Asad U
Interdisciplinary Biotechnology Unit, Medical Microbiology and Molecular Biology Laboratory, Aligarh Muslim UniversityAligarh, India.
Front Pharmacol. 2017 Jul 5;8:449. doi: 10.3389/fphar.2017.00449. eCollection 2017.
CTX-M-15 type β-lactamase has the ability to hydrolyse cefotaxime, a third generation cephalosporin. The infections caused by multidrug resistant strains, especially CTX-M-15 producing strains are being treated with carbapenem group of β-lactam antibiotics. The objective of the study was to know if cefotaxime in combination with doripenem (carbapemen antibiotic) at very low concentration, inhibits the CTX-M-15 producing bacterial strains. gene was cloned to express CTX-M-15 enzyme and construct CTX-M-15 producing strain. The clone carrying CTX-M-15 was found susceptible to doripenem. Doripenem and CTX-M-15 binding was an endothermic and spontaneous process leading to change in polarity in the micro-environment and conformational changes of enzyme as shown by fluorescence, UV and CD spectroscopic study. The catalytic efficiency of CTX-M-15 enzyme was reduced to about 15.86% when it was treated with doripenem along with cefotaxime (in 5 times molar ratio each of doripenem and cefotaxime w.r.t CTX-M-15), as compared to the studies where enzyme's efficiency was increased by 33% when treated with cefotaxime alone. Hence, doripenem in combination with cefotaxime reduces enzyme's efficiency to hydrolyse cefotaxime by about 48%. FIC study showed that doripenem paired with cefotaxime showed synergistic effect against CTX-M-15 producing bacterial strain. The study concludes that doripenem at very low concentration (25 nM), induces such a structural changes in CTX-M-15 which reduced enzyme's activity to hydrolyse cefotaxime. Hence, the synergistic use of doripenem and cefotaxime plays a significant role in inhibiting the efficiency of CTX-M-15 type β-lactamase, and may provide an alternative approach to reduce the resistance against the cephalosporin type antibiotics.
CTX-M-15型β-内酰胺酶具有水解第三代头孢菌素头孢噻肟的能力。由多重耐药菌株,尤其是产CTX-M-15菌株引起的感染,正使用碳青霉烯类β-内酰胺抗生素进行治疗。本研究的目的是了解极低浓度的头孢噻肟与多利培南(碳青霉烯类抗生素)联合使用时,是否能抑制产CTX-M-15的细菌菌株。克隆基因以表达CTX-M-15酶并构建产CTX-M-15菌株。发现携带CTX-M-15的克隆对多利培南敏感。荧光、紫外和圆二色光谱研究表明,多利培南与CTX-M-15的结合是一个吸热且自发的过程,导致微环境极性改变和酶的构象变化。与单独用头孢噻肟处理时酶效率提高33%的研究相比,当用多利培南和头孢噻肟(相对于CTX-M-15,多利培南和头孢噻肟的摩尔比均为5倍)联合处理时,CTX-M-15酶的催化效率降低至约15.86%。因此,多利培南与头孢噻肟联合使用可使酶水解头孢噻肟的效率降低约48%。FIC研究表明,多利培南与头孢噻肟联用对产CTX-M-15的细菌菌株显示出协同作用。该研究得出结论,极低浓度(25 nM)的多利培南会引起CTX-M-15的结构变化,从而降低其水解头孢噻肟的酶活性。因此,多利培南与头孢噻肟的协同使用在抑制CTX-M-15型β-内酰胺酶的效率方面发挥着重要作用,并且可能为降低对头孢菌素类抗生素的耐药性提供一种替代方法。