de Andrade João Paulo Lopes, de Macêdo Farias Luiz, Ferreira João Fernando Gonçalves, Bruna-Romero Oscar, da Glória de Souza Daniele, de Carvalho Maria Auxiliadora Roque, dos Santos Kênia Valéria
Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627 - Pampulha, C.P. 486, Belo Horizonte, MG, CEP 31270-901, Brazil.
Centro de Ciências Biológicas/MIP, Universidade Federal de Santa Catarina, Campus Universitário do Córrego Grande, sn, sala05, Bl. A, MIP, C.P. 476, Florianópolis, SC, CEP: 88040-970, Brazil.
Curr Microbiol. 2016 Jan;72(1):19-28. doi: 10.1007/s00284-015-0912-9. Epub 2015 Sep 12.
Sub-inhibitory concentrations of antibiotics are always generated as a consequence of antimicrobial therapy and the effects of such residual products in bacterial morphology are well documented, especially the filamentation generated by beta-lactams. The aim of this study was to investigate some morphological and pathological aspects (virulence factors) of Escherichia coli cultivated under half-minimum inhibitory concentration (1.0 µg/mL) of piperacillin-tazobactam (PTZ sub-MIC). PTZ sub-MIC promoted noticeable changes in the bacterial cells which reach the peak of morphological alterations (filamentation) and complexity at 16 h of antimicrobial exposure. Thereafter the filamentous cells and a control one, not treated with PTZ, were comparatively tested for growth curve; biochemical profile; oxidative stress tolerance; biofilm production and cell hydrophobicity; motility and pathogenicity in vivo. PTZ sub-MIC attenuated the E. coli growth rate, but without changes in carbohydrate fermentation or in traditional biochemical tests. Overall, the treatment of E. coli with sub-MIC of PTZ generated filamentous forms which were accompanied by the inhibition of virulence factors such as the oxidative stress response, biofilm formation, cell surface hydrophobicity, and motility. These results are consistent with the reduced pathogenicity observed for the filamentous E. coli in the murine model of intra-abdominal infection. In other words, the treatment of E. coli with sub-MIC of PTZ suggests a decrease in their virulence.
抗生素的亚抑制浓度总是抗菌治疗的结果,此类残留产物对细菌形态的影响已有充分记录,尤其是β-内酰胺类抗生素所导致的丝状化。本研究旨在调查在哌拉西林-他唑巴坦半最小抑菌浓度(1.0µg/mL,PTZ亚抑菌浓度)下培养的大肠杆菌的一些形态学和病理学方面(毒力因子)。PTZ亚抑菌浓度促使细菌细胞发生显著变化,在抗菌暴露16小时时达到形态改变(丝状化)和复杂性的峰值。此后,对丝状细胞和未用PTZ处理的对照细胞进行生长曲线、生化谱、氧化应激耐受性、生物膜产生和细胞疏水性、运动性及体内致病性的比较测试。PTZ亚抑菌浓度降低了大肠杆菌的生长速率,但碳水化合物发酵或传统生化测试无变化。总体而言,用PTZ亚抑菌浓度处理大肠杆菌产生了丝状形态,同时伴随着毒力因子如氧化应激反应、生物膜形成、细胞表面疏水性和运动性的抑制。这些结果与在腹腔内感染小鼠模型中观察到的丝状大肠杆菌致病性降低一致。换句话说,用PTZ亚抑菌浓度处理大肠杆菌表明其毒力下降。