Morgan Radwa N, Farrag Hala A, Aboulwafa Mohammad M, Saleh Sarra E
National Centre for Radiation Research and Technology (NCRRT), Drug Radiation Research Department, Egyptian Atomic Energy Authority (EAEA), Ahmed El-Zomor Street, Nasr city, Cairo, 11787, Egypt.
Microbiology and Immunology Department, Faculty of Pharmacy, Ain Shams University, African union organization Street, Abbassia, Cairo, 11566, Egypt.
Curr Microbiol. 2021 Feb;78(2):544-557. doi: 10.1007/s00284-020-02331-6. Epub 2021 Jan 3.
Colibactin and cytotoxic necrotizing factor 1 (Cnf 1) are cyclomodulins secreted by uropathogenic E. coli. In this study, uropathogenic E. coli expressing colibactin and Cnf 1 was exposed to antibiotics subMICs and gamma radiation to investigate their effects on its cytotoxicity and expression of colibactin. The test isolate was exposed to three subMIC levels of levofloxacin, ciprofloxacin, trimethoprim/sulfamethoxazole and ceftriaxone and irradiated with gamma rays at 10 and 24.4 Gy. The cytotoxicity for either antibiotic or gamma rays treated cultures was measured using MTT assay and the expression of colibactin encoding genes was determined by RT-PCR. Treatment with fluoroquinolones nearly abolished the cytotoxicity of E. coli isolate and significantly downregulated clbA gene expression at the tested subMICs (P ≤ 0.05) while trimethoprim/sulfamethoxazole treated cultures exerted significant downregulation of clbA and clbQ genes at 0.5 MIC only (P ≤ 0.05). Ceftriaxone treated cultured exhibited reduction in the cytotoxicity and insignificant effects on expression of clbA, clbQ and clbM genes. On contrast, significant upregulation in the expression of clbA and clbQ genes was observed in irradiated cultures (P ≤ 0.05). Fluoroquinolones reduced both the cytotoxicity of UPEC isolate and colibactin expression at different subMICs while ceftriaxone at subMICs failed to suppress the expression of genotoxin, colibactin, giving an insight to the risks associated upon their choice for UTI treatment. Colibactin expression was enhanced by gamma irradiation at doses resembling these received during pelvic radiotherapy which might contribute to post-radiotherapy complications.
大肠杆菌素和细胞毒性坏死因子1(Cnf 1)是由尿路致病性大肠杆菌分泌的环调节素。在本研究中,将表达大肠杆菌素和Cnf 1的尿路致病性大肠杆菌暴露于亚抑菌浓度的抗生素和γ射线中,以研究它们对其细胞毒性和大肠杆菌素表达的影响。将测试菌株暴露于左氧氟沙星、环丙沙星、甲氧苄啶/磺胺甲恶唑和头孢曲松的三个亚抑菌浓度水平,并分别用10 Gy和24.4 Gy的γ射线进行辐照。使用MTT法测定经抗生素或γ射线处理的培养物的细胞毒性,并通过RT-PCR测定大肠杆菌素编码基因的表达。氟喹诺酮类药物处理几乎消除了大肠杆菌分离株的细胞毒性,并在测试的亚抑菌浓度下显著下调了clbA基因的表达(P≤0.05),而甲氧苄啶/磺胺甲恶唑处理的培养物仅在0.5 MIC时显著下调了clbA和clbQ基因的表达(P≤0.05)。头孢曲松处理的培养物细胞毒性降低,对clbA、clbQ和clbM基因的表达影响不显著。相比之下,在辐照培养物中观察到clbA和clbQ基因的表达显著上调(P≤0.05)。氟喹诺酮类药物在不同亚抑菌浓度下均降低了尿路致病性大肠杆菌分离株的细胞毒性和大肠杆菌素表达,而亚抑菌浓度的头孢曲松未能抑制基因毒素大肠杆菌素的表达,这为其在治疗尿路感染时的选择所带来的风险提供了见解。类似于盆腔放疗期间所接受的剂量的γ射线辐照可增强大肠杆菌素的表达,这可能导致放疗后并发症。