Gopichand Pallam, Agarwal Girija, Natarajan Mailan, Mandal Jharna, Deepanjali Surendran, Parameswaran Sreejith, Dorairajan L N
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), Pondicherry, India.
Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER) , Pondicherry, India.
Infect Drug Resist. 2019 Jul 9;12:2005-2013. doi: 10.2147/IDR.S207569. eCollection 2019.
Rising rates of resistance to antimicrobial drugs among limit the choice of therapeutic agents to treat urinary tract infections. In this context we assessed the in-vitro effect of fosfomycin against extended-spectrum beta-lactamases, AmpC beta-lactamases and carbapenemase-producing strains of spp, and isolated from the patients with urinary tract infection (UTI) and also studied the effect of fosfomycin on their biofilm formation.
A total of 326 multidrug-resistant (MDR) isolates comprising of spp, and from the urine samples of the patients with a diagnosis of UTI were included in the study. MIC 50 and MIC 90 were detected by agar dilution method and the capacity to form biofilm in the presence of fosfomycin by these MDR isolates was assessed by the tissue culture plate method.
The MIC50 for meropenem (0.5 µgm/mL) and nitrofurantoin (32 µgm/mL) was within the susceptible range only for . Fosfomycin was the only antibiotic that inhibited 100% , 70% spp, and 50% spp and 40% spp which included the extended-spectrum beta-lactamases producers. It showed a similar effect on carbapenemase producers and AmpC producers. Fosfomycin disrupted biofilm in 67% (n=141) , 74% (n=50) spp, 88% (n=27) spp and 36% (n=23) spp at 24 hrs of incubation with a concentration of 2 fold dilution lower than that of the MIC.
Fosfomycin showed a good inhibitory effect on the biofilms produced by the MDR organisms studied here.
尿路致病性大肠埃希菌、肺炎克雷伯菌和奇异变形杆菌对抗菌药物的耐药率不断上升,限制了治疗尿路感染的治疗药物选择。在此背景下,我们评估了磷霉素对产超广谱β-内酰胺酶、AmpCβ-内酰胺酶和碳青霉烯酶的尿路致病性大肠埃希菌、肺炎克雷伯菌和奇异变形杆菌菌株的体外抗菌效果,并研究了磷霉素对其生物膜形成的影响。
本研究共纳入326株多重耐药(MDR)菌株,包括从诊断为尿路感染的患者尿液样本中分离出的尿路致病性大肠埃希菌、肺炎克雷伯菌和奇异变形杆菌。采用琼脂稀释法检测MIC50和MIC90,并通过组织培养板法评估这些MDR菌株在磷霉素存在下形成生物膜的能力。
美罗培南(0.5µg/mL)和呋喃妥因(32µg/mL)的MIC50仅在对尿路致病性大肠埃希菌的敏感范围内。磷霉素是唯一一种能100%抑制尿路致病性大肠埃希菌、70%肺炎克雷伯菌、50%奇异变形杆菌和40%阴沟肠杆菌的抗生素,其中包括产超广谱β-内酰胺酶的菌株。它对产碳青霉烯酶菌株和产AmpC酶菌株也有类似作用。在浓度比MIC低2倍稀释度的情况下孵育24小时后,磷霉素破坏了67%(n=141)的尿路致病性大肠埃希菌、74%(n=50)的肺炎克雷伯菌、88%(n=27)的奇异变形杆菌和36%(n=23)的阴沟肠杆菌的生物膜。
磷霉素对本研究中的MDR菌株产生的生物膜具有良好的抑制作用。