Rajendran R, Sherry L, Nile C J, Sherriff A, Johnson E M, Hanson M F, Williams C, Munro C A, Jones B J, Ramage G
School of Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Public Health England, Southwest Laboratory, Bristol, UK.
Clin Microbiol Infect. 2016 Jan;22(1):87-93. doi: 10.1016/j.cmi.2015.09.018. Epub 2015 Sep 30.
Bloodstream infections caused by Candida species remain a significant cause of morbidity and mortality in hospitalized patients. Biofilm formation by Candida species is an important virulence factor for disease pathogenesis. A prospective analysis of patients with Candida bloodstream infection (n = 217) in Scotland (2012-2013) was performed to assess the risk factors associated with patient mortality, in particular the impact of biofilm formation. Candida bloodstream isolates (n = 280) and clinical records for 157 patients were collected through 11 different health boards across Scotland. Biofilm formation by clinical isolates was assessed in vitro with standard biomass assays. The role of biofilm phenotype on treatment efficacy was also evaluated in vitro by treating preformed biofilms with fixed concentrations of different classes of antifungal. Available mortality data for 134 patients showed that the 30-day candidaemia case mortality rate was 41%, with predisposing factors including patient age and catheter removal. Multivariate Cox regression survival analysis for 42 patients showed a significantly higher mortality rate for Candida albicans infection than for Candida glabrata infection. Biofilm-forming ability was significantly associated with C. albicans mortality (34 patients). Finally, in vitro antifungal sensitivity testing showed that low biofilm formers and high biofilm formers were differentially affected by azoles and echinocandins, but not by polyenes. This study provides further evidence that the biofilm phenotype represents a significant clinical entity, and that isolates with this phenotype differentially respond to antifungal therapy in vitro. Collectively, these findings show that greater clinical understanding is required with respect to Candida biofilm infections, and the implications of isolate heterogeneity.
念珠菌属引起的血流感染仍然是住院患者发病和死亡的重要原因。念珠菌属形成生物膜是疾病发病机制中的一个重要毒力因素。对苏格兰(2012 - 2013年)217例念珠菌血流感染患者进行了前瞻性分析,以评估与患者死亡率相关的危险因素,特别是生物膜形成的影响。通过苏格兰11个不同的卫生委员会收集了280株念珠菌血流分离株和157例患者的临床记录。用标准生物量测定法在体外评估临床分离株的生物膜形成。还通过用固定浓度的不同类别的抗真菌药物处理预先形成的生物膜,在体外评估生物膜表型对治疗效果的作用。134例患者的现有死亡率数据显示,念珠菌血症30天病例死亡率为41%,诱发因素包括患者年龄和拔除导管。对42例患者进行的多变量Cox回归生存分析显示,白色念珠菌感染的死亡率显著高于光滑念珠菌感染。生物膜形成能力与白色念珠菌死亡率显著相关(34例患者)。最后,体外抗真菌敏感性测试表明,低生物膜形成者和高生物膜形成者受唑类和棘白菌素类药物的影响不同,但不受多烯类药物的影响。本研究提供了进一步的证据,表明生物膜表型是一个重要的临床实体,并且具有这种表型的分离株在体外对抗真菌治疗有不同的反应。总体而言,这些发现表明,对于念珠菌生物膜感染以及分离株异质性的影响,需要有更深入的临床认识。