van der Mee-Marquet Nathalie L, Blanc Dominique S, Gbaguidi-Haore Houssein, Dos Santos Borges Sandra, Viboud Quentin, Bertrand Xavier, Quentin Roland
Service de Bactériologie et Hygiène, Centre Hospitalier Universitaire de Tours, UMR 1282 Tours, France ; Réseau des Hygiénistes du Centre, Centre Hospitalier Universitaire de Tours France.
Service of Hospital Preventive Medicine, Lausanne University Hospital Lausanne, Switzerland.
Front Microbiol. 2015 Jun 30;6:646. doi: 10.3389/fmicb.2015.00646. eCollection 2015.
We conducted a survey including 3334 bloodstream infections (BSIs) due to E. coli diagnosed in 2005-2014 at a stable cohort of hospitals. Marked increases in incidence were observed for community-acquired (CA) BSIs in patients aged >75 years, CA-BSIs of digestive origin in patients aged 60-74 years, healthcare-associated BSIs, and BSIs associated with ESBL (extended-spectrum B-lactamase)-producing E. coli (ESBLEc). Using MLST, we studied the genetic diversity of 412 BSI isolates recovered during the 2014 survey: 7 major sequence type complexes (STCs) were revealed in phylogenetic group B2, 3 in group A/B1 and 2 in group D. Among the 31 ESBLEc isolates, 1/3 belonged to STC 131. We searched for possible associations between clonal groups, clinical determinants and characteristics of BSIs: isolates from groups B2 (except STC 131) and D were susceptible to antibiotics and associated with BSIs of urinary origin in patients <60 years. STC 131 and group A/B1 isolates were multi-drug resistant and associated with CA-BSIs of digestive origin in patients aged 60-74 with a recent history of antibiotic treatment. STC 131 isolates were associated with HCA-BSIs in patients with recent/present hospitalization in a long-stay unit. We provide a unique population-based picture of the epidemiology of E. coli BSI. The aging nature of the population led to an increase in the number of cases caused by the B2 and D isolates generally implicated in BSIs. In addition, the association of a trend toward increasing rates of gut colonization with multi drug-resistant isolates revealed by the rise in the incidence of BSIs of digestive origin caused by STC 131 and A/B1 (STCs 10, 23, and 155) isolates, and a significant increase in the frequency of BSIs in elderly patients with recent antibiotic treatment suggested that antibiotic use may have contributed to the growing incidence of BSI.
我们对2005年至2014年期间在一组稳定的医院中诊断出的3334例大肠杆菌所致血流感染(BSIs)进行了调查。观察到75岁以上患者的社区获得性(CA)BSIs、60至74岁患者的消化源性CA-BSIs、医疗保健相关BSIs以及与产超广谱β-内酰胺酶(ESBL)大肠杆菌(ESBLEc)相关的BSIs的发病率显著增加。我们使用多位点序列分型(MLST)研究了2014年调查期间分离出的412株BSI菌株的遗传多样性:在系统发育群B2中发现了7个主要序列类型复合体(STCs),在群A/B1中发现了3个,在群D中发现了2个。在31株ESBLEc菌株中,三分之一属于STC 131。我们寻找克隆群、临床决定因素与BSIs特征之间的可能关联:来自群B2(STC 131除外)和群D的菌株对抗生素敏感,且与60岁以下患者的泌尿道源性BSIs相关。STC 131和群A/B1菌株具有多重耐药性,且与60至74岁近期有抗生素治疗史的患者的消化源性CA-BSIs相关。STC 131菌株与近期/目前在长期住院病房住院的患者的医疗保健相关BSIs相关。我们提供了一份独特的基于人群的大肠杆菌BSI流行病学情况。人口老龄化导致通常与BSIs相关的B2和D分离株引起的病例数增加。此外,STC 131和A/B1(STCs 10、23和155)分离株引起的消化源性BSIs发病率上升揭示了肠道定植率增加与多重耐药分离株之间的关联,以及近期接受抗生素治疗的老年患者中BSIs频率的显著增加,这表明抗生素使用可能导致了BSI发病率的上升。