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尿路感 染 小鼠模型中大肠杆 菌对磷霉素耐药性的生物学代价。

Biological cost of fosfomycin resistance in Escherichia coli in a murine model of urinary tract infection.

机构信息

INSERM, IAME, UMR 1137, F-75018 Paris, France; Université Paris Diderot, IAME, UMR 1137, Sorbonne Paris Cité, F-75018 Paris, France.

Université de Caen Normandie, EA 4655 (équipe « Antibio-résistance »), F-14032 Caen, France; CHU de Caen, Service de Microbiologie, F-14033 Caen, France.

出版信息

Int J Med Microbiol. 2017 Dec;307(8):452-459. doi: 10.1016/j.ijmm.2017.09.019. Epub 2017 Sep 29.

DOI:10.1016/j.ijmm.2017.09.019
PMID:28986014
Abstract

Prevalence of fosfomycin resistance in E. coli clinical isolates from UTIs remains very low. Our hypothesis was that fosfomycin resistance may be associated with a biological cost. Three groups of strains of E. coli belonging to the B2 phylogenetic group were used: clinical wild-type (WT) isolates, clinical multidrug-resistant isolates and in vitro fosfomycin-resistant derivatives from the uropathogen clinical strain E. coli CFT073. In each group fosfomycin-susceptible and -resistant isolates were compared. In vitro, we found a significantly decreased growth rate for fosfomycin-resistant strains as compared with susceptible strains in the WT group. In a murine model of ascending UTI, there was a significant reduction in infection rates with fosfomycin-resistant isolates as compared with susceptible ones, in all 3 study groups, ranging from 28 to 39% (P<0.03). All fosfomycin-susceptible clinical strains were virulent in vivo (13/13), while fosfomycin-resistant clinical strains were either virulent (2/7) or non-virulent (5/7) (P<0.002). This difference was not explained by the number of virulence factors or pathogenicity-associated islands. In conclusion, fosfomycin resistance appears to carry some biological cost in E. coli, which may explain in part the apparent paradox of the low prevalence of fosfomycin resistance despite a high rate of spontaneous mutants.

摘要

尿路感染中大肠埃希菌临床分离株对磷霉素的耐药率仍然很低。我们的假设是,磷霉素耐药可能与生物学成本有关。使用了属于 B2 系统发育群的三组大肠埃希菌菌株:临床野生型(WT)分离株、临床多药耐药分离株和来自尿路病原体临床株大肠杆菌 CFT073 的体外磷霉素耐药衍生物。在每组中,比较了磷霉素敏感和耐药的分离株。在体外,与 WT 组中的敏感株相比,耐药株的生长速度明显降低。在鼠上升性尿路感染模型中,与敏感株相比,所有 3 个研究组中耐药株的感染率均显著降低,范围为 28%至 39%(P<0.03)。所有磷霉素敏感的临床分离株在体内均具有毒力(13/13),而磷霉素耐药的临床分离株要么具有毒力(2/7),要么无毒性(5/7)(P<0.002)。这种差异不能用毒力因子或致病性相关岛的数量来解释。总之,磷霉素耐药在大肠埃希菌中似乎存在一些生物学成本,这部分解释了尽管自发突变率很高,但磷霉素耐药率似乎很低的明显悖论。

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