Thingholm Karen Rønø, Hertz Frederik Boëtius, Løbner-Olesen Anders, Frimodt-Møller Niels, Nielsen Karen Leth
Department of Clinical Microbiology, Rigshospitalet, Copenhagen 2100, Denmark.
Department of Clinical Microbiology, Herlev and Gentofte Hospital, Herlev 2730, Denmark.
Infect Drug Resist. 2019 Aug 6;12:2429-2435. doi: 10.2147/IDR.S208536. eCollection 2019.
Extended spectrum beta-lactamase (ESBL)-producing () causing urinary tract infections often belong to sequence type 131 (ST131), serotype O25, carrying .
The main aim of this study was to examine the conjugational frequencies of with plasmids carrying to isolates from the fecal flora of healthy humans to determine whether ST131 is more likely to uptake or donate ESBL resistance compared to other clones.
Donors and recipients were all clinical isolates and did not harbor plasmids with identical incompatibility groups (Inc-groups) based on in silico analyses of Inc-groups and restriction/modification systems (R/M-systems). The in vitro conjugation experiments were performed as filter conjugation with verification of transconjugants by random amplified polymorphic DNA (RAPD) PCR and PCR.
The frequencies of conjugation with -carrying plasmids were found to be very rare with detectable conjugation frequencies in the range of 4x10-7x10 transconjugants/recipient. Recipients of O25/ST131 type yielded significantly lower conjugation frequencies compared to recipients of other O-types (=0.004). The applied ST131/O25 donors did not yield detectable levels of transconjugants regardless of the applied recipient. Presence of sub-MIC levels of ampicillin increased plasmid transfer frequencies x100 fold (=0.07).
The results indicate that is rarely transferred by conjugation to isolates of the intestinal flora, even when the gene is plasmid-borne.
产超广谱β-内酰胺酶(ESBL)的引起尿路感染的菌株通常属于序列型131(ST131),血清型O25,携带。
本研究的主要目的是检测携带的质粒与健康人粪便菌群分离株之间的接合频率,以确定与其他克隆相比,ST131是否更有可能摄取或传递ESBL耐药性。
供体和受体均为临床分离株,根据Inc组和限制/修饰系统(R/M系统)的计算机分析,它们不携带具有相同不相容组(Inc组)的质粒。体外接合实验采用滤膜接合进行,通过随机扩增多态性DNA(RAPD)PCR和PCR验证转接合子。
发现携带质粒的接合频率非常低,可检测到的接合频率范围为4×10 - 7×10转接合子/受体。与其他O型受体相比,O25/ST131型受体产生的接合频率显著降低(=0.004)。无论应用何种受体,所应用的ST131/O25供体均未产生可检测水平的转接合子。亚抑菌水平的氨苄青霉素的存在使质粒转移频率增加了100倍(=0.07)。
结果表明,即使该基因是质粒携带的,也很少通过接合转移到肠道菌群的分离株中。