Yalcin Metin, Enginler Sinem Özlem, Kuşkucu Mert Ahmet, Sarılar Mert, Yalçın Selma, Küçükbasmacı Ömer
Department of Medical Microbiology, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Faculty of Veterinary Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Vet Med Sci. 2025 Sep;11(5):e70523. doi: 10.1002/vms3.70523.
The increasing prevalence of antimicrobial resistance in animals, particularly the spread of multidrug-resistant Enterobacterales, poses a significant zoonotic and public health risk.
The aim of this study was to investigate extended-spectrum β-lactamase (ESBL), carbapenem and colistin resistance among Enterobacterales in faecal swabs of dairy cattle.
A total of 400 samples were cultured on Mac Conkey screening media for ESBL, carbapenem and colistin resistance. The grown Enterobacterales were identified by MALDI-TOF-MS, followed by ceftriaxone, cefotaxime and ceftazidime resistance and double disk synergy. ESBL resistance genes were identified by polymerase chain reaction (PCR) and Sanger sequencing. Bacteria grown on colistin screening media were investigated for colistin resistance by EUCAST microbroth dilution method.
A total of 89 (22.25%) of the bacteria grown from 400 samples were identified as potential ESBL-producing Enterobacterales members. A number of 53 (59.5%) of them were identified as ESBL blaCTX-M as a result of PCR, and 10 of them were identified as blaCTX-M-15/28/36/66 as a result of sequencing. None of the samples cultured on carbapenem medium grew. A total of 18 samples grown in colistin medium were found to be colistin sensitive by broth microdilution. Genotypes were not included in the study. All isolated bacteria were identified as Escherichia coli.
In this study, blaCTX-M-15 and its derivatives, which are common in humans, were also found to be the predominant ESBL type in animals. Monitoring resistance in animals together with resistance in human infections may provide more important data on the spread of resistance.
动物中抗菌药物耐药性的日益普遍,尤其是多重耐药肠杆菌科细菌的传播,构成了重大的人畜共患病和公共卫生风险。
本研究旨在调查奶牛粪便拭子中肠杆菌科细菌对超广谱β-内酰胺酶(ESBL)、碳青霉烯类和黏菌素的耐药情况。
总共400份样本在麦康凯筛选培养基上培养,以检测对ESBL、碳青霉烯类和黏菌素的耐药性。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)鉴定生长的肠杆菌科细菌,随后检测其对头孢曲松、头孢噻肟和头孢他啶的耐药性以及双纸片协同试验。通过聚合酶链反应(PCR)和桑格测序鉴定ESBL耐药基因。采用欧洲抗菌药物敏感性试验委员会(EUCAST)微量肉汤稀释法研究在黏菌素筛选培养基上生长的细菌对黏菌素的耐药性。
从400份样本中培养出的细菌共有89株(22.25%)被鉴定为潜在产ESBL肠杆菌科细菌成员。其中53株(59.5%)经PCR鉴定为ESBL blaCTX-M,10株经测序鉴定为blaCTX-M-15/28/36/66。在碳青霉烯培养基上培养的样本均未生长。在黏菌素培养基上生长的18份样本经肉汤微量稀释法检测对黏菌素敏感。本研究未纳入基因型分析。所有分离出的细菌均鉴定为大肠埃希菌。
在本研究中,在人类中常见的blaCTX-M-15及其衍生物在动物中也是主要的ESBL类型。对动物耐药性与人类感染耐药性一起进行监测,可能会提供关于耐药性传播的更重要数据。