Wang Mengtao, Ma Mengjuan, Yu Lijie, He Kun, Zhang Tengli, Feng Yiming, Hu Gongzheng, He Dandan, Pan Yushan, Zhai Yajun
College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.
Vet Microbiol. 2025 Apr;303:110443. doi: 10.1016/j.vetmic.2025.110443. Epub 2025 Feb 25.
Antimicrobial resistance (AMR) poses a significant global health threat, particularly due to increasing bacterial resistance to β-lactam and aminoglycoside antibiotics, primarily mediated by extended-spectrum β-lactamases (ESBLs) and 16S rRNA methylases in Enterobacteriaceae. In this study, a multidrug resistant (MDR) E. coli strain HN257 isolated from chicken belonging to ST224 and serotype O88:H23 was characterized. SNP-based phylogenetic analysis revealed two distinct clades among poultry-associated E. coli ST224 in this study and others from Genbank, with strain HN257 closely related to chicken-derived E. coli YH17148 (serotype O78:H23), from China. The E. coli HN257 harbored four plasmids with 16 resistance determinants. Two bla genes were located on different plasmids with an IS26-bracketed resistance module IS26-traI-fip-∆ISEcp1-bla-IS903D-iroN-IS26. The plasmid pHN257-2 belonged to the IncI1 ST71 epidemic lineage and carried bla, bla, rmtB, fosA3, floR, aac(3)-IV and oqxAB, while plasmid pHN257-4 belonged to the non-conjugative IncX1 and carried bla and fosA3. Under experimental conditions, a rmtB-positive conjugative helper IncI1 ST136 plasmid could fuse with the non-conjugative pHN257-4 carrying bla, resulting in the formation of a cointegrate pHN257-F mediated by IS26. Importantly, both single and fused plasmids in transconjugants showed minimal impact on bacterial growth. This study highlights the first identification of a non-conjugative IncX1 plasmid carrying bla and fosA3 in MDR E. coli ST224 from poultry, offering critical insights into the presence and transmission dynamics of bla.
抗菌药物耐药性(AMR)对全球健康构成重大威胁,尤其是由于细菌对β-内酰胺类和氨基糖苷类抗生素的耐药性不断增加,这主要由肠杆菌科中的超广谱β-内酰胺酶(ESBLs)和16S rRNA甲基化酶介导。在本研究中,对一株从鸡中分离出的属于ST224和血清型O88:H23的多重耐药(MDR)大肠杆菌菌株HN257进行了特征分析。基于单核苷酸多态性(SNP)的系统发育分析揭示了本研究中的家禽相关大肠杆菌ST224与来自Genbank的其他菌株之间存在两个不同的进化枝,菌株HN257与来自中国的鸡源大肠杆菌YH17148(血清型O78:H23)密切相关。大肠杆菌HN257携带四个含有16个耐药决定簇的质粒。两个bla基因位于不同的质粒上,带有一个由IS26包围的耐药模块IS26-traI-fip-∆ISEcp1-bla-IS903D-iroN-IS26。质粒pHN257-2属于IncI1 ST71流行谱系,携带bla、bla、rmtB、fosA3、floR、aac(3)-IV和oqxAB,而质粒pHN257-4属于非接合性IncX1,携带bla和fosA3。在实验条件下,一个rmtB阳性的接合性辅助IncI1 ST136质粒可以与携带bla的非接合性pHN257-4融合,导致由IS26介导形成共整合体pHN257-F。重要的是,转接合子中的单个质粒和融合质粒对细菌生长的影响都很小。本研究首次鉴定出家禽多重耐药大肠杆菌ST224中携带bla和fosA3的非接合性IncX1质粒,为bla的存在和传播动态提供了关键见解。