Furlan João Pedro Rueda, Bueno Giovanna Carrasco, Sousa-Carmo Rubens Renato, Silva Renan Lourenço Oliveira, Barbosa Mikaela Renata Funada, Sato Maria Ines Zanoli, Brunetti Florencia, Power Pablo, Lincopan Nilton, Schenkman Sergio
Paulista School of Medicine, Federal University of São Paulo, São Paulo, Brazil.
Antimicrobial Resistance Institute of São Paulo (ARIES), São Paulo, Brazil.
Mol Biol Rep. 2025 Jul 11;52(1):705. doi: 10.1007/s11033-025-10801-y.
While novel KPC variants continue to emerge among clinically relevant Enterobacterales from hospital settings, their occurrence in impacted aquatic environments has been poorly investigated. We hereby report KPC-157 and KPC-181, allelic variants of KPC-2, produced by Citrobacter freundii and Klebsiella pneumoniae isolated from wastewater in Brazil.
Antimicrobial susceptibility was determined by disk diffusion and broth microdilution, whereas carbapenemase production was evaluated by inhibitor-based methods. Genome sequencing was performed combining short-read (Illumina HiSeq) and long-read (Oxford Nanopore) technologies, with further bioinformatic analyses. In silico KPC modeling was carried out using Yasara/PyMOL. Horizontal transfer and plasmid stability were assessed by conjugation and serial passage experiments, respectively. Epidemiological tracking of KPC-2 allelic variants and KPC-bearing plasmids was performed using publicly available genomes.
Carbapenem-resistant C. freundii strain M21 [sequence type (ST) 522] and K. pneumoniae strains M16 and M18 (ST258), harboring bla and bla genes, respectively, were recovered from a sewage treatment plant. KPC-157 and KPC-181 differed from KPC-2 by single amino acid substitutions (Asn132Ser and Glu275Asp, respectively) that do not affect the main kinetic behavior, preserving the classical KPC-2 resistance phenotype (i.e., carbapenem resistance and ceftazidime-avibactam susceptibility). KPC-2 allelic variants were embedded in Tn4401 transposons. KPC-157 was carried on an IncN2 plasmid, while KPC-181 was associated with an IncFIB(pQil)/IncFII(K) plasmid.
The identification of KPC-157 and KPC-181 in wastewater highlights the role of polluted environments in harboring novel KPC variants from high-risk Enterobacterales clones and reinforces the importance of continued antimicrobial resistance surveillance beyond hospital settings.
虽然新型KPC变体在医院环境中具有临床相关性的肠杆菌科细菌中不断出现,但它们在受影响的水生环境中的出现情况却鲜有研究。在此,我们报告了从巴西废水中分离出的弗氏柠檬酸杆菌和肺炎克雷伯菌产生的KPC-2等位变体KPC-157和KPC-181。
采用纸片扩散法和肉汤微量稀释法测定抗菌药物敏感性,通过基于抑制剂的方法评估碳青霉烯酶的产生。结合短读长(Illumina HiSeq)和长读长(Oxford Nanopore)技术进行基因组测序,并进行进一步的生物信息学分析。使用Yasara/PyMOL进行KPC的计算机模拟。分别通过接合实验和连续传代实验评估水平转移和质粒稳定性。利用公开可用的基因组对KPC-2等位变体和携带KPC的质粒进行流行病学追踪。
从一家污水处理厂分离出了分别携带bla和bla基因的耐碳青霉烯弗氏柠檬酸杆菌菌株M21[序列类型(ST)522]以及肺炎克雷伯菌菌株M16和M18(ST258)。KPC-157和KPC-181与KPC-2的区别在于单个氨基酸取代(分别为Asn132Ser和Glu275Asp),这些取代不影响主要动力学行为,保留了经典的KPC-2耐药表型(即碳青霉烯耐药和头孢他啶-阿维巴坦敏感)。KPC-2等位变体嵌入Tn4401转座子中。KPC-157携带在IncN2质粒上,而KPC-181与IncFIB(pQil)/IncFII(K)质粒相关。
在废水中鉴定出KPC-157和KPC-181突出了污染环境在容纳来自高风险肠杆菌科克隆的新型KPC变体方面的作用,并强化了在医院环境之外持续进行抗菌药物耐药性监测的重要性。