Furlan João Pedro Rueda, Bueno Giovanna Carrasco, Sousa-Carmo Rubens Renato, Silva Renan Lourenço Oliveira, Barbosa Mikaela Renata Funada, Sato Maria Ines Zanoli, Lincopan Nilton, Schenkman Sergio
Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
ARIES, Antimicrobial Resistance Institute of São Paulo, São Paulo, Brazil.
Curr Microbiol. 2025 Jul 28;82(9):416. doi: 10.1007/s00284-025-04394-9.
Comamonas species have been isolated from different sources, with Comamonas testosteroni and Comamonas resistens commonly related to human diseases and multidrug resistance, respectively. During a surveillance study to monitor carbapenem resistance in bacteria from wastewater samples in Brazil, a carbapenem-resistant strain, named M13, was obtained and identified as C. resistens (ANI 98.90%, dDDH 94.60%) by genomic analysis, being a species distinct from C. testosteroni. It exhibited multidrug resistance and presented small inhibition zones around disks containing novel β-lactams and β-lactam-β-lactamase inhibitor combinations. Comparative genomics showed significant single nucleotide polymorphism divergence between M13 and other C. resistens genomes, suggesting geographically driven genomic diversity. Strain M13 uniquely harbored genes related to antimicrobial resistance and metal tolerance as follows: bla (carbapenem resistance), bla (third-generation cephalosporin resistance), mer operon (mercury tolerance), and pco operon (copper tolerance). The bla and bla genes were located on distinct plasmids that lacked conjugative genes but contained mobilization elements, indicating the potential for horizontal transfer. Unlike C. resistens strains from China, M13 strain may have acquired clinically relevant antimicrobial resistance genes via interactions with Brazilian microbial communities. These findings highlight the relevance of monitoring Comamonas species as potential reservoirs and disseminators of clinically relevant antimicrobial resistance genes and underscore the need for environmental monitoring of carbapenem-resistant strains.
丛毛单胞菌属已从不同来源分离得到,其中睾丸酮丛毛单胞菌和耐药丛毛单胞菌通常分别与人类疾病和多重耐药性相关。在一项监测巴西废水样本中细菌碳青霉烯耐药性的研究中,获得了一株碳青霉烯耐药菌株,命名为M13,并通过基因组分析鉴定为耐药丛毛单胞菌(ANI 98.90%,dDDH 94.60%),是一种与睾丸酮丛毛单胞菌不同的物种。它表现出多重耐药性,在含有新型β-内酰胺类和β-内酰胺-β-内酰胺酶抑制剂组合的药敏纸片周围呈现出小的抑菌圈。比较基因组学显示,M13与其他耐药丛毛单胞菌基因组之间存在显著的单核苷酸多态性差异,表明存在地理驱动的基因组多样性。菌株M13独特地携带了与抗菌药物耐药性和金属耐受性相关的基因,如下所示:bla(碳青霉烯耐药性)、bla(第三代头孢菌素耐药性)、mer操纵子(汞耐受性)和pco操纵子(铜耐受性)。bla和bla基因位于不同的质粒上,这些质粒缺乏接合基因,但含有转移元件,表明存在水平转移的潜力。与来自中国的耐药丛毛单胞菌菌株不同,M13菌株可能通过与巴西微生物群落的相互作用获得了临床相关的抗菌药物耐药基因。这些发现突出了监测丛毛单胞菌属作为临床相关抗菌药物耐药基因潜在储存库和传播者的相关性,并强调了对碳青霉烯耐药菌株进行环境监测的必要性。