Valdezate Sylvia, Cobo Fernando, Monzón Sara, Medina-Pascual María J, Zaballos Ángel, Cuesta Isabel, Pino-Rosa Silvia, Villalón Pilar
National Centre of Microbiology, Reference and Research Laboratory for Taxonomy, Instituto de Salud Carlos III, Majadahonda, 280220 Madrid, Spain.
Department of Microbiology, Instituto Biosanitario de Granada, University Hospital of Virgen de las Nieves, Avda. Fuerzas Armadas s/n, 18014 Granada, Spain.
Antibiotics (Basel). 2021 Mar 16;10(3):304. doi: 10.3390/antibiotics10030304.
shows high antimicrobial resistance (AMR) rates and possesses numerous AMR mechanisms. Its carbapenem-resistant strains (metallo-β-lactamase A-positive) appear as an emergent, evolving clade.
This work examines the genomes, taxonomy, and phylogenetic relationships with respect to other genomes of two strains (CNM20180471 and CNM20200206) resistant to meropenem+EDTA and other antimicrobial agents.
Both strains possessed A genes (A14b and the new A28), along with other AMR mechanisms. The presence of other efflux-pump genes, AB/JK/XY-M, EF/EF-C, and especially R, which reduces the entry of carbapenem via the repression of porin OprD, may be related to meropenem-EDTA resistance. None of the detected insertion sequences were located upstream of A. The genomes of these and other strains that clustered together in phylogenetic analyses did not meet the condition of >95% average nucleotide/amino acid identity, or >70% in silico genome-to-genome hybridization similarity, to be deemed members of the same species, although <1% difference in the genomic G+C content was seen with respect to the reference genome NCTC 9343T.
Carbapenem-resistant strains may be considered a distinct clonal entity, and their surveillance is recommended given the ease with which they appear to acquire AMR.
显示出较高的抗菌耐药性(AMR)发生率,并拥有多种AMR机制。其耐碳青霉烯菌株(金属β-内酰胺酶A阳性)表现为一个新兴的、不断进化的分支。
这项工作研究了两株对美罗培南+乙二胺四乙酸及其他抗菌剂耐药的菌株(CNM20180471和CNM20200206)的基因组、分类学以及与其他基因组的系统发育关系。
两株菌株均拥有A基因(A14b和新的A28)以及其他AMR机制。其他外排泵基因AB/JK/XY-M、EF/EF-C,尤其是R的存在,可能与美罗培南-乙二胺四乙酸耐药性有关,R通过抑制孔蛋白OprD减少碳青霉烯的进入。检测到的插入序列均不在A基因上游。在系统发育分析中聚集在一起的这些菌株和其他菌株的基因组,不符合被视为同一物种成员的条件,即平均核苷酸/氨基酸同一性>95%,或电子基因组到基因组杂交相似性>70%,尽管相对于参考基因组NCTC 9343T,基因组G+C含量的差异<1%。
耐碳青霉烯菌株可能被视为一个独特的克隆实体,鉴于它们似乎很容易获得AMR,建议对其进行监测。