Hernández-García Marta, García-Fernández Sergio, García-Castillo María, Bou Germán, Cercenado Emilia, Delgado-Valverde Mercedes, Mulet Xavier, Pitart Cristina, Rodríguez-Lozano Jesús, Tormo Nuria, López-Mendoza Diego, Díaz-Regañón Jazmín, Cantón Rafael
Servicio de Microbiología, Hospital Ramón y Cajal-IRYCIS, Madrid, Spain.
Servicio de Microbiología, Hospital Universitario A Coruña, A Coruña, Spain.
JAC Antimicrob Resist. 2020 Oct 22;2(4):dlaa084. doi: 10.1093/jacamr/dlaa084. eCollection 2020 Dec.
To analyse by WGS the ceftolozane/tazobactam (C/T) resistance mechanisms in and spp. isolates recovered from complicated intra-abdominal and urinary tract infections in patients from Spanish ICUs (SUPERIOR surveillance study, 2016-17).
The clonal relatedness, the resistome and the virulome of 45 and 43 spp. isolates with different C/T susceptibility profiles were characterized.
In , two (C/T susceptible) carbapenemase producers (VIM-2-CC23, OXA-48-ST38) were detected. The most relevant clone was ST131-B2-O25:H4-H30 (17/45), particularly the CTX-M-15-ST131-H30-Rx sublineage (15/17). ST131 strains were mainly C/T susceptible (15/17) and showed an extensive virulome. In non-ST131 strains (28/45), CTX-M enzymes [CTX-M-14 (8/24); CTX-M-15 (6/24); CTX-M-1 (3/24); CTX-M-32 (2/24)] were found in different clones. C/T resistance was detected in non-clonal isolates (13%, 6/45) with ESBL (4/6) and non-ESBL (2/6) genotypes. Among spp., (42/43) and (1/43) species were identified; 42% (18/43) were carbapenemase producers and 58% showed a C/T resistance phenotype (25/43). OXA-48-ST11 (12/18), OXA-48-ST392 (2/18), OXA-48-ST15 (2/18), NDM-1-ST101 (1/18) and OXA-48+VIM-2-ST15 (1/18) isolates were found, all C/T resistant. Correlation between carbapenemase detection and resistance to C/T was demonstrated ( < 0.001). In non-carbapenemase-producing (25/43), C/T resistance (28%, 7/25) was detected in ESBL (3/7) and AmpC (2/7) producers. Overall, an extensive virulome was found and was correlated with carbapenemase carriage ( < 0.001) and C/T resistance ( < 0.05), particularly in OXA-48-ST11 strains ( < 0.05).
Prediction of antimicrobial susceptibility profiles using WGS is challenging. Carbapenemase-encoding genes are associated with C/T resistance in , but other resistance mechanisms might be additionally involved.
通过全基因组测序(WGS)分析从西班牙重症监护病房(ICU)患者的复杂性腹腔内感染和尿路感染中分离出的大肠埃希菌和肺炎克雷伯菌菌株对头孢洛扎/他唑巴坦(C/T)的耐药机制(SUPERIOR监测研究,2016 - 2017年)。
对45株大肠埃希菌和43株肺炎克雷伯菌菌株的克隆相关性、耐药组和毒力组进行了特征分析,这些菌株具有不同的C/T敏感性谱。
在大肠埃希菌中,检测到两株(对C/T敏感)产碳青霉烯酶菌株(VIM - 2 - CC23、OXA - 48 - ST38)。最相关的克隆是ST131 - B2 - O25:H4 - H30(17/45),特别是CTX - M - 15 - ST131 - H30 - Rx亚系(15/17)。ST131菌株主要对C/T敏感(15/17),并表现出广泛的毒力组。在非ST131菌株(28/45)中,在不同克隆中发现了CTX - M酶[CTX - M - 14(8/24);CTX - M - 15(6/24);CTX - M - 1(3/24);CTX - M - 32(2/24)]。在非克隆性大肠埃希菌分离株(13%,6/45)中检测到C/T耐药,其基因型为ESBL(4/6)和非ESBL(2/6)。在肺炎克雷伯菌中,鉴定出肺炎克雷伯菌(42/43)和产酸克雷伯菌(1/43);42%(18/43)为产碳青霉烯酶菌株,58%表现出C/T耐药表型(25/43)。发现了OXA - 48 - ST11(12/18)、OXA - 48 - ST392(2/18)、OXA - 48 - ST15(2/18)、NDM - 1 - ST101(1/18)和OXA - 48 + VIM - 2 - ST15(1/18)分离株,均对C/T耐药。证实了碳青霉烯酶检测与对C/T耐药之间的相关性(P < 0.001)。在不产碳青霉烯酶的肺炎克雷伯菌(25/43)中,在ESBL(3/7)和AmpC(2/7)产生菌中检测到C/T耐药(28%,7/25)。总体而言,发现了广泛的毒力组,并且与碳青霉烯酶携带(P < 0.001)和C/T耐药(P < 0.05)相关,特别是在OXA - 48 - ST11菌株中(P < 0.05)。
使用WGS预测抗菌药物敏感性谱具有挑战性。编码碳青霉烯酶的基因与大肠埃希菌和肺炎克雷伯菌对C/T的耐药相关,但可能还涉及其他耐药机制。