Nolasco-Romero Carolina G, Prado-Galbarro Francisco-Javier, Jimenez-Juarez Rodolfo Norberto, Gomez-Ramirez Uriel, Cancino-Díaz Juan Carlos, López-Marceliano Beatriz, Apodaca Magali Reyes, Aguayo-Romero Mónica Anahí, Rodea Gerardo E, Pichardo-Villalon Lilia, Parra-Ortega Israel, Santos Fortino Solórzano, Moreno-Galván Mónica, Velázquez-Guadarrama Norma
Laboratorio de Investigación en Microbiología y Resistencia Antimicrobiana, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.
Posgrado en Ciencias Quimicobiológicas, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Mexico City 11350, Mexico.
Pathogens. 2024 Nov 22;13(12):1030. doi: 10.3390/pathogens13121030.
The poor prognosis of infections associated with multidrug-resistant can be attributed to several conditions of the patient and virulence factors of the pathogen, such as the type III secretion system (T3SS), which presents the ability to inject four effectors into the host cell: ExoS, ExoT, ExoU and ExoY. The aim of this study was to analyze the distribution of genes through multiplex polymerase chain reaction in strains isolated from patients at a third-level pediatric hospital and their relationships with clinical variables, e.g., the origin of the sample, susceptibility profile and outcome, through a multinomial logistic regression model. A total of 336 bacterial strains were obtained from cystic fibrosis (CF; n = 55) and bloodstream infection (BSI; n = 281) samples, and eleven presence (+)/absence (-) virulotype patterns were identified. The virulotype V3 () was observed in 64.28%, followed by V1 () with 11.60%. Additionally, V2 () was present in 11.60%, and V7 () was present in 4.17%. The remaining virulotypes (8.33%) identified were clustered in the other virulotype (OV) group (V4, V5, V6, V8, V9, V10 and V11). The clinical records of 100 patients and their outcomes were reviewed. Fifteen patients died (CF = 4; BSI = 11). V2 and V1 were the virulotypes most related to pandrug resistance (PDR), whereas the V1 relative risk of death was determined to be almost four-fold greater than that of V3, followed by V2 and OV. In summary, the virulotypes V1, V2 and CF are related to death. This study highlights the association of T3SS virulotypes with the susceptibility profile, clinical origin and their potential for predicting a poor prognosis.
与多重耐药相关感染的预后不良可归因于患者的多种状况及病原体的毒力因子,如III型分泌系统(T3SS),它具有向宿主细胞注射四种效应蛋白的能力:ExoS、ExoT、ExoU和ExoY。本研究的目的是通过多重聚合酶链反应分析从一家三级儿科医院患者中分离出的菌株中相关基因的分布,并通过多项逻辑回归模型分析它们与临床变量的关系,如样本来源、药敏谱和转归。共从囊性纤维化(CF;n = 55)和血流感染(BSI;n = 281)样本中获得336株细菌菌株,并鉴定出11种存在(+)/缺失(-)的毒力型模式。毒力型V3()占64.28%,其次是V1()占11.60%。此外,V2()占11.60%,V7()占4.17%。鉴定出的其余毒力型(8.33%)聚集在其他毒力型(OV)组(V4、V5、V6、V8、V9、V10和V11)中。回顾了100例患者的临床记录及其转归。15例患者死亡(CF = 4;BSI = 11)。V2和V1是与全耐药(PDR)最相关的毒力型,而V1的死亡相对风险被确定几乎是V3的四倍,其次是V2和OV。总之,毒力型V1、V2和CF与死亡相关。本研究强调了T3SS毒力型与药敏谱、临床来源的关联及其预测预后不良的可能性。