Monroy-Pérez Eric, Herrera-Gabriel Jennefer Paloma, Olvera-Navarro Elizabeth, Ugalde-Tecillo Lorena, García-Cortés Luis Rey, Moreno-Noguez Moisés, Martínez-Gregorio Héctor, Vaca-Paniagua Felipe, Paniagua-Contreras Gloria Luz
Facultad de Estudios Superiores Iztacala, Universidad Nacional Autónoma de México, Tlalnepantla 54090, Mexico.
Coordinación de Investigación del Estado de México Oriente, Insitituto Mexicano del Seguro Social, Tlalnepantla de Baz 50090, Mexico.
Pathogens. 2024 Oct 3;13(10):868. doi: 10.3390/pathogens13100868.
The increase in the number of hospital strains of hypervirulent and multidrug resistant (MDR) is a major health problem that reduces medical treatment options and increases mortality. The molecular profiles of virulence and multidrug resistance of -associated hospital and community infections in Mexico have been poorly studied. In this study, we analyzed the different molecular profiles associated with the virulence genotypes related to multidrug resistance and the genotypes of multidrug efflux pumps () in causing clinically critical infections isolated from Mexican patients with community- and hospital-acquired infections. Susceptibility to 12 antibiotics was determined using the Kirby-Bauer method. The identification of and the detection of virulence and efflux pump system genes were performed using conventional PCR. All strains isolated from patients with hospital-acquired (n = 67) and community-acquired infections (n = 57) were multidrug resistant, mainly to beta-lactams (ampicillin [96.7%], carbenicillin [98.3%], cefalotin [97.5%], and cefotaxime [87%]), quinolones (norfloxacin [78.2%]), phenicols (chloramphenicol [91.9%]), nitrofurans (nitrofurantoin [70.9%]), aminoglycosides (gentamicin [75%]), and sulfonamide/trimethoprim (96.7%). Most strains (95.5%) isolated from patients with hospital- and community-acquired infections carried the adhesion () and biofilm formation () genes. Outer membrane proteins ( and ) were present in 100% of cases, elastases ( and ) in 100% and 98.3%, respectively, alkaline protease () and alginate () in 99.1% and 97.5%, respectively, and chaperone () and epoxide hydrolase () in 100% and 97.5%, respectively. Overall, 99.1% of the strains isolated from patients with hospital- and community-acquired infections carried the efflux pump system genes and , while 98.3% of the strains carried and . These findings show a wide distribution of the virulome related to the genotypic and phenotypic profiles of antibiotic resistance and the origin of the strains isolated from patients with hospital- and community-acquired infections, demonstrating that these molecular mechanisms may play an important role in high-pathogenicity infections caused by .
高毒力和多重耐药(MDR)医院菌株数量的增加是一个重大的健康问题,它减少了医疗治疗选择并增加了死亡率。墨西哥医院和社区感染相关的毒力和多重耐药的分子特征研究较少。在本研究中,我们分析了与多重耐药相关的毒力基因型以及多重耐药外排泵()基因型相关的不同分子特征,这些特征存在于从墨西哥社区获得性感染和医院获得性感染患者中分离出的引起临床严重感染的菌株中。使用 Kirby-Bauer 方法测定对 12 种抗生素的敏感性。使用常规 PCR 进行菌株鉴定以及毒力和外排泵系统基因的检测。从医院获得性感染患者(n = 67)和社区获得性感染患者(n = 57)中分离出的所有菌株均为多重耐药,主要对β-内酰胺类(氨苄西林 [96.7%]、羧苄西林 [98.3%]、头孢噻吩 [97.5%] 和头孢噻肟 [87%])、喹诺酮类(诺氟沙星 [78.2%])、酚类(氯霉素 [91.9%])、硝基呋喃类(呋喃妥因 [70.9%])、氨基糖苷类(庆大霉素 [75%])以及磺胺类/甲氧苄啶(96.7%)耐药。从医院获得性感染和社区获得性感染患者中分离出的大多数菌株(95.5%)携带黏附()和生物膜形成()基因。外膜蛋白(和)在所有病例中均存在,弹性蛋白酶(和)分别在所有病例中的 100% 和 98.3% 中存在,碱性蛋白酶()和藻酸盐()分别在 99.1% 和 97.5% 中存在,伴侣蛋白()和环氧水解酶()分别在 100% 和 97.5% 中存在。总体而言,从医院获得性感染和社区获得性感染患者中分离出的 99.1% 的菌株携带外排泵系统基因和,而 98.3% 的菌株携带和。这些发现表明与抗生素耐药的基因型和表型特征以及从医院获得性感染和社区获得性感染患者中分离出的菌株来源相关的毒力组广泛分布,表明这些分子机制可能在由引起的高致病性感染中起重要作用。