Juzbašić Tajana, Andrijašević Nataša, Ferenčak Ivana, Jurić Dragan, Šoprek Silvija, Poje Janeš Vlatka, Žmak Ljiljana, Tambić Andrašević Arjana, Gverić Grginić Ana
Department of Microbiology, Croatian Institute of Public Health, 10000 Zagreb, Croatia.
Department for Clinical Microbiology, University Hospital for Infectious Diseases, 10000 Zagreb, Croatia.
Trop Med Infect Dis. 2025 Jun 12;10(6):165. doi: 10.3390/tropicalmed10060165.
is a leading cause of bacterial gastroenteritis worldwide which usually presents as mild, and self-limiting disease in immunocompetent individuals. However, in immunocompromised patients, such as those with common variable immunodeficiency, can cause severe recurrent infections requiring antibiotic treatment. Our study reports a case of a 37-year-old male patient with CVID, who had multiple episodes of intestinal infections over a 3.5-year period. A total of 27 stool samples were collected and analyzed between December 2020 and July 2024 during acute febrile diarrheal episodes, with isolated in 15 samples. Antimicrobial susceptibility testing (AST) during the course of the disease revealed three different antimicrobial resistance profiles including multi-drug-resistant phenotype. Whole genome sequencing was performed on three representative isolates, all identified as MLST type 367, ST-257 complex, with minimal genetic divergence, indicating a clonal origin. Genes and point mutations conferring resistance to macrolides, fluoroquinolones, beta-lactams, and tetracycline were identified in different isolates, along with key virulence factors linked to adherence, invasion, motility, and immune evasion. The genetic analysis of macrolide phenotypic resistance revealed different resistance mechanisms. Genotypic and phenotypic analyses of the same clone from single patient, and identified multidrug resistance pattern, present the first documented case of in vivo resistance development of in Croatia. This case highlights the role of prolonged antibiotic pressure in driving resistance evolution and underscores the need for careful antimicrobial stewardship and genomic monitoring in immunocompromised patients. Further research is needed to correlate phenotypic resistance with genetic determinants in spp.
是全球细菌性肠胃炎的主要病因,在免疫功能正常的个体中通常表现为轻度自限性疾病。然而,在免疫功能低下的患者中,如患有常见可变免疫缺陷的患者,可导致严重的反复感染,需要使用抗生素治疗。我们的研究报告了一例37岁患有常见可变免疫缺陷的男性患者,在3.5年的时间里发生了多次肠道感染。在2020年12月至2024年7月期间,在急性发热性腹泻发作期间共收集并分析了27份粪便样本,其中15份样本中分离出[病原体名称未给出]。疾病过程中的抗菌药物敏感性测试(AST)显示出三种不同的抗菌药物耐药谱,包括多重耐药表型。对三个代表性分离株进行了全基因组测序,所有分离株均被鉴定为MLST型367,ST-257复合体,遗传差异最小,表明为克隆起源。在不同的分离株中鉴定出了赋予对大环内酯类、氟喹诺酮类、β-内酰胺类和四环素耐药的基因和点突变,以及与黏附、侵袭、运动和免疫逃避相关的关键毒力因子。对大环内酯类表型耐药的遗传分析揭示了不同的耐药机制。对来自单一患者的同一克隆进行基因型和表型分析,并确定多重耐药模式,这是克罗地亚首例记录在案的[病原体名称未给出]体内耐药发展病例。该病例突出了长期抗生素压力在推动耐药性进化中的作用,并强调了在免疫功能低下患者中进行谨慎的抗菌药物管理和基因组监测的必要性。需要进一步研究以关联[病原体名称未给出]种表型耐药与遗传决定因素。