Background/Objectives: Healthcare-associated infections caused by multidrug-resistant (MDR) bacteria pose a significant and growing public health challenge, particularly in high-risk settings such as Intensive Care Units (ICUs). Colonization is often asymptomatic but can precede infection and contribute to hospital outbreaks, making early detection critical for infection control and containment. The aim of the study is to evaluate the antibiotic susceptibility patterns of MDR bacteria involved in colonization and/or infection among patients admitted to the ICU at a tertiary care hospital in Northeastern Romania and to investigate the relationship between MDR bacterial colonization and subsequent infection. Methods: A total of 118 patients from ICU were included in this study and a total of 609 bacterial strains were isolated, involved in both colonization and infection, with multiple isolates per patient included if obtained from different sites or time points. Results: A predominance of Gram-negative bacilli was found to be involved in both colonization and infection in the ICU, with Acinetobacter baumannii (n = 146; 26.64%), Klebsiella pneumoniae (n = 146; 26.64%), Escherichia coli (n = 60; 10.95%), and Pseudomonas aeruginosa (n = 56; 10.22%) as the main bacteria involved in colonization, and A. baumannii (n = 23; 37.7%), K. pneumoniae (n = 19; 31.1%), and P. aeruginosa (n = 15; 24.6%) as the main bacteria involved in infections. The study revealed a high diversity of antibiotypes among K. pneumoniae (43 distinct antibiotypes), E. coli (35 distinct antibiotypes) and P. aeruginosa (27 distinct antibiotypes). In contrast, only 6 antibiotypes were identified for A. baumannii, with most strains belonging to a single dominant antibiotype. For K. pneumoniae, E. coli and A. baumannii, infections mainly involved the same antibiotype as that found in colonization, while infections with P. aeruginosa were often linked to different antibiotypes than those involved in colonization. Conclusions: This study demonstrates a high colonization-to-infection link among ICU patients in a Northeastern Romanian tertiary care hospital, and these findings underscore the importance of systematic colonization screening to identify patients at high risk in ICU settings.

Even with significant advances in therapeutic interventions and monitoring protocols, cystic fibrosis (CF) remains a critical pediatric health challenge affecting respiratory function and long-term patient outcomes. CF, caused by mutations in the CFTR gene, disrupts normal mucociliary clearance and creates conditions for chronic respiratory infections. The disorder affects individuals globally, with pediatric patients facing particularly complex microbial challenges that evolve throughout childhood growth. CF poses significant risks with progressive lung function decline and increased mortality, leading to potential short- and long-term respiratory complications. There is a growing concern among clinicians about the dynamic nature of airway microbial communities, with classical pathogens like Pseudomonas aeruginosa and Staphylococcus aureus showing sequential emergence patterns that complicate treatment strategies, highlighting an urgent need for microbiome-informed therapeutic approaches. Our review aims to provide a comprehensive overview of airway microbiome evolution in pediatric CF patients. We outline the molecular and ecological mechanisms involved in microbial community progression, as well as the age-related trajectories leading to pathogen-dominated ecosystems and the subsequent complications associated with microbial dysbiosis. Given the widespread implications of disrupted microbial balance on disease progression, our review also presents the temporal landscape of airway microbiome changes, including age-related microbial succession patterns, and explores the underlying mechanisms driving these ecological shifts. The progressive nature of microbial simplification frequently leads to treatment challenges, emphasizing the importance of investigating microbiome-targeted therapeutic interventions. Therefore, in this review, we also explore established therapeutic strategies, including CFTR modulators and probiotics, which could offer promising approaches to maintaining microbial balance and improving outcomes in pediatric CF patients.

Non-typhoidal Salmonella (NTS) represents a growing public health concern worldwide due to its increasing antimicrobial resistance and substantial disease burden, yet data from Romania remain limited. We conducted the first regional 7-year retrospective study of NTS-associated diarrhea among hospitalized patients, focusing on resistance trends and clinical factors associated with disease severity. This study included all laboratory-confirmed Salmonella infections admitted for acute diarrheal disease to the “Sfânta Parascheva” Clinical Hospital of Infectious Diseases, Iași (January 2018–December 2024). Patient data were extracted from electronic medical records and analyzed using SPSS (v31.0), with statistical significance set at p < 0.05. Among the isolates obtained from the 698 included patients, most belonged to serogroup D (63.6%), followed by B (21.8%) and C (14.0%). Overall resistance rates were 12.3% for ampicillin, 3.6% for trimethoprim–sulfamethoxazole and 29.9% for ciprofloxacin, with a significant yearly increase observed only for ciprofloxacin (OR = 1.21, p < 0.001). Cardiovascular comorbidities were independently associated with prolonged hospitalization (>5 days) (OR = 2.25, p = 0.007). Invasive infections occurred in 14 patients (2%). Given the high ciprofloxacin resistance and the additional impact of comorbidities on disease severity, there is a need for ongoing surveillance and targeted management strategies.