Uropathogenic Escherichia coli (UPEC) strains are among the leading causes of urinary tract infections (UTIs) worldwide. They can colonize the urinary tract and form biofilms that allow bacteria to survive and persist, causing relapses of infections and life-threatening sequelae. Here, we analyzed biofilm production, antimicrobial susceptibility, virulence factors, and phylogenetic groups in 74 E. coli isolated from diagnosed patients with UTIs to describe their microbiological features and ascertain their relationship with biofilm capabilities. High levels of ceftazidime resistance are present in hospital-acquired UTIs. Isolates of multidrug resistance strains (p = 0.0017) and the yfcV gene (p = 0.0193) were higher in male patients. All the strains tested were able to form biofilms. Significant differences were found among higher optical densities (ODs) and antibiotic resistance to cefazolin (p = 0.0395), ceftazidime (p = 0.0302), and cefepime (p = 0.0420). Overall, the presence of fimH and papC coincided with strong biofilm formation by UPEC. Type 1 fimbriae (p = 0.0349), curli (p = 0.0477), and cellulose (p = 0.0253) production was significantly higher among strong biofilm formation. Our results indicated that high antibiotic resistance may be related to male infections as well as strong and moderate biofilm production. The ability of E. coli strains to produce biofilm is important for controlling urinary tract infections.

The leaves of Psidium guajava L. are an agro-industrial by-product with an outstanding content of polyphenolic compounds; however, there are many factors which can affect the phytochemical profile when valuing this type of plant material, such as temperatures and extraction times involving in the extraction methods applied. In this context, this study analyzed the impact of different extraction methods (Soxhlet, maceration and ultrasound-assisted extraction) on the phytochemical profile (FTIR and UPLC-MS) and the antioxidant activity (ABTS, FRAP and Folin–Ciocalteu) of guava leaf extracts. A yield of phenolic compounds per gram of guava leaf was obtained within the range of 16 to 45 mg/g; on the other hand, the ${IC}_{50}$ values determined with the ABTS assay ranged between 78 ± 4 to 152 ± 12 µg/mL. The methanolic extract obtained by Soxhlet was the one with the best reducing power, both in the FRAP assay and in the Folin–Ciocalteu assay. Finally, bioactive compounds such as quercetin, kaempferol and avicularin were identified in the guava leaf extract. It was concluded that the purification of polyphenolics compounds improves the antioxidant capacity, and that the extraction method greatly influences the phytochemical profile and activity of the extracts.

Currently, a global health crisis is being caused by microbial resistance, in which Acinetobacter baumannii plays a crucial role, being considered the highest-priority microorganism by the World Health Organization (WHO) for discovering new antibiotics. As a result, phytochemicals have emerged as a potential alternative to combat resistant strains, since they can exert antimicrobial activity through various mechanisms and, at the same time, represent a more natural and safe option. This study analyzes the antimicrobial effects of guava leaf extract in ten clinical isolates of extensively drug-resistant (XDR) A. baumannii, using the agar diffusion technique and the microdilution method to determine the minimum inhibitory concentrations (MICs). Additionally, possible improvements in antimicrobial activity after the purification of polyphenolic compounds and potential synergy with the antibiotic gentamicin are examined in this research. Moreover, the effect of the plant extract in cell line A549 derived from lung tissue was also evaluated. The extract exhibited antimicrobial activity against all the strains studied, and the purification of polyphenols along with the combination with gentamicin improved the extract activity. The presence of the plant extract induced morphological changes in the lung cells after 24 h of exposure. Therefore, Psidium guajava L. leaf extract is a potential antimicrobial agent.

Pseudomonas aeruginosa is a leading cause of healthcare-associated infections, which are related to substantial morbidity and mortality. The incidence of Plasmid-Mediated Quinolone Resistance (PMQR) determinants has been previously reported in this bacterium. However, there is limited information regarding the presence of PMQR and carbapenemase-encoding genes simultaneously. This study aims to analyze the prevalence of these determinants on P. aeruginosa strain isolated from clinical patients in the State of Aguascalientes, Mexico. Fifty-two P. aeruginosa isolates from nosocomial patients were collected from Centenario Hospital Miguel Hidalgo. This is a retrospective observational study conducted at a single center. Antibiotic susceptibility was tested using the Vitek-2 system. Only carbapenem-resistant isolates were included in this study. Carbapenemase-encoding genes and PMQR determinants were screened by polymerase chain reaction (PCR). Resistance rates of 100% were found on tigecycline and ceftriaxone. Of the 52 isolates, 34.6% were positive for the qnr genes, 46.2% for the oqxA gene, and 25% for the aac-(6′)-lb gene. The most frequent carbapenemase genes found in the samples were bla_OXA-51 (42.3%), bla_OXA-1 (15.4%), and bla_VIM (15.4%). bla_OXA-51 co-carrying oqxA was detected in 21.1% of the isolates, bla_OXA-51 co-carrying aac-(6’)-lb in 11.5%, bla_VIM co-carrying aac-(6′)-lb in 3.8%, and bla_KPC co-carrying oqxA in 5.8%. Systematic surveillance to detect carbapenemase-encoding genes and PMQR determinants, and rational prescription using the last-line drugs could help in preventing the dissemination of multidrug-resistant determinants.

Synthetic colorants are widely used globally by different industries for the dyeing process. However, these chemicals pollute the environment and affect human health by causing allergies, hives, dermatitis, and cancer. This study aims to compare the effectiveness of duckweed (Lemna minor) in the removal of the Methylene Blue (MB) and Congo red (CR) dyes at different concentrations (1 mg/L, 5 mg/L, 10 mg/L, and 15 mg/L). Absorbance values were determined at 665 nm for MB and 497 nm for CR after 96 hours. The results show higher removal of MB compared to CR for all concentrations (95.49 % vs. 59.32%, 1 mg/L; 97.24% vs. 39.43%, 5mg/L; 91.30% vs 28.47%, 10mg/L; y 85.42% vs 20.27%, 15mg/L). The removal of MB was observed after 30 min of contact with duckweed, while the removal of CR was observed after 24 hours in all concentrations. Los colorantes sintéticos son altamente utilizados a nivel global por distintas industrias para el proceso de tinción. Sin embargo, estos químicos son altamente contaminantes para el ambiente y afectan la salud humana provocando alergias, urticaria, dermatitis y cáncer. Este estudio tiene como objetivo comparar la efectividad de la lenteja de agua (Lemna minor) en la remoción de los colorantes azul de metileno (AM) y rojo Congo (RC), a distintas concentraciones (1mg/L, 5mg/L, 10 mg/L y 15 mg/L). Los valores de absorbancia fueron determinados a 665 nm para AM y 497 nm para RC. Los resultados muestran que el porcentaje de remoción de AM fue mayor que el de CR (95.49 % vs 59.32%, 1 mg/L; 97.24% vs 39.43%, 5mg/L; 91.30% vs 28.47%, 10mg/L; y 85.42% vs 20.27%, 15mg/L). La remoción del AM se observó a los 30 minutos de contacto, mientras que el RC redujo la absorbancia a partir de las 24 horas.