Vigilancia de la resistencia a los antimicrobianos en cepas de Neisseria gonorrhoeae aisladas en Paraguay. Año 2021

Neisseria gonorrhoeae (N. gonorrhoeae) es el agente causal de la gonorrea, infección de transmisión sexual (ITS) que corresponde a la segunda causa más frecuente de ITS a nivel mundial, provocando una alta morbilidad y costo en atención de salud. En las últimas décadas han aumentado los reportes a nivel mundial de cepas resistentes a penicilina, sulfonamidas, tetraciclina, macrólidos y fluoroquinolonas, y más recientemente a azitromicina y cefalosporinas de espectro extendido como ceftriaxona y cefixima. El objetivo principal de este estudio fue determinar la sensibilidad a los antimicrobianos en cepas de N. gonorrhoeae que fueron enviadas al Laboratorio Central de Salud Pública (LCSP), por los centros colaboradores de la Red de Vigilancia Laboratorial de la Resistencia a los Antimicrobianos (RAM). Para ello, se realizó un estudio prospectivo de corte transversal de enero a diciembre de 2021. Se caracterizaron 128 cepas como N. gonorrhoeae a las cuales se le realizaron pruebas de susceptibilidad obteniéndose 48% de resistencia y 52% de sensibilidad intermedia a penicilina. El 70% presentó resistencia a ciprofloxacina y el 19% a tetraciclina. Se obtuvo 100% de sensibilidad a ceftriaxona y cefixima. El fenotipo de resistencia de mayor prevalencia fue QRNG, asociado con resistencia a ciprofloxacina, seguido del fenotipo PPNG-QRNG, asociado con resistencia a penicilina y ciprofloxacina. Ante estos hallazgos y frente a la emergencia mundial de la resistencia a los antimicrobianos, especialmente de cefalosporinas de espectro extendido, se recomienda que los laboratorios de bacteriología fortalezcan la vigilancia para apoyar la detección de casos y proporcionar el tratamiento adecuado.

Neisseria gonorrhoeae (N. gonorrhoeae) is the causal agent of gonorrhea, a sexually transmitted infection (STI) that is the second most common cause of STIs worldwide, causing high morbidity and cost in health care. In recent decades, reports of strains resistant to penicillin, fluoroquinolones, sulfonamides, tetracycline, macrolides, and more recently to azithromycin and extended-spectrum cephalosporins such as ceftriaxone and cefixime have increased worldwide. The main objective of this study was to determine the sensitivity to antimicrobials in N. gonorrhoeae strains that were sent to the Central Laboratory of Public Health (LCSP), by the collaborating centers of the Antimicrobial Resistance Laboratory Surveillance Network (RAM). For this, a prospective cross-sectional study was carried out from January to December, 2021. One hundred eighty strains were characterized as N. gonorrhoeae, which were subjected to sensitivity tests, obtaining 48% resistance and 52% intermediate sensitivity to penicillin while 70% presented resistance to ciprofloxacin and 19% to tetracycline. Also, 100% sensitivity to ceftriaxone and cefixime was obtained. The most prevalent resistance phenotype was QRNG, associated with resistance to ciprofloxacin, followed by the PPNG-QRNG phenotype, associated with resistance to penicillin and ciprofloxacin. Given these findings and the global emergence of antimicrobial resistance, especially extended-spectrum cephalosporins, it is recommended that bacteriology laboratories fortify surveillance to support case detection and provide appropriate treatment.

Pranlukast Antagonizes CD49f and Reduces Stemness in Triple-Negative Breast Cancer Cells.

INTRODUCTION: Cancer stem cells (CSCs) drive the initiation, maintenance, and therapy response of breast tumors. CD49f is expressed in breast CSCs and functions in the maintenance of stemness. Thus, blockade of CD49f is a potential therapeutic approach for targeting breast CSCs. In the present study, we aimed to repurpose drugs as CD49f antagonists. MATERIALS AND METHODS: We performed consensus molecular docking using a subdomain of CD49f that is critical for heterodimerization and a collection of pharmochemicals clinically tested. Molecular dynamics simulations were employed to further characterize drug-target binding. Using MDA-MB-231 cells, we evaluated the effects of potential CD49f antagonists on 1) cell adhesion to laminin; 2) mammosphere formation; and 3) cell viability. We analyzed the effects of the drug with better CSC-selectivity on the activation of CD49f-downstream signaling by Western blot (WB) and co-immunoprecipitation. Expressions of the stem cell markers CD44 and SOX2 were analyzed by flow cytometry and WB, respectively. Transactivation of SOX2 promoter was evaluated by luciferase reporter assays. Changes in the number of CSCs were assessed by limiting-dilution xenotransplantation. RESULTS: Pranlukast, a drug used to treat asthma, bound to CD49f in silico and inhibited the adhesion of CD49f+ MDA-MB-231 cells to laminin, indicating that it antagonizes CD49f-containing integrins. Molecular dynamics analysis showed that pranlukast binding induces conformational changes in CD49f that affect its interaction with ß1-integrin subunit and constrained the conformational dynamics of the heterodimer. Pranlukast decreased the clonogenicity of breast cancer cells on mammosphere formation assay but had no impact on the viability of bulk tumor cells. Brief exposure of MDA-MB-231 cells to pranlukast altered CD49f-dependent signaling, reducing focal adhesion kinase (FAK) and phosphatidylinositol 3-kinase (PI3K) activation. Further, pranlukast-treated cells showed decreased CD44 and SOX2 expression, SOX2 promoter transactivation, and in vivo tumorigenicity, supporting that this drug reduces the frequency of CSC. CONCLUSION: Our results support the function of pranlukast as a CD49f antagonist that reduces the CSC population in triple-negative breast cancer cells. The pharmacokinetics and toxicology of this drug have already been established, rendering a potential adjuvant therapy for breast cancer patients.

Cost of medical attention in patients with Chronic Obstructive Pulmonary Disease / Costo de la atención médica en pacientes con enfermedad pulmonar obstructiva crónica

Background: The chronic obstructive pulmonary disease is a preventable entity, when it develops the patient suffers severe complications, with a high economic impact for the patient and for health services. Objetive: To determine the cost of medical care in patients with chronic obstructive pulmonary disease (COPD). Methods: Using a cost design, the files of patients with COPD who attended the pulmonology clinic were analyzed. The size of the sample (n = 265) was calculated with the formula of averages of a finite population. The sample units were captured with the simple random technique. The study variables were: sociodemographic characteristics, characteristics of COPD, annual use profile, unit cost per service, total cost per service and total cost of medical care. The analysis plan included averages, percentages, confidence intervals and health expenditure projections. Results: The average annual cost of patient care with COPD was $ 89 479.08, of which $ 61 267.63 corresponded to medications. With a COPD prevalence of 25% in a population of 46 million, the calculated cost of care was $ 347 805 183 960. Conclusion: The cost of medical care in patients with COPD was high, at the expense of medications.

Introducción: la enfermedad pulmonar obstructiva crónica es una entidad prevenible, cuando se desarrolla, el enfermo sufre complicaciones severas, con un alto impacto económico para el paciente y para los servicios de salud. Objetivo: determinar el costo de la atención médica en pacientes con enfermedad pulmonar obstructiva crónica (EPOC). Métodos: con un diseño de costos se analizaron los expedientes de pacientes con EPOC que acudieron a consulta de neumología. El tamaño de la muestra (n = 265) se calculó con la fórmula de promedios de una población finita. Las unidades muestrales se capturaron con la técnica aleatoria simple. Las variables de estudio fueron: características sociodemográficas, características de la EPOC, perfil de uso anual, costo unitario por servicio, costo total por servicio y costo total de la atención médica. El plan de análisis incluyó promedios, porcentajes, intervalos de confianza y proyecciones del gasto en salud. Resultados: el costo promedio anual de la atención del paciente con EPOC fue $89 479.08, de los cuales $61 267.63 correspondieron a medicamentos. Con una prevalencia de EPOC de 25% en una población de 46 millones, el costo calculado de la atención fue $347 805 183 960. Conclusión: el costo de la atención médica en pacientes con EPOC fue alto en buena medida a expensas de los medicamentos.

Involvement of Melatonin in the Regulation of the Circadian System in Crayfish.

Melatonin (MEL) is an ancient molecule, broadly distributed in nature from unicellular to multicellular species. MEL is an indoleamine that acts on a wide variety of cellular targets regulating different physiological functions. This review is focused on the role played by this molecule in the regulation of the circadian rhythms in crayfish. In these species, information about internal and external time progression might be transmitted by the periodical release of MEL and other endocrine signals acting through the pacemaker. We describe documented and original evidence in support of this hypothesis that also suggests that the rhythmic release of MEL contributes to the reinforcement of the temporal organization of nocturnal or diurnal circadian oscillators. Finally, we discuss how MEL might coordinate functions that converge in the performance of complex behaviors, such as the agonistic responses to establish social dominance status in Procambarus clarkii and the burrowing behavior in the secondary digging crayfish P. acanthophorus.