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Background and Aim: Salmonella has been identified as one of the most widely distributed zoonotic pathogens in broiler litter. Multidrug-resistant strains have been isolated from salmonellosis outbreaks, compromising the success of their treatment. This study aimed to isolate and identify Salmonella spp. serovars in healthy broiler litter in Tolima (Colombia), determine their resistance to different antimicrobials, and detect genes associated with b-lactam resistance that could be useful to control Salmonella spp. in poultry. Materials and Methods: In total, 45 broiler litter samples were collected. Salmonella spp. was isolated and identified using selective and differential culture media and biochemical tests. Molecular confirmation of the pathogen was performed with the invA gene and serotyping by Kauffman-White scheme. Antimicrobial susceptibility to 15 antibiotics was determined by Kirby-Bauer method. In cefotaxime-resistant strains, blaCTX-M-F, blaCTX-M-1, blaCMY, and blaTEM genes were evaluated by polymerase chain reaction (PCR). Results: In total, 817 presumptive strains were obtained from xylose lysine deoxycholate and Salmonella Shigella agars and subcultured on xylose-lysine-tergitol 4 and MacConkey agars, from which 150 strains were isolated; 29 of these strains were presumptive for Salmonella spp. after performing biochemical tests and 16 were confirmed by PCR as Salmonella Infantis (15) and Gallinarum (1). All strains were found to be multiresistant to antibiotics, showing three different profiles and isolates resistant to cefotaxime, and the blaCTX-M gene was detected. Conclusion: This is the first study to isolate S. Infantis from broiler litter in Colombia. All isolates exhibited resistance to the evaluated antimicrobials, suggesting the misuse of antimicrobials in small- and medium-sized poultry farms. The presence of Salmonella enterica serovar Infantis is a public health problem. Thus, regular monitoring of poultry litter is recommended, as these bacteria can be transmitted to humans through animal products or contaminated environments.

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(1) Background: During the COVID-19 outbreak, several studies showed an increased prevalence of extended-spectrum ß-lactamase producing Enterobacterales (ESBL-PE) carriage in intensive care units (ICUs). Our objective was to assess the impact of antibiotic prescriptions on the acquisition of ESBL-PE in ICUs during the COVID-19 crisis. (2) Methods: We conducted an observational study between 1 April 2020, and 31 December 2021, in the medical-surgical ICU of the Cayenne General Hospital. We defined two periods: Period 1 with routine, empirical antibiotic use, and Period 2 with no systematic empiric antibiotic prescription. (3) Results: ICU-acquired ESBL-PE carriage was 22.8% during Period 1 and 9.4% during Period 2 (p = 0.005). The main isolated ESBL-PE was Klebsiella pneumoniae (84.6% in Period 1 and 58.3% in Period 2). When using a generalized linear model with a Poisson family, exposure to cefotaxime was the only factor independently associated with ESBL-PE acquisition in ICU (p = 0.002, IRR 2.59 (95% IC 1.42-4.75)). The propensity scores matching estimated the increased risk for cefotaxime use to acquire ESBL-PE carriage at 0.096 (95% CI = 0.02-0.17), p = 0.01. (4) Conclusions: Exposure to cefotaxime in patients with severe COVID-19 is strongly associated with the emergence of ESBL-PE in the context of maximal infection control measures.

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The natural diversification of CTX-M ß-lactamases led to the emergence of Asp240Gly variants in the clinic that confer reduced susceptibility to ceftazidime (CAZ). In this study, we compared the impact of this substitution on CAZ and ceftazidime-avibactam (CZA) MICs against isogenic Escherichia coli strains with different porin deficiencies. Our results show a noticeable increase in CAZ resistance in clones expressing Asp240Gly-harboring CTX-M when combined with OmpF porin deficiency. Kinetic analysis revealed that the kcat/Km for CAZ was 5- to 15-fold higher for all Asp240Gly variants but remained 200- to 725-fold lower than that for cefotaxime (CTX). In vitro selection of CAZ-resistant clones yielded nonsusceptible CTX-M producers (MIC of >16 µg/ml) only after overnight incubation; the addition of avibactam (AVI) decreased MICs to a susceptible range against these variants. In contrast, the use of CZA as a selective agent did not yield resistant clones. AVI inactivated both CTX-M-12 and CTX-M-96, with an apparent inhibition constant comparable to that of SHV-2 and 1,000-fold greater than that of PER-2 and CMY-2, and k2/K for CTX-M-12 was 24- and 35-fold higher than that for CTX-M-96 and CTX-M-15, respectively. Molecular modeling suggests that AVI interacts similarly with CTX-M-96 and CTX-M-15. We conclude that the impact of Asp240Gly in resistance may arise when other mechanisms are also present (i.e., OmpF deficiency). Additionally, CAZ selection could favor the emergence of CAZ-resistant subpopulations. These results define the role of Asp240 and the impact of the -Gly substitution and allow us to hypothesize that the use of CZA is an effective preventive strategy to delay the development of resistance in this family of extended-spectrum ß-lactamases.

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The aim of this work is to evaluate simple, sensitive, effective and validated procedures for the determination of cefotaxime, cefoperazone, ceftazidime and cefadroxil. In this study, the methods based on the ability of the cited drugs to reduce Ag+ ions to silver nanoparticles (Ag-NPs) in the presence of Polyvinyl Pyrrolidone (PVP) as a stabilizing agent producing very intense surface plasmon resonance peak of Ag-NPs (λmax. = 410-430 nm). The plasmon absorbance of the Ag-NPs allows the quantitative spectrophotometric determination of the cited drugs. The calibration curves are linear with concentration ranges of 0.4-3.2, 1-8, 0.5-4.0 and 1.5-9.0 µg/mL for cefotaxime, cefoperazone, ceftazidime and cefadroxil, respectively. Apparent molar absorptivity, detection and quantitative limits are calculated. Applications of the proposed methods to representative pharmaceutical formulations are successfully presented. The extracellular synthesis of nanoparticles is fast, and the method doesn't require various elaborate treatments and tedious extraction procedures.

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The reaction between the antibiotic cefotaxime and the CTX-M-14 class A serine hydrolase is addressed from a theoretical point of view, by means of hybrid quantum mechanics/molecular mechanical (QM/MM) calculations, adopting a new approach that postulates that the residue Ser70 itself should play the role of the acid-base species required for the cefotaxime acylation. The proposed mechanism differs from earlier proposals existing in literature for other class A ß-lactamases. The results confirm the hypothesis, and show that the reaction should occur via a concerted mechanism in which the acylation of the lactam carbonyl carbon, protonation of the N7 lactam atom, and opening of the ß-lactam ring occurs simultaneously. Exploration of the potential energy surface shows three critical points, associated with reactants, transition state and product. The transition state is characterized by frequency, intrinsic reaction coordinate, atomic charge, and bond orders calculations. The calculated activation barrier is 20 kcal mol-1, and the reaction appears to be slightly endothermic by about 12 kcal mol-1. We conclude that this approach is feasible, and should be considered as an alternative mechanism or may exist in competition with others already published in the literature. This information should be useful for the design of novel antibiotics and ß-lactamase inhibitors. Graphical abstract Three-dimensional view of the potential energy surface of cefotaxime.

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Bacterial resistance to antibiotics is a growing phenomenon in the world. Considering the relevance of antimicrobials for population and the reduction in the registration of new antimicrobials by regulatory, proper quality control is required in order to minimize the spread of bacterial resistance and ensure the effectiveness of a treatment, as well as safety for the patient. Among the antimicrobials is cefotaxime, a drug belonging to third-generation cephalosporins, which is highly active against Gram-negative bactéria and is used to treat central nervous system infections such as meningitis and septicemia. Due to the critical importance of quality control in regard to drugs and pharmaceutical products, combined with bacterial resistance to antibiotics, this study aims to conduct a detailed review of analytical methods for cefotaxime. Using a critical review of literature, this paper describes the analytical methods published to quantify cefotaxime in different matrices; a large number of methods by HPLC and spectrophotometry were observed. Despite the advantages of the techniques, most methods reported have large environment and occupational impact, which enfatizes the need to adopt green procedures in quantifying cefotaxime.

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In this work an "in house" rapid test based on the change in pH that is due to hydrolysis for detecting Enterobacteriaceae susceptible to cefotaxime is evaluated. The strains of Enterobacteriaceae from 1947 urine cultures were assessed using MicroScan panels and the "in house" test. This rapid test includes red phenol solution and cefotaxime. Using MicroScan panels, 499 Enterobacteriaceae isolates were evaluated, which included 27 isolates of Escherichia coli producing extended-spectrum beta-lactamases (ESBL), 16 isolates of Klebsiella pneumoniae ESBL and 1 isolate of Klebsiella oxytoca ESBL. The "in house" test offers the following values: sensitivity 98% and specificity 97%, with negative predictive value 100% and positive predictive value 78%. The "in house" test based on the change of pH is useful in our area for detecting presumptively cefotaxime-resistant Enterobacteriaceae strains.

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En este trabajo se evalúa una prueba rápida in house para la detección de enterobacterias sensibles a cefotaxima, basada en el cambio de pH del rojo fenol debido a la hidrólisis de este antibiótico. Las cepas de enterobacterias procedentes de 1.947 urocultivos se evaluaron mediante los paneles MicroScan y esta prueba in house. Mediante los paneles de MicroScan se estudiaron 499 aislados de enterobacterias, entre los cuales había 27 aislados de Escherichia coli productora de β-lactamasa de espectro extendido (BLEE), 16 de Klebsiella pneumoniae BLEE y una de Klebsiella oxytoca BLEE. La prueba in house mostró una sensibilidad del 98% y una especificidad del 97%, con un valor predictivo negativo del 100% y un valor predictivo positivo del 78%. La prueba in house basada en el cambio de pH es útil en nuestro medio para detectar presuntivamente de forma rápida cepas de enterobacterias con cierta resistencia a cefotaxima.

In this work an "in house" rapid test based on the change in pH that is due to hydrolysis for detecting Enterobacteriaceae susceptible to cefotaxime is evaluated. The strains of Enterobacteriaceae from 1947 urine cultures were assessed using MicroScan panels and the "in house" test. This rapid test includes red phenol solution and cefotaxime. Using MicroScan panels, 499 Enterobacteriaceae isolates were evaluated, which included 27 isolates of Escherichia coli producing extended-spectrum beta-lactamases (ESBL), 16 isolates of Klebsiella pneumoniae ESBL and 1 isolate of Klebsiella oxytoca ESBL. The "in house" test offers the following values: sensitivity 98% and specificity 97%, with negative predictive value 100% and positive predictive value 78%. The "in house" test based on the change of pH is useful in our area for detecting presumptively cefotaxime-resistant Enterobacteriaceae strains.

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We report an H. parainfluenzae clinical isolate resistant to cefotaxime and with decreased susceptibility to ciprofloxacin recovered from a patient with cystic fibrosis. The isolate had elevated MICs of ampicillin (256mg/L), amoxicillin-clavulanate (8mg/L), cefuroxime (8mg/L) and cefotaxime (4mg/L), and showed a ß-lactamase-producing amoxicillin-clavulanic acid-resistant (BLPACR) phenotype. A blaTEM-1 plus five amino acid substitutions in the PBP3 were found: Ser385Thr, Val511Ala, Ile519Val, Asn526Lys and Asp551Leu. MIC of ciprofloxacin was 0.5mg/L, and substitutions in gyrA (Ser84Tyr) and parC (Ser84Phe) genes were detected.

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Introducción. Las secuencias de inserción tales como IS CR1 promueven la captura, transposición y expresión de los genes bla CTX-M, facilitando, de esta manera, su diseminación rápida en la población bacteriana. Objetivo. Se determinó la presencia del elemento IS CR1 y su asociación con genes bla CTX-M-1 y bla CTX-M-2 en plásmidos de diferentes grupos de incompatibilidad en Klebsiella pneumoniae de origen hospitalario. Materiales y métodos. Se aislaron tres cepas de K. pneumoniae con sensibilidad disminuida a cefalosporinas de amplio espectro, de neonatos con septicemia hospitalaria. La presencia de β -lactamasas de espectro expandido (BLEE) fue determinada fenotípicamente. Los plásmidos se aislaron y clasificaron según grupos de incompatibilidad por tipificación del replicón por reacción en cadena de la polimerasa (PCR). Los genes bla BLEE y su asociación a IS CR1 se determinaron por PCR y secuenciación directa, usando varios juegos de iniciadores. Resultados. Todas las cepas demostraron un perfil fenotípico indicativo de producción de BLEE, transferibles por conjugación. Los ensayos de PCR para para cefotaximasas (CTX-M) y el análisis de la secuenciación, revelaron que las cepas portaban genes bla CTX-M-1 y bla CTX-M-2. Estos genes se encontraron en plásmidos conjugados de 150 kb, aproximadamente, relacionados con los grupos IncN e IncFIIA, respectivamente. IS CR1 se encontró ´aguas arriba´ ( upstream ) y asociado con los genes bla CTX-M-1 y bla CTX-M-2. Conclusión. Este es el primer reporte realizado en Venezuela donde la presencia de IS CR1 está estrechamente asociada con la movilización de los genes bla CTX-M-1 y bla CTX-M-2 en plásmidos conjugativos IncN y IncFIIA en cepas de K. pneumoniae que circulan en una Unidad de Alto Riesgo Neonatal.

Introduction: Insertion sequences such as IS CR1 promote capture, transposition and expression of bla CTX-M genes. Thus, gene dissemination in bacterial populations occurs rapidly. Objective: To determine the presence of IS CR1 sequence genes and their association with bla CTX-M-1 and bla CTX-M-2 on plasmids IncN and IncFIIA from K. pneumoniae of nosocomial origin, was determined. Materials and methods: Three strains of K. pneumoniae with reduced susceptibility to extendedspectrum cephalosporins were isolated from neonatal sepsis cases of nosocomial origin. Phenotypic tests showed the presence of ESBLs. Plasmids were isolated and classified according to incompatibility groups by PCR replicon typing. Detection and association of IS CR1 with bla CTX-M genes were determined by PCR and direct sequencing through the use of several sets of PCR primers. Results: All strains showed phenotypic profile consistent with ESBL-producing transferred by conjugation. PCR amplification assay for CTX-M together with sequencing analysis revealed that strains carrying bla CTX-M-1 y bla CTX-M-2 genes were localized in plasmids of approximately 150 kb related to IncN and IncFIIA groups, respectively. IS CR1 was found upstream and associated with bla CTX-M-1 y bla CTX-M-2 genes. Conclusion. Thus far, this is the first Venezuelan report, in which IS CR1 presence is closely related to bla CTX-M-1 y bla CTX-M-2 gene mobilization in IncN and IncFIIA conjugative plasmids located in K. pneumonaiae strains circulating at a neonatal high risk unit.

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Fundamento y objetivo: El mayor aislamiento y la diseminación de gérmenes multirresistentes en unidades de atención a pacientes críticos, contribuyen al incremento de estadía, costos, morbilidad y mortalidad hospitalarias que solo pueden ser controlados con el trabajo eficiente de grupos médicos de trabajo, multidisciplinario e interdisciplinario. Métodos: Se muestran los principales microorganismos aislados de pacientes hospitalizados, durante el año 2008, con sus patrones de resistencia. Se presenta la metodología para el control de la sepsis hospitalaria por los diferentes grupos interdisciplinarios según el algoritmo de trabajo propuesto. Resultados: Acinetobacter sp pasó a ocupar el primer lugar en el año 2008 dentro de los gérmenes más frecuentemente aislados, a su vez resultó el agente responsable de mayores reportes de infección hospitalaria, con patrones de resistencia elevados frente a todos los antibióticos estudiados in vitro, particularmente al ceftriaxone con el 98,1 por ciento. Para colistina, la resistencia fue solo 2 por ciento. La resistencia de Escherichia coli, Klebsiella sp y Enterobacter sp frente al ceftriaxone fue 59,4, 75 y 83,3 por ciento, respectivamente. Conclusión: El trabajo multidisciplinario e interdisciplinario de todas las especialidades médicas y de grupos de expertos, resulta fundamental para controlar la aparición y diseminación de infecciones nosocomiales provocadas por gérmenes multirresistentes, de mayor frecuencia de aislamiento en la actualidad. La elevada resistencia bacteriana frente al ceftriaxone, de los principales microorganismos aislados, constituye un objetivo de trabajo para su control por los diferentes comités o grupos de expertos médicos

Basis and objective: The great isolation and spreading of multiresistance germs in care units to critical patients, contribute to increase of stay, costs, hospital morbidity and mortality only controlled with an efficient, multidisciplinary and interdisciplinary work by physician groups. Methods: The main microorganisms are showed isolated in 2008, with its resistance patterns of admitted patients. A methodology for the hospital sepsis control is presented by the interdisciplinary groups according to the proposed work algorithm. Results: Acinetobacter sp was in the first place over 2008 included into the more frequent isolated germs being the causal agent of more reports on hospital infection with high patterns of resistance to all in vitro study antibiotics, in particular, to Ceftriaxione with the 98.1 percent; for Colistin the resistance was only of 2 percent. The resistance of Escherichia coli, Klebsiella sp and Enterobacter sp to Ceftriaxione was of 59.4, 75 and 83.3 percent, respectively. Conclusion: The multidisciplinary and interdisciplinary work of all medical specialties and expert groups is essential to control the appearance and spreading of nosocomial infections provoked by multiresistance germs of great isolation frequency at present time. The high bacterial resistance of main isolated microorganisms to Ceftriaxone is a work objective for its prevention by the different committees or medical expert groups

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The objectives of the present work were to establish the minimal lethal dose of the selective agent to determine the type and concentration of appropriate antibiotics for the elimination of Agrobacterium tumefaciens inoculated explants, without interfering with the regenerative potential of the E. camaldulensis cotyledonary explants. Non-transformed explants were cultivated in medium supplemented with kanamycin. The results showed that the antibiotic was suitable for the selection of transformed cells in the concentration of 9 mg L-1 as it inhibited the growth of non-transformed cells. Cotyledons infected with A. tumefaciens were cultivated in MS N/2 medium supplemented with BAP, ANA, Km and cefotaxime or AugmentinÒ . The highest average of regenerated shoots by explant (5,4) was observed in the presence of 300 mg L-1 of AugmentinÒ /15 days, followed by 150 mg L-1/15 days and 100 mg L-1/30 days.

O presente trabalho teve como objetivos determinar o tipo e a concentração de antibióticos adequados para a eliminação de Agrobacterium tumefaciens de explantes inoculados e estabelecer a dose letal mínima do agente seletivo canamicina (Km), sem interferir com o potencial regenerativo do explante cotiledonar de E. camaldulensis. Para a avaliação da eficiência dos antibióticos, cotilédones infectados com A. tumefaciens foram cultivados em meio MS N/2 com BAP, ANA, canamicina e cefotaxima ou AugmentinaÒ . Foi observada a maior média de brotos regenerados por explante (5,4) na presença de 300 mg.L-1 de AugmentinaÒ /15 dias, seguido por 150 mg.L-1/30 dias, e 100 mg.L-1/30 dias. Explantes cotiledonares não transformados foram cultivados em meio de cultura suplementado com antibiótico canamicina onde a concentração adequada para a seleção de células transformadas foi de 9 mg.L-1.

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We report a term neonate who developed early-onset sepsis due to Morganella morganii. The child was vaginally delivered after a short labor, and presented signs of perinatal asphyxia. Blood cultures taken soon after birth and from mother's lochia were positive for this microorganism. The infection was unresponsive to treatment with cefotaxime, to which the microorganism was susceptible, and the infant died at 17 days of age. M morganii is an opportunistic and uncommon pathogen, causing disease mainly in patients with underlying illness or after surgery. It is a rare perinatal pathogen, causing severe disease in premature infants, in association with maternal chorioamnionitis and premature rupture of the membranes (RevMéd Chile 2009; 137: 1201-4).

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Fundamentación: El uso profiláctico perioperatorio de antimicrobianos en la apendicitis aguda no complicada, lidera la reducción de las infecciones del sitio quirúrgico. Se obtienen mejores o iguales resultados desde el punto de vista farmacoeconómico con la utilización de monoterapia con la familia de las cefalosporinas. Objetivo: Determinar la relación costo-efectividad entre dos cefalosporinas utilizadas como profilaxis en enfermos apendicectomizados. Método: Se realizó un estudio descriptivo retrospectivo de todos los enfermos tratados según la guía de profilaxis antimicrobiana para la apendicitis aguda durante el período comprendido entre enero de 2000 y diciembre de 2005, en el Servicio de Cirugía Pediátrica del Hospital Pediátrico Provincial Docente Dr Eduardo Agramonte Piña de la ciudad de Camagüey. Para la evaluación económica comparativa, se utilizó la técnica de análisis de costo-efectividad. El análisis de costo-efectividad medio y el análisis costo-efectividad incremental fueron hallados según las fórmulas establecidas. Resultados: En el estudio 245 niños recibieron tratamiento profiláctico con Ceftriaxona 3006,15 pesos y 364 con Cefotaxima 4036, 76 pesos.El análisis de costo-efectividad medio fue de 12,47pesos/por ciento de infección evitada con la utilización de la Ceftriaxona, mientras que para el uso de la Cefotaxima fue de 11,37pesos/por ciento infección evitada. Conclusiones: Las cefalosporinas comparadas mostraron similar relación costo-efectividad como profilaxis en la apendicitis aguda.

Background: The perioperative prophylactic use of antimicrobial in non complicated acute appendicitis, leads the reduction of the infections of the surgical place. Better or equal results from the pharmacoeconomic point of view with the monotherapy use of the cephalosporin family are obtained. Objective: To determine the cost-effectiveness relationship between two cefalosporins used as prevention in appendicectomized sickpeople. Method: A descriptive retrospective study of all the sick persons treated according to the antimicrobial guide of prevention for acute appendicitis was carried out from January 2000 and December 2005, in the Pediatric Surgery Service at Dr Eduardo Agramonte Piña Educational Provincial Pediatric Hospital of Camagüey city. For the economic comparative evaluation, the cost-effectiveness analysis technique was used. The cost-effectiveness mean analysis and the cost-effectiveness increasing analysis were found according to the established formulas. Results: In the study 245 children received prophylactic treatment with Ceftriaxone $ 3006,15 and 364 with Cefotaxime $ 4036, 76. The cost-effectiveness mean analysis was about 12,47 $ /percent of avoided infection with the use of Ceftriaxone, while the use of Cefotaxime was about 11,37 $ /percent of avoided infection. Conclusions: The compared cefalosporins showed similar cost-effectiveness relationship as prophylaxis in acute appendicitis.

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