Actividad bactericida de superficies de cobre frente a bacterias asociadas a infecciones nosocomiales, en un modelo in vitro de adherencia y sobrevivencia / Adherence to copper and stainless steel metal coupons of common nosocomial bacterial strains

Background: Copper has a bactericidal activity against a series of bacterial strains. Aim: To measure resistance to bacterial adherence of copper (Cu) and stainless steel (SS) metal coupons. Material and Methods: Bacterial strains causing nosocomial infections in Chile were analyzed. Bacterial adherence was studied using apreviously described method based on a system of metal coupons that are immersed in culture media containing the bacteria ofinterest at room temperature. Results: Adherence to Cu and SS coupons was differentfor Methicillin-resistant Staphylococcus aureus (MRSA), Klebsiella pneumoniae and Acinetobacter baumannii strains. For these strains, no adherence to Cu coupons occurred during the 48 h observation period compared to a rapidly increasing adherence to SS coupons, with a final colony count of 1.00E + 07 cfu/mL. For two different Pseudomonas aeruginosa clinical strains, inhibition of adherence was not observed on Cu coupons, and colony counts were similar for Cu and SS using the standard inoculum (2-3 xlO7 cfu).Apartial decrease in adherence was observed for Cu but not for SS coupons, when a lower inoculum was used. Conclusions: Copper surfaces represent an interesting option to reduce bacterial contamination in the hospital environment due to its resistance to bacterial adhesión ofmost ofthe common nosocomial bacterial strains.

Detection of metallo-β-lactamases producing Acinetobacter baumannii using microbiological assay, disc synergy test and PCR.

Background: One leading factor responsible for resistance in Acinetobacter baumannii, an important opportunist in health care institutions globally, is the production of carbapenamases like metallo-β-lactamases (MBLs), which hydrolyze a variety of β-lactams including penicillin, cephalosporins and carbapenems. However, neither any standard guidelines are available nor any method has been found to be perfect for their detection. Various methods have shown discordant results, depending upon the employed methodology, β-lactamase substrate and MBL inhibitor used. This study aims to evaluate two phenotypic methods against PCR as gold standard among carbapenem resistant A. baumannii for identifying MBL producers. Materials and Methods: A total of 130 A. baumannii were screened for imipenem and meropenem resistance by Kirby-Bauer disc diffusion method. Phenotypic expression of MBL was detected by EDTA-imipenem-microbiological (EIM) assay and extended EDTA disc synergy (eEDS) test and presence of bla-IMP and bla-VIM was detected by PCR in all the carbapenem resistant isolates. Results: Of the 43 imipenem and/or meropenem resistant A. baumannii isolates, 4 (9.3%) were found to be MBL producers by EIM and 3 (6.97%) by eEDS. Only bla-VIM gene was detected in 7 (16.28%) by PCR. In addition EIM detected 14 (32.56%) carbapenem resistant non-metallo enzyme producers. Conclusion: Of the two MBL genes targeted, bla-VIM was only detected and that too in isolates resistant to both imipenem and meropenem. Further, EIM was useful in differentiating MBL from non-metalloenzymes producers.

Biotransformación de carbón de bajo rango por bacterias aisladas de microhábitats influenciados por residuos de carbón / Biotransformation of low rank coal by bacteria isolated from environments influenced by coal residue

Se describió la capacidad de cinco cepas bacterianas para transformar un carbón de bajo rango (CBR), para ello se evaluaron cepas aisladas de microhábitats con presencia de partículas procedentes de los procesos de almacenamiento y lavado de carbón en la mina El Cerrejón (Colombia). Se realizaron ensayos de solubilización de CBR en medio de cultivo sólido y líquido, además de la decoloración de sustancias húmicas (SH) extraídas del CBR. Todas las bacterias evaluadas presentaron capacidad para biotransformar CBR en medio sólido, esta actividad es mayor cuando el CBR ha sido pretratado con ácido nítrico; en medio líquido se alcanzó una pérdida de peso de CBR hasta del 37% por acción de una cepa de Acinetobacter baumannii, acompañada de la aparición de hasta 8,06 mg/ml-1 de sustancias solubles con absorbancia a 465 nm; los cambios en el pH del medio sugieren que la actividad biotransformadora de CBR está asociada a la liberación de sustancias alcalinas; finalmente, se encontró evidencia para sugerir que las SH presentes en el CBR son transformadas por cometabolismo, posiblemente mediante reacciones de depolimerización, decoloración y repolimerización.

in this study were evaluated five bacterial strains isolated from microhabitats with high content of coal particles generated from storage and washing processes, in "The Cerrejón” open coal mine (Colombia), their ability to biotransform a low rank coal (LRC) was described by testing solubilization on solid and liquid culture medium, as well as bleaching of humic substances (HS) extracted from LRC. All tested bacteria showed ability to biotransform LRC on solid medium, this activity is greater when the LRC has been pretreated with nitric acid; in liquid medium LRC reached 37% of weight loss by Acinetobacter baumannii strain, accompanied by the appearance of up to 6.8 mg/ml-1 of soluble substances with absorbance at 465 nm, changes in culture medium pH suggest that LRC biotransformations activity is associated with alkaline substances release, finally found evidence to suggest that HS contained within LRC are transformed by cometabolism, possibly by depolymerization reactions, bleaching and repolimerization.

The genomic identification of Colombian Acinetobacter baumannii clinical isolates by RFLP-PCR analysis of the 16S-23S rRNA gene spacer region / Identificación genómica de aislamientos colombianos de Acinetobacter baumannii mediante RFLP-PCR de la región intergénica espaciadora de los genes 16S y 23S rRNA

The 16S-23S rRNA gene intergenic spacer (ITS) was analysed by RFLP in this study to identify A. baumannii from 139 isolates from four hospitals (identified as A, B, C and D). One hundred and twenty of these isolates (86.3%) belonged to the A. baumannii species; those identified as being A. baumannii were found to be polyclonal (19 clone groups) when determining the genetic relationships, 16 of them being found in hospital C. Hospitals A, B and D shared two clone groups isolated during different years. This study describes a rapid and easy method for genospecies identification of Acinetobacter baumannii.

Con el objeto de identificar la genomoespecie Acinetobacter baumannii, se estudiaron 189 aislamientos pertenecientes al Complejo Acinetobacter baumannii-Acinetobacter calcoaceticus provenientes de cuatro hospitales colombianos (denominados A,B,C,D) mediante el análisis por RFLP-PCR de la región intergénica espaciador (ITS) de los genes 16S y 23S rRNA. Se encontraron 120 aislamientos (86.3%) pertenecientes a la especie A. baumannii. La estructura de la población fue policlonal, con 19 grupos clonales, 16 de los cuales se hallaron en el hospital C. En los hospitales A,B y D se encontraron 2 grupos clonales aislados durante diferentes años. En este estudio se propone un método rápido y fácil para la identificación de Acinetobacter baumannii.