ABSTRACT
Abstract INTRODUCTION: This study aimed to determine the role of genes encoding aminoglycoside-modifying enzymes (AMEs) and 16S rRNA methylase (ArmA) in Acinetobacter baumannii clinical isolates. METHODS: We collected 100 clinical isolates of A. baumannii and identified and confirmed them using microbiological tests and assessment of the OXA-51 gene. Antibiotic susceptibility testing was carried out using disk agar diffusion and micro-broth dilution methods. The presence of AME genes and ArmA was detected by PCR and multiplex PCR. RESULTS: The most and least effective antibiotics in this study were netilmicin and ciprofloxacin with 68% and 100% resistance rates, respectively. According to the minimum inhibitory concentration test, 94% of the isolates were resistant to gentamicin, tobramycin, and streptomycin, while the highest susceptibility (20%) was observed against netilmicin. The proportion of strains harboring the aminoglycoside resistance genes was as follows: APH(3′)-VIa (aphA6) (77%), ANT(2")-Ia (aadB) (73%), ANT(3")-Ia (aadA1) (33%), AAC(6′)-Ib (aacA4) (33%), ArmA (22%), and AAC(3)-IIa (aacC2) (19%). Among the 22 gene profiles detected in this study, the most prevalent profiles included APH(3′)-VIa + ANT(2")-Ia (39 isolates, 100% of which were kanamycin-resistant), and AAC(3)-IIa + AAC(6′)-Ib + ANT(3")-Ia + APH(3′)-VIa + ANT(2")-Ia (14 isolates, all of which were resistant to gentamicin, kanamycin, and streptomycin). CONCLUSIONS: High minimum inhibitory concentration of aminoglycosides in isolates with the simultaneous presence of AME- and ArmA-encoding genes indicated the importance of these genes in resistance to aminoglycosides. However, control of their spread could be effective in the treatment of infections caused by A. baumannii.
Subject(s)
Acinetobacter baumannii/genetics , Bacterial Proteins , RNA, Ribosomal, 16S/genetics , Microbial Sensitivity Tests , Drug Resistance, Bacterial/genetics , Aminoglycosides/pharmacology , Methyltransferases , Anti-Bacterial Agents/pharmacologyABSTRACT
Background and Aims: Plants as medicines have always played a vital role in human life. Tumor necrosis factor alpha [TNF]- alpha; is one of the macrophage-derived inflammatory cytokine with pleotropic effects in the inflammation process. Some studies have been demonstrated that some of the Echinops species have anti-inflammatory activity. In fact, Echinops lasilepis is introduced as one of the native plants of Yazd. Thus, the present study intended to assess the inflammatory activity of Echinops lasiolepis on TNF-alpha; secretion in J774 A.1 mouse macrophages
Materials and Methods: At first, methanol extract was prepared by maceration. 105 cells/ well were seeded in 96-well plate in triplicate and were treated with different concentrations of extract and 100 ng/ml Lipopolysaccharides. MTT cytotoxicity assay was used to determine the cell viability. Concentrations of extract with cell viability of more than 90% were used to evaluate the level of TNF- and alpha; in the macrophage culture using enzyme-linked immunosorbent assay
Results: Viability of cells at different extract concentrations of 0.1, 1, 10, 50, 100 and 200 µg/ml were 91.68, 95.27, 94.2, 90.8, 85.38 and 71.38, respectively. Therefore, cells treated with 50 mu;g/ml and lower concentrates of extracts showed more than 90% of viability and their supernatants were used for TNF-alpha; assay. The study results revealed that all concentrations of extract reduced the production of TNF-alpha
Conclusions: Our findings showed that methanol extract of Echinops lasiolepis may have anti-inflammatory activity via reducing TNF-alpha; production
ABSTRACT
Background: Stearic acid is known as a potent anti-inflammatory lipid. This fatty acid has profound and diverse effects on liver metabolism. The aim of this study was to investigate the effect of stearic acid on markers of hepatocyte transplantation in rats with acetaminophen [APAP]-induced liver damage
Methods: Wistar rats were randomly assigned to 10-day treatment. Stearic acid was administered to the rats with APAP-induced liver damage. The isolated liver cells were infused intraperitoneally into rats. Blood samples were obtained to evaluate the changes in the serum liver enzymes, including activities of aspartate aminotransferase [AST], alanine aminotransferase [ALT] and alkaline phosphatase [ALP] and the level of serum albumin. To assess the engraftment of infused hepatocytes, rats were euthanized, and the liver DNA was used for PCR using sex-determining region Y [SRY] primers
Results: The levels of AST, ALT and ALP in the serum of rats with APAP-induced liver INJURY were significantly increased and returned to the levels in control group by day six. The APAP-induced decrease in albumin was significantly improved in rats through cell therapy, when compared with that in the APAP-alone treated rats. SRY PCR analysis showed the presence of the transplanted cells in the liver of transplanted rats
Conclusion: Stearic acid-rich diet in combination with cell therapy accelerates the recovering of hepatic dysfunction in a rat model of liver injury