Dual Application of 24-Epibrassinolide and Spermine Confers Drought Stress Tolerance in Maize (<Emphasis Type="Italic">Zea mays</Emphasis> L.) by Modulating Polyamine and Protein Metabolism

No information is available concerning the influence of dual application of 24-epibrassinolide (EBL) and spermine (Spm) on the nitrogen metabolism in plants subjected to drought conditions. As a first report, this investigation assesses the role of EBL, Spm, and their dual application on polyamine and protein pools in water-stressed plants. It explores the ameliorative effects of these foliar applications under water deficiency. Two maize hybrids (Giza 10 and Giza 129) were treated with or without EBL and/or Spm foliar applications under well-irrigated and drought-stressed conditions (75 and 50 % of field capacity). Dual application (25 mg l^?1 Spm + 0.1 mg l^?1 EBL) significantly relieved the drought-induced inhibition on the activities of ribulose-1,5-bisphosphate carboxylase and nitrate reductase and the contents of relative water, nitrate, and protein, particularly in hybrid Giza 129. Changes in the content of free polyamines and in the activity of polyamine biosynthetic and catabolic enzymes were detected when water-stressed plants were treated with EBL and/or Spm. Putrescine content and arginine decarboxylase activity were significantly increased in stressed hybrid Giza 10 plants treated by the dual application. However, spermidine and Spm levels as well as ornithine decarboxylase and S-adenosylmethionine decarboxylase activities were significantly increased in stressed hybrid Giza 129 plants treated with the dual application. Diamine oxidase, polyamine oxidase, protease activity, carbonyl content, and ethylene formation were increased in response to water stress and significantly decreased when stressed plants were treated by the dual application. Total free amino acids, phenols, and flavonoids concentration were increased with the increasing water stress level; moreover, they further increased in stressed plants treated with the dual application. Overall, the combined utilization of EBL and Spm serves as complementary tools to confer plant drought tolerance by altering polyamine, ethylene, and protein levels.     

Screening of mcr-1 Among Gram-Negative Bacteria from Different Clinical Samples from ICU Patients in Alexandria,Egypt: One-Year Study

Antimicrobial resistance represents a global dilemma. Our present study aimed to investigate the presence of mcr-1 among different Gram-negative bacteria including Enterobacteriaceae (except intrinsically resistant to colistin) and Pseudomonas aeruginosa. Gram-negative bacterial isolates were collected from different ICUs in several Alexandria hospitals from June 2019 to June 2020. The identification of these Gram-negative isolates was made using the VITEK-2^® system (BioMérieux, France). SYBR Green-based PCR was used to screen for the presence of mcr-1 using a positive control that we amplified and sequenced earlier in our pilot study. All isolates were screened for the presence of mcr-1 regardless of their colistin susceptibility. Isolates that harbored mcr-1 were tested for colistin susceptibility and for the presence of some beta-lactamase genes. Klebsiella pneumoniae isolates harboring mcr-1 were capsule typed using the wzi sequence analysis. Four hundred eighty isolates were included in this study. Only six isolates harbored mcr-1.1. Of these, four were resistant to colistin, while two (K. pneumoniae and P. aeruginosa) were susceptible to colistin. Five of the six isolates were resistant to carbapenems. They harbored bla_OXA-48, and three of them co-harbored bla_NDM-1. K-58 was the most often found among our K. pneumoniae harboring mcr-1.1. To our knowledge, this is the first time to report colistin susceptible P. aeruginosa and K. pneumoniae harboring the mcr-1.1 gene in Egypt. Further studies are needed to investigate the presence of the mcr genes among colistin susceptible isolates to shed more light on its significance as a potential threat. Open in a separate window     

Genbank accession #: AF139098

Plant Molecular Biology -     

Simultaneous quantification of emtricitabine and tenofovir nucleotides in peripheral blood mononuclear cells using weak anion-exchange liquid chromatography coupled with tandem mass spectrometry

Emtricitabine (FTC) and tenofovir (TFV) are widely used antiviral agents that require intracellular phosphorylation to become active. This article describes the development and validation of an assay for the simultaneous quantification of FTC mono-, di- and triphosphate (FTC-MP, -DP and -TP), TFV and TFV mono- and diphosphate (TFV-MP and -DP) in peripheral blood mononuclear cells. Reference compounds and internal standards were obtained by thermal degradation of FTC-TP, TFV-DP, stable isotope-labeled TFV-DP and stable isotope-labeled cytosine triphosphate. Cells were lysed in methanol:water (70:30, v/v) and the extracted nucleotides were analyzed using weak anion-exchange chromatography coupled with tandem mass spectrometry. Calibration ranges in PBMC lysate from 0.727 to 36.4, 1.33 to 66.4 and 1.29 to 64.6 nM for FTC-MP, FTC-DP and FTC-TP and from 1.51 to 75.6, 1.54 to 77.2 and 2.54 to 127 nM for TFV, TFV-MP and TFV-DP, respectively, were validated. Accuracies were within ?10.3 and 16.7% deviation at the lower limit of quantification at which the coefficients of variation were less than 18.2%. At the other tested levels accuracies were within ?14.3 and 9.81% deviation and the coefficients of variation lower than 14.7%. The stability of the compounds was assessed under various analytically relevant conditions. The method was successfully applied to clinical samples.