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1.
Acta Trop ; 207: 105500, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32330451

ABSTRACT

In the scientific literature, a small amount of information is found concerning mycoplasmosis in camel species. A variety of pathogens could be causative agents for pneumonia, but walking pneumonia is mostly caused by Mycoplasma with slow development and mild symptoms. The aim of this study was to identify mycoplasmas from camels (Camelus dromedarius) and extending the arsenal of factors implicated in pathogenicity of M. arginini to shed light on the current knowledge gap. 460 lung samples (pneumonic; n=210 and apparently healthy; n=250) were randomly collected from the one-humped camels (C. domedarius) that have been imported from Sudan and slaughtered at Cairo Slaughterhouse. 48 out of 210 isolates (22.9%) recovered from the pneumonic lungs were recorded as M. arginini. Positive PCR results were obtained for all 48 isolates. On the other hand, infection with the organism was not detected in the apparently healthy lungs. Hemolysis and hydrogen sulphide (H2S) production, a compound that has previously not been identified as a virulence factor in M. arginini, was evident in 100% of the isolates. The 48 M. arginini isolates were weak in their ability to form biofilm on polystyrene surfaces. All isolates were 100% susceptible to florfenicol and streptomycin and 100% resistant to ciprofloxacin. Resistance to lincomycin, spiromycin, tylosin, doxacyclin and erythromycin was observed at different frequencies. 13 different combinations of antibiotics representing one to four classes were evident with the Macrolide erythromycin being the most represented. It also should be noted that the ciprofloxacin, doxacyclin, lincomycin, erythromycin combination was the most noted in 21/48 isolates. Surprisingly, none of the virulence genes (vsp, uvrC and gapA) and quinolone resistance genes (parC and gyrA) were detected by PCR.


Subject(s)
Camelus/microbiology , Mycoplasma/isolation & purification , Animals , Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial/drug effects , Mycoplasma/drug effects , Mycoplasma/genetics , Mycoplasma/pathogenicity , Phylogeny , Virulence/genetics
2.
J Environ Manage ; 258: 110043, 2020 Mar 15.
Article in English | MEDLINE | ID: mdl-31929075

ABSTRACT

Two types of chitosan-based composites (chitosan/ZnO and chitosan/Ce-ZnO composites) were synthesized under microwave irradiation and characterized as advanced catalysts of enhanced photocatalytic activity under the visible light. The morphological investigation reflected the formation of ZnO and Ce doped ZnO at stunning micro flowers of nano limps. Additionally, the optical studies reflected a reduction in the bandgap of ZnO from 3.3 eV to 2.85 eV and 2.5 eV after supporting it onto chitosan chains and after doping it with cerium, respectively. The synthetic composites were applied in photocatalytic removal of malachite green dye under a visible light source. The synthetic CH/ZnO and CH/Ce-ZnO showed enhancement in the photocatalytic removal of M.G by 54% and 87%, respectively, as compared to the pure ZnO. The synthetic composites are of high stability and can be reused for five photocatalytic degradation cycles at stunning removal percentages. The main oxidizing radicals during the removal of M.G by CH/ZnO are the generated electron-hole pairs as well as the hydroxyl radicals. The effective species in CH/Ce-ZnO photocatalytic system are the photogenerated hydroxyl radicals followed by the electron-hole pairs.


Subject(s)
Chitosan , Zinc Oxide , Flowers , Light , Rosaniline Dyes
3.
Curr Res Transl Med ; 68(2): 77-80, 2020 04.
Article in English | MEDLINE | ID: mdl-31501046

ABSTRACT

BACKGROUND: Preeclampsia (PE) is a common pregnancy complication and one of the main causes of maternal and fetal morbidity and mortality, worldwide. While the pathogenesis of PE is unclear, it has been suggested that hypercoagulability due to Factor V Leiden (FVL) and prothrombin gene mutation (FII G20210A) play a role in its progression. PURPOSE: This study aimed to determine if there is an association between FVL and FII G20210A mutations and severe PE. PATIENTS AND METHODS: This case-control study enrolled 50 women with severe PE and 50 healthy pregnant women as the control, at Khartoum North Teaching Hospital, in Khartoum State, Sudan, from January 2017 to June 2017. The presence of point mutations in FVL and FII G20210A were determined for each of the participants. Deoxyribonucleic acid (DNA) was extracted, and then an allele-specific polymerase chain reaction (PCR) was used to detect the point mutations in FVL and FII G20210A. RESULTS: The results revealed a significant difference between the subjects in the severe PE group and the control group for the means of parity, gestational age/ week and hemoglobin concentration (P < 0.05). No statistically significant body mass index (BMI) differences were found between the groups (P > 0.05). Women with severe PE were found to have a significant difference in FVL (16%; P value = 0.0058; OR: 20.20; 95%CI: 1.132-360.5) and FII G20210A (14%; P value = 0.0125; OR: 17.41; 95%CI: 0.9659-314.0) in comparison to the women in the control group (0%). CONCLUSION: Our findings intensely indicate that there is a statistically proven significant association between FVL, FII G20210A mutations and the development of severe preeclampsia in Sudanese pregnant women.


Subject(s)
Activated Protein C Resistance/genetics , Factor V/genetics , Pre-Eclampsia/genetics , Pregnancy Complications, Hematologic/genetics , Prothrombin/genetics , Activated Protein C Resistance/epidemiology , Adult , Body Mass Index , Case-Control Studies , Comorbidity , Disease Progression , Female , Gestational Age , Hemoglobins/analysis , Humans , Parity , Point Mutation , Pre-Eclampsia/epidemiology , Pregnancy , Pregnancy Complications, Hematologic/epidemiology , Promoter Regions, Genetic/genetics , Sudan/epidemiology
4.
Environ Sci Pollut Res Int ; 26(15): 14823-14834, 2019 May.
Article in English | MEDLINE | ID: mdl-30499087

ABSTRACT

The objective of this study is to assess the environmental sustainability of a large water treatment plant through life cycle assessment (LCA) approach. This study is a pioneering one that explores the environmental impacts of a water treatment plant in Turkey by using the data collected from an actual plant. Decision makers of the treatment plant under investigation, operators of similar installations, and the scientific researchers that work on LCA of water treatment facilities are defined as the target audience. GaBi software is used for the LCA model, and CML 2001 method is adopted to calculate the results given per 1 m3 water ready to be distributed to the city. The plant serves about 2,600,000 people generating a maximum potable water flow rate of 400,000 m3/day. In the facility, 0.57 kWh of electricity is required to obtain 1 m3 of water. Of this total electricity consumption, 85% is allocated to inlet and outlet pumping stations. The results denote that the environmental impacts are dominated by electricity consumption that in turn depends on the energy source/s adopted. Sensitivity analysis on energy sources reveals the following outcomes: In case of using hard coal as energy source rather than grid mix, impacts are increased apart from freshwater aquatic ecotoxicity potential, ozone layer depletion potential, and abiotic depletion potential elements. Once solar panels are used instead of grid mix, values for all impact categories except abiotic depletion potential elements and human toxicity potential are lowered. The usage of wind turbines in place of grid mix results in 29 to 84% reductions in all investigated impact categories. The best option to decrease the environmental impacts is attained when energy is generated using wind turbines. As pumps having 90% efficiency replace the pumps with 60% efficiency, reductions ranging from 15 to 24% on all impact categories are obtained. The work performed for this study should be further pursued to obtain more representative inventory data for countries with scarce LCA studies.


Subject(s)
Environment , Water Purification/methods , Cities , Coal , Electricity , Fresh Water , Turkey , Water Purification/instrumentation
5.
Ann Clin Microbiol Antimicrob ; 16(1): 35, 2017 May 10.
Article in English | MEDLINE | ID: mdl-28486995

ABSTRACT

BACKGROUND: The objectives of this study were to characterize the diversity and magnitude of antimicrobial resistance among Staphylococcus species recovered from imported beef meat sold in the Egyptian market and the potential mechanisms underlying the antimicrobial resistance phenotypes including harboring of resistance genes (mecA, cfr, gyrA, gyrB, and grlA) and biofilm formation. RESULTS: The resistance gene mecA was detected in 50% of methicillin-resistant non-Staphylococcus aureus isolates (4/8). Interestingly, our results showed that: (i) resistance genes mecA, gyrA, gyrB, grlA, and cfr were absent in Staphylococcus hominis and Staphylococcus hemolyticus isolates, although S. hominis was phenotypically resistant to methicillin (MR-non-S. aureus) while S. hemolyticus was resistant to vancomycin only; (ii) S. aureus isolates did not carry the mecA gene (100%) and were phenotypically characterized as methicillin- susceptible S. aureus (MSS); and (iii) the resistance gene mecA was present in one isolate (1/3) of Staphylococcus lugdunensis that was phenotypically characterized as methicillin-susceptible non-S. aureus (MSNSA). CONCLUSIONS: Our findings highlight the potential risk for consumers, in the absence of actionable risk management information systems, of imported foods and advice a strict implementation of international standards by different venues such as CODEX to avoid the increase in prevalence of coagulase positive and coagulase negative Staphylococcus isolates and their antibiotic resistance genes in imported beef meat at the Egyptian market.


Subject(s)
Anti-Bacterial Agents/pharmacology , Coagulase/metabolism , Drug Resistance, Bacterial/genetics , Red Meat/microbiology , Staphylococcus aureus/drug effects , Staphylococcus aureus/genetics , Virulence/genetics , Animals , Bacterial Proteins/genetics , Biofilms/growth & development , Cattle , Chlorocebus aethiops , DNA Gyrase/genetics , Egypt , Food Microbiology , Genes, Bacterial/genetics , Hemolysin Proteins/metabolism , Methicillin/pharmacology , Methicillin Resistance/drug effects , Methicillin Resistance/genetics , Microbial Sensitivity Tests , Penicillin-Binding Proteins/genetics , Phenotype , RNA, Ribosomal, 16S/genetics , Staphylococcal Infections/microbiology , Staphylococcus/classification , Staphylococcus/drug effects , Staphylococcus/genetics , Staphylococcus/isolation & purification , Staphylococcus aureus/enzymology , Staphylococcus aureus/isolation & purification , Staphylococcus haemolyticus/drug effects , Staphylococcus haemolyticus/genetics , Staphylococcus haemolyticus/isolation & purification , Staphylococcus lugdunensis/drug effects , Staphylococcus lugdunensis/genetics , Staphylococcus lugdunensis/isolation & purification , Vancomycin/pharmacology , Vero Cells/microbiology
6.
APMIS ; 125(5): 499-505, 2017 May.
Article in English | MEDLINE | ID: mdl-28295668

ABSTRACT

This study was designed to investigate the prevalence of metallo-ß-lactamase (MBL) in Pseudomonas aeruginosa isolates collected from Suez Canal University Hospital in Ismailia, Egypt. Antibiotic susceptibility testing and phenotypic and genotypic screening for MBLs were performed on 147 isolates of P. aeruginosa. MICs were determined by agar dilution method for carbapenem that was ≥2 µg/mL for meropenem. MBL genes were detected by multiplex and monoplex PCR for P. aeruginosa-harbored plasmids. Mutation profile of sequenced MBL genes was screened using online software Clustal Omega. Out of 147 P. aeruginosa, 39 (26.5%) were carbapenem-resistant isolates and 25 (64%) were confirmed to be positive for MBLs. The susceptibility rate of P. aeruginosa toward polymyxin B and norfloxacin was 99% and 88%, respectively. Identification of collected isolates by API analysis and constructed phylogenetic tree of 16S rRNA showed that the isolates were related to P. aeruginosa species. The frequency of blaGIM-1, blaSIM-1, and blaSPM-1 was 52%, 48%, and 24%, respectively. BlaVIM and blaIMP-like genes were 20% and 4% and the sequences confirm the isolate to be blaVIM-1, blaVIM-2, blaVIM-4, and blaIMP-1. Three mutations were identified in blaVIM-4 gene. Our study emphasizes the high occurrence of multidrug-resistant P. aeruginosa-producing MBL enzymes.


Subject(s)
Pseudomonas Infections/epidemiology , Pseudomonas aeruginosa/enzymology , Pseudomonas aeruginosa/genetics , beta-Lactamases/analysis , beta-Lactamases/genetics , Anti-Bacterial Agents/pharmacology , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Egypt/epidemiology , Hospitals, University , Humans , Microbial Sensitivity Tests , Mutation , Plasmids/analysis , Polymerase Chain Reaction , Pseudomonas Infections/microbiology , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
7.
Jundishapur J Microbiol ; 9(11): e30257, 2016 Nov.
Article in English | MEDLINE | ID: mdl-28138370

ABSTRACT

BACKGROUND: Resistant Pseudomonas aeruginosa is a serious concern for antimicrobial therapy, as the common isolates exhibit variable grades of resistance, involving beta-lactamase enzymes, beside native defense mechanisms. OBJECTIVES: The present study was designed to determine the occurrence of Metallo-ß- Lactamases (MBL) and Amp C harboring P. aeruginosa isolates from Suez Canal university hospital in Ismailia, Egypt. METHODS: A total of 147 P. aeruginosa isolates, recovered from 311 patients during a 10-month period, were collected between May 2013 and February 2014; the isolates were collected from urine, wound and sputum. Minimum inhibitory concentration (MIC) determined by agar dilution methods was ≥2 µg/mL for meropenem and imipenem. Identification of P. aeruginosa was confirmed using API 20NE. Metallo-ß- Lactamases and Amp C were detected based on different phenotypic methods. RESULTS: Overall, 26.5% of P. aeruginosa isolates (39/147) were carbapenem resistant isolates. Furthermore, 64.1% (25/39) were MBL producers, these isolates were screened by the combined disc and disc diffusion methods to determine the ability of MBL production. Both MBL and Amp C harbored P. aeruginosa isolates were 28% (7/25). Sixty-four percent of P. aeruginosa isolates were multidrug resistant (MDR) (16/25). The sensitivity toward polymyxin, imipenem, norfloxacin, piperacillin-tazobactam and gentamicin was 99%, 91%, 88%, 82% and 78%, respectively. The resistance rate towards cefotaxime, ceftazidime, cefepime, aztreonam and meropenem was 98.6%, 86%, 71.4%, 34% and 30%, respectively. CONCLUSIONS: Multidrug resistance was significantly associated with MBL production in P. aeruginosa. Early detection of MBL-producing P. aeruginosa and hospital antibiotic policy prescription helps proper antimicrobial therapy and avoidance of dissemination of these multidrug resistance isolates.

8.
Mutagenesis ; 28(2): 233-9, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23408845

ABSTRACT

AZD9708 is a new chemical entity with selective and long-acting ß2-agonistic properties currently being evaluated by AstraZeneca for potential use in treatment of respiratory diseases by the inhaled route. As part of the toxicological characterisation of this compound, an increased incidence of micronucleated immature erythrocytes (MIEs) was seen in the bone marrow of rats following single intravenous doses near the maximum tolerated. This effect was seen in the absence of in vitro genotoxicity in bacterial and mammalian cells and no consistent evidence of in vivo DNA damage in the the bone marrow or liver using the comet assay was observed. Because of the lack of signals for mutagenic potential, combined with the observation that MIE frequencies appeared to be increased in only some of the rats and the clearest response was seen at the intermediate dose, it was hypothesised that the effect was secondary to ß2-adrenergic receptor overstimulation. Because it appears that this has not been previously described for ß2-agonists and because pharmacodynamic/pharmacokinetic factors may influence the response, studies using repeated dosing were performed to investigate whether this would lead to compound-induced tachyphylaxis with tolerance induction and decreased responses indicated by ß2-effect biomarkers. A series of experiments confirmed that a sequence of five escalating daily doses leading to systemic exposure corresponding to that after a single dose led to symptomatic tolerance, declining or diminished effects on plasma biomarkers of ß2-effects (plasma glucose and potassium) and elimination of the micronucleus response. This suggests that the increased MIE frequencies after single doses of AZD9708 are secondary to physiological overstimulation of ß2-adrenergic receptors, not a consequence of genotoxicity.


Subject(s)
Adrenergic beta-2 Receptor Agonists/pharmacology , Benzothiazoles/pharmacology , Bone Marrow/drug effects , Micronucleus Tests/methods , beta-Alanine/analogs & derivatives , Animals , Blood Glucose/analysis , Blood Glucose/drug effects , Comet Assay , DNA Damage/drug effects , Dose-Response Relationship, Drug , Erythrocytes/drug effects , Liver/drug effects , Male , Mutagens/toxicity , Potassium/blood , Rats , Rats, Wistar , Receptors, Adrenergic/metabolism , beta-Alanine/pharmacology
9.
Angiology ; 61(3): 304-13, 2010 Apr.
Article in English | MEDLINE | ID: mdl-19689996

ABSTRACT

A total of 30 patients with chronic hepatitis C (HCV) thrombocytopenia (TP) and 20 healthy controls were studied. Both groups were subjected to complete medical history, clinical examination in addition to assessment of hepatitis markers: level of thrombopoietin (Tpo), Geimsa-stained bone marrow smears, and in vitro short-term megakaryocytic progenitors culture (CFU-MK). Serum Tpo level was significantly elevated in patients with TP HCV. Short-term CFU-MK showed an evident depression in the colony-forming unit-megakaryocyte (CFU-meg). There is a positive correlation between the number of CFU-meg and the platelet count and between serum Tpo level and prothrombin time, transaminase, albumin, and the Child Pugh score of liver disease; a negative correlation between serum Tpo level and the number of CFU-meg and between serum Tpo level and the platelet count. Thus, the level of Tpo could be an indicator of intact functional response of the hepatocytes.


Subject(s)
Blood Platelets/physiology , Hepacivirus/physiology , Hepatitis C, Chronic/complications , Stem Cells/physiology , Thrombocytopenia/virology , Colony-Forming Units Assay , Hepatitis C, Chronic/blood , Humans , Megakaryocytes/physiology , Platelet Count , Prothrombin Time , Thrombocytopenia/blood , Thrombocytopenia/complications , Thrombopoietin/blood
10.
J Cardiovasc Dis Res ; 1(4): 177-80, 2010 Oct.
Article in English | MEDLINE | ID: mdl-21264181

ABSTRACT

BACKGROUND AND AIM: Rheumatic fever is still a common cause of acquired heart disease in children and young adult in many developing countries. The aim was to investigate the role of myocardial involvement in the hemodynamic changes in patients with acute rheumatic fever using cardiac troponin assay and echocardiography. DESIGN: A prospective cohort study was designed. PATIENTS AND METHODS: Thirty-four children with acute rheumatic fever, 20 with carditis, and 14 without carditis. Level of cardiac troponin T (cTnT) and echocardiographic measurement of left ventricular function were the main outcome measure. RESULTS: The level of cardiac troponin in children with carditis was 0.051 ± 0.01 ng/dL, and it was 0.039 ± 0.02 ng/dL in those without carditis. The difference is not significant. In addition, there was no significant difference between the children with carditis and those without carditis regarding left ventricular ejection and shortening fractions. CONCLUSION: There are no significant echocardiographic measurements abnormalities or cTnT levels elevation suggesting clinically relevant hemodynamic abnormalities due to myocardial involvement during acute rheumatic fever.

11.
Biochem Biophys Res Commun ; 349(2): 825-32, 2006 Oct 20.
Article in English | MEDLINE | ID: mdl-16945327

ABSTRACT

Using the mouse as a model organism in pharmaceutical research presents unique advantages as its physiology in many ways resembles the human physiology, it also has a relatively short generation time, low breeding and maintenance costs, and is available in a wide variety of inbred strains. The ability to genetically modify mouse embryonic stem cells to generate mouse models that better mimic human disease is another advantage. In the present study, a comprehensive phenotypic screening protocol is applied to elucidate the phenotype of a novel mouse knockout model of hepatocyte nuclear factor (HNF) 4-gamma. HNF4-gamma is expressed in the kidneys, gut, pancreas, and testis. The first level of the screen is aimed at general health, morphologic appearance, normal cage behaviour, and gross neurological functions. The second level of the screen looks at metabolic characteristics and lung function. The third level of the screen investigates behaviour more in-depth and the fourth level consists of a thorough pathological characterisation, blood chemistry, haematology, and bone marrow analysis. When compared with littermate wild-type mice (HNF4-gamma(+/+)), the HNF4-gamma knockout (HNF4-gamma(-/-)) mice had lowered energy expenditure and locomotor activity during night time that resulted in a higher body weight despite having reduced intake of food and water. HNF4-gamma(-/-) mice were less inclined to build nest and were found to spend more time in a passive state during the forced swim test.


Subject(s)
Hepatocyte Nuclear Factor 4/genetics , Hepatocyte Nuclear Factor 4/metabolism , Animals , Behavior, Animal , Body Weight , Bone Marrow/metabolism , Calorimetry , Female , Hepatocyte Nuclear Factor 4/chemistry , Heterozygote , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Models, Genetic , Oxygen Consumption , Phenotype
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