scholarly journals Антимікробна активність нового хіміотерапевтичного препарату на основі флюмеквіну щодо Aeromonas Hydrophila

2017 ◽  
Vol 19 (82) ◽  
pp. 66-70
Author(s):  
H. Solopova ◽  
O. Vishchur ◽  
T.I. Stetsko ◽  
G.P. Ugrin ◽  
O.I. Hom’jak
Keyword(s):  
Antimicrobial Activity ◽  
Active Substance ◽  
Aeromonas Hydrophila ◽  
Clinical Signs ◽  
High Sensitivity ◽  
Minimum Inhibitory Concentrations ◽  
Pure Cultures ◽  
Meat Peptone Agar ◽  
Pathological Material ◽  
Peptone Broth

In the article presented results of study of the antimicrobial activity of the chemotherapeutic drug on the basis of the active substance – flumequine.The sensitivity of the microflora of the biomaterial to antibiotics was determined and the minimum inhibitory concentrations of flumequin, the active substance of the drug «Flyumek», were determined.For the study were selected 5 fish – carps affected by aeromonosis. The diagnosis for aeromonosis was based on epizootological data, clinical signs of the disease, pathological and anatomical changes and the results of bacteriological research. The fish were slaughtered and crops were made from the affected parts of the skin, liver and kidneys. Sowing was carried out on meat-peptone broth (MPB) and meat-peptone agar (MPA). The seeds were incubated in a thermostat at a temperature of 26 °C for 48 hours. The sensitivity of the microflora of the biomaterial to antibiotics was determined by agar diffusion using standard antibiotic disks and the Müller-Hinton medium. In order to isolate and identify the Aeromonas hydrophila bacterium, the primary culture of the pathological material was performed on the MPA, which was incubated in the thermostat at 26 °C for 24 hours. The next step was to isolate pure cultures of microorganisms and make smears that were stained with Gram in the Björk modification. The method of serial dilutions in a liquid nutrient medium was determined by the minimum inhibitory concentrations (MICs) of flumequine in the preparation of «Flyumek» for Aeromonas hydrophila isolates.The results of the test for the sensitivity of the microflora of the biomaterial from the patient to the aeromonosis of the fish showed high sensitivity of the microorganisms to flumequin, tetracycline, fluorophenicol and trimethoprim, moderate neomycin sensitivity and resistance to amoxicilline, tylosine, lincomycine and colistine. The diameter of the growth retardation zone around the disks with flumequin was – 23,2 mm in the crop sown from the skin, from the kidneys – 30,0 mm, from the liver – 30,4 mm.According to the obtained values of the minimum inhibitory concentrations of flumequine, all investigated isolates of Aeromonas hydrophila were sensitive to the drug «Flyumek» and amounted to 1.0–2.0 μg ml.The results of the conducted studies indicate that fluoroquinolone antibiotic flumequin has a high antimicrobial activity against the bacterium Aeromonas hydrophila, an aeromonosis agent of carp fish. 

ANTIMICROBIAL ACTIVITIES OF METHANOL EXTRACT FROM UNIDENTIFIED SPONGE ASSOCIATED BACTERIA IN LEMUKUTAN ISLAND, KALIMANTAN BARAT

2009 ◽  
Vol 1 (2) ◽  
Author(s):  
Risa Nofiani ◽  
Siti Nurbetty ◽  
Ajuk Sapar
Keyword(s):  
Antimicrobial Activity ◽  
Bacillus Subtilis ◽  
Pathogenic Bacteria ◽  
Methanol Extract ◽  
Agar Medium ◽  
Antimicrobial Activities ◽  
Antimicrobial Compounds ◽  
Associated Bacteria ◽  
Minimum Inhibitory Concentrations ◽  
Sponge Associated Bacteria

<p>The increase of issues on the antibiotics resistant pathogenic bacteria has triggered high exploration for new antimicrobial compounds. One of the potential sources is sponge-associated bacteria. The aim of this study was to get sponge-associated bacteria extract containing antimicrobial activities. On the basis screening of antimicrobial activity using by streaking on agar medium, there were two potential isolates with antimicrobial activities namely LCS1 and LCS2. The two isolates were cultivated,then secondary metabolite product were extracted using methanol as a solvent. Minimum inhibitory concentrations (MICs) of extract LCS 1 were 1,000 μg/well for S. aureus, 950 μg/well for Salmonella sp.and 800 μg/well for Bacillus subtilis. Minimum inhibitory concentrations of extract LCS 2 were 500 μg/well for S. aureus, 1,050 μg/well for Salmonella sp., 750 μg/well for Bacillus subtilis, 350 μg/well for P. aeruginosa, 750 μg/sumur terhadap B. subtilis. Based on the MIC values, the two assay extracts have a relatively low antimicrobial activity.</p> <p>Keywords:Antimicrobial,Sponges associated bacteria,MICs</p>

Markers of the early stage of rheumatoid arthritis

2016 ◽  
Vol 51 (4) ◽  
pp. 305-314
Author(s):  
Beata Polińska ◽  
Joanna Matowicka-Karna ◽  
Halina Kemona
Keyword(s):  
Rheumatoid Arthritis ◽  
Human Population ◽  
Early Stage ◽  
Clinical Signs ◽  
High Sensitivity ◽  
Unknown Etiology ◽  
Serological Tests ◽  
Citrullinated Peptide ◽  
Peptide Antibodies

Rheumatoid arthritis (RA) is a chronic, autoimmune connective tissue disease of unknown etiology. RA affects about 1% of the human population, women suffer three times more often than men, with the peak incidence between the age of 40 to 50. The up-to-date criteria from 2010 for the diagnosis of RA include: occurrence and duration of clinical signs, indicators of inflammation and serological tests. Neopterin, a protein released by macrophages, is a sensitive indicator of inflammation and the severity of RA. Regarding the serological tests, anti-cyclic citrullinated peptide antibodies represent a well-known marker with the specificity for RA of about 98%. The antibodies may be present in the serum of patients even a few years before the first clinical signs of the disease, heralding erosive changes in the joints and more severe course of RA. The literature also contains reports about autoantibodies anti-CarP and anti-Sa/ anti-MCV, which may occur in people with pain and swelling of joints and precede full-blown development of RA as well as reflect disease activity. Serological diagnosis of RA may be supported by some genetic tests based on PCR for detecting mutations e.g. C1858T in the PNPN22 gene. In turn, the quantitative analysis of different classes of miRNAs seems justified in order to better classify patients showing symptoms of RA. Further studies are needed that take into account the role of different markers in the development of RA, and confirm the high sensitivity and specificity of these markers in the diagnosis of the disease.

scholarly journals Coherent fluctuation nephelometry in clinical microbiology

2019 ◽  
Vol 9 (2) ◽  
pp. 385-392
Author(s):  
A. S. Gur’ev ◽  
O. Yu. Shalatova ◽  
E. V. Rusanova ◽  
I. V. Vasilenko ◽  
A. Yu. Volkov
Keyword(s):  
Antibiotic Susceptibility ◽  
Clinical Microbiology ◽  
Urine Analysis ◽  
Growth Curves ◽  
High Sensitivity ◽  
Pure Cultures ◽  
Susceptibility Tests ◽  
Express Methods ◽  
Coherent Fluctuation

In this article data concerning coherent fluctuation nephelometry (CFN) use in clinical microbiology is presented. CFN-analyzer allows to solve two important problems – fast urine screening for bacteriuria within 2-4 hours and antibiotic susceptibility testing within 3-6 hours. Altogether more than 650 urine samples were tested, and the effectivity of CFN-analyzer for preliminary selection of samples for further analysis was shown. Method allows to detect negative samples, reducing the number of urine analyses by 70-80%. Simultaneous analysis of growth curves and concentration of microorganisms shows high sensitivity and specificity (95.2% и 96.9%). Also more than 250 antibiotic susceptibility tests were performed using CFN-analyzer to show its effectiveness for determination of resistant properties of both pure cultures and urine microflora without isolation of bacteria. The agreement with traditional methods was from 84% to 88%. The use of CFN-analyzer with express methods of identification of microorganisms (chromogenic nutrient broths or mass-spectrometry) allows to make full urine analysis within 1-2 days. In the future CFN-analyzer gives an opportunity to screen different human biological liquids, and finds an application for other microbiological tasks, including standardization and speeding-up in sanitary bacteriology.

scholarly journals Investigation of the Antimicrobial Activity and Hematological Pattern of Nano-Chitosan and its Developed Nano-Copper Composite

2021 ◽  
Author(s):  
Somia Ahmed ◽  
Hadeer Mohamed ◽  
Abeer Al-Subaie ◽  
Ahoud Al-Ohali ◽  
Nesrine Mahmoud
Keyword(s):  
Antimicrobial Activity ◽  
High Sensitivity ◽  
Ionic Gelation ◽  
Clotting Time ◽  
Blood Samples ◽  
Gram Negative ◽  
Inhibition Concentration ◽  
Copper Composite ◽  
Biogenic Nanoparticles

Abstract Novel synthesized Chitosan-Copper oxide nanocomposite (Cs-CuO) was prepared using pomegranate peels extract as green precipitating agents to improve the biological activity of Cs-NP's which was synthesized through ionic gelation method. The characterization of biogenic nanoparticles Cs-NP's and Cs-CuO-NP's were investigated structurally, morphologically to determine the full descriptive features of those nanoparticles. Antimicrobial activity was tested for both Cs-NP's and Cs-CuO-NP's via Minimum inhibition concentration and zone analysis against fungus, gram positive and gram negative. The results of the antimicrobial test showed high sensitivity of Cs-CuO-NP's to all microorganisms that are tested in concentration less than 20 mg/ml while the sensitivity of Cs-NP's against all microorganisms under test started from a concentration of 20 mg/ml to 40 mg/ml except for the C.albicans species. Hematological activity was also tested in via measuring the RBCs, platelets count and clotting time against healthy, diabetic and hypercholesterolic blood samples. Measurement showed a decrease in RBCs and platelets count by adding Cs-NP’s or Cs-CuO-NP's to the three blood samples. Cs-NP’s success to decrease the clotting time for healthy and diabetic blood acting as a procoagulant agent, while adding biogenic CuO-NP’s to Cs-NP’s increased clotting time considering as an anticoagulant agent for hyperchloesterolic blood samples.

Synthesis and antimicrobial activity of 4-trifluoromethylpyridine nucleosides

2017 ◽  
Vol 23 (3) ◽  
pp. 197-203 ◽  
Author(s):  
Shaikha S. Alneyadi ◽  
Anas A. Abdulqader ◽  
Alaa A. Salem ◽  
Ibrahim M. Abdou
Keyword(s):  
Escherichia Coli ◽  
Staphylococcus Aureus ◽  
Antimicrobial Activity ◽  
Stenotrophomonas Maltophilia ◽  
Antibacterial Agents ◽  
Antibacterial Activities ◽  
Nucleoside Analogues ◽  
Reference Drug ◽  
Minimum Inhibitory Concentrations

Abstract4-Trifluoromethylpyridine derivatives 4–8 represent good candidates for the discovery of new antibacterial agents. Fluorinated pyridine nucleosides 4–7 and non-nucleoside analogues 8a,b were synthesized and evaluated for their antibacterial activities against Staphylococcus aureus, Bacillus infantis, Escherichia coli and Stenotrophomonas maltophilia. The minimum inhibitory concentrations (MICs) of the new nucleosides 4–7 range from 1.3 to 4.9 μg/mL and MICs of fluoroaryl derivatives 8a,b are in the range of 1.8–5.5 μg/mL. Activity of amoxicillin, the reference drug, is 1.0–2.0 μg/mL under similar conditions.

scholarly journals Synthesis, structural chemistry and antimicrobial activity of −(−) borneol derivative

2010 ◽  
Vol 8 (5) ◽  
pp. 1127-1133 ◽  
Author(s):  
Khalid Al-Farhan ◽  
Ismail Warad ◽  
Saud Al-Resayes ◽  
Moustafa Fouda ◽  
Mohamed Ghazzali
Keyword(s):  
Escherichia Coli ◽  
Antimicrobial Activity ◽  
Hydrogen Bonding ◽  
Reference Material ◽  
High Sensitivity ◽  
Structural Determinants ◽  
Single Crystal Diffraction ◽  
Methane Sulfonate ◽  
X Ray ◽  
Hirshfeld Surfaces

AbstractBorneol is a monoterpene that is a part of traditional Chinese and Japanese medicine. (−) borneol reacted with methanesulfonyl chloride in THF/pyridine to afford the new 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate derivative in excellent yield. The product is characterized by H1NMR, C13NMR, mass spectroscopy as well as elemental analysis and its structure was identified by X-ray single crystal diffraction. The packing of 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methanesulfonate exhibits the non-classical C-H···O hydrogen bonding in C(4) and R22(8) chain and ring motifs as structural determinants. This was also confirmed by the analysis of Hirshfeld surfaces. The 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate antimicrobial activity was tested and compared with its parent (−) borneol against three different pathogens. Particularly, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl methane sulfonate showed high sensitivity, compared to Chloramphenicol reference material, against Escherichia coli.

Antimicrobial Activity of Extracts of the Lichen Xanthoparmelia pokornyi and its Gyrophoric and Stenosporic Acid Constituents

2006 ◽  
Vol 61 (5-6) ◽  
pp. 319-323 ◽  
Author(s):  
Mehmet Candan ◽  
Meral Yılmaz ◽  
Turgay Tay ◽  
Merih Kıvança ◽  
Hayrettin Türk
Keyword(s):  
Staphylococcus Aureus ◽  
Antimicrobial Activity ◽  
Bacillus Subtilis ◽  
Candida Albicans ◽  
Aeromonas Hydrophila ◽  
Candida Glabrata ◽  
Proteus Vulgaris ◽  
Ethanol Extracts ◽  
Bacteria And Fungi ◽  
Gyrophoric Acid

The antimicrobial activity of the diethyl ether, acetone, chloroform, petroleum ether, and ethanol extracts of the lichen Xanthoparmelia pokornyi and its gyrophoric acid and stenosporic acid constituents has been screened against some foodborne bacteria and fungi. Both the extracts and the acids showed antimicrobial activity against Aeromonas hydrophila, Bacillus cereus, Bacillus subtilis, Listeria monocytogenes, Proteus vulgaris, Staphylococcus aureus, Streptococcus faecalis, Yersinia enterocolitica, Candida albicans and Candida glabrata. The extracts were inactive against the tested filamentous fungi. The MIC values of the extracts and the acids for the bacteria have also been determined.

scholarly journals Molecular Detection of Apiosporina morbosa, Causal Agent of Black Knot in Prunus virginiana

Plant Disease ◽  
2005 ◽  
Vol 89 (8) ◽  
pp. 815-821 ◽  
Author(s):  
J. X. Zhang ◽  
W. G. D. Fernando ◽  
W. R. Remphrey
Keyword(s):  
Pcr Amplification ◽  
High Sensitivity ◽  
Its Region ◽  
Fungal Species ◽  
Causal Agent ◽  
Diseased Plant ◽  
Pcr Assay ◽  
Single Spore ◽  
Prunus Virginiana ◽  
Pure Cultures

A specific and sensitive polymerase chain reaction (PCR) assay was developed to detect Apiosporina morbosa, the causal agent of black knot disease on chokecherry, Prunus virginiana (including the cultivar ‘Shubert Select’). A pair of A. morbosa-specific forward and reverse primers (AMF and AMR) was designed from the internal transcribed spacer (ITS) regions of A. morbosa, preamplified by universal ITS primers ITS1 and ITS4, and compared with the ITS region sequences of Fusarium, Alternaria, Phoma, and Cladosporium species associated with black knots. The primers were tested for their specificity to A. morbosa detection in the PCR assays using DNA derived from 64 pure cultures, including 42 single-spore isolates of A. morbosa and 22 isolates of other fungi, as well as healthy and diseased plant branches collected from the field. A product of ~400 bp was amplified from DNA of all isolates belonging to A. morbosa. No product was amplified from DNA of other fungal species, confirming the specificity of the newly designed primers. Within plant tissues, the pathogen was detected at further distances from the edges of knots on thicker branches bearing larger knots compared with thinner branches bearing smaller knots. The PCR assay has shown high sensitivity, needing only 100 fg of the A. morbosa DNA for a reliable PCR amplification with the AMF and AMR primers.

Evaluation of the Antimicrobial Activity of the Acetone Extract of the Lichen Ramalina farinacea and its (+)-Usnic Acid, Norstictic Acid, and Protocetraric Acid Constituents

2004 ◽  
Vol 59 (5-6) ◽  
pp. 384-388 ◽  
Author(s):  
Turgay Tay ◽  
Ayşen Özdemir Türk ◽  
Meral Yılmaz ◽  
Hayrettin Türk ◽  
Merih Kıvanç
Keyword(s):  
Staphylococcus Aureus ◽  
Antimicrobial Activity ◽  
Bacillus Subtilis ◽  
Candida Albicans ◽  
Yersinia Enterocolitica ◽  
Aeromonas Hydrophila ◽  
Candida Glabrata ◽  
Usnic Acid ◽  
Acetone Extract ◽  
Ramalina Farinacea

The acetone extract of the lichen Ramalina farinacea and its (+)-usnic acid constituent showed antimicrobial activity against Bacillus subtilis, Listeria monocytogenes, Proteus vul­garis, Staphylococcus aureus, Streptococcus faecalis. Yersinia enterocolitica, Candida albicans, and Candida glabrata. Norstictic acid was active against Aeromonas hydrophila as well as the above microorganisms except Yersinia enterocolitica. Protocetraric acid showed activity only against the tested yeasts Candida albicans and Candida glabrata. The MIC values of the extract as well as of the three substances were determined. No antifungal activity of the acetone extract has been observed against ten filamentous fungi.

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