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Rapid Diagnosis of Acute Respiratory Infections by Multiplex Endpoint PCR Technology
Current Issue
Volume 1, 2014
Issue 5 (December)
Pages: 41-45   |   Vol. 1, No. 5, December 2014   |   Follow on         
Paper in PDF Downloads: 45   Since Aug. 28, 2015 Views: 2205   Since Aug. 28, 2015
Authors
[1]
Aurelian Udristioiu, Clinical Laboratory Department, Emergency County Hospital Targu Jiu & UCB University, City Targu Jiu, Romania.
[2]
Manole Cojocaru, Physiology Department, Faculty of Medicine, Titu Maiorescu University, City Bucharest, Romania.
[3]
Dana Alexandra Maria Panait, Microbiology Department, Faculty of Medicine, Titu Maiorescu University, City Bucharest, Romania.
[4]
Nica Badea Delia, Biochemistry Department, Faculty of Medical Science, Behavioral Constantin Brancusi University, City Targu Jiu, Romania.
Abstract
Introduction: The multiplex endpoint PCR technology offers a number of potential advantages, results are available in a matter of hours rather than days, the extreme sensibility facilitates detection of even minutes the amounts of pathogen DNA in clinical samples and the test is not significantly affected by prior administration of antibiotics. Aim: The aim of this work was to rapidly identify the antibiotic resistance the monitoring of pathogen growth at the patients admitted in Hospitalization Intensive Care Unit of Emergency County Hospital Targu Jiu with the diagnosis of Community Acquired Pneumonia, (CAP), in months December/2013-March/2014. Method: The Analyzer Unyvero™ Pneumonia Application was used in detection of pneumonia associated pathogens and their antibiotic resistance genes using the Pneumonia Unyvero™ System, following PCR pathogen species with sequencing of the amplified microbial DNA. Results: The main pathogens of community acquired pneumonia from the cohort study, 36 cases, (20 males in mean age 35-66 years and 16 females in mean age 40-55 mean years) were Streptococcus pneumonia (16 cases), Staphilococcus aureus, (10 cases), Klebsiella pneumonia (5 cases), and other important agents were “atypical”, such as Haemophilus Influenzae, Chlamidophila pneumonie and Moraxela cataralis. A case with Acinetobacter baumani and Proteus Sp. was also widely resistance to mefA gene / ermB gene as all cases of analyzed. The more frequency of genes resistant (29 cases) are ermA gene / ermC / ermB for Staphilococcus aureus and the gene tem+shv / gene / ctx-M with the Chromosomal mutation (7 cases), as gyrA83_87 Ecoli / Pseu for Klebsiella pneumonia agents. Also most resistance antibiotics were Makrolides, (29 cases and Lincosamides (6 cases) and this cases have had the chromosomial integrates. The most resistance microbe, Pseudomonas aeruginosa(1 case), has been registered as multi drugs resistance [MDR]*. Conclusion: The Unyvero™ results have been available 2 days before the primary microbiology report and 3 days before the final confirmation results, obtained by microbiology culture. The Unyvero Analyzer only provides rapid data to support the therapeutic decision of currant medic.
Keywords
Antibiotic Resistance, PCR, Gene, DNA, Resistance Markers, Microbiology Report
Reference
[1]
Caliendo AM. Multiplex PCR and emerging technologies for the detection of respiratory pathogen. Clin Infect 2011; (4):5326-5330.
[2]
Rulls© Curetis AG, 2013 Unyvero ™ P50 Pneumonia Application Guide 00118 V2.0, Hamburg, Germany, 2013, http://www.curetis.com/
[3]
Kugelberg, E, Löfmark S, Wretlind B, Andersson ID. Reduction of the fitness burden of quinolone resistance in Pseudomonas aeruginosa. J. Antimicrob. Chemother 2005; 55 (1): 22-30.
[4]
Gerzova L, Videnska P, Faldynova M, Sedlar K et al. Characterization of Microbiota Composition and Presence of Selected Antibiotic Resistance Genes in Carriage Water of Ornamental Fish. PLOS ONE Journal Information 2014; 9(8): e103865
[5]
M. van Hoek AHA, Mevius D, Guerra B, Mullany P et al. Acquired Antibiotic Resistance Genes: An Overview. Front Microbiol 2011; 2: 203.
[6]
Davies J, Davies D. Origins and Evolution of Antibiotic Resistance. Microbiol Mol Biol Rev. Sep 2010; 74(3): 417–433.
[7]
Wright G. D. Bacterial resistance to antibiotics: enzymatic degradation and modification. Adv Drug Deliv Rev 2005; 57, 1451–1470.
[8]
Roberts M.C. Update on macrolide-lincosamide, treptogramin, ketolide,and oxazolidinone resistance genes, -ermA, ermB, ermC Makrolides / Lincosamides, gyrA83 of E. coli . FEMS Microbiol. Lett 2008; 282: 147–159.
[9]
Jacoby AG. AmpC β-Lactamases. Clin Microbiol Rev. Jan 2009; 22(1): 161–182.
[10]
Bonnet R, Dutour C, Sampaio MLJ, Chanal C et al. Novel Cefotaximase (CTX-M-16) with Increased Catalytic Efficiency Due to Substitution Asp-240®Gly. Antimicrob Agents Chemother 2001; 45(8):2269.
[11]
Breurec S, Guessennd N, Timinouni M, Le TAH. Klebsiella pneumoniae resistant to third-generation cephalosporins in five African and two Vietnamese major towns: multiclonal population structure with two major international clonal groups, CG15 and CG258. Clinical Microbiology and Infection 2013; 19(4): 349–355.
[12]
Oliviera JE, Silva CA, Oliviera GM, Zaneta DM et al. Antimicrob Agents Chemoter 2009; 53(7): 2887-289.
[13]
Livermore MD. Pneumonia-causing pathogens and their resistance. Curetis Symposium, ECCMID, 01/04/2014, London, UK.
[14]
Radu Popescu AM, Dumitriu S, Simona ES, Bancescu G, Udristioiu A, Cojocaru M, Vagu C. Phenotypic and Genotipc Caracterisation of Antibiotics. Farmacia 2010; (57); 3: 420-427
[15]
Radu Popescu AM, Dumitriu S, Simona ES, Bancescu G, Udristioiu A, Cojocaru M, Vagu C Resistance Patterns in Acinetobacter baumani Strains isolated in a Romanian Hospital. Farmacia 2010; (58); 4: 422-429
[16]
David A. Relman. Actionable Sequence Data on Infectious Diseases in the Clinical Workplace. Clin Chem 2014; 61:38-40.
[17]
Gavin R. Oliver, Steven N. Hart, and Eric W. Klee. Bioinformatics for Clinical Next Generation Sequencing. Clin Chem 2014; 61:124-135.
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