期刊论文详细信息
BMC Microbiology
A novel, nested, multiplex, real-time PCR for detection of bacteria and fungi in blood
Małgorzata Bulanda1  Monika Brzychczy-Włoch2  Agnieszka Sroka2  Danuta Jurkiewicz-Badacz3  Tomasz Gosiewski2 
[1] Department Epidemiology of Infection, Chair of Microbiology Jagiellonian University Medical College, Czysta 18 Str, 31-121 Kraków, Poland;Department of Bacteriology, Microbial Ecology and Parasitology, Chair of Microbiology Jagiellonian University Medical College, Czysta 18 Str, 31-121 Kraków, Poland;The John Paul II Hospital in Krakow, Pradnicka 80 Str, 31-202 Kraków, Poland
关键词: Gram differentiation;    Fungi;    Bacteria;    Sepsis;    Multiplex PCR;    Nested PCR;   
Others  :  1140988
DOI  :  10.1186/1471-2180-14-144
 received in 2014-03-02, accepted in 2014-05-28,  发布年份 2014
PDF
【 摘 要 】

Background

The study describes the application of the PCR method for the simultaneous detection of DNA of Gram-negative bacteria, Gram-positive bacteria, yeast fungi and filamentous fungi in blood and, thus, a whole range of microbial etiological agents that may cause sepsis. Material for the study was sterile blood inoculated with four species of microorganisms (Escherichia coli, Staphylococcus aureus, Candida albicans and Aspergillus fumigatus) and blood collected from patients with clinical symptoms of sepsis. The developed method is based on nested-multiplex real-time PCR .

Results

Analysis of the obtained data shows that sensitivity of nested-multiplex real-time PCR remained at the level of 101 CFU/ml for each of the four studied species of microorganisms and the percentage of positive results of the examined blood samples from the patients was 70% and 19% for the microbiological culture method. The designed primers correctly typed the studied species as belonging to the groups of Gram-positive bacteria, Gram-negative bacteria, yeast fungi, or filamentous fungi.

Conclusions

Results obtained by us indicated that the designed PCR methods: (1) allow to detect bacteria in whole blood samples, (2) are much more sensitive than culture method, (3) allow differentiation of the main groups of microorganisms within a few hours.

【 授权许可】

   
2014 Gosiewski et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150325173544886.pdf 217KB PDF download
【 参考文献 】
  • [1]Jamal W, Tamaray G, Pazhoor A, Rotimi VO: Comparative evaluation of BacT/ALERT 3D and BACTEC systems for the recovery of pathogens causing bloodstream infections. Med Princ Pract 2006, 15:223-227.
  • [2]Zieliński A, Czarkowski MP: Infectious diseases in Poland in 2007. Przegl Epidemiol 2009, 63:161-167.
  • [3]Klouche M, Schroder U: Rapid methods for diagnosis of bloodstream infections. Clin Chem Lab Med 2008, 46:888-908.
  • [4]Gosiewski T, Szała L, Pietrzyk A, Brzychczy-Włoch M, Heczko PB, Bulanda M: Comparison of methods for isolation of bacterial and fungal DNA from human blood. Curr Microbiol 2014, 68:149-155.
  • [5]Gosiewski T, Brzychczy-Włoch M, Pietrzyk A, Sroka A, Bulanda M: Evaluation the activity of the thermostable DNA polymerases in the presence of heme as a key inhibitor in the real time PCR method in diagnostics of sepsis. Acta Biochim Pol 2013, 60:603-606.
  • [6]Opel KL, Chung D, McCord BR: A Study of PCR Inhibition Mechanisms Using Real Time PCR. J Forensic Sci 2010, 55:25-33.
  • [7]Schrader C, Schielke A, Ellerbroek L, Johne R: PCR inhibitors - occurrence, properties and removal. J Appl Microbiol 2012, 113:1014-1026.
  • [8]Mauro MV, Cavalcanti P, Perugini D, Noto A, Sperli D, Giraldi C: Diagnostic utility of LightCycler SeptiFast and procalcitonin assays in the diagnosis of bloodstream infection in immunocompromised patients. Diagn Microbiol Infect Dis 2012, 73:308-311.
  • [9]Wellinghausen N, Kochem AJ, Disque C, Muhl H, Gebert S, Winter J, Matten J, Sakka SG: Diagnosis of Bacteremia in Whole-Blood Samples by Use of a Commercial Universal 16S rRNA Gene-Based PCR and Sequence Analysis. J Clin Microbiol 2009, 47:2759-2765.
  • [10]Bispo P, de Melo G, Hofling-Lima A, Pignatari A: Detection and Gram Discrimination of Bacterial Pathogens from Aqueous and Vitreous Humor Using Real-Time PCR Assays. Invest Ophthalmol Vis Sci 2011, 52:873-881.
  • [11]Sugita S, Kamoi K, Ogawa M, Watanabe K, Shimizu N, Mochizuki M: Detection of Candida and Aspergillus species DNA using broad-range real-time PCR for fungal endophthalmitis. Graefes Arch Clin Exp Ophthalmol 2012, 250:391-398.
  • [12]Westh H, Lisby G, Breysse F, Boeddinghaus B, Chomarat M, Gant V, Goglio A, Raglio A, Schuster H: Multiplex real-time PCR and blood culture for identification of bloodstream pathogens in patients with suspected sepsis. Clin Microbiol Infect 2009, 15:544-551.
  • [13]Mancini N, Carletti S, Ghidoli N, Cichero P, Ossi C, Ieri R, Poli E, Burioni R, Clementi M: Molecular Diagnosis of Polymicrobial Sepsis. J Clin Microbiol 2009, 47:1274-1275.
  • [14]Chang S, Hsieh W, Liu T, Lee S, Wang C, Chou H, Yeo Y, Tseng C, Lee C: Multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis - a systemic review and meta-analysis. Plos One 2013., 8doi: 10.1371/journal.pone.0062323
  • [15]Previsdomini M, Gini M, Cerutti B, Dolina M, Perren A: Predictors of positive blood cultures in critically ill patients: a retrospective evaluation. Croat Med J 2012, 53:30-39.
  • [16]Valle DL, Andrade JI, Cabrera EC, Rivera WL: Evaluation of buffy coat 16S rRNA PCR, buffy coat culture and whole blood PCR for detection of bacteraemia. Mem Inst Oswaldo Cruz 2010, 105:117-122.
  文献评价指标  
  下载次数:11次 浏览次数:14次