Rapid screening by real-time 16S rDNA PCR for bacterial contamination of blood products / Schnelles Screening von Blutprodukten nach bakteriellen Kontaminationen mit real-time PCR von 16S rDNA

2006 ◽  
Vol 30 (6) ◽  
pp. 402-411
Author(s):  
Hendrik W. Reesink ◽  
Tamimount Mohammadi ◽  
Rubyn N.I. Pietersz ◽  
Paul H.M. Savelkoul
Author(s):  
Hendrik W. Reesink ◽  
Tamimount Mohammadi ◽  
Rubyn N.I. Pietersz ◽  
Paul H.M. Savelkoul

2019 ◽  
Vol 14 ◽  
Author(s):  
Martina Oriano ◽  
Leonardo Terranova ◽  
Antonio Teri ◽  
Samantha Sottotetti ◽  
Luca Ruggiero ◽  
...  

Background: The analysis of microbiome in respiratory samples is a topic of great interest in chronic respiratory diseases. The method used to prepare sputum samples for microbiome analysis is very heterogeneous. The selection of the most suitable methodology for DNA extraction is fundamental to have the most representative data. The objective of this study was to compare different conditions for DNA extraction from sputum in adult patients with bronchiectasis. Methods: Five sputum samples from bronchiectasis patients were collected at the Policlinico Hospital in Milan, Italy. Eighteen conditions for DNA extraction were compared, including two enzyme-based (Roche and Zymo) and one beads-based (Mobio) technique. These techniques were tested with/without Dithiothreitol (DTT) and with/without lysostaphin (0.18 and 0.36 mg/mL) step. DNA was quantified, tested using Real-time PCR for 16S rDNA and S. aureus and, then, microbiome was evaluated. Results: Although 16S rDNA was similarly detected across all the different techniques, Roche kit gave the highest DNA yield. The lowest Ct values for Real-time PCR for S. aureus was identified when lysostaphin was added. Considering genera from microbiome, alpha diversity indices did not show any significant differences between techniques, while relative abundances were more similar in presence of DTT. Conclusions: None of the conditions emerged to be superior to the others even if enzyme-based kits seem to be needed in order to have a higher extraction yield.


2016 ◽  
Vol 33 (1) ◽  
pp. 12-18
Author(s):  
Chiaki KOJIMA ◽  
Michiru KISHIMOTO ◽  
Machiko MIYATA ◽  
Sayumi NOMURA ◽  
Takayuki EZAKI

2017 ◽  
Vol 72 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Luis Jimenez ◽  
Theranda Jashari ◽  
Jenifer Vasquez ◽  
Stephanie Zapata ◽  
Joy Bochis ◽  
...  

Foods ◽  
2020 ◽  
Vol 9 (1) ◽  
pp. 67 ◽  
Author(s):  
Marina Torresi ◽  
Anna Ruolo ◽  
Vicdalia Aniela Acciari ◽  
Massimo Ancora ◽  
Giuliana Blasi ◽  
...  

From January 2015 to March 2016, an outbreak of 23 human cases of listeriosis in the Marche region and one human case in the Umbria region of Italy was caused by Listeria monocytogenes strains showing a new pulsotype never described before in Italy. A total of 37 clinical strains isolated from patients exhibiting listeriosis symptoms and 1374 strains correlated to the outbreak were received by the Italian National Reference Laboratory for L. monocytogenes (It NRL Lm) of Istituto Zooprofilattico Sperimentale dell’Abruzzo e del Molise (IZSAM) for outbreak investigation. A real-time PCR assay was purposely designed for a rapid screening of the strains related to the outbreak. PCR-positive strains were successively typed through molecular serogrouping, pulsed field gel electrophoresis (PFGE), and Next Generation Sequencing (NGS). Applying the described strategy, based on real-time PCR screening, we were able to considerably reduce time and costs during the outbreak investigation activities.


BioTechniques ◽  
2005 ◽  
Vol 38 (1) ◽  
pp. 29-31 ◽  
Author(s):  
Oliver Goldenberg ◽  
Olfert Landt ◽  
Ralf R. Schumann ◽  
Ulf B. Göbel ◽  
Lutz Hamann

2002 ◽  
Vol 43 (12) ◽  
pp. 2291-2299 ◽  
Author(s):  
Kazuoki Osumi ◽  
Takafumi Fukui ◽  
Hitoshi Kiyoi ◽  
Masanobu Kasai ◽  
Yoshihisa Kodera ◽  
...  

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