Multidisciplinary Respiratory Medicine (Jan 2019)

Comparison of different conditions for DNA extraction in sputum - a pilot study

  • Martina Oriano,
  • Leonardo Terranova,
  • Antonio Teri,
  • Samantha Sottotetti,
  • Luca Ruggiero,
  • Camilla Tafuro,
  • Paola Marchisio,
  • Andrea Gramegna,
  • Francesco Amati,
  • Fabrizio Nava,
  • Elisa Franceschi,
  • Lisa Cariani,
  • Francesco Blasi,
  • Stefano Aliberti

DOI
https://doi.org/10.1186/s40248-018-0166-z
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 8

Abstract

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Abstract 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.

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