Evaluation of an Environmental Transport Medium for Recovery.

Marianna Martinelli, Enrico Calaresu, Rosario Musumeci, Chiara Giubbi, Federica Perdoni, Sergio Frugoni, Santina Castriciano, Maria Scaturro, Maria Luisa Ricci, Clementina E Cocuzza
Author Information
  1. Marianna Martinelli: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. ORCID
  2. Enrico Calaresu: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
  3. Rosario Musumeci: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. ORCID
  4. Chiara Giubbi: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. ORCID
  5. Federica Perdoni: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
  6. Sergio Frugoni: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy.
  7. Santina Castriciano: Copan Italia SpA, 25125 Brescia, Italy.
  8. Maria Scaturro: Istituto Superiore di Sanità, 00161 Roma, Italy.
  9. Maria Luisa Ricci: Istituto Superiore di Sanità, 00161 Roma, Italy.
  10. Clementina E Cocuzza: Department of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. ORCID

Abstract

The collection and storage of water-related matrices such as biofilm from collection to processing are critical for the detection of by cultural and molecular tests. SRK™ is a liquid medium that acts both as an antimicrobial neutralizing agent and a transport medium for bacterial culture enumeration and is useful to maintain the stability of the sample from collection to analysis. The aims of this study were to evaluate viability and bacterial nucleic acids' stability in SRK™ medium over time at different storage conditions. Artificial bacterial inoculates with an approximate concentration of 10, 10 and 10 CFU/mL were made using certified reference material suspended in SRK™ medium. Bacteria recovery was analyzed by cultural and molecular methods at time 0, 24 and 48 h at room temperature and at 0, 24, 48 and 72 h at 2-8 °C, respectively. SRK™ medium supported culture viability with CFU counts within the expected range. The recovery after 72 h at 2-8 °C was 83-100% and 75-95% after 48 h at room temperature. Real-time PCR appropriately detected DNA at each temperature condition, dilution and time point. Results demonstrated a good performance of SRK™ medium for the reliable recovery of environmental .

Keywords

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MeSH Term

Culture Media
Legionella
Legionella pneumophila
Real-Time Polymerase Chain Reaction
Water Microbiology

Chemicals

Culture Media

Word Cloud

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