Detection and enumeration of Legionella in water samples is of great importance for risk assessment analysis. The plate culture method is the gold standard, but has received several well-known criticisms, which have induced researchers to develop alternative methods. The purpose of this study was to compare Legionella counts obtained by the analysis of potable water samples through the plate culture method and through the IDEXX liquid culture Legiolert method. Legionella plate culture, according to ISO 11731:1998, was performed using 1 L of water. Legiolert was performed using both the 10 mL and 100 mL Legiolert protocols. Overall, 123 potable water samples were analyzed. Thirty-seven (30%) of them, positive for L. pneumophila, serogroups 1 or 2–14 by plate culture, were used for comparison with the Legiolert results. The Legiolert 10 mL test detected 34 positive samples (27.6%) and the Legiolert 100 mL test detected 37 positive samples, 27.6% and 30% respectively, out of the total samples analyzed. No significant di_erence was found between either the Legiolert 10 mL and Legiolert 100 mL vs. the plate culture (p = 0.9 and p = 0.3, respectively) or between the Legiolert 10 mL and Legiolert 100 mL tests (p = 0.83). This study confirms the reliability of the IDEXX Legiolert test for Legionella pneumophila detection and enumeration, as already shown in similar studies. Like the plate culture method, the Legiolert assay is also suitable for obtaining isolates for typing purposes, relevant for epidemiological investigations.

Performance of Legiolert Test vs. ISO 11731 to Confirm Legionella pneumophila Contamination in Potable Water Samples / Maria Scaturro, Matteo Buffoni, Antonietta Girolamo, Sandra Cristino, Luna Girolamini, Marta Mazzotta, Maria Antonietta Bucci Sabattini, Cristina Maria Zaccaro, Leonarda Chetti, Microbiology Arpa Novara Laboratory, Antonino Bella, Maria Cristina Rota, Maria Luisa Ricci. - In: PATHOGENS. - ISSN 2076-0817. - ELETTRONICO. - 9:9(2020), pp. 690.1-690.8. [10.3390/pathogens9090690]

Performance of Legiolert Test vs. ISO 11731 to Confirm Legionella pneumophila Contamination in Potable Water Samples

Maria Scaturro;Sandra Cristino;Luna Girolamini;Marta Mazzotta;
2020

Abstract

Detection and enumeration of Legionella in water samples is of great importance for risk assessment analysis. The plate culture method is the gold standard, but has received several well-known criticisms, which have induced researchers to develop alternative methods. The purpose of this study was to compare Legionella counts obtained by the analysis of potable water samples through the plate culture method and through the IDEXX liquid culture Legiolert method. Legionella plate culture, according to ISO 11731:1998, was performed using 1 L of water. Legiolert was performed using both the 10 mL and 100 mL Legiolert protocols. Overall, 123 potable water samples were analyzed. Thirty-seven (30%) of them, positive for L. pneumophila, serogroups 1 or 2–14 by plate culture, were used for comparison with the Legiolert results. The Legiolert 10 mL test detected 34 positive samples (27.6%) and the Legiolert 100 mL test detected 37 positive samples, 27.6% and 30% respectively, out of the total samples analyzed. No significant di_erence was found between either the Legiolert 10 mL and Legiolert 100 mL vs. the plate culture (p = 0.9 and p = 0.3, respectively) or between the Legiolert 10 mL and Legiolert 100 mL tests (p = 0.83). This study confirms the reliability of the IDEXX Legiolert test for Legionella pneumophila detection and enumeration, as already shown in similar studies. Like the plate culture method, the Legiolert assay is also suitable for obtaining isolates for typing purposes, relevant for epidemiological investigations.
2020
Performance of Legiolert Test vs. ISO 11731 to Confirm Legionella pneumophila Contamination in Potable Water Samples / Maria Scaturro, Matteo Buffoni, Antonietta Girolamo, Sandra Cristino, Luna Girolamini, Marta Mazzotta, Maria Antonietta Bucci Sabattini, Cristina Maria Zaccaro, Leonarda Chetti, Microbiology Arpa Novara Laboratory, Antonino Bella, Maria Cristina Rota, Maria Luisa Ricci. - In: PATHOGENS. - ISSN 2076-0817. - ELETTRONICO. - 9:9(2020), pp. 690.1-690.8. [10.3390/pathogens9090690]
Maria Scaturro, Matteo Buffoni, Antonietta Girolamo, Sandra Cristino, Luna Girolamini, Marta Mazzotta, Maria Antonietta Bucci Sabattini, Cristina Maria Zaccaro, Leonarda Chetti, Microbiology Arpa Novara Laboratory, Antonino Bella, Maria Cristina Rota, Maria Luisa Ricci
File in questo prodotto:
File Dimensione Formato  
pathogens-09-00690.pdf

accesso aperto

Descrizione: Full-text
Tipo: Versione (PDF) editoriale
Licenza: Licenza per Accesso Aperto. Creative Commons Attribuzione (CCBY)
Dimensione 241.13 kB
Formato Adobe PDF
241.13 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/769795
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 21
  • ???jsp.display-item.citation.isi??? 16
social impact