2021
DOI: 10.1016/j.mimet.2021.106242
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Comparative study of Legiolert with ISO 11731-1998 standard method-conclusions from a Public Health Laboratory

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Cited by 8 publications
(7 citation statements)
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“…L. pneumophila was quantified using the Legiolert most probable number assay (IDEXX Laboratories, Inc., Westbrook, ME, USA) according to manufacturer protocols [IDEXX]. Legiolert is a liquid-based culture most probable number (MPN) method that correlates well with standard culture methods and has a low (3–4%) false positivity rate [ 21 , 22 , 23 , 24 , 25 , 26 , 27 ].…”
Section: Methodsmentioning
confidence: 99%
“…L. pneumophila was quantified using the Legiolert most probable number assay (IDEXX Laboratories, Inc., Westbrook, ME, USA) according to manufacturer protocols [IDEXX]. Legiolert is a liquid-based culture most probable number (MPN) method that correlates well with standard culture methods and has a low (3–4%) false positivity rate [ 21 , 22 , 23 , 24 , 25 , 26 , 27 ].…”
Section: Methodsmentioning
confidence: 99%
“…However, alternative methods such as the IDEXX Legiolert ® kit, a liquid culture method that yields results in most probable number (MPN) per volume, has become more widely used in recent years due to its ease of use and reported specificity for L. pneumophila. [34][35][36][37][38][39][40] DNA-based methods (e.g., quantitative polymerase chain reaction [qPCR] and droplet digital polymerase chain reaction [ddPCR]) have also become more common due to fast turnaround times, the possibility to detect cells in the viable but non-culturable (VBNC) state, and the potential for increased specificity. [41][42][43] However, comparison and interpretation of results obtained with different methods are generally lacking.…”
Section: Introductionmentioning
confidence: 99%
“…At present, culture analysis techniques are the only option that yields L. pneumophila concentrations, which may be compared against action levels. Legiolert ® has emerged as a viable analysis method that may be implemented at the utility level and with sensitivity consistent with action levels proposed in this study and in other protocols for responding to positive samples (Barrette, 2019;Boczek et al, 2021;Checa et al, 2021;Dowdell et al, 2022;Hirsh et al, 2021;Inoue et al, 2020;LeChevallier, 2019aLeChevallier, , 2019bMapili et al, 2020;Maqbool, 2019;McCuin et al, 2021;Niu et al, 2022;Omoregie et al, 2022;Petrisek & Hall, 2017;Rech et al, 2018;Sartory et al, 2017;Scaturro et al, 2020;Spies et al, 2018). Because most qPCR assays do not distinguish between genetic material from live and dead organisms, surveys with qPCR indicate very high occurrence (proportion positive samples) of Legionella, making the results less useful in diagnosing and controlling Legionella growth.…”
Section: Discussionmentioning
confidence: 59%