Ulster University Logo

Legionella jordanis inactivation in water by solar driven processes: EMA-qPCR versus culture-based analyses for new mechanistic insights

Polo-López, María Inmaculada, Castro-Alférez, María, Nahim-Granados, Samira, Malato, Sixto and Fernandez-Ibanez, Pilar (2016) Legionella jordanis inactivation in water by solar driven processes: EMA-qPCR versus culture-based analyses for new mechanistic insights. Catalysis Today, N/A . [Journal article]

Full text not available from this repository.

URL: http://dx.doi.org/10.1016/j.cattod.2016.10.029

DOI: doi:10.1016/j.cattod.2016.10.029


In this contribution, the validation of EMA-qPCR method for the quantification of viable Legionella spp. in water after solar treatments was carried out. EMA-qPCR was used to evaluate the different effects of several solar water disinfection processes over this bacterium, and furthermore their mode of action. Inactivation of Legionella jordanis in water by solar photocatalytic (TiO2 and TiO2/H2O2) and solar photochemical (solar/H2O2 and solar disinfection) processes have been investigated under natural sunlight. Culture-based and molecular (EMA-qPCR) techniques were systematically compared for the analysis of treated water samples. Solar tests were done under natural solar radiation (clear sky) and ambient temperature (20–35 °C) for 2 h, using H2O2/Solar (10, 20 and 50 mg/L), TiO2/Solar (100, 200, 300, 400, and 500 mg/L) and TiO2/H2O2/Solar (100/10, 200/10, 500/10 mg/L). According to culture-based method, the best results of bacterial inactivation were obtained for 500/10 mg/L of TiO2/H2O2. The order of efficiency to reach complete inactivation was: TiO2/H2O2/solar (5 min) > TiO2/solar (15 min) ≈ H2O2/solar (15 min) > Solar only disinfection (90 min). Moreover, EMA-qPCR and culturable counting results showed a direct correlation for samples treated with TiO2/solar for those catalyst concentrations that generate a strong oxidative attack over the cell wall. EMA-qPCR results demonstrated to be a good method to detect damaged and dead cells when the treatment affects the integrity of the cell’s membrane, as occurs under photocatalysis. Meanwhile for solar disinfection and solar/H2O2 (at non-toxic concentrations, <1.5 mM), where membrane integrity remained unaltered, EMA-qPCR results couldn’t discriminate between alive and dead cells, even when the bacteria were not culturable.

Item Type:Journal article
Keywords:EMA; Legionella jordanis; Real time qPCR; TiO2; Hydrogen peroxide
Faculties and Schools:Faculty of Computing & Engineering > School of Engineering
Faculty of Computing & Engineering
Research Institutes and Groups:Engineering Research Institute
Engineering Research Institute > Nanotechnology & Integrated BioEngineering Centre (NIBEC)
ID Code:36762
Deposited By: Dr Pilar Fernandez-Ibanez
Deposited On:02 Feb 2017 09:24
Last Modified:17 Oct 2017 16:27

Repository Staff Only: item control page