Journal: Italian Journal of Food Safety

Article Title: Presence of enteric bacterial pathogens in meat samples of wild boar hunted in Campania region, southern Italy

doi: 10.4081/ijfs.2022.9967

Figure Lengend Snippet: Gender, age (years (Y)/months (M)) and weight (kg) of the shot animals, presence of foodborne bacteria genes detected using Real-Time PCR.

Article Snippet: From each enrichment broth, the “iQ-Check Real-Time PCR Kits” were used for the detection of Salmonella (BR3578123, Bio-Rad, Hercules, CA, USA), STEC (BR3578139, Bio-Rad, Hercules, CA, USA), and Campylobacter (BR3578135, Bio-Rad, Hercules, CA, USA), following manufacturer’s recommendations.

Techniques: Bacteria, Isolation, Real-time Polymerase Chain Reaction

Journal: The Science of the total environment

Article Title: Verification and application of qPCR and viability-qPCR for Legionella monitoring in evaporative cooling systems complementing the conventional culture method.

doi: 10.1016/j.scitotenv.2024.176011

Figure Lengend Snippet: Fig. 1. Recovery of L. pneumophila in Evian water and artificial process water (aPW) using qPCR and viability-qPCR. Ten samples per concentration level and matrix were produced by spiking with cryopreserved L. pneumophila Sg 1 standards. Additionally, DNA of three aliquots of the stock suspension (105 Legionella/100 mL) were extracted using the direct method without filtration steps and used as a reference value for the calculation of the recovery of L. pneumophila.

Article Snippet: The iQ-Check® Free DNA Removal Solution (FDRS) (Bio-Rad Laboratories), an enzyme -based approach to v-qPCR was used according to the manufacturer's instructions in combination with iQ-Check® Quanti L. pneumophila Real-Time PCR Quantification Kit (Bio-Rad Laboratories).

Techniques: Concentration Assay, Produced, Suspension, Filtration

Journal: The Science of the total environment

Article Title: Verification and application of qPCR and viability-qPCR for Legionella monitoring in evaporative cooling systems complementing the conventional culture method.

doi: 10.1016/j.scitotenv.2024.176011

Figure Lengend Snippet: Fig. 2. Verification of linearity for the Bio-Rad L. pneumophila qPCR kit using artificial samples based on Evian water or artificial process water (aPW). Matrices were spiked with L. pneumophila Sg 1, Sg 4 or Sg 6 cryopreserved standards over a range of seven concentrations (102, 5 × 102, 103, 5 × 103, 104, 5 × 104, 105 TLC/100 mL). Each concentration was spiked in triplicates for qPCR (T1 to T3) using dilutions based on one stock suspension (105 TLC/mL) and the resulting DNA extracts were run as triplicates. Results of the qPCR in genomic units (GU) for each triplicate (n = 3) are plotted against spiked concentrations (m) based on total Legionella count (TLC). The reference value is indicating the curve if TLC and GU were identical. For linear regression, results below the limit of quantification were omitted.

Article Snippet: The iQ-Check® Free DNA Removal Solution (FDRS) (Bio-Rad Laboratories), an enzyme -based approach to v-qPCR was used according to the manufacturer's instructions in combination with iQ-Check® Quanti L. pneumophila Real-Time PCR Quantification Kit (Bio-Rad Laboratories).

Techniques: Concentration Assay, Suspension

Journal: The Science of the total environment

Article Title: Verification and application of qPCR and viability-qPCR for Legionella monitoring in evaporative cooling systems complementing the conventional culture method.

doi: 10.1016/j.scitotenv.2024.176011

Figure Lengend Snippet: Fig. 3. Verification of linearity for the Hygiena qPCR kit using artificial samples based on Evian water or artificial process water (aPW). Matrices were spiked with L. pneumophila Sg 1 cryopreserved standards over a range of seven concentrations (102, 5 × 102, 103, 5 × 103, 104, 5 × 104, 105 ILC/100 mL). Each concentration was spiked in duplicates per matrix for viability-qPCR (V1, V2) and once for qPCR (T) and all resulting DNA extracts were run as duplicates. Results of the viability-qPCR or qPCR in genomic units (GU) for each reaction duplicate (n = 2) are plotted against spiked concentrations (m = 6) based on intact Legionella count (ILC). The reference value is indicating the curve if ILC and GU were identical. For linear regression results below the limit of quantification were omitted.

Article Snippet: The iQ-Check® Free DNA Removal Solution (FDRS) (Bio-Rad Laboratories), an enzyme -based approach to v-qPCR was used according to the manufacturer's instructions in combination with iQ-Check® Quanti L. pneumophila Real-Time PCR Quantification Kit (Bio-Rad Laboratories).

Techniques: Concentration Assay

Journal: The Science of the total environment

Article Title: Verification and application of qPCR and viability-qPCR for Legionella monitoring in evaporative cooling systems complementing the conventional culture method.

doi: 10.1016/j.scitotenv.2024.176011

Figure Lengend Snippet: Fig. 4. Verification of linearity for the culture method using artificial samples based on Evian water or artificial process water (aPW) spiked with L. pneumophila Sg 1 cryopreserved standards over a range of seven concentrations (102, 5 × 102, 103, 5 × 103, 104, 5 × 104, 105 ILC/100 mL). For each concentration the weighted mean of evaluable plating (on GVPC agar) of a series of five (2 × 0.1 mL, 2 × 0.5 mL, membrane filtration of 20 mL) was used for linear regression. Results of the culture method (colony forming units, CFU) are plotted against spiked concentrations (m = 7) based on intact Legionella count (ILC). One additional run (Run3) was performed in Evian mineral water due to bigger deviations between the first two runs compared to aPW.

Article Snippet: The iQ-Check® Free DNA Removal Solution (FDRS) (Bio-Rad Laboratories), an enzyme -based approach to v-qPCR was used according to the manufacturer's instructions in combination with iQ-Check® Quanti L. pneumophila Real-Time PCR Quantification Kit (Bio-Rad Laboratories).

Techniques: Concentration Assay, Membrane, Filtration

Journal: The Science of the total environment

Article Title: Verification and application of qPCR and viability-qPCR for Legionella monitoring in evaporative cooling systems complementing the conventional culture method.

doi: 10.1016/j.scitotenv.2024.176011

Figure Lengend Snippet: Fig. 6. qPCR (A) and viability-qPCR (B) results for environmental samples of evaporative cooling systems spiked with cryopreserved L. pneumophila Sg 1 to con centrations of 103 and 104 ILC/100 mL. Bar chart on the left is showing determined GU/100 mL for samples 18 to 25 for Bio-Rad (BR) and Hygiena (HG) kit. Results below Limit of quantification (

Article Snippet: The iQ-Check® Free DNA Removal Solution (FDRS) (Bio-Rad Laboratories), an enzyme -based approach to v-qPCR was used according to the manufacturer's instructions in combination with iQ-Check® Quanti L. pneumophila Real-Time PCR Quantification Kit (Bio-Rad Laboratories).

Techniques: Environmental Sampling, Concentration Assay

Journal: Microbiology Resource Announcements

Article Title: Draft genome sequences from 127 Legionella spp. strains isolated in water systems linked to legionellosis outbreaks

doi: 10.1128/mra.01154-23

Figure Lengend Snippet: Statistics of assembled genomes

Article Snippet: Presumptive positive colonies were further confirmed by qualitative real-time PCR using the IQ-Check screen L. pneumophila Kit (Bio-Rad, Italy) and serologically identified using Legionella rapid latex test Kit (Biolife, Italy) monovalent antisera ( ).

Techniques: Isolation