TY - JOUR
T1 - Useful molecular tools for facing next pandemic events
T2 - Effective sample preparation and improved RT-PCR for highly sensitive detection of SARS-CoV-2 in wastewater environment
AU - Rusková, Magdaléna
AU - Bučková, Mária
AU - Achs, Adam
AU - Puškárová, Andrea
AU - Wu, Jer Horng
AU - Kuchta, Tomáš
AU - Šubr, Zdeno
AU - Pangallo, Domenico
N1 - Publisher Copyright:
© 2022 Elsevier GmbH
PY - 2022/8
Y1 - 2022/8
N2 - Viral pandemics can be inevitable in the next future. Considering SARS-CoV-2 pandemics as an example, there seems to be a need to develop a surveillance system able to monitor the presence of potential pathogenic agents. The sewage and wastewater environments demonstrated to be suitable targets for such kind of analysis. In addition, it is important to have reliable molecular diagnostic tools and also to develop a robust detection strategy. In this study, an effective sample preparation procedure was selected from four options and combined with a newly developed improved RT-PCR. First, a model viral system was constructed, containing a fragment of the SARS-CoV-2 gene encoding for the Spike protein. The encapsidated S RNA mimic (ESRM) was based on the plum pox virus (PPV) genome with the inserted targeted gene fragment. ESRM was used for seeding wastewater samples in order to evaluate the viral recovery of four different viral RNA concentration/extraction methods. The efficiency of individual approaches was assessed by the use of a quantitative reverse transcription PCR (qRT-PCR) and by a one-step single-tube nested quantitative reverse transcription PCR (OSN-qRT-PCR). For the detection of viruses in wastewater samples with low viral loads, OSN-qRT-PCR assay produced the most satisfactory results and the highest sensitivity.
AB - Viral pandemics can be inevitable in the next future. Considering SARS-CoV-2 pandemics as an example, there seems to be a need to develop a surveillance system able to monitor the presence of potential pathogenic agents. The sewage and wastewater environments demonstrated to be suitable targets for such kind of analysis. In addition, it is important to have reliable molecular diagnostic tools and also to develop a robust detection strategy. In this study, an effective sample preparation procedure was selected from four options and combined with a newly developed improved RT-PCR. First, a model viral system was constructed, containing a fragment of the SARS-CoV-2 gene encoding for the Spike protein. The encapsidated S RNA mimic (ESRM) was based on the plum pox virus (PPV) genome with the inserted targeted gene fragment. ESRM was used for seeding wastewater samples in order to evaluate the viral recovery of four different viral RNA concentration/extraction methods. The efficiency of individual approaches was assessed by the use of a quantitative reverse transcription PCR (qRT-PCR) and by a one-step single-tube nested quantitative reverse transcription PCR (OSN-qRT-PCR). For the detection of viruses in wastewater samples with low viral loads, OSN-qRT-PCR assay produced the most satisfactory results and the highest sensitivity.
UR - http://www.scopus.com/inward/record.url?scp=85135939725&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85135939725&partnerID=8YFLogxK
U2 - 10.1016/j.ijheh.2022.114017
DO - 10.1016/j.ijheh.2022.114017
M3 - Article
C2 - 35939897
AN - SCOPUS:85135939725
SN - 1438-4639
VL - 245
JO - International Journal of Hygiene and Environmental Health
JF - International Journal of Hygiene and Environmental Health
M1 - 114017
ER -