2023
DOI
bib
abs
Realizing the value in “non-standard” parts of the qPCR standard curve by integrating fundamentals of quantitative microbiology
Philip J. Schmidt,
Nicole Acosta,
Alex H. S. Chik,
Patrick M. D’Aoust,
Robert Delatolla,
Hadi A. Dhiyebi,
Melissa B. Glier,
Casey R. J. Hubert,
Jennifer Kopetzky,
Chand S. Mangat,
Xiaoli Pang,
Shelley Peterson,
Natalie Prystajecky,
Yuanyuan Qiu,
Mark R. Servos,
Monica B. Emelko,
Philip J. Schmidt,
Nicole Acosta,
Alex H. S. Chik,
Patrick M. D’Aoust,
Robert Delatolla,
Hadi A. Dhiyebi,
Melissa B. Glier,
Casey R. J. Hubert,
Jennifer Kopetzky,
Chand S. Mangat,
Xiaoli Pang,
Shelley Peterson,
Natalie Prystajecky,
Yuanyuan Qiu,
Mark R. Servos,
Monica B. Emelko
Frontiers in Microbiology, Volume 14
The real-time polymerase chain reaction (PCR), commonly known as quantitative PCR (qPCR), is increasingly common in environmental microbiology applications. During the COVID-19 pandemic, qPCR combined with reverse transcription (RT-qPCR) has been used to detect and quantify SARS-CoV-2 in clinical diagnoses and wastewater monitoring of local trends. Estimation of concentrations using qPCR often features a log-linear standard curve model calibrating quantification cycle (Cq) values obtained from underlying fluorescence measurements to standard concentrations. This process works well at high concentrations within a linear dynamic range but has diminishing reliability at low concentrations because it cannot explain "non-standard" data such as Cq values reflecting increasing variability at low concentrations or non-detects that do not yield Cq values at all. Here, fundamental probabilistic modeling concepts from classical quantitative microbiology were integrated into standard curve modeling approaches by reflecting well-understood mechanisms for random error in microbial data. This work showed that data diverging from the log-linear regression model at low concentrations as well as non-detects can be seamlessly integrated into enhanced standard curve analysis. The newly developed model provides improved representation of standard curve data at low concentrations while converging asymptotically upon conventional log-linear regression at high concentrations and adding no fitting parameters. Such modeling facilitates exploration of the effects of various random error mechanisms in experiments generating standard curve data, enables quantification of uncertainty in standard curve parameters, and is an important step toward quantifying uncertainty in qPCR-based concentration estimates. Improving understanding of the random error in qPCR data and standard curve modeling is especially important when low concentrations are of particular interest and inappropriate analysis can unduly affect interpretation, conclusions regarding lab performance, reported concentration estimates, and associated decision-making.
DOI
bib
abs
Realizing the value in “non-standard” parts of the qPCR standard curve by integrating fundamentals of quantitative microbiology
Philip J. Schmidt,
Nicole Acosta,
Alex H. S. Chik,
Patrick M. D’Aoust,
Robert Delatolla,
Hadi A. Dhiyebi,
Melissa B. Glier,
Casey R. J. Hubert,
Jennifer Kopetzky,
Chand S. Mangat,
Xiaoli Pang,
Shelley Peterson,
Natalie Prystajecky,
Yuanyuan Qiu,
Mark R. Servos,
Monica B. Emelko,
Philip J. Schmidt,
Nicole Acosta,
Alex H. S. Chik,
Patrick M. D’Aoust,
Robert Delatolla,
Hadi A. Dhiyebi,
Melissa B. Glier,
Casey R. J. Hubert,
Jennifer Kopetzky,
Chand S. Mangat,
Xiaoli Pang,
Shelley Peterson,
Natalie Prystajecky,
Yuanyuan Qiu,
Mark R. Servos,
Monica B. Emelko
Frontiers in Microbiology, Volume 14
The real-time polymerase chain reaction (PCR), commonly known as quantitative PCR (qPCR), is increasingly common in environmental microbiology applications. During the COVID-19 pandemic, qPCR combined with reverse transcription (RT-qPCR) has been used to detect and quantify SARS-CoV-2 in clinical diagnoses and wastewater monitoring of local trends. Estimation of concentrations using qPCR often features a log-linear standard curve model calibrating quantification cycle (Cq) values obtained from underlying fluorescence measurements to standard concentrations. This process works well at high concentrations within a linear dynamic range but has diminishing reliability at low concentrations because it cannot explain "non-standard" data such as Cq values reflecting increasing variability at low concentrations or non-detects that do not yield Cq values at all. Here, fundamental probabilistic modeling concepts from classical quantitative microbiology were integrated into standard curve modeling approaches by reflecting well-understood mechanisms for random error in microbial data. This work showed that data diverging from the log-linear regression model at low concentrations as well as non-detects can be seamlessly integrated into enhanced standard curve analysis. The newly developed model provides improved representation of standard curve data at low concentrations while converging asymptotically upon conventional log-linear regression at high concentrations and adding no fitting parameters. Such modeling facilitates exploration of the effects of various random error mechanisms in experiments generating standard curve data, enables quantification of uncertainty in standard curve parameters, and is an important step toward quantifying uncertainty in qPCR-based concentration estimates. Improving understanding of the random error in qPCR data and standard curve modeling is especially important when low concentrations are of particular interest and inappropriate analysis can unduly affect interpretation, conclusions regarding lab performance, reported concentration estimates, and associated decision-making.
2022
DOI
bib
abs
Emergence and Spread of the SARS-CoV-2 Omicron Variant in Alberta Communities Revealed by Wastewater Monitoring
Casey R. J. Hubert,
Nicole Acosta,
Barbara Waddell,
Maria E. Hasing,
Yuanyuan Qiu,
Meghan Fuzzen,
Nathanael B.J. Harper,
María A. Bautista,
Tiejun Gao,
Chloe Papparis,
Jenn Van Doorn,
Kristine Du,
Kevin Xiang,
Leslie Chan,
Laura Vivas,
Puja Pradhan,
Janine McCalder,
Kashtin Low,
Whitney England,
Darina Kuzma,
John Conly,
M. Cathryn Ryan,
Gopal Achari,
Jia Hu,
Jason Cabaj,
Chris Sikora,
Lawrence W. Svenson,
Nathan Zelyas,
Mark R. Servos,
Jon Meddings,
Steve E. Hrudey,
Kevin J. Frankowski,
Michael D. Parkins,
Xiaoli Pang,
Bonita E. Lee
Abstract Wastewater monitoring of SARS-CoV-2 allows for early detection and monitoring of COVID-19 burden in communities and can track specific variants of concern. Targeted assays enabled relative proportions of SARS-CoV-2 Omicron and Delta variants to be determined across 30 municipalities covering >75% of the province of Alberta (pop. 4.5M) in Canada, from November 2021 to January 2022. Larger cities like Calgary and Edmonton exhibited a more rapid emergence of Omicron relative to smaller and more remote municipalities. Notable exceptions were Banff, a small international resort town, and Fort McMurray, a more remote northern city with a large fly-in worker population. The integrated wastewater signal revealed that the Omicron variant represented close to 100% of SARS-CoV-2 burden prior to the observed increase in newly diagnosed clinical cases throughout Alberta, which peaked two weeks later. These findings demonstrate that wastewater monitoring offers early and reliable population-level results for establishing the extent and spread of emerging pathogens including SARS-CoV-2 variants.
DOI
bib
abs
Tracking Emergence and Spread of SARS-CoV-2 Omicron Variant in Large and Small Communities by Wastewater Monitoring in Alberta, Canada
Casey R. J. Hubert,
Nicole Acosta,
Barbara Waddell,
Maria E. Hasing,
Yuanyuan Qiu,
Meghan Fuzzen,
Nathanael B.J. Harper,
María A. Bautista,
Tiejun Gao,
Chloe Papparis,
Jenn Van Doorn,
Kristine Du,
Kevin Xiang,
Leslie Chan,
Laura Vivas,
Puja Pradhan,
Janine McCalder,
Kashtin Low,
Whitney England,
Darina Kuzma,
John Conly,
M. Cathryn Ryan,
Gopal Achari,
Jia Hu,
Jason Cabaj,
Chris Sikora,
Lawrence W. Svenson,
Nathan Zelyas,
Mark R. Servos,
Jon Meddings,
Steve E. Hrudey,
Kevin J. Frankowski,
Michael D. Parkins,
Xiaoli Pang,
Bonita E. Lee
Emerging Infectious Diseases, Volume 28, Issue 9
Abstract Wastewater monitoring of SARS-CoV-2 enables early detection and monitoring of the COVID-19 disease burden in communities and can track specific variants of concern. We determined proportions of the Omicron and Delta variants across 30 municipalities covering >75% of the province of Alberta (population 4.5 million), Canada, during November 2021–January 2022. Larger cities Calgary and Edmonton exhibited more rapid emergence of Omicron than did smaller and more remote municipalities. Notable exceptions were Banff, a small international resort town, and Fort McMurray, a medium-sized northern community that has many workers who fly in and out regularly. The integrated wastewater signal revealed that the Omicron variant represented close to 100% of SARS-CoV-2 burden by late December, before the peak in newly diagnosed clinical cases throughout Alberta in mid-January. These findings demonstrate that wastewater monitoring offers early and reliable population-level results for establishing the extent and spread of SARS-CoV-2 variants.