tetano
Editor, Senior Moderator
Food Environ Virol
. 2026 Jun 8;18(2):28.
doi: 10.1007/s12560-026-09699-x.
Development of Fit-for-Purpose, High Quality Proficiency Samples for Interlaboratory Evaluation of RT-PCR Detection of HPAI H5N1 in Milk
Emily L Smith[SUP] 1 [/SUP], Yuhan Jin[SUP] 2 [/SUP], Megan R Miller[SUP] 3 [/SUP], Kirstin Frost[SUP] 4 [/SUP], Jodie Ulaszek[SUP] 2 [/SUP], Sarah M Nemser[SUP] 3 [/SUP], Laura B Goodman[SUP] 5 [/SUP], Steffen Uhlig[SUP] 4 [/SUP], Anja Schlierf[SUP] 4 [/SUP], Karina Hettwer[SUP] 4 [/SUP], Matthew Kmet[SUP] 6 [/SUP], Andriy Tkachenko[SUP] 3 [/SUP], Olgica Ceric[SUP] 3 [/SUP], Gregory H Tyson[SUP] 3 [/SUP], Ravinder Reddy[SUP] 6 [/SUP]
Affiliations
The increased demand for highly pathogenic avian influenza (HPAI) testing in milk highlights the critical need for well-characterized samples that enable meaningful evaluation of current detection methods. In this study, we focus on the development and rigorous characterization of artificially contaminated spiked milk samples, forming the foundation for reliable assessment of assay performance. By using reverse transcriptase digital PCR (RT-dPCR), we obtained precise genome copy (GC) measurements of our virus stock and of spiked samples, producing accurate quantification even at low viral loads. In parallel, the U.S. Department of Agriculture National Veterinary Services Laboratories' (USDA-NVSL's) influenza A matrix gene (IAV M) real-time reverse transcriptase (rRT-PCR) assay was employed as the main detection assay, serving as a tool to validate the sample preparation methodology. The goal of this work is to show that robust, reproducible, and analytically traceable samples can be generated to support HPAI method evaluation in proficiency exercises (PEs) distributed nationwide. Low between-sample standard deviations, ranging from 0 to 0.10 rRT-PCR Ct values for replicate samples, fall below the theoretical threshold indicative of heterogeneity, along with RT-dPCR determinations of sample GCs affirm the homogeneity of the developed samples. Parallel analysis of corresponding milk-based and phosphate buffered saline (PBS)-based samples showed no indication of a matrix effect. No significant shifts of Ct value or of measured GCs were observed over time, proving samples to be stable for at least 28 days when stored at -80 °C. The defined assay sensitivity, expressed as the level of detection 50% (LOD[SUB]50%[/SUB]), of the USDA-NVSL's IAV M rRT-PCR assay was determined to be 3.2 GCs/rRT-PCR reaction for milk samples and 5.5 GCs/rRT-PCR reaction for PBS samples, but this difference is not significant. This work sets the basis for determining laboratory competency, providing confidence in HPAI testing results for ongoing and future surveillance.
Keywords: Digital PCR; H5N1; HPAI; Milk; Proficiency; Real-time PCR.
. 2026 Jun 8;18(2):28.
doi: 10.1007/s12560-026-09699-x.
Development of Fit-for-Purpose, High Quality Proficiency Samples for Interlaboratory Evaluation of RT-PCR Detection of HPAI H5N1 in Milk
Emily L Smith[SUP] 1 [/SUP], Yuhan Jin[SUP] 2 [/SUP], Megan R Miller[SUP] 3 [/SUP], Kirstin Frost[SUP] 4 [/SUP], Jodie Ulaszek[SUP] 2 [/SUP], Sarah M Nemser[SUP] 3 [/SUP], Laura B Goodman[SUP] 5 [/SUP], Steffen Uhlig[SUP] 4 [/SUP], Anja Schlierf[SUP] 4 [/SUP], Karina Hettwer[SUP] 4 [/SUP], Matthew Kmet[SUP] 6 [/SUP], Andriy Tkachenko[SUP] 3 [/SUP], Olgica Ceric[SUP] 3 [/SUP], Gregory H Tyson[SUP] 3 [/SUP], Ravinder Reddy[SUP] 6 [/SUP]
Affiliations
- PMID: 42258002
- DOI: 10.1007/s12560-026-09699-x
The increased demand for highly pathogenic avian influenza (HPAI) testing in milk highlights the critical need for well-characterized samples that enable meaningful evaluation of current detection methods. In this study, we focus on the development and rigorous characterization of artificially contaminated spiked milk samples, forming the foundation for reliable assessment of assay performance. By using reverse transcriptase digital PCR (RT-dPCR), we obtained precise genome copy (GC) measurements of our virus stock and of spiked samples, producing accurate quantification even at low viral loads. In parallel, the U.S. Department of Agriculture National Veterinary Services Laboratories' (USDA-NVSL's) influenza A matrix gene (IAV M) real-time reverse transcriptase (rRT-PCR) assay was employed as the main detection assay, serving as a tool to validate the sample preparation methodology. The goal of this work is to show that robust, reproducible, and analytically traceable samples can be generated to support HPAI method evaluation in proficiency exercises (PEs) distributed nationwide. Low between-sample standard deviations, ranging from 0 to 0.10 rRT-PCR Ct values for replicate samples, fall below the theoretical threshold indicative of heterogeneity, along with RT-dPCR determinations of sample GCs affirm the homogeneity of the developed samples. Parallel analysis of corresponding milk-based and phosphate buffered saline (PBS)-based samples showed no indication of a matrix effect. No significant shifts of Ct value or of measured GCs were observed over time, proving samples to be stable for at least 28 days when stored at -80 °C. The defined assay sensitivity, expressed as the level of detection 50% (LOD[SUB]50%[/SUB]), of the USDA-NVSL's IAV M rRT-PCR assay was determined to be 3.2 GCs/rRT-PCR reaction for milk samples and 5.5 GCs/rRT-PCR reaction for PBS samples, but this difference is not significant. This work sets the basis for determining laboratory competency, providing confidence in HPAI testing results for ongoing and future surveillance.
Keywords: Digital PCR; H5N1; HPAI; Milk; Proficiency; Real-time PCR.