Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise

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Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise. / Abend, M.; Amundson, S. A.; Badie, C.; Brzoska, K.; Hargitai, R.; Kriehuber, R.; Schüle, S.; Kis, E.; Ghandhi, S. A.; Lumniczky, K.; Morton, S. R.; O’Brien, G.; Oskamp, D.; Ostheim, P.; Siebenwirth, C.; Shuryak, I.; Szatmári, T.; Unverricht-Yeboah, M.; Ainsbury, E.; Bassinet, C.; Kulka, U.; Oestreicher, U.; Ristic, Y.; Trompier, F.; Wojcik, A.; Waldner, L.; Port, M.

I: Scientific Reports, Vol. 11, 9756, 12.2021.

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

Harvard

Abend, M, Amundson, SA, Badie, C, Brzoska, K, Hargitai, R, Kriehuber, R, Schüle, S, Kis, E, Ghandhi, SA, Lumniczky, K, Morton, SR, O’Brien, G, Oskamp, D, Ostheim, P, Siebenwirth, C, Shuryak, I, Szatmári, T, Unverricht-Yeboah, M, Ainsbury, E, Bassinet, C, Kulka, U, Oestreicher, U, Ristic, Y, Trompier, F, Wojcik, A, Waldner, L & Port, M 2021, 'Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise', Scientific Reports, vol. 11, 9756. https://doi.org/10.1038/s41598-021-88403-4

APA

Abend, M., Amundson, S. A., Badie, C., Brzoska, K., Hargitai, R., Kriehuber, R., Schüle, S., Kis, E., Ghandhi, S. A., Lumniczky, K., Morton, S. R., O’Brien, G., Oskamp, D., Ostheim, P., Siebenwirth, C., Shuryak, I., Szatmári, T., Unverricht-Yeboah, M., Ainsbury, E., ... Port, M. (2021). Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise. Scientific Reports, 11, [9756]. https://doi.org/10.1038/s41598-021-88403-4

CBE

Abend M, Amundson SA, Badie C, Brzoska K, Hargitai R, Kriehuber R, Schüle S, Kis E, Ghandhi SA, Lumniczky K, Morton SR, O’Brien G, Oskamp D, Ostheim P, Siebenwirth C, Shuryak I, Szatmári T, Unverricht-Yeboah M, Ainsbury E, Bassinet C, Kulka U, Oestreicher U, Ristic Y, Trompier F, Wojcik A, Waldner L, Port M. 2021. Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise. Scientific Reports. 11:Article 9756. https://doi.org/10.1038/s41598-021-88403-4

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Author

Abend, M. ; Amundson, S. A. ; Badie, C. ; Brzoska, K. ; Hargitai, R. ; Kriehuber, R. ; Schüle, S. ; Kis, E. ; Ghandhi, S. A. ; Lumniczky, K. ; Morton, S. R. ; O’Brien, G. ; Oskamp, D. ; Ostheim, P. ; Siebenwirth, C. ; Shuryak, I. ; Szatmári, T. ; Unverricht-Yeboah, M. ; Ainsbury, E. ; Bassinet, C. ; Kulka, U. ; Oestreicher, U. ; Ristic, Y. ; Trompier, F. ; Wojcik, A. ; Waldner, L. ; Port, M. / Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise. I: Scientific Reports. 2021 ; Vol. 11.

RIS

TY - JOUR

T1 - Inter-laboratory comparison of gene expression biodosimetry for protracted radiation exposures as part of the RENEB and EURADOS WG10 2019 exercise

AU - Abend, M.

AU - Amundson, S. A.

AU - Badie, C.

AU - Brzoska, K.

AU - Hargitai, R.

AU - Kriehuber, R.

AU - Schüle, S.

AU - Kis, E.

AU - Ghandhi, S. A.

AU - Lumniczky, K.

AU - Morton, S. R.

AU - O’Brien, G.

AU - Oskamp, D.

AU - Ostheim, P.

AU - Siebenwirth, C.

AU - Shuryak, I.

AU - Szatmári, T.

AU - Unverricht-Yeboah, M.

AU - Ainsbury, E.

AU - Bassinet, C.

AU - Kulka, U.

AU - Oestreicher, U.

AU - Ristic, Y.

AU - Trompier, F.

AU - Wojcik, A.

AU - Waldner, L.

AU - Port, M.

PY - 2021/12

Y1 - 2021/12

N2 - Large-scale radiation emergency scenarios involving protracted low dose rate radiation exposure (e.g. a hidden radioactive source in a train) necessitate the development of high throughput methods for providing rapid individual dose estimates. During the RENEB (Running the European Network of Biodosimetry) 2019 exercise, four EDTA-blood samples were exposed to an Iridium-192 source (1.36 TBq, Tech-Ops 880 Sentinal) at varying distances and geometries. This resulted in protracted doses ranging between 0.2 and 2.4 Gy using dose rates of 1.5–40 mGy/min and exposure times of 1 or 2.5 h. Blood samples were exposed in thermo bottles that maintained temperatures between 39 and 27.7 °C. After exposure, EDTA-blood samples were transferred into PAXGene tubes to preserve RNA. RNA was isolated in one laboratory and aliquots of four blinded RNA were sent to another five teams for dose estimation based on gene expression changes. Using an X-ray machine, samples for two calibration curves (first: constant dose rate of 8.3 mGy/min and 0.5–8 h varying exposure times; second: varying dose rates of 0.5–8.3 mGy/min and 4 h exposure time) were generated for distribution. Assays were run in each laboratory according to locally established protocols using either a microarray platform (one team) or quantitative real-time PCR (qRT-PCR, five teams). The qRT-PCR measurements were highly reproducible with coefficient of variation below 15% in ≥ 75% of measurements resulting in reported dose estimates ranging between 0 and 0.5 Gy in all samples and in all laboratories. Up to twofold reductions in RNA copy numbers per degree Celsius relative to 37 °C were observed. However, when irradiating independent samples equivalent to the blinded samples but increasing the combined exposure and incubation time to 4 h at 37 °C, expected gene expression changes corresponding to the absorbed doses were observed. Clearly, time and an optimal temperature of 37 °C must be allowed for the biological response to manifest as gene expression changes prior to running the gene expression assay. In conclusion, dose reconstructions based on gene expression measurements are highly reproducible across different techniques, protocols and laboratories. Even a radiation dose of 0.25 Gy protracted over 4 h (1 mGy/min) can be identified. These results demonstrate the importance of the incubation conditions and time span between radiation exposure and measurements of gene expression changes when using this method in a field exercise or real emergency situation.

AB - Large-scale radiation emergency scenarios involving protracted low dose rate radiation exposure (e.g. a hidden radioactive source in a train) necessitate the development of high throughput methods for providing rapid individual dose estimates. During the RENEB (Running the European Network of Biodosimetry) 2019 exercise, four EDTA-blood samples were exposed to an Iridium-192 source (1.36 TBq, Tech-Ops 880 Sentinal) at varying distances and geometries. This resulted in protracted doses ranging between 0.2 and 2.4 Gy using dose rates of 1.5–40 mGy/min and exposure times of 1 or 2.5 h. Blood samples were exposed in thermo bottles that maintained temperatures between 39 and 27.7 °C. After exposure, EDTA-blood samples were transferred into PAXGene tubes to preserve RNA. RNA was isolated in one laboratory and aliquots of four blinded RNA were sent to another five teams for dose estimation based on gene expression changes. Using an X-ray machine, samples for two calibration curves (first: constant dose rate of 8.3 mGy/min and 0.5–8 h varying exposure times; second: varying dose rates of 0.5–8.3 mGy/min and 4 h exposure time) were generated for distribution. Assays were run in each laboratory according to locally established protocols using either a microarray platform (one team) or quantitative real-time PCR (qRT-PCR, five teams). The qRT-PCR measurements were highly reproducible with coefficient of variation below 15% in ≥ 75% of measurements resulting in reported dose estimates ranging between 0 and 0.5 Gy in all samples and in all laboratories. Up to twofold reductions in RNA copy numbers per degree Celsius relative to 37 °C were observed. However, when irradiating independent samples equivalent to the blinded samples but increasing the combined exposure and incubation time to 4 h at 37 °C, expected gene expression changes corresponding to the absorbed doses were observed. Clearly, time and an optimal temperature of 37 °C must be allowed for the biological response to manifest as gene expression changes prior to running the gene expression assay. In conclusion, dose reconstructions based on gene expression measurements are highly reproducible across different techniques, protocols and laboratories. Even a radiation dose of 0.25 Gy protracted over 4 h (1 mGy/min) can be identified. These results demonstrate the importance of the incubation conditions and time span between radiation exposure and measurements of gene expression changes when using this method in a field exercise or real emergency situation.

U2 - 10.1038/s41598-021-88403-4

DO - 10.1038/s41598-021-88403-4

M3 - Article

C2 - 33963206

AN - SCOPUS:85105485567

VL - 11

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 9756

ER -