An RT-PCR based microchip test system for the detection of SARS-CoV-2 offers pre-loaded and lyophilized reagents in the microchip. However, the 30- and 48-microwell formats of the microchip being miniaturized and performing 1.2 μl reaction, seek visual attention during sample addition. Therefore, adding colorants as color indicator in the lyophilized matrix in the microchips or adding to sample or master mix can impart not only user-friendliness to the task of liquid handling but also precision, and color-codes for easy identification of multiple kits in the layout of the microchip without compromising PCR data quality. A panel of colorants was screened for their background intensity, spectral inertness towards detection channels of AriaDNATM analyzer, interference with the reporter dyes (FAM, Cy5 and ROX), and visibility of optimal concentration in the microwell. The concentration of the colorant displaying insignificant impact on the quality of the amplification (Ct, fluorescence, and sensitivity) in comparison to no-colorant control was chosen for inclusion in the test kit. Tartrazine, Acid Red, Brilliant Blue and FAST Green colorants lyophilized with the reagents in the SARS-CoV-2 microchips were found to be stable and suitable. Storage of microchips with Fast Green colorant was tested at 40°C, 22°C, 4°C, and -20°C for 70 days and was found to be suitable and compatible with different master mixes available as liquid or lyophilized. Additionally, the microchips pre-loaded with lyophilized reagents in the presence and absence of two colorants Tartrazine and Fast Green were validated with clinical samples of SARS-COV-2. No significant impact of these colorants both intra- and inter-microchips was observed on the Ct and intensity of amplification for the tested samples in comparison to no-colorant control. The data suggested that the tested colorants can be used to color the sample, or the master mix or PCR mix for user-friendly liquid handling in empty microchips. For the microchip with pre-loaded and lyophilized reagents, the colorant can be added to lyophilized mixture for precision liquid handling and color-coding of lyophilized kits in the microchips. The manufacturing quality of the lyophilized microchips can also improve with colorant loaded reagent mix.
References
[1]
Razvan, C., Yaseen, I., Unrau, P.J., Lowe, C.F., Ritchie, G., Romney, M.G., Sin, D.D., Gill, S. and Slyadnev, M. (2012) Microchip RT-PCR Detection of Nasopharyngeal SARS-CoV-2 Samples. Journal of Molecular Diagnostics, 8, S1525-S1578.
[2]
Gill, R., Gill, S., Slyadnev, M. and Stroganov, A. (2018) Identification and Quantitation of Cashmere (Pashmina) Fiber and Wool Using Novel Microchip Based Real-Time PCR Technology. Journal of Textile Science and Technology, 4, 141-150. https://doi.org/10.4236/jtst.2018.44010
[3]
Nikitin, M.M., Statsyuk, N.V., Frantsuzov, P.A., Dzhavakhiya, V.G. and Golikov, A.G. (2018) Matrix Approach to the Simultaneous Detection of Multiple Potato Pathogens by Real-Time PCR. Journal of Applied Microbiology, 124, 797-809. https://doi.org/10.1111/jam.13686
[4]
Nikitin, M.M., Statsyuk, N.V., Frantsuzov, P.A., Pridannikov, M.V. and Golikov, A.G. (2017) Rapid and Simple Detection of Two Potato Cyst Nematode Species by Real-Time Multiplex PCR Using Preserved Microarray-Based Test Systems. Russian Journal of Nematology, 25, 51-60. http://www.russjnematology.com/Articles/rjn251/Nikitin_RJN2017_1_FIN2.pdf
[5]
Bogdanov, K.V., Nikulina, T.S., Lomaia, E.G., Slyadnev, M.N. and Zaritskey, A.Y. (2017) Identification of Oncogene Mutations in Leukemia Patients Using Microchip-Based PCR Analysis. Russian Journal of Bioorganic Chemistry, 43, 544-551. https://doi.org/10.1134/S1068162017040033
[6]
Abdulina, D.R., Iutynska, G.O., Anjskina, A.I. and Nikitin, M.M. (2020) Detection of Sulfate-Reducing Bacteria from Various Ecotopes by Real-Time PCR. Biotechnologia Acta, 13, 38-47. https://doi.org/10.15407/biotech13.02.038
[7]
Tong, R., Zhang, L., Song, Q., Hu, C., Chen, X., Lou, K., Gong, X., Gao, Y. and Wen, W. (2019) A Fully Portable Microchip Real-Time Polymerase Chain Reaction for Rapid Detection of Pathogen. Electrophoresis, 40, 1699-1707. https://doi.org/10.1002/elps.201900090
[8]
Babiker, A., Myers, C.W., Hill, C.E. and Guarner, J. (2020) SARS-CoV-2 Testing. American Journal of Clinical Pathology, 153, 706-708. https://doi.org/10.1093/ajcp/aqaa052
[9]
Zhou, P., Yang, X.-L., Wang, X.-G., Hu, B., Zhang, L., Zhang, W., Si, H.-R., Zhu, Y., Li, B., Huang, C.-L., Chen, H.-D., Chen, J., Luo, Y., Guo, H., Jiang, R.-D., Liu, M.-Q., Chen, Y., She, X.-R., Wang, X., Zheng, X.-S., Zhao, K., Chen, Q.-J., Deng, F., Liu, L.-L., Yan, B., Zhan, F.-X., Wang, Y.-Y., Xiao, G.-F. and Shi, Z.-L. (2020) A Pneumonia Outbreak Associated with a New Coronavirus of Probable Bat Origin. Nature, 579, 270-273. https://doi.org/10.1038/s41586-020-2012-7
[10]
Zhang, Y., Odiwuor, N., Xiong, J., Sun, L., Nyaruaba, R.O., Wei, H. and Tanner, N.A. (2020) Rapid Molecular Detection of SARS-CoV-2 (COVID-19) Virus RNA Using Colorimetric LAMP. https://doi.org/10.1101/2020.02.26.20028373
[11]
Lamb, L.E., Bartolone, S.N., Ward, E. and Chancellor, M.B. (2020) Rapid Detection of Novel Coronavirus (COVID-19) by Reverse Transcription-Loop-Mediated Isothermal Amplification. https://doi.org/10.1101/2020.02.19.20025155
[12]
El-Tholoth, M., Bau, H.H. and Song, J. (2020) A Single and Two-Stage, Closed- Tube, Molecular Test for the 2019 Novel Coronavirus (COVID-19) at Home, Clinic, and Points of Entry. https://doi.org/10.26434/chemrxiv.11860137.v1
[13]
Yu, L., Wu, S., Hao, X., Dong, X., Mao, L., Pelechano, V., Chen, W.H. and Yin, H. (2020) Rapid Detection of COVID-19 Coronavirus Using a Reverse Transcriptional Loop-Mediated Isothermal Amplification (RT-LAMP) Diagnostic Platform. Clinical Chemistry, 66, 975-977. https://doi.org/10.1093/clinchem/hvaa102
[14]
Rabe, B.A. and Cepko, C. (2020) SARS-CoV-2 Detection Using an Isothermal Amplification Reaction and a Rapid, Inexpensive Protocol for Sample Inactivation and Purification. https://doi.org/10.1101/2020.04.23.20076877
[15]
Bustin, S.A. and Nolan, T. (202) RT-qPCR Testing of SARS-CoV-2: A Primer. International Journal of Molecular Sciences, 21, 3004. https://doi.org/10.3390/ijms21083004
[16]
Udugama, B., Kadhiresan, P., Kozlowski, H.N., Malekjahani, A., Osborne, M., Li, V.Y.C., Chen, H. and Mubareka, S. (2020) Diagnosing COVID-19: The Disease and Tools for Detection. ACS Nano, 14, 3822-3835. https://doi.org/10.1021/acsnano.0c02624
[17]
European Centre for Disease Prevention and Control, Stockholm (2020) An Overview of the Rapid Test Situation for COVID-19 Diagnosis in the EU/EEA. https://www.ecdc.europa.eu/sites/default/files/documents/Overview-rapid-test-situation-for-COVID-19-diagnosis-EU-EEA.pdf
[18]
Jaggi, N., Yadav, K. and Giri, M.K. (2014) Static Studies of Absorption and Emission Spectra of Acid Yellow 17-An Azo Dye. Journal of Pure and Applied Physics, 52, 742-746. http://nopr.niscair.res.in/bitstream/123456789/29597/1/IJPAP%2052%2811%29%20742-746.pdf
[19]
Ntrallou, K., Gika, H. and Tsochatzis, E. (2020) Analytical and Sample Preparation Techniques for the Determination of Food Colorants in Food Matrices. Foods, 9, 58. https://doi.org/10.3390/foods9010058
[20]
Gill, S., Slyadnev, M. and Stroganov, A. (2017) Lumex Instruments Canada. Laboratory Focus May/June 2017. https://laboratoryfocus.ca/validation-of-colorants-for-colour-coding-of-lyophilized-reagents-in-microchips-for-real-time-pcr-ariadna