Performance Evaluation of Kawsar DNA Banking Card (DBC) for Preservation of DNA from Multiple Biological Matrices: Application in PCR-Based Assays
DOI:
https://doi.org/10.63053/ijhes.215Keywords:
DNA, Specimen shipping, Polymerase Chain Reaction, Inhibitors, Quality ControlAbstract
DNA preservation cards provide a practical alternative to traditional cold storage methods for molecular applications. This study assessed the performance of the locally produced Kawsar DNA Banking Card (DBC) for preserving DNA from whole blood, saliva, tissue, cell lysate, and tissue homogenate at room temperature for one month. DNA quality was evaluated by spectrophotometry and PCR amplification of the human GAPDH gene.
Washed punches yielded measurable DNA concentrations (53.59–188.81 ng/µL), though with low purity ratios. Direct PCR from unwashed punches showed minimal amplification. By using the washing step, clear GAPDH bands (235 bp) were obtained from saliva, tissue, and cell lysate samples, while tissue homogenate mainly produced off-target products. All DBC-derived signals were weaker than the positive control.
The Kawsar DBC effectively preserves amplifiable DNA from various biological matrices when a washing procedure is applied. It offers a cost-effective, room-temperature solution suitable for biobanking and PCR-based diagnostics, particularly in resource-limited settings
References
Ataei, S., Nateghpour, M., Hajjaran, H., Edrissian, G. H., & Rahimi Foroushani, A. (2011). High specificity of semi-nested multiplex PCR using dried blood spots on DNA banking card in comparison with frozen liquid blood for detection of Plasmodium falciparum and Plasmodium vivax. Journal of Clinical Laboratory Analysis, *25*(3), 185–190. DOI: 10.1002/jcla.20454
Atavliyeva, S., Mukhamedyarov, D., Anuarbekova, A., & Tarlykov, P. (2018). Cards for collection of biomaterial samples: Areas of application. National Center for Biotechnology.
Choi, E.-H., Lee, S. K., Ihm, C., & Sohn, Y.-H. (2014). Rapid DNA extraction from dried blood spots on filter paper: Potential applications in biobanking. Osong Public Health and Research Perspectives, *5*(6), 331–337. DOI: http://dx.doi.org/10.1016/j.phrp.2014.09.005
da Cunha Santos, G. (2018). FTA cards for preservation of nucleic acids for molecular assays: A review on the use of cytologic/tissue samples. Archives of Pathology & Laboratory Medicine, *142*(3), 308–312. DOI: 10.5858/ arpa.2017-0303-RA
de Flamingh, A., Ishida, Y., Pecnerova, P., Vilchis, S., Siegismund, H. R., van Aarde, R. J., Malhi, R. S., & Roca, A. L. (2023). Combining methods for non-invasive fecal DNA enables whole genome and metagenomic analyses in wildlife biology. Frontiers in Genetics, *13*, 1021004. DOI: 10.3389/fgene.2022.1021004
Fata, A., Bojdy, A., Maleki, M., Hosseini Farash, B. R., Ghazvini, K., Tajzadeh, P., Vakili, V., Moghaddas, E., Mastroeni, P., & Rahmani, S. (2019). Fish tank granuloma: An emerging skin disease in Iran mimicking cutaneous leishmaniasis. PLoS ONE, *14*(9), e0221367. DOI: https://doi.org/10.1371/journal.pone.0221367
Fata, A., Khamesipour, A., Mohajery, M., Hosseininejad, Z., Afzalaghaei, M., Berenji, F., Ganjbakhsh, M., Akhavan, A. A., Eskandari, E., & Amin-Mohammad, A. (2009). Whatman paper (FTA cards) for storing and transferring Leishmania DNA for PCR examination. Iranian Journal of Parasitology, *4*(4), 37–42.
Green, H., Tillmar, A., Pettersson, G., & Montelius, K. (2019). The use of FTA cards to acquire DNA profiles from postmortem cases. International Journal of Legal Medicine. DOI: https://doi.org/10.1007/s00414-019-02015-2
Harty, L. C., Garcia-Closas, M., Rothman, N., Reid, Y. A., Tucker, M. A., & Hartge, P. (2000). Collection of buccal cell DNA using treated cards. Cancer Epidemiology, Biomarkers & Prevention, *9*(5), 501–506.
Jozwiak, M., Wyrostek, K., Domanska-Blicharz, K., Olszewska-Tomczyk, M., Smietanka, K., & Minta, Z. (2016). Application of FTA® Cards for detection and storage of avian influenza virus. Journal of Veterinary Research. DOI: 10.1515/jvetres-2016-0001
Karimian, F., Sedaghat, M. M., Oshaghi, M. A., Mohtarami, F., Sanei Dehkordi, A., Koosha, M., Akbari, S., & Hashemi-Aghdam, S. S. (2011). Utility of filter paper for preserving insects, bacteria, and host reservoir DNA for molecular testing. Iranian Journal of Arthropod-Borne Diseases, *5*(2), 42–50.
Naddaf, S. R., Ghazinezhad, B., Kazemira, E., & Cutler, S. J. (2020). Development of a loop-mediated isothermal amplification (LAMP) assay for the rapid detection of tick-borne relapsing fever in resource-limited areas. Iranian Journal of Parasitology, *15*(4), 496–504.
Patel, Y. K., Nammi, N. L., Mane, S. R., & Dalton, D. L. (2026). Investigation of six-week DNA degradation patterns in tissue exposed to indoor and outdoor conditions using FTA™ Cards. protocols.io. DOI: https://dx.doi.org/10.17504/protocols.io.q26g7o7xkvwz/v1
Saieg, M. A., Geddie, W. R., Boerner, S. L., Bailey, D., Crump, M., & da Cunha Santos, G. (2012). The use of FTA cards for preserving unfixed cytological material for high-throughput molecular analysis. Cancer Cytopathology, *120*(3), 206–214. DOI: 10.1002/cncy.20205, wileyonlinelibrary.com
Shahab, Z., Zeynali, S., & Aslani, M. M. (2011). Evaluation of stability of Escherichia coli DNA on DNA Banking Card (DBC) for molecular assays. Modares Journal of Medical Sciences: Pathobiology, *14*(4), 99–107.
Sharafi Farzad, M., Tomas, C., Borsting, C., Zeinali, Z., Malekdoost, M., Zeinali, S., & Morling, N. (2013). Analysis of 49 autosomal SNPs in three ethnic groups from Iran: Persians, Lurs and Kurds. Forensic Science International: Genetics, *7*(4), 471–473. DOI: http://dx.doi.org/10.1016/j.fsigen.2013.04.001
Singh, H. N. (2021). Collection, preservation and transportation of biological evidence for forensic DNA analysis. Forensic Science Laboratory, Kolkata.
Stringer, O. W., Bosse, J. T., Lacouture, S., Gottschalk, M., Fodor, L., Angen, O., Velazquez, E., Penny, P., Lei, L., Langford, P. R., & Li, Y. (2021). Rapid detection and typing of Actinobacillus pleuropneumoniae serovars directly from clinical samples: Combining FTA® card technology with multiplex PCR. Frontiers in Veterinary Science, *8*, 728660. DOI: 10.3389/fvets.2021.728660
Zeinali, S., Kharazi Tavakol, Z., Kianfar, S., Kariminejad, A., Mahdieh, N., Hashemi, M., & Zeinali, Z. (2012). Detection of numerical aneuploidy of chromosomes X, Y, 13, 18 and 21 in 100 blood and fetal samples by QF-PCR method. Journal of Proteomics & Bioinformatics, *5*(6), 147–151. DOI: 10.4172/jpb.1000227
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