Deciphering dengue: novel RNA barcoding segments for enhanced serotype-specific identification and global surveillance of dengue viruses

Front Microbiol. 2024 Dec 23:15:1474406. doi: 10.3389/fmicb.2024.1474406. eCollection 2024.

Abstract

Introduction: Dengue viruses (DENVs), the causative agents of dengue hemorrhagic fever and dengue shock syndrome, undergo genetic mutations that result in new strains and lead to ongoing global re-infections.

Objectives: To address the growing complexity of identifying and tracking biological samples, this study screened RNA barcode segments for the four DENV serotypes, ensuring high specificity and recall rates for DENV identification using segments.

Results: Through analyzing complete genome sequences of DENVs, we screened eight barcode segments for DENV, DENV-1, DENV-2, DENV-3, and DENV-4 identification. Comparing the screened barcode segments to sequences of known strains and determining the proportion of correctly or incorrectly identified nucleotides, these segments demonstrated an average recall rate at nucleotide level of 91.34% for four DENV serotypes, a specificity of 99.50% at species level within the Flaviviridae family, and a precision rate of 100% for identifying DENVs. For arboviruses, the nucleotide-level specificity was 63.58%. We designed and used the "Barcoding" software to streamline segment design, integrating automated sequence preprocessing, evaluation of barcode segments, and primer design, significantly reducing manual intervention and enhancing overall efficiency. We also established an online database called "Barcodes" for storing and preparing barcode segments.

Conclusion: This work established a standard framework for DENV identification and barcode segment selection, promising significant advancements in the real-time management and control of DENVs, thereby enhancing surveillance capabilities and facilitating targeted interventions in dengue outbreak-prone regions.

Keywords: RNA barcoding technology; four DENV serotypes; genetic information visualization; population genetic tests; species-specific molecule markers.

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This research was supported by grants from the Key Research & Development Project of Nanhua Biomedical Co., Ltd., (No. H202191490139), the National Natural Science Foundation of China (No. 32372124), China Postdoctoral Science Foundation (Nos. 2021M701160 and 2022M721101), and the Undergraduate Innovation and Entrepreneurship Training Program (XCX2024138).