# Unexpected diversification of DENV2 genotype III in Colombia: New Insights and application of the globalized nomenclature

**Authors:** Eliana P. Calvo, Leidy Johana Madroñero, Lenny Marcela Hernández, Jhann Andrés Arturo, Hernando Pinzón, Félix Giovanni Delgado, Myriam Lucia Velandia-Romero, Verity Hill, Nathan D. Grubaugh, Jaime Eduardo Castellanos

PMC · DOI: 10.1371/journal.pone.0343528 · PLOS One · 2026-02-24

## TL;DR

This study explores the genetic diversity of DENV-2 genotype III in Colombia and highlights the importance of globalized nomenclature for tracking dengue virus lineages.

## Contribution

The study introduces a globalized nomenclature system for DENV-2 genotype III and identifies new lineages in Colombia.

## Key findings

- Phylogenetic analyses revealed a major lineage (D) and four minor lineages (D.2.1, D.2.2, D.3.1, D.3.2) in Colombia.
- D.2.1 and D.2.2 lineages differ by about 20 mutations, but their functional implications are unknown.
- The study emphasizes the need for genomic surveillance to monitor emerging dengue lineages.

## Abstract

Dengue is the most prevalent mosquito-borne viral disease worldwide and constitutes a major public health concern in Colombia. The disease is caused by four antigenically distinct dengue virus serotypes (DENV-1 to DENV-4), which share more than 65% genome identity. Although all four serotypes co-circulate in Colombia, secondary infections with DENV-2 have frequently been associated with more severe clinical outcomes. DENV-2 comprises six genotypes, of which genotype III has been the dominant lineage in the Americas over the past two decades. In this study, we investigated the evolutionary dynamics of DENV-2 genotype III in Colombia by analyzing available whole-genome coding sequences together with twenty-six newly generated genomes. Bayesian and maximum-likelihood phylogenetic approaches were applied to infer evolutionary relationships and temporal patterns. To harmonize lineage definitions and facilitate regional comparisons, we adopted the recently proposed hierarchical lineage nomenclature and used the Genome Detective Dengue typing tool for automated classification and consolidation of sequences from Colombia, Ecuador, and Venezuela. Phylogenetic analyses revealed a broadly distributed major lineage (previously designated D) circulating across the three countries, together with ongoing diversification and repeated introductions of genotype III within Colombia. Four minor lineages were identified, designated D.2.1, D.2.2, D.3.1, and D.3.2. Notably, the diversification of these minor lineages was accompanied by multiple non-synonymous substitutions. In particular, the two lineages currently circulating in Colombia, D.2.1 and D.2.2, are distinguished by approximately 20 mutations; however, the functional implications of these substitutions for viral virulence, pathogenicity, or vector competence remain unknown. These findings support the need for sustained and targeted genomic surveillance to detect and monitor emerging dengue virus lineages, prioritize them for epidemiological follow-up, and inform geographically focused public-health strategies. Overall, this study highlights the value of a globalized nomenclature, which enables the integration of genomic data across countries, facilitates the identification of emerging lineages in the region, and supports molecular surveillance efforts aimed at assessing their potential impact on disease presentation and public health.

## Linked entities

- **Diseases:** dengue (MONDO:0005502)

## Full-text entities

- **Genes:** ERVK-6 (endogenous retrovirus group K member 6, envelope) [NCBI Gene 64006] {aka ERVK6, HERV-K(C7), HERV-K108, K-Rev, c-orf, cORF}, SOS1 (SOS Ras/Rac guanine nucleotide exchange factor 1) [NCBI Gene 6654] {aka GF1, GGF1, GINGF, HGF, NS4, SOS-1}, SPINK5 (serine peptidase inhibitor Kazal type 5) [NCBI Gene 11005] {aka LEKTI, LETKI, NETS, NS, VAKTI}
- **Diseases:** deaths (MESH:D003643), viral disease (MESH:D014777), hepatic impairment (MESH:D008107), DHF (MESH:D019595), ascites (MESH:D001201), hypovolemic shock (MESH:D012769), infections (MESH:D007239), pleural effusion (MESH:D010996), bleeding (MESH:D006470), DENV infection (MESH:D003715), endothelial (MESH:D005642), burn (MESH:D002056), hypotension (MESH:D007022), mosquito (MESH:D000079426), febrile illness (MESH:D005334)
- **Chemicals:** RPMI medium (-), water (MESH:D014867), CO2 (MESH:D002245)
- **Species:** Aedes aegypti (yellow fever mosquito, species) [taxon 7159], Homo sapiens (human, species) [taxon 9606], Dothidea sp. ENV1 (species) [taxon 154308], Mus musculus (house mouse, species) [taxon 10090], Dengue virus (no rank) [taxon 12637]
- **Mutations:** I462V, I277V, A811V, T2496I, K3140R, N3367T, V26M, E3298D, T450I, T2510A
- **Cell lines:** C6/36 — Aedes albopictus (Asian tiger mosquito), Spontaneously immortalized cell line (CVCL_Z230), C6 — Rattus norvegicus (Rat), Rat malignant glioma, Cancer cell line (CVCL_0194)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12931762/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC12931762/full.md

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Source: https://tomesphere.com/paper/PMC12931762