# Bluetongue in the Mediterranean Basin: An Overview of Recent Hotspots and Advances in Vaccine Technologies

**Authors:** Ikram Joubair, Abdellatif Errabbani, Soukaina Daif, Jesus Zueco, Salim Bounou, Ouafaa Fassi Fihri, Ismaïl Moukadiri

PMC · DOI: 10.3390/microorganisms14020437 · Microorganisms · 2026-02-12

## TL;DR

Bluetongue is a viral disease in ruminants, and this paper reviews recent outbreaks and new vaccine technologies to better control the disease in the Mediterranean region.

## Contribution

The paper provides a critical assessment of next-generation bluetongue vaccines with DIVA compatibility and multiserotype coverage.

## Key findings

- Bluetongue virus serotypes BTV-1, -4, -8, and the emerging BTV-3 pose risks to Mediterranean herds.
- Next-generation vaccines like subunit and viral-vectored constructs offer improved safety and cross-protection.
- Integrated surveillance and vector control are recommended alongside new vaccines for effective disease management.

## Abstract

Bluetongue (BT) is a noncontagious, arthropod-borne viral disease of domestic and wild ruminants caused by bluetongue virus (BTV), an arbovirus of the Orbivirus genus within the Sedoreoviridae family. At least 36 serotypes have been identified globally; recurrent circulation of BTV-1, -4, and -8, along with the recent emergence of BTV-3 in northern Europe, underscores a persistent incursion risk for Mediterranean herds. Key drivers include climate-driven expansion of Culicoides vector niches, windborne dispersal, animal movements, and subclinical reservoirs in cattle and goats. As no specific treatment is currently available, control of bluetongue disease still relies largely on vaccination. Live-attenuated vaccines and inactivated vaccines have reduced incidence, but important limitations persist: risk of reversion and the possibility of reassortment for LAVs; requirement for multiple doses and limited cross-protection for inactivated products; and the absence of DIVA capability for both. As an alternative, next-generation platforms are under active evaluation. Subunit formulations, often VP2 combined with VP5 and/or NS1/NS2 virus-like particles (VLPs), and viral-vectored constructs demonstrate favorable safety, strong humoral and cellular responses, inherent or engineered DIVA compatibility, and potential for rapid updating against emergent serotypes. This review synthesizes recent bluetongue activity across the Mediterranean Basin and provides a critical assessment of both existing and emerging vaccine strategies, with a focus on recommending next-generation platforms that emphasize DIVA-compliant, multiserotype, and adaptable vaccination approaches, supported by integrated surveillance and vector control in the region.

## Linked entities

- **Proteins:** VP2 (vacuolar H+-pyrophosphatase 2), VP5 (VP5), PTPN11 (protein tyrosine phosphatase non-receptor type 11), LZTR1 (leucine zipper like post translational regulator 1)
- **Diseases:** Bluetongue (MONDO:0025385)
- **Species:** Culicoides (taxon 41820)

## Full-text entities

- **Genes:** CD4 [NCBI Gene 443509], IVNS1ABP (influenza virus NS1A binding protein) [NCBI Gene 10625] {aka ARA3, FLARA3, HSPC068, IMD70, KLHL39, ND1}, NS2 [NCBI Gene 57762]
- **Diseases:** PPR (MESH:D029021), yellow fever (MESH:D015004), malaria (MESH:D008288), deaths (MESH:D003643), viral disease (MESH:D014777), weight loss (MESH:D015431), malarial catarrhal fever (MESH:D008304), infected (MESH:D007239), COVID-19 (MESH:D000086382), abortions (MESH:D000026), viremia (MESH:D014766), fetal abortions (MESH:D005315), BT disease (MESH:D001819), influenza (MESH:D007251), injury to (MESH:D014947), hepatitis B (MESH:D006509), reproductive failures (MESH:D051437)
- **Chemicals:** lipid (MESH:D008055), aluminum hydroxide (MESH:D000536), formaldehyde (MESH:D005557), saponin (MESH:D012503), BioRender (-), Oil (MESH:D009821), hydroxylamine (MESH:D019811), beta-propiolactone (MESH:D011420)
- **Species:** Nicotiana benthamiana (species) [taxon 4100], Bos taurus (bovine, species) [taxon 9913], Capra hircus (domestic goat, species) [taxon 9925], Gallus gallus (bantam, species) [taxon 9031], Bluetongue virus (no rank) [taxon 40051], hepatitis E virus [taxon 12461], Mivirus boleense (species) [taxon 2845619], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Homo sapiens (human, species) [taxon 9606], Ovis aries (domestic sheep, species) [taxon 9940], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Culicoides (subgenus) [taxon 58271], Bluetongue virus 2 (no rank) [taxon 35328], Bacillus sp. T (species) [taxon 1071724], Meleagris gallopavo (common turkey, species) [taxon 9103], Orbivirus (genus) [taxon 10892], Human immunodeficiency virus 1 (no rank) [taxon 11676], Hepatitis B virus (no rank) [taxon 10407], Escherichia coli (E. coli, species) [taxon 562], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Human papillomavirus (species) [taxon 10566], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Ebola virus [taxon 186536], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** CHO- — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0213), Chinese hamster — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0212)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942964/full.md

## References

126 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942964/full.md

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Source: https://tomesphere.com/paper/PMC12942964