First report of blueberry red ringspot virus (Soymovirus maculavaccinii) in highbush blueberries in Türkiye


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Çağlayan K., Akkan R., Tunç B., Roumi V.

Journal of Plant Pathology, vol.108, no.1, pp.877-878, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Publication Type: Article / Technical Note
  • Volume: 108 Issue: 1
  • Publication Date: 2026
  • Doi Number: 10.1007/s42161-025-02110-x
  • Journal Name: Journal of Plant Pathology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Environment Index
  • Page Numbers: pp.877-878
  • Keywords: Blueberry red ringspot virus, PCR/sequencing, Phylogenetic analysis, Vacciniumspp
  • Open Archive Collection: AVESIS Open Access Collection
  • Hatay Mustafa Kemal University Affiliated: Yes

Abstract

Blueberry red ringspot virus (BRRV) (Soymovirus maculavaccinii) belongs to the

Soymovirus genus in the Caulimoviridae family, causes red ringspot disease in

highbush blueberry (Vaccinium corymbosum L.), and has been reported in blueberrygrowing

regions in the United States, Japan, and some European countries. Intensive

virus surveillance conducted since 2015 in Türkiye, where wild and cultivated

blueberries are widely grown, has identified blueberry mosaic-associated virus (BlMaV)

as the most prevalent virus, with blueberry leaf mottle virus (BLMoV) recently reported

(Çağlayan et al. 2025). In August 2023, red ringspot symptoms (Supplementary Fig. 1)

resembling BRRV infection were observed on leaves and stems of the Darrow cultivar

in Kocaeli province in Turkiye, although the fruits were symptomless. To confirm the

presence of BRRV, DNA was extracted from 290 symptomatic and asymptomatic

blueberry plants using DNeasy Plant Mini Kit (Qiagen, Germany) and subjected to PCR

using primers targeting the putative translational transactivator (BRRSV3F/BRRSV4R:

Polashock et. al., 2009) and coat protein (BRRSV 13F/BRRSV 14R: Glasheen et al.

2002) genes of BRRV. DNA fragments of the expected sizes were successfully

amplified from only five symptomatic plants using both primer pairs (Supplementary

Fig. 2), and were sequenced in both orientations and submitted to GenBank (Acc. No.

OR684355-59 for the putative translational transactivator gene and OR886932-36 for

the coat protein gene). Sequence and phylogenetic analysis (Supplementary Fig. 3)

revealed that the Turkish BRRV isolates were closely related to an isolate from

Slovenia (Acc. No. JF421559), exhibiting 99.79% (coat protein) to 100% (translational

transactivator) nucleotide sequence identity. These findings represent the first

detection of BRRV in highbush blueberries in Türkiye. Considering rapid expansion of

blueberry cultivation in the country, results of this study highlight the importance of

implementing strict propagation and management strategies. Effective measures will

be essential to mitigate the spread of BRRV and other blueberry viruses, thereby

protecting crop health and ensuring sustainable production.