Vol. 65 No. 2 (2026)
Articles

Identification and characterization of two isolates of Bougainvillea chlorotic vein banding virus (Badnavirus venabougainvilleae) in bougainvillea plants from Italy

Amani BEN SLIMEN
International Centre for Advanced Mediterranean Agronomic Studies (CIHEAM of Bari), Valenzano, Italy
Reem YAZBECK
International Centre for Advanced Mediterranean Agronomic Studies (CIHEAM of Bari), Valenzano, Italy
Toufic ELBEAINO
International Centre for Advanced Mediterranean Agronomic Studies (CIHEAM of Bari), Valenzano, Italy
Michele DIGIARO
International Centre for Advanced Mediterranean Agronomic Studies (CIHEAM of Bari), Valenzano, Italy

Published 2026-09-10

Keywords

  • BCVBV,
  • HTS,
  • Badnavirus,
  • genetic diversity,
  • Apulia

How to Cite

[1]
A. BEN SLIMEN, R. YAZBECK, T. ELBEAINO, and M. DIGIARO, “Identification and characterization of two isolates of Bougainvillea chlorotic vein banding virus (Badnavirus venabougainvilleae) in bougainvillea plants from Italy”, Phytopathol. Mediterr., vol. 65, no. 2, pp. 301–308, Sep. 2026.

Abstract

Ornamental plants can be reservoirs of plant viruses, facilitating virus dissemination through international trade. In this bougainvillea study, 58 samples collected from six ornamental nurseries in Apulia (southern Italy) were screened for the presence of known bougainvillea-infecting viruses, using PCR assays. Among the viruses tested, only Bougainvillea chlorotic vein banding virus (BCVBV) was detected, occurring in five (8.6%) of the samples, whereas Impatiens necrotic spot virus (INSV), Clerodendron yellow mosaic virus (ClYMV), tomato yellow ring virus (TYRV), and cucumber mosaic virus (CMV) were not detected. High-throughput sequencing (HTS) of one BCVBV-positive sample (O54) enabled reconstruction of a complete viral genome, designated BCVBV Mini-Thai (GenBank accession no. PQ682517). A second HTS analysis of a pooled set of PCR-negative samples revealed a genetically distinct BCVBV isolate that was not detected by PCR using previously published primers. The complete genome of this isolate was reconstructed through contig assembly and gap-filling PCR using newly designed primers, and was named BCVBV Apulia 1 (PQ682518). The genome of Mini-Thai was 8,822 nucleotides long, and had high nucleotide (98.5%) and amino acid (98.7%) similarities with the Malaysian isolate BCVBV-UKM. In contrast, BCVBV Apulia 1 (PQ682518) was 8,694 nucleotides long and had greatest nucleotide similarity (81.6%) with the Brazilian isolate BCVBV UNB-01, with 84.0% amino acid similarity in the polyprotein. Both isolates had typical Badnavirus genome organization, with four open reading frames, and clustered in distinct phylogenetic clades. Further screening of the 58 collected samples using primers designed on the Apulia 1 isolate detected seven (12.1%) additional infected samples. A primer set targeting conserved genomic regions was also developed, enabling detection of both isolates. This report is the first detection of BCVBV in Italy and Europe, and also reveals the presence of a genetically divergent isolate of this virus.

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