Characterization of virus species associated with sweet potato virus disease in Costa Rica and riboprobe development for its rapid detection

[EN] Sweet potato (Ipomoea batatas) is a crucial crop for food security and economic stability in many regions, including Costa Rica. This study aimed to assess the prevalence and genetic diversity of two major viruses associated with sweet potato virus disease (SPVD) in Costa Rica: sweet potato fea...

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Detalhes bibliográficos
Autores: Méndez-Navarro, Daniela, Chacón-Cerdas, Randall, Alvarado-Ulloa, Carlos, Camacho-Montero, José Roberto, Alvarado-Marchena, Luis Fernando, Sánchez-Navarro, Jesús-Ángel|||0000-0002-3320-2827
Formato: artículo
Fecha de publicación:2025
País:España
Recursos:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/212855
Acesso em linha:https://riunet.upv.es/handle/10251/212855
Access Level:acceso abierto
Palavra-chave:Genetic diversity
Sweet potato chlorotic stunt virus
Sweet potato feathery mottle virus
Sweet potato virus disease
Viral detection methods
Virus prevalence
Descrição
Resumo:[EN] Sweet potato (Ipomoea batatas) is a crucial crop for food security and economic stability in many regions, including Costa Rica. This study aimed to assess the prevalence and genetic diversity of two major viruses associated with sweet potato virus disease (SPVD) in Costa Rica: sweet potato feathery mottle virus (SPFMV) and sweet potato chlorotic stunt virus (SPCSV). A total of 50 leaf samples displaying typical viral disease symptoms were collected from major sweet potato-growing regions. Using multiplex reverse transcription (RT)-PCR, SPFMV was detected in 82% of the samples and SPCSV in 52%, with a coinfection rate of 48%. Genetic analysis revealed that SPFMV isolates belonged predominantly to phylogenetic group B, while SPCSV isolates clustered with the West African (WA) strain. The low genetic diversity within these viral populations suggests a limited number of initial infection events followed by local spread. Riboprobe technology was evaluated as an alternative to RT-PCR for virus detection. While the riboprobes for SPFMV demonstrated sensitivity comparable to RT-PCR, the SPCSV riboprobes showed slightly lower sensitivity, particularly when using crude leaf extracts. Despite this, riboprobes offer significant advantages in terms of cost and ease of use for large-scale screening. Our findings underscore the need for robust diagnostic and management strategies to control SPVD and highlight the importance of continuous monitoring and research to mitigate the impact of viral diseases on sweet potato production in Costa Rica. These insights contribute to the global understanding of SPVD and support collaborative efforts in plant pathology research.