First Report of Crinivirus Tomatichlorosis Infecting Tomato Plants in Argentina

ABSTRACT Tomato is mainly produced in five main areas distributed in western, northern, eastern and south Argentina. In Jujuy, Argentina, tomato plants with yellowing, rolling, brittleness leaves symptoms were observed and samples were taken to the lab. Total RNA was extracted from symptomatic plants, and reverse transcription–PCR was done in order to detect simultaneously Crinivirus tomatichlorosis , Crinivirus contagichlorosis. Degenerate primers (HS‐11/HS‐12) and specific primers (TIC‐3/TIC‐4 and ToC‐5/ToC‐6) were used together to detect these two viruses in a nested‐PCR. Only a PCR fragment of the expected size for Crinivirus tomatichlorosis (463 bp) was amplified from symptomatic diseased plants. The sequence of the amplicon blasted with Crinivirus tomatichlorosis virus protein (97.6%). Phylogenetic analysis supported this finding. So, here we report for the first time the Crinivirus tomatichlorosis infecting tomato cultivars in our country.

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Publication Details

Journal
Journal of Phytopathology
Published
2025-03-01
DOI
https://doi.org/10.1111/jph.70064
Primary Topic
Plant Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

First Report of Crinivirus Tomatichlorosis Infecting Tomato Plants in Argentina

Juan Manuel Reparaz, Silvina Marianela Yanil López, Pedro Alberto Balatti, Rocío Medina et al.
Journal of Phytopathology
Plant Virus Research Studies
article

First Report of Crinivirus Tomatichlorosis Infecting Tomato Plants in Argentina

Juan Manuel Reparaz, Silvina Marianela Yanil López, Pedro Alberto Balatti, Rocío Medina, César Gustavo Lucentini
article en

Abstract

ABSTRACT Tomato is mainly produced in five main areas distributed in western, northern, eastern and south Argentina. In Jujuy, Argentina, tomato plants with yellowing, rolling, brittleness leaves symptoms were observed and samples were taken to the lab. Total RNA was extracted from symptomatic plants, and reverse transcription–PCR was done in order to detect simultaneously Crinivirus tomatichlorosis , Crinivirus contagichlorosis. Degenerate primers (HS‐11/HS‐12) and specific primers (TIC‐3/TIC‐4 and ToC‐5/ToC‐6) were used together to detect these two viruses in a nested‐PCR. Only a PCR fragment of the expected size for Crinivirus tomatichlorosis (463 bp) was amplified from symptomatic diseased plants. The sequence of the amplicon blasted with Crinivirus tomatichlorosis virus protein (97.6%). Phylogenetic analysis supported this finding. So, here we report for the first time the Crinivirus tomatichlorosis infecting tomato cultivars in our country.

Journal of PhytopathologyVol. 173(2)
Universidad Nacional de La Plata (AR)
Consejo Nacional de Investigaciones Científicas y Técnicas, Agencia Nacional de Promoción Científica y Tecnológica
Openalex Percentile: Top 94%
Plant Virus Research Studies
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