Tracking early cytological changes following expression of NSm and N proteins from tomato spotted wilt virus field isolates

Tomato spotted wilt virus (TSWV) is a major yield-limiting pathogen of peanut in the southeastern USA. To assess viral variability, field isolates were collected from symptomatic peanut plants at three locations in Alabama. Sequence analysis identified mutations in the non-structural movement protein (NSm) and the nucleocapsid protein (N). Subcellular localization studies showed that NSm fused to GFP (NSm:GFP) localized to plasmodesmata and co-localized with callose deposits by 2 days post-infiltration (dpi). By 4 dpi, NSm:GFP formed cytoplasmic aggregates, and callose deposition appeared more consistent with basal plasmodesmatal patterns. The N protein localized to the nuclear periphery and cell margins at 2 dpi and later aggregated in the cytoplasm by 4 dpi. The early callose accumulation associated with NSm expression suggests a potential plant defence response, warranting further investigation.

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Publication Details

Journal
Journal of General Virology
Published
2025-09-12
DOI
https://doi.org/10.1099/jgv.0.002151
Citations
1
Primary Topic
Plant Virus Research Studies
Type
article
Field-Weighted Citation Impact
1.75
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article

Tracking early cytological changes following expression of NSm and N proteins from tomato spotted wilt virus field isolates

A Ríos, Kathleen Martin, Amanda Strayer-Scherer, Asmaa M. Shehata
1 citations
Journal of General Virology
Plant Virus Research Studies
1.75
article

Tracking early cytological changes following expression of NSm and N proteins from tomato spotted wilt virus field isolates

A Ríos, Kathleen Martin, Amanda Strayer-Scherer, Asmaa M. Shehata
article en
1 citations

Abstract

Tomato spotted wilt virus (TSWV) is a major yield-limiting pathogen of peanut in the southeastern USA. To assess viral variability, field isolates were collected from symptomatic peanut plants at three locations in Alabama. Sequence analysis identified mutations in the non-structural movement protein (NSm) and the nucleocapsid protein (N). Subcellular localization studies showed that NSm fused to GFP (NSm:GFP) localized to plasmodesmata and co-localized with callose deposits by 2 days post-infiltration (dpi). By 4 dpi, NSm:GFP formed cytoplasmic aggregates, and callose deposition appeared more consistent with basal plasmodesmatal patterns. The N protein localized to the nuclear periphery and cell margins at 2 dpi and later aggregated in the cytoplasm by 4 dpi. The early callose accumulation associated with NSm expression suggests a potential plant defence response, warranting further investigation.

Journal of General VirologyVol. 106(9)
Auburn University (US), Assiut University (EG)
Openalex Percentile: Top 12%
Plant Virus Research Studies
1.75
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