Evidence map›Paper›PMID 41012588›Full record

ArticleViruses2025

Topography and Nanomechanics of the Tomato Brown Rugose Fruit Virus Suggest a Fragmentation-Driven Infection Mechanism.

Péter Puskás, Katalin Salánki, Levente Herényi, Tamás Hegedűs, Miklós Kellermayer

Abstract read
In one paragraph

Article in Viruses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Péter PuskásDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.
Katalin SalánkiDepartment of Plant Pathology, Plant Protection Institute, Centre for Agricultural Research, Hungarian Research Network (HUN-REN), H-1525 Budapest, Hungary.
Levente HerényiDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.
Tamás HegedűsDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.ORCID 0000-0002-5195-749X
Miklós KellermayerDepartment of Biophysics and Radiation Biology, Semmelweis University, H-1094 Budapest, Hungary.

Funding

Hungarian Ministry for Culture and Innovation 2024-2.1.1-EKÖP-2024-00004Hungarian National Research, Development and Innovation Office K143321, 150826Ministry for Innovation and Technology in Hungary 2020-4.1.1.-TKP2020
6 · The paper itself

Abstract

Tomato brown rugose fruit virus (ToBRFV) has been causing severe agricultural damage worldwide since its recent discovery. While related to tobacco mosaic virus, its properties and infection mechanisms are poorly understood. To uncover their structure and nanomechanics, we carried out atomic force microscopy (AFM) measurements on individual ToBRFV particles. The virions are rod-shaped with a height and width of 9 and 30 nm, respectively. Length is widely distributed (5-1000 nm), with a mode at 30 nm. ToBRFV rods displayed a 22.4 nm axial periodicity related to structural units. Force spectroscopy revealed a Young's modulus of 8.7 MPa, a spring constant of 0.25 N/m, and a rupture force of 1.7 nN. In the force curves a step was seen at a height of 3.3 nm, which is related to virion wall thickness. Wall thickness was also estimated by predicting coat protein structure with AlphaFold, yielding a protein with a length of 7.3 nm. Accordingly, the structural element of ToBRFv is a right circular cylinder with an equal height and diameter of ~22 nm and a wall thickness between 3.3 and 7.3 nm. Thus, at least four to nine serially linked units are required to encapsidate a single, helically organized RNA genome. Fragmentation of ToBRFV into these cylindrical structural units may result in a facilitated release of the genome and thus efficient infection.

Indexed as

Plant DiseasesSolanum lycopersicumTombusviridaeCapsid ProteinsMicroscopy, Atomic ForceVirionCapsid ProteinsAlphaFoldatomic force microscopyforce mapforce spectroscopytomato brown rugose fruit virus

Identifiers

PMID41012588
PMCPMC12474120

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.