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A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features
A novel cytorhabdovirus, tentatively named Actinidia virus D (AcVD), was identified from kiwifruit (Actinidia chinensis) in China using high‐throughput sequencing technology. The genome of AcVD consists of 13,589 nucleotides and is organized into seven open reading frames (ORFs) in its antisense str...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435229/ https://www.ncbi.nlm.nih.gov/pubmed/34288324 http://dx.doi.org/10.1111/mpp.13110 |
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author | Wang, Yanxiang Wang, Guoping Bai, Jianyu Zhang, Yongle Wang, Ying Wen, Shaohua Li, Liu Yang, Zuokun Hong, Ni |
author_facet | Wang, Yanxiang Wang, Guoping Bai, Jianyu Zhang, Yongle Wang, Ying Wen, Shaohua Li, Liu Yang, Zuokun Hong, Ni |
author_sort | Wang, Yanxiang |
collection | PubMed |
description | A novel cytorhabdovirus, tentatively named Actinidia virus D (AcVD), was identified from kiwifruit (Actinidia chinensis) in China using high‐throughput sequencing technology. The genome of AcVD consists of 13,589 nucleotides and is organized into seven open reading frames (ORFs) in its antisense strand, coding for proteins in the order N‐P‐P3‐M‐G‐P6‐L. The ORFs were flanked by a 3′ leader sequence and a 5′ trailer sequence and are separated by conserved intergenic junctions. The genome sequence of AcVD was 44.6%–51.5% identical to those of reported cytorhabdoviruses. The proteins encoded by AcVD shared the highest sequence identities, ranging from 27.3% (P6) to 44.5% (L), with the respective proteins encoded by reported cytorhabdoviruses. Phylogenetic analysis revealed that AcVD clustered together with the cytorhabdovirus Wuhan insect virus 4. The subcellular locations of the viral proteins N, P, P3, M, G, and P6 in epidermal cells of Nicotiana benthamiana leaves were determined. The M protein of AcVD uniquely formed filament structures and was associated with microtubules. Bimolecular fluorescence complementation assays showed that three proteins, N, P, and M, self‐interact, protein N plays a role in the formation of cytoplasm viroplasm, and protein M recruits N, P, P3, and G to microtubules. In addition, numerous paired proteins interact in the nucleus. This study presents the first evidence of a cytorhabdovirus infecting kiwifruit plants and full location and interaction maps to gain insight into viral protein functions. |
format | Online Article Text |
id | pubmed-8435229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84352292021-09-15 A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features Wang, Yanxiang Wang, Guoping Bai, Jianyu Zhang, Yongle Wang, Ying Wen, Shaohua Li, Liu Yang, Zuokun Hong, Ni Mol Plant Pathol Original Articles A novel cytorhabdovirus, tentatively named Actinidia virus D (AcVD), was identified from kiwifruit (Actinidia chinensis) in China using high‐throughput sequencing technology. The genome of AcVD consists of 13,589 nucleotides and is organized into seven open reading frames (ORFs) in its antisense strand, coding for proteins in the order N‐P‐P3‐M‐G‐P6‐L. The ORFs were flanked by a 3′ leader sequence and a 5′ trailer sequence and are separated by conserved intergenic junctions. The genome sequence of AcVD was 44.6%–51.5% identical to those of reported cytorhabdoviruses. The proteins encoded by AcVD shared the highest sequence identities, ranging from 27.3% (P6) to 44.5% (L), with the respective proteins encoded by reported cytorhabdoviruses. Phylogenetic analysis revealed that AcVD clustered together with the cytorhabdovirus Wuhan insect virus 4. The subcellular locations of the viral proteins N, P, P3, M, G, and P6 in epidermal cells of Nicotiana benthamiana leaves were determined. The M protein of AcVD uniquely formed filament structures and was associated with microtubules. Bimolecular fluorescence complementation assays showed that three proteins, N, P, and M, self‐interact, protein N plays a role in the formation of cytoplasm viroplasm, and protein M recruits N, P, P3, and G to microtubules. In addition, numerous paired proteins interact in the nucleus. This study presents the first evidence of a cytorhabdovirus infecting kiwifruit plants and full location and interaction maps to gain insight into viral protein functions. John Wiley and Sons Inc. 2021-07-20 /pmc/articles/PMC8435229/ /pubmed/34288324 http://dx.doi.org/10.1111/mpp.13110 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wang, Yanxiang Wang, Guoping Bai, Jianyu Zhang, Yongle Wang, Ying Wen, Shaohua Li, Liu Yang, Zuokun Hong, Ni A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title | A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title_full | A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title_fullStr | A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title_full_unstemmed | A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title_short | A novel Actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
title_sort | novel actinidia cytorhabdovirus characterized using genomic and viral protein interaction features |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8435229/ https://www.ncbi.nlm.nih.gov/pubmed/34288324 http://dx.doi.org/10.1111/mpp.13110 |
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