{"title":"Genetic diversity, genotyping and evolutionary history of the global population of Orthotospovirus tomatomaculae genomic segments","authors":"Majid Siampour, Sajedeh Noorbakhsh, Keramatollah Izadpanah","doi":"10.1111/aab.12960","DOIUrl":null,"url":null,"abstract":"<p>Tomato spotted wilt virus (<i>Orthotospovirus tomatomaculae</i>; TSWV) is a destructive pathogen that affects over 1000 plant species worldwide. To elucidate its evolutionary mechanisms, genetic diversity and emergence timeline, we examined around 100 TSWV isolates with complete genome sequences available in GenBank. This study also included the complete genome of a TSWV isolate, IRP4, which has recently been implicated in an outbreak affecting greenhouse-grown bell peppers in Iran. Pairwise genetic divergence analysis revealed varying levels of genetic differences among TSWV RNA segments. Phylogenetic and sequence analysis determined that the global TSWV population consists of three major groups based on each of the three RNA segments (L, M, and S). Results suggested multiple introductions of the virus into different regions, indicating that the geographical origin of the isolates is not the sole factor determining their phylogenetic grouping. The large incongruences observed in the phylogeny of the TSWV segments and the analysis of genetic diversity patterns highlight extensive reassortment events in TSWV. As a result, 11 genotypes were identified within the TSWV population. The Iranian IRP4 isolate, along with nine other isolates from Europe, Asia, and South America shared a common genotype designated L3-M1-S1. This suggests that this potentially reassortant genotype has undergone long-distance intercontinental movement. Similar to IRP4, the majority of TSWV isolates with the L3-M1-S1 genotype were also obtained from pepper, suggesting a potential role of the host plant in the evolution of this genotype. Furthermore, temporal analysis suggests that the existing population of TSWV, circulating between 1996 and 2023, originated from a common ancestor that existed 107–284 years ago. The population size of TSWV experienced a significant expansion for 10–15 years since 1980 and then remained constant until recently.</p>","PeriodicalId":7977,"journal":{"name":"Annals of Applied Biology","volume":"186 3","pages":"232-247"},"PeriodicalIF":2.2000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Applied Biology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/aab.12960","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Tomato spotted wilt virus (Orthotospovirus tomatomaculae; TSWV) is a destructive pathogen that affects over 1000 plant species worldwide. To elucidate its evolutionary mechanisms, genetic diversity and emergence timeline, we examined around 100 TSWV isolates with complete genome sequences available in GenBank. This study also included the complete genome of a TSWV isolate, IRP4, which has recently been implicated in an outbreak affecting greenhouse-grown bell peppers in Iran. Pairwise genetic divergence analysis revealed varying levels of genetic differences among TSWV RNA segments. Phylogenetic and sequence analysis determined that the global TSWV population consists of three major groups based on each of the three RNA segments (L, M, and S). Results suggested multiple introductions of the virus into different regions, indicating that the geographical origin of the isolates is not the sole factor determining their phylogenetic grouping. The large incongruences observed in the phylogeny of the TSWV segments and the analysis of genetic diversity patterns highlight extensive reassortment events in TSWV. As a result, 11 genotypes were identified within the TSWV population. The Iranian IRP4 isolate, along with nine other isolates from Europe, Asia, and South America shared a common genotype designated L3-M1-S1. This suggests that this potentially reassortant genotype has undergone long-distance intercontinental movement. Similar to IRP4, the majority of TSWV isolates with the L3-M1-S1 genotype were also obtained from pepper, suggesting a potential role of the host plant in the evolution of this genotype. Furthermore, temporal analysis suggests that the existing population of TSWV, circulating between 1996 and 2023, originated from a common ancestor that existed 107–284 years ago. The population size of TSWV experienced a significant expansion for 10–15 years since 1980 and then remained constant until recently.
期刊介绍:
Annals of Applied Biology is an international journal sponsored by the Association of Applied Biologists. The journal publishes original research papers on all aspects of applied research on crop production, crop protection and the cropping ecosystem. The journal is published both online and in six printed issues per year.
Annals papers must contribute substantially to the advancement of knowledge and may, among others, encompass the scientific disciplines of:
Agronomy
Agrometeorology
Agrienvironmental sciences
Applied genomics
Applied metabolomics
Applied proteomics
Biodiversity
Biological control
Climate change
Crop ecology
Entomology
Genetic manipulation
Molecular biology
Mycology
Nematology
Pests
Plant pathology
Plant breeding & genetics
Plant physiology
Post harvest biology
Soil science
Statistics
Virology
Weed biology
Annals also welcomes reviews of interest in these subject areas. Reviews should be critical surveys of the field and offer new insights. All papers are subject to peer review. Papers must usually contribute substantially to the advancement of knowledge in applied biology but short papers discussing techniques or substantiated results, and reviews of current knowledge of interest to applied biologists will be considered for publication. Papers or reviews must not be offered to any other journal for prior or simultaneous publication and normally average seven printed pages.