Integration of transcriptomics and network analysis reveals co-expressed genes in Frankliniella occidentalis larval guts that respond to tomato spotted wilt virus infection

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Publicado en:bioRxiv (Aug 15, 2021), p. n/a
Autor principal: Han, Jinlong
Otros Autores: Rotenberg, Dorith
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Cold Spring Harbor Laboratory Press
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Acceso en línea:Citation/Abstract
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022 |a 2692-8205 
024 7 |a 10.1101/2021.08.14.456355  |2 doi 
035 |a 2561332630 
045 0 |b d20210815 
100 1 |a Han, Jinlong 
245 1 |a Integration of transcriptomics and network analysis reveals co-expressed genes in Frankliniella occidentalis larval guts that respond to tomato spotted wilt virus infection 
260 |b Cold Spring Harbor Laboratory Press  |c Aug 15, 2021 
513 |a Working Paper 
520 3 |a Background: The arthropod gut is the first barrier to infection by viruses that are internally borne and transmitted persistently by arthropod vectors to plant and animal hosts. Tomato spotted wilt virus (TSWV), a plant-pathogenic virus, is transmitted exclusively by thrips vectors in a circulative-propagative manner. Frankliniella occidentalis (western flower thrips), the principal thrips vector of TSWV, is transmission-competent only if the virus is acquired by young larvae. To begin to understand the larval gut response to TSWV infection and accumulation, a genome-assisted, transcriptomic analysis of F. occidentalis gut tissues of first (early L1) and second (early L2 and late L2) instar larvae was conducted using RNA-Seq to identify differentially-expressed transcripts (DETs) in response to TSWV compared to non- exposed cohorts. Results: The larval gut responded in a developmental stage-dependent manner, with the majority of DETs (71%) associated with the early L1 stage at a time when virus infection is limited to the midgut epithelium. Provisional annotations of these DETs inferred roles in digestion and absorption, insect innate immunity, and detoxification. Weighted gene co-expression network analysis using all assembled transcripts of the gut transcriptome revealed eight gene modules that distinguish the larval development. Intra-module interaction network analysis of three most DET-enriched modules revealed ten central hub genes. Droplet digital PCR-expression analyses of select network hub and connecting genes revealed temporally-dynamic changes in gut expression during and post exposure to TSWV. Conclusion: These findings expand our understanding of the developmentally-mediated interaction between thrips vectors and orthotospoviruses, and provide opportunities for probing pathways for biomarkers of thrips vector competence. Competing Interest Statement The authors have declared no competing interest. 
653 |a Infections 
653 |a Transcriptomes 
653 |a Disease transmission 
653 |a Genomes 
653 |a Innate immunity 
653 |a Host plants 
653 |a Epithelium 
653 |a Arthropods 
653 |a Viruses 
653 |a Midgut 
653 |a Wilt 
653 |a Digestive system 
653 |a Genes 
653 |a Vectors 
653 |a Detoxification 
653 |a Developmental stages 
653 |a Plant viruses 
653 |a Transcriptomics 
653 |a Gastrointestinal tract 
653 |a Frankliniella occidentalis 
653 |a Tospovirus 
653 |a Orthotospovirus 
700 1 |a Rotenberg, Dorith 
773 0 |t bioRxiv  |g (Aug 15, 2021), p. n/a 
786 0 |d ProQuest  |t Biological Science Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/2561332630/abstract/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full text outside of ProQuest  |u https://www.biorxiv.org/content/10.1101/2021.08.14.456355v1