Tomato spotted wilt orthotospovirus shifts sex ratio toward males in the western flower thrips, Frankliniella occidentalis, by down‐regulating a FSCB‐like gene

BACKGROUND Plant viruses can facilitate their transmission by modulating the sex ratios of their insect vectors. Previously, we found that exposure to tomato spotted wilt orthotospovirus (TSWV) in the western flower thrips, Frankliniella occidentalis, led to a male‐biased sex ratio in the offspring....

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Veröffentlicht in:Pest management science 2022-11, Vol.78 (11), p.5014-5023
Hauptverfasser: Tao, Min, Wan, Yanran, Zheng, Xiaobin, Qian, Kanghua, Merchant, Austin, Xu, Baoyun, Zhang, Youjun, Zhou, Xuguo, Wu, Qingjun
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Sprache:eng
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Zusammenfassung:BACKGROUND Plant viruses can facilitate their transmission by modulating the sex ratios of their insect vectors. Previously, we found that exposure to tomato spotted wilt orthotospovirus (TSWV) in the western flower thrips, Frankliniella occidentalis, led to a male‐biased sex ratio in the offspring. TSWV, a generalist pathogen with a broad host range, is transmitted primarily by F. occidentalis in a circulative‐propagative manner. Here, we integrated proteomic tools with RNAi to comprehensively investigate the genetic basis underlying the shift in vector sex ratio induced by the virus. RESULTS Proteomic analysis exhibited 104 differentially expressed proteins between F. occidentalis adult males with and without TSWV. The expression of the fiber sheath CABYR‐binding‐like (FSCB) protein, namely FoFSCB‐like, a sperm‐specific protein associated with sperm capacitation and motility, was decreased by 46%. The predicted FoFSCB‐like protein includes 10 classic Pro‐X‐X‐Pro motifs and 42 phosphorylation sites, which are key features for sperm capacitation. FoFSCB‐like expression was gradually increased during the development and peaked at the pupal stage. After exposure to TSWV, FoFSCB‐like expression was substantially down‐regulated. Nanoparticle‐mediated RNAi substantially suppressed FoFSCB‐like expression and led to a significant male bias in the offspring. CONCLUSION These combined results suggest that down‐regulation of FoFSCB‐like in virus‐exposed thrips leads to a male‐biased sex ratio in the offspring. This study not only advances our understanding of virus‐vector interactions, but also identifies a potential target for the genetic management of F. occidentalis, the primary vector of TSWV, by manipulating male fertility. © 2022 Society of Chemical Industry. The expression level of FoFSCB‐like was decreased by 46% in viruliferous male Frankliniella occidentalis. Nanomaterial‐mediated RNAi substantially suppressed FoFSCB‐like expression and led to a significant male‐biased offspring.
ISSN:1526-498X
1526-4998
DOI:10.1002/ps.7125