Your browser doesn't support javascript.
loading
Altering of host larval (Spodoptera exigua) calcineurin activity in response to ascovirus infection.
Yu, Huan; He, Lei; Li, Zi-Qi; Li, Ni; Ou-Yang, Yi-Yi; Huang, Guo-Hua.
Affiliation
  • Yu H; Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, P.R. China.
  • He L; College of Plant Protection, Hunan Agricultural University, Changsha, P.R. China.
  • Li ZQ; Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, P.R. China.
  • Li N; College of Plant Protection, Hunan Agricultural University, Changsha, P.R. China.
  • Ou-Yang YY; Hunan Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Hunan Agricultural University, Changsha, P.R. China.
  • Huang GH; College of Plant Protection, Hunan Agricultural University, Changsha, P.R. China.
Pest Manag Sci ; 76(3): 1048-1059, 2020 Mar.
Article in En | MEDLINE | ID: mdl-31515935
BACKGROUND: Calcineurin (CaN) is involved in numerous cellular processes and Ca2+ -dependent signal transduction pathways. According to our previous transcriptome studies, thousands of host larval (Spodoptera exigua) transcripts were downregulated after the infection of Heliothis virescent ascovirus 3h (HvAV-3h), while the Spodoptera exigua calcineurin genes (SeCaNs) were significantly upregulated. To understand the regulation of SeCaNs in S. exigua larvae during the infection of HvAV-3h, the functions of CaN subunit A (SeCaN-SubA) and CaN binding protein (SeCaN-BP) were analysed. RESULTS: The in vitro assays indicated that the bacterial expressed SeCaN-SubA is an acid phosphatase, but no phosphatase activity was detected with the purified SeCaN-BP. The transcription level of SeCaN-SubA was upregulated after HvAV-3h infection and the CaN activity was significantly increased after HvAV-3h infection in S. exigua larvae. Interestingly, the SeCaN-BP transcripts were only detectable in the HvAV-3h infected larvae. Further immunoblotting results consistently agree with those obtained by qPCR, indicating that the infection of HvAV-3h causes the upregulated expression of SeCaN-SubA and the appearance of SeCaN-BP. An interaction between the cleaved SeCaN-SubA and SeCaN-BP was detected by co-immunoprecipitation assays, and the expression of SeCaN-BP in Spodoptera frugiperda-9 (Sf9) cells can help to increase the CaN activity of SeCaN-SubA. Further investigations with CaN inhibitors suggested that HvAV-3h. Further investigations with CaN inhibitors suggested that the inhibition on host larval CaN activity can also inhibit the viral replication of HvAV-3h. CONCLUSION: The increase in CaN activity caused by HvAV-3h infection might be due to the upregulation of SeCaN-SubA and the induced expression of SeCaN-BP, and increased CaN activity is essential for ascoviral replication. © 2019 Society of Chemical Industry.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ascoviridae Limits: Animals Language: En Journal: Pest Manag Sci Journal subject: TOXICOLOGIA Year: 2020 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ascoviridae Limits: Animals Language: En Journal: Pest Manag Sci Journal subject: TOXICOLOGIA Year: 2020 Document type: Article Country of publication: