- Plasmatocyte spreading peptide does not induce Microplitis demolitor polydnavirus-infected plasmatocytes to spread on foreign surfaces
- 作者: Strand, M.R.; Clark, K.C. and Gardiner, E.M.M
- literature id: 43902
- catalog nub: TPL_STRAND1999PSPDN41005200
- 文献库: Taxapad收录文献
- type: article
- publication name: Archives of Insect Biochemistry and Physiology
- publish date: 1999-01-01
- pages: 41-52
- volume: I
- 创建时间: 2021-03-02 15:00:32
- create by: zxmlmq (admin)
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comment:
Pseudoplusia includens; PROTEINS-; Plasmatocyte spreading peptide, role in parasite encapsulation; Effect of infection by hymenopteran parasite virus; HAEMOCYTES-; HYMENOPTERAN-PARASITES; Microplitis demolitor; Parasite encapsulation by host plasmatocyte, effect of parasite virus; VIRAL-DISEASES; Polydnavirus of hymenopteran parasite; Plasmatocyte infection, effect on parasite encapsulation; ENCAPSULATION-; Plasmatocyte response to hymenopteran parasite; Effect of plasmatocyte infection by parasite virus Microplitis demolitor; MUTUALISM-; Polydnavirus; Lepidopteran host plasmatocyte infection, effect on parasite encapsulation; LEPIDOPTERAN-HOSTS; Pseudoplusia includens; Parasite encapsulation by host plasmatocyte, effect of parasite virus Capsule formation by the moth Pseudopulsia includens requires that plasmatocytes change from being nonadhesive cells in circulation to strongly adhesive cells capable of attaching to the foreign target and one another. This change in adhesive state is induced by Plasmatocyte Spreading Peptide (PSP1); a 23 amino acid peptide isolated from P. includens plasma. Plasmatocytes from hosts parasitized by Microplitis demolitor remain in a nonadhesive state after infection by Microplitis demolitor polydnavirus (MdPDV). This alteration in plasmatocyte function prevents P. includens from encapsulating the developing parasitoid. In the current study, we examined whether MdPDV infection eliminates PSP1-responsive plasmatocytes from circulation or disrupts the ability of PSP1 to induce adhesion and spreading of plasmatocytes to foreign surfaces. In vivo experiments revealed that infection of P. includens by MdPDV induced an increase in the total number of hemocytes in circulation but reduced the proportion of hemocytes in circulation that were plasmatocytes. However, plasmatocytes normally capable of responding to PSP1 were not eliminated from circulation. Both in vivo and in vitro experiments indicated that plasmatocytes inoculated with MdPDV lost the capacity to respond to PSP1 4-6 h post-infection. Infection of P. includens with MdPDV reduced expression levels of prepro-PSP1 mRNA in hemocytes but did not appear to alter expression levels in fat body. none
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