4.5 Article

Transcriptional response of BmTo119-1 and RNAi machinery genes to exogenous dsRNA in the midgut of Bombyx mori

期刊

JOURNAL OF INSECT PHYSIOLOGY
卷 59, 期 6, 页码 646-654

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jinsphys.2013.03.013

关键词

Bombyx mori; To119-1; dsRNA; LPS Immune response

资金

  1. Research Council of Ghent University (BOF-UGent)
  2. Fund for Scientific ResearchFlanders (FWO-Vlaanderen, Belgium)
  3. General Secretariat for Research and Technology
  4. Hellenic Republic Ministry of National Education and Religious Affairs
  5. China Scholarship Council (CSC)
  6. Research Council of Ghent University

向作者/读者索取更多资源

Injection of dsRNA is widely applied to silence endogenous genes and study gene function in insects. However, it is not yet clear to what extent it can also exert non-specific effects, for instance by interference with the innate immune response. In this study, we report on the transcriptional response of BmTo119-1 to lipopolysaccharide (LPS) and dsRNA in the silkmoth, Bombyx mori. BmTo119-1 encodes a Toll receptor highly expressed in midgut tissue and that shows limited similarity to the mammalian TLR3 endolysosome receptor for dsRNA; while Dcr2 and Ago2 encode two key components of the RNAi machinery. An expression pattern study of all 14 Toll receptors in B. mori showed that BmTo119-1 was expressed in different larval and pupal tissues with the highest expression level detected in the midgut, indicating a possible function in immunity against pathogens taken up by the food. In order to investigate the response of BmTo119-1, different ways to deliver dsRNA, specific for GFP (dsGFP), and LPS were applied in Bombyx 5th instar larvae. The feeding experiments suggested that dsGFP did not suppress the expression of BmTo119-1 significantly, while LPS could suppress the expression of BmTo119-1 after 3 h of feeding. On the other hand, the injection experiments showed that dsGFP, as well as LPS, could significantly inhibit the expression of BmTo119-1 in 3 h. Bacteria that constantly expressed dsGFP could also down-regulate the expression of BmTo119-1 to a greater extent than bacteria that do not express dsGFP. The failure of dsGFP by-feeding to-affect the-expression-of BmTo119-1 was-correlated with-the-rapid-degradation-of-dsGFPby dsRNase in the midgut juice. Expression of the RNAi machinery genes Dcr2 and Ago2, as well as dsRNase, was also affected by injection of dsRNA and not by feeding, but in these cases an induction was observed instead of a down-regulation. Because LPS is a well-known pathogen-associated molecular pattern (PAMP), it suggested that the decrease in BmTo119-1 expression is a consequence of the activation of the innate immune response by LPS. The similar response of BmTo119-1 between the two triggers, LPS and dsRNA, suggests that dsRNA can also act as a PAMP in the midgut of Bombyx. Furthermore, induction of the genes Dcr2,Ago2 and dsRNase may also constitute a defense mechanism against invading dsRNA. (C) 2013 Elsevier Ltd. All rights reserved.

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