Immune depression in Rhodnius prolixus by seco-steroids, physalins

J Insect Physiol. 2008 Mar;54(3):555-62. doi: 10.1016/j.jinsphys.2007.12.004. Epub 2007 Dec 14.

Abstract

A comparative study of the effects of physalins, seco-steroidal substances of Physalis angulata (Solanaceae), on the immune reactions of R. prolixus was carried out. Ecdysis and mortality were not affected by treatment with physalins B, D, F or G (1-10 microg/ml of blood meal). R. prolixus larvae fed with blood containing physalins and inoculated with 1 microl of Enterobacter cloacae beta12 (5 x 10(3)/insect) exhibited mortality rates three times higher than controls. The insects treated with physalin B, and F (1 microg/ml) and inoculated with E. cloacae beta12 showed significant differences on lysozyme activity in the hemolymph compared to untreated insects. Furthermore, physalin D (1 microg/ml) significantly reduced the antibacterial activity. Concerning cellular immune reactions, all insects treated with physalins (1 microg/ml), exhibited drastic reductions in the quantity of yeast cell-hemocyte binding and subsequent internalization. Insects inoculated with bacteria and treated with physalins B, F and G showed reductions of microaggregate formation but physalin D did not. Physalins B and F also reduced total hemocyte count in the hemolymph. These results suggest that, in different ways, probably due to their different chemical structures, physalin B, D, F and G are immunomodulatory substances for the bloodsucking insect, R. prolixus.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enterobacter / immunology
  • Enterobacteriaceae Infections / immunology
  • Hemocytes / drug effects*
  • Host-Pathogen Interactions / drug effects
  • Host-Pathogen Interactions / immunology
  • Muramidase / metabolism*
  • Phagocytosis / drug effects*
  • Rhodnius / drug effects*
  • Rhodnius / microbiology
  • Rhodnius / physiology
  • Secosteroids / pharmacology*

Substances

  • Secosteroids
  • Muramidase