IMMUNOFLUORESCENT VISUALIZATION OF THE EXCRETORY AND GUT SYSTEM OF SCHISTOSOMA-MANSONI BY CONFOCAL LASER-SCANNING MICROSCOPY

Conventional epifluorescence microscopy (CEM) and confocal laser scann ing microscopy (CLSM) were used to visualize the excretory system and the gut on whole organisms of different life-cycle stages of Schistoso ma mansoni. To visualize the gut system, an anti-circulating anodic an tigen (CAA) monoclonal antibody (MAb) (120-1B10-A) was used, whereas t he excretory system was immunohistochemically stained with an antiflam e cell MAb (51-4H8-A) and with a recently described anti-egg MAb (114- 5B1-A). The CEM procedure resulted in clear images at low magnificatio n but the signal-to-noise ratio on the higher magnification images was very poor. Using CLSM on the adult worm, the 114-581-A MAb demonstrat ed a well-defined system of canals that could be morphologically ident ified as the excretory system. The flame eels terminating the branches of the excretory canals showed a clear immunoreactivity with the 114- 5B1-A MAb as well as with the specific flame cell MAb. The gut system could be visualized, using an anti-CAA MAb, as two well-defined bands throughout the length of the parasite. Application of the 114-5B1-A MA b on cercariae revealed a strong fluorescence on the cercarial surface , whereas no immunoreactivity could be detected on internal structures . Whole eggs showed a bright fluorescence of the egg shell, whereas mi racidia showed immunoreactivity of the germinal cells located in the c enter of the organism. The CLSM procedure, especially with the recentl y introduced fast photon-counting option, provides a superior tool to investigate the three-dimensional localization of different epitopes o n immunofluorescently stained whole mounts of multicellular organisms in comparison with CEM. The advent of new visualization techniques to exactly localize epitopes of newly discovered MAbs can be of great sig nificance in the development of new screening tests. The identificatio n of epitopes on the different life-cycle stages of this clinically im portant trematode is valuable for the improvement of therapeutic and p rophylactic strategies.