“…Since its isolation, H. roitmani has appeared to be quite a remarkable trypanosomatid: (a) it is a member of a restricted group of symbiont-bearing trypanosomatids, which includes Crithidia deanei (Carvalho 1973), C. desouzai (Fiorini et al 1989), C. oncopelti (Newton and Horne 1957), Blastocrithidia culicis (Novy et al 1907), and T. cobitis (Lewis and Ball 1980); (b) it was ®rst described as a member of the Crithidia genus, mainly due its morphology that closely resembles choanomastigotes (Fiorini et al 1989); (c) it was reclassi®ed as Herpetomonas (Faria-e-Silva et al 1991) based on the opisthomastigote forms and on isoenzymatic analysis; (d) opisthomastigotes of H. roitmani could be obtained in a high yield (98%) and it was shown that they can proliferate in culture, unlike other Herpetomonas species (Faria-e-Silva et al 1996); (e) recent studies (Teixeira et al 1997) suggest that H. roitmani may represent a new group of¯agellates, and it was suggested to use the term opisthomorph (OPM) to designate forms in which the kinetoplast is located posteriorly to the nucleus (as in opisthomastigotes) but have a body shape somewhat resembling choanomastigote forms. In view of these characteristics, we decided to analyze further the transformation process of promastigote (PRO) into OPM forms in H. roitmani, investigating the changes that occur on the surface-exposed carbohydrate residues and also in the surface anionic sites.…”