Prochilodus lineatus (Valenciennes, 1836) is a detritivorous teleost popularly known as curimba or curimbatá, is widely distributed in South American rivers and attains a relatively large size, with some specimens measuring 75 cm in length and weighing 8.2 kg (Godoy 1975). It has a high reproductive capacity, rapid growth, good acceptance on the market and is one of the most consumed fish species in Brazil. Its consumption has led to increased interest in its cultivation in fish farms throughout the country.Until recently, Myxobolus porofilus Adriano, Aranas, Ceccarelli et Cordeiro, 2002 was the only myxosporean species reported to parasitize P. lineatus. However, during a survey of myxosporean parasites of fish species cultivated in Brazil, we found a new species of Henneguya parasitizing the gills of P. lineatus. This species is described based on light microscopy, scanning electron microscopy, transmission electron microscopy, and on the histopathological effects produced in the host.
MATERIALS AND METHODSFour-month old specimens of P. lineatus (curimbatá), Piaractus mesopotamicus (Holmberg, 1887) (pacu), Brycon cephalus (Günther, 1869) (matrinxã) and Leporinus macrocephalus Garavello et Britski, 1988 (piauçu) obtained from artificial reproduction programs were released in a pond at the Center for the Research and Management of Continental Fishing Resources (Cepta/Ibama) located in the municipality of Pirassununga, state of São Paulo, Brazil. Each month, five specimens of each fish species were examined for the presence of myxozoan parasites from March 2000 to February 2002. Immediately after collection, the fish were transported alive to the laboratory where they were killed by transection of the spinal cord, before being measured and necropsied. Of 120 curimbatá examined, 20 were 7-15 cm long, 78 were 15.1-25 cm long and 22 were 25.1-30.5 cm long.The parasite was identified according to Lom and Arthur (1989). Measurements from 40 fresh mature spores were obtained using a ocular micrometer and are givem in micrometres (mm) as the mean ± standard deviation (SD). Smears containing free spores were stained with a Giemsa solution and mounted in low-viscosity mounting medium (Cytoseal) as permanent preparations. For histological analysis, the gills were fixed in 10% buffered formalin for 24 h, embedded in paraffin, cut into sections 4 µm thick and stained with sirius red (Adriano et al. 2002), haematoxylin and eosin, and PAS. For scanning electron microscopy, free spores were deposited on a coverslip coated with poly-L-lysine and fixed for 2 h at room temperature with glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.2). After washing in the same buffer, the preparations were dehydrated in ethanol, critical point dried by CO 2 , coated with metallic gold and examined in JEOL JSM 35 microscope operated at 15 kV. For transmission electron microscopy, fragments of gills containing plasmodia were fixed in 2.5% glutaraldeyde in cacodylate buffer (2 h), dehydrated in increasing concentrations of acetone and embe...