Native carp species cultured in Indian farms in Punjab (catla Catla catla, rohu Labeo rohita, mrigal Cirrhinus mrigala, exotic carps such as silver carp Hypophthalmichthys molitrix, grass carp Ctenopharyngodon idella, common carp Cyprinus carpio and a catfish Sperata seenghala) were examined for the presence of myxozoan parasites infecting gills. Firstly, the gills were examined under a zoom-stereomicroscope for the presence of plasmodia. The number of plasmodia per gill was counted to determine the index for the intensity of infection. Infected tissues were processed for histology, and 3−4 µm sections of infected gills were stained with haematoxylin & eosin and Luna's method. A total of 19 species of myxosporean were found infecting various cell types in the gills. Of these, 14 species belonged to the genus Myxobolus, 3 species to the genus Thelohanellus and 2 species to the genus Henneguya. Species belonging to the genus Myxobolus formed the interlamellar and intralamellar vascular (LV) type plasmodia, and species belonging to the genus Thelohanellus and Henneguya formed intrafilamental vascular (FV) type plasmodia. Mixed infections comprising 2, 3 or 4 different myxozoan species were noted in individual fish. The most common type of parasitism was polyparasitism due to 4 myxobolids co-occuring in fish with an infection rate of 23.16%. All species caused mild to severe haemorrhagic gill disease with little clinical symptomatology.KEY WORDS: Aquaculture · Parasite · Myxozoa · Gills · Freshwater fish
Resale or republication not permitted without written consent of the publisherDis Aquat Org 118: [129][130][131][132][133][134][135][136][137] 2016 analysis. The selected ponds were polyculture having Labeo rohita Hamilton (1882), Catla catla Hamilton (1882), Cirrhinus mrigala Hamilton (1882), Ctenopharyngodon idella Valenciennes in Cuvier & Valenciennes (1844), Cyprinus carpio Linnaeus (1758), Hypophthalmichthys molitrix Valenciennes (1844) and Sperata seenghala Sykes (1839). Organs such as gills, gall bladder, liver, heart, gut, eyes, fins, scales and skin were examined and were fixed in Bouin's fixative for histopathological studies. Besides gills, the infection was also recorded in the scales, fins, liver and gall bladder. Each plasmodium was picked under a stereozoom binocular with fine forceps and ruptured in normal saline (0.85%) on a glass slide and examined under a light microscope for the presence of spores. Fresh spores were studied under a phase contrast microscope (Magnus MLX-TR). Polar filaments were extruded by treating the spores with 8% KOH. The number of spores per plasmodium were counted under low magnification on a glass slide. One plasmodium was ruptured on a slide with the help of a fine needle then covered with a coverslip, and the number of spores were counted; 3 to 4 plasmodia were ruptured to obtain the average number of spores.To make dry preparations, thin smears were air dried, fixed in methanol and stained with Giemsa. In the case of permanent (wet) preparations, smears we...