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Light and electron microscopic study on Henneguya suprabranchiae Landsberg, 1987 (Myxozoa: Myxosporea) infecting Oreochromis niloticus, a new host record

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Abstract

Out of 58 live tilapia fish, five Oreochromis niloticus were found to be naturally infected with Henneguya suprabranchiae (8.62%). Such infection was recorded only during winter season from Bahr Shebin, a tributary of the River Nile at Menoufia Governorate, Nile Delta, Egypt. Based on the structure and measurements of fresh spores, this parasite was identified as H. suprabranchiae. Spores are oval in shape and they measure 15 (13–16) × 5 (4–6) µm length by width. It has two polar capsules inside and they measure 4 (5–7) × 1 (2–3) μm length by width. Each polar capsule has spirally coiled (7–9 turns) polar filament. The plasmodia as well as all other parasitic stages were described using light and transmission electron microscopy and discussed regarding to those of other fish hosts especially those of Africa.

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References

  • Abdel-Ghaffar F, El-Shahawi G, Naas S (1995) Myxosporidia infecting some Nile fishes in Egypt. Parasitol Res 81:163–166

    Article  PubMed  CAS  Google Scholar 

  • Abdel-Ghaffar F, Abdel-Baki, El-Garhy M (2005) Ultrastructural characteristics of the sporogenesis of genus Myxobolus infecting some Nile fishes in Egypt. Parasitol Res 88:617–626

    Google Scholar 

  • Ali MA (1999) Henneguya ghaffari sp. n. (Myxozoa: Myxosporea) infecting the Nile perch Lates niloticus (Teleostei: Centropomidae). Dis Aquat Org 38:225–230

    Article  PubMed  CAS  Google Scholar 

  • Adriano EA, Arana S, Cordeiro NS (2005) Histology, ultrastructure and prevalence of Henneguya piaractus (Myxosporea) infecting the gills of Piaractus mesopotamicus (Characidae) cultivated in Brazil. Dis Aquat Org 64:229–235

    Article  PubMed  CAS  Google Scholar 

  • Ashmawy KI, Abu-Elwafa A, Imam EA, El-Otifi YZ (1989) Description of newly recorded myxosporidian protozoa of freshwater fishes in Behera Province. J Egyp Vet Med Ass 49:43–53

    Google Scholar 

  • Azevedo C, Matos E (1989) Some ultrastructural data on the spore development in a Henneguya sp. parasite of the gill of a Brazilian fish. Parasitol Res 76:131–134

    Article  PubMed  CAS  Google Scholar 

  • Cheissin EM, Shulman SS, Vinnichenko LN (1961) Structure of Myxobolus spores. Tsitologiya 3:662–667 (in Russian, English summary)

    Google Scholar 

  • Cuadrado M, Albinyana G, Padrós F, Redondo MJ, Sitjà-Bobadilla A, Álvarez-Pellitero P, Palenzuela O, Diamant A, Crespo S (2007) An unidentified epi-epithelial myxosporean in the intestine of gilthead sea bream Sparus aurata L. Parasitol Res 101:403–411

    Article  PubMed  CAS  Google Scholar 

  • Current WL, Janovy J Jr (1976) Ultrastructure of interlamellar Henneguya exilis in the channel catfish. J Parasitol 62:975–981

    Article  PubMed  CAS  Google Scholar 

  • Current WL, Janovy J Jr (1978) Comparative study of ultrastructure of interlamellar and intralamellar types of Henneguya exilis Kudo from channel catfish. J Protozool 25:56–65

    PubMed  CAS  Google Scholar 

  • Current WL, Janovy J Jr, Knight SA (1979) Myxosoma funduli Kudo (Myxosporida) in Fundulus kansae: ultrastructure of the plasmodium wall and sporogenesis. J Protozool 26:574–583

    Google Scholar 

  • Desser SS, Paterson WB (1978) Ultrastructural and cytochemical observation on sporogenesis of Myxobolus sp. (Myxosporidia) from common shiner Natropis coronutus. J Protozool 25:314–326

    PubMed  CAS  Google Scholar 

  • Desser SS, Molnar K, Weller I (1983) Ultrastructure of sporogenesis of Thelobanellus nikolskii Akkhmerov, 1955 (Myxozoa: Myxosporea) from the common carp Cyprinus carpio. J Parasitol 69:504–518

    Article  Google Scholar 

  • Dykova I, Lom J (1987) Host cell hypertrophy induced by contact with trophozoites of Thelohanellus pyriformis (Myxozoa: Myxosporea). Arch Protistenkd 133:285–293

    Google Scholar 

  • El-Mansy A (2002) Immature stages and re-description of Henneguya suprabranchiae (Myxosporea: Myxobolidae), an intestinal parasite of the catfish Clarias gariepinus in the River Nile, Egypt. Dis Aquat Org 51:179–186

    Article  PubMed  Google Scholar 

  • El-Mansy AIE, Bashtar AR (2002) Histopathological and ultrastructural studies of Henneguya suprabranchiae Landsberg, 1987 (Myxosporea: Myxobolidae) parasitizing the suprabranchial organ of the freshwater catfish Clarias gariepinus Burchell, 1822 in Egypt. Parasitol Res 88:617–626

    Article  PubMed  CAS  Google Scholar 

  • El-Matbouli M, Hoffmann R (1989) Experimental transmission of two Myxobolus spp. developing bisporogeny via tubificid worms. Parasitol Res 75:461–464

    Article  PubMed  CAS  Google Scholar 

  • El-Matbouli M, Fisher-Scherl T, Hoffmann R (1990) Light and electron microscopic studies on Myxobolus cotti El-Matbouli and Hoffmann, 1987 infecting the central nervous system of the bullhead (Cottus gobio). Parasitol Res 76:219–227

    Article  PubMed  CAS  Google Scholar 

  • Fomena A, Bouix G (1997) Myxosporea (Protozoa: Myxozoa) of freshwater fishes in Africa: keys to genera and species. Syst Parasitol 37:161–178

    Article  Google Scholar 

  • Grupcheva G, Dykova I, Lom J (1985) Seasonal fluctuation in the prevalence of Sphaerospora renicola and myxosporean bloodstream stages in carp fingerlings in Bulgaria. Folia Parasitol 32:193–203

    Google Scholar 

  • Hulbert WC, Kommourdjian MP, Moon TW, Fenwich JC (1977) The fine structure of sporogony in Myxidium zealandicum (Protozoa: Myxosporidia). Can J Zool 55:438–447

    Article  Google Scholar 

  • Kent ML, Andree KB, Omewc JLB, El-Matbouli M, Desser SS, Devlin RH, Feist SW, Hedrick RP, Hoffmann RW, Khattra J, Hallett SL, Lester RJG, Longshaw M, Palenzeula O, Siddall ME, Xiao C (2001) Recent advances in our knowledge of the Myxozoa. J Eukaryot Microbiol 48(4):395–413

    Article  PubMed  CAS  Google Scholar 

  • Klontz GW, Rourke AW, Eckblad W (1986) The immune response during proliferative kidney disease in rainbow trout: a case history. Vet Immunol Immunopathol 12:387–383

    Article  PubMed  CAS  Google Scholar 

  • Komourdijia NP, Hulbert WC, Fenwick JC, Moon TW (1977) Description and first occurrence of Myxidium zealandicum (Protozoa: Myxosporidia) in the North American eel Anguilla rostrata Le Sueur. Can J Zool 55:52–59

    Google Scholar 

  • Kostoingue B, Diebakate C, Faye N, Toguebaye BS (2001) presence of Myxosporidea (Myxozoa: Myxosporea) of the genus Henneguya Thelohan, 1892 in freshwater fishes from Chad (Central Africa). Acta Protozool 40:117–123

    Google Scholar 

  • Listebarger JK, Mitchell LG (1981) Plasmodial ultrastructure and cytochemistry of the myxozoan, Chloromyxum trijugum. In Progress in Protozoology, VIth International Congress of Protozoology, Warsaw, p. 219

  • Lom J (1969) Notes on the ultrastructure and sporoblast development in fish parasitizing myxosporidian of the genus Sphaeromyxa. Z Zellforsch 97:416–437

    Article  PubMed  CAS  Google Scholar 

  • Lom J, Vavra J (1963) Mucous envelopes of spores of the subphylum cnidospora (Doflein, 1901). Vestin Ceskoslov Spol Zoo1 27:4–6

    Google Scholar 

  • Lom J, de Puytorac P (1965) Studies on the myxosporidian ultrastructure and polar capsule development. Protistologica 1:53–65

    Google Scholar 

  • Lom J, Arthur JR (1989) A guideline for the preparation of species descriptions in Myxosporea. J Fish Dis 12:151–156

    Article  Google Scholar 

  • Lom J, Noble ER (1984) Revised classification of the class Myxosporea Bütschli, 1881. Folia Parasitol 31:193–205

    Google Scholar 

  • Lom J, Dykova I (1992) Protozoan parasites of fish. Elsevier, Amsterdam

    Google Scholar 

  • Lom J, Dykova I, Lhotakova S (1982) Fine structure of Sphaerospora renicola Dykova and Lom, 1982. A myxosporean pansporoblasts. Protistologica 18:489–502

    Google Scholar 

  • Lom J, Molnar K, Dykova I (1986) Hoferellus gilsoni (Debaissieux, comb. n.) (Myxozoa, Myxosporea): redescription and mode of attachment to the epithelium of the urinary bladder of its host, the European eel. Protistologica 22:405–413

    Google Scholar 

  • Luft JH (1961) Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol 9:409–410

    Article  PubMed  CAS  Google Scholar 

  • Martins ML, Onaka EM (2006) Henneguya garavelli n. sp. and Myxobolus peculiaris n. sp. (Myxozoa: Myxobolidae) in the gills of Cyphocharax nagelli (Osteichthyes: Curimatidae) from Rio do Peixe Reservoir, Sao José do Rio Pardo, Sao Paulo, Brazil. Vet Parasitol 137:253–261

    Article  PubMed  CAS  Google Scholar 

  • Martins ML, Souza VN, Moraes JRE, Moraes FR (1999) Gill infection of Leporinus macrocephalus Garavello & Britski, 1998 (Osteichthyes: Anostomidae) by Henneguya leporinicola n. sp. (Myxozoa: Myxobolidae). Description, histopathology and treatment. Rev Bras Biol 59:527–534

    PubMed  CAS  Google Scholar 

  • Matos E, Tajdari J, Azevedo C (2005) Ultrastructural studies of Henneguya rhamdi n. sp. (Myxozoa) a parasite from the Amazon teleost fish, Rhamdia quelen (Pimelodidae). J Eukaryot Microbiol 52:532–537

    Article  PubMed  Google Scholar 

  • Pulsford A, Matthews RA (1982) An ultrastructure study of Myxobolus exiguus Thelohan, 1895 (Myxosporea) from gray mullet, Crenimugil labrosus (Risso). J Fish Dis 5:509–526

    Article  Google Scholar 

  • Schmahl G, Mehlhorn H, Taraschewski H (1989) Treatment of fish parasites. 7. Effects of sym. Triazinone (Toltrazuril) on developmental stages of Myxobolus sp. Butschli, 1882 (Myxosporea, Myxozoa): a light and electron microscopic study. Europ J Protistol 25:26–32

    Google Scholar 

  • Schubert G (1968) Elektronenmikroskopische Untersuchungen zur Sporenentwicklung von Henneguya pinnae Schubert (Sporozoa, Myxosporidia, Myxobolidae). Parasitol Res 30:57–77

    CAS  Google Scholar 

  • Seagrave C, Bucke D, Alderman D (1980) The causative agent of proliferative kidney disease may be a member of the Haplosporidia. In: Ahne W (ed) Fish diseases. Springer, Berlin, pp 174–181

    Google Scholar 

  • Wessels NS, Spooner BS, Ash KR, Bradley MO, Luduena MA, Taylor EL, Wrenn JT, Yamada, KM (1971) Microfilaments in cellular and developmental processes. Science 171:135–143

    Article  Google Scholar 

  • Williams JA, Wolff J (1970) Possible role of microtubules in thyroid secretion. Proc Nat Acad Sci USA 67:1901–1908

    Google Scholar 

  • Wolf K, Markiw ME, Hiltunen JK (1986) Salmonid whirling disease: Tubifex tubifex (Müller) identified as the essential oligochaete in the protozoan life cycle. J Fish Dis 9:83–85

    Article  Google Scholar 

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Acknowledgement

The authors are thankful for the funding support of Center of Excellence for Biodiversity Research, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.

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Correspondence to Fathy Abdel-Ghaffar.

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Abdel-Ghaffar, F., Abdel-Baki, AA.S., Bayoumy, E.M. et al. Light and electron microscopic study on Henneguya suprabranchiae Landsberg, 1987 (Myxozoa: Myxosporea) infecting Oreochromis niloticus, a new host record. Parasitol Res 103, 609–617 (2008). https://doi.org/10.1007/s00436-008-1019-z

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  • DOI: https://doi.org/10.1007/s00436-008-1019-z

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