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Morphological Studies of Developmental Stages of Oculotrema hippopotami (Monogenea: Polystomatidae) Infecting the Eye of Hippopotamus amphibius (Mammalia: Hippopotamidae) Using SEM and EDXA with Notes on Histopathology

  • Rubtsova, Nataliya Yu. (Institute of Parasitic Diseases (IPD)) ;
  • Heckmann, Richard A. (Department of Biology, Brigham Young University) ;
  • Smit, Willem J. (Department of Biodiversity, University of Limpopo) ;
  • Luus-Powell, Wilmien J. (Department of Biodiversity, University of Limpopo) ;
  • Halajian, Ali (Department of Biodiversity, University of Limpopo) ;
  • Roux, Francois (Mpumalanga Tourism and Parks Agency)
  • Received : 2018.05.19
  • Accepted : 2018.10.09
  • Published : 2018.10.31

Abstract

The present study was performed to observe histopathological effects of Oculotrema hippopotami Stunkard, 1924 infection in the eye of Hippopotamus amphibius, as well as to reveal new details of morphology and structural features of this monogenean and its comparison between 2 age stages of the parasite. This was done using both light and scanning electron microscopy, energy dispersive X-ray analysis (EDXA) and histopathology. The presence of a mixture of different generations (adult and sub-adult) in one host individual is common for Oculotrema Stunkard, 1924 in contrast to Polystoma Zeder, 1800. New metrical and graphical information obtained for adults and sub-adults compared with the previous studies. Here we show the presence of genital papillae in adults, metrical data on the distal part of the vas deferens. SEM micrographs of sperm ejaculatory structures and information about the flattened dorsal side of the body provided for the first time. Histopathological changes, such as necrosis and hemorrhage in host tissues as a result of O. hippopotami attachment structures are described. Structural analysis of different body parts of O. hippopotami of both age groups are also included. We show qualitative differences in the presence of hardening ions (S, P, Ca) in attachment structures (oral and haptor suckers) that increase with the age of the worm. The presence of sub-adults and adults on the same host, together with high levels of infection without high pathogenicity may account for Oculotrema being one of the most successful parasites among the Monogenea.

Keywords

References

  1. Thurston JP, Laws RM. Oculotrema hippopotami (Trematoda: Monogenea) in Uganda. Nature 1965; 205: 1127.
  2. Jooste R. A checklist of the helminth parasites of the larger domestic and wild mammals of Zimbabwe. Trans Zimbabwe Sci Assoc 1990; 64: 15-32.
  3. McCully RW, van Niekerk JW, Kruger SP. Observation of the pathology of bilharsiasis and other parasitic infestations of Hippopotamus Linnaeus, 1758, from the Kruger National Park. Onderstepoort J Vet Res 1967; 34: 563-617.
  4. Du Preez LH, Moeng IA. Additional morphological information on Oculotrema hippopotami Stunkard, 1924 (Monogenea: Polystomatidae) parasitic on the African hippopotamus. Afr Zool 2004; 39: 225-233. https://doi.org/10.1080/15627020.2004.11657219
  5. Stunkard HW. A new trematode, Oculotrema hippopotami n.g., n.sp, from the eye of the hippopotamus. Parasitology 1924; 16: 436-440. https://doi.org/10.1017/S0031182000020333
  6. Tinsley RC. The oncomiracidium of Oculotrema hippopotami Stunkard, 1924 and relationships within the Polystomatidae (Monogenea). Syst Parasitol 2013; 84: 123-135. https://doi.org/10.1007/s11230-012-9392-5
  7. Thurston JP. The larva of Oculotrema hippopotami (Monogenea: Polystomatidae). J Zool 1968; 154: 475-480.
  8. Thurston JP. Haemoglobin in a Monogenean, Oculotrema hippopotami. Nature 1970; 228: 578-579. https://doi.org/10.1038/228578a0
  9. Theunissen M. Morphology and functioning of attachment organs of the Polystomatidae (Monogenea) [master's thesis]. [Potchefstroom]: North-West University; 2014, pp 1-159.
  10. Halajian A, Luus-Powell WJ, Roux F, Nakao M, Sasako M, Lavikainen A. Echinococcus felidis in hippopotamus, South Africa. Vet Parasitol 2017; 243: 24-28. https://doi.org/10.1016/j.vetpar.2017.06.001
  11. Lee RE. Scanning Electron Microscopy and X-ray Microanalysis. Englewood Cliff, USA. Prentice Hall. 1993, pp 1-458.
  12. Bancroft JD, Gamble M. Theory and Practice of Histological Techniques. 5th ed. Edinburgh, UK. Churchill Livingston. 2001, pp 1-800.
  13. Keinan JA. Histological and Histochemical Methods: Theory and Practice. Edinburgh, UK. Churchill Livingston. 2001, pp 1-520.
  14. Galigher AE, Kozloff EN. Essentials of Practical Microtechnique. 2nd ed. Philadelphia, USA. Lee & Febiger. 1971, pp 1-531.
  15. Miroshnichenko AI. Monogeneans of freshwater fish of Crimea. In Scarlato OA ed, Studies of Monogeneans in the USSR. Leningrad, USSR. Zoological Institute of Academy of Sciences of USSR. 1977, pp 102-103 (in Russian).
  16. Tinsley RC, Jackson JA. Host factors limiting monogenean infections: a case study. Int J Parasitol 2002; 32: 353-365. https://doi.org/10.1016/S0020-7519(01)00336-8
  17. Halton DW, Jennings JB. Observation on the nutrition of monogenetic trematodes. Biol Bull 1965; 129: 257-272. https://doi.org/10.2307/1539843
  18. Moeng IA, Du Preez LH. Oral sucker morphology of two polystomatids (Monogenea): one blood feeding and one mucous feeding. Microsc Soc South Africa 1997; 27: 116.
  19. Rubtsova NYu, Heckmann RA. Morphological and structural differences of normal adult and sub-adult bladder forms of Polystoma integerrimum (Frohlich, 1798) (Monogenea: Polystomatidae) from the common frog, Rana temporaria. Sci Parasitol 2017; 18: 38-53.
  20. Moeng IA. Aspects of the morphology and life history of Oculotrema hippopotami (Polystomatidae: Monogenea) [master's thesis]. [Bloemfontein]: University of the Orange Free State Bloemfontein; 1999, pp 1-108.
  21. Rubtsova NYu. Redescription and variability of Polystoma mazurmovici and P. skuratovitchi (Monogenea, Polystomatidae), with a key to Polystoma from anurans of Ukraine. Vestn Zool 2018; 52: 91-100. https://doi.org/10.2478/vzoo-2018-0011
  22. Roberts LS, Janovy J Jr. Foundations of Parasitology. 5th ed. Boston, USA. Wm. C. Brown Publishers. 1996, pp 281-296.
  23. Amin OM, Heckmann RA, Bannai MA. Cavisoma magnum (Cavisomidae), a unique Pacific acanthocephalan redescribed from an unusual host, Mugil cephalus (Mugilidae), in the Arabian Gulf, with notes on histopathology and metal analysis. Parasite 2018; 25: 5. https://doi.org/10.1051/parasite/2018006
  24. Amin OM, Heckmann RA, Mohammed O, Evans RP. Morphological and molecular descriptions of Moniliformis saudi sp. n. (Acanthocephala: Moniliformidae) from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg) in Saudi Arabia, with a key to species and notes on histopathology. Folia Parasitol 2016; 63: 14.
  25. Amin OM, Heckmann RA. Neoandracantha peruensis n. gen. n. sp. (Acanthocephala, Polymorphidae) described from cystacanths infecting the ghost crab Ocypode gaudichaudii on the Peruvian coast. Parasite 2017; 24: 40. https://doi.org/10.1051/parasite/2017038
  26. Amin OM, Heckmann RA. Rhadinorhynchus oligospinosus n. sp. (Acanthocephala, Rhadinorhynchidae) from mackerels in the Pacific Ocean off Peru and related rhadinorhynchids in the Pacific, with notes on metal analysis. Parasite 2017; 24: 19. https://doi.org/10.1051/parasite/2017022

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