Hostname: page-component-8448b6f56d-wq2xx Total loading time: 0 Render date: 2024-04-25T04:57:50.051Z Has data issue: false hasContentIssue false

Pathophysiology of Marshallagia marshalli in experimentally infected lambs

Published online by Cambridge University Press:  05 September 2013

NONA MORADPOUR
Affiliation:
Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Iran
HASSAN BORJI*
Affiliation:
Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Iran
GHOLAMREZA RAZMI
Affiliation:
Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Iran
MOHSEN MALEKI
Affiliation:
Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Iran
HOSSEIN KAZEMI
Affiliation:
Department of Clinical Sciences, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran
*
*Corresponding author: Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, P.O. Box 9177948974, Iran. E-mail: hborji@um.ac.ir

Summary

Species of Marshallagia are abomasal parasites in free-ranging and domesticated ungulates in temperate climatic zones throughout the world. Pervasiveness of these nematodes is significant in various parts of the world. There has been limited research in the area of Marshallagi amarshalli pathogenesis. The aim of this study was to investigate the effects of M. marshalli on the acid secretory capacity of the abomasal mucosa and the morphological changes due to parasitic migration to different parts of abomasal tissue in sheep. Ten lambs, approximately around 6 months old, were allotted to two groups of five (A and B). The sheep from group A were infected orally with a dose of 5000 third-stage larvae (L3) of M. marshalli whereas the sheep of group B were not infected. The results indicated that the development of M. marshalli in the abomasal glands of ruminants causes pathophysiological changes, which include a reduced acidity of the abomasal contents, increased abomasal pH and increased serum pepsinogen concentrations. The reduced acid secretion is explained by a replacement of functional parietal cells by undifferentiated cells. Histology changes include mucosal cell hyperplasia, loss of parietal cells and inflammatory cell infiltration, which includes numerous granulocytes and lymphocytes.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Altaş, M. G., Sevgili, M., Gökçen, A., Aksin, N. and Bayburs, H. C. (2009). The prevalence of gastro-intestinal nematodes in hair goats of the Sanliurfa region. Turkiye Parazitologii Dergisi 33, 2024.Google ScholarPubMed
Anderson, N., Reynolds, G. W. and Titchen, D. A. (1988). Changes in gastrointestinal mucosal mass and mucosal and serum gastrin in sheep experimentally infected with Ostertagia circumcincta. International Journal for Parasitology 18, 325331.CrossRefGoogle ScholarPubMed
Anderson, R. C. (2000). Nematode Parasites of Vertebrates, their Development and Transmission. CABI, Wallingford, UK.CrossRefGoogle Scholar
Armour, J., Jarrett, W. F. H. and Jennings, F. W. (1966). Experimental Ostertagia circumcincta infections in sheep: development and pathogenesis of a single infection. American Journal of Veterinary Research 27, 12671278.Google Scholar
Berghen, P., Dorny, P. and Vercruysse, J. (1987). Evaluation of a simplified blood pepsinogen assay. American Journal of Veterinary Research 48, 664669.Google ScholarPubMed
Borji, H., Raji, A. R. and Naghibi, A. (2011). The comparative morphology of Marshallagia marshalli and Ostertagia occidentalis (Nematoda: Strongylida, Trichostrongylidae) by scanning electron microscopy. Parasitology Research 108, 13911395. doi: 10.1007/s00436-010-2186-2.CrossRefGoogle ScholarPubMed
Conceição, M. A., Durão, R. M., Costa, I. H. and da Costa, J. M. (2002). Evaluation of a simple sedimentation method (modified McMaster) for diagnosis of bovine fascioliosis. Veterinary Parasitology 105, 337343.CrossRefGoogle ScholarPubMed
Dallas, J. F., Irvine, R. J. and Halvorsen, O. (2001). DNA evidence that Marshallagia marshalli Ransom, 1907 and M. occidentalis Ransom, 1907 (Nematoda: Ostertagiinae) from Svalbard reindeer are conspecific. Systematic Parasitology 51, 101103.CrossRefGoogle Scholar
Dunn, A. M. (1978). Veterinary Helminthology, 2nd Edn. William Heinemann Medical Books, London, UK.Google Scholar
El-Azazy, O. M. (1995). Seasonal changes and inhibited development of the abomasal nematodes of sheep and goats in Saudi Arabia. Veterinary Parasitology 58, 9198.CrossRefGoogle ScholarPubMed
Eslami, A., Meydani, M., Maleki, S. and Zargarzadeh, A. (1979). Gastrointestinal nematodes of wild sheep (Ovis orientalis) from Iran. Journal of Wildlife Diseases 15, 263265.CrossRefGoogle ScholarPubMed
Fox, M. T., Carroll, A. P., Hughes, S. A., Uche, U. E., Jacobs, D. E. and Vaillant, C. (1993). Gastrin and gastrin-related responses to infection with Ostertagia ostertagi in the calf. Research in Veterinary Science 54, 384391.CrossRefGoogle ScholarPubMed
Khalafalla, R. E., Elseify, M. A. and Elbahy, N. M. (2010). Seasonal prevalence of gastrointestinal nematode parasites of sheep in Northern region of Nile Delta, Egypt. Parasitology Research 108, 337340. doi: 10.1007/s00436-010-2066-9.CrossRefGoogle ScholarPubMed
Khan, M. N., Sajid, M. S., Khan, M. K., Iqbal, Z. and Hussain, A. (2010). Gastrointestinal helminthiasis: prevalence and associated determinants in domestic ruminants of district Toba Tek Singh, Punjab, Pakistan. Parasitology Research 107, 787794. doi: 10.1007/s00436-010-1931-x.CrossRefGoogle ScholarPubMed
Lawton, D. E. B., Reynolds, G. W., Hodgkinson, S. M., Pomroy, W. E. and Simpson, H. V. (1996). Infection of sheep with adult and larval Ostertagia circumcincta: effects on abomasal pH and serum gastrin and pepsinogen. Int ernational Journal of Parasitology 26, 10631074.Google Scholar
Levecke, B., Rinaldi, L., Charlier, J., Maurelli, M. P., Bosco, A., Vercuysse, J. and Cringoli, G. (2012). The bias, accuracy and precision of faecal egg count reduction test results in cattle using McMaster, Cornell–Wisconsin and FLOTAC egg counting method. Veterinary Parasitology 188, 194199. doi: 10.1016/j.vetpar.2012.03.017.CrossRefGoogle Scholar
Lichtenfels, J. R., Pilitt, P. A. and Lancaster, M. B. (1988). Systematics of the nematodes that cause ostertagiasis in cattle, sheep and goats in North America. Veterinary Parasitology 27, 312.CrossRefGoogle ScholarPubMed
Mead, R. and Curnow, R. N. (1983). Statistical Methods in Agriculture and Experimental Biology. Chapter 1. Chapman and Hall, London, UK.CrossRefGoogle Scholar
Nishikawa, N., Gruner, L., Giangaspero, M. and Tabbaa, D. (1995). Parasite nematode infections in Awassi adult sheep: distribution through Syrian farm flocks. Veterinary Research 26, 162167.Google ScholarPubMed
Orloff, I. W. (1933). Sur la reconstruction de la systématique du genre Ostertagia Ransom, 1907. Annales de Parasitology 11, 96111.Google Scholar
Rahman, W. A. and Collins, G. H. (1990). The establishment and development of Haemonchus contortus in goats. Veterinary Parasitology 35, 189193.CrossRefGoogle ScholarPubMed
Scott, I., Hodgkinson, S. M., Khalaf, S., Reynolds, G. W., Pomroy, W. E. and Simpson, H. V. (1998). Infection of sheep with adult and larval Ostertagia circumcincta: abomasal morphology. International Journal for Parasitology 28, 13831392.CrossRefGoogle ScholarPubMed
Scott, I., Khalaf, S., Simcock, D. C., Knight, C. G., Reynolds, G. W., Pomroy, W. E. and Simpson, H. V. (2000). A sequential study of the pathology associated with the infection of sheep with adult and larval Ostertagia circumcincta. Veterinary Parasitology 89, 7994.CrossRefGoogle ScholarPubMed
Simpson, H. V., Lawton, D. E. B., Simcock, D. C., Reynolds, G. W. and Pomroy, W. E. (1997). Abomasal secretion in sheep receiving adult that are prevented from contact with the mucosa. New Zealand Veterinary Journal 27, 825831.Google Scholar
Tariq, K. A., Chishti, M. Z., Ahmad, F. and Shawl, A. S. (2008). Epidemiology of gastrointestinal nematodes of sheep managed under traditional husbandry system in Kashmir valley. Veterinary Parasitology 158, 138143.CrossRefGoogle ScholarPubMed
Taylor, M. A., Coop, R. L. and Wall, R. L. (2007). Veterinary Parasitology. Blackwell, Oxford, UK.Google Scholar
Yamaguti, S. (1961). The Nematodes of Vertebrates, Part I and II. In Systema Helminthum, Vol. III, part 5, pp. 429430. Interscience, New York, USA.Google Scholar