The use of primary murine fibroblasts to ascertain if Spirocerca lupi secretory/excretory protein products are mitogenic ex vivo.

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  • Additional Information
    • Source:
      Publisher: BioMed Central Country of Publication: England NLM ID: 101249759 Publication Model: Electronic Cited Medium: Internet ISSN: 1746-6148 (Electronic) Linking ISSN: 17466148 NLM ISO Abbreviation: BMC Vet Res Subsets: MEDLINE
    • Publication Information:
      Original Publication: London : BioMed Central, 2005-
    • Subject Terms:
    • Abstract:
      Background: Spirocerca lupi is a nematode that parasitizes vertebrates in particular canids, by forming nodules in the thoracic cavity specifically in the oesophagus. In 25% of Spirocerca infections of the domestic dog, nodules progress from inflammatory to pre-neoplastic to sarcomatous neoplasia. With the mechanism of neoplastic transformation being incompletely understood, this study investigates if S. lupi parasite proteinaceous secretory/excretory products (ESPs) play a role in the neoplastic transformation.
      Methods: To facilitate collection of ESPs, we maintained naturally harvested adult parasites in the laboratory under artificial conditions. Media in which the parasites were grown was subsequently evaluated for the presence of proteinaceous compounds using a mass spectroscopy library as well as for their ability to be mitogenic in primary murine fibroblastic cells.
      Results: Chromatrography of the ethyl acetate extracted incubation media showed the presence of 9 protein compounds, of which three were identified as non-specific proteins isolated from Nematostella vectensis, Caenorhabditis brenneri and Sus scrofa, with the rest being unknown. Acetone, methanol, hexane and ethylacetate extracted culture media were unable to induce a mitogenic change in primary murine fibroblasts in comparison to the controls.
      Conclusion: While no mitogenic effect was evident, further studies are required to understand the role of worm excretory/secretory products on clastogenesis under chronic exposure. In addition, while not of primary importance for this study, the observed duration of parasite survival indicates that ex vivo studies on S. lupi are possible. For the latter we believe that the worm culture method can be further optimized if longer survival times are required.
    • References:
      Parasitol Res. 2009 Apr;104(5):1011-6. (PMID: 19066964)
      Appl Environ Microbiol. 2003 Jan;69(1):92-6. (PMID: 12513981)
      J Parasitol. 1972 Feb;58(1):3-22. (PMID: 5012526)
      Vet Parasitol. 2004 Jan 30;119(2-3):209-21. (PMID: 14746980)
      Vet Parasitol. 2012 Nov 23;190(1-2):185-90. (PMID: 22770706)
      Vet Parasitol. 2010 Feb 26;168(1-2):71-7. (PMID: 19963322)
      World J Gastroenterol. 2006 Jun 14;12(22):3585-92. (PMID: 16773716)
      Vet J. 2008 Jun;176(3):294-309. (PMID: 17512766)
      J Vet Intern Med. 2011 Jul-Aug;25(4):963-6. (PMID: 21615495)
      Parasite Immunol. 2011 Oct;33(10):545-53. (PMID: 21770972)
      Vet Parasitol. 2002 Aug 2;107(3):235-50. (PMID: 12127253)
      Vet Parasitol. 1996 May;63(1-2):83-94. (PMID: 8792583)
      Science. 1985 Apr 5;228(4695):89-91. (PMID: 3975633)
      Int J Parasitol. 1996 Jan;26(1):25-35. (PMID: 9198593)
      Vet Radiol Ultrasound. 2001 Mar-Apr;42(2):119-29. (PMID: 11327359)
      Mol Biochem Parasitol. 1992 Jul;53(1-2):135-48. (PMID: 1501633)
    • Contributed Indexing:
      Keywords: Ex vivo culture; Mitogenic; Murine fibroblasts; Spirocerca lupi; Viability
    • Accession Number:
      0 (Helminth Proteins)
      0 (Mitogens)
    • Publication Date:
      Date Created: 20170824 Date Completed: 20180322 Latest Revision: 20181202
    • Publication Date:
      20231215
    • Accession Number:
      PMC5568052
    • Accession Number:
      10.1186/s12917-017-1162-9
    • Accession Number:
      28830546