The aim of this study was to ascertain if the S. lupi adult parasite changed its surrounding environment through the release of secretory/excretory protein products, and whether any of these products could be the reason for the parasites ability to induce carcinogenic changes in the host. The latter was undertaken by placing live adult worms into specific media/saline for a limited period. Only the Iscoves’s and RPMI media showed a difference in their protein content in comparison to the said media prior to culture. Of the two, the Iscove’s media was selected for further analysis for the presence of a mitogenic effect, as preliminary TLC separation demonstrated the most intense staining bands (results not shown). In all cases the proteins identified were above 160 m/z. While in total nine additional proteins were identified on the spectra through LC-MSMS, only three of these were previously identified from other organisms. The three proteins have, however, thus far not been subjected to any further testing for the purpose of this study, nor could any published studies on the function or significance of these proteins be found. Another important question that should be answered is whether these proteins were from parasite or bacterial origin.
In an attempt to establish if these proteins could be mitogenic a cell culture assay was used. Following the exposure of fibroblasts to adult S. lupi ESPs (at various dilutions, 10, 20 and 30 μl), the in vitro fibroblasts were investigated in cytological preparation for an increase in mitotic rate, which would have been indicative of clastogenesis. For the exposure, murine fibroblasts were harvested and exposed to extracts of excretory/secretory substances for a period of 48 h. The principle of the assay was based on use of primary fibroblast cultures to ascertain the mitogenic effect of environmental chemicals, under in vitro conditions [13]. As an increase in fibroblast proliferation was evident in both the adult S. lupi ESPs extracts and in the organic solvent groups, we concluded that S. lupi ESPs had no additional mitogenic effect over and above that of the solvents alone under the conditions of the study design. While the absence of a mitogenic effect tends to suggest that the parasite is not inducing its effect via the release of secretory/excretory proteinaceous substances, the time progression of infection to tumour development in vivo still needs to be taken into consideration. As such we believe that to conclusively rule out the effect of potentially mitogenic compounds, it may be necessary to undertake repeated exposure of the primary fibroblast cultures, in such a manner that with the periodical media change, the excretory/secretory products are replenished over a longer period of time.
While the main objective of the study was to ascertain if the parasites were releasing potentially mitogenic secretory/excretory products, to achieve this the parasite had to be maintained outside of its host for a period of time. To our knowledge this is the first description of an attempt to maintain adult S. lupi worms alive outside of the host animal, even for the short periods required for this study, and thus warrants some discussion. The worms in question were collected opportunistically from recently euthanized dogs through dissection of their esophageal nodules and the physical removal of the worms, without the necessity for collagenase digestion. Following nodule dissection, the harvested worms were deemed viable according to our established criteria of being pink in color, having an intact esophagus and showing some, albeit varied, motility. It would therefore appear that the physical harvesting of the worms had no adverse effect on parasite viability. A qualitative difference in movement was present between the worms, possibly due to the delay to time of nodule dissection and/or the pre-cooling that happens on placement of carcasses into a refrigerator at 4 °C, indicating that delays in harvesting should preferably be avoided.
Following harvest, the worms were placed in saline as the control or within Ham’s F12 medium, DMEM, RPMI 1640 medium and / or Iscove’s modification of DMEM for five to 7 days under serum free conditions. These media were selected based on prior reports of their use in in vitro culture of other parasites such as Onchocerca spp. and Schistosoma spp., and these media are also the most commonly used media in mammalian cell culture. The media differed from each other in their amino acid and glucose content and in their buffering systems. For example, DMEM contained only sodium pyruvate and no buffer, RPMI 1640 medium contained only sodium bicarbonate as the buffer, Iscove’s modification of DMEM contained lower concentrations of bicarbonate as HEPES was included as the buffer and Ham’s F12 medium contained no buffer. In terms of their nutrient contents, the media contained different amino acids to support the growth of different cell types. Since S. lupi must survive off nutrients within their environment in esophageal nodules and with the selected cell media best representing the nutrient content within tissue fluid, it was speculated that these media would be able to meet the nutritional requirements of the parasite. Despite this, the parasites failed to thrive within the selected media with the worms progressively becoming weaker and more opaque until they died.
While we’re uncertain as to the exact reason for the earlier death of the parasites in the various media, this was most likely an indication of the parasite’s inability to utilise the nutrients within the media. This theory is supported by the measured change in pH of the media, as in all cases the parasites failed to modify the pH of the environment in which they were resident. From studies on Ascaris suum and H. contortus, one would have expected the parasite to modify their external environment to being a more acidic pH (circa pH 5 was reported for A. suum) [14, 15]. This pH modification is meant to arise from the excretion of the end-products of carbohydrate metabolism across the cuticle, in order to maintain the functionality of cuticle transporters. This would also explain why the parasites survived longer in the acidic saline, as the lower pH would have allowed for optimal functionality of the cuticle transporters for a longer period, with death probably eventually resulting from starvation as the incubation media was devoid of added nutrients. Support for the latter is evident by progressive increases in the parasite opaqueness, which from studies on H. contortus is an indication of glycogen stores depletion during starvation [16].
We propose some recommendations pertaining to future studies that potentially need the parasites to survive for a longer period of time. Firstly, the presence of E. coli, E. faecalis, P. aeruginosa and S. marcescens, indicates that the harvest of the parasites does result in the transfer of bacterial contaminants and that washing alone is not sufficient to remove them, warranting the need for antimicrobials in the media. Based on the organisms cultured, the aminoglycosides may a good antibiotic to include in the media. Nonetheless, we cannot at this stage associate the death of the parasite with the presence of the bacteria, as the four bacteria species were cultured equally well from all the media and the saline. The implication is that the bacteria cultured may be associated with the parasite, which is not uncommon as other nematode parasites have been reported to have bacteria attached to their cuticle e.g. urinary cysts caused by Strongylus edentatus are associated with genera such as Escherichia, Enterobacter and Streptococcus that are attached to the cuticle, while E coli and Pseudomonas have been associated with swine ascarids [17]. We also consider it unlikely that the bacteria were the cause of death of the parasites, especially since an intact cuticle purportedly protects nematode parasites against environmental insult [18]. Furthermore, living S. lupi parasites within esophageal nodules in infected dogs are routinely associated with purulent inflammation, necrotic cell debris and assorted bacteria in migratory tracts within these nodules. It may even be possible that the S. lupi parasite is the source of esophageal nodule contamination in a similar manner as described for S. edentatus cysts above.
A second consideration would be to lower the pH of the incubation media to 5 or 6, as the parasite may only be able to mobilise nutrients from the media at a lower pH, as seen with studies on Ascaris where it has been demonstrated that trans-cuticle transport is dependent on the pH of the surrounding environment [14]. Lastly perhaps the media should be supplemented with fetal calf serum (FCS). For this study, with the attempt being the characterization of excretory/secretory protein products, we kept the additions of exogenous proteins to the media to a minimum. This is in contrast with other studies for which fetal calf serum is commonly added to mammalian and parasite cell cultures as a source of albumin and growth factors. For the parasite Schistosoma spp., it has been shown that the parasite needs albumin for glycogen production, while supplementation with 10% FCS was vital for the prolonged viability of Oesophagostomum gutturosa adult parasites cultured in vitro using RPMI 1640 medium, Iscove’s Modified Dulbecco’s Medium and Minimum Essential Medium for 39 days [17]. The FCS is believed to provide parasites with necessary growth factors, e.g. platelet-derived growth factor (PDGF), epidermal growth factor (EGF), transforming growth factor-β (TGF-β) and insulin-like growth factor (IGF) [11].
