Stage-specific cuticular proteins of Ostertagia circumcincta and Ostertagia ostertagi

In this study we have shown that NHS-biotin and I¹²⁵-streptavidin can detect cuticular polypeptides of Ostertagia spp. The labelled polypeptide profile of intact nematodes is simple compared to the profile obtained by labelling homogenates. None of the major internal polypeptides are labelled and the subset of proteins labelled in intact nematodes appears to be mainly surface associated. The results presented here demonstrate that NHS-biotin may be used as a reagent for the analysis of surface polypeptides. The surface polypeptide profiles of the five major developmental stages (L1, L2, L3, L4 and adult) of Ostertagia circumcincta show a series of stage-specific molecules with no polypeptides common to all stages, indicating that the cuticle is a dynamic structure which changes throughout the life cycle. Similarity comparison of Ostertagia ostertagi L3 and L4 stage surface profiles showed that each stage is clearly distinct; comparison of these stages between the two species shows an overall similarity.     

The glucose metabolism of adult Ostertagia circumcincta, in vitro

Adult Ostertagia circumcincta from freshly killed sheep were incubated at 39 degrees C in a medium containing inorganic salts, antibiotics and D-[U-14C] glucose. The worms appeared healthy even after incubation for as long as 72 h. All the radioactivity was recovered either within the worms or in the incubation vessel in the form of metabolic products or unmetabolized glucose. Incubations were carried out at low oxygen tension except for those in which CO2 was measured. These were either aerobic or anaerobic. In terms of both quantity and radioactivity the main metabolic products of glucose were CO2, propan-1-ol, acetate and propionate. Smaller amounts of ethanol, lactate and succinate were formed. The results are compared with those found for the similar nematode Haemonchus contortus.     

Comparative morphology of Ostertagia mossi and Ostertagia dikmansi (trichostrongylidae) from Odocoileus virginianus and comments on other Ostertagia spp. from the Cervidae

The synlophes of Ostertagia mossi Dikmans, 1931 and O. dikmansi Becklund & Walker, 1968 were found to be identical supporting recognition of these as the major and minor morphotypes, respectively, of a putative species pair within the Ostertagiinae. The cervical synlophe included three narrowly spaced, continuous, parallel ridges laterally and three parallel but more widely spaced ridges in the dorsal and ventral fields (Type II and Type A patterns, respectively). The disposition of the synlophe in conjunction with a long oesophageo-intestinal valve, and attributes of the genital cone and spicules are characteristics shared among other Ostertagia spp. from cervids in the Holarctic region that allow recognition of a species group morphologically distinct from the Ostertagiinae of domestic ruminants. The morphological similarity of O. mossi/O. dikmansi, O. leptospicularis Assadov, 1953/O. kolchida Popova, 1937 and O. gruehneri Skrjabin, 1929/O. arctica Mitzkewitsch, 1929 is substantial, but these species can be differentiated by small but constant differences in the synlophe and genital complex of males; females cannot be easily distinguished. The morphological similarity of this cryptic complex of species and their relatively restricted distribution among cervids suggests a coevolutionary history for hosts and parasites in the Holarctic region.     

Experimental studies on the interaction between infections of Ostertagia leptospicularis and other bovine Ostertagia species

Experimental infections of calves were carried out with either isolates of predominantly Ostertagia ostertagi, pure O. leptospicularis or a mixed isolate of equal numbers of both these species. The total worms established on day 21 for the mixed species from a total inoculum of 100 000 infective larvae, was 1.2 times greater than from 100 000 larvae of the O. ostertagi isolate and 3.3 times that of the pure O. leptospicularis isolate. The increased establishment in the mixed inoculum referred to both O. ostertagi and O. leptospicularis (days 17 and 21). These differences were both highly significant (P less than 0.01). The severity of the pathological changes was also greater in the mixed infections. It is suggested that these findings must be taken into account when control measures involving alternate grazing of sheep and cattle are being employed.     

Ostertagia ostertagi: protective immunity in calves. The development in calves of a protective immunity to infection with Ostertagia ostertagi

Resistance to the establishment of Ostertagia ostertagi was tested in calves which had been infected daily with 1000 larvae for 30, 80, 150, and 250 days. The proportion of a challenge dose of 30,000 larvae which became established decreased steadily and by Day 250 was only $\text{1}\text{20}$ of the proportion that became established in susceptible control animals. Neither the age of the host nor the age of the larvae used affected the proportion that became established. It is shown that the increasing resistance to the establishment of worms, and an average life span of 28 days, of worms which developed beyond the early fourth stage, adequately account for the course of infections in calves infected daily. Evidence is presented which suggests that the host's previous experience of infection increases the proportion of the worms that are inhibited in their development.     

First sign in Italy of Nematodirus roscidus, Apteragia quadrispiculata and Ostertagia drozdzi, found in Dama dama

The authors refer the first report in Italy of Nematodirus roscidus Railliet, 1911, Apteragia quadrispiculata Jansen, 1958 and Ostertagia drozdzi Jancev, 1977 from Dama dama. In fallow deer they found also: Trichostrongylus axei, Trichostrongylus colubriformis, Trichostrongylus vitrinus, Spiculopteragia asymmetrica, Skrjabinagia arctica, Oesophagostomum venulosum, Trichuris ovis. Trichostrongylus axei, Trichostrongylus colubriformis, Trichostrongylus vitrinus and Skrjabinagia arctica were not found before in Dama dama in Italy.     

DNA evidence that Ostertagia gruehneri and Ostertagia arctica (Nematoda: ostertagiinae) in reindeer from Norway and Svalbard are conspecific

DNA sequences of ITS-1 and ITS-2 of rDNA were determined for 16 individual adult males each of Ostertagia gruehneri and Ostertagia arctica from Svalbard reindeer (Rangifer tarandus platyrhynchus) and Eurasian tundra reindeer (R. t. tarandus). Each ITS was virtually identical in O. gruehneri and O. arctica and the three mixed bases detected were shared by both species. Our results strongly suggest that O. gruehneri and O. arctica are dimorphic males of the same species.     

Hypergastrinaemia, abomasal bacterial population densities and pH in sheep infected with Ostertagia circumcincta.

Serum gastrin and pepsinogen concentrations, food intake, abomasal pH and abomasal aerotolerant and anaerobic bacterial populations were measured in sheep infected with Ostertagia circumcincta to search for links between hypergastrinaemia, food intake and changes in the abomasal environment. Abomasal pH and serum gastrin and pepsinogen concentrations were elevated in each of five sheep infected via abomasal cannulae with 150000 exsheathed larval stage three, followed 11 days later by 100000 sheathed larvae given intraruminally. Unparasitised abomasa contained aerotolerant bacterial population densities of between 10(3) and 10(6) cells ml(-1) and these did not change significantly following parasitism. In contrast, anaerobic bacterial population densities increased markedly by about 10(4)-fold following parasitism. Anaerobic numbers changed rapidly when abomasal pH increased from 2.5 to 3.5. At pH 4 and above, anaerobic bacterial numbers approached levels expected in rumen contents but parameters other than pH did not relate to bacterial numbers. Brief periods when serum gastrin was lower than expected, coinciding with raised abomasal pH, were not explicable by increased bacterial numbers. Food intake, which decreased for a variable period from around Day 5 p.i., correlated poorly with serum gastrin concentration, suggesting hypergastrinaemia is not the sole cause of anorexia in parasitised animals. The survival of substantial numbers of rumen bacteria in the abomasum at only slightly raised pH may significantly lower the bacterial protein available to the sheep.     

Gender-enriched transcription of activation associated secreted proteins in Ostertagia ostertagi

Activation associated secreted proteins (ASP) are members of a nematode-specific protein family belonging to the SCP/Tpx-1/Ag5/PR-1/Sc7 family. Three different types of molecules have been identified in this family: two-domain ASPs and single-domain ASPs showing homology to either the C-terminal or N-terminal domain of the two-domain ASP. The function of these proteins is still unclear, but a role in transition to parasitism and a role as allergen are often suggested. Here we report that the abomasal cattle parasite Ostertagia ostertagi produces at least 15 ASPs, including two-domain and C- and N-type single-domain ASPs. Ten of these are highly transcribed in the L4 stage, whereas others are highly enriched in adult male worms. The latter was especially the case for the N-type single-domain ASPs Oo-ASP1 and Oo-ASP2 and also for Oo-ASP3, which is homologous with the Haemonchus contortus and Ancylostoma caninum C-type single-domain ASPs. Immunohistochemistry showed that Oo-ASP3 was localised in the oesophagus. Oo-ASP1 and Oo-ASP2 on the other hand were localised in the reproductive tract of both male and female worms, suggesting a role in reproduction or in the development of the reproductive tract.