Heterologous transmission with Dictyocaulus capreolus from roe deer (Capreolus capreolus) to cattle (Bos taurus).

Eight Swedish Red Breed cattle, about 2 months old, were experimentally infected with a Swedish isolate of Dictyocaulus viviparus (Dviv-Se) from cattle and D. capreolus from roe deer. The aims were to determine whether the roe deer lungworm is infective to cattle or if it can induce seroconversion in cattle against D. viviparus as measured with an ELISA. Four calves which were given 500 Dviv-Se infective larvae (L3) each by larval dosing for two successive days developed patent infection between days 23 and 25 post-inoculation (PI). Larval output varied among the calves and during the patent period. However, maximum recovery occurred between 28 and 56 days PI with peak shedding on day 37 PI. Shedding ceased at day 58 PI and adult worms were recovered from one calf at necropsy (day 67 PI). No immature worms were recovered from the lungs at necropsy. Seroconversion was detected on days 35-42 PI. One Dviv-Se infected calf became seronegative on day 67 PI whereas the other calves still remained seropositive during this period. Prepatency and patency periods of D. viviparus and serological findings in this study basically conform to previous studies. Each calf that was infected with 400 L3 of D. capreolus for two successive days, and about 800 L3 of the same species about 8 weeks later, did not develop to patency based on faecal and post-mortem examinations. Consequently, under the conditions of this study, D. capreolus was not infective to cattle. Two of the four calves that were infected with L3 from roe deer were challenged with L3 cultured from faeces of the Dviv-Se-infected calves. This infection did not develop to patency. Whether this was due to cross-protection as a result of the prior priming with L3 from roe deer is not clear. However, if it is so, it opens up the possibility of using D. capreolus L3 for preventing bovine dictyocauliasis.

Identification of Dictyocaulus spp. in ruminants by morphological and molecular analyses.

Lungworms of the genus Dictyocaulus from cattle, roe deer, and moose in Sweden were subjected to morphological and molecular analyses. The objectives of the study were to investigate whether mixed or monospecific Dictyocaulus infections occur in Swedish cattle and whether wild cervids may act as reservoirs. The morphological characters examined were thickness and shape of the buccal capsule wall (BCW) and total spicular length (TSL). Morphometry was also done on the total body length, and BCW thickness and length. In the molecular identification, we used a PCR-linked hybridization assay to probe worm DNA with species-specific oligonucleotide probes to the second internal transcribed spacer (1TS2). The results showed that the BCW shape was the most reliable morphological character for identification. Significant differences were observed in this character, but an overlap occurred between lungworms from each of the host species. With the hybridization assay, all lungworms from cattle were identified as D. viviparus, whereas those from roe deer represented a novel Dictyocaulus species demonstrating that each host had a monospecific lungworm infection. In moose, 61 (78.2%) worms belonged to the new species and 17 (21.8%) were D. eckerti. This study shows the usefulness of hybridization assay as an epidemiological tool for the specific identification of lungworms of cattle and wild cervids.

Potential for cross-transmission of Dictyocaulus viviparus between cattle and white-tailed deer.

Development of an in vitro culture system for infectious Dictyocaulus viviparus larvae made it possible to study the potential cross-transmission of D. viviparus between white-tailed deer (Odocoileus virginianus) and cattle (Bos taurus). Between 26 September 1995-29 February 1996, six parasite-free bull calves were individually inoculated with 15 to 50 infective third stage larvae (L3)/kg of body weight cultured from adult D. viviparus collected from white-tailed deer. Three bull calves were simultaneously inoculated with 45 L3/kg of body weight recovered from cattle either by the Baermann technique or by in vitro culture as above. All three calves inoculated with the homologous cattle strain became patently infected while all six calves inoculated with the heterologous deer strain remained negative for the presence of D. viviparus in the feces and in the lungs upon necropsy.

Cross-infections between fallow deer and domestic ruminants with large lungworms (Dictyocaulus spp.).

Groups of four deer each were experimentally infected with larvae of Dictyocaulus (D.) eckerti (from fallow deer) or D. viviparus (from cattle) or D. filaria (from sheep), groups of four cattle each with D. viviparus or D. eckerti and groups of 4 lambs each with D. filaria or D. eckerti. The animals were daily examined coprologically following the 16th day post infectionem. The animals were slaughtered at different times and the lungs were dissected. With the exception of the infection of the sheep with D. eckerti from fallow deer, the mutual infections of the different hosts with the lungworm species became patent. Lungworms could be isolated. Fallow deer proved to be more susceptible to an infection with D. viviparus than cattle to an infection with D. eckerti. The large lungworms which naturally infest fallow deer and cattle, D. eckerti and D. viviparus respectively, can be distinguished according to the morphology of their mouth capsules, especially in the structure of the buccal ring. These features were also present after infection of the heterologous hosts.

Study on the causes of outbreaks of lungworm disease on commercial dairy farms in The Netherlands.

The causes of outbreaks of lungworm disease were determined from the herd histories of 25 affected herds of young cattle. The results indicate that light pasture contamination by carriers and subsequent auto-infections are the most prominent cause of lungworm disease, followed by heavy pasture contamination by carriers. Overwintered pasture infections seem to play a minor role. Adult dairy cows seem to be the predominant carrier animal when light pasture infections are concerned. Heavy pasture infections are almost always caused by calves and yearlings.

Isolation of Pilobolus spp. from the northern elk herd in Yellowstone National Park.

Pilobolus spp. were recovered from all fecal samples collected from an elk (Cervus elaphus nelsoni) herd in Yellowstone National Park (USA) with a high prevalence of Dictyocaulus viviparus infection. Pilobolus spp. have been shown to be important in the epizootiology of D. viviparus infections in cattle because these fungi aid in dissemination of larvae away from feces to areas where animals are more likely to ingest them, and protect larvae against dehydration and thus prolong survival. The same mechanism of dissemination of D. viviparus larvae may play a role in the epizootiology of these infections in elk.

Epidemiology of Dictyocaulus viviparus in Louisiana (U.S.A.).

An epidemiological investigation was conducted during a 1-year period on a permanent pasture naturally contaminated with Dictyocaulus viviparus and grazed by a varying number of yearling cattle. Seasonal variation in pasture infectivity to cattle was monitored by monthly slaughter of tracer calves, slaughter of pairs of resident yearlings at 30-60-day intervals, herbage larval recovery and by counts of first stage larvae in feces (modified Baermann technique) of resident cattle. A clinical outbreak of dictyocauliasis occurred during January-March 1986 and was associated with peak levels of pasture infectivity. Carrier animals were considered responsible for the survival of infection over summer. Although soil samples were taken regularly on a monthly basis to study the epidemiological importance of the soil as a source of infection, infective larvae were not recovered at any time. The epidemiological pattern observed in the present study provides basic information on the factors involved in infection and diseases outbreaks under sub-tropical conditions.

Diseases of wapiti utilizing cattle range in southwestern Alberta.

Specimens from 28 wapiti (Cervus elaphus canadensis) were collected by hunters in southwestern Alberta in 1984. Various tests were performed to detect infections and conditions that could affect cattle sharing the range or cause disease in wapiti. Serum antibodies were present against leptospiral serovars autumnalis (25%), bratislava (4%), and icterohaemorrhagiae (8%), and the viruses of bovine virus diarrhea (52%), infectious bovine rhinotracheitis (45%), and parainfluenza type 3 (13%). No serological evidence of bovine respiratory syncytial virus, Brucella, Anaplasma, bluetongue virus, or epizootic hemorrhagic disease virus was found, nor were any lesions of vesicular diseases, necrotic stomatitis or nutritional myopathy evident. Focal interstitial nephritis and sarcocystosis were diagnosed histologically in 40% and 75%, respectively, of the wapiti tested. The prevalence of giant liver flukes (Fascioloides magna) was 50% and of lungworms (Dictyocaulus viviparus) 32%. Leptospiral serology on cattle in the area did not indicate that wapiti or cattle were a serious source of infection to each other. The giant liver fluke was the parasite most likely to be amplified by wapiti for cattle. Within the limits of this study, the results indicated that wapiti in the Waterton area do not pose a disease threat to the cattle with which they range, but periodic observational studies in these wapiti would be a useful means of early detection of any changes in the interspecies relationship.

Dispersal of Dictyocaulus viviparus larvae from bovine faeces in Ireland.

An involvement of Pilobolus species fungus in the dispersal of Dictyocaulus viviparus third stage larvae from dung to surrounding herbage under Irish conditions was investigated. The presence of Pilobolus kleinii on artificial dung pats containing first stage larvae of D viviparus was associated with a 19-fold increase (P less than 0.05) in numbers of third stage larvae recovered from the surrounding herbage. A subjective examination of natural dung pats showed that the presence of Pilobolus species was significantly correlated with hours of bright sunshine (r = -0.5, P less than 0.01), total rainfall (r = 0.41, P less than 0.05) and the height of herbage surrounding the pats (r = 0.31, P less than 0.001). A multiple regression analysis showed that meteorological parameters and the height of surrounding herbage accounted for 38 per cent of the variation in growth of Pilobolus species on dung pats. The incidence of extensive damage to natural dung pats within five days of deposition, caused by biotic factors, another possible cause of D viviparus third stage larvae dispersal, varied from 0 to 92 per cent of the pats depending on their degree of dryness.

Spread of equine lungworm (Dictyocaulus arnfieldi) larvae from faeces by Pilobolus fungi.

Between 10 and 25% of the Dictyocaulus arnfieldi larvae excreted in faeces from a naturally infected donkey were harvested as infective stages from faecal cultures by means of Pilobolus fungi. The faeces were collected between 24 and 56 hours after drenching the donor animal with Pilobolus spores and kept at 16 +/- 2 degrees C. Most larvae were collected between the 5th and the 8th day of culturing during which period fructification and sporangium discharge also peaked. The sporangia and the adhering larvae were collected in Petri dishes inserted between the faecal mass and a light source. All recovered larvae were viable. A mean larval length of 368 microns (range 312-440 microns) and width of 14.6 microns (range 12-20 microns) was recorded for the infective stage. The method was found suitable for the recovery of infective stages for experimental purposes. The authors suggest that the Pilobolus mechanism play an important part in the spread of equine lungworm infection under field conditions similar to the situation in bovine lungworm (Dictyocaulus viviparus) infection.

Spread of infective Dictyocaulus viviparus larvae in pasture and to grazing cattle: experimental evidence of the role of Pilobolus fungi.

Four calves experimentally infected with Dictyocaulus viviparus were made Pilobolus-free by hygienic measures and by feeding them irradiation sterilized feed. Two of the calves were only administered laboratory cultured Pilobous sporangia daily. As a result, the faeces from one pair contained D. viviparus larvae and Pilobolus sores, and the faeces from the other one pair contained D. viviparus larvae, but no Pilobolus spores. Two identical plots were used for deposition of the two kinds of faeces, and one of them remained free of Pilobolus fructification. Herbage sampling and the use of tracer calves revealed that on this plot the larval contamination and the infectivity of the pasture were greatly reduced. A mean larval count of 1321 near the faecal pats (0-5 cm) in the plot where Pilobolus was observed was reduced to 69 per kg of herbage on the Pilobolus-free plot. At a distance of 100 cm from the pats, a reduction from 99 to 3 larvae per kg herbage was found. Each plot was grazed by four parasite-free tracer calves for 3 days. During the subsequent stabling period of these calves, the lungworm larval excretion of those from the Pilobolus-free plot was reduced by 90% and the clinical symptoms were milder than those which grazed the plot which contained the fungus. The mean post mortem worm counts after 4 weeks of stabling showed a reduction from 167 to 25 worms. A more marked effect of Pilobolus fungi on the transmission of D. viviparus infection is to be expected under field conditions where calves are grazing more selectively than in the present study.

Natural infection with Dictyocaulus arnfieldi in pony and donkey foals.

From June to October 1978 four pony mares and foals and two donkey mares and foals grazed a paddock contaminated with Dictyocaulus arnfieldi larvae. No signs of respiratory disease were seen in the foals but within 11 weeks of exposure to the paddock all six developed patent lungworm infections. In October 1978 one donkey and two pony foals were killed. At post mortem examination parasites in various stages of development and measuring up to 8 cm in length were found in the lungs. At this time the three surviving foals were stabled for the remainder of the experiment. Two of these ceased passing D arnfieldi larvae during the winter months but in one pony foal patency persisted until the study ended in August 1979. Patent lungworm infections were not seen in the pony mares, although two started to cough four to six weeks after starting to graze the infected paddock. One of the affected mares was killed in October 1978 when seven small (less than 7 mm) D arnfieldi were recovered. The other continued to cough until the end of the study over a year later.

The bionomics of the free-living larvae and the transmission of Dictyocaulus filaria between lambs in North-East England.

The bionomics of the free-living larvae of Dictyocaulus filaria on pasture, and the transmission of infection between lambs, were studied during different seasons of the year in North-East England. The rate of development of first-stage larvae to the third stage took 4-9 days in late spring and summer, 1 1/2-4 weeks in autumn and 5 1/2-7 weeks in winter. The proportion of first-stage larvae developing to the third stage ranged from 10-28% in autumn and winter, and 2-25% in spring and summer. The rate of mortality of the third-stage larvae was approximately logarithmic in nature, although the survival time was shorter in spring and summer than in autumn and winter. Third stage larvae were able to survive from autumn until the spring of the following year in sufficient numbers to perpetuate transmission but not to cause clinical disease. In a transmission study, the survival of the infective larvae on the experimental plot was poor in summer, but the larval population increased in the autumn and then declined slowly throughout the winter. Infection in the susceptible lambs was related to the level of infection on the herbage increasing in severity from early summer to late autumn. However, those lambs infected in the summer were resistant to the heavy autumn challenge of larvae on pasture.