Parelaphostrongylus Andersoni Research Articles

DNA sequencing confirms meningeal worm (Parelaphostrongylus tenuis) and muscle worm (Parelaphostrongylus andersoni) in white-tailed deer (Odocoileus virginianus): Implications for moose (Alces alces) management.

In North America, some moose populations are declining, and meningeal worm (Parelaphostrongylus tenuis) infections may be contributing. Moose are aberrant hosts for meningeal worm and develop severe pathology whereas white-tailed deer (WTD) are definitive hosts that experience minimal pathology and spread parasite larvae into the environment. Analyses of harvested WTD heads confirmed meningeal worm in Western Manitoba, Canada including in areas where moose have experienced population declines and are currently of management concern. The prevalence of larval meningeal worm from WTD feces in these areas are unknown, particularly because the dorsal-spined larvae (DSL) are morphologically indistinguishable from muscle worm (Parelaphostrongylus andersoni). To assess transmission risk of DSL, we investigated the spatial and temporal variation of prevalence in WTD feces from four areas (two with historical moose population declines and two without) sampled across two summers. We predicted higher prevalence of DSL in areas where moose are of management concern and surveys have shown higher meningeal worm prevalence in WTD heads. Further, we expected to only recover meningeal worm, as muscle worm has only been reported from caribou in more northern areas of Manitoba. We collected WTD feces by transect sampling, used the Baermann technique to obtain larvae, and sequenced partial cytochrome oxidase 1 and internal transcribed spacer 2 genes to confirm species identity. Zero-inflated models revealed that DSL prevalence did not differ temporally but was higher in areas where moose are of management concern. Genetic analyses revealed that meningeal worm and muscle worm were both present in Western Manitoba and co-occurred in three areas. Our results reveal novel insights into the geographic distribution of muscle worm and emphasize the importance of DNA sequencing for DSL identification. We suggest that concern for moose populations is warranted given the increased risk of parasite infection in some management areas.

The biogeography of the caribou lungworm, Varestrongylus eleguneniensis (Nematoda: Protostrongylidae) across northern North America.

Varestrongylus eleguneniensis (Nematoda; Protostrongylidae) is a recently described species of lungworm that infects caribou (Rangifer tarandus), muskoxen (Ovibos moschatus) and moose (Alces americanus) across northern North America. Herein we explore the geographic distribution of V. eleguneniensis through geographically extensive sampling and discuss the biogeography of this multi-host parasite. We analyzed fecal samples of three caribou subspecies (n = 1485), two muskox subspecies (n = 159), and two moose subspecies (n = 264) from across northern North America. Protostrongylid dorsal-spined larvae (DSL) were found in 23.8%, 73.6%, and 4.2% of these ungulates, respectively. A portion of recovered DSL were identified by genetic analyses of the ITS-2 region of the nuclear rDNA or the cytochrome oxidase c subunit I (COI) region of the mtDNA. We found V. eleguneniensis widely distributed among caribou and muskox populations across most of their geographic prange in North America but it was rare in moose. Parelaphostrongylus andersoni was present in caribou and moose and we provide new geographic records for this species. This study provides a substantial expansion of the knowledge defining the current distribution and biogeography of protostrongylid nematodes in northern ungulates. Insights about the host and geographic range of V. eleguneniensis can serve as a geographically extensive baseline for monitoring current distribution and in anticipating future biogeographic scenarios under a regime of accelerating climate and anthropogenic perturbation.

PREVALENCE OF PARELAPHOSTRONGYLUS ANDERSONI IN WHITE-TAILED DEER, OTHER CERVIDS, AND BOVIDS IN NORTHERN FLORIDA.

Parelaphostrongylus andersoni, the muscleworm, commonly infects white-tailed deer (Odocoileus virginianus) and also infects caribou (Rangifer tarandus [R.t.] groenlanicus, R.t. grantii, R.t. tarandus, and R.t. caribou). Heavy infection with P. andersoni leads to weakness in the hindquarters, abnormal gait, and pulmonary lesions. The geographical range and full host spectrum of this parasite are not fully known. This study aims to understand host specificity better, especially in nonnative cervids and bovids. This study involved the collection of 140 fecal samples from native and nonnative cervid and bovid species, and 34 snail specimens. With the use of real-time PCR, we found 4/47 (8.5%) O. virginianus fecal samples were positive for P. andersoni. No previously undocumented species of cervids or bovids were found to be infected. Further research is warranted to understand P. andersoni range, host distribution, and potential impact on host health.

HEALTH SURVEY OF BOREAL CARIBOU (RANGIFER TARANDUS CARIBOU) IN NORTHEASTERN BRITISH COLUMBIA, CANADA.

Boreal woodland caribou (Rangifer tarandus caribou) are listed as threatened across Canada, and a basic understanding of their health status is lacking. From December 2012 to April 2013, we investigated multiple health indices for adult female boreal caribou (n=163) captured from seven herds in NE British Columbia, Canada. Health indices included physical characteristics, physiologic and trace mineral status, exposure to or infection with selected pathogens, and measures of chronic stress and inflammation, including serum amyloid A, haptoglobin, and hair cortisol concentration. Key findings were exposure to the bacterium Erysipelothrix rhusiopathiae in 14% of individuals, mild to severe hair loss associated with winter tick (Dermacentor albipictus) infestations in 76% of caribou from December to early February and 81% from late February to early April, and evidence of trace mineral deficiencies with 99% and 34% of individuals deficient in copper and selenium, respectively. Seroprevalence for exposure to selected pathogens was: alphaherpesvirus (63%), pestivirus (1%), Besnoitia spp. (60%), and Neospora caninum (2%). All animals were seronegative to Brucella spp. and Toxoplasma gondii. Mycobacterium avium ssp. paratuberculosis was not detected in any fecal samples. Parasite eggs or larvae, including Parelaphostrongylus andersoni (36%), Skrjabinema spp. (1%), Strongyle-type eggs (11%), Moniezia-type eggs (8%), and nematodirines (3%), were detected on fecal examination, but at low intensity. Blood biochemistry values and hair cortisol concentrations were within ranges previously reported in Rangifer tarandus sspp. Some significant differences among herds were noted, including antler morphology, exposure to Besnoitia spp., and concentrations of serum amyloid A, copper, cobalt, manganese, and iron.

Parasite prevalence, infection intensity and richness in an endangered population, the Atlantic-Gaspésie caribou.

The Atlantic-Gaspésie caribou (Rangifer tarandus caribou) population is a small isolated relict herd considered endangered according to the Canadian Species at Risk Act (SARA). This population has low recruitment and survival rates but the potential role of parasites on individual fitness is unknown. In this context, we explored the parasite status of this population with the aim of 1) assessing the occurrence and intensity of parasite infections and the spatial, temporal and individual variations, 2) quantifying parasite richness and investigating factors such as sex and host body condition that may be associated with this variable and 3) evaluating the effects of parasite infections on survival in the Atlantic-Gaspésie caribou population. We examined fecal samples from 32 animals captured in 2013–2014 for eggs, oocysts and larvae of parasites and detected 7 parasite species: dorsal-spined larvae protostrongylids, presumably Parelaphostrongylus andersoni based on PCR identification of a subset, Nematodirus odocoilei and other unidentified Strongyles, Trichuris sp., Capillaria sp., Moniezia sp. and Eimeria sp. For each caribou, mean parasite species richness was 1.8 ± 1.1 (SD). Sex, body condition, year and capture location did not explain parasite prevalence, intensity of infection or richness except for intensity of infection of Capillaria sp. that was positively influenced by body condition. Parasites did not influence survival although mortality was higher for males than for females. We suggest that the relatively low and common gastrointestinal and protostrongylid parasite infections will not be a short-term threat leading to extinction.

Morphological keys to advance the understanding of protostrongylid biodiversity in caribou (Rangifer spp.) at high latitudes.

The Protostrongylidae is a diverse family of nematodes capable of causing significant respiratory and neuromuscular disease in their ungulate and lagomorph hosts. Establishing the species diversity and abundance of the protostrongylid fauna has been hindered because the first stage larvae, commonly referred as dorsal spined larvae (DSL), that are shed in the feces are morphologically very similar among several genera. We aimed to determine the protostrongylid diversity and distribution in caribou (Rangifer tarandus groenlandicus and R. t. pearyi) in the central and high Canadian Arctic. We first developed, tested and validated a morphological diagnostic guide for the DSL of two important protostrongylids, Parelaphostrongylus andersoni and Varestrongylus eleguneniensis, and then applied this guide to determine the prevalence and intensity of infection of these parasites in fecal samples from 242 caribou. We found that DSL of V. eleguneniensis and P. andersoni can be differentiated morphologically based on the structural differences at the caudal extremity. The presentation and morphology of the dorsal spine, and caudoventral bulging at the start of the tail extension were identified as the key identifying features. The two species were found in caribou on the arctic mainland and southern Victoria Island in single and co-infections, but the prevalence and intensity of infection was low. No protostrongylids were detected in caribou from the high arctic islands. Through this study, we provide a simple, efficient, and robust method to distinguish the DSL of the two protostrongylids, and present the current status of infection in different herds of caribou of the central Canadian Arctic. We report new geographic and host records for P. andersoni infection in Dolphin and Union caribou herd.

A Nearctic parasite in a Palearctic host: Parelaphostrongylus andersoni (Nematoda; Protostrongylidae) infecting semi-domesticated reindeer in Alaska

Parelaphostrongylus andersoni is a muscle-dwelling protostrongylid nematode that infects caribou and white-tailed deer across North America, and can cause significant muscular and pulmonary pathology in these species. We collected 44 fecal samples from semi-domesticated reindeer (Rangifer tarandus tarandus) from the Kakarak herd of western Seward Peninsula, Alaska, USA. This herd has no record of historical contact and extremely limited possibility of contemporary contact with native Grant's caribou (Rangifer tarandus granti) of the Western Arctic herd. Fecal samples were processed using the Baermann technique, and 22.7% (n=10) were positive for protostrongylid dorsal-spined larvae (DSL). Genomic DNA extracted from individual DSL from each of the ten positive reindeer (total of 48 DSL) was amplified by PCR targeting the ITS-2 region of ribosomal RNA. Forty of 48 DSL were successfully sequenced and confirmed as P. andersoni and one representative sequence for each of the ten positive samples was deposited in GenBank. No other protostrongylids, including Varestrongylus sp., presumed to be widespread across caribou range, and Elaphostrongylus rangiferi, which could have been introduced with reindeer from Eurasia, were detected in these samples. P. andersoni is likely widespread among introduced reindeer in Alaska, potentially causing subtle but deleterious effects with negative economic impacts on commercial herding activities.

MUSCLEWORMS, PARELAPHOSTRONGYLUS ANDERSONI (NEMATODA: PROTOSTRONGYLIDAE), DISCOVERED IN COLUMBIA WHITE-TAILED DEER FROM OREGON AND WASHINGTON: IMPLICATIONS FOR BIOGEOGRAPHY AND HOST ASSOCIATIONS

Parelaphostrongylus andersoni is considered a characteristic nematode infecting white-tailed deer (Odocoileus virginianus). Host and geographic distribution for this parasite, however, remain poorly defined in the region of western North America. Fecal samples collected from Columbia white-tailed deer (O. v. leucurus) in a restricted range endemic to Oregon and Washington, USA, were examined for dorsal-spined larvae characteristic of many protostrongylid nematodes. Multilocus DNA sequence data (internal transcribed spacer 2 and cytochrome c oxidase subunit 1) established the identity and a new record for P. andersoni in a subspecies of white-tailed deer previously unrecognized as hosts. Populations of P. andersoni are now recognized along the basin of the lower Columbia River in Oregon and Washington and from south-central Oregon on the North Umpqua River. Current data indicate a potentially broad zone of sympatry for P. andersoni and Parelaphostrongylus odocoilei in the western region of North America, although these elaphostrongylines seem to be segregated, respectively, in white-tailed deer or in black-tailed and mule deer (Odocoileus hemionus) at temperate latitudes. The geographic range for P. andersoni in white-tailed deer is extended substantially to the west of the currently defined limit in North America, and we confirm an apparently extensive range for this elpahostrongyline. These observations are explored in the broader context of host and geographic associations for P. andersoni and related elaphostrongylines in North American cervids.

Serendipitous discovery of a novel protostrongylid (Nematoda: Metastrongyloidea) in caribou, muskoxen, and moose from high latitudes of North America based on DNA sequence comparisons

Fecal samples are often the only feasible means to assess diversity of parasites in wildlife; however, definitive identification of egg or larval stages in feces by morphology is rarely possible. We determined partial sequences from the second internal transcribed spacer region (ITS-2) of nuclear ribosomal DNA for first-stage, dorsal-spined larvae (DSL) in feces from caribou ( Rangifer tarandus tarandus (L., 1758), Rangifer tarandus caribou (Gmelin, 1788), Rangifer tarandus grantii (Allen, 1902)), muskoxen ( Ovibos moschatus moschatus (Zimmermann, 1780), Ovibos moschatus wardi Lydekker, 1900), moose ( Alces alces gigas Miller, 1899 and Alces alces andersoni Peterson, 1952), and from the tissue of one slug ( Deroceras laeve (Müller, 1774)) in Arctic–Subarctic North America. A previously uncharacterized, genetically distinct species was recognized based on sequences of 37 DSL from 19 ungulate hosts and the slug. Sequence similarity among individuals of this novel species was 91%–100%. For many individual DSL, paralogues of ITS-2 were detected. ITS-2 sequences from the novel species were 72%–77% similar to those of Varestrongylus alpenae (Dikmans, 1935) and 51%–61% similar to those of other protostrongylids known in North American and some Eurasian ungulates. Results indicate a discrete lineage of an undescribed protostrongylid infecting muskoxen, caribou, and moose from Alaska to Labrador. Sympatric infections with Parelaphostrongylus andersoni Prestwood, 1972 were found in three caribou herds.

Bighorn Sheep, a New Host Record for Parelaphostrongylus odocoilei (Nematoda: Protostrongylidae)

Larval nematodes with a dorsal spine on the tail were recovered from fecal samples of California bighorn sheep (Ovis canadensis californiana) in northeastern Washington State, USA. The identity of these dorsal-spined larvae (DSL) was established by single-strand conformation polymorphism (SSCP) analyses of a partial fragment of the first internal transcribed spacer of the ribosomal DNA. The SSCP profiles of individual DSL from bighorn sheep were compared with those of DSL of five protostrongylid species (Parelaphostrongylus andersoni, P odocoilei, P. tenuis, Elaphostrongylus rangiferi, and Muellerius capillaris) but were identical to only those of P. odocoilei. This study represents the first confirmed identification of P. odocoilei in bighorn sheep.

REGULAR ARTICLES / ARTICLES RÉGULIERSFactors affecting the distribution and transmission ofElaphostrongylus rangiferi(Protostrongylidae) in caribou (Rangifer tarandus caribou) of Newfoundland, Canada

Elaphostrongylus rangiferi was introduced to caribou (Rangifer tarandus caribou) of Newfoundland by infected reindeer (R. t. tarandus) from Norway and has caused at least two epizootics of cerebrospinal elaphostrongylosis (CSE), a debilitating neurologic disease. In an attempt to understand the conditions necessary for such outbreaks, we examined the effects of herd density and climatic factors on parasite abundance. The abundance of E. rangiferi was represented by counts of first-stage larvae in feces collected from young caribou (calves and yearlings) in 7 distinct caribou herds in Newfoundland. Abundance of E. rangiferi was highest in February and in the Avalon (632 ± 14 (mean ± SE)) and St. Anthony (526 ± 145) herds, the 2 herds in which CSE was most frequently reported. Mean abundance in February samples from young animals correlated positively with mean annual minimum temperature (rS= 0.829, df = 6, P = 0.04) and the number of days per year above 0°C (rS= 0.812, df = 6, P = 0.05) and negatively with mean summer temperatures (rS= –0.830, df = 6, P = 0.04). Results suggest that abundance of E. rangiferi and the likelihood of cases of CSE are increased by moderate summer temperatures suitable for the activity and infection of gastropod intermediate hosts and by mild winters with little snow that extend the transmission period. Abundance of larvae was not correlated with herd density. Animals in all 7 herds also had the muscle worm Parelaphostrongylus andersoni, a related nematode with similar dorsal-spined larvae. In 2 additional herds (Cape Shore and Bay de Verde), P. andersoni occurred alone and larvae were passed only by young caribou. In herds with dual infections, numbers of P. andersoni larvae were depressed, declined more quickly in young animals, and were considered to be present in only low numbers in February samples used for E. rangiferi analysis. Upon initial infection, young caribou develop a resistance to E. rangiferi that prevents or reduces reinfection later in life. This was demonstrated by examining the brains of caribou for recently acquired worms, which must develop there for up to 90 days before continuing their tissue migration into the skeletal muscles. Recent infections were detected in only calves and yearlings in all herds with E. rangiferi except the Avalon herd, where developing worms were also found on the brains of older caribou. The infection of older animals in the Avalon herd may reflect a lower immunocompetence of a naive herd that has only recently been exposed to E. rangiferi.

Serological Diagnosis of Parelaphostrongylus tenuis Infection in White-Tailed Deer and Identification of a Potentially Unique Parasite Antigen

Serological diagnosis of Parelaphostrongylus tenuis infection should offer many advantages over the currently used method of fecal analysis that relies on a patent infection. Toward this end, we investigated the presence of P. tenuis-specific antibodies in experimentally infected white-tailed deer (WTD) and of unique P. tenuis antigens that may be exploited for serodiagnosis. WTD infected with 6, 20 or 100-150 P. tenuis third-stage larvae (L3) had anti-parasite antibodies from as early as 21 days postinoculation (dpi) until the end of the experiment (147 dpi). Peak anti-P. tenuis enzyme-linked immunosorbent assay (ELISA) titers in individual animals ranged from 1:70 to 1:5,700. Serum from infected WTD reacted with 5 distinct P. tenuis L3 antigens (105, 45, 37, 32, and 19 kDa) as detected by the immunoblotting technique. Serum from caribou infected with Parelaphostrongylus andersoni or Elaphostrongylus rangiferi reacted with all antigens except the 37-kDa antigen of L3, indicating that it may be unique to P. tenuis and can serve as a serodiagnostic antigen. The 37-kDa antigen appears to be present in the adult P. tenuis but not adult E. rangiferi or E. cervi. The development of an ELISA utilizing the unique antigen of P. tenuis should lead to a reliable diagnostic assay for P. tenuis infection in WTD.

A search for Parelaphostrongylus andersoni in white-tailed deer from Maine.

Longissimus dorsi muscles from 42 white-tailed deer (Odocoileus virginianus) from Maine (USA) were examined for the Parelaphostrongylus andersoni. No adult nematodes were found. Prevalence based on the Poisson approximation of a binomial distribution could have been between 0 and 9% (95% C.I.). However, based on prevalence documented elsewhere (10 to 18%), it is unlikely that P. andersoni occurs in white-tailed deer in central Maine.

Parelaphostrongylus andersoni (Nematoda: Protostrongylidae) in White-tailed Deer from Michigan

Dorsal-spined larvae in fecal samples from free-ranging white-tailed deer (Odocoileus virginianus) in Michigan and Pennsylvania were used as a source of larvae to infect a hand-raised white-tailed deer fawn. The fawn receive 200 third-stage larvae and passed dorsal-spined larvae in feces 66 days later. Muscleworm (Parelaphostrongylus andersoni), and meningeal worm (Parelaphostrongylus tenuis) were recovered at necropsy. Two white-tailed deer and seven wapiti (Cervus elaphus) exposed to larvae of the source from Pennsylvania harbored only P. tenuis. This is the first report of P. andersoni in the midwestern United States and extends the known range of this muscleworm in free-ranging white-tailed deer. Concurrent infections of P. andersoni and P. tenuis have not been established previously in experimentally infected fawns.

Parelaphostrongylus andersoni (Nematoda: Protostrongylidae) in caribou (Rangifer tarandus) of northern and central Canada

Woodland (Rangifer tarandus caribou) and barren ground (R. t. groenlandicum) caribou are reported for the first time as hosts of Parelaphostrongylus andersoni, greatly extending the known geographic range of this muscle nematode. Up to 56% of caribou in the Beverly herd, central Northwest Territories, passed dorsal-spined first-stage larvae in their feces. Animals less than 3 years old were more frequently infected and passed greater numbers of larvae than older animals. Larval output in winter and spring did not differ. Adults of the four elaphostrongyline nematodes known to occur in caribou are distinguished by their location in the host, the size of the worms, and the size and morphology of the male copulatory structures. There is an urgent need for tested and improved methods of differentiating larvae of P. andersoni and other elaphostrongyline nematodes from those of P. tenuis that cause neurologic disease in various North American cervids. Demonstration of the occurrence of P. andersoni in Rangifer sp. in North America raises the possibility that it originated in Eurasian cervids and may still occur in the Old World.

Efficacy of ivermectin against Parelaphostrongylus andersoni (Nematoda, Metastrongyloidea) in white-tailed deer (Odocoileus virginianus).

Ivermectin was injected subcutaneously at 200 and 400 micrograms/kg of body weight into seven white-tailed deer (Odocoileus virginianus) in an attempt to control the muscle nematode Parelaphostrongylus andersoni. Counts of first-stage larvae in feces dropped to zero at 17 to 18 days posttreatment. Larvae reappeared in feces 1.5 to 6 wk later in six deer. Four deer were treated again approximately 9 wk after the first treatment; larval counts dropped to zero in 12 to 18 days. Larvae reappeared in low numbers 45 to 55 days after the second treatment. Because deer were held indoors on cement and the prepatent period of these worms is approximately 2 mo, the reappearance of larvae was not due to reinfection by accidental ingestion of gastropod intermediate hosts. Results suggest that ivermectin at dosages of 200 or 400 micrograms/kg of body weight suppressed larval production by adult female nematodes for several weeks or destroyed first-stage larvae in the lungs.

Diagnostic Morphology of the Third-Stage Larvae of Three Species of Parelaphostrongylus (Nematoda, Metastrongyloidea)

In North America, adults of meningeal worm Parelaphostrongylus tenuis (Dougherty, 1945) and muscleworm Parelaphostrongylus andersoni Prestwood, 1972 occur in white-tailed deer (Odocoileus virginianus) of eastern regions (Anderson and Prestwood, 1981. In Diseases and parasites of white-tailed deer, W. R. Davidson, F. A. Hayes, V. F. Nettles, and F. E. Kellogg (eds.). Misc. Pub. No. 7, Tall Timbers Res. Stat., Tallahassee, Florida, pp. 266-317) and adults of P. andersoni and muscleworm P. odocoilei (Hobmaier and Hobmaier, 1934) occur in white-tailed and mule and black-tailed deer (0. hemionus subspp.), respectively, of the West (Pybus and Samuel, 1981, J. Wildl. Mgmt 45: 537-542; Platt, 1978. Ph.D. Thesis, Univ. of Alberta, Edmonton, Alberta, 233 p.). Parelaphostrongylus tenuis and P. andersoni are found concurrently in whitetailed deer of the southeastern United States (Prestwood et al., 1974, J. Wildl. Dis. 10: 404409) and, based on experimental work (Pybus, 1983. Ph.D. Thesis, Univ. of Alberta, Edmonton, Alberta, 185 p.), the potential exists for concurrent infections of P. andersoni and P. odocoilei in mule deer. First-stage larvae (L1s) of these nematodes are passed in the feces of the definitive host and, later, develop to the third (=infective)-stage (L3) in terrestrial gastropods. Clearly, the ability to distinguish these larval stages would be advantageous for parsitologists and wildlife biologists. Unfortunately, first-stage larvae of all 3 species are similar (Anderson, 1963, Can. J. Zool. 41: 775-991; Prestwood, 1972, J. Parasit. 58: 897902; Platt, loc. cit.). Prestwood (loc. cit.) distinguished L3s of P. andersoni from those of P. odocoilei by size and P. andersoni from P. tenuis by a slight swelling on the dorsal surface of the tail of P. andersoni. In the present study, we compared the L3s of all 3 species using light microscopy and found that the shape of the tails was different. Laboratory-raised Triodopsis multilineata (Say) (Pulmonata: Stylommatophora) were used as intermediate hosts. Snails were infected by placing them in a dish containing L,s on moistened filter paper. The number of L1s exposed to each snail ranged from 10 to 1,000. Larvae of P. tenuis were recovered from frozen feces of whitetailed deer collected in the Rachelwood Wildlife

Attempts to find a laboratory host for Parelaphostrongylus andersoni and Parelaphostrongylus odocoilei (Nematoda: Protostrongylidae)

Twenty guinea pigs (Cavia porcellus) and eight domestic rabbits (Oryctolagus cuniculus) were each exposed to 100 or 200 third-stage larvae of Parelaphostrongylus andersoni or Parelaphostrongylus odocoilei. A few larvae penetrated the stomach and caecal walls and were found in the mesentery, liver, and diaphragm. However, most were recovered from the lungs and pleurae of the pleural cavity. Larvae did not appear to grow or develop and they did not reach the skeletal muscles, the usual site of adult P. andersoni and P. odocoilei in deer. All larvae in tissues were encapsulated (after 36 days) and overcome (after 59 days) by a local host response. Larvae appeared to migrate via the circulatory system and by direct penetration of tissues and organs. Patent infections were not found in three domestic goats (Capra hircus) up to 101 days after exposure to 300 or 1000 third-stage larvae of P. odocoilei.

Repeated Low-Level Infection of White-Tailed Deer with Parelaphostrongylus andersoni

Two white-tailed deer (Odocoileus virginianus) were given 5 infective larvae of Parelaphostrongylus andersoni each weekday for 13 weeks. At 23 weeks one of these deer and a control were challenged with single doses of 200 third-stage larvae. Repeated low-level infection of P. andersoni resulted in a sustained leukocytosis with an absolute eosinophilia which declined only after administration of larvae ceased, partial failure of worms to become established in the musculature, reduced numbers and reduced viability of eggs in the lungs, and an apparent active immunity which enabled the deer to resist challenge. The results of this study suggest that wild deer become infected with P. andersoni by isolated chance encounters with infected gastropods.

Experimental Parelaphostrongylus andersoni infections in white-tailed deer.

Gross and microscopic lesions caused by Parelaphostrongylus andersoni were studied in white-tailed deer (Odocoileus virginianus) infected with large (1000 or 5000) and moderate (200-356) numbers of third-stage larvae. In heavy infections, adult worms caused eosinophilic myositis in the loin and thigh. Masses of eosinophils underwent caseous necrosis surrounded by a granulomatous border. Adult worms, eggs, and larvae were in the lesions. Muscle damage caused by moderate doses was slight. One deer given a moderate dose maintained a patent infection for more than 1 year and was reinfected. Gross lung damage caused by eggs and larvae occurred with both degrees of infection and consisted of firm miliary nodules. Microscopically, the main changes were granulomatous encapsulation of eggs and first-stage larvae in alveolar capillaries, accumulations of eosinophils and mononuclear inflammatory cells in the adjacent alveolar septa, congestion, and interstitial pneumonia.