The trematode Microphallus sp. alters the behavior of its snail intermediate host, Potamopyrgus antipodarum, in ways that seem to increase transmission to its final host, e.g., waterfowl, and decrease the probability of being eaten by other predators, e.g., fish. The parasite seems to cause the snail to move from the top to the bottom of rocks at about 0900 hr. Waterfowl feed predominantly before 0900 hr, and fish feed predominantly after 0900 hr. In the present study, we tested the hypothesis that Microphallus sp.-infected snails exhibit a change in behavior at around 0900 hr by examining their response to light and vertical orientation before and after 0900 hr. Results demonstrated that uninfected snails generally move toward light, oriented downward, and move a greater distance in the light compared with the dark at all times of day. Microphallus sp.-infected snails behaved differently from uninfected snails in the early morning but similarly to uninfected snails in the late morning with regard to downward orientation and distance moved in response to light. Snails infected with parasites other than Microphallus sp. behaved similarly to uninfected snails during both time periods. These results suggest that Microphallus sp. manipulates the behavior of Potamopyrgus sp. by altering rates of movement in response to light and vertical orientation in a manner consistent with the hypothesized 0900-hr shift.

In order to identify the early stages of Taenia solium metacestodes, 12 pigs were each fed 100,000 viable eggs and later killed and necropsied at different times after infection. Hematoxylin–eosin (HE) and immunohistochemical techniques (IHCs) were used to identify onchospheres and cysticerci in different tissues. At 2 days postinfection (dpi) structures compatible with onchospheres were found in the lumen of the small intestine, and in the mesenteric blood vessels and lymph nodes. At 4 dpi, these same structures were observed in the small intestine, the liver, and skeletal muscles. Between 6 and 39 dpi, they were found only in skeletal muscles. Between 2 and 6 dpi the postonchospheres were circular and oval shaped and measured between 6 and 34 × 27 μm. From 14 to 39 dpi, well-developed metacestodes 550 × 750 μm were observed. IHCs support the identification of early stages of T. solium.

Population density, or crowding, was examined to determine its effect on the morphometric variability of Echinostoma caproni (Digenea) in ICR mice. Six mice were infected with 25 and 100 metacercariae, and a single mouse was infected with 300 metacercariae. All mice were infected at necropsy 22 days postinfection with recoveries of 77%, 69%, and 7.3%, respectively. Whole mounts were prepared, and 31 characters were evaluated (25 direct measurements and 6 ratios). Univariate and multivariate statistical analysis revealed significant differences between adult worms from all 3 groups. Twenty-seven of 31 characters showed significant within-group differences, with the primary differences between worms from 25/100 versus 300 metacercariae infections. Discriminant function analysis yielded a 100% correct classification based on infection size, which is consistent with studies on distinct species of Echinostoma. The low recovery from the mouse infected with 300 metacercariae suggests inflammatory expulsion of juvenile worms and the possibility of immunity as a factor in the crowding effect. These results suggest that external factors may affect morphometric variability of digenetic trematodes to a larger degree than previously recognized.

The male and female of Haemodipsis brachylagi n. sp. (Phthiraptera: Anoplura) are described from specimens collected from a pygmy rabbit, Brachylagus idahoensis (Merriam) (Lagomorpha: Leporidae), from Nevada. Morphological features that differentiate the new species from other known species of Haemodipsus are elucidated, and an identification key to both sexes of the 3 species now known from this genus in North America is included. Geographical distributions of the other 4 species of Haemodipsus known from other parts of the world are highlighted.

Udonella australis is a platyhelminth that lives on the surface of the ectoparasite copepods Caligus rogercresseyi and Lepeophtheirus mugiloidis, which coexist on the Chilean rock cod Eleginops maclovinus. The absence of a planktonic oncomiracidium stage in the life cycle of udonellids may limit their dispersal ability. However, the high prevalence and intensity of U. australis on C. rogercresseyi suggest they have developed dispersal strategies to compensate for the lack of a free-living larval stage. The goals of this study were to determine the main dispersal mechanisms of U. australis in 1 copepod species and to compare the dispersal ability of U. australis between 2 different copepod species. Chilean rock cods were infected with female (without udonellids) and male (with and without udonellids) C. rogercresseyi. Other fishes were also infected with this copepod (with U. australis) and with L. mugiloidis (without U. australis). The dispersal of udonellids among copepods occurs through both intraspecific and interspecific processes. The main dispersal mechanism appears to be copepod mating; contact between same-sex individuals is less important. Intraspecific dispersal seems to be more dependent on the number of udonellids per fish than on copepod abundance, as observed for interspecific dispersal.

Questing behavior of Ixodes uriae and their associated seasonal, host-feeding patterns are crucial to our understanding of tick life history strategies and the ecology of diseases that they transmit. Consequently, we quantified questing behavior of nymphs and adult female I. uriae ticks at Gull Island, a seabird colony in Newfoundland, Canada, to examine seasonal variation of off-host and on-host tick activity. We sampled a total of 133 adult Atlantic puffins (Fratercula arctica), 152 puffin chicks, and 145 herring gull (Larus argentatus) chicks for ticks during the breeding seasons of 2004 and 2005. Questing ticks were sampled by dragging a white flannel cloth across the grassy breeding areas during the mo of May, June, July, and August. Nymph questing activity reached a peak during mid-July (79 and 110 individuals/hr in 2004 and 2005, respectively). The prevalence of nymphs and adult female ticks on different seabird hosts varied between years and during the seasons. Puffin chicks had the highest prevalence (above 70% in July) of nymphs in both years and this was correlated with questing activity. Female ticks rarely fed on puffin chicks, but were prevalent on adult puffins and gulls, although prevalence and questing of ticks were not correlated in these hosts. These patterns of off-host and on-host tick activity suggests that I. uriae ticks likely use a combination of questing and passive waiting, e.g., in puffin burrows, to detect hosts, depending on the tick stage and the host species.

I investigated spatial variation in the prevalence and abundance of 4 species of parasites in the sand crab, Emerita analoga, on 8 sandy beaches along 800 km of the California coast, to assess the importance of bird abundance for the distribution of parasites among sand crab populations. I collected sand crabs and counted shorebirds and gulls at each beach during June and November 1994. Sand crabs served as intermediate hosts for 4 species of parasites, including a trematode, Spelotrema nicolli (Cable and Hunnienen, 1938); an acanthocephalan, Polymorphus kenti (Van Cleave, 1947); a nematode, Proleptus sp., and an unidentified trypanorhynch tapeworm. Among sand crab populations, there was substantial spatial variation in the prevalence and abundance of each parasite species. No latitudinal pattern was apparent for any of the 4 species observed. Temporally, parasite prevalence and abundance was significantly different between dates for all 4 parasites. Specifically, sand crab populations experienced higher trematode, nematode, and trypanorhynch prevalence and abundance in November than in June. In contrast, prevalence and abundance of acanthocephalans were higher in June than in November. There were strong positive associations between bird abundance and prevalence of parasitic infection for trematodes and acanthocephalans for some dates but not for nematodes or trypanorhynchs, which use elasmobranchs as definitive hosts. The spatial variation in prevalence and abundance of trematodes and acanthocephalans observed among sand crab populations may be attributed to the distribution and abundance of shorebirds and gulls that serve as definitive hosts.

Pterygodermatites (Paucipectines) jägerskiöldi Lent and Freitas, 1935, a parasitic nematode of the small intestine of the marsupial Gracilinanus agilis (Mammalia: Didelphidae) from the Pantanal of Mato Grosso do Sul state, and G. microtarsus from Atlantic Forest of Rio de Janeiro state, Brazil, were analyzed by light and scanning electron microscopy. Details of the surface topography such as the oral aperture, cephalic papillae, 2 papillae in posterior end, and longitudinal cuticular elements represented by combs and spines are presented along with measurements, adding new taxonomic characters to the previous diagnostic feature of P. (P.) jägerskiöldi based on light microscopy. In addition, two new hosts records and two new geographical distributions for this nematode are reported.

Premunition in Plasmodium spp. is the prevention of superinfection by novel genotypes entering an already established infection in a vertebrate host. Evidence for premunition was sought for the lizard malaria parasite, P. mexicanum, in its natural host, the fence lizard, Sceloporus occidentalis. Clonal diversity (= alleles for the haploid parasite) was determined with the use of 3 microsatellite markers. Both naturally infected lizards (N = 25) and previously noninfected lizards (N = 78) were inoculated intraperitoneally (IP) with blood from donor infections and followed over a 3-mo period. Compared to the success of clonal establishment in all the naive lizards (78/78 successful), clones entering preexisting infections had a significant disadvantage (9/25 successful). The number of preexisting clones (1–2 vs. 3–4) within recipient infections had no effect on the success of superinfection. Infections that excluded entering novel clones did not have higher initial asexual parasitemia, but had a higher initial density of gametocytes, suggesting they were older. Infections allowing superinfection experienced a higher final parasitemia.

The life cycle of the apicomplexan protozoon Hepatozoon canis in its natural hosts Rhipicephalus sanguineus (tick) and Canis familiaris (domestic dog) was studied in an experimental infection. Tick nymphs were fed on a naturally infected dog, or they were infected by percutaneous injection of blood. Dogs were inoculated by ingestion of adult ticks containing mature oocysts. Gamonts were in syzygy 24 hr after percutaneous injection of ticks. Early oocysts were detected 96 hr after nymph repletion, and mature oocysts in adult ticks were infective to dogs 40 days postmolt. Merogony was detected in dog bone marrow from 13 days postinoculation (PI) and included meronts containing 20–30 micromerozoites, and a second type with 2–4 macromerozoites. Monozoic cysts were observed in the spleen in conjunction with merogony. Gamontogony with infection of leukocytes by micromerozoites occurred from 26 days PI, and gamont parasitemia, which completed the life cycle, was detected 28 days PI. The length of the life cycle from nymphal attachment to parasitemia in dogs was 81 days. Increased body temperatures were evident from 16 to 27 days PI and paralleled the time of intensive bone marrow merogony. Skeletal pain and recumbency were manifested in 2 dogs. This study further elucidates the life cycle of H. canis and provides a sequential morphologic description of H. canis merogony, gamontogony, and sporogony.

Studies on the life cycles and epizootiology of North American frog lung flukes indicate that most species utilize odonates as second intermediate hosts; adult frogs become infected by ingesting odonate intermediate hosts. Newly metamorphosed frogs are rarely infected with these parasites, predominantly because they are gape-limited predators that cannot feed on large intermediate hosts such as dragonflies. We examined the role of the frog diet and potential intermediate hosts in the recruitment of the frog lung fluke, Haematoloechus coloradensis, to metamorphosed northern leopard frogs (Rana pipiens), Woodhouse's toads (Bufo woodhousii), and bullfrogs (Rana catesbeiana) from western Nebraska. Because of the uncertain validity of H. coloradensis as a distinct species from Haematoloechus complexus, morphological characters of both species were reevaluated and the life cycles of both species were completed in the laboratory. The morphological data on H. coloradensis and H. complexus indicate that they differ in their oral sucker to pharynx ratio, uterine loop distribution, and placement of vitelline follicles. However, in terms of their life cycles, both species are quite similar in their use of physid snails as first intermediate hosts, a wide range of nonodonate and odonate arthropods as second intermediate hosts, and leopard frogs and toads as definitive hosts. These results indicate that H. coloradensis and H. complexus are generalists at the second intermediate host level and might be able to infect newly metamorphosed leopard frogs and toads by using small nonodonate arthropods more commonly than other frog lung fluke species. Comparisons of population structure of adult flukes in newly metamorphosed leopard frogs indicate that the generalist nature of H. coloradensis metacercariae enables it to colonize young of the year leopard frogs more commonly than other Haematoloechus spp. that only use odonates as second intermediate hosts. In this respect, the generalist nature of H. coloradensis and H. complexus at the second intermediate host level is an avenue for the colonization of young of year frogs.

Four parasite species (Crepidostomum cooperi, Cystidicoloides ephemeridarum, Acanthocephalus dirus, Salmincola edwardsii) infected 215 juvenile brook trout (105 young-of-year; 110, 1-yr-old) from Hunt Creek, Michigan, in 2003, 2004, and 2005. Prevalences of these species in 2004 (main study year) varied from 29 to 37%. Crepidostomum cooperi had the highest mean intensity and mean abundance, followed by C. ephemeridarum. The number of fish infected with each parasite species was significantly higher in 1-yr-old fish than in young-of-year fish. Also, the mean intensities and mean abundances of C. cooperi and C. ephemeridarum and the mean abundance of A. dirus were significantly higher in older fish. The mean intensity of C. cooperi and prevalence of A. dirus were significantly higher in fish between creek sections. Fish length had a significant positive effect on the abundances of C. cooperi and C. ephemeridarum; parasite species richness, on the abundances of A. dirus and S. edwardsii; and parasite species richness in the 2003 and 2004 trout cohorts, respectively. Crepidostomum cooperi, C. ephemeridarum, A. dirus, and S. edwardsii commonly infect Michigan brook trout. The small number of parasite species infecting Hunt Creek brook trout is similar to the number of parasite species of brook trout from other Michigan creeks.

Cercaria sevillana is the cercaria larval stage that infects the gonads and the digestive gland of its first intermediate host, Nassarius reticulatus. In this study the decapodous crustacean Carcinus maenas was used to determine if it would serve as second intermediate host in the parasite's life cycle. The latter hypothesis was based on the knowledge that C. maenas is the second intermediate host of several other digenean species. After dissection, it was possible to observe encysted metacercariae in the antennal glands of the green crab. After biochemical excystment, the metacercariae were processed for light and scanning electron microscopy. The morphological features observed led us to conclude that this species was a microphallid fluke, and it was identified as Gynaecotyla longiintestinata. To establish a possible relationship between C. sevillana and this metacercariae, the ITS1 region was analyzed. Thus, DNA was extracted from C. sevillana and from the cysts isolated from the antennal glands. The ITS1 region was amplified and sequenced, and the alignment clearly demonstrated that the cercaria and the metacercariae belonged to the same species, G. longiintestinata.

The partial life cycle of an echinostomatid found in Lymnaea viatrix from Patagonia, Argentina, was experimentally clarified. Emerging cercariae were exposed to laboratory-reared specimens of Biomphalaria sp. Metacercariae obtained from both naturally and experimentally infected snails were force-fed to chicks. Specimens recovered from the chicks belong to Echinoparyphium sp. on the basis of morphological features. The studied species possesses 43 collar spines arranged in 4-4-27-4-4 at all stages, a cercariae with over 100 small corpuscles in the excretory system, a cercariae tail without finfolds, and a metacercariae with a thin cyst wall. The present species cannot be assigned to Echinoparyphium megacirrus despite their morphological similarity because of differences in the habitats of L. viatrix and the intermediate hosts of E. megacirrus, namely Chilina dombeiana, Diplodon chilensis, and Temnocephala chilensis. More information on some life cycle stages and on the ecology of the intermediate hosts is needed to clarify the taxonomic status of the parasite. This study represents the first detailed description of parasites other than Fasciola hepatica in L. viatrix from Argentina.

Lipid rafts are detergent-resistant, liquid-ordered microdomains in plasma membranes that are enriched in cholesterol and sphingolipids and involved in intracellular signal transduction, membrane trafficking, and molecular sorting. In this study, we investigated the possibility that lipid rafts on Eimeria tenella sporozoites may act as platforms for host cell invasion. Flotillin-1, a resident protein of lipid rafts, was identified on E. tenella sporozoites and was prominently expressed at the apex of the cells, a region mediating host cell invasion. Pretreatment of sporozoites with antibody against flotillin-1 blocked parasite invasion. Furthermore, the anticoccidial drug, monensin, disrupted the localization of flotillin-1 within raft structures resulting in loss of invasion. We conclude that Eimeria sporozoites utilize lipid rafts containing flotillin-1 for internalization into host cells.

A number of complex processes are involved in Eimeria spp. survival, including control of sporulation, intracellular invasion, evasion of host immune responses, successful reproduction, and nutrition. Proteases have been implicated in many of these processes, but the occurrence and functions of serine proteases have not been characterized. Bioinformatic analysis suggests that the Eimeria tenella genome contains several serine proteases that lack homology to trypsin. Using RT-PCR, a gene encoding a subtilisin-like and a rhomboid protease-like serine protease was shown to be developmentally regulated, both being poorly expressed in sporozoites (SZ) and merozoites (MZ). Casein substrate gel electrophoresis of oocyst extracts during sporulation demonstrated bands of proteolytic activity with relative molecular weights (Mr) of 18, 25, and 45 kDa that were eliminated by coincubation with serine protease inhibitors. A protease with Mr of 25 kDa was purified from extracts of unsporulated oocysts by a combination of affinity and anion exchange chromatography. Extracts of SZ contained only a single band of inhibitor-sensitive proteolytic activity at 25 kDa, while the pattern of proteases from extracts of MZ was similar to that of oocysts except for the occurrence of a 90 kDa protease, resistant to protease inhibitors. Excretory-secretory products (ESP) from MZ contained AEBSF (4-[2-Aminoethyl] benzenesulphonyl fluoride)–sensitive protease activity with a specific activity about 10 times greater than that observed in MZ extracts. No protease activity was observed in the ESP from SZ. Pretreatment of SZ with AEBSF significantly reduced SZ invasion and the release of the microneme protein, MIC2. The current results suggest that serine proteases are present in all the developmental stages examined.

Musculoskeletal symptoms such as myalgia are well-known features in the course of trichinellosis; however, the characteristics of musculoskeletal findings have been described in detail in only 1 study. The present study was aimed to determine the joint and muscle symptoms in subjects diagnosed with acute trichinellosis at our rheumatology unit during a Trichinella britovi outbreak that occurred in Izmir, Turkey, in 2004. In total, 98 patients (55 females, 43 males; mean age 32.3 ± 10.9 yr) were included in the study. A detailed history and full musculoskeletal examination were obtained in each patient. A self-administered questionnaire developed for recording the musculoskeletal symptoms was completed monthly until all the symptoms were resolved. Pain at the joints, restriction of movements (in shoulders, elbows, wrists, knees, ankles, and temporomandibular joints), myalgia, and muscle weakness (neck and shoulder girdle, muscles of the upper and forearm, back, thigh, and calf muscles) were assessed in every patient. Eosinophil counts, serum levels of creatine kinase, and lactate dehydrogenase also were analyzed. The most frequent musculoskeletal symptoms were muscle pain (86 cases [87.8%]), joint pain (83 [84.7%]), subjective muscle weakness (75 [76.5%]), and restriction of joint movements (63 [64.3%]). Calves, upper arm, neck and shoulder girdle, and forearms were the most affected muscle groups. Muscle pain was reported more frequently in the upper than in the lower extremities and during activity. The most frequent painful joints were shoulders, knees, wrists, and ankles. Upper extremity joints were affected more frequently than the lower extremity joints (77.6 vs. 70.4%). Joint pain occurred more frequently at rest. Both muscle weakness and restriction of joint movements were reported in and around the most frequently affected regions. No evidence of arthritis and objective muscle weakness was noted on physical examination in any patient. Musculoskeletal symptoms in the course of T. britovi infection are frequent but with an excellent prognosis. Joint pain in people suffering from acute trichinellosis may occur more frequently than reported previously.

Canine intestinal coccidiosis is a cause of diarrhea in young dogs and dogs that are immunocompromised. Reports in the literature indicate that experimental reproduction of clinical coccidiosis with Cystoisospora canis (syn. Isospora canis) is difficult, and few studies have been done with C. canis. Experimental oral infections were attempted in 22, 6- to 8-wk-old female beagles with 5 × 10⁴ (n = 2) or 1 × 10⁵ (n = 20) sporulated C. canis oocysts. Diarrhea was observed in all inoculated dogs. Diarrhea began 2–3 days before oocyst excretion. Five of the 22 dogs were given an anticoccidial (sulfadimethoxine) because of their clinical signs. The mean prepatent period was 9.8 days (range, 9–11 days, n = 22 dogs), and the patent period was 8.9 days (range, 7–18 days, n = 20 dogs). Two dogs exhibiting clinical coccidiosis were examined at necropsy 10 days after infection. Developmental stages of C. canis were present in cells in the lamina propria throughout the entire small intestine in both dogs. Microscopic lesions observed in both of these dogs were villous atrophy, dilation of lacteals, and hyperplasia of lymph nodes in Peyer's patches. Results of bacterial and viral examinations of these 2 dogs were negative, indicating that intestinal coccidiosis was the cause of the diarrhea. Our study indicates that C. canis can be a primary cause of diarrhea in young dogs.

A new species of dracunculoid nematode, Moravecia argentinensis n. sp. (Guyanemidae), is described from the blood vessels and body cavity of Brazilian flathead, Percophis brasiliensis Quoy et Gaimard (Perciformes: Percophidae), from off the coast of Argentina. The new species differs from the only other congeneric species, Moravecia australiensis Ribu et Lester, 2004, mainly in the number (14) of cephalic papillae, the length ratio of the muscular and glandular portions of esophagus (1:1–2), more numerous (3–5 pairs) genital papillae in the male, and the presence of a sclerotized copulatory plate. This is the second known species of Moravecia Ribu et Lester, 2004 and the first species of this genus reported from South American waters.

New material of Yorkeria Southwell, 1927, collected from Chiloscyllium Müller & Henle species, i.e., bamboo sharks, from Malaysian Borneo and eastern Australia was found to include specimens that appear to be consistent with, and thus allow redescription of, the poorly characterized type of the genus, Yorkeria parva Southwell, 1927, as well as 7 new species of tetraphyllidean cestodes from the genus Yorkeria. Discovered in Borneo were Y. parva and Yorkeria teeveeyi n. sp. from Chiloscyllium indicum (Gmelin), Yorkeria garneri n. sp. from Chiloscyllium hasselti Bleeker, Yorkeria pusillulus n. sp., Yorkeria saliputium n. sp., and Yorkeria yubodohensis n. sp. from Chiloscyllium punctatum Müller & Henle. In Australia, a shark species tentatively identified as Chiloscyllium cf. punctatum was found to host Yorkeria izardi n. sp. and Yorkeria longstaffae n. sp. Three of the new species resemble Yorkeria kelleyae Caira & Tracy, 2002, described from sharks identified as C. punctatum in Thailand, in their possession of medial and lateral hooks that are approximately equal in length. All 3 can be distinguished from Y. kelleyae, however, in their possession of vitelline follicles that are not interrupted at the level of the ovary; they differ from one another in that 1 is hyperapolytic (Y. saliputium n. sp.), and the other 2 possess round (Y. pusillulus n. sp.) versus tapered (Y. longstaffae n. sp.) bothridia. Among species with medial and lateral hooks that are conspicuously unequal in length, only Y. izardi n. sp. possesses bothridia that taper posteriorly and almost completely overlap the cephalic peduncle, stopping just short of its posterior margin. Yorkeria garneri n. sp. is distinctive in its possession of mature proglottids that are only slightly longer than wide, rather than distinctly longer than wide. Particularly notable is Y. teeveeyi n. sp., which bears a stobila on which 2–3 of the subterminal proglottids are consistently more mature than the terminal proglottid. Yorkeria yubodohensis n. sp. most closely resembles Y. parva, differing in the pattern of microtriches seen on its scolex, and also in its possession of relatively fewer proglottids. This brings the total number of Yorkeria species described worldwide to 12. The host associations of these cestodes raise questions about the conspecificity of bamboo shark specimens identified as C. punctatum in Thailand, Borneo, and Australia, since individuals in each of these 3 regions appear to host distinctive, nonoverlapping Yorkeria faunas. A key to the 12 known species of Yorkeria is provided.

Huffmanela moraveci n. sp. (Nematode: Trichosomoididae) is described from the skin of fins and gills of the silversides Odontesthes smitti Lahille, 1949, and Odontesthes nigricans Richardson, 1848 (Pisces: Atheriniformes), from southwestern Atlantic coast, on the basis of the morphology of adults and eggs found in the host tissues. Huffmanela moraveci n. sp. can be distinguished from Huffmanela carcharini, H. banningi, H. japonica, H. mexicana, H. paronai, H. schouteni, H. shikokuensis, H. branchialis, H. filamentosa, H. ossicola, and H. lata by the size and shape of the eggs. The adult stage of H. moraveci n. sp. can be differentiated from H. huffmani and H. canadensis by the position of the nerve ring and by the total esophagus length/body length ratio. Huffmanela moraveci n. sp. also differs from H. huffmani by the presence of bacillary bands and by the body length. This is the first report of a species of Huffmanela in South America, the first report of a species of Huffmanela with Odontesthes spp. as host, and the third known adult form in the genus.

Eight species of Syphacia (Nematoda: Oxyuridae) have been reported from South America in rodents of the Sigmodontinae, only 1 of which has been recorded in Argentina. Syphacia (Syphacia) carlitosi n. sp. is described from the ceca of Akodon azarae bibianae and Akodon azarae hunteri (Sigmodontinae: Akodontini) captured in 3 provinces in the northeast region of Argentina. The new species is differentiated principally by the shape of the cephalic plate; distribution of submedian papillae and amphids; presence, extent, and shape of cervical alae in females; absence of lateral alae; absence of deirids; spicular and gubernaculum length; shape and structure of accessory hook of gubernaculum; and distance of mamelons, excretory pore, and vulva from the anterior extremity. This is the second record of Syphacia parasitizing rodents of the tribe Akodontini.

In a survey of 1,732 amphibians and reptiles collected across São Paulo Province, Brazil, and 7 provinces in Paraguay, 26 species were found infected with acanthocephalans. Of 1,510 anurans, 14 anurans, representing 11 species, were infected with cystacanths of Centrorhynchus spp. and 1 anuran with cystacanths of Oligacanthorhynchus sp. Of 107 lizards, 1 lizard was infected with cystacanths of Centrorhynchus sp. and 1 lizard with cystacanths of Oligacanthorhynchus sp. Acanthocephalus caspanensis was found in 3 anurans (3 species) and Acanthocephalus lutzi in 3 anurans (2 species) and 2 snakes (2 species). The systematic position of A. lutzi cannot be resolved using presently available morphological data. Acanthocephalus saopaulensis n. sp. was found in a single individual of Bufo ictericus. The new species can be differentiated from all its congeners except A. caspanensis in having a sigmoid-shaped male posterior end and from A. caspanensis in having a proboscis armature of 16 rows of 5–7 hooks rather than 18–19 rows of 6–7 hooks and larger eggs. The status of Acanthocephalus and Pseudoacanthocephalus continues to be problematic.

Neosychnocotyle maggiae, n. gen., n. sp., (Aspidogastrea) is described from the pig-nosed turtle, Carettochelys insculpta, and reported from the Victoria River red-faced turtle, Emydura victoriae, all from the Daly River, Northern Territory, Australia. Neosychnocotyle n. gen. is differentiated from all aspidogastrean genera but one by the absence of a cirrus sac. The similar Sychnocotyle also lacks a cirrus sac, but Neosychnocotyle n. gen. differs from the former genus by possessing a narrow, tapered anterior end, a ventral disk that covers the posterior end of the body, a genital pore that is displaced anteriorly, and a vas deferens that is less convoluted and less robust. Analysis of ribosomal DNA sequences demonstrates substantial sequence variability between representatives of Sychnocotyle and Neosychnocotyle maggiae, n. gen., n. sp. It is possible that this new parasite may reach sexual maturity only in C. insculpta. This is only the second aspidogastrean species reported from Australian freshwater turtles.

Aptorchis megacetabulus n. sp. is described from the intestine of the northern long-necked turtle, Chelodina rugosa (Pleurodira: Chelidae), in Northern Territory, Australia. This is the first helminth species reported from C. rugosa. This plagiorchioidean digenean differs from the 3 previously known species of Aptorchis in the relative size of the ventral sucker, overall body proportions, nature of the cirrus sac, and egg size. Comparison of approximately 2,700 bases of ribosomal DNA obtained from all known Aptorchis species strongly supports the status of Aptorchis megacetabulus n. sp. as a new species.

Taeniasis diagnosis is an important step in the control and elimination of both cysticercosis and taeniasis. We report the development of 2 serological taeniasis diagnostic tests using recombinant antigens rES33 and rES38 expressed by baculovirus in insect cells in an EITB format. In laboratory testing with defined sera from nonendemic areas, rES33 has a sensitivity of 98% (n = 167) and a specificity of 99% (n = 310) (J index: 0.97); rES38 has a sensitivity of 99% (n = 146) and a specificity of 97% (n = 275) (J index: 0.96). Independent field testing in Peru showed 97% (n = 203) of the taeniasis sera were positive with rES33, and 100% of the nontaeniasis sera (n = 272) were negative with rES33; 98% (n = 198) of taeniasis sera were positive with rES38, and 91% (n = 274) of the nontaeniasis sera were negative with rES38. Among the Peruvian sera tested, 17 of 26 Peruvian Taenia saginata sera were false positive with rES38 test. Both tests were also examined with cysticercosis sera, with a positive rate ranging from 21% to 46%. rES33 and rES38 tests offer sensitive and specific diagnosis of taeniasis and easy sample collection through finger sticks that can be used in large-scale studies. They are currently being used in cysticercosis elimination programs in Peru.

The infection of Myxobolus galaxii Szidat, 1953, from the musculature and abdominal organs of northwestern Patagonian Galaxias maculatus is described. Plasmodia are histozoic and intercellular. Spores are pyriform in valvar view and biconvex in sutural view, with 4–9 edge notches in the sutural line, varying in shape within the same plasmodium. Myxobolus galaxii was detected in fish from 7 of 17 Andean Patagonian lakes, with prevalences ranging between 2 and 17%. A repeating pattern of summer increment in prevalence was observed, which could be explained by the ontogenetic migratory movements of the fish in Lake Gutiérrez. Also, accumulation of plasmodia through the life span of fish was detected.

Organic remains attributable to one regurgitated pellet were examined. The pellet, belonging to a bird of prey and collected from a cave of Southern Patagonia, was dated at 6,540 ± 110 yr. With standard paleoparasitological procedures, eggs of Capillaria sp. and a mite, Demodex sp., were found. The parasites found in the pellet belong to a rodent ingested by the bird. The present report constitutes the first paleoparasitological study of a regurgitated pellet.

Studies reporting numbers of eggs in vagina and utero in nematodes often give little information of the technique used for the estimations. This situation hampers comparison among studies, because, so far, differences in estimations provided by different techniques have not been assessed. This note examines whether a manual method based on visual counts in aliquots and an automated method using a Coulter counter yield equivalent estimations of egg numbers in vagina and utero of 3 anisakid nematode species (Anisakis simplex, Pseudoterranova decipiens, and Contracaecum osculatum). The number of eggs from 50 females per nematode species was estimated using both techniques. The automated and manual methods yielded similar egg counts (correlation coefficients >0.9 in the 3 species), but the methods were not always statistically equivalent. The automated method was more precise and seemed less dependent on egg density, whereas the manual method was less time-consuming (contrary to previous perceptions) and less expensive. Despite the higher precision of automated counts, the manual technique seemed to produce similar estimates; thus, it may be particularly useful in developing countries where nematode parasitism is prevalent in humans and domestic animals, but scientific resources are limited.

The molecular identification of species and genotypes of Giardia spp. infecting wild mammals represents the most reliable tool to understand the role played by these animals as reservoirs of cysts infectious for human and other animals. Of 139 fecal samples collected from fallow deer (Dama dama L.) hunted in a Natural Reserve of northern Italy, the prevalence of Giardia sp. was 11.5% (16 of 139 animals), and it was higher in fawns than in older animals. Fragments of the β-giardin and triose phosphate isomerase (tpi) genes were successfully polymerase chain reaction amplified and sequenced from 8 isolates. No sequence variation was observed between isolates at the 2 genetic loci. Sequence and phylogenetic analyses identified a Giardia duodenalis subtype that clusters with assemblage A isolates and that shows homologies of 98 and 97% at the β-giardin and tpi loci, respectively, compared with the A1 subtype. Because the G. duodenalis subtype found in fecal samples of fallow deer has never been detected previously, its role as a pathogen for humans and domestic animals is unknown, but, considering its genetic distinctiveness, it is likely to be low.

It is known that excretory/secretory antigens of Fasciola hepatica (ESFh) trigger a Th2-like immune response. Anapsos® (A) is an aqueous hydrosoluble extract obtained from the rhizomes of the fern Polypodium leucotomos that has shown immunomodulator effects in some parasitic infections and immunological disorders. In this work we assess the effect of Anapsos® and ESFh and Quillaja saponaria extract (Qs) on BALB/c mice and rat alveolar macrophages. Anapsos® modulates the response of mice immunized with ESFh, decreasing IgG1 antibodies in A ESFh− and A Qs ESFh−treated mice and triggering high levels of γIFN in spleen cell culture in comparison with ESFh− and Qs ESFh−treated groups. Moreover, Anapsos® showed statistically significant inhibitory effects on the nitrite production by rat alveolar macrophages prestimulated with lipopolysaccharide (LPS) as well as ESFh antigen in comparison with macrophages stimulated only with LPS. The application of ESFh and Anapsos® combined avoids this inhibitory effect. Thus, Anapsos® modulates the immune response against ESFh in naive mice and on the nitrite production in prestimulated rat alveolar macrophages.

Canine heartworm (Dirofilaria immitis) is a nematode that naturally parasitizes in the pulmonary arteries and the right ventricle of domestic dogs (Canis familiaris) as final hosts. Japanese raccoon dogs (Nyctereutes procyonoides viverrinus) also are known to be susceptible to infection by the parasite. However, prevalence of this infection among free-ranging raccoon dogs is low and so is the worm burden. To examine the susceptibility of the raccoon dog to D. immitis infection, 3 raccoon dogs and 2 beagles were inoculated 4 times with 25 third-stage larvae (L3s) of D. immitis at 3-wk intervals. Worms were recovered from 2 raccoon dogs and both domestic dogs. The average percentage of recovery (2.3%) of the raccoon dogs was almost 10 times lower (24.5%) than that of the domestic dogs, but there was no significant difference in the body length of worms recovered from 2 types of hosts. To examine microfilaremia, 2 raccoon dogs were infected with 100 L3s. Microfilaremia was observed for 180 days postinoculation (PI) but disappeared at about 300 days PI. The raccoon dog was mildly susceptible to infection with D. immitis, but surviving worms developed and matured normally.

Most procedures that have been described for purifying Cryptosporidium parvum oocysts are designed to either identify the parasites in clinical specimens or isolate oocysts from a small volume of feces from infected animals. The present study describes a rapid method for purifying high numbers of C. parvum oocysts from feces of infected calves that contains minimal contaminating fecal material and bacteria. The isolation method is based on differential flotation of C. parvum oocysts in NaCl, followed by ether extraction to solubilize lipids in calf feces. This procedure regularly yields >10⁹ purified C. parvum oocysts within 1–2 days of feces collection.

The infection dynamics of Centrocestus armatus cercariae with respect to second intermediate fish hosts were investigated using cercariae collected from naturally infected Semisulcospira libertina. Cercariae survival and infectivity were recorded at 2-hr intervals. Survival remained constant but decreased abruptly at 30 hr of age. An age-dependent model presented the best-fit curve for the survival data (r² = 0.936), implying that cercariae tended to allocate resources equally among themselves and then died once those resources were depleted. Cercariae infectivity remained constant over the first 10 hr of life and then declined; an age-dependent model also provided a better fit (r² = 0.956). The transmission rate of C. armatus cercariae to the fish host was relatively low near the time of emergence from the snail host but peaked at 85% after 1 hr and then maintained a plateau period until 5 hr of exposure to fish. The pattern of transmission was also investigated initially at varying densities of cercariae and then by maintaining a constant cercariae density but varying the total number. Results revealed that the pattern of transmission was frequency-dependent.

In June 2005, we collected 115 fecal samples from wild primates in western Uganda and examined them for Cryptosporidium sp. and Giardia sp. with the use of immunofluorescent antibody (IFA) detection. We sampled primates from an undisturbed forest in Kibale National Park and from 3 highly disturbed forest fragments outside the park. Of disturbed forest samples, red colobus (Pilocolobus tephrosceles) and red-tailed guenons (Cercopithecus ascanius) harbored species of Cryptosporidium or Giardia, but black-and-white colobus (Colobus guereza) did not. All primate samples from undisturbed forest were negative for both parasites. Seven of 35 (20%) red colobus and 1 of 20 red-tailed guenons (5%) from forest fragments were infected with either Cryptosporidium sp. or Giardia sp. The presence of Cryptosporidium and Giardia species in primates living in forest fragments, but not in primates in undisturbed forest, suggests that habitat disturbance may play a role in transmission or persistence of these pathogens.

Fifteen cases of human pseudoterranovosis are reported for Chile, representing an emerging parasitic infection in this country caused by larvae of the nematode Pseudoterranova sp. Our observations also included an outbreak of pseudoterranovosis in 3 of 4 individuals who shared the same raw fish dish (cebiche). Most of the cases occurred in adult patients. The main source of infection was from consumption raw or fried marine fish, including hakes (Merluccius australis or Merluccius gayi), pomfret (Brama australis), Inca scad (Trachurus murphyi), and corvina (Cilus gilberti). Seasonal distribution showed most of the cases to occur in fall and spring. Parasite larvae were isolated from the mouths of most of the patients after they reported a pharyngeal tickling sensation, coughing, vomiting, or a foreign body in the mouth or throat.