Investigating the development of Eustrongylides ignotus in its definitive host would enable us to trace the complete life cycle of this nematode. Fourth-stage larvae isolated from naturally infected swamp eels (Monopterus albus) were used to infect domestic ducks (Anas platyrhynchos domestica [L.]). We observed that male and female worms exhibited different developmental patterns in host ducks. In males, the fourth molt occurred at day 1–2 post-infection (PI), after which they attained maturity on day 4 PI and died between day 7 and 9 PI. However, females underwent the fourth molt at day 2–4 PI, produced eggs from day 9 to 17 PI, and then degenerated and died. When compared to fourth-stage female larvae, adult females demonstrated a considerable increase in total body size with a 151% increase in average body width and a 17% increase in average body length. However, the increase in size of the male larvae was not as significant as that in females. The average body width in adult males exhibited only a 45% increase over that in the larval stage.

Neoechinorhynchus golvani is an intestinal parasite of freshwater and brackish water fishes distributed in Mexico. The genetic variability of 40 samples representing 12 populations from north, south, and central Mexico, and 1 from Costa Rica, was estimated by sequencing 2 nuclear genes (ITS1, 5.8S, ITS2, and LSU rDNA, including the domain D2 D3). The length of both genes ranged from 700 to 779 base pairs (bp) and from 813 to 821 bp, for ITSs and LSU, respectively. The genetic divergence among populations ranged from 19.5 to 35.3% with ITSs and from 9.28 to 19.58% with LSU. Maximum likelihood and maximum parsimony analyses were performed for each data set and also for 2 combined data sets (ITSs LSU rDNA with and without outgroups), showing strong similarities among trees, with high bootstrap support in all cases. Genetic divergence, in combination with phylogenetic analyses, suggested that the acanthocephalan N. golvani represents a complex of cryptic species, which is composed of at least 3 lineages. The first lineage, corresponding with N. golvani, shows a wide distribution, including localities from northeastern Mexico, southwards through central and southeastern Mexico, and further down to Costa Rica. This lineage is associated with cichlid fishes in strictly freshwater environments. Lineages 2 and 3 are distributed in brackish water systems along the Gulf of Mexico and Pacific slopes, respectively; both are associated with eleotrid fishes, and apparently represent 2 cryptic species. The diversification of the eleotrid and cichlid lineages seems to be the result of independent host-switching events from the ancestral population.

The population dynamics of Ascaris suum was studied by long-term exposure of pigs to infective eggs. The pigs were experimentally inoculated with 25 A. suum eggs/kg/day, and 7, 8, and 8 pigs were necropsied at weeks 4, 8, and 14 postinoculation (PI), respectively. Despite the fact that the pigs were continuously reinfected, dramatic reductions in numbers of liver lesions (white spots) and migrating lung larvae were observed as a function of time. However, even at the end of the study, a few larvae were able to complete migration, but these larvae seemed unable to mature in the small intestine. Thus, the adult worm population seemed to consist of worms from the first part of the exposure period. The noticeable decrease in number of white spots suggests that the level of exposure is not reflected in the number of white spots in the late phase of a continuous infection. The serum levels of A. suum L₃-specific IgG1 and IgA were significantly elevated by week 4 PI, after which the antibody levels declined. The population dynamics and parasite regulating mechanisms are discussed for A. suum in pigs as well as for the closely related species A. lumbricoides in humans.

The influence of ontological diet shifts on infracommunity nestedness was examined by comparing the infracommunity structure of Lepomis gulosus and Lepomis macrochirus at 2 localities in Par Pond, South Carolina, United States. Fill-constrained, occurrence-constrained, and abundance-constrained null models were used to evaluate the degree of nestedness. The presence–absence matrices from all 4 component communities had significantly fewer discrepancies than those produced by the fill-constrained model, and none had significantly fewer discrepancies than those produced by the occurrence-constrained model. Only the presence–absence matrix for the infracommunities of L. gulosus from the Cold Dam locality had significantly fewer discrepancies than those produced by the abundance-constrained null model. The nestedness of the 4 samples could not be distinguished from that expected under a hypothesis of passive sampling. A positive correlation between host size and total parasite abundance indicates the passive mechanism has a deterministic basis. Thus, even in the absence of habitat or diet shifts, nestedness can arise in infracommunities of freshwater fishes when older, larger fish have sampled more individuals from an uneven distribution of infective stages.

An epidemiologic case-control study was conducted to identify factors that predispose Peromyscus spp. to the risk of infection with Giardia sp. in watersheds. A total of 200 Giardia sp.–positive mice (cases) and a similar number of Giardia sp.–negative mice (controls) were selected from a population 2,528 mice captured in a watershed in southeastern New York State. The Giardia sp. infection status of the mice was determined by centrifugation concentration flotation and an enzyme-linked immunosorbent assay. The mice were later classified into 2 species, Peromyscus maniculatus and P. leucopus, using cellulose acetate electrophoresis of individual saliva samples. The risk of infection was evaluated while controlling for indigenous factors (age and sex) and exogenous factors (habitat and land use) that were hypothesized to influence the likelihood of infection with Giardia sp. The study population consisted of 257 (59%) P. leucopus and 165 (41%) P. maniculatus. Peromyscus leucopus mice were at a higher risk of becoming infected with Giardia in comparison to P. maniculatus (adjusted odds ratio  =  40). The risk of Giardia sp. infection varied with the age of the animals, since adult animals were at higher risk than juvenile animals. This study suggested a difference in susceptibility to Giardia sp. between different species of mice.

During March 2002 and November 2005, teleost fishes were collected at Lizard Island, Great Barrier Reef (GBR), Australia. Gnathiid isopod juveniles were allowed to detach from these host fishes and were maintained in fresh seawater until they molted into adults. Adult males emerged 5 days post-detachment (d.p.d.) and females 10 d.p.d. of juveniles from host fish. The adults and juveniles were identified as new to science and described as Gnathia aureamaculosa n. sp. The species description is based on brightfield and scanning electron microscopy observations primarily of males, since the taxonomy of gnathiids is based on male morphology. This species has been widely employed in various studies on the Great Barrier Reef, from its involvement in feeding patterns in reef fish to its role in transmitting blood parasites, and has been referred to as Gnathia sp. A. Distinctive features of the male include gold-spotted pigmentation on the dorsal pereon of live specimens, a cephalosome with a conical superior fronto-lateral process, an inferior and conical medio-frontal process, and mandibles, each with an armed carina and an internal lobe. The female is characterized by its broad, rounded shape and cephalosome setae. The mandible of the third stage juvenile has 2 small teeth on the tip and 7 large teeth on the mesial margin. Differential pigmentation occurs in live male and female third-stage juveniles; females have greenish-yellow spots distributed over the pereon and males have white blotches and light brown and yellow spots on the pereon.

The original description of Henneguya adiposa, a myxozoan parasitizing channel catfish Ictalurus punctatus, is supplemented with new data on spore morphology, including photomicrographs and line drawings, as well as 18S small-subunit (SSU) ribosomal DNA (rDNA) sequence. Elongate, translucent, linear plasmodia were situated between the connective tissue bands of the adipose fin. The myxospore possessed an elongate, lanceolate spore body, flattened parallel to the suture line: 17.1 ± 1.6 µm (range 14.7–20.5) in length, 4.1 ± 0.3 µm (range 3.4–4.6) wide in valvular view, and 3.7 ± 0.3 µm (range 3.2–4.0) thick in sutural view. Polar capsules were pyriform and unequal in length, measuring 7.2 ± 0.6 µm (range 5.8–8.3) long and 1.3 ± 0.2 µm (range 0.9–1.9) wide, with at least 8 turns in the polar filament coil. The caudal appendages were 38.0 ± 6.2 µm (range 23.2–48.8) and split posteriorly. The total length of the spore was 55.6 ± 6.5 µm (range 40.7–65.8). Phylogenetic analysis of 18S SSU rDNA sequence data placed this isolate within the Myxobolidae, indicating a close relationship to a group of Henneguya species parasitizing channel catfish in the southeast United States.

Antarctophthirus microchir was originally described from Phocarctos hookeri on the basis of 1 female and 1 male only. We redescribe adults and describe, for the first time, the 3 nymphal stages from specimens collected from Otaria flavescens from Patagonia, using light and scanning electron microscopy. The present material can be distinguished from other Antarctophthirus species by the presence of a fringe of setae on the back of the head, only present in Antarctophthirus trichechi and Antarctophthirus callorhini. However, A. trichechi also possess a prominent proboscis with large hooks, and A. callorhini presents less abundant and nonuniform abdominal scales in shape and size. Other differential features of A. microchir are the pattern of ovoid and uniform scales and longitudinal grooves in the surface of spines. Nymphal stage 1 differs from 2 and 3 mainly by the absence of scales and thorax without ventral spines or hairs. Nymphal stages 2 and 3 may be distinguished by the disposition of the occipital apophyses. Antarctophthirus microchir has been reported from 5 sea lion species from both hemispheres. Considering the conservative morphology, and ecological and evolutionary features of sucking lice, we raise the question of whether A. microchir from different sea lion hosts may represent a complex of cryptic species.

Three new species of the feather mite genus Proterothrix Gaud, 1968 (Proctophyllodidae: Pterodectinae) are reported from parrotbills (Passeriformes: Paradoxornithidae) in China. We describe Proterothrix paradoxornis n. sp. from Paradoxornis webbianus (type host) and Par. alphonsianus, P. longicaula n. sp. from Par. gularis, and P. sarahbushae n. sp. from Par. verreauxi (type host) and Par. alphonsianus. These are the first records of mites of the Pterodectinae from the Paradoxornithidae. Within Proterothrix, the new species constitutes a distinct complex, characterized by the presence of a long, whip-like aedeagus and spindle-shaped setae e on tarsi I in males.

Two new species, Choricotyle scapularis and Choricotyle isaciencis (Monogenea: Diclidophoridae), are described from the gills of haemulid fishes, Anisotremus scapularis and Isacia conceptionis, respectively, in San Jorge Bay, northern Chile (23°42′S, 70°24′W); they are compared with the known species in the genus. Diagnostic characters for C. scapularis includes the number of hooks in the male copulatory organ, a developed isthmus, the shape of the haptor, and the number of testes. The diagnostic characters for C. isaciensis include the presence of an oval accesory sclerite in the clamps, the number of testes, the number of hooks in the male copulatory organ, and the relative clamp peduncle size.

Two new species of Gyrodactylus Nordmann, 1832 (Gyrodactylidae, Monogenoidea) are described, i.e., Gyrodactylus coriicepsi n. sp. from gills of black rockcod, Notothenia coriiceps Richardson, 1844, and Gyrodactylus nudifronsi n. sp. from gills of gaudy notothen, Lepidonotothen nudifrons Lönnberg, 1905, collected in waters surrounding the South Shetland Islands, Antarctica. Gyrodactylus coriicepsi n. sp. is characterized by a long, narrowing membrane of the ventral bar and a marginal hook sickle with beveled heel and toe. Gyrodactylus nudifronsi n. sp. is characterized by a conspicuous ventral bar process and barely curved marginal hook sickle with curved heel and toe. Definitive species identification and phylogenetic position were based on sequences of the rDNA region (ITS1-5.8S-ITS2). Both new species belong to a monophyletic group (bootstrap support 99%) that includes the European marine species Gyrodactylus perlucidus Bykhovskiy and Polyanskiy, 1953 (on Zoarces viviparus), Gyrodactylus flesi Malmberg, 1957 and G. robustus Malmberg, 1957 (both on Platichthys flesus), and the freshwater species Gyrodactylus hrabei Ergens, 1957 and Gyrodactylus mariannae Winger, Hansen, Bachmann and Bakke, 2008 (both on Cottus poecilopus). The observations suggest an evolutionary continuum of the marine Gyrodactylus spp. fauna in the northern and southern hemispheres, which indicates the marine origin of some freshwater Gyrodactylus species.

Sexual selection is an influential agent of evolution, often shaping the sex ratio, sexual size dimorphism (SSD), and genital size in animals. To explore its effects in ectoparasites, we quantified SSD and male genital size in relation to intensity and sex ratio across subpopulations of Philopterus coarctatus, a philopterid louse of the great grey shrike. SSD was calculated separately for the width and length of the head and abdomen. Presuming that sexual selection affects the evolution of avian lice, we would expect that infestation intensities should covary with sex ratio, relative male size, and relative male genital size, either positively or negatively depending upon presumptions. Contrary to former studies, there was a weak negative relationship between infestation intensity and sex ratio. The relative width of male abdomens exhibited a highly significant negative interaction with the intensity of infestations. In contrast, sex ratio did not predict any of the dimorphism measures. Similarly, male genital size did not covary with the intensity of infestations or sex ratios. These findings may indicate that intensity covaries positively with levels of inbreeding in this species, suggesting that more-inbred subpopulations, wasting less energy for sexual rivalry, can multiply more intensively. Thus, small subpopulations have more frequent males which also possess larger abdomens. Alternatively, however, the same pattern may also arise due to male-biased starvation in overcrowded habitats; thus, males are rarer and have smaller abdomens in larger infrapopulations.

Ticks were collected from 38 black bears (Ursus americanus floridanus) from northwestern Florida (n  =  18) from 2003 to 2005 and southern Georgia (n  =  20) in 2006. Five species (Amblyomma americanum, A. maculatum, Dermacentor variabilis, Ixodes scapularis, and I. affinis) were collected from Florida bears, and 4 species (A. americanum, A. maculatum, D. variabilis, I. scapularis) were collected from bears in Georgia. Ixodes scapularis was the most frequently collected tick, followed by D. variabilis, A. americanum, A. maculatum, and I. affinis. The collection of I. affinis from a Florida bear represents a new host record. A subset of ticks was screened for pathogens and putative symbionts by polymerase chain reaction (PCR). The zoonotic tick-borne pathogens Ehrlichia chaffeensis and Rickettsia parkeri were detected in 1 of 23 (4.3%) A. americanum and 1 of 12 (8.3%) A. maculatum, respectively. The putative zoonotic pathogen “Rickettsia amblyommii” was detected in 4 (17.4%) A. americanum and 1 (8.3%) A. maculatum. Other putative symbiotic rickettsiae detected included R. bellii and R. montanensis in D. variabilis, a Rickettsia cooleyi–like sp. and Rickettsia sp. Is-1 in I. scapularis, and Rickettsia TR39–like sp. in I. scapularis and A. americanum. All ticks were PCR-negative for Anaplasma phagocytophilum, Panola Mountain Ehrlichia sp., E. ewingii, Francisella tularensis, and Borrelia spp.

Toxoplasma gondii and Bartonella spp. are zoonotic pathogens of cats. Feline immunodeficiency virus (FIV) and feline leukemia virus (FeLv) are related to human immunodeficiency virus, and human leukemia virus, respectively; all of these viruses are immunosuppressive. In the present study, the prevalence of antibodies to T. gondi, Bartonella spp., FIV, as well as FeLv antigen were determined in sera from 75 domestic and 101 feral cats (Felis catus) from the Caribbean island of Grenada, West Indies. Using a modified agglutination test, antibodies to T. gondii were found in 23 (30.6%) of the 75 pet cats with titers of 1:25 in 1, 1:50 in 3, 1:400 in 4, 1:500 in 12, 1:800 in 2, and 1:1,600 in 1, and 28 (27.7%) of 101 feral cats with titers of 1:25 in 4, 1:50 in 7, 1:200 in 4, 1:400 in 1, 1:500 in 3, 1:800 in 2, 1:1,600 in 3, and 1:3,200 in 4. Overall, in both pet and feral cats, the seroprevalence increased with age. Antibodies to Bartonella spp. were found in 38 (50.6%) of the 75 pet cats and 52.4% of 101 feral cats. Antibodies to FIV were found in 6 domestic and 22 feral cats. None of the 176 cats was positive for FeLv antigen. There was no correlation among T. gondii, Bartonella spp., and FIV seropositivity.

In larvae of Drosophila paramelanica, eggs and larvae of the endoparasitic wasp Leptopilina heterotoma succumb to an effective host reaction that does not involve blood cell–mediated melanotic encapsulation, a response that characterizes cellular immunity in various species of Drosophila and in many insects and other arthropods. A significant increase occurs, however, in the number of lamellocytes, a type of blood cell that functions in encapsulation reactions. The appearance of activated lamellocytes in D. paramelanica is viewed as an early response to infection, one most likely initiated by non–self-recognition processes that similarly function in other wasp-infected Drosophila. However, ensuing cytotoxic responses, about which little is presently known, are not accompanied by melanotic encapsulation in D. paramelanica. Concurrent analyses of the cell-signaling molecule nitric oxide (^.NO) revealed significant alterations in the levels of this free radical during the early stages of infection, most notably a dramatic increase immediately upon infection, and precipitous decreases occurring at times when parasites were killed. Injections of a specific inhibitor of nitric oxide synthase (NOS) into the host's body cavity prior to infection significantly increased parasite survival. These observations suggest some involvement of ^.NO in the host immune response, either in recruiting hemocytes to sites of infection or as a component of the insect's cytotoxic arsenal, given the capacity of the radical to generate toxic molecules through interactions with various intermediates of oxygen and nitrogen.

Parahaemoproteus lophortyx (formerly Haemoproteus lophortyx) is known to infect populations of bobwhite quail (Colinus virginianus) in California and to lead to considerable mortalities in these birds. Populations of bobwhite quail in Florida have never been surveyed for the presence of this parasite. The goal of this study was to determine whether P. lophortyx is present in populations of bobwhite quail in north Florida. To achieve this goal, blood was drawn from 294 bobwhite quail from 4 study sites in north Florida from 19 June 2007 to 1 August 2007. Blood smears were made, stained with Giemsa, and examined under ×1,000 magnification for the presence of Parahaemoproteus lophortyx. No gametocytes were noted in any of the blood smears. Thirty randomly chosen samples were examined via polymerase chain reaction (PCR). This procedure may detect parasitemias too low to detect by microscopy. No PCR-positive samples were detected, however, adding support to the absence of hematozoa in Florida populations of bobwhite quail.

The present study used experimental infections to compare the life cycles and life histories of 6 Rhabdias spp. infecting snakes and anurans. Free-living development of anuran lungworms was primarily limited to heterogonic reproduction, and females utilized matricidal endotoky exclusively, whereas snake lungworms primarily reproduced homogonically and, when heterogonic reproduction occurred, females used a combination of releasing eggs and matricidal endotoky. Infective snake lungworms survived for longer periods in fresh water compared to anuran worms. Infective anuran lungworms penetrated into the skin of frogs and toads; few infections resulted from per os infections. In contrast, snake lungworms were unable to penetrate skin; instead, infective juveniles penetrated into snake esophageal tissue during per os infections. Despite separate points of entry, anuran and snake lungworms both migrated and developed in the fascia, eventually penetrating into the body cavity of the host. Worms molted to adulthood inside the body cavity and subsequently penetrated into the host's lungs, where they fed on blood while becoming gravid. Adult lungworm survival varied among lungworm species, but, in general, snake lungworms were longer lived than anuran worms. Anuran lungworms were poorly suited for transmission via transport hosts, whereas snake lungworms were consistently capable of establishing infections using transport hosts. Overall, these observations suggest that snake and anuran lungworms have discrepant life cycles and life history strategies.

Africana dardanelosi n. sp. is described from the intestine of the lizard Hoplocercus spinosus Fitzinger, 1843 collected from southern Amazon, Brazil. Africana dardanelosi is the third species of the genus occurring in the Neotropical realm and is the tenth species assigned to the genus. From other species of Africana from Africa, and especially from the Neotropical species (A. telfordi Bursey and Goldberg, 2002 and A. chabaudi Baker, 1981), A. dardanelosi is easily distinguished by spicule size (2,157–2,403 µm versus 366–458 µm and 644–869 µm, respectively) and by the number of caudal papillae (13 versus 17 and 10, respectively).

Pristicola bruchi n. sp. (Trematoda: Deropristiidae) is described from the spiral-valved intestine of the lake sturgeon, Acipenser fulvescens, from the Wolf River in Wisconsin, United States. It differs from the only other species of the genus, Pristicola sturionis, a parasite of the European Atlantic sturgeon Acipenser sturio, in being smaller and in possessing the following characters: a single row of conspicuous peg-like oral spines instead of 2 rows; vitelline follicles that are dorsally confluent over only a small region and that barely overlap the testes instead of extending beyond the posterior testes; and a shorter hermaphroditic duct. Comparisons are hindered by the fact that the type material of P. sturionis is no longer available. This is the first report of the genus in North America and is, apparently, the first time the genus has been reported in sturgeon anywhere since the description of P. sturionis in 1930. The presence of a species of Pristicola in North America means that all 3 genera of deropristiids, Deropristis, Pristicola, and Skrjabinopsolus, now have 2 described species, 1 in North America and another in Europe, reinforcing the amphi-Atlantic biogeography of the family. This, in turn, supports the contention that the deropristiids had diversified into the 3 generic lineages before the establishment of the North Atlantic, and that the present day distribution was likely effected by historical vicariance processes. The association of species of Pristicola and Skrjabinopsolus with the exclusively freshwater lake sturgeon in the interior of the continent also indicates their considerable geological age.

Granulocytic anaplasmosis (GA) is a potentially fatal tick-borne rickettsial disease that occurs sporadically in the far western United States. We evaluated the prevalence of Anaplasma phagocytophilum in multiple species of lizards and snakes from enzootic sites in northern California, described the infestation prevalence of its tick vector Ixodes pacificus on reptiles, and conducted an experimental challenge of western fence lizards (Sceloporus occidentalis) and Pacific gopher snakes (Pituophis catenifer) with A. phagocytophilum delivered via needle inoculation or tick bite. Both serologically and polymerase-chain reaction (PCR)–positive lizards (seroprevalence  =  10.8%, PCR prevalence  =  10.2%) and snakes (seroprevalence  =  5.8%, PCR prevalence  =  11.7%) were detected among wild-caught animals. A DNA sequence of the A. phagocytophilum groESL gene from a PCR-positive snake was 100% homologous to that of the human-derived A. phagocytophilum. Experimental attempts to infect naïve animals were unsuccessful for snakes (n  =  2), but 1 of 12 lizards became infected for 1 wk only by tick bite. Xenodiagnostic I. pacificus larvae that fed on a PCR-positive lizard did not acquire or transmit rickettsiae. Our findings suggest that lizards and snakes are exposed to A. phagocytophilum by infected ticks, but that they do not serve as primary reservoir hosts of this rickettsia.

Haemosporidian parasite diversity among raptorial birds (hawks and owls), as estimated by DNA sequencing, is proving to be greater than previously anticipated from taxonomic assessments based on parasite morphology. Here, we place raptor parasites in a phylogenetic context, including new parasite cytochrome b (cyt b) sequences from North America and Europe and from a variety of host species not previously sampled. Mitochondrial DNA sequences reveal raptor-specific parasite clades within Parahaemoproteus, but not within Plasmodium. We also recovered a strikingly divergent clade of raptor parasites that aligns with neither genus, but groups with both as a sister clade to Leucocytozoon. Different cyt b primer sets recovered additional sequences from 3 of these samples, which grouped with Parahaemoproteus in 2 cases and with Plasmodium in 1 case. Possible explanations (after excluding contamination) include multiple infections, alternative cyt b copies within the mitochondrial genome, and nuclear copies of mitochondrial genes. We believe the latter 2 explanations are unlikely because these divergent cyt b lineages form a single clade and were also recovered with several additional genomic markers.

Plagioporus kolipinskii n. sp. (Trematoda: Opecoelidae) is described from the intestine of the threespine stickleback, Gasterosteus aculeatus L., from Lobos Creek, a freshwater stream in Presidio, San Francisco County, California. Plagioporus kolipinskii is morphologically somewhat similar to 4 (P. serotinus Stafford, 1904, P. angusticollis Hausmann, 1896, P. macrouterinus Haderlie, 1953, and P. shawi [McIntosh, 1939]) of the 12 currently recognized North American species of the genus, but can be readily distinguished from all 4 in possessing a much larger acetabulum and a larger ovary relative to the testes. In addition, the new species can be distinguished from P. angusticollis by a smaller cirrus sac; from P. macrouterinus by the elongated shape of its body and reduced extent of its uterus (the uterus of P. macrouterinus extends posteriorly to the intersection of the testes); from P. shawi by a much-shorter cirrus sac (which reaches the ovary in P. shawi), an unlobed ovary (as opposed to a quadrilobed ovary in P. shawi), and fewer eggs that are also larger relative to body size.

A novel Babesia species is described from blood collected from 3 common murres (also known as common guillemots) (Uria aalge) from California. This is the first report of a Babesia species from the Alcidae and the second from the Charadriiformes. Babesia uriae n. sp. is morphologically similar to several other avian Babesia species but can be differentiated from Babesia bennetti, the only other species from a host in the Charadriiformes, by size of round and amoeboid forms. Phylogenetic analysis of near–full length 18S rRNA, ITS-1, 5.8S rRNA, and ITS-2 sequences indicated that the Babesia sp. from the common murre is closely related to Babesia poelea, a parasite of brown boobies (Sula leucogaster).

Two (33.3%) of 6 blue-crowned motmots (Momotus momota) sampled from Costa Rica were positive for a new species of Isospora. Oocysts of Isospora momotana n. sp. have a double, thick, yellow to orange, 2.3 µm ± 0.5 µm (2–3 µm) wall, contain 1 to 3 globular polar granules (1–4 µm), are ovoid with heavy pitting on the outer surface, and measure 29.4 ± 2.3 × 27.5 ± 2.3 (25–33 × 23–31) with an average length∶width ratio of 1.1 (1.0–1.35). Sporocysts are ovoid, contain a residuum composed of large, equal-sized granules, and measure 19.4 ± 1.3 × 12.2 ± 1.1 (16–22 × 10–14) with an average length∶width ratio of 1.6 (1.2–1.91). A small rounded stieda body, continuous with the sporocyst wall, and a prominent triangular substieda body are present. A second Isospora species was observed in 1 bird, but because only a few oocysts were present, a full description is not provided. This is the first report of coccidia from a motmot (Momotidae) and only the third Ispospora species described from the Coraciiformes.

Fifty-two fecal samples from the Plateau pika, Ochotona curzoniae, collected in the Haibei Area, Qinghai Province, China, were examined for the presence of coccidia (Apicomplexa: Eimeriidae). Five distinct morphotypes, all Eimeria species, were distinguished based on the structure of their sporulated oocysts. Three of these included Eimeria banffensis, Eimeria calentinei, and Eimeria cryptobarretti, all of which have been described previously from other Ochotona species. We also studied 2 morphotypes that we feel have sufficient qualitative and quantitative characters to distinguish them from all previously described species; herein, we identify them as putative new species. Eimeria qinghaiensis n.sp. was found in 18/52 (35%) O. curzoniae. It has ovoidal oocysts with a 3-layered wall, with a rough outermost layer and a micropyle, ∼9 µm wide. Sporulated oocysts are 37.2 × 27.2 (34–41 × 24–32) µm; 1 polar granule is present, but an oocyst residuum is absent. Sporocysts are ovoidal, 16.6 × 9.8 (14–19 × 9–11) µm with a Stieda body; sporocyst residuum and sporozoites have 2 refractile bodies. Eimeria haibeiensis n. sp. was found in 21/52 (40%) pikas. It has ellipsoidal to ovoidal oocysts, with a 2-layered smooth wall and a micropyle, 3.9 µm wide. Oocysts are 22.2 × 16.2 (20–24 × 15–18) µm; polar granule and oocyst residuum are both absent. Sporocysts are ovoidal, 11.6 × 6.6 (10–13 × 5–7) µm, with a Stieda body; sporocyst residuum and sporozoites each have 2 refractile bodies, 1 at each end. The 5 eimerian species we discovered in O. curzoniae in China all represent new host and locality records.

Five assemblages of Giardia duodenalis were identified from cysts in cattle, dog, cat, sheep, and reindeer feces using ribosomal DNA (rDNA) sequencing. Assemblage A was present in cattle and reindeer feces, Assemblages C and D were present in dog feces, Assemblage E was present in cattle and sheep feces, and Assemblage F was present in cat feces. Giardia virus, originally referred to as Giardia lamblia virus (GLV), is a double-stranded RNA virus. Primers designed for the GLV capsid protein gene identified GLV sequences in G. lamblia from a reindeer (Assemblage A) and from a dog (Assemblage C). Two distinct GLV sequences were identified in the dog specimen and 1 sequence was identified in the reindeer specimen. None of these GLV sequences was identical with previously published GLV sequences. It appears that GLVs are genetically diverse and that more than 1 virion can be present in a single sample. Because many of the specimens that contained cysts were found to be negative for GLV, it appears that this test for capsid protein is of limited value for the purposes of detecting G. lamblia.

Helminth infections are generally characterized by dominant T-helper type 2 (Th2) immune response polarization and have been shown in some cases to modulate immune responses to vaccines, i.e., the Bacillus Calmette-Guerin (BCG) vaccine. The filarial nematode secreted product ES-62 has been shown to possess immunomodulatory activities, such as the ability to inhibit pro-inflammatory/Th1 immune responses and to have therapeutic potential against diseases associated with such responses. This study aimed to investigate the ability of ES-62 to modulate the immune response to purified protein derivative (PPD), a component of the BCG vaccine designed to provoke a Th1 response. Overall, the results show that ES-62 was not capable of modulating the Th1 immune response induced by PPD, demonstrating that the helminth product, if employed therapeutically, is unlikely to interfere with the protective effects of the vaccine.

The taxonomic status of Profilicollis ( =  Falsifilicollis Webster, 1948) species in crustaceans in Chile is examined. Mole crabs, Emerita analoga (Stimpson 1857), living in the splash zone of a sandy beach at Lenga off the coast of central Chile, harbor Polymorphus (Profilicollis) bullocki Mateo, Córdova and Guzmán 1982, while the estuarine crabs, Hemigrapsus crenulatus (Milne-Edwards, 1837), living in an oligohaline inlet at the same site, harbor Profilicollis spp. cystacanths which cannot be distinguished specifically to either Profilicollis antarcticus Zdzitowiecki 1985 or P. chasmagnathi Holcman-Spector, Mañé-Garzón and Dei-Cas 1977. We found no morphological data supporting records of P. altmani along the coast of Chile. Therefore, and after examination of both their morphology and the literature, we consider that P. bullocki must be reinstated as a valid species in the genus. There is a widespread distribution of habitats, such as sandy beaches and inlets, as well as a variety of host taxa involved in the life cycle of Profilicollis spp. Consequently, they provide an interesting scenario for testing hypotheses regarding the coevolution and host specificity of these parasites.

Deepwater sculpin (Myoxocephalus thompsonii) were collected from 19 lakes across the species' distribution in Canada and examined for parasites. Six helminth species (Crepidostomum farionis, Bothriocephalus cuspidatus, Proteocephalus sp., Cyathocephalus truncatus, Raphidascaris acus, and Echinorhynchus salmonis), 1 crustacean species (Ergasilus nerkae), and 1 molluscan species (glochidia) parasitized these hosts. Crepidostomum farionis, Proteocephalus sp., R. acus, E. nerkae, and the glochidia represent new parasite records for this host species. Overall parasite prevalence was 78.0% while mean intensity was 6.1 ± 7.1 SD. Bothriocephalus cuspidatus was the most prevalent parasite and was recorded from 62.2% of the deepwater sculpin and found in 17 of the 19 lakes. The low-productivity habitat of this host limits the parasites available for transmission, and the infra- and component communities were generally species poor. With the exception of the Proteocephalus sp., all of the helminth parasites recovered have been reported as adults in lake trout (Salvelinus namaycush) or burbot (Lota lota), suggesting that, in the lakes where they occur, deepwater sculpin may play an important role in energetic transfer and parasitic transmission to higher trophic levels.

The sensitivity of fecal examination methods can be influenced by both technician error and methodology. In this analysis, we compared the results of 335 passive fecal flotation examinations performed on the feces of stray dogs by 3rd-yr veterinary students at the University of Pennsylvania, School of Veterinary Medicine, to the results obtained through zinc-sulfate centrifugation performed by the diagnostic parasitology laboratory on the same fecal samples. The students' passive flotation results agreed with the laboratory zinc-sulfate centrifugation for only 62.4% of samples. Students were able to diagnose 75.0% of Ancylostoma caninum cases, 71.4% of Toxocara canis cases, 54.2% of Trichuris vulpis cases, 26.7% of Cystoisospora spp. (C. ohioensis-like and C. canis) cases, and 14.7% of Giardia lamblia cases. There were also 70 instances where students reported the presence of parasites in the sample that were not diagnosed by zinc-sulfate centrifugation. Based on the overall study findings, passive fecal flotation examinations run in private practice could be missing up to 50.5% of infected dogs, due to either technician error or inherent limitations to the passive fecal flotation technique.

Dwarf razor clams (Ensis minor) in the Gulf of Mexico are known to be infected with plerocercoid larvae of a tetraphyllidean tapeworm. Here, we show that these larvae live unencysted in the intestinal lumen of the clam. Morphologically, the larvae are similar to (although significantly larger than) tapeworm larvae previously described living in the gut of amphioxus (Branchiostoma floridae) from the same habitat. Sequence data from the D2 region of the 28S rDNA from clam-infecting larvae were identical to the sequence of Acanthobothrium brevissime isolated as larvae from amphioxus and as adults from a stingray (Dasyatis say). The sequence data leave little doubt that the dwarf razor clam and the amphioxus are alternative intermediate hosts in the life cycle of A. brevissime.

Scanning electron microscopy was used to analyze superficial features of Gordius dimorphus Poinar, 1991, larvae that might serve as generic or specific diagnostic characters. Three adults of G. dimorphus (2 males and 1 female) were maintained under laboratory conditions until oviposition, which occurred within long strings commonly referred to as egg strings. Larvae have a cylindrical body, annulated and divided into 2 sections, plus an anterior preseptum and a posterior postseptum. Three concentric rings with 6 spines each surround the proboscis. The proboscis is retractile, dorsoventrally flattened, with 1 pair of forceps-like projections on its distal-most portion. On the surface of each projection, 3 pairs of aculeiforms spines are aligned and lean toward the proboscis opening. One large spine is present on the posterior portion of the postseptum. Papillae were not observed. Gordius dimorphus larvae are similar to previous light microscope descriptions. This is the first record of G. dimorphus in Brazil.

Six helminth species were recorded during the helminthological examination of 35 specimens of the goodeid Xenotaenia resolanae from Arroyo Durazno, Jalisco, Mexico, a tributary of the Cuzalapa River. Helminth species identified included: 4 species of digeneans, i.e., Posthodiplostomum minimum (metacercariae), Clinostomum companatum (metacercariae), Dendrorchis sp. (adult), and Margotrema guillerminae (adult); and 2 species of nematodes, i.e., Spiroxys sp. (larvae) and Rhabdochona ahuehuellensis (adult). A very low number of individual larvae were found. The observed species richness, individual parasite abundance, and diversity were low at both component community and infracommunity levels. The values of similarity between infracommunities were relatively high because of the predominance of the digenean M. guillerminae, the species that reached the higher values of both prevalence and abundance. High water flow of the collecting site is suggested as the main factor determining the depauperate helminth assemblage in this fish species.

We investigated the intestinal parasites of a wild fish population in a Kansas stream to determine the prevalence and abundance of potentially harmful parasites. In total, 180 red shiners (Cyprinella lutrensis) were collected from 6 sites in October–November 2007. Fifteen Asian tapeworms (Bothriocephalus acheilognathi) were recovered from 13 fish (prevalence of 7.2%). Prevalence did not differ among sites; however, B. acheilognathi abundance was greatest at the site of a public fishing area. A total of 39 roundworms (Rhabdochona canadensis) were recovered from 28 fish (prevalence of 15.6%). Prevalence did not differ among sites, nor did abundance. However, mean abundance tended to be about 50% greater at the site of a public fishing area compared to all other sites. This paper documents the presence of both B. acheilognathi and R. canadensis in Kansas and offers a compilation of the known potential impacts these parasites may have on the native, federally endangered Topeka shiner (Notropis topeka).

The Alaska pollock, Theragra chalcogramma (Pallas), is an important raw source for surimi and other food products in Japan. However, Alaska pollock caught in the Atlantic and Mediterranean regions has been reported to harbor Anisakis species that pose considerable food safety problems. Here, we identified the third-stage (L3) Anisakis spp. sampled from Alaska pollock caught in northern Japan using a combination of morphological and molecular analyses which included PCR-RFLP and sequencing of the ITS (ITS1-5.8S rDNA-ITS2) region and mtDNA cox2 gene markers. Four Anisakis spp. were confirmed, namely Anisakis simplex (sensu stricto [s.s.]), A. pegreffii, A. brevispiculata, and an Anisakis sp. belonging to the Anisakis Type II group. The identification of 4 different Anisakis spp. occurring in Alaska Pollock, and the identification of A. brevispiculata and an Anisakis sp. (Anisakis Type II) in the northwest Pacific region, are first reports. Anisakis simplex (s.s.) composed the majority of Anisakis spp. in Alaska pollock at 91.0%, followed by A. pegreffii (5.2%), Anisakis sp. (Anisakis Type II) (2.4%), and A. brevispiculata (1.4%).

This is the first host record of Gymnophallus choledochus metacercariae infecting the polychaete Diopatra neapolitana in the Aveiro estuary (Portugal). The metacercariae were found unencysted, and their morphology is similar to that presented by metacercariae harbored by Nereis diversicolor and Cerastoderma edule, although they are larger in size. In D. neapolitana, the prevalence and mean intensity of the infection was very high, at 100% and 202 ± 139 metacercariae per host, respectively, suggesting that this polychaete is the most suitable host for G. choledochus in the Aveiro estuary. In terms of distribution within the host, the metacercariae were found almost exclusively in the branchial segments (97.4%). This, in conjunction with the close relationship between the mean intensity and branchial surface area, suggests that the branchiae may be the site of entry into the polychaete. Within the branchial segments, the sites selected by the metacercariae are the parapodia (68.9%), where they are mostly located inside the setal sac, and the longitudinal muscles (22.3%), causing hypertrophy and rupture of the muscle bundles, respectively. These histological changes suggest a reduction in polychaete mobility, which should aid the easy predation of infected hosts by birds and thus facilitate the continuity of the G. choledochus life cycle.

Stomach nematodes were collected from 151 live American alligators, Alligator mississippiensis, from 3 lakes (Apopka, Griffin, and Woodruff) in north-central Florida using a gastric lavage technique. Four species were identified: Dujardinascaris waltoni, Ortleppascaris antipini, Brevimulticaecum tenuicolle, and larvae of Contracaecum sp. Of these, D. waltoni was the most prevalent species in all 3 lakes and was more prevalent in Lake Apopka than in the other 2 lakes. This is the first record of Contracaecum larvae in the American alligator and the second record of O. antipini.

The lack of robust methods for culturing Cryptosporidium parasites remains a major challenge and is hampering efforts to screen for anti-cryptosporidial drugs. In existing culture methods, monolayers of mammalian epithelial cells are inoculated with oocysts. The system supports an initial phase of asexual proliferation of the parasite. For reasons that are not clear, development rapidly declines within 2–3 days. The unexpected report of Cryptosporidium parvum culture in the absence of host cells, and the failure of others to reproduce the method, prompted us to apply quantitative PCR to measure changes in C. parvum DNA levels in cell-free cultures, and parasite-specific antibodies to identify different life cycle stages. Based on this approach, which has not been applied previously to analyze C. parvum growth in cell-free culture, we found that the concentration of C. parvum DNA increased by about 5-fold over 5 days of culture. Immuno-labeling of cultured organisms revealed morphologically distinct stages, only some of which reacted with Cryptosporidium-specific monoclonal antibodies. These observations are indicative of a modest proliferation of C. parvum in cell-free culture.

An important obstacle in studying Cryptosporidium parvum is the lack of a permanent in vitro cultivation system of the parasite. While short-term cultures using various host cell lines have been widely employed, long-term cultures that would facilitate the immortalization of C. parvum isolates have not yet been developed. The description of the complete development of C. parvum in cell-free culture in 2004 has been received with great interest and also with some astonishment. Unfortunately, attempts to reproduce these results with different isolates of C. parvum and also C. hominis have failed. In this report, we provide an alternative interpretation of the nature of a parasite stage that occurs 24 hr after excystation of oocysts which, morphologically, is similar to stages that have been regarded as being extracellular trophozoites or merozoites by other investigators.