Some parasites modify the behavior of intermediate hosts to increase the probability of transmission to the next host in their life cycle. In habitats where this is common, parasites play an important role in predator-prey links and food web dynamics. In this study we used laboratory observations to investigate the behavior of longnose killifish, Fundulus similis, that were naturally infected with metacercariae of the trematode, Euhaplorchis sp. A, from Laguna Madre, south Texas. In particular, we examined whether there was a relationship between the number of metacercariae lodged on the brain of the infected fish and behaviors that made the fish more conspicuous to avian final hosts. We also quantified the abundance and cercariae production of this parasite in its first intermediate snail host, Cerithidea pliculosa, and examined the seasonal variation of Euhaplorchis sp. A in F. similis. Our data demonstrated that Euhaplorchis sp. A affected the surfacing behavior of F. similis in an intensity-dependent manner. Fish with many infections spent longer time at the surface of the water than fish with few infections. Our data also show that Euhaplorchis sp. A is a common parasite in the first intermediate host and produces close to 4,000 cercariae m⁻² day⁻¹. Consequently 97% of all fish collected and necropsied were infected, with little seasonal variation in the mean abundance of the parasite. Based on our data, Euhaplorchis sp. A is likely important to predator-prey links in Gulf of Mexico estuary food webs, similar to the closely related Euhaplorchis californiensis in southern California. We expect that other closely related species elsewhere may have similar effects on other fish hosts, emphasizing the need for incorporating trophically transmitted parasites in estuarine food web studies.

Ecological investigations regarding the parasite fauna of grey mullets are scarce. The present study provides a detailed description of the helminth communities of Liza aurata in the Spanish western Mediterranean and analyzes the role of spatial, temporal, and host variables in shaping the infracommunities. In total, 204 fish were collected in 2 localities, situated ca. 290 km apart, in spring and fall of 2004 and 2005. A non-metric multidimensional scaling (NMDS) was used to visualize an ordination of the infracommunities according to their relative similarities in parasite abundances. The relationship between infracommunity composition and explanatory variables (host size, locality, year, and season of harvest) was examined by permutational analysis of variance (PERMANOVA) applied to species abundances. Permutational tests for homogeneity of multivariate dispersion were used to test the null hypothesis of no differences in dispersion among groups formed by the factors whose effects were significant in PERMANOVA. A total of 33,241 helminth parasites, belonging to 18 species, was collected, i.e., 12 species of adult digeneans (23% of the parasite specimens), 3 digeneans as metacercariae (68%), 1 acanthocephalan (2.1%), and 2 monogeneans (6.5%). An important part of this helminth fauna is specialized to grey mullets, with a sizable portion of the component community restricted to the Mediterranean and northeast Atlantic. The NMDS ordination indicated high heterogeneity among infrapopulations. However, most differences at both the component and infracommunity level were related to geographic locality. In fact, the PERMANOVA showed that, among the explanatory variables considered, sampling locality accounted for the largest share of variation. The geographical differences observed may be related to local environmental characteristics or to the limited spatial dispersal of the species forming the component community. The latter was supported by the significant portion of variation explained by a 3-way interaction term. Thus, the spatial structure of our helminth infracommunities seems to be determined by a combination of differences in local environmental conditions and the transmission ability of each species at small local and time scales.

Hepatozoon spp. (Apicomplexa: Haemogregarinidae) are the most commonly reported hemoparasites from snakes. Of over 300 Hepatozoon species identified, more than 120 were described from snakes. However, recent genetic assessments have found Hepatozoon lineages recovered from both prey and predators, indicating that diet may play an important role in the infection of final vertebrate hosts. Here 4 different snake genera with different diets were assessed. Hepatozoon spp. prevalence varied greatly between the genera, but only lineages already identified from potential prey, i.e., gecko and lacertid lizards, were recovered from the snakes. Interestingly, the Hepatozoon spp. lineage known from geckos was the most common in the snakes, but this does not reflect their diet. Higher parasitemia levels, reported for some geckos relative to lacertid lizards, may play a role. Alternatively, this lineage may be more effective at parasitizing snakes or may occur, despite being unrecorded, in other vertebrate groups consumed by snakes.

Nothoaspis reddelli Keirans and Clifford, 1975, was described from 3 males collected in Grutas de Xtacumbilxunaán, Campeche, Mexico, although females have remained undescribed for 37 yr. Recently adult females of this species were collected from Cueva de Villa Luz ( =  Cueva de las Sardinas, Cueva del Azufre), in Tapijulapa, Tabasco, Mexico. Here we present a morphological description of the female stage, together with 16S rDNA sequences that confirm the conspecificity of our female, male, and nymphal specimens. The female integument of the anterior portion of the dorsal surface is smooth (nothoaspis), appearing to consist of 3 large “subunits,” 1 anterior and 2 posterior, each with a small sublateral “subunit” on either side. The remaining dorsal covered integument is a cell-like configuration. The hood is large and bluntly rounded, and visible dorsally. The spiracular plate is oval. It possesses 1 pair of posthypostomal setae. The palpal trochanter has 1 pair of setae and a 5/5 hypostome decreasing to 4/4 at the apex. There is a single central pore at the base of the hypostome.

The prevalence of hemosporidian parasites varies among different host species, geographic locations, habitats, and host life histories, and yet we do not have a firm understanding of the ultimate causes of the variation. Seabirds are not typically found infected with hemosporidian parasites; however, frigatebird species have been repeatedly documented with Hemoproteus spp. infections. Hemoproteus iwa in Galapagos great frigatebirds (Fregata minor) is vectored by a hippoboscid fly, Olfersia spinifera, an obligate ectoparasite of the bird host. Five populations of Galapagos great frigatebirds, and flies collected from the birds, were sampled and tested for H. iwa. Prevalence did not differ across 4 yr or between 5 islands, but males were found to have a significantly higher prevalence of infection than did females. Additionally, juveniles were more likely to be infected than were adults and chicks. Because the invertebrate vector is an obligate parasite, we were able to estimate prevalence in the vector as well as in the particular host upon which it fed, a task that is impossible, or nearly impossible, in hemosporidian parasites vectored by midges or mosquitoes. We tested the correlation between the infection status of the bird host and the infection status of the fly collected from the bird. More often than not the 2 were correlated, but some mismatches were found. Using the occurrence of infected flies on uninfected birds (12/99) as a proxy for transmission potential, we can estimate the transmission rate to be between 5 and 20% (95% confidence intervals) among individual vertebrate hosts.

Parasitic lice have been valuable informants of their host's evolutionary history because they complete their entire life cycle on the host and move between hosts primarily through direct host-to-host contact. Therefore, lice are confined to their hosts both in ecological and evolutionary time. Lice on great apes have been studied to examine details of their host's evolutionary history; however, species of Pedicinus, which parasitize the Old World monkeys, are less well known. We sampled lice from 2 groups of red colobus (Procolobus spp.) in Kibale National Park in Uganda and from red colobus and black and white colobus (Procolobus polycomos) in Taï National Park in Côte d'Ivoire. We used next-generation sequencing data analysis and the human body louse (Pediculus humanus humanus) genome to search for microsatellites for population genetic studies of Pedicinus lice. The 96 primer sets for microsatellite loci designed from the human body louse genome failed to amplify microsatellites in Pedicinus sp., perhaps due to the fast rate of evolution in parasitic lice. Of 63 microsatellites identified by next-generation sequencing data analysis of Pedicinus sp., 12 were variable among populations and 9 were variable within a single population. Our results suggest that these loci will be useful across the genus Pedicinus. We found that the lice in Uganda are not structured according to their hosts' social group; rather, 2 non-interbreeding populations of lice were found on both groups of red colobus. Because direct host-to-host contact is usually required for lice to move among hosts, these lice could be useful for identification and study of behavioral interactions between primate species.

Vitellogenesis of Aphallus tubarium, an intestinal parasite of Sparidae (Dentex dentex), was studied by transmission electron microscopy. The ultrastructural features allowed us to distinguish 4 stages in the vitellogenesis process. In stage 1, vitellocytes have a cytoplasm mainly filled with ribosomes, but few mitochondria. In stage 2, there is an increase in amount of endoplasmic reticulum and few Golgi complexes. There is production of shell globules that coalesce into clusters in stage 3; some glycogen particles are observed via the Thiéry method. Finally, in stage 4, mature vitellocytes are filled with shell globule clusters and generally contain a large lipid droplet. Glycogen particles are grouped at the periphery of the cell.

The seroprevalence of Toxoplasma gondii infection in horses in Mexico is unknown. Therefore, antibodies to T. gondii were assessed in 495 horses in Durango State, Mexico, using the modified agglutination test (MAT). Horses were from 18 farms in 3 municipalities in the valley region of Durango State. Antibodies to T. gondii were found in 30 (6.1%) of 495 horses, with MAT titers of 1∶25 in 19, 1∶50 in 6, and 1∶100 in 5. Seropositive horses were found in 8 (44.4%) of 18 farms sampled in all 3 municipalities. Age, gender, and breed of horses did not influence significantly the seroprevalence of T. gondii infection. The seroprevalence in horses was higher in rural (7.8%) versus urban (0%) areas, and in larger herds (30–64 horses, 7.8%) versus smaller ones (3–28, 3.5%). The seroprevalence was higher in stall fed (16.5%) than in pastured horses (3.1%). Results indicate that infected horses represent a potential source of T. gondii infection for humans in Mexico. This is the first report of T. gondii infection in horses in Mexico.

An experimental excystation assay was used to test the potential species isolating effects of excystation signaling among gregarines. Oocysts of a single gregarine species, Blabericola migrator, were tested for activation, excystation, and sporozoite motility by using intestinal extracts from 11 species of cockroaches representing a cohesive phylogeny of 7 genera, 3 subfamilies, and 2 families of Blattodea. Sporozoite activation, excystation, and motility were observed for all excystation assay replications using intestinal fluid from blaberid hosts, but delayed activation or excystation was observed for all assay replications using intestinal fluid from hosts in the family Blattidae. The results illustrate a trend toward a generalized excystation signal among gregarines that is conserved across the host clade at a subfamily or family level but that is unlikely to play a significant role as a species-isolating mechanism among sibling gregarine species.

Sarcocystis bunopusi n. sp. from the muscle fibres of the rock gecko (Bunopus tuberculatus) in Saudi Arabia is described. Sarcocysts were found in skeletal muscles of the tail and fore and hind limbs in 3 of 30 geckos. Sarcocysts were microscopic, 42–45 µm long and 22–25 µm wide. Using light microscopy, the cyst wall was thin and smooth. Ultrastructurally, the primary cyst wall consisted of a thin parasitophorous vacuolar membrane with osmiophilic 100 nm × 50 nm knob-like papillae, and no perpendicular protrusions. Septae were indistinct. Bradyzoites were 5–7 × 1.5–2.0 µm in size. This is the first description of a Sarcocystis species from this gecko.

A 5-yr retrospective study in livestock slaughtered in abattoirs was carried out in Khuzestan Province (southwestern Iran) to determine the prevalence of parasitic infections responsible for condemnation of slaughtered animals' carcasses and viscera. The economic importance of such infections in terms of lost meat and offal were also estimated. Between 20 March 2006 and 19 March 2011, 125,593 cattle, 1,191,871 sheep, 240,221 goats, and 25,010 buffalos were slaughtered in the study area; the livers of 58,753 (3.7%; 95% confidence interval [CI]: 3.7–3.8%), the lungs of 34,522 (2.2%; 95% CI: 2.1–2.2%), and the carcasses of 78 (0.0049% 95% CI: 0.0048–0.0049%) of these animals were condemned. Proportions of liver, lung, and carcass condemnations during the 5-yr study period in buffalos were significantly greater than the other species (P < 0.001). Frequency of liver condemnation during the 5-yr period for cattle was greater than sheep and goats (P < 0.001), but condemnation of lungs in goat was significantly greater than sheep and cattle (P < 0.001). The parasitic lesions observed in the condemned livers were attributed to Echinococcus granulosus, Fasciola hepatica, or Dicrocoelium dendriticum, or some combination of these species. All the parasitic lesions observed in the condemned lungs from cattle, sheep, goats, and buffalos are ascribed to E. granulosus. Sarcocystis spp. cysts were found in ovine and buffalo muscles, whereas Taenia sp. cysticerci were detected in bovine muscle. Muscles of goats were devoid of any parasitic lesions. Parasites were responsible for 54.1% of the condemned organs or carcasses, with a retail value (based on market prices in 2011) of $1,148,181 (U.S.) ($137,880 for cattle, $602,699 for sheep, $280,955 for goats, and $126,647 for buffalos). The parasites contributing most to the condemnation of otherwise marketable organs and flesh were E. granulosus (29.2%) and F. hepatica (18.6%). These parasites clearly remain the most common, causing considerable economic loss in Khuzestan Province and, presumably, other areas of Iran.

Few data are available on the prevalence of Eimeria spp. in yaks. An observational study was conducted to determine the prevalence of coccidial infection in yaks on the Qinghai-Tibet Plateau of China. A total of 324 fecal samples from 4 counties was examined, and oocysts were identified to the species level on the basis of morphological features. Eimeria oocysts were found in 113 (34.9%) samples. The species detected and their prevalence values included the following: Eimeria zuernii (54.9%), E. pellita (35.4%), E. canadensis (33.6%), E. bovis (23.0%), E. cylindrica (16.8%), E. subspherica (16.8%), E. ellipsoidalis (14.1%), E. brasiliensis (13.3%), E. wyomingensis (8.0%), E. alabamensis (7.1%), E. illinoisensis (5.3%), E. auburnensis (4.4%), E. bombayansis (3.5%), and E. bukidnonensis (2.7%). Mixed infections of 2 to 7 species were found in 66.4% of the animals. There was an age-related difference in the prevalence of infection. The highest prevalence (53.3%) was observed in calves, an intermediate prevalence in yearlings (36.1%), and the lowest was in adults (15.6%). The number of oocysts per g of feces was significantly higher in calves than in adults. More Eimeria species were indentified in calves. Eimeria zuernii was the most prevalent species in calves and adults, whereas in yearling yaks E. pellita was most common. The majority of calves and yearlings showed mixed infection, but adults tended to be infected with 1 species. The prevalence and intensity of Eimeria species were found to show statistically significant differences among different regions in Qinghai Province.

The prevalence of coccidial infections in dairy cattle was examined in Shanghai from November 2010 to March 2011. In total, 626 fecal samples from 24 dairy farms were examined; oocysts were identified to the species level based on morphological features. All herds were infected with Eimeria species. The overall prevalence of coccidia was 47.1%, with the highest prevalence in <4-mo-old calves (51.8%) and the lowest in >12-mo-old cattle (27.0%). The number of oocysts per gram of feces was significantly higher in young calves than in weaners and adults. Ten species of Eimeria were identified, among which Eimeria ellipsoidalis, Eimeria bovis, Eimeria zuernii, and Eimeria alabamensis were the predominant species. Concurrent infection with 2–8 species was common.

An unidentified xiphidio-type cercaria, previously thought inconsequential to catfish health, was found to be released from marsh rams-horn snails (Planorbella trivolvis) inhabiting ponds on a commercial catfish operation in the Mississippi Delta. A preliminary challenge of cohabiting channel catfish (Ictalurus punctatus) with snails actively shedding the unidentified cercariae resulted in death of some fish. A second cohabitation trial yielded similar results, as did a third challenge of 250 cercariae/fish. Histopathology revealed developing metacercariae concentrated in the cranial region, especially within the branchial chamber, with several metacercariae at the base of the branchial arches within, or adjacent to, blood vessels, possibly the proximate cause of death. Genetic sequence analysis of the 18S small subunit ribosomal DNA (ssDNA), 28S large subunit rDNA (lsDNA), and cytochrome oxidase (Cox1) genes all matched the cercariae to Drepanocephalus spathans (Digenea: Echinostomatidae), a parasite of the double-crested cormorant (Phalacrocorax auritus), a piscivorous bird endemic on most catfish farms. This is the first commentary regarding pathology of D. spathans in juvenile channel catfish as well as the first report of the marsh rams-horn snail as an intermediate host in the D. spathans life cycle. The data presented here suggest this parasite could have limiting effects on catfish production, further supporting the need for adequate snail control programs to reduce trematode prevalence on commercial catfish operations.

Megalobatrachonema papuaensis n. sp. (Ascaridida: Kathlaniidae) from the small intestine of Fojia bumui (Squamata: Scincidae) collected in Papua New Guinea is described and illustrated. Megalobatrachonema papuaensis represents the first species from the Australian realm and the third species assigned to the genus. It is distinguished from other species of Megalobatrachonema by the distribution pattern of caudal papillae (8 precloacal, 10 postcloacal, and 1 median), length of spicules (201–226 µm), and absence of a pseudosucker.

Four specimens of wild leporids, Lepus capensis Linnaeus, 1758, in Longde County, Ningxia Hui Autonomous Region (NXHAR), and 40 domestic rabbits, Oryctolagus cuniculus (Linnaeus, 1758) (20 from Xiji County, NXHAR, and 20 from Jingning County, Gansu Province) were examined for the presence of helminth parasites. Two new cestode species of Schizorchis Hansen, 1948 (Anoplocephalidae), were found: Schizorchis sinensis sp. n. from L. capensis and Schizorchis oryctolagi sp. n. from domestic rabbits. Schizorchis sinensis sp. n. is distinguished from all the species in the genus from pikas, Ochotona spp. (Lagomorpha: Ochotonidae) by having much longer strobila, a larger cirrus sac, a greater number of segments, and more numerous testes. The morphology of S. oryctolagi n. sp. is most similar to that of S. sinensis. It is distinguished from the latter species by its relatively small strobila, larger number of segments, smaller size of eggs, and much larger cirrus sac, which is substantially extending in a medial direction. In addition, a genital papilla is present in S. sinensis, but absent in S. oryctolagi. These findings indicate that species of Schizorchis are widespread in leporid mammals, contrary to the widespread opinion that the latter genus is specific to ochotonid lagomorph mammals. They are congruent, however, with the hypothesis of a close phylogenetic relationship between species of Schizorchis and Mosgovoyia. The occurrence of Schizorchis spp. in leporids is considered relict, vestigial from wider geographical and host ranges of this parasite genus during the Pleistocene.

Two species of Guerrerostrongylus Sutton and Durette-Desset, 1991, are reported in cricetid rodents from the Atlantic rain forest of Misiones, Argentina. Guerrerostrongylus zetta (Travassos, 1937) is redescribed on the basis of material collected from Oligoryzomys nigripes from Argentina and material loaned by CHIOC from Brazil. It is characterized by a synlophe with about 40–45 (35–48) well-developed cuticular ridges, caudal bursa with long rays 6 and dorsal ray divided at mid-length, and well-sclerotized spicules with marked twisting. It was found with a prevalence of 100% in O. nigripes (14 hosts examined); however, it was not found in its type host Nectomys squamipes (4 hosts examined). Guerrerostrongylus ulysi n. sp., which is described from Sooretamys angouya, differs from the remaining species in the genus mainly by a synlophe with a strong reduction of the cuticular ridges and struts on the right side, and by a heart-shaped caudal bursa, with short rays 6 and a dorsal ray divided distally. It was found with a prevalence of 100% in 5 hosts examined.

A new microphallid species of Maritrema is described from the native southern river otter, Lontra provocax (Thomas). A naturally infected otter was found dead in the Nahuel Huapi National Park, Argentina. Ovigerous adult worms were recovered from the anterior portion of the intestine. Specimens of Maritrema huillini n. sp. have an unarmed genital pore and glabrous cirrus. They can be distinguished from all other species in the genus by having a long intestinal ceca extending up to three-quarters of the testes length to the level of the posterior border of the testes and a metraterm composed of a proximal sphincter, a non-muscular sac, and a distal muscular portion. This microphallid is the first species recovered from a South American eutherian host and the first digenean recorded for L. provocax.

Riouxgolvania kapapkamui sp. n. (Nematoda: Muspiceoidea: Muspiceidae), a peculiar intradermal parasite, is described based on gravid adults, eggs, and first-, second-, and third-stage larvae collected from dermal nodules formed in Myotis macrodactylus and Myotis ikonnikovi bats from Hokkaido, Japan. The nematode is readily distinguished from 3 previously described congeners in having a globular body with brown, transverse striae in the anterior region of fully grown females. The third-stage larva is also distinguished from other congeners by having a round tail end. Nucleotide sequences of the analyzed partial SSU rDNA-ITS1 region and partial cytochrome c oxidase subunit 1 of mtDNA showed greater similarity to chromadoreans rather than to enopleans. This is the first report of muspiceoid nematodes from Asia.

A captive specimen of Meller's chameleon, Trioceros melleri (Gray), originally from Tanzania and housed at the Oklahoma City Zoological Park Herpetarium, Oklahoma County, Oklahoma, was found to be passing an undescribed species of Choleoeimeria in its feces. Oocysts of Choleoeimeria steveuptoni n. sp. were cylindroidal, 38.5 × 17.8 (36–42 × 17–19) µm with a bilayered wall and a shape index (length/width) of 2.2. A micropyle and oocyst residuum were absent, but a fragmented polar granule was often present. Ovoidal sporocysts were composed of 2 valves joined by a suture and measured 11.3 × 9.1 (11–12 × 9–10) µm; shape index of 1.3. Stieda, sub-Stieda, and para-Stieda bodies were absent. The sporocyst residuum consists of multiple globules dispersed along the perimeter of the sporocyst and between sporozoites. Sporozoites were elongate, 13.1 × 2.9 (12–15 × 2.6–3.2) µm with an elongate posterior refractile body. The new species represents the second coccidian documented from this lizard.

During September 2004, 4 adult northern myotis, Myotis septentrionalis, were collected from LeFlore County, Oklahoma (n  =  2), and Logan (n  =  1) and Yell (n  =  1) counties, Arkansas, and their feces examined for coccidian parasites. Three of 4 bats (75%) were passing oocysts of Eimeria spp. Oocysts of Eimeria tumlisoni n. sp. were subspherical, 17.6 × 16.8 (16–19 × 14–18) µm with a shape index of 1.0 (1.0–1.1). A micropyle and oocyst residuum were absent, although 1–2 bilobed polar granules were often present. Sporocysts were ovoidal, 10.5 × 5.9 (9–12 × 5–7) µm with a shape index of 1.8 (1.6–2.0). A Stieda body was present, but substieda and parastieda bodies were absent. A sporocyst residuum was present consisting of compact to dispersed granules between the sporozoites. The sporozoites were elongate, with subspherical anterior refractile body and spherical posterior refractile body; a nucleus was not discernable. This is the second coccidian reported from this host and the first instance of a bat coccidian reported from Oklahoma. We also document a new geographic record for Eimeria catronensis in Oklahoma and provide an emended description.

A new nematode species, Spirura mexicana n. sp., is described from specimens recovered from the esophageal mucosa of the Parnell's mustached bat Pteronotus parnellii, Davy's naked-backed bat Pteronotus davyi, Wagner's mustached bat Pteronotus personatus, and the ghost-faced bat Mormoops megalophylla in the State of Morelos, Mexico. This nematode is characterized by having a relatively short prostoma, 5–6 pairs of caudal papillae, and a smooth distal end of the tail in females. This is the first species of Spirura described from bats in the New World.

The objectives of this study were: (1) to determine the prevalence and factors associated with Rhipicephalus microplus, resistant to cypermethrin and amitraz, from cattle farms in Veracruz, Mexico, and (2) to determine in vitro mortality percentages of field populations of R. microplus exposed to discriminating doses (DD) of cypermethrin and amitraz. Fifty-three populations of R. microplus were tested by bioassays using DD of cypermethrin (0.05%) and amitraz (0.0002%). The prevalence of cattle farms with R. microplus ticks that were resistant to cypermethrin and amitraz, and co-resistant to both acaricides, was 90.6, 54.7, and 47.2%, respectively. The level of cypermethrin resistance, measured as a survival percentage, was higher as compared to amitraz. Cattle farms with ≤50 animals (odds ratio [OR]  =  3.84, 95% confidence interval [CI]  =  1.07–13.70, P  =  0.038) and a stocking density of >1 animal unit per ha (AU/ha) (OR  =  4.21, 95% CI  =  1.0–17.71, P  =  0.050) had a higher probability to develop R. microplus tick populations co-resistant to both acaricides. In conclusion, there is a high prevalence of R. microplus populations on cattle farms in Veracruz, Mexico that are both resistant to cypermethrin and amitraz and co-resistant to both acaricides. The level of cypermethrin resistance is critical, and the exposition variables of ≤50 cattle and a stocking density of >1 AU/ha were factors associated with R. microplus co-resistant to both acaricides.

In total, 241 sera from clinically healthy adult horses were collected from 6 locations in Saudi Arabia and examined for Theileria equi and Babesia caballi antibodies by an indirect fluorescent antibody test. Antibodies to Theileria equi were detected in 25 horses (10.4%) while the antibodies to Babesia caballi were observed in 18 horses (7.5%). In addition, 7 serum samples were positive for antibodies to both parasites (3%). The horses sampled in Al-Janadriah had the highest prevalence of infection with T. equi at 16.5% and with B. caballi at 8.8%, while the lowest prevalence of infection with T. equi (4.7%) and B. caballi (3.1%) was observed among horses examined from the Dyrab district. However, significant differences (P < 0.05) in seroprevalence were not observed between these districts. This study represents the first report on the status of T. equi and B. caballi infection in the central province of Saudi Arabia.

The aim of this study was to evaluate the concentrations of copper, iron, and zinc in blood serum of dogs experimentally infected with Rangelia vitalii (n  =  7) compared with uninfected controls (n  =  5). Serum metal levels were determined in blood samples collected at days 0, 10, 15, and 20 post-infection (PI). Inductively coupled plasma optical emission spectrometry was used to measure the levels of copper, iron, and zinc. Significant differences (P < 0.05) were observed among groups PI. Increased levels of copper and decreased levels of iron and zinc were observed in the infected animals. The infection by R. vitalii may, therefore, alter the serum metal levels, resulting in metabolic disorders in dogs. These metals are directly involved in many enzymatic systems; accordingly, alterations in their blood concentrations may also influence the pathogenesis of disease.

Plagiorchis elegans has been shown to decrease the fecundity and survivorship of the incompatible snail host Biomphalaria glabrata. Furthermore, a prior infection with P. elegans was shown to render the snails resistant to the compatible parasite Schistosoma mansoni. Here, we test the hypothesis that infection with P. elegans stimulates the immune system of B. glabrata. Our findings indicate that infection by P. elegans significantly increased the number of free hemocytes in the hemolymph of B. glabrata by an average of ∼60%. Furthermore, this immuno-stimulated state lasted from the first day post-infection (PI) to some time between 7 and 21 days PI. This is one of the few reported examples of a parasite stimulating the immune response of an incompatible host.

Consumption of raw freshwater fish produced in both rural farm and urban wastewater ponds is a common practice in Vietnam. The present study assessed the risk of fish-borne zoonotic trematode (FZT) infection from fish raised in both these aquaculture systems in northern Vietnam. The diversity, prevalence, and infection intensity of FZT metacercariae in 1,500 freshwater fish collected from 6 sites located in rural and urban areas in northern Vietnam were investigated. The specific diagnosis of species was made by morphologic methods. The overall FZT prevalence in fish from both urban wastewater ponds and rural farm ponds was 11.2%. In wastewater ponds, the overall prevalence was 5.1%, ranging from 2.0% in tilapia to 7.3% in common and grass carp. In fish from farm ponds, the prevalence was 17.3%, and ranged from 6.7% in mud carp to 26.7% in common carp. The mean intensity of FZT infection was also higher in fish from farm ponds than that in fish from wastewater ponds (6.0% and 8.4%, respectively). The FZT species recovered from infected fish included both liver (Clonorchis sinensis) and intestinal flukes (Haplorchis taichui, Haplorchis pumilio, and Centrocestus formosanus). The prevalence of FZT in fish raised in these common farm systems represents a significant public health risk for a population with a strong cultural preference for consuming raw or inadequately prepared fish. These research results should encourage the public health and agriculture sectors to conduct the risk factor research required to develop control programs for FZT.

During a study of the endohelminths of aquatic birds from the central flyway of North America, the details of the paranephridial systems of 3 immature specimens of Prohyptiasmus sp. were examined; the worms had been collected by the late Dr. J. Teague Self, former Professor, Department of Zoology, University of Oklahoma, Norman, Oklahoma from an American coot, Fulica americana (Raillidae), from the Cheyenne Bottoms, Roger Mills County, Oklahoma and deposited in the Harold W. Manter Laboratory of Parasitology. The excretory vesicle was Y-shaped and had a reduced stem. There were 3 main excretory canals on each side that, in the case of the most lateral 2 pairs, reached anteriorly to the level of the oral sucker. The most lateral canals entered the excretory vesicle about halfway down the stem on each side; the middle canals entered the vesicle at the tips of the branches of the vesicle; and the most medial canals entered the vesicle on the anterior edge about halfway between the branch point and the tips of the branches. There were numerous smaller secondary canals that interconnected with each other and with the 6 main paranephridial canals, forming a net-like system.

The fleas of the Malacopsyllidae are known only by their adults. In this study, we describe the eggs of Malacopsylla grossiventris and Phthiropsylla agenoris and compare their surface ultrastructure using scanning electron microscopy. Eggs of both flea species are similar in their general appearance, i.e., the presence of disks and absence of lateral aeropyles, but they differ in size, texture of the surface, and number of micropyles and aeropyles. In addition, the eggs of M. grossiventris and P. agenoris are larger (719–800 µm) than most of the flea eggs known (<600 µm), and the length/width ratio is 2.0, while it varies between 1.6 and 1.8 in other species. As opposed to other large species, malacopsyllids have expandable (telescoping) abdomens that display growth. It is possible that a clutch of eggs has more than 2 eggs. Females of M. grossiventris were observed fixed with their mouthparts to the skin of their hosts. Indeed, some of these specimens were observed copulating on the venter of their hosts. These results contribute to the knowledge about the biology of malacopsyllids.

A convenience sampling of fecal specimens from 40 cats in northern Florida was examined for the presence of Ancylostoma braziliense eggs by using centrifugal sugar flotation and polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). Of the 40 samples, 26 (65%) contained hookworm eggs. DNA from 24 samples was successfully amplified using PCR; using RFLP, 10 samples were identified as containing DNA of A. braziliense (41.7% of the 24 samples that successfully amplified). Of these, 6 samples contained DNA of both Ancylostoma tubaeforme and A. braziliense, and 4 samples contained only DNA of A. braziliense. The remaining samples (n  =  14) contained only the DNA of A. tubaeforme, except for 1 sample that had no discernible bands after RFLP.

Isolation of a specific Ancylostoma species typically requires death of the source animal, or holding an animal long enough to collect feces after treatment, for worm recovery and identification. The reason for collecting worms is that the eggs are not easy to distinguish morphologically. In keeping with the 3 Rs of laboratory animal research (reduction, refinement, replacement), the objective of this study was to obtain an isolate of Ancylostoma braziliense from 1-time field-collected samples of canine feces without the need for killing the host. During a collection trip to Florida, fecal samples (n  =  148) were collected and identified as containing eggs of Ancylostoma species (n  =  64) using centrifugal sugar flotation. Eggs from hookworm-positive slides were washed into tubes, DNA was extracted, and 2 samples were identified as A. braziliense using restriction fragment length polymorphism (RFLP) with Hinf1. Larval cultures were initiated from these samples, and larvae from the cultures were returned to New York and used to inoculate a purpose-bred kitten with the goal of inhibiting the growth of any contaminating Ancylostoma caninum that might be present in the culture. The infection was patent at 15 days, and eggs were identified as A. braziliense by RFLP and DNA sequencing. Using forceps during endoscopy, 2 adult worms (1 male, 1 female) were recovered from the cat and identified morphologically as A. braziliense. Larvae were cultured from the feces of this cat and used to infect a laboratory-reared beagle dog. Additionally, worms recovered from the feces of the cat post-treatment were confirmed to be A. braziliense, except for 1 female A. caninum containing infertile eggs. The dog (patent 14 days post-infection) was also infected with A. braziliense as determined by RFLP and DNA sequencing of eggs and cultured larvae. Both the cat and dog were treated, verified to be no longer shedding eggs, and then placed into adoptive homes.

Because the eggs of Ancylostoma species of dogs and cats are difficult to readily distinguish morphologically, isolation of a certain species often requires the humane death of the source animal or holding an animal after treatment to obtain worms for specific identification or to harvest ex utero eggs. The objective of this study was to obtain an isolate of Ancylostoma braziliense from 1-time, field-collected samples of feline feces without the need for the killing of any animals. During a collection trip to Florida, fecal samples (n  =  40) were collected and identified as containing A. braziliense eggs (n  =  26) using centrifugal sugar flotation. Eggs from hookworm-positive slides were washed into tubes, DNA was extracted, and 10 samples were identified as containing A. braziliense using restriction fragment length polymorphism (RFLP) with Hinf1. Six of these samples also contained DNA of Ancylostoma tubaeforme and, thus, only 4 samples were from cats infected only with A. braziliense. Larvae cultured from two of the latter samples were used to subcutaneously inoculate a purpose-bred puppy with the intention to inhibit the growth of any potentially contaminating A. tubaeforme larvae in the culture. The infection was patent at 14 days after inoculation, and the eggs were identified as A. braziliense by RFLP and DNA sequencing. Larvae were cultured from the feces of this dog and used to infect a laboratory-reared, specific-pathogen-free cat; the eggs and larvae produced by the cat were also identified molecularly as those of A. braziliense. The larvae from this cat were used to infect other cats to maintain the isolate for further research. Both the puppy and the first cat used in this study were treated to clear their infections and have since been adopted by new owners.

A convenience collection of fecal samples from 148 dogs in northern Florida was examined for the presence of Ancylostoma braziliense eggs by using centrifugal sugar flotation and polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP). Of the 148 samples, 64 (43.2%) contained hookworm eggs. DNA from 42 samples was successfully amplified using PCR; using RFLP, 2 samples were identified as containing DNA of A. braziliense (4.8% of the 42 successfully amplified samples).

The establishment of cat- and dog-derived laboratory strains of Ancylostoma braziliense allowed for a morphological comparison of the eggs of A. braziliense, Ancylostoma caninum, and Ancylostoma tubaeforme. The length, width, and perimeter were determined for images of 10 eggs each of A. braziliense from the feces of a dog infected with a canine isolate and a cat infected with a feline isolate, A. caninum from dog feces, and A. tubaeforme from cat feces. The specific identity of the eggs was verified by polymerase chain reaction and restriction fragment length polymorphism by using HinfI and RsaI restriction digests followed by gel electrophoresis and sequencing. The mean (±SD) length, width, and perimeter and the length-to-width ratio (±SD) (all measurements are in micrometers) for the eggs of each species were as follows: A. braziliense eggs (combined cat and dog source), 53.03 ± 2.33, 36.37 ± 1.35, 140.43 ± 2.56, and 1.46 ± 0.11; A. caninum eggs, 63.92 ± 5.28, 39.21 ± 1.52, 161.99 ± 9.30, and 1.63 ± 0.13; and A. tubaeforme eggs, 61.44 ± 3.05, 39.14 ± 1.40, 157.98 ± 5.81, and 1.57 ± 0.08. The eggs of A. braziliense were significantly (P < 0.001) smaller than the eggs of A. caninum and A. tubaeforme in all dimensions. Thus, the eggs seem to be readily distinguishable using light microscopy, thereby aiding in species identification in fecal samples for a more comprehensive clinical picture and assessment of zoonotic risk.

A cDNA encoding the Babesia microti 32-kDa protein was identified by serological immunoscreening of a cDNA expression library and designated as BmP32. The full length of BmP32 contains an open reading frame of 918 base pairs consisting of 306 amino acids having a significant homology with B. microti secreted antigen 1. Antiserum raised against recombinant protein (rBmP32) specifically reacted with a 32-kDa native protein of the parasite lysate using western blot analysis. The indirect immunofluorescent antibody test showed a preferable localization of BmP32 in the cytoplasm of the intra- and extracellular parasites. Moreover, BmP32 was secreted in the cytosol of infected erythrocytes, especially during the peak parasitemia and the recovery phase of the infection. Next, the antigenicity of rBmP32 was examined by an enzyme-linked immunosorbent assay (ELISA) and sera from mice experimentally infected with either B. microti or closely related parasites. ELISA was highly specific and sensitive when used for the detection of B. microti antibody in a mouse model. Furthermore, mice immunized with rBmP32 emulsified with Freund's adjuvant were not significantly protected against challenge infection with B. microti. However, high antibody titer was detected just before the challenge infection. Our data suggest that rBmP32 may be a specific diagnostic antigen but not a subunit vaccine.

While Schistosoma rodhaini is typically considered a parasite of small mammals and is very scantly distributed in the Lake Victoria basin, it is known to hybridize with the more widespread Schistosoma mansoni, the causative agent of intestinal schistosomiasis. As part of broader parasitological and malacological surveys for S. mansoni across Lake Victoria, schistosome cercariae were harvested from a field-caught Biomphalaria choanomphala taken on Ngamba Island Chimpanzee Sanctuary, Uganda. Upon DNA barcoding, these cercariae were found to be a mixture of both S. rodhaini and S. mansoni, with further phylogenetic analysis revealing a hitherto unknown sub-lineage within S. rodhaini. Despite repeated sampling for eggs and miracidia from both chimpanzees and staff on Ngamba Island Sanctuary, detection of S. rodhaini within local definitive hosts awaits additional efforts, which should be mindful of a potential host role of spotted-necked otters.

Translating research advances to natural systems using experimental laboratory studies is often difficult because of the variability between the natural environment and experimental conditions. Because environmental conditions have a large effect on an organism's physiology, responses to stressors like nutrient limitation, temperature, oxygen deprivation, predation, and parasite/pathogen infection are likely to be context dependent. Therefore, it is essential to examine the impact the study environment has on the experimental outcome. Here, we explored the effect of light exposure on susceptibility to parasite infection. The Biomphalaria glabrata/Schistosoma mansoni study system is a well-established model for studying schistosomiasis. It has been general practice to maintain the vector, B. glabrata, in dark conditions after exposure to miracidia of the human pathogen S. mansoni. We evaluated susceptibility of B. glabrata to S. mansoni under 3 different light conditions during the prepatent period, light (125 lx) on a 12–12 cycle, dim light (3 lx) on a 12–12 cycle, and no light (24 hr at 0 lx). We hypothesized that stress due to photoperiod disruption (24 hr of darkness) would result in compromised immune function and lead to higher susceptibility to infection. Prevalence of infected snails differed significantly between the light conditions, and higher susceptibility was observed in the full light and complete dark conditions compared with the low light conditions. The dim conditions are representative of current methods for evaluating susceptibility in this system. Our results indicate that light exposure during the prepatent period can affect infection outcomes, and environmental conditions must therefore be considered when assessing fitness and immune response due to interactions between host genotype and environment.