Levisunguis subaequalisCurran, Overstreet, Collins & Benz, 2014, was recently described from the lungs of the definitive hosts, softshell turtles, Apalone ferox (Schneider, 1783), and Apalone spinifera aspera (Agassiz, 1857) as well as the viscera of an intermediate host, the western mosquitofish, Gambusia affinis (Baird and Girard, 1853). However, the original account lacked molecular data. Furthermore, histological examination of infected host tissues in the original account of L. subaequalis did not reveal any pathological changes in the intermediate host. The present work provides a robust morphological description of the nymph and novel molecular data from the 18S and 28S ribosomal gene regions and the cytochrome c oxidase subunit 1 (COI) mitochondrial gene. Phylogenetic analyses using Bayesian inference and maximum likelihood analysis with concatenated sequence data from these 3 regions, as well as each region individually, placed the turtle pentastomid L. subaequalis as a sister clade to the crocodilian pentastomids of the genus Sebekia Sambon, 1922. While only concatenated phylogenetic analyses agreed with the currently accepted classification of the Eupentastomida and phylogenetic signal assessment indicated that the concatenated data set yielded the most phylogenetic signal, data from more taxa are still needed for robust phylogenetic inferences to be made. The intensity of infection ranged from 2 to 171 nymphs per fish, compared with the highest previously reported intensity of 6. These high-intensity infections with L. subaequalis were characterized by the nymphs occupying 5–50% of the coelomic cavity of G. affinis. However, despite this heavy parasite infection, fish exhibited minimal pathology. Observed pathology was characterized by compression or effacement of organs adjacent to the nymphs, particularly liver, swim bladder, and intestines, as well as the formation of granulomas around shed pentastomid cuticles. Nonetheless, the morphological and molecular data provided in the present work will bolster future efforts to identify this pentastomid in other hosts where pathology may be present in addition to aiding in the advancement of the field of molecular pentastomid systematics.

The genus Sarahcultrix n. gen. (Phthiraptera: Ischnocera) is described and illustrated based on 2 new species of chewing lice from New Guinean birds in the genus Peltops Wagler, 1829 (Passeriformes: Artamidae). These species are: Sarahcultrix ypsilophora n. sp. ex Peltops montanus Stresemann, 1921, and Sarahcultrix sphenura n. sp. ex Peltops blainvillii (Garnot, 1827).

Five new species of Guimaraesiella Eichler, 1949 are described and illustrated from hosts in the Eurylaimidae and Calyptomenidae. They are Guimaraesiella corydoni n. sp. from Corydon sumatranus laoensisMeyer de Schauensee, 1929; Guimaraesiella latirostris n. sp. from Eurylaimus ochromalusRaffles, 1822; Guimaraesiella cyanophoba n. sp. from Cymbirhynchus macrorhynchus malaccensisSalvadori, 1874 and C. m. siamensisMeyer de Schauensee and Ripley, 1940; Guimaraesiella altunai n. sp. from Calyptomena viridis caudacutaSwainson, 1838; and Guimaraesiella forcipata n. sp. from Eurylaimus steerii steeriiSharpe, 1876. These represent the first species of Guimaraesiella described from the Calyptomenidae and Eurylaimidae, as well as the first species of this genus described from the Old World suboscines.

Nine new species of chewing lice in the genus BrueeliaKéler, 1936, are described from North American hosts. They are Brueelia thorini n. sp. from Haemorhous mexicanus frontalis (Say, 1822) and Haemorhous mexicanus potosinus Griscom, 1928; Brueelia straseviciusi n. sp. from Haemorhous purpureus (Gmelin, 1789); Brueelia mattsonae n. sp. from Coccothraustes vespertinus brooksi (Grinnell, 1917); Brueelia novemstriata n. sp. from Icterus wagleri wagleri Sclater, 1857, and I. parisorum Bonaparte, 1838; Brueelia benkmani n. sp. from Pheucticus melanocephalus (Swainson, 1827); Brueelia arizonae n. sp. from Passerina caerulea (Linnaeus, 1758); Brueelia hellstromi n. sp. from Piranga ludoviciana (Wilson, 1811); Brueelia dolorosa n. sp. from Spinus pinus pinus (Wilson, 1810); and Brueelia melancholica n. sp. from Spinus tristis (Linnaeus, 1758). Brueelia limbata (Burmeister, 1838) is redescribed and illustrated from North American material. A key for these North American species is provided.

Knowledge of helminth life cycles is essential to understanding their host specificity, geographic distribution, and transmission. Many helminth life cycle descriptions are based on field collections in a limited part of the parasite's range. However, it is important to determine whether helminth life cycles and host specificity remain consistent across their geographic range so that we may better understand their life history and transmission ecology. Here, we investigated whether the life cycle of a widespread trematode, Quinqueserialis quinqueserialis (Notocotylidae) varies across its geographic range. Four species of planorbid snails; Gyraulus circumstriatus, Gyraulus crista, Planorbula sp., and Promenetus exacuous, were collected at 5 locations in Canada (3 in Manitoba, 2 in Northwest Territories). Snails and parasite larvae were morphologically and genetically identified to species. The total prevalence of Q. quinqueserialis infections in snail hosts among the 5 locations was 2.3% (n = 1,017). Three species of snails were infected with Q. quinqueserialis rediae: G. circumstriatus, G. crista, and P. exacuous. Two of the 3 species of snails were infected in central (Manitoba) and northern locations (Northwest Territories) within Canada, which indicates limited life cycle variation across a large geographic range. This is the first report of snails naturally infected with Q. quinqueserialis in Canada. These novel host records demonstrate that this trematode species is not as host-specific for first intermediate host species as previously described.

The microsporidium Nosema sp. SE is a pathogen that infects the beet armyworm Spodoptera exigua. The complete sequence of its 4,302-base pair (bp) ribosomal ribonucleic acid (rRNA) gene region was obtained by polymerase chain reaction amplification and sequencing. The rRNA organization of Nosema sp. SE was 5′-large subunit (LSU) rRNA-internal transcribed spacer-small subunit (SSU) rRNA-intergenic spacer-5S-3′, which corresponded to the pattern of Nosema bombycis. Phylogenetic analysis based on LSU rRNA and SSU rRNA both indicated that the parasite had a close relationship with other true Nosema species, confirming that Nosema sp. SE belongs to true Nosema group of the genus Nosema.

The genus Eustrongylides includes nematodes known as the etiological agent of the “big red worm disease.” The aim of this work was to identify Eustrongylides spp. larvae from fish and adults from great cormorant (Phalacrocorax carbo) sampled at Lake Trasimeno, Italy, by morphological and molecular analysis. Histopathological description of the lesions in birds was also provided. We described adults of Eustrongylides excisus for the first time in Italy, and we also linked larval stages 3 and 4 to adults. The use of molecular tools combined with the traditional taxonomy will help the identification of the species, including species inquirendae. Moreover, molecular analysis can also help to investigate the role of intermediate and paratenic hosts, to deepen the knowledge about geographical distribution of the different Eustrongylides spp. and to define the zoonotic potential of E. excisus, which has not yet been identified as causal agent of human cases.

Toxoplasma gondii infections are prevalent in most warm-blooded animals worldwide. During the 2018 November hunting season in Pennsylvania, fresh (unfixed, not frozen) samples obtained from 99 harvested elk (Cervus canadensis) were tested for T. gondii infection. Antibodies to T. gondii were detected in 69 of 99 (69.7%) elk tested by the modified agglutination test (MAT, 1:25 cut-off). Tongues and hearts from 16 elk with high MAT titers (>1:200) were bioassayed for T. gondii by inoculation in outbred Swiss Webster (SW) and interferon-gamma gene knockout (KO) mice. Viable T. gondii was isolated from tongues of 2 elk with MAT titers of 1:200 and 1:3,200. Toxoplasma gondii from both isolates were successfully propagated in cell culture. Genetic typing on DNA extracted from culture-derived tachyzoites using the PCR restriction fragment length polymorphism with 10 genetic markers (SAG1, SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, and Apico) revealed that both isolates belonged to ToxoDB PCR-RFLP genotype #5 that is widely prevalent in wildlife in the United States. Our results suggest that elk may clear T. gondii organisms from their tissues.

Five new species of chewing lice in the genus BrueeliaKéler, 1936, are described from North American jays and allies. They are Brueelia mexicana n. sp. from Aphelocoma woodhouseii cyanotisRidgway, 1887; Brueelia bonnevillensis n. sp. from Aphelocoma woodhouseii nevadaePitelka, 1945; Brueelia diblasiae n. sp. from Cyanocitta stelleri frontalis (Ridgway, 1873); Brueelia tempestwilliamsae n. sp. from Gymnorhinus cyanocephalaWied-Neuwied, 1841; Brueelia mcnewae n. sp. from Nucifraga columbiana (Wilson, 1811). An identification key to the Brueelia on corvid hosts is provided.

From the small intestines of both Ctenomys boliviensis and Ctenomys steinbachi collected from August 1984 through June 1990 from the eastern lowlands of the Department of Santa Cruz, Bolivia a total of 36 specimens of Ancylostoma were recovered. Morphological investigation and comparisons with known species described and reported from mammals in the Neotropical Region show that this is an undescribed species, herein described as new. These nematans were collected from individuals of C. steinbachi collected from near a locality called Caranda (northwest of Santa Cruz de la Sierra) and from C. boliviensis from near Santa Rosa de la Roca (northeast of Santa Cruz de la Sierra) and from cajuchis collected from 3 km west of Estación El Pailón, 30 km east of Santa Cruz de la Sierra. The new species of Ancylostoma differs from all other species of Ancylostoma known from the Neotropical Region in the presence of paired sub-terminal papillae on the dorsal ray of males.

Hemosporidians are a monophyletic group of protozoan parasites infecting all terrestrial vertebrate orders. Although Plasmodium is the most studied genus within the Haemosporidia, this research effort is heavily biased toward mammal and bird hosts. We screened 205 specimens of at least 18 reptile species from Brazil using a partial mitochondrial cytochrome b gene marker. Positive samples were sequenced and included in a phylogenetic assessment. Four positive PCR products matched others identified as Plasmodium using BLAST from 3 different host species, Ameiva ameiva, Tropidurus hispidus, and Hemidactylus mabouia. Recovery of similar haplotypes in the native T. hispidus and exotic H. mabouia (99.9%) indicate potential host-switching.

The pirate perch Aphredoderus sayanus is a relatively small fish species found in rivers throughout much of the eastern United States. Due to their cryptic nature, relatively little is known regarding their parasite fauna. A survey of pirate perch from the upper Mississippi River revealed 2 novel myxozoans. Hennegoides flockae n. sp. was observed in heavily infected gills where the lamellae featured irregular expansion by bulbous myxozoan polysporic plasmodia, typically affecting the middle to distal half of the filaments. When severe, infection of sequential filaments was such that the filaments were fused, forming what appeared as multicystic/lobular parasitic aggregates subdivided by fine epithelial cords. The total myxospore length of Hennegoides flockae was 35.4–46.4 (41.3 ± 3.3) and the spore body, asymmetrically ovoid in valvular view, was 15.4–18.7 (17.0 ± 0.7) × 7.1–8.7 (7.9 ± 0.4). Henneguya marcquenskiae n. sp. was observed in the liver with plasmodia present randomly and infrequently in the hepatocellular parenchyma. The total myxospore length for Henneguya marcquenskiae was 39.5–55.9 (48.4 ± 4.2), with the spore body being lanceolate, 13.9–16.5 (15.4 ± 0.7) × 7.1–9.0 (8.3 ± 0.5). Phylogenetic analysis of the SSU rRNA gene placed both Hennegoides flockae and Henneguya marcquenskiae as sisters to each other in a clade containing other Myxozoans known to infect the gills of esocids, percids, and centrarchids. These parasites represent the first reports of Henneguya and Hennegoides from pirate perch, with the latter being the first report of this genus outside of the Asian continent.