Acanthocephalans are common intestinal parasites of marine mammals, the most widespread of which is the genus Corynosoma. In this study, parasite infrapopulations of two closely related species of Corynosoma were examined: Corynosoma enhydri from sea otters (Enhydra lutris) in Alaska (n = 12) and California (n = 19), and Corynosoma strumosum from seals in Germany (n = 22). Prevalence of C. enhydri was 100% in Californian otters, with a mean abundance of 30, and 83% in Alaskan otters, with a mean abundance of 232. In seals, C. strumosum had a prevalence of 65%, with a mean abundance of 33. Female C. enhydri dominated both Californian (82%) and Alaskan (79%) infections, while, in seals, female C. strumosum made up 68% of the parasite population. Reproduction rates for C. enhydri, with 16% (California) and 18% (Alaska) of females mated, were low compared to C. strumosum in seals, of which 40% of females were mated. Habitat selection also differed significantly between the two species. Corynosoma enhydri was found most frequently in the second and third fifths of the small intestine, while C. strumosum was found most frequently in the fourth. The differences in habitat selection and prevalence analysed in this study may be related to a trade-off between growth and reproduction between the two species.

During nematode surveys of natural vegetation in forests of La Cima de Copey de Dota, San José, San José province, Costa Rica, a Xenocriconemella species closely resembling X. macrodora and related species was found. Integrative taxonomical approaches demonstrated that it is a new species described herein as X. costaricense sp. nov. The new species is parthenogenetic (only females have been detected) and characterised by a short body (276–404 μm); lip region with two annuli, not offset, not separated from body contour; first lip annulus partially covering the second lip annulus. Stylet thin, very long (113–133 μm) and flexible, occupying 30.5–47.8% of body length. Excretory pore located from one or two annuli anterior to one or two annuli posterior to level of stylet knobs, at 42 (37–45) μm from anterior end. Female genital tract monodelphic, prodelphic, outstretched, and occupying 35–45% of body length, with vagina slightly ventrally curved (14–18 μm long). Anus located 6–11 annuli from the tail terminus. Tail conoid and bluntly rounded terminus, the last 2–3 annuli oriented dorsally. Results of molecular characterisation and phylogenetic analyses of D2-D3 expansion segments of 28S rRNA, ITS, and partial 18S rRNA, as well as cytochrome oxidase c subunit 1 gene sequences further characterised the new species and clearly separated it from X. macrodora and other related species (X. iberica, X. paraiberica, and X. pradense).

Adult specimens of Andracantha gravida (Alegret, 1941) were recorded from the intestines of the double-crested cormorant Nannopterum auritus (Lesson) (type host) and brown pelican Pelecanus occidentalis L. in two localities from Mexico: Celestún, Yucatan (south-eastern) and Punta Piedra, Tamaulipas (north-eastern). The specimens of A. gravida are morphologically characterized by having a pipe-shaped body without swellings, the absence of small trunk spines between the two fields of spines on the foretrunk and a cylindrical proboscis with 14–16 rows of 10–12 hooks per row. Newly generated partial sequences of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene were generated from adult isolates of A. gravida from Mexico and compared with one sequence of A. gravida and with sequences of other polymorphid acanthocephalans available in GenBank. Phylogenetic analyses based on maximum likelihood and Bayesian inference methods of the cox1 dataset placed all the species of Andracantha in a single clade, with weak support. The analyses of the cox1 dataset placed Andracantha sigma Presswell, García-Varela & Smales, 2018, as sister to the clade formed by A. gravida, Andracantha phalacrocoracis (Yamaguti, 1939), Andracantha leucocarboi Presswell, García-Varela & Smales, 2018 and an unidentified species of Andracantha from Japan. The newly generated cox1 sequences of A. gravida from piscivorous birds of Mexico formed a strongly supported clade with the published sequence of A. gravida from the double-crested cormorant from the south-eastern coast of Mexico. The intraspecific genetic divergence among isolates identified as A. gravida ranged from 0.0% to 2.2%. A cox1 haplotype network inferred with 14 sequences revealed the presence of nine haplotypes, two of which were shared between the populations of piscivorous birds from the north-eastern and south-eastern coasts of Mexico and seven of which were unique. The fixation index between the populations from north-eastern and south-eastern Mexico was low (0.06949), which suggests genetic flow. This can be explained by the migration patterns of the brown pelican and the double-crested cormorant along the coasts of the Gulf of Mexico.

A simple method for the collection of third-stage larvae of Necator americanus has been described. This technique provides repeated recovery of very clean larvae from cultures in moderate numbers.

The breed differences in post-parturient rise (PPR) in faecal egg counts in lambing ewes of different breeds naturally infected with Haemonchus contortus were compared. The ewes of Nali, 50% Nali × 50% Russian Merino/Corriedale and 37.5% Nali × 62.5% Russian Merino/Corriedale were treated with fenben-dazole while ewes of the above three breeds as well as 25% Nali × 75% Russian Merino/Corriedale, were kept untreated. Observations from 3 weeks before lambing to 12 weeks post-lambing at weekly intervals revealed that in treated ewes, egg counts of Nali did not differ significantly with 50% Nali whereas 37.5% Nali had significantly higher egg counts than those of Nali and 50% Nali. In untreated ewes egg counts of 50% Nali were significantly higher than that of Nali on some occasions, while 25% Nali had significantly higher egg counts than the other three breeds. None of the ewes from the Nali breed showed signs of haemonchosis, whereas few lambing ewes of the three Nali crosses (50%, 37.5% and 25% Nali) showed signs of haemonchosis and one ewe of the latter breed died.

Examination of naturally infected felids and viverrids in Malaysia confirmed previously published records which indicated that P. westermani occured only in felid cats. Felis planiceps and F. temnickii were reported as new host records. Analysis of stomach contents revealed no crab remains in either family of cats, but confirmed that felids were strictly carnivorous while viverrids were often omnivorous. In feeding experiments, only viverrids ate the host crabs Potamiscus johorensis and Parathelphusa maculata. The probable transmission of P. westermani to felids via paratenic hosts was discussed.

Neoheterakis chapini n.g., n.sp. (Nematoda: Heterakoidea) is described from the caecum of a Congopeacock Afropavo congensis Chapin, 1936. The diagnostic features of the subfamily Spinaspidoderinae are extended to accomodate the new genus.

Attempts have been made to increase the survival rate of third-stage larvae of Parastrongylus cantonensis during cryopreservation. Parasites were obtained from experimentally infected snails, Biomphalaria glabrata. The maximum non-toxic concentrations of cryoprotectants dimethyl sulphoxide (DMSO) and glycerol were determined as 10% v/v in NCTC 109 medium. Different pre-cooling times and serum additives were assayed to determine their effects on the viability of larvae. Larvae pre-cooled at –20°C for 15–20 minutes before transfer to –70°C had the optimum survival rate. The presence of serum was essential for further cooling to –196°C. There were no differences between native and heat-inactivated sera on the larval viability. The survival of larvae recovered after storage at –196°C was higher in sera collected from the rat, man, or fetal calf than in sera collected from the mouse, dog, or horse. Viability assessed by mouse-infections showed that thawed larvae retained infectivity for susceptible hosts, but it was significantly lower than that of unfrozen control worms.

Tetraspanins are a superfamily of transmembrane proteins that in flatworms have structural roles in the development, maturation or stability of the tegument. Several tetraspanins are considered as potential candidates for vaccines or drugs against helminths. Monopisthocotylean monogeneans are ectoparasites of fish that are health hazards for farmed fish. The aim of this study was to identify in silico putative tetraspanins in the genomic datasets of four monopisthocotylean species. The analysis predicted and classified 40 tetraspanins in Rhabdosynochus viridisi, 39 in Scutogyrus longicornis, 22 in Gyrodactylus salaris and 13 in Neobenedenia melleni, belonging to 13 orthologous groups. The high divergence of tetraspanins made it difficult to annotate their function. However, a conserved group was identified in different metazoan taxa. According to this study, metazoan tetraspanins can be divided into 17 monophyletic groups. Of the 114 monogenean tetraspanins, only seven were phylogenetically close to tetraspanins from non-platyhelminth metazoans, which suggests that this group of proteins shows rapid sequence divergence. The similarity of the monopisthocotylean tetraspanins was highest with trematodes, followed by cestodes and then free-living platyhelminths. In total, 27 monopisthocotylean-specific and 34 flatworm-specific tetraspanins were identified. Four monogenean tetraspanins were orthologous to TSP-1, which is a candidate for the development of vaccines and a potential pharmacological target in trematodes and cestodes. Although studies of tetraspanins in parasitic flatworms are scarce, this is an interesting group of proteins for the development of new methods to control monogeneans.

A new genus and species of filarioid worm is described from the peritoneal cavity of fruit bats, Pteropus hawaiiensis from Fiji and the name Chiropterofilaria brevicaudata n. sp. is given to it. The microfilaria is described. This appears to be the first record of a nematode from this host. The new genus is differentiated from its nearest genus Lemdana in that the spicules are only slightly unequal; and in the female worms, the oesophagus usually make several turns around the vagina before joining the intestine. From the same host, a second microfilaria, Microfilaria fijiensis n. sp. is described, the adults of which were not found.

Two species of the genus Aporcella, one new and one previously known, collected from cultivated fields in Iran are studied. Description, morphometrics, illustrations (both line and microphotographs) and D2–D3 sequences are provided for Aporcella talebii sp. n., which is characterized by its 1.66–2.02-mm-long body, lip region offset by constriction and 15–17 μm broad, odontostyle 14–17.5 μm long, neck 412–484 μm long, pharyngeal expansion occupying 46–50% of total neck length, uterus simple and 1.6–2.0 times the corresponding body diameter long, V = 52–59, tail conical (40–50 μm, c = 37–47, c′ = 1.1–1.4) with a weak but perceptible dorsal concavity at the end and male absent. Morphometrics, microphotographs and D2–D3 sequences of Aporcella simplex are also presented, this being its first Asian record. Molecular analyses confirm the monophyly of the genus, its close relationship with other taxa lacking pars refringens vaginae and the polyphyly of Aporcelaimidae.

Detailed studies were carried out to assess the infection characteristics of the antelope schistosomes in BALB/c mice and Mastomys coucha. Both schistosome species reached sexual maturity in these hosts. However, they differed markedly in terms of egg production rates and preferred sites of tissue egg deposition. Tissue egg deposition commenced between 4 and 5 weeks in the case of Schistosoma margrebowiei and between 6 and 7 weeks in the case of S. leiperi. Tissue egg accumulation rates of S. leiperi were calculated to be 334 and 311 eggs/gravid worm pair/day in mice and M. coucha, respectively. The fecundity of S. margrebowiei was found to be substantially greater (approximately 5 times; daily output ranging from 1600–1900 eggs/gravid worm pair). While S. leiperi infections remained relatively stable in both hosts during the study period (i.e. up to 15 weeks after onset of egg laying), S. margrebowiei infections were observed to deteriorate rapidly in M. coucha.

In this study, we report the first complete mitochondrial genome of the tapeworm Nippotaenia mogurndae in the order Nippotaeniidea Yamaguti, 1939. This mitogenome, which is 14,307 base pairs (bp) long with an A + T content of 72.2%, consists of 12 protein-coding genes, 22 transfer RNA (tRNA) genes, two rRNA genes, and two non-coding regions. Most tRNAs have a conventional cloverleaf structure, but trnS1 and trnR lack dihydrouridine arms of tRNA. The two largest non-coding regions, NCR1 (220 bp) and NCR2 (817 bp), are located between trnY and trnS2 and between nad5 and trnG, respectively. Phylogenetic analyses of mitogenomic data indicate that N. mogurndae is closely related to tapeworms in the order Cyclophyllidea.

Interspecific interactions between parasites sharing the same host are often antagonistic; the presence of one species decreases the number of individuals or negatively affects both the distribution and reproduction of the other species. Antagonistic interactions between co-infecting parasites may translate into direct competition or interactive segregation, but elements of both may be present. Potential interactions between two acanthocephalan species, Pomphorhynchus laevis and Acanthocephalus anguillae, were studied in the field in two of their natural fish definitive hosts. There was no evidence for competitive exclusion between P. laevis and A. anguillae. However, a negative interaction was found for the first time in the field between these two species. Based on the analysis of parasite abundance and total biomass using a static regression approach, I found that the abundance and total biomass of parasites was also limited by host characteristics. These results are consistent with previous laboratory studies on competition between P. laevis and A. anguillae.

Brachylaemus arcuatus and Plagiorchis (Multiglandidmns) mmris are recorded for the first time from the fox and sheep respectively.

By combining a number of well-known but scattered results, a theoretical model has been constructed to explain the observed quadratic increase in sample variance of egg counts over sample mean with increasing egg concentration. Our contention is that the over-dispersion arises because of inherent variation in volumetric deliveries of faecal suspension onto the counting slide. Even though the observed variation of volumetric deliveries appears to be small, we have shown that it is adequate to cause a considerable increase in egg count variance over mean at not unreasonably high concentrations.

Global programmes to eliminate lymphatic filariasis (GPELF) require mapping, monitoring and evaluation using filarial antigen diagnostic kits. To meet this objective, a functional single-chain fragment variable (ScFv) specific for filarial Wuchereria bancrofti SXP-1 (Wb-SXP-1) antigen was constructed for the diagnosis of active filarial infection, an alternative to the production of complete antibodies using hybridomas. The variable heavy chain (VH) and the variable light chain (kappa) (Vκ) genes were amplified from the mouse hybridoma cell line and were linked together with a flexible linker by overlap extension polymerase chain reaction (PCR). The ScFv construct (Vκ–Linker–VH) was expressed as a fusion protein with N-terminal His tag in Escherichia coli and purified using immobilized metal affinity chromatography (IMAC) without the addition of reducing agents. Immunoblotting and sandwich enzyme-linked immunosorbent assay (ELISA) were used to analyse the antigen binding affinity of purified ScFv. The purified ScFv was found to recognize recombinant and native Wb-SXP-1 antigen in microfilariae (Mf)-positive patient sera. The affinity of ScFv was comparable with that of the monoclonal antibody. The development of recombinant ScFv to replace monoclonal antibody for detection of filarial antigen was achieved. The recombinant ScFv was purified, on-column refolded and its detection ability validated using field samples.