During investigations at the Bussey Institution on the rôle played by certain dipterous larvae in experimentally induced myiasis, with the object if possible of clearing a little of the doubt with which so much of the question is shrouded, the need of good diagnostic characters for these larvae was brought forcibly to my attention.

The priority of the names of the fishes in the following list has been determined from Jordan in Part II of the Report of the United States Commissioner of Fisheries for the year 1928: A check list of Fishes. In determining the names of those not mentioned in this list I have to thank Mr J. R. Norman of the British Museum for his kind assistance.

1. Axenic strains of Entamoeba invadens can be maintained indefinitely, by serial culture, in saline containing a slice of liver. Growth in this medium is poor, the amoebae are vacuolated, and few cysts are formed.

2. The optimum concentration of NaCl for amoebic growth in this medium is 0·75–1·0%, and the optimum pH is 5·7–6·1.

3. The source of the liver tissue in the medium is unimportant, but, of several tissues tested, liver was the only one which supported amoebic growth in serial culture.

4. Suspensions of minced liver also supported amoebic growth, but the growth-promoting activity of the liver was removed completely by centrifugation, autoclaving, and Seitz- or glass-filtration. Heat treatment at 50–60° C. and prolonged storage at 8° C. partially inactivated the liver.

5. Growth in axenic saline-liver medium does not affect the ability of E. invadens to grow and undergo mass encystation when reassociated with suitable bacteria.

Early in January of the present year Professor Minchin kindly gave me for examination a portion of tissue and a mounted section taken from a case of the above disease and sent him by Dr J. Burton Cleland, then of Perth, W. Australia. The tissue was already embedded in paraffin, and both it and the section were stained by Levaditi's method and showed the presence of numerous spirochaetes.

The following descriptions relate to a new species of Amblyomma in all its stages, to two species of Haemaphysalis of which diagnoses of the males and females are given, and to the hitherto unknown larva of Ixodes putus:

Many herpetomonads have been recorded from various insects belonging chiefly to the Diptera and Hemiptera, but until the present instance, members of this genus of flagellates have not been found in the Mollusca and very few in other Invertebrata. Also the habitat of the herpetomonads has usually been either the main alimentary tract or the haemocoel of their hosts. Digestive glands hitherto have not been recorded as being infected.

In this investigation, the host–parasite relationship of ninespine stickleback fish Pungitius pungitius and the cestode parasite Schistocephalus pungitii was studied using samples from Dog Bone Lake, Kenai Peninsula, Alaska, to test the hypothesis that S. pungitii is a castrator of ninespine stickleback. Infected, adult females of all sizes (ages) were capable of producing clutches of eggs. S. pungitii had a negative effect on the ability of host females to produce a clutch, which was related to increasing parasite:host mass ratio (parasite index, PI). Among infected females with egg clutches, both clutch size and egg size were reduced; and the reduction increased with greater PI. The results of this study are consistent with the hypothesis that S. pungitii causes host sterility as a result of simple nutrient theft and is not a true castrator as hypothesized in earlier reports. The degree of parasite-induced sterility appears to vary among populations of the ninespine stickleback, perhaps reflecting differences in resource availability. Populations of ninespine stickleback appear to show a greater reduction in host reproductive capacity with PI than populations of the threespine stickleback infected by Schistocephalus solidus, possibly owing, in part, to the length-adjusted somatic mass of the threespine stickleback being greater.

Pats of pig faeces containing known numbers of Oesophagostomum dentatum eggs were placed on plots with bare soil, short or tall herbage on 8 occasions during 1 year. The number of eggs and larvae and the relative distribution of larvae in faeces, soil and herbage was monitored for 1 year after deposition. On 2 occasions soil from 8 selected plots was given to pigs, which were later slaughtered and examined for the presence of adult O. dentatum. Less than 1% of the deposited eggs could be recovered as infective larvae. The highest recoveries were generally made on tall herbage plots. The majority of infective larvae was found within the faecal pats, which indicates that infective O. dentatum larvae, to a large extent, do not disperse onto the herbage or into soil. The infective larval stage was reached only when the mean temperature in the weeks post-deposition was above 10 °C. This stage was reached within 1 week when the mean weekly temperature was above 13 °C. After the winter period no infective larvae could be recovered from any plots and no parasitic worms could be isolated from pigs fed soil from 8 selected plots.

Toxoplasma gondii rhoptry protein TgROP18 is a polymorphic virulence effector that targets immunity-related GTPases (IRGs) in rodents. Given that IRGs are uniquely diversified in rodents and not in other T. gondii intermediate hosts, the role of TgROP18 in manipulating non-rodent cells is unclear. Here we show that in human cells TgROP18I interacts with the interferon-gamma-inducible protein N-myc and STAT interactor (NMI) and that this is a property that is unique to the type I TgROP18 allele. Specifically, when expressed ectopically in mammalian cells only TgROP18I co-immunoprecipitates with NMI in IFN-γ-treated cells, while TgROP18II does not. In parasites expressing TgROP18I or TgROP18II, NMI only co-immunoprecipitates with TgROP18I and this is associated with allele-specific immunolocalization of NMI on the parasitophorous vacuolar membrane (PVM). We also found that TgROP18I reduces NMI association with IFN-γ-activated sequences (GAS) in the IRF1 gene promoter. Finally, we determined that polymorphisms in the C-terminal kinase domain of TgROP18I are required for allele-specific effects on NMI. Together, these data further define new host pathway targeted by TgROP18I and provide the first function driven by allelic differences in the highly polymorphic ROP18 locus.

Leishmaniasis development is multifactorial; nonetheless, the establishment of the infection, which occurs by the survival and replication of the parasite inside its main host cell, the macrophage, is mandatory. Thus, the importance of studying the molecular mechanisms involved in the Leishmania–macrophage interaction is highlighted. The aim of this study was to characterize a cellular model of macrophages derived from U937 cells that would allow for the identification of infection phenotypes induced by genetic silencing with interference RNA in the context of macrophages infected with Leishmania (Viannia) braziliensis. The model was standardized by silencing an exogenous gene (gfp), an endogenous gene (lmna) and a differentially expressed gene between infected and non-infected macrophages (gro-β). The silencing process was successful for the three genes studied, obtaining reductions of 88·9% in the GFP levels, 87·5% in LMNA levels and 74·4% for Gro-β with respect to the corresponding control cell lines. The cell model revealed changes in the infection phenotype of the macrophages in terms of number of amastigotes per infected macrophage, number of amastigotes per sampled macrophage and percentage of infected macrophages as a result of gene silencing. Thus, this cell model constitutes a research platform for the study of parasite–host interactions and for the identification of potentially therapeutic targets.

In vitro maintenance of helminth parasites enables a variety of molecular, pharmaceutical and immunological analyses. Currently, the nutritional and environmental in vitro requirements of the equine ascarid parasite, Parascaris spp., have not been determined. Additionally, an objective method for assessing viability of Parascaris spp. intestinal stages does not exist. The purpose of this study was to ascertain the in vitro requirements of intestinal stages of Parascaris spp., and to develop a viability assessment method. A total of 1045 worms were maintained in a total of 212 cultures. Worms obtained from naturally infected foals at necropsy were immediately placed in culture flasks containing 200 mL of culture media. A variety of media types, nutrient supplementation and environmental conditions were examined. A motility-based scoring system was used to assess worm viability. Worms maintained in Roswell Park Memorial Institute-1640 had significantly better viability than any other media (P < 0.0001) and all media types supplemented with any of the nutrients examined (P < 0.0001). The use of a platform rocker also significantly improved viability (P = 0.0305). This is the first study to examine the requirements for maintaining Parascaris spp. intestinal stages in vitro and to evaluate their viability based on movement using an objective scoring system.

Fibres isolated from the ventral sucker of Fasciola hepatica were identified as muscle on the basis of their contractility, and their actin and myosin staining. They were voltage-clamped at a holding potential of −40 mV and depolarization-activated outward currents were characterized both electrophysiologically and pharmacologically. Activation was well fitted by a Boltzmann equation with a half-maximal potential of +9 mV and a slope factor of −14·3 mV, and the kinetics of activation and deactivation were voltage-sensitive. Tail current analysis showed that the reversal potential was shifted by +46±3 mV when EK was increased by 52 mV, confirming that this was a K+-current with electrophysiological characteristics similar to delayed rectifier and Ca2+-activated K+-currents in other tissues. The peak current at +60 mV was inhibited by 76±6% by tetrapentylammonium chloride (1 mM) and by 84±7% by Ba2+ (3 mM), but was completely resistant to block by tetraethylammonium (30 mM), 3,4-diaminopyridine (100 μM) and 4-aminopyridine (10 mM). Penitrem A, a blocker of high-conductance Ca2+-activated K+-channels reduced the current at +60 mV by 23±5%. When the effects of Ca2+-channel blocking agents were tested, the peak outward current at +60 mV was reduced by 71±7% by verapamil (30 μM) and by 59±4% by nimodipine (30 μM). Superfusion with BAPTA-AM (50 μM), which is hydrolysed intracellularly to release the Ca2+-buffer BAPTA, also decreased the current by 44±16%. We conclude that voltage-and Ca2+-sensitive K+-channels are expressed in this tissue, but that their pharmacology differs considerably from equivalent channels in other phyla.

While parasite infection can have substantial fitness consequences in organisms, the predictors of parasite prevalence and intensity are often complex and vary depending on the host species. Here, we examined correlates of Haemoproteus (a common malaria parasite) prevalence and intensity in an opportunistically breeding songbird, the red crossbill (Loxia curvirostra). Specifically, we quantified Haemoproteus prevalence and intensity in crossbills caught in the Grand Teton National Park from 2010 to 2013. We found that parasite prevalence varies seasonally and across years, with the highest number of infected individuals occurring in the summer, although there was variation across summers sampled, and that prevalence was positively related to annual mean cone crop sizes (a measure of crossbill food abundance) and daily ambient temperature (a correlate of vector abundance). Parasite intensity was significantly and positively related to one measure of innate immunity, leucocyte counts per blood volume. Finally, neither crossbill age, ecomorph, nor sex had significant effects on parasite infection intensity; however, parasite prevalence did significantly vary among ecomorph and age classes. These results support the interpretation that a combination of physiological (specifically immune activity) and environmental factors affects parasite prevalence and infection intensity in this opportunistically breeding avian species.

1. A local population of Gammarus pulex, infected with Heliospora longissima and Rotundula gammari, was found to have an intracellular developmental stage.

2. Experimental infections of G. pulex were made with the two species of gregarines. In the case of R. gammari infections, large numbers of intracellular developmental stages were found.

3. The taxonomic relationship of the genera Cephaloidophora and Rotundula is discussed.

Thanks are due to Dr P. Tate for constant encouragement and guidance during the course of this work and for the many helpful suggestions in the preparation of the manuscript. Thanks are also due to Mr D. W. T. Crompton for kindly giving me the infected material. The work was completed during the tenure of a Royal Society and Nuffield Foundation Commonwealth Bursary.

R. carnivoralis has been shown to be capable of transmitting T. parva under experimental conditions and stages of the protozoon have been found in sections of salivary glands of the tick.

The monocystid here described was found in the coelom of Pheretima heterochaeta (Mich.).

The following account is based wholly on material fixed in vapour of osmic acid and methyl alcohol—other fixatives like Bouin's and Schaudinn's gave bad results.