Serum-free media were used to culture Plasmodium falciparum. A commercial preparation, Daigo's GF21 developed as a growth-promoting factor for many kinds of mammalian cells, and consisting of the 55–70% ammonium sulphate fraction of adult bovine serum, insulin, transferrin, ethanolamine and sodium selenite, was found to sustain growth of the parasite when Daigo's T was employed as a basal medium. The optimal Daigo's GF21 concentration for parasite growth was between 5 and 20% (v/v), with the best results at 10%. Differential counts indicated that Daigo's GF21 is essential for schizogony. Established serum-free medium, GIT, consisting of Daigo's T basal medium and Daigo's GF21, yielded good parasite growth without any supplementation. Growth-promoting factor derived from adult bovine serum in Daigo's GF21 was shown to be crucial to parasite growth. The results presented here will not only be of practical value, but will provide important information about the developmental requirements for the parasite.

A passive transfer system, dependent upon hyperimmune rat serum, was used to study in vivo protective humoral immunity to Schistosoma mansoni infection in Fischer rats. Infected recipients of hyperimmune serum exhibited a significant reduction (51%) in the number of recovered adult schistosomes relative to infected recipients of normal rat serum. Furthermore, schistosomula were equally sensitive to the effects of hyperimmune serum injected up to and including 7 days post-infection, a phenomenon which was termed ‘extended sensitivity’. Schistosomula were beginning to lose sensitivity to the effects of hyperimmune serum by the 8th day post-infection and were completely refractile by the 9th day. In addition, it was demonstrated that parasite elimination occurred after the lung stage. Some protection was also observed when hyperimmune rat serum was transferred to mice as late as 5 days post-infection.

Comparisons were made of the infectivity and antigenicity of 4 Trichinella spiralis isolates (S, D, Y, W), of quite different geographical origins, and T. pseudospiralis (P) in rapid- and slow-responder inbred mice. Infectivity was measured by the Index of Reproductive Capacity (ICR) expressed as the ratio between the number of muscle larvae recovered on day 30 post-infection (p.i.) and the numbers of larvae given at infection. Antigen recognition was measured by the degree of proliferation of mesenteric lymph node cells (MLNC) to in vitro stimulation with crude muscle larvae antigen (CMLA) and by the total antibody responses to CMLA at day 25 p.i. as measured by ELISA. Regarding infectivity the isolates fell into two groups, high infectivity (S, D and Y) and low infectivity (W and P). Analysis of CMLA, detergent-stripped (CTAB) and I-labelled surface larval proteins was made by SDS—PAGE under reducing conditions. Differences in antigen profiles were seen in all antigen preparations, being most noticeable in CTAB and 125I-labelled proteins from W and P isolates. Antigen recognition by polyclonal infection-derived antisera and by monoclonal antibodies raised against the T. spiralis London strain (L) was studied in the W (Arctic) and S (Spanish) isolates. Polyclonal antisera recognized different antigens in the S and W isolates, as did the monoclonal antibody, although recognition was more restricted. Neither antibody recognized a 64 kDa band in the W isolate which was clearly visible in the others tested.

A survey of tick activity curve data for Britain shows:

There are usually two peaks of female activity per annum, one peak in ‘spring’ and a lesser one in ‘autumn’, the date limits of the ‘seasons’ being slightly elastic. For a greater or lesser period in summer female-tick activity is low or practically absent, while in winter it is practically absent.

There are exceptions to the biannual type of female activity. In three areas, only one annual peak occurs. At Hethpool, north-eastern Northumberland, and in Ettrick Valley, southern Scotland, this single peak is in April–May; in the Hill o'Fare area, north-eastern Scotland, it is in July.

The theory of temperature control of activity (the limits being the range 45–60° F. average weekly maximum shade temperature, i.e. corresponding to spring and autumn conditions in Britain) does not stand up to the following facts: At Hethpool, following a spring female activity confined to the range 45–60° F., there was no autumn recrudescence when temperatures again passed through the same range. About half the annual female activity at Crag, south-western Cumberland, and practically all in the Hill o'Fare area occurred at temperatures of 60–70° F. and 60–65° F. respectively.

Solar radiation, evaporativity and humidity, as well as temperatures, of the macro-climate were investigated in relation to female activity. The tentative conclusion is that the duration of humidity level during daylight, in conjunction with temperature, may partly decide the amount and extent of activity in summer.

In spring, where spring activity obtains, males and females appear in small numbers a few weeks before nymphs. The bulk of male, female and nymphal spring activity, however, is concurrent, the curves having peaks at approximately the same date.

Again, where spring activity obtains, spring larval activity commences later than that of males, females and nymphs, the peak being about 1 month later.

Theories of seasonal activity are discussed.

Eight species of coccidia were recognized in 596 faeces samples from 3 commercial rabbitries in South East England. The level of infection was related to management methods and at one site it was reduced by an outbreak of mucoid enteritis and/or its treatment with oxytetracycline. In samples from rabbits managed conventionally in wire cages over droppings-pits, 96% contained oocysts and of these, 60% had 1000–10000 oocysts/g. Mixed infections were common, 67% of the animals carrying 2–4 different species. Eimeria media, E. magna and E. perforans occurred most frequently; E. coecicola, E. irresidua and E. flavescens were less common and E. intestinalis and E. piriformis were relatively rare. E. stiedai was not recorded.

1. The osmotic behaviour of three parasites in normal and experimental media has been studied with a view to understanding the relationship with their hosts.

2. Angusticaecum sp., a nematode frpm the intestine of the tortoise, is hypertonic in media of very low concentrations (1·1–1·3 % NaCl in tap water), but becomes isotonic in sea water and slightly hypertonic in 50 % sea water. Ligaturing experiments show that its cuticle is permeable to water and probably to salts.

3. Lernaeocera branchialis, a blood-feeding copepod from Gadus spp., is hypotonic to the surrounding sea water so long as it remains attached to its host, its blood showing an osmotic pressure equivalent to 2·O–2·8 % NaCl. Isotonicity with the medium is established when the parasite is excised and kept alive. Hypotonicity of Lernaeocera is probably caused by the low osmotic pressure of the blood of its host (1·443 % NaCl in Gadus pollachius), to which it is permanently attached.

4. Bopyrus squillarum, a blood-sucking isopod from Leander serratus, is isotonic or slightly hypotonic to sea water, the tendency towards hypotonicity being probably the result of the hypotonic nature of the blood of the host.

5. The osmotic properties of Lerpaeocera and Bopyrus would suggest their ability to survive in dilute sea water, a fact which is supported by their occurrence on hosts living in inshore or estuarine habitats.

The immune status of a host infected with Trypanosoma spp. or Leishmania spp. can play an important role in successful chemotherapy. In animal models, treatment of African trypanosomiasis with difluoromethylornithine or melarsoprol requires an appropriate antibody-mediated immune response. An intact immune system is also necessary for rapid clearance of trypanosomes from the bloodstream following treatment with suramin or quinapyramine. Similarly, an efficient cell-mediated immune response is required for maximal efficacy of pentavalent antimonials in the treatment of leishmaniasis. However, the potential relationship between parasite-induced or acquired immunosuppression and effective chemotherapy has been poorly studied. Macrophages which have been activated by bacterial cell wall components or gamma-interferon are known to display increased activity against Leishmania donovani or Trypanosoma cruzi. In experimental and clinical visceral leishmaniasis, use of macrophage activators together with pentavalent antimonials has lowered the dose of antimony required to cure the infection.

Before the discovery of Toxoplasma gondii as a coccidium of the cat in 1970, cat and dog coccidia were classified in the genus Isospora and considered of little clinical or zoonotic significance. Since 1970, several new (Hammondia sp., Neospora sp.) and previously described species, including Sarcocystis, Besnoitia, and Cryptosporidium have been found as coccidians of cats and dogs with clinical and zoonotic significance. In the present paper I review salient features of the evolution of cat and dog coccidia.

Chagas' disease, caused by Trypanosoma cruzi, affects 16–18 million people in Central and South America. Patient treatment is based on drugs that have toxic effects and limited efficacy. Therefore, new chemotherapeutic agents need to be developed. Snake venoms are sources of natural compounds used in various medical treatments. We observed that Crotalus viridis viridis venom was effective against all developmental forms of T. cruzi. Ultrastructural analysis revealed swelling of mitochondria, blebbing and disruption of the plasma membrane, loss of cytoplasm components and morphological changes of the cell. Staining with propidium iodide and rhodamine 123 confirmed the observed alterations in the plasma and mitochondrial membranes, respectively. The effects of the venom on the parasite intracellular cycle were also analysed. Pre-infected LLC-MK2 cells incubated with Cvv venom showed a 76–93% reduction in the number of parasites per infected cell and a 94–97·4% reduction in the number of parasites per 100 cells after 96 h of infection. Free trypomastigotes harvested from the supernatants of Cvv venom-treated cells were incapable of initiating a new infection cycle. Our data demonstrate that Cvv venom can access the host cell cytoplasm at concentrations that cause toxicity only to the amastigote forms of T. cruzi, and yields altered parasites with limited infective capacity, suggesting the potential use of Cvv venom in Chagas' disease chemotherapy.

This study compared the prevalence and intensity of infections of helminths in 2 chicken breeds in Vietnam, the indigenous Ri and the exotic Luong Phuong. Also, possible correlations with the Major Histocompatibility Complex (MHC) were tested. The most prevalent helminths were Ascaridia galli, Heterakis beramporia, Tetrameres mothedai, Capillaria obsignata, Raillietina echinobothrida and Raillietina tetragona. Differences in prevalence and intensity of infection were found between the 2 breeds. Comparing the 2 groups of adult birds, Ri chickens were observed to have higher prevalence and infection intensities of several species of helminths, as well as a higher mean number of helminth species. In contrast, A. galli and C. obsignata were shown to be more prevalent in Luong Phuong chickens. Furthermore, an age-dependent difference was indicated in the group of Ri chickens in which the prevalence and the intensity of infection was higher for the adult than the young chickens for most helminths. The most notable exception was the significantly lower prevalence and intensities of A. galli in the group of adult chickens. In contrast, the prevalence and intensity were very similar in both age groups of Luong Phuong chickens. Using a genetic marker located in the MHC, a statistically significant correlation between several MHC haplotypes and the infection intensity of different helminth species was inferred. This is the first report of an association of MHC haplotype with the intensity of parasite infections in chickens.

The present study addresses the effect of varying temperature and host species on the size and shape of the opisthaptoral hard-parts in isogenic strains of Gyrodactylus salaris and G. thymalli. Variation in shape was examined using geometric morphometrics. Since the opisthaptoral hard-parts of Gyrodactylus have few specific landmarks, their shape information mostly being represented by outlines and surfaces, a method based on sliding semi-landmarks was applied. The ventral bars of G. salaris did not follow the previously postulated negative correlation between size and temperature, and the largest hamuli and marginal hooks from G. salaris and the smallest from G. thymalli clearly overlapped in size. Consistent shape differences with temperature were detected for the hard-parts from G. thymalli but not from G. salaris. The hard-parts of G. salaris were similar in size but significantly different in shape when grown on secondary hosts rather than the primary host.

The composition of the fatty acid methyl ester (FAME) and alcohol fractions of the cuticular and internal lipids of Calliphora vomitoria larvae, pupae and male/female adults was obtained by separating these two fractions by HPLC–LLSD and analysing them quantitatively using GC–MS. Analysis of the cuticular lipids of the worldwide, medically important ectoparasite C. vomitoria revealed 6 FAMEs with odd-numbered carbon chains from C15:0 to C19:0 in the larvae, while internal lipids contained 9 FAMEs ranging from C15:1 to C19:0. Seven FAMEs from C15:0 to C19:0 were identified in the cuticular lipids of the pupae, whereas the internal lipids of the pupae contained 10 FAMEs from C13:0 to C19:0. The cuticular lipids of males and females and also the internal lipids of males contained 5, 7 and 6 FAMEs from C15:0 to C19:0 respectively. Seven FAMEs from C13:0 to C19:0 were identified in the internal lipids of females, and 7, 6, 5 and 3 alcohols were found in the cuticular lipids of larvae, pupae, males and females respectively. Only saturated alcohols with even-numbered carbon chains were present in these lipids. Only 1 alcohol (C22:0) was detected in the internal lipids of C. vomitoria larvae, while just 4 alcohols from – C18:0 to C24:0 – were identified in the internal lipids of pupae, and males and females. We also identified glycerol and cholesterol in the larvae, pupae, males and females of C. vomitoria. The individual alcohols and FAMEs, as well as their mixtures isolated from the cuticular and internal lipids of larvae, pupae, males and females of C. vomitoria, demonstrated antimicrobial activity against entomopathogenic fungi.

The use of aromatic plants and their essential oils for ectoparasite treatment is a field of growing interest. Several species of birds regularly introduce aromatic herbs into their nests putatively to reduce parasites. The behaviour is most often seen in cavity nesting birds and after nest building has finished. The plants are included in a non-structural manner and are often strongly aromatic. Various different hypotheses have been proposed regarding the function of this behaviour; from the plants altering some non-living factor in the nest (crypsis, water loss and insulation hypotheses) to them being involved in mate selection (mate hypothesis) or even having a beneficial effect, direct or indirect, on chicks (drug or nest protection hypothesis, NPH). Many studies have been carried out over the years observing and experimentally testing these hypotheses. This review focuses on studies involving the most popular of these hypotheses, the NPH: that plants decrease nest parasites or pathogens, thereby conveying positive effects to the chicks, allowing the behaviour to evolve. Studies providing observational evidence towards this hypothesis and those experimentally testing it are discussed.

Cestodes of the genus Taenia are parasites of mammals, with mainly carnivores as definitive and herbivores as intermediate hosts. Various medium-sized cats, Lynx spp., are involved in the life cycles of several species of Taenia. The aim of the present study was to identify Taenia tapeworms in the Eurasian lynx (Lynx lynx) from Finland. In total, 135 tapeworms from 72 lynx were subjected to molecular identification based on sequences of 2 mtDNA regions, the cytochrome c oxidase subunit 1 and the NADH dehydrogenase subunit 1 genes. Available morphological characters of the rostellar hooks and strobila were compared. Two species of Taenia were found: T. laticollis (127 samples) and an unknown Taenia sp. (5 samples). The latter could not be identified to species based on mtDNA, and the rostellar hooks were short relative to those described among other Taenia spp. recorded in felids from the Holarctic region. In the phylogenetic analyses of mtDNA sequences, T. laticollis was placed as a sister species of T. macrocystis, and the unknown Taenia sp. was closely related to T. hydatigena and T. regis. Our analyses suggest that these distinct taeniid tapeworms represent a putative new species of Taenia. The only currently recognized definitive host is L. lynx and the intermediate host is unknown.

Sequence variation within 3 morphologically defined species of the anoplocephalid cestode genus Progamotaenia (P. ewersi, P. macropodis and P. zschokkei) was investigated using the cytochrome c oxidase subunit 1 gene. The magnitude of genetic variation detected within each morphospecies suggests that, in each instance, several cryptic species are present. Within P. ewersi, 5 genetically distict groups of cestodes were detected, 1 shared by Macropus robustus and M. parryi in Queensland, 1 in M. agilis from Queensland, 1 in Petrogale assimilis from Queensland, 1 in Macropus fuliginosus from South Australia and 1 in Wallabia bicolor from Victoria. In P. macropodis, cestodes from M. robustus from Queensland, Western Australia and the Northern Territory, M. parryi from Queensland and M. eugenii from South Australia were genetically distinct from those in Wallabia bicolor from Queensland and Victoria and from M. fuliginosus from South Australia. P. zschokkei consisted of a number of genetically distinct groups of cestodes, 1 in Lagorchestes conspicillatus and L. hirsutus from Queensland and the Northern Territory respectively, 1 in Petrogale herberti, P. assimilis and M. dorsalis from Queensland, 1 in Onychogalea fraenata from Queensland, 1 in M. agilis from Queensland and 1 in Thylogale stigmatica and T. thetis from Queensland. In general, genetic groups within each morphospecies were host specific and occurred predominantly in a particular macropodid host clade. Comparison of genetic relationships of cestodes with the phylogeny of their hosts revealed examples of colonization (P. zschokkei in M. agilis) and of host switching (P. zschokkei in M. dorsalis).

Irrigation for intensive sugar cultivation started in the early 1980s at Richard Toll, some 100 km from the mouth of the Senegal River. Infections with Schistosoma mansoni were first seen in late 1988. This study records quantitative snail surveys for over 3 years from 1992 at sites representing different habitats in and around the irrigation scheme. Populations of both Biomphalaria pfeifferi (the intermediate host of S. mansoni) and Bulinus spp. (mainly B. truncatus, the local host of S. bovis) peaked in late ‘spring' or early ‘summer', depending on the habitat, and then remained low until the following ‘spring'. B. pfeifferi favoured smaller, man-made habitats with most transmission between May and August each year. The less abundant Bulinus spp. favoured larger natural and man-made habitats with most S. bovis transmission between April and July. S. mansoni infections were more, but S. bovis infections were less abundant than other trematodes in their respective snail hosts. Ecological changes in the early 1980s due to sugar irrigation pre-dated similar, more widespread changes in the late 1980s when the completion of dams across the Senegal River prevented seasonal rain fed floods and sea water intrusion. S. mansoni has since spread rapidly around Richard Toll. The incompatibility of the local S. haematobium strains with the dominant bulinid snails has so far prevented an epidemic of urinary schistosomiasis at Richard Toll, but the invasion of similar downstream habitats by susceptible B. globosus is worrying. The principal control measure, chemotherapy, given in the ‘winter' would minimise the rate of reinfection. It could be reinforced by judicious mollusciciding within the sugar irrigation scheme but not elsewhere.

The usual host of this new parasite, Helicosporidium parasiticum, is the larva of a Ceratopogonid, Dasyhelea obscura Winnertz, which lives in the decomposed sap filling the wounds of trees—elm and horse-chestnut. All the material used for this study was derived from the wounds of two trees only: (1) an elm tree standing on the Caius College ground at Newnham, facing Church Rate Walk, and (2) a horse-chestnut standing between the School of Agriculture and Downing College.

1. The period which elapses between a blood-meal and oviposition on the part of the female bed-bug affects the duration of the egg stage. Eggs laid soon after the meal take longer to hatch than those laid later. It is supposed that embryonic development of eggs inside the female occurs at a rate relatively greater than that of oviposition.

2. Atmospheric humidity is without effect on the duration of the egg stage. Although the temperature-velocity graph appears to be fairly linear between 18 and 30° C. the thermal constants show considerable variation.

3. A daily alternation of temperature with a range of 10° C, between the threshold and optimum temperatures results in an acceleration of development; this can, however, be accounted for by the non-linearity of the temperature-velocity relationship, if the usual methods of thermal summation are used.

4. Eggs have been exposed to temperatures between 1 and 12° C. and the time taken to hatch on subsequent incubation at 23° C. has been ascertained. When these times are compared with times for hatching of control eggs kept at 23° C. from oviposition there is some evidence that a slight amount of development may occur at as low a temperature as 4° C.; i.e. 9° below the developmental-hatching threshold. Times after exposure are shorter than times for control eggs.

5. Thermal summation, however, suggests that temperatures between 13 and 11·7° C. result in a retardation of development since the times after exposure at which hatching occurs at 23° C. are longer than would be expected.

6. The method of thermal summation is criticized mainly on the grounds that it assumes that a temperature has the same accelerating effect on all stages of embryonic development. A retardation of development such as that mentioned in the preceding paragraph may be either a true retardation or due to errors resulting from the assumption that the reciprocal of the time for complete development represents the true amount of daily development at all stages of embryonic growth.

7. The lowest constant temperature at which complete development with hatching, of eggs laid at 23° C, can occur is 13° C. I have called this temperature the developmental-hatching threshold. The developmental threshold may be as low as 4° C, while the hatching threshold is at approximately 8° C.

8. Alternating temperatures such as occur in English houses are unlikely to affect the position of the developmental-hatching threshold. Atmospheric humidity does, however, affect it and 75–90% r.h. appear to be the only humidities at which development with hatching can take place at a constant temperature of 13° C.

9. Mortalities near the developmental-hatching threshold appear to depend also on the temperature at which eggs are laid (or perhaps the temperatures at which they develop within the female). Eggs laid at 15° C. and incubated at 15° C. and 7% r.h. suffer 97·1% mortality while those laid at 23° C. and incubated under identical conditions have 32·9% mortality.

10. If eggs are laid at 23° C. and are incubated at 15, 18 and 23° C. until nearly ready to hatch, the percentage hatch at temperatures near the batching threshold is higher with those eggs previously kept at 18° C. than with those from 15 or from 23° C. At 8° C, the lowest observed temperature for hatching, preliminary incubation at 15° C. is probably more favourable than one at 23° C.

11. Mortality of eggs above 13° C. is only slightly affected by atmospheric humidity over the optimal range. But the effects are more noticeable near the upper and lower temperature limits. 99–100% r.h. appears to be associated with a higher mortality than 90% r.h. The extreme temperature limits for eggs laid at 23° C. are 13 and 37° C. With eggs laid at 15° C. the range is restricted at both upper and lower temperature limits compared with the range for eggs laid at 23° C. The temperature of oviposition, whether it is 15 or 25° C, seems to make no difference to mortalities between 18 and 28° C.

12. The mortalities of eggs exposed for varying periods to temperatures between 1 and 13° C. and various humidities are discussed. By means of probits estimates of the times for 50 and 99·99% mortalities have been made for each of the temperature and humidity combinations.

13. Exposure for 50% mortality is affected slightly by humidity below 13° C, but no simple law relating survival to humidity has been found either above or below 13° C. Variations in temperature within the range 0—34° C. are likely to influence survival more than the humidity variations possible within this temperature range.

14. At constant saturation deficiencies the eggs survive longer at the higher temperatures between 1 and 13° C. The median exposure for death (i.e. exposure for 50% mortality) increases by 1·5–1·8 days per 1° C. rise of temperature.

15. The scatter of mortalities about the median exposure for death as measured by the regression coefficient of probits on exposure times is slightly influenced by humidity, but is not affected by temperatures between 1 and 13° C. Much of the variation in the slopes of the mortality curves is thought to be due to inherent variation in the eggs themselves.

16. With eggs laid at 23° C. and exposed to temperatures below 13° C. the longest exposure necessary to produce 99·99% mortality (as judged by subsequent incubation at 23° C.) was estimated at 79.8 days. This occurred at 12·1° C. and 73% r.h. The actual observed times for exposure for 100% mortality are somewhat shorter than the estimated times.

17. Eggs with embryos in an advanced state of development are more quickly killed by exposure to 7·7° C. and 90% r.h. than are newly laid eggs.

18. Ovipositional temperatures of 15, 18 and 23° C. produced no different effects on the mortality rates of eggs exposed to 10° C. and 90% r.h.

19. Future problems and the ecological significance of the experimental results are discussed.

To assess ectoparasite impact on individuals and populations of Gerbillus andersoni allenbyi under natural conditions, I addressed the following questions. Do ectoparasites affect their host fitness and, if so, how? Do ectoparasites affect host population level? Does this parasite–host interaction support the traditional concept of parasite evolution towards avirulence? For this purpose, host infestation, infection, survival, haematological indices, and physical condition were recorded. A field experiment which included manipulating host infestation while recording host survival was conducted to determine the causal relations between these variables. G. a. allenbyi was infested by 2 fleas (Synosternus cleopatrae and Stenoponia tripectinata), 5 mesostigmatid mites (Androlaelaps centrocarpus, A. hirsti, A. insculptus, A. marshalli and Hirstionyssus carticulatus), 1 tick (Rhipicephalus sanguineus), and 1 louse (Polyplax gerbilli). Ectoparasite burden significantly reduced host survival and red blood cell indices (red cell concentration, haemoglobin concentration and haematocrit). Ectoparasite burden did not significantly affect white blood cell concentration. Gerbils were not infected by haemoparasites or gut helminths which potentially could cause anaemia. The causal relationship between S. cleopatrae burden and host survival was established by manipulation of host infestation. Both ectoparasite removal and initial level of infestation significantly affected host survival. Ectoparasites that caused anaemia were not associated with host physical condition (PC), measured as weight/length3. None of the red blood cell indices was correlated with host PC. These results suggest both that host PC was not affected by ectoparasite burden and that exsanguination leading to anaemia was the main effect of the ectoparasites. Ectoparasite pressure on the host population (based on the ectoparasite effects as estimated by statistical models, combined with dispersion of the infestation within the host population) changed seasonally and was greatest when host density was the highest. A large segment of the gerbil population was affected by ectoparasites during the entire year. An explanation for the evolution of parasite virulence, contrasting parasites that evolve towards increased virulence with parasites that evolve towards avirulence is presented. This classification is primarily based on whether parasite impact is equated with a higher efficiency of host exploitation, or whether it is a ‘side effect’ of parasite biology.

Two species of Schizotrypanum, T. (S.) dionisii and T. (S.) vespertilionis, were identified from British bats. Laboratory studies on stocks of isolated trypanosomes from 5 species of bat (Pipistrellus pipistrellus, Nyctalus leisleri, N. noctula, Eptesicus serotinus and Myotis brandti) indicated that the predominant species was T. d. dionisii. Collections and dissection of the bat bug Cimex pipistrelli from bat roosts revealed flagellate infection in a total of 12 out of 20 bugs; 7 of these bugs had metacyclic trypanosomes present. C. pipistrelli and the human bed bug, C. lectularius were reared in the laboratory and allowed to feed on wild-caught bats known to be infected with T. d. dionisii. Development occurred in both species of Cimex. Cimex spp. could be used to detect subpatent Schizotrypanum infections by xenodiagnosis. This technique was used to test the parasitological status of bats collected in the wild or reared in captivity. On a single occasion an apparent transmission of T. d. dionisii to an uninfected (by xenodiagnosis) laboratory reared bat was achieved. A stock of Schizotrypanum isolated from a wild-caught C. pipistrelli collected in a N. leisteri roost was identified by DNA buoyant density centrifugation as T. (S.) vespertilionis. A P. pipistrellus known to be infected with T. d. dionisii was found to have cyst-like structures in thoracic skeletal muscle containing amastigotes. The study provided the strongest evidence yet that C. pipistrelli is the vector of Schizotrypanum in British bats.