Four laboratory-hatched European kestrels Falco tinnunculus L. were fed on laboratory mice and common voles Microtus arvalis Pallas previously inoculated with different doses of sporulated oocysts of Caryospora kutzeri Böer, 1982. Two kestrels that were fed infected mice shed C. kutzeri oocysts 6 days after ingesting murine tissues. To compare direct and indirect transmissions, two of the kestrels were subsequently directly inoculated with 105 sporulated C. kutzeri oocysts and became patent on days 8 and 9 and shed caryosporan oocysts up to day 25 post inoculation. Additionally, four mice were inoculated with 106 oocysts in order to examine mouse tissues for the presence of developmental stages of C. kutzeri. No coccidian stages were found in the tissues of inoculated mice. The experiment showed that developmental stages of C. kutzeri are able to survive in mouse tissues and cause infection of suitable host after their ingestion.
The effect of host variables such as size and density, on the transmission of cercariae of Diplostomum spathaceum (Rudolphi, 1819) into a second intermediate fish host, rainbow trout, Oncorhynchus mykiss (Walbaum), was studied quantitatively in laboratory experiments under varying exposure conditions. Differences in the number of established metacercariae were noted in differently sized fish exposed singly to the same number of cercariae and in water volumes related to the body surface area of the host. When exposed (1) singly in an equal water volume or, (2) simultaneously in the same tank, no differences in recovery of metacercariae per fish were found between “small” and “large" hosts. The latter observation is valid for three water volumes tested using the same number of cercariae per host. No significant difference in metacercarial infection was revealed in similar sized fish exposed at different host densities. It appears that transmission is more influenced by cercarial density (number of cercariae per water volume) and fish size than by fish density. These experimental findings support the view that cercarial infection offish occurs by chance, presumably mainly in the gill region. Accordingly, in the field, individual fish size and cercarial density rather than fish population density, prevail in parasite transmission from snail to fish. This is of interest in coastal areas heated by cooling water, where fish growth and fish population density are enhanced.
This paper reviews past, current and likely future research on the fish haemogregarine, Haemogregarina bigemina Laveran et Mesnil, 1901. Recorded from 96 species of fishes, across 70 genera and 34 families, this broad distribution for H. bigemina is questioned. In its type hosts and other fishes, the parasite undergoes intraerythrocytic binary fission, finally forming mature paired gamonts. An intraleukocytic phase is also reported, but not from the type hosts. This paper asks whether stages from the white cell series are truly H. bigemina. A future aim should be to compare the molecular constitution of so-called H. bigemina from a number of locations to determine whether all represent the same species. The transmission of H. bigemina between fishes is also considered. Past studies show that young fish acquire the haemogregarine when close to metamorphosis, but vertical and faecal-oral transmission seem unlikely. Some fish haemogregarines are leech-transmitted, but where fish populations with H. bigemina have been studied, these annelids are largely absent. However, haematophagous larval gnathiid isopods occur on such fishes and may be readily eaten by them. Sequential squashes of gnathiids from fishes with H. bigemina have demonstrated development of the haemogregarine in these isopods. Examination of histological sections through gnathiids is now underway to determine the precise development sites of the haemogregarine, particularly whether merozoites finally invade the salivary glands. To assist in this procedure and to clarify the internal anatomy of gnathiids, 3D visualisation of stacked, serial histological sections is being undertaken. Biological transmission experiments should follow these processes.
A new haemogregarine species Hepatozoon affluomaloti sp. n. is described from erythrocytes in the peripheral blood of crag lizards Pseudocordylus melanotus (Smith) and Pseudocordylus subviridis (Smith) (Sauria: Cordylidae) from mountainous regions in the Eastern Free State, South Africa. This species can be distinguished from all other congeners based on its large size, staining properties and life cycle development in its vector, Culex (Afroculex) lineata (Theobald) (Diptera: Culicidae). Mature gamonts stain mostly uniformly pinkish-purple with Giemsa, sometimes containing darker azurophilic granules anterior and posterior to the nucleus. The reflexed posterior extremity of the gamont stage sometimes stains slightly deeper purple and the nucleus is dense and placed in the posterior third of the parasite body. Merogonic stages of this haemogregarine occur in the liver tissues of P. melanotus with dizoic meronts. Macromeronts contains 2-7 macromerozoites and micromeronts contains 9-24 micromerozoites. Sporogonic developmental stages found in the proposed final host and vector, C. lineata, include large oocysts, measuring 54 × 48 µm on average. Sporulating oocysts with 8 nuclei are present in mosquitoes 6-7 days post-feeding on infected lizards. Sporocysts with mature sporozoites measure 31.0 × 21.8 µm on average and each contains 2-8 large sporozoites. It is suggested that transmission of infective sporozoites is achieved through predation of lizards on mosquitoes., Johann Van As, Angela J. Davies, Nico J. Smit., and Obsahuje bibliografii
Ileterosporous (polymorphic) microsporidia in mosquitoes are characterized by intricate life cycles involving multiple spore types responsible for horizontal (per os) and vertical (transovarial) transmission. They affect two generations of the mosquito and some involve an obligate intermediate host. Heterosporous microsporidia are generally very host and tissue specific with complex developmental sequences comprised of unique stages and events. Full details on the intricate relationships between heterosporous microsporidia and their mosquito hosts have only recently been elucidated. Edhazardia aedis (Kudo, 1930) and Culicospora magna (Kudo, 1920) have developmental sequences in larvae that involve gametogony followed by plasmogatny and nuclear association to form diplokarya. These diplokaryotic stages then undergo karyogamy and form binucleate spores responsible for transovarial transmission. In the filial generation, haplosis occurs as a result of nuclear dissociation to produce uninucleate spores infectious to larval mosquitoes. Amblyospora cali-fornica (Kellen et Lipa, 1960) has similar sequences except that haplosis is by meiosis to produce spores infectious for a copepod intermediate host. A third spore type is formed in the intermediate host responsible for infection in a new generation of the mosquito host.
Caryospora duszynskii Upton, Current et Barnard, 1984 was successfully transmitted to snakes of the genus Elaphe by feeding them previously infected mice. Fifty thousand oocysts were orally administered to two mouse strains, BALB/c and Crl:CD-1(ICR)BR, which were subsequently fed to captive-born coccidia-free Elaphe guttata (L.) in two respective independent experiments. Both E. guttata expelled C. duszynskii oocysts in their faeces, beginning on day 18 and 26 post infection (p.i.) and shed oocysts continuously through the end of the experiment, day 230 and 135 p.i., respectively. There were no parasitic stages or lesions in mice, as revealed by histological examination. Experiments proved that rodents serve as paratenic hosts for C. duszynskii. In summary we discuss the life-cycle strategies of Caryospora spp. in reptiles and present three general modes of their development.
A series of laboratory experiments was conducted to investigate the possibility of post-cyclic transmission in Pomphorhynchus laevis (Muller, 1776). Rainbow trout Oncorhynchus mykiss (Walbaum) were exposed to P. laevis in naturally infected Coitus gobio Linnaeus, Noemacheiius barhalulus (Linnaeus), Phoxinus phoxinus (Linnaeus) and heuciscus cephalus (Linnaeus) and sacrificed one month alter infection. Post-cyclic transmission was possible from all four species even though they came from three families and differed in respect of their status and suitability as hosts of P. laevis. There was no selection for or against cither sex of P. laevis, parasites grew in the rainbows and they occupied the same, normal site in the intestine of rainbows irrespective of source host. Post-cyclic transmission of gravid parasites could occur from C. gobio but not from L. cephalus. It is believed that this failure to transmit larger parasites of either sex reflects the age and so development of the proboscis bulb of P. laevis and the extent of the host encapsulation response rather than size or stage of maturity per se. Post-cyclic transmission has the potential to be important in nature.
Sandfly females, while feeding on the host, excrete urine to concentrate proteins of the bloodmeal and restore weight and water balance. This process, analogous to prediuresis in mosquitoes, was observed in 100% of Phlebotomus papatasi (Scopoli) and 85% of P. duboscqi Neveu-Lemaire females studied. Individual females, however, differed in duration of prediuresis and in the number of ejected urine droplets. In both species the prediuresis generally started 1-2 min after the commencement of feeding and the variation in urine production was positively correlated with the length of feeding. The first one or two droplets were opaque whitish while the remaining ones were clear. Erythrocytes were found sporadically in first droplets of some females. Representative prediuresis in P. duboscqi included 27 droplets, i.e., about 325 nl urine in total, ejected during 8 min of feeding. The study revealed prediuresis in P. papatasi and P. duboscqi as a regular physiological process which may have consequences in transmission of infective diseases.
Two experimental trials were performed to elucidate the role of rodents in the life cycle of Hepatozoon species using snakes as intermediate hosts. In one trial, two ball pythons, Python regius Shaw, 1802 were force fed livers of laboratory mice previously inoculated with sporocysts of Hepatozoon ayorgbor Sloboda, Kamler, Bulantová, Votýpka et Modrý, 2007. Transmission was successful in these experimentally infected snakes as evidenced by the appearance of intraerythrocytic gamonts, which persisted until the end of trial, 12 months after inoculation. Developmental stages of haemogregarines were not observed in histological sections from mice. In another experimental trial, a presence of haemogregarine DNA in mice inoculated with H. ayorgbor was demonstrated by PCR in the liver, lungs and spleen.
In order to elucidate the transmission and dispersion routes used by the myxozoan parasite Enteromyxum scophthalmi Palenzuela, Redondo et Alvarez-Pellitero, 2002 within its host (Scophthalmus maximus L.), a detailed study of the course of natural and experimental infections was carried out. Purified stages obtained from infected fish were also used in in vitro assays with explants of uninfected intestinal epithelium. The parasites can contact and penetrate loci in the intestinal epithelium very quickly. From there, they proliferate and spread to the rest of the digestive system, generally in an antero-posterior pattern. The dispersion routes include both the detachment of epithelium containing proliferative stages to the intestinal lumen and the breaching of the subepithelial connective system and local capillary networks. The former mechanism is also responsible for the release of viable proliferative stages to the water, where they can reach new fish hosts. The finding of parasite stages in blood smears, haematopoietic organs, muscular tissue, heart and, less frequently, skin and gills, suggests the existence of additional infection routes in transmission, especially in spontaneous infections, and indicates the role of vascular system in parasite dispersion within the fish. The very high virulence of this species in turbot and the rare development of mature spores in this fish may suggest it is an accidental host for this parasite. This may also question the existence of a two-host life cycle involving an actinosporean stage in this species. Further studies are needed to clarify this open point of the life cycle.