Host's Body Cavity Research Articles

Microsporidian coinfection reduces fitness of a fungal pathogen due to rapid host mortality.

Infection outcomes can be strongly context dependent, shifting a host-symbiont relationship along a parasitism-mutualism continuum. Numerous studies show that under stressful conditions, symbionts that are typically mutualistic can become parasitic. The reverse possibility, a parasite becoming mutualistic, has received much less study. We investigated whether the parasitic microsporidium Ordospora pajunii can become beneficial for its host Daphnia dentifera in the presence of the more virulent fungal pathogen Metschnikowia bicuspidata. We found that, even though infection with O. pajunii reduces the frequency of penetration of M. bicuspidata spores into the host body cavity, it does not improve the survival or reproduction of the host; conversely, coinfection increased the mortality of Daphnia. This shorter lifespan of coinfected hosts disrupted the life cycle of M. bicuspidata, greatly reducing its fitness. Thus, coinfection with both pathogens was detrimental to the host at the individual level but might be beneficial for the host population as a result of greatly reduced production of M. bicuspidata spores. If so, this would mean that O. pajunii outbreaks should delay or prevent M. bicuspidata outbreaks. In support of this, in an analysis of dynamics of naturally occurring outbreaks in two lakes where these pathogens co-occur, we found a time lag in occurrence between O. pajunii and M. bicuspidata, with M. bicuspidata epidemics only occurring after the collapse of O. pajunii epidemics. Thus, these results suggest that the interaction between co-occurring symbionts, and the net impact of a symbiont on a host, might be qualitatively different at different scales.IMPORTANCEUnderstanding the factors that modify infection probability and virulence is crucial for identifying the drivers of infection outbreaks and modeling disease epidemic progression, and increases our ability to control diseases and reduce the harm they cause. One factor that can strongly influence infection probability and virulence is the presence of other pathogens. However, while coexposures and coinfections are incredibly common, we still have only a limited understanding of how pathogen interactions alter infection outcomes or whether their impacts are scale dependent. We used a system of one host and two pathogens to show that sequential coinfection can have a tremendous impact on the host and the infecting pathogens and that the outcome of (co-)infection can be negative or positive depending on the focal organization level.

Characterization of the serosal cells surrounding Cotesia kariyai larvae and their role in host immunosuppression

About half of the serosal cells (Scs) of Cotesia kariyai (Ck) eggs are released as teratocytes into the host body cavity after hatching, and another half remain attached to the larval epidermis until the 1st instar larvae of Ck ecdysis to 2nd instars. To investigate the role of the serosal cells surrounding Ck 1st instar larvae (1st Scs) in immune avoidance, Ck 1st instar larvae with and without Scs removed using dispase were transplanted into Mythimna separata larvae (MsLrv), respectively. As a result, Ck 1st instar larvae surrounded by Scs were less susceptible to the MsL encapsulation than Ck 1st instar larvae without the Scs, suggesting that the Scs are involved in suppressing the encapsulation of the MsL. Furthermore, when the granular cells and plasmatocytes of the MsL involved in the encapsulation were incubated in a medium supplemented with proteins extracted from 1st Scs, the plasmatocytes failed to adhere to glass slides, and did not spread their filopodium and lamellipodium. These findings suggest that 1st Scs express proteins that inhibit filopodium and lamellipodium spreading to prevent the MsL plasmatocytes from adhering to Ck larvae.

Dispersal and invasive stages of Urospora eugregarines (Apicomplexa) from brown bodies of a polychaete host

Urosporid eugregarines (Apicomplexa: Urosporidae) are unicellular eukaryotic parasites inhabiting the coelom or the intestine of marine invertebrates such as annelids, molluscs, nemerteans, and echinoderms. Despite the availability of published morphological and phylogenetical analyses of coelomic gregarines, their long-term survival in the host body cavity and dispersal routes into the marine environment remain unclear. Here, we focus on Urospora gametocysts and oocysts with sporozoites, which were found viable inside the so-called brown bodies floating in the body cavity of the polychaete Travisia forbesii. Brown bodies form as a result of host defence where coelomocytes encapsulate dead host cells and foreign objects including potential pathogens. We hypothesise the long-term persistence of Urospora eugregarines in brown bodies through evasion of the host immunity and outline possible pathways for their egress into the marine environment, applicable as dispersal routes for other parasites as well. Unique features revealed by detailed ultrastructural analysis of detected eugregarine stages include asynchronous sporogony, a massive sporozoite secretion apparatus, as well as the presence of free (possibly autoinfective) sporozoites within the gametocyst. The assignment to the genus Urospora and the complete identity with U. ovalis and U. travisiae were confirmed by analysing 18S rDNA sequences obtained from isolated gametocysts. The 18S rDNA phylogeny confirmed the affiliation of Urosporidae to Lecudinoidea and the grouping of all Urospora sequences with Difficilina from nemerteans and environmental sequences from the Artic region. We also enriched the Apicomplexa set by partial 28S rDNA sequences of two Urospora species enabling more complex phylogenetic analyses prospectively.

The proof is in the poo: Non-invasive method to detect endoparasitic infection.

Almost every animal trait is strongly associated with parasitic infection or the potential exposure to parasites. Despite this importance, one of the greatest challenges that researchers still face is to accurately determine the status and severity of the endoparasitic infection without killing and dissecting the host. Thus, the precise detection of infection with minimal handling of the individual will improve experimental designs in live animal research. Here, we quantified extracellular DNA from two species of endoparasitic worm that grow within the host body cavity, hairworms (phylum Nematomorpha) and mermithids (phylum Nematoda), from the frass of their insect host, a cave wētā (Orthoptera: Rhaphidophoridae) and an earwig (Dermaptera: Forficulidae), respectively. Frass collection was done at two successive time periods, to test if parasitic growth correlated with relative DNA quantity in the frass. We developed and optimized two highly specific TaqMan assays, one for each parasite-specific DNA amplification. We were able to detect infection prevalence with 100% accuracy in individuals identified as infected through post-study dissections. An additional infection in earwigs was detected with the TaqMan assay alone, probably because some worms were either too small or degraded to observe during dissection. No difference in DNA quantity was detected between sampling periods, although future protocols could be refined to support such a trend. This study demonstrates that a noninvasive and minimally stressful method can be used to detect endoparasitic infection with greater accuracy than dissection alone, helping improve protocols for live animal studies.

Paraphyly of Marimermithida refines primary routes of transition to parasitism in roundworms

AbstractParasitic life-strategies in the phylum Nematoda (roundworms) are remarkably diverse and intricate in terms of evolution and taxonomy. By analysing novel rDNA data obtained on rare host-associated groups with unusual biology, we reveal paraphyly of the last major taxon with uncertain higher-rank classification that united solely parasitic nematodes (Marimermithida) to show that primarily marine parasitism only emerged independently and repeatedly in a few free-living lineages. We report secondary seaward ingression of land-based parasites (Mermithida) via invading hosts in the subtidal zone to illustrate the host-borne scenario of oceanic fish and mammal colonization by primarily terrestrial parasites (Spiruria). We also present the first molecular data on marine nematodes from unicellular hosts (foraminiferan protozoans) to demonstrate the independent origins of exploitative nematode associations at a microscopic scale. We argue that, in contrast with primarily intestinal associations arising from saprotrophy and commensalism, non-intestinal host capture (colonization of host body cavity or internal organs) is likely to be a primary route of transition to truly exploitative parasitism in roundworms. Predispositions to host capture in nematode morphology, ecology and life cycles imply its evolution as part of innate pre-adaptations to crossing environmental boundaries to enable multiple successful transitions to parasitism in the phylum history.

Dive into the sea: first molecular phylogenetic evidence of host expansion from terrestrial/freshwater to marine organisms in Mermithidae (Nematoda: Mermithida).

We report the first mermithid nematode found to be parasitic in a marine tanaidacean crustacean. Ten host tanaidaceans were collected from a depth of 52 m in Otsuchi Bay, Iwate, Japan, north-western Pacific, and identified as a species in the tanaidid genus Zeuxo Templeton, 1840. Nematodes occurred in the host's body cavity; in one case, at least two individuals inhabited a single host. We provide a brief description and illustrations of the morphology of the nematode. In a phylogenetic reconstruction based on the 18S ribosomal RNA gene, the nematode nested in a clade otherwise containing mermithids from terrestrial or freshwater hosts, showing an expansion in host utilization in Mermithidae Braun, 1883 from terrestrial/freshwater hosts to a marine organism.

Host age alters disease life history. A case study in zooplankton and a castrating pathogen

Host age alters disease life history. A case study in zooplankton and a castrating pathogen

DYNAMICS OF SECRETION OF PROSTAGLANDINS E2 AND D2 WITH DIBOTHRIOCHEPHALLUS DENDRITICUS (CESTODA) PLEROCERCOIDS IN RESPONSE TO EXPOSURE OF BLOOD SERUM OF BAIKAL CISCO, THE HOST

Parasites regulate host immune response via secretion of soluble mediators which interact in a certain way with cells and molecules of the immune system. The aim of the study was to determine changes of prostaglandins E2 и D2 content in Dibothriochephallus dendriticus plerocercoids and also in the incubation media during incubation of tapeworms with addition of blood serum from the intermediate host – Baikal cisco. D. dendriticus plerocercoids were retrieved from the host body cavity, ashed in the physiological solution and placed in incubation media. Microcolumn high-performance liquid chromatography was used to detect prostaglandins. Concentration of prostaglandins in the plerocercoid organism increased insignificantly after incubation in the Hanks’ solution with addition of blood serum, when compared with incubation in the Hanks’ solution only. Concentration of prostaglandin E2 increased significantly in the incubation media after incubation of plerocercoids in the Hanks’ solution with addition of blood serum. Prostaglandin D2 was also identified in high concentrations after 12 h and 24 h of incubation, whereas prostaglandin D2 was not quite detected during incubation in Hanks’ solution only.

Understanding trophic interactions in host-parasite associations using stable isotopes of carbon and nitrogen

BackgroundStable isotope analysis of carbon and nitrogen can deliver insights into trophic interactions between organisms. While many studies on free-living organisms are available, the number of those focusing on trophic interactions between hosts and their associated parasites still remains scarce. In some cases information about taxa (e.g. acanthocephalans) is completely missing. Additionally, available data revealed different and occasionally contrasting patterns, depending on the parasite’s taxonomic position and its degree of development, which is most probably determined by its feeding strategy (absorption of nutrients through the tegument versus active feeding) and its localization in the host.MethodsUsing stable isotope analysis of carbon and nitrogen we provided first data on the trophic position of an acanthocephalan species with respect to its fish host. Barbels (Barbus barbus) infected only with adult acanthocephalans Pomphorhynchus laevis as well as fish co-infected with the larval (L4) nematodes Eustrongylides sp. from host body cavity were investigated in order to determine the factors shaping host-parasite trophic interactions. Fish were collected in different seasons, to study also potential isotopic shifts over time, whereas barbels with single infection were obtained in summer and co-infected ones in autumn.ResultsAcanthocephalans as absorptive feeders showed lower isotope discrimination values of δ15N than the fish host. Results obtained for the acanthocephalans were in line with other parasitic taxa (e.g. cestodes), which exhibit a similar feeding strategy. We assumed that they feed mainly on metabolites, which were reprocessed by the host and are therefore isotopically lighter. In contrast, the nematodes were enriched in the heavier isotope δ15N with respect to their host and the acanthocephalans, respectively. As active feeders they feed on tissues and blood in the body cavity of the host and thus showed isotope discrimination patterns resembling those of predators. We also observed seasonal differences in the isotope signatures of fish tissues and acanthocephalans, which were attributed to changes in food composition of the host and to seasonality in the transmission and development of acanthocephalans.ConclusionsThis study provided first data on trophic interaction between an acanthocephalan species and its associated host, which support the tendency already described for other taxa with similar nutrition strategy (e.g. cestodes). Actively feeding taxa such as larval Eustrongylides sp., appear to act like predators as it can be seen from their isotope discrimination values. However, future research on additional host-parasite systems and especially on acanthocephalans is needed in order to corroborate these conclusions.

Glugea jazanensis sp. nov. infecting Lutjanus bohar in the Red Sea: ultrastructure and phylogeny.

During a survey of the microsporean fauna of the two-spot red snapper Lutjanus bohar Forsskål, 1775, from the Red Sea off Jizan (Saudi Arabia), a species of Glugea Thélohan, 1891 was found that did not conform to any known species. The species is characterized by the presence of spherical xenomas (ca. 2-5 mm in diameter) in the host body cavity. Examination of the lifecycle stages and mature spores using light and transmission electron microscopy also revealed morphological characteristics typical of species of the genus Glugea. Spores were elongated-ovoid with a posterior vacuole surrounded by the polar filament coils. Mature spores were 4.5 (4.0-4.8) µm long and 2.5 (2.0-2.5) µm wide. The polar filament was isofilar with 28 to 30 coils, although in most cases 29 coils, organized in 3 rows. Phylogenetic study based on the partial sequence of the small subunit (SSU) rRNA gene clustered the new microsporidia within the clade grouping species of the genus Glugea. The comprehensive analysis of the parasite's ultrastructural characteristics, together with molecular data for the SSU rDNA gene, suggests that this parasite is a new species of the genus Glugea, for which the name Glugea jazanensis sp. nov. is proposed.

Microbiomes, plausible players or not in alteration of host behavior.

Many parasites can affect the physiology and behavior of their hosts in ways that seem to improve the parasites' chances of completing their life cycle (Biron and Loxdale, 2013; Lafferty and Shaw, 2013; Webster et al., 2013). These parasite species are so-called “manipulative parasites.” Common habitats of manipulative parasites are the host's body cavity, muscles and brain (Lafferty and Shaw, 2013). Typically the host's neural, endocrine, neuromodulatory, and immunomodulatory systems are targeted (Adamo, 2013; Lafferty and Shaw, 2013). In evolutionary biology, manipulation of host behavior by parasites is considered to be an example of the “extended phenotype” concept (Dawkins, 1982; Libersat et al., 2009). There are numerous fascinating cases of alteration of host behavior induced by a parasite; for instance, the suicidal behavior of crickets induced by hairworms (Thomas et al., 2002; Biron and Loxdale, 2013). Many studies on strategies used by manipulative parasites assume that only two organisms are involved in crosstalk based on Dawkins' assumption: the host and a manipulative parasite. However, hosts are frequently invaded by more than one species of parasite (Ferrari and Vavre, 2011; Cezilly et al., 2014). The interests of different parasitic species may conflict; for example, two parasites may share an intermediate host but require a different definitive host. Parasite-parasite interactions in the intermediate host can result in perturbation of the parasite infection process for each parasite species (Lafferty and Shaw, 2013; Cezilly et al., 2014). As far as we know, microbiomes are not considered to be taking part in crosstalk between an aquatic host and a manipulative parasite. Therefore, we first briefly present the background for microbiomes as plausible and underestimated players in the crosstalk in host-manipulative parasite associations in aquatic ecosystems, and secondly we discuss concepts and -omics methods to determine whether or not host microbiomes can influence host behavior in aquatic models. Finally, we discuss the importance of considering context-dependent changes in the analysis of -omics data to decode and understand the role of a host microbiome in the alteration of host behavior in aquatic ecosystems.

New Features ofNeoechinorhynchus(Neoechinorhynchus)dimorphospinus(Acanthocephala: Neoechinorhynchidae) from Recent Collections in the Arabian Gulf Using SEM, with Notes on Histopathology

Neoechinorhynchus dimorphospinus Amin and Sey, 1996, was described from 4 species of marine fishes in the Arabian Gulf off Kuwait. Specimens of N. dimorphospinus have been reported only twice since then from marine and freshwater fishes also from the Arabian Gulf and brackish waters associated with it. The 2 latter reports offered no new descriptive accounts. SEM studies based on recent collections of N. dimorphospinus from Klunzinger's mullets, Liza klunzingeri (Day, 1888) (Mugiliformes) (new host record), revealed many new features that were not possible to include in the original description using optical microscopy. These new features include an apical organ in the proboscis, a broad prominent collar at the anterior end of the trunk, prominent longitudinal grooves on proboscis hooks, a pair of sensory structures in the neck, the subterminal position of the female gonopore with a minute lipless vulva, micropores on the trunk not showing differentiation in various trunk regions, and eggs in different stages of development. There is extensive damage to the host intestine due to invading specimens of N. dimorphospinus. Worms destroy the epithelial lining of L. klunzingeri and migrate through the thin smooth muscle wall of the intestine into the host body cavity. Extensive host hemorrhaging, tissue necrosis, villi compression, and loss of host epithelial cells appears to be the typical pathology in intestinal sites occupied by this worm.

Differential responses of the whitefly Bemisia tabaci symbionts to unfavorable low and high temperatures.

The whitefly Bemisia tabaci complex contains many cryptic species, of which the Middle East-Asia Minor 1 (MEAM1) and Mediterranean (MED) are notorious invasive pests. In our field-collected whitefly samples, MEAM1 harbors an obligate primary symbiont "Candidatus Portiera aleyrodidarum" and two secondary symbionts, "Candidatus Hamiltonella defensa" and Rickettsia sp., whereas MED has only "Ca. Portiera aleyrodidarum" and "Ca. Hamiltonella defensa." Both "Ca. Portiera aleyrodidarum" and "Ca. Hamiltonella defensa" are intracellular endosymbionts residing in the bacteriomes, whereas Rickettsia sp. has a scattered distribution throughout the host body cavity. We examined responses of these symbionts to adverse temperatures as well as survival of the host insects. After cold treatment at 5 or 10 °C or heat treatment at 35 or 40 °C for 24 h, respectively, the infection rates of all symbionts were not significantly decreased based on diagnosis PCR. However, quantitative PCR assays indicated significant reduction of "Ca. Hamiltonella defensa" at 40 °C, and the reduction became greater as the duration increased. Compared with "Ca. Hamiltonella defensa," "Ca. Portiera aleyrodidarum" was initially less affected in the first day but then showed more rapid reduction at days 3-5. The density of Rickettsia sp. fluctuated but was not reduced significantly at 40 °C. Meanwhile, the mortality rates of the host whiteflies elevated rapidly as the duration of exposure to heat treatment increased. The differential responses of various symbionts to adverse temperatures imply complex interactions among the symbionts inside the same host insect and highlight the importance of taking the whole bacterial community into account in studies of symbioses.

A new oomycete species parasitic in nematodes, Chlamydomyzium dictyuchoides sp. nov.: Developmental biology and phylogenetic studies

The genus Chlamydomyzium is a little studied holocarpic oomycete parasite of nematodes of uncertain phylogenetic and taxonomic position. A new holocarpic species, Chlamydomyzium dictyuchoides, is described which has usually refractile cytoplasm and a dictyuchoid pattern of spore release. This new species infects bacteriotrophic rhabditid nematodes and was isolated from diverse geographical locations. Infection was initiated by zoospore encystment on the host surface and direct penetration of the cuticle. A sparsely branched, constricted, refractile thallus was formed which eventually occupied almost the entire host body cavity, often accompanied by complete dissolution of the host cuticle. Walled primary cysts formed throughout the thallus and each cyst released a single zoospore via an individual exit papillum, leaving a characteristic dictyuchoid wall net behind. At later stages of infection some thalli formed thick-walled stellate resting spores in uniseriate rows. Resting spore formation appeared to be parthenogenetic and was not accompanied by the formation of antheridial compartments. These spores had ooplast-like vacuoles and thick multi-layered walls, both of which suggest they were oospores. The maximum likelihood tree of sequences of the small ribosomal subunit (SSU) gene placed this new isolate in a clade before the main saprolegnialean and peronosporalean lines diverge. A second undescribed Chlamydomyzium sp., which has direct spore release forms a paraphyletic clade, close to C. dictyuchoides and Sapromyces. The fine structure of other documented Chlamydomyzium species was compared, including an undescribed (but sequenced) isolate, SL02, from Japan, Chlamydomyzium anomalum and Chlamydomyzium oviparasiticum. Chlamydomyzium as currently constituted is a paraphyletic genus that is part of a group of phylogenetically problematic early diverging clades that lie close to both the Leptomitales and Rhipidiales.

Parasitism and phenotypic change in colonial hosts

Changes in host phenotype are often attributed to manipulation that enables parasites to complete trophic transmission cycles. We characterized changes in host phenotype in a colonial host–endoparasite system that lacks trophic transmission (the freshwater bryozoan Fredericella sultana and myxozoan parasite Tetracapsuloides bryosalmonae). We show that parasitism exerts opposing phenotypic effects at the colony and module levels. Thus, overt infection (the development of infectious spores in the host body cavity) was linked to a reduction in colony size and growth rate, while colony modules exhibited a form of gigantism. Larger modules may support larger parasite sacs and increase metabolite availability to the parasite. Host metabolic rates were lower in overtly infected relative to uninfected hosts that were not investing in propagule production. This suggests a role for direct resource competition and active parasite manipulation (castration) in driving the expression of the infected phenotype. The malformed offspring (statoblasts) of infected colonies had greatly reduced hatching success. Coupled with the severe reduction in statoblast production this suggests that vertical transmission is rare in overtly infected modules. We show that although the parasite can occasionally infect statoblasts during overt infections, no infections were detected in the surviving mature offspring, suggesting that during overt infections, horizontal transmission incurs a trade-off with vertical transmission.

Morphology and Development of a Termite Endoparasitoid Misotermes mindeni (Diptera: Phoridae)

Abstract The morphology and developmental stages of Misotermes mindeni Disney & Neoh (Diptera: Phoridae), a newly described endoparasitoid of the fungus-growing termite Macrotermes gilvus (Hagen) (Termitidae: Macrotermitinae) were studied, and biometric descriptors of eggs, larvae, and pupae were recorded. The larvae of M. mindeni exhibit three larval stages. Larvae complete their first instar development in fourth larval instars and major presoldiers, whereas the second and third instars develop entirely in major soldiers' head capsule and abdomen, respectively. The second instar can be readily differentiated from the first by the presence of a posterior spiracular base and more defined body segments, and the third instar can be discriminated from the second by the presence of respiratory horns and a well-developed posterior spiracular base. Differentiation of the larval instars is further supported by morphometric measurements. The first instar moves freely within the host's body cavity and head capsule, whereas the last two instars remain in the host's head capsule and abdomen, respectively. Termite developmental stages were used as a model to determine the developmental time of M. mindeni larvae. Duration between the first and second instars was 19.00 ± 2.28 d and between second and third instars was 36.88 ± 5.17 d. It took the third instar, 0.53 ± 0.08 d to reach pupation. The pupal stage lasted for an average of 13.51 ± 0.74 d. Mean adult longevity was 1.47 ± 0.57 d and 3.00 ± 0.98 d for females and males, respectively. Longevity of males was significantly longer than that of females.

An ultrastructural study of polyembryonic parasitoid embryo and host embryo cell interactions

The morula-stage embryo of the polyembryonic egg-larval parasitoid Copidosoma floridanum forms outside the host embryo and secondarily invades the host body. Electron microscopic analyses of cellular interactions between the extraembryonic syncytium of the parasitic morula and the host embryonic epithelial cells showed that morula penetration into the host embryo did not cause obvious damage to the host cells, except for the abrasion of the embryonic cuticle. Epithelial cells of the host embryo extended microvilli toward the invading C. floridanum morula and also adjacent host cells in the same way. Shortly after settlement of the morula within the host body cavity, gap junctions and adherens junctions with host cells were formed. The morula was then surrounded by a cyst comprised of host cells into which host tracheoles were invaginated.

Parasite-Induced Changes in Nitric Oxide Levels in Drosophila paramelanica

In larvae of Drosophila paramelanica, eggs and larvae of the endoparasitic wasp Leptopilina heterotoma succumb to an effective host reaction that does not involve blood cell-mediated melanotic encapsulation, a response that characterizes cellular immunity in various species of Drosophila and in many insects and other arthropods. A significant increase occurs, however, in the number of lamellocytes, a type of blood cell that functions in encapsulation reactions. The appearance of activated lamellocytes in D. paramelanica is viewed as an early response to infection, one most likely initiated by non-self-recognition processes that similarly function in other wasp-infected Drosophila. However, ensuing cytotoxic responses, about which little is presently known, are not accompanied by melanotic encapsulation in D. paramelanica. Concurrent analyses of the cell-signaling molecule nitric oxide (*NO) revealed significant alterations in the levels of this free radical during the early stages of infection, most notably a dramatic increase immediately upon infection, and precipitous decreases occurring at times when parasites were killed. Injections of a specific inhibitor of nitric oxide synthase (NOS) into the host's body cavity prior to infection significantly increased parasite survival. These observations suggest some involvement of *NO in the host immune response, either in recruiting hemocytes to sites of infection or as a component of the insect's cytotoxic arsenal, given the capacity of the radical to generate toxic molecules through interactions with various intermediates of oxygen and nitrogen.

The parasitic polychaete known as Asetocalamyzas laonicola (Calamyzidae) is in fact the dwarf male of the spionid Scolelepis laonicola (comb. nov.)

Abstract. The morphology of the obligately ectoparasitic polychaete Asetocalamyzas laonicola was studied by light and electron microscopy, and its taxonomic position was determined using molecular methods. The parasite has an extensive coelomic cavity, complete septae, and well‐developed segmental nephridia, circulatory, and digestive systems. The nervous system is rudimentary and without ganglia. The parasite's anterior region penetrates the tissues of the host, and opens into the host's body cavity. The epidermal tissues of the parasite and the host are highly integrated in the area of contact, and the parasite's cuticle is continuous with that of the host. Blood vessels of the parasite and the host may interlace in the fusion zone. The dorsal side of the parasite faces the dorsal side of the host. All parasites were males, but all hosts were females. In order to elucidate the uncertain systematic position of the parasite, molecular systematic studies were conducted. Parasite and host 18S rDNA sequences were virtually identical and revealed that both belong to the spionid cluster. These sequences differed from those of Scolelepis squamata and Scolelepis bonnieri by 2.7% and 0.9%, respectively. In addition, of seven partial sequences of the mitochondrial COI gene obtained from three parasites and four hosts, six were identical, and in one host–parasite pair, COI sequences differed by one substitution. Partial ITS2 sequences from one host–parasite pair were analyzed and also found to be similar but not identical, with two indels in a 645‐bp alignment. We conclude that the parasite is in fact a dwarf male of its conspecific spionid female host. Consequently, A. laonicola is transferred to Scolelepis (Spionidae), forming the new combination Scolelepis laonicola.

Cotesia kariyai larvae need an anchor to emerge from the host Pseudaletia separata

Mature larvae of the gregarious endoparasitoid Cotesia kariyai construct cocoons for pupation approximately 10 days after parasitization and emerge from their host Pseudaletia separata under a long day photo-regime (16L8D) at 25 +/- 1 degrees C. The parasitoid larvae make capsules in the host hemocoel just prior to their emergence. These capsules function as "anchors," which enable them to press against the host integument from inside the host. It was predicted that this anchor might be composed of silk proteins secreted from the parasitoid larvae, because a previous study showed that the anchor was made up of a glycoprotein and that the silk gland of parasitoid larvae developed from 2nd larval stage. Fibroin-like proteins in C. kariyai larva mainly consist of two proteins with molecular masses of the 300.6 and 46.7 kDa estimated by SDS-PAGE. The fibroin-like proteins with the same molecular mass were detected from the anchor proteins just prior to parasitoid emergence. These results indicate that the anchor was assembled with fibroin-like proteins and was formed just before parasitoid emergence while in the host body cavity. Injection of bovine pancreatic trypsin inhibited the emergence of parasitoid larvae from the host because the anchor was decomposed by trypsin. Trypsin activity in the parasitized host hemolymph increased only after parasitoid emergence.