A NEW SPECIES OF ALLINTOSHIUS (NEMATODA: HELIGMOSOMOIDEA) FROM TWO SPECIES OF BATS IN BRAZIL.

Allintoshius Chitwood, 1937 is the only genus of the family Ornithostrongylidae (Travassos, 1937) Durette-Desset and Chabaud, 1981 that parasitizes bats. Currently, there are 10 valid species in the genus, of which 3 were described from Brazil. This study describes a new species of Allintoshius and records the first occurrence of a nematode of this genus parasitizing Artibeus lituratus (Olfers). Allintoshius gomesae n. sp. is characterized by having anterior region coiled, cephalic vesicle with cuticular dilation striated transversely, and claviform esophagus. Synlophe in females consists of 16 cuticular ridges at the mid-body. Males have large caudal bursa, and conic and small spicules, and the gubernaculum is absent. Females have uterus didelphic, amphidelphic, tail tip tapered, and ovijector divided into 2 divergent branches, subequal in length. The new species differs from its congeners especially by the shape of the tail tip, vulvar opening, and size of spicules. Allintoshius gomesae is the fourth species of Allintoshius from Brazil and the first report in Ar. lituratus, increasing the number of species recognized of the genus.

Contrasting patterns of structural host specificity of two species of Heligmosomoides nematodes in sympatric rodents.

Host specificity is a fundamental property of parasites. Whereas most studies focus on measures of specificity on host range, only few studies have considered quantitative aspects such as infection intensity or prevalence. The relative importance of these quantitative aspects is still unclear, mainly because of methodological constraints, yet central to a precise assessment of host specificity. Here, we assessed simultaneously two quantitative measures of host specificity of Heligmosomoides glareoli and Heligmosomoides polygyrus polygyrus infections in sympatric rodent hosts. We used standard morphological techniques as well as real-time quantitative PCR and sequencing of the rDNA ITS2 fragment to analyse parasite infection via faecal sample remains. Although both parasite species are thought to be strictly species-specific, we found morphologically and molecularly validated co- and cross-infections. We also detected contrasting patterns within and between host species with regard to specificity for prevalence and intensity of infection. H. glareoli intensities were twofold higher in bank voles than in yellow-necked mice, but prevalence did not differ significantly between species (33 vs. 18%). We found the opposite pattern in H. polygyrus infections with similar intensity levels between host species but significantly higher prevalence in mouse hosts (56 vs. 10%). Detection rates were higher with molecular tools than morphological methods. Our results emphasize the necessity to consider quantitative aspects of specificity for a full view of a parasites' capacity to replicate and transmit in hosts and present a worked example of how modern molecular tools help to advance our understanding of selective forces in host-parasite ecology and evolution.

Maternal protein deficiency during a gastrointestinal nematode infection alters developmental profile of lymphocyte populations and selected cytokines in neonatal mice.

Neonatal immune development begins in pregnancy and continues into lactation and may be affected by maternal diet. We investigated the possibility that maternal protein deficiency (PD) during a chronic gastrointestinal (GI) nematode infection could impair neonatal immune development. Beginning on d 14 of pregnancy, mice were fed protein-sufficient (PS; 24%) or protein-deficient (PD; 6%) isoenergetic diets and were infected weekly with either 0 (sham) or 100 Heligmosomoides bakeri larvae. Pups were killed on d 2, 7, 14, and d 21 and dams on d 20 of lactation. Lymphoid organs were weighed. Cytokine concentration in maternal and pup serum and in milk from pup stomachs and lymphoid cell populations in pup spleen and thymus were determined using luminex and flow cytometry, respectively. GI nematode infection increased Th2 cytokines (IL-4, IL-5, IL-13), IL-2, IL-10, and eotaxin in serum of dams whereas PD reduced IL-4 and IL-13. The lower IL-13 in PD dams was associated with increased fecal egg output and worm burdens. Maternal PD increased vascular endothelial growth factor in pup milk and eotaxin in pup serum. Maternal infection increased eotaxin in pup serum. Evidence of impaired neonatal immune development included reduced lymphoid organ mass in pups associated with both maternal infection and PD and increased percentage of T cells and T:B cell ratio in the spleen associated with maternal PD. Findings suggest that increases in specific proinflammatory cytokines as a result of the combination of infection and dietary PD in dams can impair splenic immune development in offspring.

Description of two new species of Nippostrongylinae (Nematoda: Heligmonellidae) coparasites in three sympatric species of Mastomys spp. (Rodentia: Muridae) from Senegal.

Two new species of heligmosomoid Trichostrongylina nematodes belonging to the genera Neoheligmonella Durette-Desset, 1970 and Heligmonina Baylis, 1928 are described. They are parasitic in the small intestine of three species of Mastomys from Senegal living in sympatry: M. natalensis (Smith, 1834), M. erythroleucus (Temminck, 1853) and M. huberti (Wroughton, 1909). Neoheligmonella granjoni n. sp. is closely related to three species from Senegal. They concern: N. bai Diouf & Durette-Desset, 2002 and N. dielmensis Diouf, Bâ & Durette-Desset, 1998, both parasitic in Arvicanthis niloticus Geoffroy, 1903 and N. mastomysi Diouf et al., 1998, a parasite of M. erythroleucus. N. granjoni n. sp. differs from these species by having 15 cuticular ridges at mid-body versus 13, a large carene and spicules taking up 10-15% of body length versus 5.3-7.1%. Heligmonina kanei n. sp. differs from the most related species H. kotoensis Diouf, Daouda & Durette-Desset 2005, a parasite of M. natalensis from Benin in the following features: spicules taking up 11.6% of body length on average versus 16.8%; a female tail three times longer than the distance anus-vulva versus a tail of equivalent size to this distance. In N. granjoni n. sp., where the material is abundant in all three hosts, the infra-specific variations observed (morphological or morphometrical) were not related to the host species. This is the first report of the genera Neoheligmonella and Heligmonina in M. huberti. The relevance of the phenomenon of host capture concerning the evolution of these two genera is confirmed.

New Pudicinae (Trichostrongylina, Heligmosomoidea), Pudica ctenomydis n. sp. parasite of Ctenomys talarum (Rodentia: Octodontidae) from Argentina.

A total of 138 nematodes were found in the small intestine of Ctenomys talarum (Octodontidae) from Mar de Cobo, Argentina. A new nematode species, Pudica ctenomydis n. sp., is described. The new species more closely resembles P. pujoli Durette-Desset, 1990, parasite of Microcavia niata Thomas, from Bolivia. It can be distinguished from P. pujoli by the number of ridges and characteristics of the synlophe, the spicular morphology, differences in length between rays 9 and 10, and by the presence of a symmetrical caudal bursa and a cuticular expansion surrounding the body between vulva and anus in females.

Description of two new species of Nippostrongylinae (Nematoda, Trichostrongyuna, Heligmosomoidea) coparasites in Arvicanthis ansorgei (Muridae) from Cameroon.

In the small intestine of a single Arvicanthis ansorgei from Cameroon, two new species of Nippostrongylinae were found: Neoheligmonella zero n. sp. and Heligmonina comerounensis n. sp. N. zero belongs to the Neoheligmonella species in which the right dorsal ridge is poorly developed. Among these species, N. bainae (Durette-Desset, 1970), a parasite of Steatomys opinus from Burkina Fasso, is a closely related species. It is differentiated by the presence of vulvar alae, the ratio uterus length/body length and the separation of rays 2 and 3 at two thirds of their length. N. zero is also closely related to N. kenyae (Yeh, 1958) a parasite of Rattus rattus kijabius from Kenya by the pattern of the caudal bursa and the ratio spicules length/body length. The synlophe of N. kenyae was not described in detail but it is differentiated from N. zero by the position of the excretory pore, situated just posteriorly to the nerve ring and in the female by the ratio ovejector length/body length which is smaller. H. camerounensis n. sp. is characterised by the ratio dorsal ridges/ventral ridges which is 4/7. It is differentiated from the species of which the synlophe has not been described by the pattern of the caudal bursa (type 1-4 with tendancy 1-3-1). It is the first report of Nippostrongylinae species in Cameroon and the first record of a species of the genus Heligmonina in an Arvicanthis.

Two new species of Nippostrongylinae (Nematoda, Trichostrongylina) parasites of Cricetomys gambianus and Arvicanthis niloticus (Muridae) from Senegal.

Two new Nippostrongylinae (Heligmosomoidea, Heligmonellidae) originating from Senegal are described. Heligmonina bioccai n. sp., a parasite of Cricetomys gambianus (Cricetomyinae) found in the surroundings of Dakar and Neoheligmonella bai n. sp., a parasite of Arvicanthis niloticus (Murinae) from the Province of Richard Toll. H. bioccai n. sp. is related to H. hybomysi (Durette-Desset, 1966) a parasite of Hybomys univittatus from the Central African Republic by some characteristics of the caudal bursa and of the synlophe. They are the only two species with the same pattern of caudal bursa: type 1-3-1 for the right lobe, 2-3 for the left lobe, and with the same number and disposition of the cuticular ridges at mid-body in the female. The two species are differentiated by the size (three times smaller in H. hybomysi), the ratio of spicule length on body length (7.6% versus 17% in H. hybomysi) and by a different synlophe in male and posterior part of female. N. bai n. sp. is differentiated from the closely related species N. dielmensis Diouf, Bâ and Durette-Desset, 1997, also a parasite of Arvicanthis niloticus from Senegal by rays 8 arising asymmetrically on the dorsal ray and by the deirids situated at the same level as the excretory pore.

The life cycle of Ohbayashinema erbaevae (Nematoda, Heligmosomoidea, Heligmosomidae) in Ochotona rufescens rufescens (Ochotonidae).

The morphogenesis and the chronology of the life cycle of Ohbayashinema erbaevoe Durette-Desset et al, 2000, a parasite of Ochotona daurica from Buriatia were studied in detail in an experimental host, Ochotona rufescens rufescens. Worm-free pikas were each infected per os with O. erbaevae larvae and were killed at one day post infection (DPI 1) and every 12 hours from 1.5 to 8 days post infection. By DPI 1, all the larvae were exsheathed and in the small intestine. The third moult occurred in 2.5-3.0 days. The last moult occurred in 4.0-4.5 days. The prepatent period was eight days and the patent period lasted between two and 12 weeks. The distribution of O. erbaevae along the small intestine of the pikas was assessed. For each experiment, a morphological description of the different stages of the life cycle was provided. The morphogenesis and the chronology of the life cycle of O. erbaevae appear to be identical with those of two other genera of the family of the Heligmosomidae, Heligmosomum Railliet & Henry, 1909 and Heligmosomoides Hall, 1916. They confirm that the three genera belong to the same family. The presence of an abortive posterior genital branch in the female of O. erbaevae, which represents the posterior part of the genital primordium of the didelphic females, supports the systematic position of the genus Ohbayashinema between the didelphic genus Citellinema Hall, 1916 and the monodelphic genera Heligmosomum and Heligmosomoides.

Detection of gastrointestinal nematodes by a coproantigen capture ELISA.

An assay is described for the quantitative detection of excretory/secretory antigens liberated by the intestinal nematode Heligmosomoides polygyrus and voided in the host's faeces. A rabbit polyclonal antiserum to the antigens detected them in a dose-dependent manner and was sufficiently sensitive to recognise infection in mice carrying a mean worm burden of nine worms. The assay was specific, giving higher optical density readings with the faeces of mice infected with H polygyrus than with faeces from mice carrying patent infections with Trichuris muris, Hymenolepsis microstoma or the intestinal phase of Trichinella spiralis, or with faeces from rats carrying Hymenolepis diminuta or hamsters carrying Necator americanus or Ancylostoma ceylanicum. It detected the parasite antigens in faeces stored for eight weeks at -20, 4 or 20 degrees C and could detect prepatent infections. The assay has potential for the development of infection intensity-sensitive assays for gastrointestinal nematodes and for the detection of animals harbouring the arrested larvae of parasites.

The influence of dietary protein on the experimental epidemiology of Heligmosomoides polygyrus (Nematoda) in the laboratory mouse.

The influence of dietary protein on the epidemiology of an intestinal helminth infection was investigated with an experimental system that allowed transmission of the nematode Heligmosomoides polygyrus to occur naturally between laboratory mice. Mortality of mice was greatly increased in infected populations that were fed ad libitum on synthetic diets containing 2% compared with 16% protein. Larger numbers of larval and adult H. polygyrus were found to infect mice in the low-protein cage compared with the high-protein cage. No evidence for density dependence in the fecundity of female worms was detected; on average the daily egg output per female worm was greater for parasites infecting mice in the low-protein cage. The rate at which naïve mice acquired infection was also higher in the low-protein cage. Pinworm (Aspiculuris tetraptera) became established in each cage, and average worm burdens were again greater in the low-protein cage. The acquisition of resistance to reinfection was not found to be an important factor influencing the survival of parasites infecting mice in either cage. The epidemiology of H. polygyrus and A. tetraptera was therefore characterized by low average worm burdens and high host survival in a well-nourished population of mice, and by a high intensity of infection and severe parasite-induced host mortality in a malnourished colony of mice. This reflects differences in the survival and fecundity of adult parasites between mice in the two cages, and suggests that malnourished mice are predisposed to acquire large numbers of several species of intestinal worm.

Immunological relationships during primary infection with Heligmosomoides polygyrus (Nematospiroides dubius): the capacity of adult worms to survive following transplantation to recipient mice.

Chronic primary infections with Heligmosomoides polygyrus (Nematospiroides dubius) are still relatively poorly documented, particularly in relation to the role of host resistance in limiting worm survival. In the present work the duration of infection with H. polygyrus was studied in CFLP mice given doses of infective larvae ranging from 50 to 500 L3. The least heavily infected (50 L3) group ceased egg production earliest (week 36) whereas eggs were still detected in the faeces of mice given 500 larvae in week 42. At autopsy (week 42) mice given 50 larvae had virtually lost their entire worm burden with 5 out of 11 mice still harbouring a single worm each. However, all the mice in the group given 500 larvae were still infected, the highest worm burden being 93. The concentration of serum IgG1 and specific antibody was highest in mice given 500 larvae, but sera taken from mice with declining worm burdens 19-38 weeks post-infection did not contain detectable host-protective antibody. During the course of infection in CFLP mice, H. polygyrus sustained irreversible changes in its capacity for subsequent survival. Thus, adult worms transferred to naive mice 2, 7, 14, 30 or 36 weeks post-infection did not live longer than worms of a comparable age in the respective donor group. In contrast, primary infection worms taken from jirds in which expulsion is usually completed by 6 weeks post-infection, re-established in mice and survived considerably longer than in the group of donor jirds. These results were discussed in relation to the possible interactions between parasite senility and immunomodulation, and host resistance in limiting primary infections with H. polygyrus in mice and jirds.