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Biomedical subjects

S Morand

Publications and source records attributed to S Morand.

At least 73 records · Page 4Linked to original sources
PubMed1999

The distribution of Schistosoma bovis Sonsino, 1876 in relation to intermediate host mollusc-parasite relationships.

Schistosoma bovis is a digenean platyhelminth that is responsible for a parasitic disease called schistosomiasis or bilharziasis in bovines. It has a natural wide mollusc intermediate host spectrum and is compatible, experimentally, with a wide range of species. Our working hypothesis is that the Mediterranean Sea and the Sahara were two physical barriers that could have separated the populations of S. bovis in three parts and may have played a role in gene flow. Experimental data were collected from earlier published studies, and the different intermediate host spectra and the mollusc-parasite geographical compatibilities were compared between the North Mediterranean zone, the South Mediterranean zone and the South Saharan zone. From our results, the three major groups of S. bovis populations that could be determined were the Iberian, the Mediterranean and the South Saharan populations. Our tested hypothesis was thus not confirmed concerning the Mediterranean sea barrier but was confirmed with the Saharan one. A paleogeographical scenario of S. bovis is proposed following three major steps from a South Saharan origin to a possible local adaptation of the parasite in the Iberian Peninsula.

Africa↗
PubMed1999

Epidemiology and genetic variability of two species of nematodes (Heligmosomoides polygyrus and Syphacia stroma) of Apodemus spp.

The epidemiology and genetic variability of 2 parasitic nematodes Heligmosomoides polygyrus and Syphacia stroma of Apodemus spp. were investigated. Both are parasites of the same host, exhibit a direct life-cycle and are dioecious. However, H. polygyrus has a diploid and S. stroma a haplodiploid mode of reproduction. Haplodiploidy may lead to a more female biased sex ratio and reduced genetic variability. Levels of genetic diversity were analysed using both isoenzyme electrophoresis and RAPDs (random amplified polymorphic DNA). Both parasites showed a female biased sex ratio with a stronger bias for the haplodiploid parasite. Results showed significantly fewer genetic polymorphisms as measured by RAPDs for the haplodiploid parasite S. stroma in comparison with H. polygyrus. Despite the observed female biased sex ratio this could not be explained by a significant amount of inbreeding. Heterozygote deficiency for individual allozyme loci--which could indicate inbreeding--was not found in either parasite species. Other features of the particular life-history of these species are likely to have an impact on the sex ratio and genetic variability too.

Animals↗
PubMed1999

Influence of the trematode Aphalloïdes caelomicola Dollfus, Chabaud & Golvan, 1957 on the fecundity and survival of Pomatoschistus microps (Krøyer, 1838) (Teleostei: Gobiidae).

Monthly data collected during 1993 in the Vaccarès lagoon (Rhône Delta, France) were used to investigate the influence of the trematode Aphalloïdes coelomicola on the survival of the common goby Pomatoschistus microps, which acts both as second intermediate and definitive host. Prevalence of the parasite did not increase with fish size in either sex. Mean abundance and variance to mean abundance ratio gave evidence that the trematode could have an impact on host mortality. Gonad weight of parasitized females was reduced and the parasite seemed to provoke a gonadal regression above a certain parasitic biomass. Fecundity and egg diameters did not differ between parasitized and unparasitized females, we thus hypothesize that the energy content of eggs (composition in lipids and proteins) was probably modified as an adaptation to energy losses. Prevalence of infection in males compared to females and influence of the parasite on host survival and reproductive effort are discussed.

Analysis of Variance↗
PubMed1999

Geographical distances and the similarity among parasite communities of conspecific host populations.

The geographical distance between conspecific host populations is no doubt a key determinant of the likelihood that exchanges of parasite species occur between these populations. This variable must therefore be taken into account in studies that compare parasite species richness or similarity among host populations. This paper presents a multivariate approach, based on the permutation of matrices, that allows all pairwise geographical distances between host populations to be included as independent variables. The method is illustrated with 3 separate data sets on parasite communities of conspecific fish from different lakes. In 2 of 3 cases, geographical distances among lakes had a significant influence on the similarity of their parasite communities. The effect of geographical distance on species richness of parasite communities also proved important in 2 of the 3 case studies. These examples demonstrate the pervasive influence of distances among host populations on their parasite communities, and the need to properly control for them in statistical analyses.

Animals↗
PubMed1999

A review of performance and pathogenicity of male and female Schistosoma mansoni during the life-cycle.

The sexual life-history traits of Schistosoma mansoni have been reviewed to compare male and female performance and pathogenicity against Biomphalaria glabrata during the life-cycle. A meta-analysis was used on pooled results from different experiments. In most cases, there was no difference between males and females but male cercariae were significantly more infectious than female cercariae. Conversely, cercarial production and cercarial life-span were significantly greater for females than for males; furthermore, females have a tendency to occur in molluscs of larger size. Each difference is discussed and interpreted when possible in terms of male and female differences in transmission strategies. The female strategy may consist of producing many long-living larvae. The male strategy may consist of producing few short-living larvae and would invest in the quality of these larvae instead of their quantity or their life-span.

Animals↗
PubMed1999

Human enterobiasis in evolution: origin, specificity and transmission.

The co-evolutionary pathway seems to be the most plausible hypothesis for the explanation of the origin of human pinworms. Of the two modes of transmission of oxyurids among humans which have been documented, the direct oral/anal route is also observed in other Primates and seems to have been favoured by selection. As indirect air-borne transmission has also been shown for human enterobiasis, the question of "How this alternative to the standard transmission method could have arisen" is examined. The results of comparative studies of prevalence of Enterobius in human coprolites, in villages of Neolithic age of the arid west of North America, show that a higher prevalence of pinworms is correlated with the lower total amount of air-exchange in caves relative to other structures. The air-borne route of transmission of pinworms among humans is interpreted as an innovation in the human/Enterobius pair. This mode of transfer could have been favoured during the time when humans changed their behaviour from a hunting-gathering to a more sedentary existence, initially associated with cave habitats.

Biological Evolution↗
PubMed1999

Do parasites live in extreme environments? Constructing hostile niches and living in them.

We develop the hypothesis that parasites do not invade extreme environments, i.e. hostile hosts, but rather 'create' them. We argue that parasites may have driven the evolution of the constitutive and adaptive immune system. This leads to several implications. First, parasites respond to 'genes to kill' by 'genes to survive' and this triggers an indefinite selection of measures and counter-measures. Second, these coevolutionary arms races may lead to local adaptation, in which parasite populations perform better on local hosts. Third, the evolution of the immune system, whose responses are predictable, may allow parasites to specialize, to evade and even to manipulate. Finally we show that the correlations between the increase in the antibody repertoire, the expansion of MHC loci and parasite pressures support our hypothesis that both host complexity and parasite pressures can be invoked to explain the diversity of antibodies, T-receptors and MHC molecules.

Adaptation, Physiological↗
PubMed1998

Comparative analysis: a tool for studying monogenean ecology and evolution.

The comparative approach has been used widely in evolutionary ecology during the last 10 years. In the first part of this study, taking monogeneans of Mediterranean marine fishes as an example, we highlight the pitfalls that may arise in interspecific studies. In the second part, the independent contrast method is used to control for phylogenetic effects in order to evaluate the determinants of monogenean species richness and their specificity. Our results show the importance of controlling data for both host sample size and phylogeny to avoid confounding effects. Thereafter, taking into account both sampling effort and phylogenetic effects, our results show that host size is the main factor affecting monogenean species richness and specificity.

Animals↗
PubMed1998

Parasite diversity/host age and size relationship in three coral-reef fishes from French Polynesia.

The parasite communities of three coral-reef fish species (Stegastes nigricans, Dascyllus aruanus and Cephalopholis argus) were on Tiahura reef, French Polynesia. The age and growth of each fish was analysed by otolith increment counts and a significant correlation between these variables was found. Stegastes nigricans was parasitised by six adult parasite species, D. aruanus by two adult parasite species and C. argus by five adult parasite species. The most common parasite species were found in all fish size classes. Ectoparasites showed a positive relationship between their abundance and host body length for all three reef fish species. A positive relationship was found only between host size and parasite abundance for common endoparasite species. Parasite species richness, Brillouin's diversity index, and host size and age were positively related. Finally, we discuss the influence of different biological (host diet, host immune response, parasite life-cycle) and ecological factors on parasite community structure in these three reef fishes. Host diet quality seems to be one of the major factors affecting the endoparasite community structure in these reef fishes. Ectoparasite communities seem to be influenced more by biological factors such as, for example, host immunity for the caligid larvae or parasite life-cycle for the gnathiid praniza larvae. In addition, the effect of ecological factors such as cleaning symbiosis on these ectoparasites cannot be dismissed.

Aging↗
PubMed1998

Determinants of Life-history Evolution in Nematodes.

What are the determinants of parasite life-history evolution? Does life-history evolution of parasitic species differ from their free-living relatives? How and why do host and parasite life-history traits covary? Here, Serge Morand and Gabriele Sorci use recent comparative studies to investigate life-history evolution in nematodes which present both parasitic and free-living groups. Application of life-history theory to nematodes suggests that the conventional wisdom concerning the high fecundity of parasitic species could simply be the result of the larger body size of the latter when compared with free-living forms. The authors also emphasize, with the use of examples, that in most cases parasite life-history evolution depends on host features.

Journal Article↗
PubMed1998

Comparative performance of species richness estimation methods.

In most real-world contexts the sampling effort needed to attain an accurate estimate of total species richness is excessive. Therefore, methods to estimate total species richness from incomplete collections need to be developed and tested. Using real and computer-simulated parasite data sets, the performances of 9 species richness estimation methods were compared. For all data sets, each estimation method was used to calculate the projected species richness at increasing levels of sampling effort. The performance of each method was evaluated by calculating the bias and precision of its estimates against the known total species richness. Performance was evaluated with increasing sampling effort and across different model communities. For the real data sets, the Chao2 and first-order jackknife estimators performed best. For the simulated data sets, the first-order jackknife estimator performed best at low sampling effort but, with increasing sampling effort, the bootstrap estimator outperformed all other estimators. Estimator performance increased with increasing species richness, aggregation level of individuals among samples and overall population size. Overall, the Chao2 and the first-order jackknife estimation methods performed best and should be used to control for the confounding effects of sampling effort in studies of parasite species richness. Potential uses of and practical problems with species richness estimation methods are discussed.

Animals↗
PubMed1998

Use of random amplified polymorphic DNA (RAPD) for generating specific DNA probes for oxyuroid species (Nematoda).

Random amplified DNA markers (RAPD; Williams et al., 1990) were used to obtained specific RAPD fragments characterising different species of oxyuroids. We tested six species of worms parasitizing vertebrates or invertebrates: Passalurus ambiguus Rudolphi, 1819, parasite of Leporids; Syphacia obvelata (Rudolphi, 1802) Seurat, 1916, a parasite of rodents; Blatticola blattae (Graeffe, 1860) Chitwood, 1932 parasite of the cockroach Blattella germanica; Hammerschmidtiella diesingi (Hammerschmidt, 1838) Chitwood, 1932 and Thelastoma bulhoesi (Magalhaes, 1990) Travassos, 1929, parasites of the cockroach Periplaneta americana, and an undescribed parasite species of a passalid insect from New Caledonia. Among 15 oligonucleotides tested, nine produced several specific bands allowing the interspecific discrimination.

Animals↗
PubMed1998

Heritable non-susceptibility in an allopatric host-parasite system: Biomphalaria glabrata (Mollusca)-Echinostoma caproni (platyhelminth Digenea).

We studied the heritability of adult nonsusceptibility/susceptibility in an allopatric host-parasite system, Biomphalaria glabrata (Brazil)-Echinostoma caproni (Egypt). In this system, the fitness of the infected host is substantially reduced because of castration. Mean frequencies of susceptibility among progeny of individual susceptible or nonsusceptible parents were compared, and heritabilities of susceptibility and nonsusceptibility were calculated under a quantitative genetic model. A Monte-Carlo simulation was used to assess the significance of the heritability estimates under the hypothesis of normal standard deviation. The results showed high heritability of both nonsusceptibility (0.56) and susceptibility (0.91).

Animals↗
PubMed1998

Cucullanin nematodes from coral reef fishes of French Polynesia, with a description of Cucullanus faliexae n. sp. (Nematoda: Chitwoodchabaudiidae).

Cucullanus faliexae n. sp. is described from the moray eel Gymnothorax javanicus (Muraenidae) collected in Rangiroa (Tuamotu Islands, French Polynesia) in the South Pacific and is reported from the same host collected in Moorea (Society Islands, French Polynesia). This nematode is distinguished from its congeners by its protrubant anus and the presence of a single pair of subdorsal postanal papillae. Cucullanus faliexae resembles C. laurotravassosi from which it is distinguished by the farther anterior position of the first pair of male caudal preanal papillae and by the greater size of its spicules. Cucullanus bourdini Petter and Le Bel, 1992 is reported from the coral reef fishes Balistapus undulatus (Balistidae), Lutjanus gibbus (Lutjanidae), and Myripristis kuntee (Holocentridae) from French Polynesia. Additionally, Cucullanus sp. is reported from the coral reef fish Sufflamen bursa (Balistidae) in Moorea and Rangiroa. Given that C. faliexae and C. bourdini have been found in widely disparate locations between which their definitive hosts cannot migrate, it would seem likely that the life cycles of these worms include an intermediate or transport host that has a greater capability for dispersal.

Animals↗
PubMed1997

Distribution and genetic diversity of Schistosoma haematobium within its bulinid intermediate hosts in Mali.

Random amplified polymorphic DNA (RAPD) markers were used to assess distribution and genetic diversity of Schistosoma haematobium populations within their bulinid intermediate hosts in Mali. Naturally infected snails (Bulinus truncatus and B. globosus) were collected at four sites in the Bamako district. S. haematobium cercariae from single snails were used to infect mice and genotypes of the resultant adult worms were characterized using RAPD markers. Diversity indices were calculated at the scale of one snail, both within and among sites. One third of the molluscs harboured multiple miracidial infections (the maximum number equal to five) with slightly overdispersed distributions in three sites and a random distribution at one site. Similarity indices revealed significantly less variation among populations compared with populations, indicative of the absence of distinct S. haematobium populations within the Bamako district. RAPD markers represent an accurate tool for determining genetic diversity and amount of gene flow among parasite populations contained within different individual snails and among intermediate host populations.

Animals↗
PubMed1997

Host-parasite coevolution: comparative evidence for covariation of life history traits in primates and oxyurid parasites.

The environmental factors that drive the evolution of parasite life histories are mostly unknown. Given that hosts provide the principal environmental features parasites have to deal with, and given that these features (such as resource availability and immune responses) are well characterized by the life history of the host, we may expect natural selection to result in covariation between parasite and host life histories. Moreover, some parasites show a high degree of host specificity, and cladistic analyses have shown that host and parasite phylogenies can be highly congruent. These considerations suggest that parasite and host life histories may covary. The central argument in the theory of life history evolution concerns the existence of trade-offs between traits. For parasitic nematodes it has been shown that larger body sizes induce higher fecundity, but this is achieved at the expense of delayed maturity. As high adult mortality would select for reduced age at maturity, the selective benefit of increased fecundity is expressed only if adult mortality is low. Parasite adult mortality may depend on a number of factors, including host longevity. Here we tested the hypothesis concerning the positive covariation between parasite body size (which reflects parasite longevity) and host longevity. To achieve this goal, we used the association between the pinworms (Oxyuridae, Nematoda) and their primate hosts. Oxyurids are highly host specific and are supposed to be involved in a coevolutionary process with their hosts. We found that female parasite body length was positively correlated with host longevity after correcting for phylogeny and host body mass. Conversely, male parasite body length and host longevity were not correlated. These results confirm that host longevity may represent a constraint on the evolution of body size in oxyurids, at least in females. The discrepancy between female and male oxyurids is likely to depend on the particular mode of reproduction of this taxon (haplodiploidy), which should result in weak (or even null) selection pressures to an increase of body size in males.

Animals↗
PubMed1997

Reduced egg counts in mixed infections with Oestrus ovis and Haemonchus contortus: influence of eosinophils?

In all, 2 groups of lambs were infected either with Oestrus ovis first-instar larvae or with 10,000 third-stage larvae (L3) of Haemonchus contortus. Another group of lambs was infected with both parasites. Fecal nematode egg counts, plasma pepsinogen concentrations, specific O. ovis enzyme-linked immunosorbent assay (ELISA) antibodies, and blood eosinophil counts were monitored and compared to with the values recorded for a control group of uninfected lambs. There was no significant difference between the burden of H. contortus found in mixed and single infections. However, the nematode egg production was significantly depressed in mixed infections. O. ovis affects the population of H. contortus at least by decreasing the parasite egg output. This effect may be mediated through the increase in eosinophil production stimulated by the presence of O. ovis.

Animals↗