Hybrids and their parasite diversity represent interesting models for evolutionary ecology. The modified immune response, shifted ecology, inheritance, and maternal ancestry of hybrid host fish are supposed to affect the diversity of their parasite communities. The pattern of metazoan parasite distribution in non-congeneric cyprinids - common bream (Abramis brama) and roach (Rutilus rutilus) (species with different morphology and ecology, and harbouring different specific parasites) - and their hybrids was analysed. Four static alternative scenarios based on parasite infection levels in hybrids and parental taxa are known. The hybrid resistance scenario predicts that hybrids are more resistant than parental taxa, resulting in low parasite infection in hybrids. This scenario is principally consistent with hybrid heterosis advantage. In accordance with this prediction, metazoan parasite abundance and prevalence were higher in parental species when compared with their hybrids. Alternatively, the dynamic Red Queen scenario of infection in hybridising systems predicts parasite adaptation to common hosts. Temporal (six sampling events) and spatial (two sampling sites) aspects as possible factors influencing parasite distribution were analysed. We found no support for this hypothesis, i.e. no changes in the frequency of hybrids or their parental species and no changes in parasite infection in parental species or hybrids were found in the different time periods. The effect of maternal ancestry on infection level was evident; hybrids exhibiting common bream mtDNA were more strongly parasitized by digeneans and crustaceans than hybrids exhibiting roach mtDNA. Hybrids harboured a majority of the specific parasites of both parental species; however, the level of infection of common bream-specific parasites (especially monogeneans) in hybrids was low. Such an asymmetrical distribution of parental species-specific parasites in hybrids may suggest the limited inheritance of protective immunological mechanisms from one parental species and reveal stronger coadaptation between common bream and its specific parasites.
- MeSH
- Cyprinidae genetics parasitology MeSH
- Adaptation, Physiological genetics MeSH
- Genetic Predisposition to Disease MeSH
- Host Specificity MeSH
- Hybridization, Genetic * MeSH
- Sea Bream genetics parasitology MeSH
- Fish Diseases genetics parasitology MeSH
- Parasitic Diseases, Animal genetics parasitology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The oral microbiome plays key roles in human biology, health, and disease, but little is known about the global diversity, variation, or evolution of this microbial community. To better understand the evolution and changing ecology of the human oral microbiome, we analyzed 124 dental biofilm metagenomes from humans, including Neanderthals and Late Pleistocene to present-day modern humans, chimpanzees, and gorillas, as well as New World howler monkeys for comparison. We find that a core microbiome of primarily biofilm structural taxa has been maintained throughout African hominid evolution, and these microbial groups are also shared with howler monkeys, suggesting that they have been important oral members since before the catarrhine-platyrrhine split ca. 40 Mya. However, community structure and individual microbial phylogenies do not closely reflect host relationships, and the dental biofilms of Homo and chimpanzees are distinguished by major taxonomic and functional differences. Reconstructing oral metagenomes from up to 100 thousand years ago, we show that the microbial profiles of both Neanderthals and modern humans are highly similar, sharing functional adaptations in nutrient metabolism. These include an apparent Homo-specific acquisition of salivary amylase-binding capability by oral streptococci, suggesting microbial coadaptation with host diet. We additionally find evidence of shared genetic diversity in the oral bacteria of Neanderthal and Upper Paleolithic modern humans that is not observed in later modern human populations. Differences in the oral microbiomes of African hominids provide insights into human evolution, the ancestral state of the human microbiome, and a temporal framework for understanding microbial health and disease.
- MeSH
- Bacteria classification genetics MeSH
- Biofilms MeSH
- Biological Evolution * MeSH
- Ecology methods MeSH
- Phylogeny MeSH
- Gorilla gorilla microbiology MeSH
- Hominidae classification microbiology MeSH
- Humans MeSH
- Metagenome genetics MeSH
- Microbiota genetics MeSH
- Pan troglodytes microbiology MeSH
- Mouth microbiology MeSH
- Geography MeSH
- Dental Plaque microbiology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Africa MeSH
1st ed. xv, 339 s.
Seasonal acclimation and thermoregulation represent major components of complex thermal strategies by which ectotherms cope with the heterogeneity of their thermal environment. Some ectotherms possess the acclimatory capacity to shift seasonally their thermoregulatory behavior, but the frequent use of constant acclimation temperatures during experiments and the lack of information about thermal heterogeneity in the field obscures the ecological relevance of this plastic response. We examined the experimentally induced seasonal acclimation of preferred body temperatures (T(p)) in alpine newts Ichthyosaura (formerly Triturus) alpestris subjected to a gradual increase in acclimation temperature from 5°C during the winter to a constant 15°C or diel fluctuations between 10° and 20°C during the spring/summer. Both the mean and range of T(p) followed the increase in mean acclimation temperature without the influence of diel temperature fluctuations. The direction and magnitude of this acclimatory capacity has the potential to increase the time window available for thermoregulation. Although thermoregulation and thermal acclimation are often considered as separate but coadapted adjustments to thermal heterogeneity, their combined response is employed by newts to tackle seasonal variation in a thermoregulatory-challenging aquatic environment.
