12 research outputs found

    Parasite spread at the domestic animal - wildlife interface: anthropogenic habitat use, phylogeny and body mass drive risk of cat and dog flea (Ctenocephalides spp.) infestation in wild mammals

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    Spillover of parasites at the domestic animal - wildlife interface is a pervasive threat to animal health. Cat and dog fleas (Ctenocephalides felis and C. canis) are among the world's most invasive and economically important ectoparasites. Although both species are presumed to infest a diversity of host species across the globe, knowledge on their distributions in wildlife is poor. We built a global dataset of wild mammal host associations for cat and dog fleas, and used Bayesian hierarchical models to identify traits that predict wildlife infestation probability. We complemented this by calculating functional-phylogenetic host specificity to assess whether fleas are restricted to hosts with similar evolutionary histories, diet or habitat niches.Over 130 wildlife species have been found to harbour cat fleas, representing nearly 20% of all mammal species sampled for fleas. Phylogenetic models indicate cat fleas are capable of infesting a broad diversity of wild mammal species through ecological fitting. Those that use anthropogenic habitats are at highest risk. Dog fleas, by contrast, have been recorded in 31 mammal species that are primarily restricted to certain phylogenetic clades, including canids, felids and murids. Both flea species are commonly reported infesting mammals that are feral (free-roaming cats and dogs) or introduced (red foxes, black rats and brown rats), suggesting the breakdown of barriers between wildlife and invasive reservoir species will increase spillover at the domestic animal - wildlife interface.Our empirical evidence shows that cat fleas are incredibly host-generalist, likely exhibiting a host range that is among the broadest of all ectoparasites. Reducing wild species' contact rates with domestic animals across natural and anthropogenic habitats, together with mitigating impacts of invasive reservoir hosts, will be crucial for reducing invasive flea infestations in wild mammals

    Evolution of South American Paucituberculata (Metatheria: Marsupialia): adaptive radiation and climate changes at the Eocene- Oligocene boundary

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    The Eocene-Oligocene boundary (EOB) marks a period of remodeling in the metatherian faunas of South America. Paucituberculata was one of the groups that successfully diversified as the climate and environment conditions changed, and they became, during the first part of the Neogene, an important component of micromammal assemblages. Among paucituberculatans, the non-pichipilid palaeothentoids (NPP) has been recognized as the clade that diversified most widely in post-EOB times. Here we explore the evolutionary response of the NPP to the climatic-environmental changes around the EOB, by analysing the temporal patterns of disparity, taxonomic diversity and body mass in a phylogenetic context. To asses the magnitude of the NPP radiation comparisons based on these macroevolutionary parameters were done with its sister-group Pichipilidae, and its next closest relative, the Caenolestidae. In all considered parameters, NPP reached values significantly higher than the remaining paucituberculatans clades. From its initial diversification in the middle Eocene, taxonomic diversity increased through time, but it was decoupled from disparity across the EOB, and from the late Oligocene to early Miocene. The Oligocene emerges as the key period in NPP evolution, which is evidenced by a significant and concordant expansion of disparity and taxonomic diversity, suggesting evolution into empty ecospace.Facultad de Ciencias Naturales y Muse

    Functional articular cartilage repair: here, near, or is the best approach not yet clear?

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    In this Review we describe three approaches for cartilage tissue repair at the rheumatology–orthopaedics interface: disease-modifying osteoarthritis (OA) drug (DMOAD) treatment; cell-based therapies, and intrinsic cartilage repair by joint distraction. DMOADs can slow the progression of joint damage. Cell-based therapies have evolved to do the same, through selection of the most potent cell types (and combinations thereof), as well as identification of permissive boundary conditions for indications. Joint distraction techniques, meanwhile, have now demonstrated the capacity to stimulate actual intrinsic tissue repair. Although this progress is promising, true biological joint reconstruction remains distant on the developmental pathway of 'regenerative medicine'. Prolonged functional repair—that is, cure of diseases such as OA—remains an unmet medical need and scientific challenge, for which comparative and constructive interaction between these physical, chemical and cellular approaches will be required. Careful selections of patients and combinations of approaches will need to be made and tested to demonstrate their cost-effectiveness. Only with such rational and integrated assessment of outcomes will the promising results of these approaches be consolidated in clinical practice
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