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Aim The world's forested area has been declining, especially in developing countries. In contrast, forest plantations are increasing, particularly exotic Eucalyptus plantations, which cover nowadays over 20 million ha worldwide. This global landscape change affects native communities, especially those at higher trophic levels that are affected by bottom–up cascading effects, such as carnivores. We seek to identify the general life‐history traits of mammalian carnivore species that use exotic Eucalyptus plantations. Location We reviewed 55 studies reporting carnivore presence in Eucalyptus plantations worldwide. Methods We consider seven species life‐history traits (generation length, social behaviour, body mass, energetic trophic level, diet diversity, habitat generalist/specialist and locomotion mode) as candidate drivers. We used generalized linear mixed models, with life‐history traits as fixed factors, and study as well as carnivore species as random factors. We obtained the carnivore occurrence data from the literature (detection of 42 different species, from seven families). We considered non‐detected species those with an IUCN Red List of Threatened Species estimated distribution range overlapping with the study areas, but not recorded by the studies. Results While we found no evidence of an effect of any of the other life‐history traits tested, our modelling procedure indicated that habitat generalist species are more likely to use Eucalyptus forests than specialist species. Main conclusions Our results, therefore, confirm an impoverishment of predator communities in disturbed environments, with the exclusion of the most specialist predators, leading to fragmentation of their populations and, ultimately contributing to their local extinction. The local extinction of specialist carnivores may lead to “functional homogenization” of communities within plantations, modifying ecosystem functioning with a negative impact on plantations’ productivity, profitability and services.

ContextThe expansion of exotic plantations can impose conservation challenges on wildlife, and the Iberian Peninsula has one of the widest planted areas of exotic Eucalyptus sp. in Europe. Since mesocarnivores are pivotal elements of ecosystems’ functioning and Eucalyptus have been modifying the Portuguese landscape context in the last half century, it is crucial to understand how these systems may affect carnivores’ range.ObjectivesWe aim to identify the drivers of five mesocarnivores’ distribution in Portugal (e.g., land-cover, ecogeographic predictors, mammal prey availability) and understand the influence of Eucalyptus plantations in their distribution range.MethodsUsing generalized linear models, we modelled the distribution range of mesocarnivores. The initial dataset was randomly split for model training and validation, and the multicollinearity between the predictors was tested. Then, we examined the potential relationship between the Eucalyptus plantations area and the predicted probability presence of each species. ResultsWe detected species-specific patterns explained by different drivers, including climatic, land cover and mammal prey related ones. Furthermore, in areas of Eucalyptus plantations, the probability of occurrence of most Portuguese mesocarnivores is lower: red fox,stone marten,European badger, and Egyptian mongoose. ConclusionsManagers must take action to adapt their management to promote native forest patches within plantation, and allow the development of some understory within stands, to improve this plantation’s permeability to mesocarnivores. This will increase the spatial heterogeneity and enhance resource availability, reducing the constraints that plantations might have on the range of mesocarnivores in Portugal.

Humans have been altering the Mediterranean landscapes for millennia. To diminish the probability of encounters with domestic animals, humans and their activities, many species adjust their behavior to become more nocturnal. Even habitat-generalist species, such as red fox and stone marten that are somehow tolerant to environmental changes, might be affected by anthropic disturbances. Nevertheless, only a small number of studies were implemented in Iberia targeting these mesocarnivores’ activity patterns, and fewer have assessed the temporal ecology of these species in Eucalyptus plantations, the current main forest cover in Portugal. Based on camera traps, we aimed to analyze: 1) the temporal and spatio-temporal activity patterns of red fox and stone marten; and 2) how they are affected by distinct human disturbances (i.e., humans, livestock, dogs, plantations, and hunting). Foxes presented a higher crepuscular activity, while martens were entirely nocturnal, suggesting some avoidance behavior. Both mesocarnivores showed a higher overlap with dogs’ activity than with humans or livestock. Foxes’ activity patterns vary between seasons and habitats but were not influenced by the hunting period. Results suggest that both mesocarnivores, besides setting apart their activity from humans related disturbances, also show a tendency to temporally avoid each other. While the increase of nocturnality may indicate an anthropic disturbance impact, a reduction of activity overlap between mesocarnivores may be a strategy to reduce competition. These results may help support the sustainable management of landscapes by highlighting critical periods where activity overlaps may occur, and thus the anthropic impacts on wildlife are higher.

The chemical classes of semicarbazones, thiosemicarbazones, and hydrazones are present in various compounds, each demonstrating diverse biological activities. Extensive studies have revealed their potential as schistosomicidal agents. Thiosemicarbazones, in particular, have shown inhibitory effects on Schistosoma mansoni's cathepsin B1 enzyme ( Sm CB1), which plays a crucial role in hemoglobin degradation within the worm's gut and its nutrition processes. Consequently, Sm CB1 has emerged as a promising target for novel schistosomiasis therapies. Moreover, chloroquinoline exhibits characteristics in its aromatic structure that hold promise for developing Sm CB1 inhibitors, along with its interaction with hemoglobin's heme group, potentially synergizing against the parasite's gut. In this context, we report the synthesis of 22 hybrid analogs combining hydrazones and quinolines, evaluated against S. mansoni . Five of these hybrids demonstrated schistosomicidal activity in vitro, with GPQF-8Q10 being the most effective, causing worm mortality within 24 h at a concentration of 25 µM. GPQF-8Q8 proved to be the most promising in vivo, significantly reducing egg presence in feces (by 52.8%) and immature eggs in intestines (by 45.8%). These compounds exhibited low cytotoxicity in Vero cells and an in in vivo animal model ( Caenorhabditis elegans ), indicating a favorable selectivity index. This suggests their potential for the development of new schistosomiasis therapies. Further studies are needed to uncover specific target mechanisms, but these findings offer a promising starting point.

Sphingolipids (SLs) are essential components of all eukaryotic cellular membranes. In fungi, plants and many protozoa, the primary SL is inositol-phosphorylceramide (IPC). Trypanosoma cruzi is a protozoan parasite that causes Chagas disease (CD), a chronic illness for which no vaccines or effective treatments are available. IPC synthase (IPCS) has been considered an ideal target enzyme for drug development because phosphoinositol-containing SL is absent in mammalian cells and the enzyme activity has been described in all parasite forms of T . cruzi . Furthermore, IPCS is an integral membrane protein conserved amongst other kinetoplastids, including Leishmania major , for which specific inhibitors have been identified. Using a CRISPR-Cas9 protocol, we generated T . cruzi knockout (KO) mutants in which both alleles of the IPCS gene were disrupted. We demonstrated that the lack of IPCS activity does not affect epimastigote proliferation or its susceptibility to compounds that have been identified as inhibitors of the L . major IPCS. However, disruption of the T . cruzi IPCS gene negatively affected epimastigote differentiation into metacyclic trypomastigotes as well as proliferation of intracellular amastigotes and differentiation of amastigotes into tissue culture-derived trypomastigotes. In accordance with previous studies suggesting that IPC is a membrane component essential for parasite survival in the mammalian host, we showed that T . cruzi IPCS null mutants are unable to establish an infection in vivo , even in immune deficient mice.

The widespread SCP/TAPS superfamily (SCP/Tpx-1/Ag5/PR-1/Sc7) has multiple biological functions, including roles in the immune response of plants and animals, development of male reproductive tract in mammals, venom activity in insects and reptiles and host invasion by parasitic worms. Plant Pathogenesis Related 1 (PR-1) proteins belong to this superfamily and have been characterized as markers of induced defense against pathogens. This work presents the characterization of eleven genes homologous to plant PR-1 genes, designated as MpPR-1, which were identified in the genome of Moniliophthora perniciosa, a basidiomycete fungus responsible for causing the devastating witches' broom disease in cacao. We describe gene structure, protein alignment and modeling analyses of the MpPR-1 family. Additionally, the expression profiles of MpPR-1 genes were assessed by qPCR in different stages throughout the fungal life cycle. A specific expression pattern was verified for each member of the MpPR-1 family in the conditions analyzed. Interestingly, some of them were highly and specifically expressed during the interaction of the fungus with cacao, suggesting a role for the MpPR-1 proteins in the infective process of this pathogen. Hypothetical functions assigned to members of the MpPR-1 family include neutralization of plant defenses, antimicrobial activity to avoid competitors and fruiting body physiology. This study provides strong evidence on the importance of PR-1-like genes for fungal virulence on plants.

Essential oils and their isolated constituents are constantly being studied for the control of insect pests. In this context, the present research reports the chemical composition of Piper marginatum (Jacq.) oil aiming to: 1) establish lethal concentrations LC30 and LC50 for this oil and the compound geraniol, 2) histologically examine the embryonic development of Spodoptera frugiperda (J.E. Smith) through light microscopy and scanning electron microscopy (SEM), as well as 3) compare the efficacy of the P. marginatum oil with that of the botanical insecticide azadirachtin, the synthetic insecticide deltamethrin, and acetone as a negative control. Semithin sections of S. frugiperda eggs revealed that the oil, geraniol, azadirachtin, and deltamethrin affected embryonic development at both concentrations. However, geraniol and the oil were more efficient because they caused more significant damage, even at lower concentrations. SEM revealed that all products altered the morphology of the eggs, modifying the structure of the chorion and making the eggs nonviable. Thus, this work demonstrates that P. marginatum oil is effective in the control of S. frugiperda because it results in embryonic damage even at the lowest concentrations.

Spinocerebellar ataxia type 3 (SCA3) is an adult-onset neurodegenerative disease caused by a polyglutamine expansion in the ataxin-3 (ATXN3) gene. No effective treatment is available for this disorder, other than symptom-directed approaches. Bile acids have shown therapeutic efficacy in neurodegenerative disease models. Here, we pinpointed tauroursodeoxycholic acid (TUDCA) as an efficient therapeutic, improving the motor and neuropathological phenotype of SCA3 nematode and mouse models. Surprisingly, transcriptomic and functional in vivo data showed that TUDCA acts in neuronal tissue through the glucocorticoid receptor (GR), but independently of its canonical receptor, the farnesoid X receptor (FXR). TUDCA was predicted to bind to the GR, in a similar fashion to corticosteroid molecules. GR levels were decreased in disease-affected brain regions, likely due to increased protein degradation as a consequence of ATXN3 dysfunction being restored by TUDCA treatment. Analysis of a SCA3 clinical cohort showed intriguing correlations between the peripheral expression of GR and the predicted age at disease onset in presymptomatic subjects and FKBP5 expression with disease progression, suggesting this pathway as a potential source of biomarkers for future study. We have established a novel in vivo mechanism for the neuroprotective effects of TUDCA in SCA3 and propose this readily available drug for clinical trials in SCA3 patients.

Background The basidiomycete Moniliophthora roreri is the causal agent of Frosty pod rot (FPR) disease of cacao ( Theobroma cacao ), the source of chocolate, and FPR is one of the most destructive diseases of this important perennial crop in the Americas. This hemibiotroph infects only cacao pods and has an extended biotrophic phase lasting up to sixty days, culminating in plant necrosis and sporulation of the fungus without the formation of a basidiocarp. Results We sequenced and assembled 52.3 Mb into 3,298 contigs that represent the M. roreri genome. Of the 17,920 predicted open reading frames (OFRs), 13,760 were validated by RNA-Seq. Using read count data from RNA sequencing of cacao pods at 30 and 60 days post infection, differential gene expression was estimated for the biotrophic and necrotrophic phases of this plant-pathogen interaction. The sequencing data were used to develop a genome based secretome for the infected pods. Of the 1,535 genes encoding putative secreted proteins, 1,355 were expressed in the biotrophic and necrotrophic phases. Analysis of the data revealed secretome gene expression that correlated with infection and intercellular growth in the biotrophic phase and invasive growth and plant cellular death in the necrotrophic phase. Conclusions Genome sequencing and RNA-Seq was used to determine and validate the Moniliophthora roreri genome and secretome. High sequence identity between Moniliophthora roreri genes and Moniliophthora perniciosa genes supports the taxonomic relationship with Moniliophthora perniciosa and the relatedness of this fungus to other basidiomycetes. Analysis of RNA-Seq data from infected plant tissues revealed differentially expressed genes in the biotrophic and necrotrophic phases. The secreted protein genes that were upregulated in the biotrophic phase are primarily associated with breakdown of the intercellular matrix and modification of the fungal mycelia, possibly to mask the fungus from plant defenses. Based on the transcriptome data, the upregulated secreted proteins in the necrotrophic phase are hypothesized to be actively attacking the plant cell walls and plant cellular components resulting in necrosis. These genes are being used to develop a new understanding of how this disease interaction progresses and to identify potential targets to reduce the impact of this devastating disease.

IntroductionOral lichen planus (OLP) is an idiopathic chronic mucocutaneous disease with a wide range of clinical manifestations, including white reticular patches, erosive/ulcerative and atrophic lesions, both associated with intense symptomatology. Topical corticosteroids are commonly used as standard therapy. However, patients frequently present relapses after the discontinuation of treatment as well as developing resistance to corticosteroid therapy. Photobiomodulation (PBM) has been shown to be a potential therapeutic tool to treat inflammatory disorders, including OLP. The aim of this study was to compare the efficacy of PBM (660 nm) with corticosteroid therapy with clobetasol propionate 0.05% for the treatment of OLP.Methods and analysisForty-four patients with symptomatic and histopathological diagnosis of OLP will be randomised into two experimental groups in a double-blind manner: control group (n=22): clobetasol propionate 0.05%+placebo PBM, and experimental group (n=22): PBM (λ=660 nm, power 100 mW, radiant exposure: 177 J/cm2 and 0.5J per point)+placebo gel. Laser will be applied 2×/week for 1 month and clobetasol propionate three times a day for 30 days and the same for placebo treatments. The primary variable (pain) and the secondary variables (clinical score, evaluation of functional scores, clinical resolution, OLP recurrence, quality of life and anxiety and depression) will be evaluated at the baseline, once a week during treatment (depending on the variables) and after 30 days and 60 days of follow-up. Pain will be evaluated using visual analogue scale and clinical characteristics will be scored using the Thongprasom Index. The quality of life and anxiety and depression will be evaluated by Oral Health Impact Profile-14 questionnaire and by Hospital Anxiety and Depression Scale for anxiety scale, respectively. The serum and salivary levels of interleukin (IL)-6, IL-10, IL-1β, INF-γ and tumour necrosis factor-α will be evaluated by ELISA at baseline and at the end of treatment.Ethics and disseminationThis protocol was approved (#2.375.410) by the Nove de Julho University (UNINOVE) Research Ethics Committee. The data gathered using this protocol will be published in a peer-reviewed journal.Trial registration number NCT03320460.