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Salinas, N.

Publications and source records attributed to Salinas, N..

10 recordsLinked to original sources

The effects of human population density on trophic interactions are contingent upon latitude

Aim: Studies conducted at a global scale are necessary to make general conclusions on the effect of urbanization on trophic interactions and explore how these effects change along latitudinal gradients. Since biotic interactions are more intense at lower latitudes, we predict that the intensity of trophic interactions will decrease in response to urbanization (quantified by human population density), with higher impacts of urbanization at higher latitudes. Location: Global (881 study sites). Time period: 2000-2021. Major taxa studied: Birds, arthropods and woody plants. Methods: We compiled global data on insect herbivory and bird predation from individual studies using similar methodologies, and fitted generalized linear mixed models to test the effect of human population density, latitude and their interaction on these two response variables. Results: The intensity of herbivory and predation decreased with the increase of human population density at lower latitudes, remained unaffected at intermediate latitudes, and increased at higher latitudes. Main conclusions: The effect of human population density on insect herbivory and bird predation consistently varies across latitudes, with a reversal of the pattern at high versus low latitudes.

ecology↗

Woody plant taxonomic, functional, and phylogenetic diversity decrease along elevational gradients in Andean tropical montane forests: environmental filtering and arrival of temperate taxa

AimMountains are paramount for exploring biodiversity patterns and their causes due to the rich mosaic of topographies and climates encompassed over short geographical distances. Biodiversity changes along elevational gradients have traditionally been explored in terms of taxonomic diversity, but other aspects must be considered. For first time, we simultaneously assessed elevational trends in the taxonomic, functional, and phylogenetic diversity of woody plants in Andean tropical montane forests (TMFs) and explored their underlying ecological and evolutionary causing processes. LocationTropical Andes Time period2011/2012 and 2017/2019 Tropical Andes Major TaxaWoody plants MethodsWe investigated taxonomic, functional, and phylogenetic diversity along four transects (traversing ca. 2,200 m altitudinal gradients) encompassing 114 0.1 ha plots across a broad latitudinal range (ca. 10{degrees}). We used Hill numbers to quantify differences in the abundance-based diversity of 37,869 woody plant individuals with DBH [≥] 2.5 cm. ResultsTaxonomic, functional, and phylogenetic diversity decreased as elevation increased. The decrease was less pronounced for Hill numbers of higher orders. The only exception was a slight increase in phylogenetic diversity when more weight was given to dominant species. These results were consistent between transects. Main conclusionsThe decrease in taxonomic and functional diversity with elevation might be due to an environmental filtering process where the increasingly harsher conditions towards highlands exclude species and functional strategies. Besides, the differences in the steepness of the decrease between Hill orders suggest that rare species contribute disproportionately to functional diversity. The shifting elevational trend in the phylogenetic diversity between Hill orders indicates a greater than previously considered influence in central tropical Andean highlands of species originated in lowlands with strong niche conservatism relative to distantly related temperate lineages. This could be explained by a decreasing presence and abundance of extratropical taxa towards the central Andes relative to northern or southern Andes. BIOSKETCHGuillermo Banares-de-Dios is a plant ecologist with interests in community assembly, biodiversity patterns, and global change. He completed his PhD in 2020 and belongs to "Grupo de Ecologia Tropical", an international network of researchers from different institutions with broad interests in tropical biology (http://www.grupoecologiatropical.com/?lang=en). Currently he works as Project Manager implementing the European Pollinator Monitoring Scheme in Spain.

ecology↗

Granulin Loss of Function in Human Mature Brain Organoids Implicates Astrocytes in TDP-43 Pathology

Loss of function (LoF) of Tar-binding protein 43 (TDP-43) and mislocalization, together with TDP-43-positive and hyperphosphorylated inclusions, are found in postmortem tissue of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) patients, including those carrying LoF variants in the progranulin gene (GRN). Modelling TDP-43 pathology has been challenging in vivo and in vitro. We present a 3D-induced pluripotent stem cell (iPSC)-derived paradigm - mature brain organoids (mbOrg) - composed of cortical-like-astrocytes (iA) and neurons (iN). When devoid of GRN, mbOrgs spontaneously recapitulate TDP-43 mislocalization, hyperphosphorylation and LoF phenotypes. Mixing-and-matching genotypes in mbOrgs showed that GRN-/- iA are drivers for TDP-43 pathology. Finally, we rescued TDP-43 LoF by adding exogenous progranulin, demonstrating a link between TDP-43 LoF and progranulin expression. In conclusion, we present an iPSC-derived platform that shows striking features of human TDP-43 proteinopathy and provides a tool for mechanistic modelling of TDP-43 pathology and patient-tailored therapeutic screening for FTD and ALS. HighlightsO_LIGRN-/- iPSC-derived 3D paradigm (mbOrg) composed of mature cortical-like astrocytes and neurons recapitulates features of TDP-43 proteinopathy C_LIO_LIGRN-/- cortical-like astrocytes are necessary and sufficient for the development of the TDP-43 loss of function phenotype in mbOrg. C_LIO_LIA TDP-43 phenotype can be rescued in neurons by treating neuron and astrocyte co-cultures with progranulin full length protein. C_LI eTOC blurbIn this article, de Majo and colleagues present a novel 3D iPSC-derived model to study neurodegenerative disorders such as ALS and FTD. When devoid of GRN expression, these cultures present features of ALS and FTD associated pathology hardly ever observed in vitro. These phenotypes are shown to be primarily driven by diseased astrocytes and can be rescued by progranulin supplementation.

neuroscience↗

The evolutionary assembly of forest communities along environmental gradients: recent diversification or sorting of pre-adapted clades?

O_LIBiogeographic events occurring in the deep past can contribute to the structure of modern ecological communities. However, little is known about how the emergence of environmental gradients shape the evolution of species that underlie community assembly. In this study, we address how the creation of novel environments lead to community assembly via two non-mutually exclusive processes: 1) the immigration and ecological sorting of pre-adapted clades (ISPC), and 2) recent adaptive diversification (RAD). We study these processes in the context of the elevational gradient created by the uplift of the Central Andes. C_LIO_LIWe develop a novel approach and method based on the decomposition of species turnover into within- and among-clade components, where clades correspond to lineages that originated before mountain uplift. Effects of ISPC and RAD can be inferred from how components of turnover change with elevation. We test our approach using data from over 500 Andean forest plots. C_LIO_LIWe found that species turnover between communities at different elevations is dominated by the replacement of clades that originated before the uplift of the Central Andes. C_LIO_LIOur results suggest that immigration and sorting of clades pre-adapted to montane habitats is the primary mechanism shaping communities across elevations. C_LI

ecology↗

A high affinity human monoclonal antibody against Pfs230 binds multiple parasite stages and blocks oocyst formation in mosquitoes

Malaria elimination requires tools that interrupt parasite transmission. Here, we characterized B cell receptor responses among Malian adults vaccinated against the first domain of the cysteine-rich 230kDa gamete surface protein Pfs2301-3 to neutralize sexual stage P. falciparum parasites and halt their further spread. We generated nine Pfs230 human monoclonal antibodies (mAbs). One mAb potently blocked transmission to mosquitoes in a complement-dependent manner and reacted strongly to gamete surface while eight mAbs showed only low or no blocking activity. This study provides a rational basis to improve malaria vaccines and develop therapeutic antibodies for malaria elimination.

immunology↗

Evolutionary heritage shapes tree distributions along an Amazon-to-Andes elevation gradient

Understanding how evolutionary constraints shape the elevational distributions of tree lineages provides valuable insight into the future of tropical montane forests under global change. With narrow elevational ranges, high taxonomic turnover, frequent habitat specialisation, and exceptional levels of endemism, tropical montane forests and trees are predicted to be highly sensitive to environmental change. Using plot census data from a gradient traversing >3000 m in elevation on the Amazonian flank of the Peruvian Andes, we employ phylogenetic approaches to assess the influence of evolutionary heritage on distribution trends of trees at the genus level. We find that closely related lineages tend to occur at similar mean elevations, with sister genera pairs occurring a mean 254 m in elevation closer to each other than the mean elevational difference for all genera pairs. We also demonstrate phylogenetic clustering both above and below 1750 m a.s.l, corresponding roughly to the cloud-base ecotone. Belying these general trends, some lineages occur across many different elevations. However, these highly plastic lineages are not phylogenetically clustered. Overall, our findings suggest that tropical montane forests are home to unique tree lineage diversity, constrained by their evolutionary heritage and vulnerable to substantial losses under environmental changes, such as rising temperatures or an upward shift of the cloud base.

ecology↗

The Amphibian Antimicrobial Peptide Uperin 3.5 is a Cross-α/Cross-β Chameleon Functional Amyloid

Antimicrobial activity is being increasingly linked to amyloid fibril formation, suggesting physiological roles for some human amyloids, which have historically been viewed as strictly pathological agents. This work reports on formation of functional cross- amyloid fibrils of the amphibian antimicrobial peptide uperin 3.5 at atomic-resolution, an architecture initially discovered in the bacterial PSM3 cytotoxin. The fibrils of uperin 3.5 and PSM3 were comprised of parallel and anti-parallel helical sheets, respectively, recapitulating properties of {beta}-sheets. Uperin 3.5 helical fibril formation was largely induced by, and formed on, bacterial cells or membrane mimetics, and led to membrane damage and cell death. Uperin 3.5 demonstrated chameleon properties, with a secondary structure switch to cross-{beta} fibrils with reduced antibacterial activity in the absence of lipids or after heat shock. These findings suggest a regulation mechanism, which includes storage of inactive peptides as well as environmentally induced activation of uperin 3.5, via chameleon cross-/{beta} amyloid fibrils.

biochemistry↗

THE INFLUENCE OF ECOSYSTEM AND PHYLOGENY ON TROPICAL TREE CROWN SIZE AND SHAPE

1The sizes and shapes of tree crowns are of fundamental importance in ecology, yet understanding the forces that determine them remains elusive. A cardinal question facing ecologists is the degree to which general and non-specific versus ecological and context-dependent processes are responsible for shaping tree crowns. Here, we test this question for the first time across diverse tropical ecosystems. Using trees from 20 plots varying in elevation, precipitation, and ecosystem type (savanna-forest transitions) across the paleo- and neo-tropics, we test the relationship between crown dimensions and tree size. By analyzing these scaling relationships across environmental gradients, biogeographic regions, and phylogenetic distance, we extend Metabolic Scaling Theory (MST) predictions to include how local selective pressures shape variation in crown dimensions. Across all sites, we find strong agreement between mean trends and MST predictions for the scaling of crown size and shape, but large variation around the mean. While MST explained approximately half of the observed variation in tree crown dimensions, we find that local, ecosystem, and phylogenetic predictors account for the half of the residual variation. Crown scaling does not change significantly across regions, but does change across ecosystem types, where savanna tree crowns grow more quickly with tree size than forest tree crowns. Crowns of legumes were wider and larger than those of other taxa. Thus, while MST can accurately describe the central tendency of tree crown size, local ecological conditions and evolutionary history appear to modify the scaling of crown shape. Importantly, our extension of MST incorporating these differences accounts for the mechanisms driving variation in the scaling of crown dimensions across the tropics. These results are critical when scaling the function of individual trees to larger spatial scales or incorporating the size and shape of tree crowns in global biogeochemical models.

ecology↗

Structural Insights into Curli Amyloid Fibrils suggest Repurposing Anti-amyloid Compounds as Anti-biofilm Agents

Curli amyloid fibrils secreted by Enterobacteriaceae mediate host cell adhesion and contribute to biofilm formation, thereby promoting bacterial resistance to environmental stressors. Here, we present crystal structures of amyloid-forming segments from the major curlin subunit, CsgA, revealing steric zipper fibrils of tightly mated {beta}-sheets, demonstrating a structural link between curli and human pathological amyloids. We propose that these cross-{beta} segments structure the highly robust curli amyloid core. D-enantiomeric peptides, originally developed to interfere with Alzheimers disease-associated Amyloid-{beta}, inhibited CsgA fibrillation and reduced biofilm formation in Salmonella typhimurium. Moreover, CsgA fibrils cross-seeded fibrillation of Amyloid-{beta}, providing further support for the proposed structural resemblance and potential for cross-species amyloid interactions. In this study, we provide structural insights into curli formation, offer a novel strategy for disrupting amyloid-structured biofilms, and hypothesize on the formation of self-propagating prion-like species originating from a microbial source that could influence neurodegenerative diseases.\n\nSignificanceAtomic resolution structural insights into the biofilm-associated curli amyloid fibril secreted by Enterobacteriaceae revealed elements of fibrillar architecture conserved between bacterial and human amyloids. This inspired us to repurpose anti-amyloid drugs designed to target human pathological amyloids as a novel class of anti-biofilm agents. Moreover, the results provide a molecular basis for understanding interspecies cross-seeding of amyloids through the generation of prion-like agents by molecular mimicry. This raises concerns regarding human exposure to exogenous sources of amyloids, such as contaminated food and amyloid-secreting microbes. Overall, we provide a novel framework for investigating interspecies amyloid interactions at the molecular level and offer novel insights into mechanisms which may underlie the evolutionary and etiological relationships between the human and microbial amylomes.

biochemistry↗

Extreme Amyloid Polymorphism in Staphylococcus aureus Virulent PSMα Peptides

Members of the Staphylococcus aureus phenol-soluble modulin (PSM) peptide family are secreted as functional amyloids that serve diverse roles in pathogenicity and may be present as full-length peptides or as naturally occurring truncations. We recently showed that the activity of PSM3, the most toxic member, stems from the formation of cross- fibrils, which are at variance with the cross-{beta} fibrils linked with eukaryotic amyloid pathologies. Here, we show that PSM1 and PSM4, involved in biofilm structuring, form canonical cross-{beta} amyloid fibrils wherein {beta}-sheets tightly mate through steric zipper interfaces, conferring high stability. Contrastingly, a truncated PSM3 has antibacterial activity, forms reversible fibrils, and reveals two polymorphic and atypical {beta}-rich fibril architectures. These architectures are radically different from both the cross- fibrils formed by full-length PSM3, and from the canonical cross-{beta} fibrils. Our results point to structural plasticity being at the basis of the functional diversity exhibited by S. aureus PSMs.

biochemistry↗