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Habitat loss due to land-use change is the greatest threat to biodiversity on a global scale, and agriculture has been the principal driver of change. In Uruguay, the conversion of native grasslands to croplands (e.g., soybean) and exotic forest plantations (Eucalyptus and Pinus) has accelerated during the last two decades. We studied the vulnerability of vertebrate and woody plant diversity to the loss of grassland areas, driven by agricultural and forestry expansion, to identify priority areas for conservation. We assessed the spatial variability of biodiversity vulnerability in function of species richness and number of focal species (i.e., prioritized species) of woody plants and terrestrial vertebrates that use grassland ecosystem as habitat. The top 17% of vulnerable sites (51 of 302 cells) were selected as priority conservation areas for Uruguay, following Aichi Target number 11. Approximately 36 % of the original continental territory of Uruguay, mainly grasslands, was converted to cropland (28%) and exotic forest plantations (8%) in 2015. Approximately 27% of the priority cells for conservation of vertebrates and woody plant diversity have been transformed, especially in three ecoregions in which habitat loss was between 35-45%. We simulated a land-use scenario for 2030, based on national production goals of soybean and exotic forest plantations, projecting that: (1) the overall loss of original habitat (mainly grasslands) would reach 48% of the country's land area, and (2) 45% of the priority cells would be converted to agricultural lands, especially in four ecoregions, with habitat losses greater than 50%. Our results suggest an urgent need to develop strategies to reduce the rate of natural grassland loss in Uruguay, as well as to conserve biodiversity and ecosystem services associated with these systems. Conservation efforts should focus on prioritized cells, especially those with no protection status and a high likelihood of agricultural conversion in 2030, through expanding public and private protected areas and promoting wildlife-friendly agricultural alternatives, such as beef production in natural grasslands. [ABSTRACT FROM AUTHOR]

Roads are one of the main causes of loss of biodiversity, with roadkill one of the main causes of mortality. The aim of this research was to identify sites with a high probability of roadkill of medium and large mammals, and the environmental variables that would explain it. We used the favourability function (F) to build the predictive models. There were 57 explanatory variables, and we collected 685 records of 10 species of medium and large native wild mammals from the ECOBIO Uruguay databases. They were grouped into native forest and grassland species, according to the main habitat. Two models were developed, one with all the variables and one with the anthropogenic variables. For both groups, the model obtained with all the variables was the most significant according to the evaluation indices used. This made it possible to identify the hot spots of roadkill (F > 0.6) for each of the groups. The anthropic variables were the ones that best explained these hot spots. This allowed the identification of sites where the probability of roadkill is high and requires a monitoring plan to implement mitigation measures in the future. [ABSTRACT FROM AUTHOR]

Macrophages (Mφs) are instrumental regulators of the immune response whereby they acquire diverse functional phenotypes following their exposure to microenvironmental cues that govern their differentiation from monocytes and their activation. The complexity and diversity of the mycobacterial cell wall have empowered mycobacteria with potent immunomodulatory capacities. A heat-killed (HK) whole-cell preparation of Mycobacterium obuense (M. obuense) has shown promise as an adjunctive immunotherapeutic agent for the treatment of cancer. Moreover, HK M. obuense has been shown to trigger the differentiation of human monocytes into a monocyte-derived macrophage (MDM) type named Mob-MDM. However, the transcriptomic profile and functional properties of Mob-MDMs remain undefined during an activation state. Here, we characterized cytokine/chemokine release patterns and transcriptomic profiles of lipopolysaccharide (LPS)/interferon γ (IFNγ)-activated human MDMs that were differentiated with HK M. obuense (Mob-MDM(LPS/IFNγ)), macrophage colony-stimulating factor M-MDM(LPS/IFNγ)), or granulocyte/macrophage colony-stimulating factor (GM-MDM(LPS/IFNγ)). Mob-MDM(LPS/IFNγ) demonstrated a unique cytokine/chemokine release pattern (interleukin (IL)-10low, IL-12/23p40low, IL-23p19/p40low, chemokine (C-x-C) motif ligand (CXCL)9low) that was distinct from those of M-MDM(LPS/IFNγ) and GM-MDM(LPS/IFNγ). Furthermore, M-MDM(LPS/IFNγ) maintained IL-10 production at significantly higher levels compared to GM-MDM(LPS/IFNγ) and Mob-MDM(LPS/IFNγ) despite being activated with M1-Mφ-activating stimuli. Comparative RNA sequencing analysis pointed to a distinct transcriptome profile for Mob-MDM(LPS/IFNγ) relative to both M-MDM(LPS/IFNγ) and GM-MDM(LPS/IFNγ) that comprised 417 transcripts. Functional gene-set enrichment analysis revealed significant overrepresentation of signaling pathways and biological processes that were uniquely related to Mob-MDM(LPS/IFNγ). Our findings lay a foundation for the potential integration of HK M. obuense in specific cell-based immunotherapeutic modalities such as adoptive transfer of Mφs (Mob-MDM(LPS/IFNγ)) for cancer treatment. [ABSTRACT FROM AUTHOR]