MORFOGÊNESE DA PLANÍCIE ALUVIAL NA REGIÃO DA CONFLUÊNCIA ENTRE OS RIOS IVAÍ E PARANÁ E EVIDÊNCIA DE SUA PALEOCONFLUÊNCIA

O estudo apresenta a morfogênese e os estágios de evolução geomorfológica na planície e confluência dos rios Ivaí e Paraná. Informações de sensoriamento remoto, análise de fácies sedimentares e geocronologia foram utilizadas para compartimentação, e elucidam a evolução geomorfológica da planície e confluência. As analises demonstram compartimentos onde o abandono da drenagem do rio Paraná possibilitou a migração da confluência e o leito encaixado e de maior profundidade do rio Ivaí

FATORES GEOMORFOLÓGICOS DETERMINANTES DO PROCESSO DE AVULSÃO: O VALE ALUVIAL DO RIO DO PEIXE, SP.

O estudo avaliou a geomorfologia do rio do Peixe, SP, e identificou aspectos que contribuíram para a formação e extensão de um processo de avulsão. Informações cartográficas, levantamentos em campo e dados hidrológicos foram usados nesta análise. Os resultados mostraram o maior processo de avulsão dos últimos 50 anos no rio do Peixe que alterou a rede de drenagem criando o único trecho multicanal. Os dados indicam a largura da planície e a reocupação de paleocanais como propulsores da avulsão

UPLC-MS-ESI-QTOF analysis and antifungal activity of the spondias tuberosa arruda leaf and root hydroalcoholic extracts

The aim of this study was to identify and evaluate the chemical compositions and effects of the S. tuberosa leaf and root hydroalcoholic extracts (HELST and HERST) against different strains of Candida. Chemical analysis was performed by Ultra-Performance Liquid Chromatography Coupled to Quadrupole/Time of Flight System (UPLC-MS-ESI-QTOF). The Inhibitory Concentration of 50% of the growth (IC50) as well as the intrinsic and combined action of the extracts with the antifungal fluconazole (FCZ) were determined by the microdilution method while the minimum fungicidal concentrations (MFCs) and the effect on fungal morphological transitions were analyzed by subculture and in humid chambers, respectively. From the preliminary phytochemical analysis, the phenols and flavonoids were the most abundant. The intrinsic IC50 values for HELST ranged from 5716.3 to 7805.8 \ub5g/mL and from 6175.4 to 51070.9 \ub5g/mL for the HERST, whereas the combination of the extracts with fluconazole presented IC50 values from 2.65 to 278.41 \ub5g/mL. The MFC of the extracts, individually, for all the tested strains was 6516384 \ub5g/mL. When fluconazole was combined with each extract, the MFC against CA URM 5974 was reduced (HELST: 2048 and HERST: 4096 \ub5g/mL). Synergism was observed against standard C. albicans (CA) and C. tropicalis (CT) strains and with the root extract against the CT isolate. The leaf extract inhibited the morphological transition of all strains while the root extract inhibited only CT strains

Guanylate-binding protein 5 licenses caspase-11 for Gasdermin-D mediated host resistance to Brucella abortus infection.

Innate immune response against Brucella abortus involves activation of Toll-like receptors (TLRs) and NOD-like receptors (NLRs). Among the NLRs involved in the recognition of B. abortus are NLRP3 and AIM2. Here, we demonstrate that B. abortus triggers non-canonical inflammasome activation dependent on caspase-11 and gasdermin-D (GSDMD). Additionally, we identify that Brucella-LPS is the ligand for caspase-11 activation. Interestingly, we determine that B. abortus is able to trigger pyroptosis leading to pore formation and cell death, and this process is dependent on caspase-11 and GSDMD but independently of caspase-1 protease activity and NLRP3. Mice lacking either caspase-11 or GSDMD were significantly more susceptible to infection with B. abortus than caspase-1 knockout or wild-type animals. Additionally, guanylate-binding proteins (GBPs) present in mouse chromosome 3 participate in the recognition of LPS by caspase-11 contributing to non-canonical inflammasome activation as observed by the response of Gbpchr3-/- BMDMs to bacterial stimulation. We further determined by siRNA knockdown that among the GBPs contained in mouse chromosome 3, GBP5 is the most important for Brucella LPS to be recognized by caspase-11 triggering IL-1β secretion and LDH release. Additionally, we observed a reduction in neutrophil, dendritic cell and macrophage influx in spleens of Casp11-/- and Gsdmd-/- compared to wild-type mice, indicating that caspase-11 and GSDMD are implicated in the recruitment and activation of immune cells during Brucella infection. Finally, depletion of neutrophils renders wild-type mice more susceptible to Brucella infection. Taken together, these data suggest that caspase-11/GSDMD-dependent pyroptosis triggered by B. abortus is important to infection restriction in vivo and contributes to immune cell recruitment and activation

Quantification of milk adulterants (starch, H2O2, and NaClO) using colorimetric assays coupled to smartphone image analysis

In this paper, a colorimetric method for the detection of milk adulterants using smartphone image analysis is reported. This is based on the reactions to detect hydrogen peroxide, sodium hypochlorite, and starch in milk, where a color variation is observed for each substance. The image analysis was performed by using lab-made apps (PhotoMetrix®, and RedGIM®) based on partial least squares regression with the histograms of the red-green-blue images. The image histograms are automatically calculated using the smartphone camera and processed within the app. The results have shown the capability of this method to predict the concentration of the three adulterants, demonstrating the potential of the use of digital images and smartphone applications associated with chemometric tools. This method presents a fast, low-cost, and portable way to quantify adulterants in Cow milk