14 research outputs found

    Immobilization of the white-rot fungus Anthracophyllum discolor to degrade the herbicide atrazine

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    Herbicides cause environmental concerns because they are toxic and accumulate in the environment, food products and water supplies. There is a need to develop safe, efficient and economical methods to remove them from the environment, often by biodegradation. Atrazine is such herbicide. White-rot fungi have the ability to degrade herbicides of potential utility. This study formulated a novel pelletized support to immobilize the white-rot fungus Anthracophyllum discolor to improve its capability to degrade the atrazine using a biopurification system (BS). Different proportions of sawdust, starch, corn meal and flaxseed were used to generate three pelletized supports (F1, F2 and F3). In addition, immobilization with coated and uncoated pelletized supports (CPS and UPS, respectively) was assessed. UPS-F1 was determined as the most effective system as it provided high level of manganese peroxidase activity and fungal viability. The half-life (t1/2) of atrazine decreased from 14 to 6 days for the control and inoculated samples respectively. Inoculation with immobilized A. discolor produced an increase in the fungal taxa assessed by DGGE and on phenoloxidase activity determined. The treatment improves atrazine degradation and reduces migration to surface and groundwater.Grant CONICYT/FONDAP/15130015Grant FONDECYT 112096

    Disease Severity in Patients Infected with Leishmania mexicana Relates to IL-1β

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    Leishmania mexicana can cause both localized (LCL) and diffuse (DCL) cutaneous leishmaniasis, yet little is known about factors regulating disease severity in these patients. We analyzed if the disease was associated with single nucleotide polymorphisms (SNPs) in IL-1β (−511), CXCL8 (−251) and/or the inhibitor IL-1RA (+2018) in 58 Mexican mestizo patients with LCL, 6 with DCL and 123 control cases. Additionally, we analyzed the in vitro production of IL-1β by monocytes, the expression of this cytokine in sera of these patients, as well as the tissue distribution of IL-1β and the number of parasites in lesions of LCL and DCL patients. Our results show a significant difference in the distribution of IL-1β (−511 C/T) genotypes between patients and controls (heterozygous OR), with respect to the reference group CC, which was estimated with a value of 3.23, 95% CI = (1.2, 8.7) and p-value = 0.0167), indicating that IL-1β (−511 C/T) represents a variable influencing the risk to develop the disease in patients infected with Leishmania mexicana. Additionally, an increased in vitro production of IL-1β by monocytes and an increased serum expression of the cytokine correlated with the severity of the disease, since it was significantly higher in DCL patients heavily infected with Leishmania mexicana. The distribution of IL-1β in lesions also varied according to the number of parasites harbored in the tissues: in heavily infected LCL patients and in all DCL patients, the cytokine was scattered diffusely throughout the lesion. In contrast, in LCL patients with lower numbers of parasites in the lesions, IL-1β was confined to the cells. These data suggest that IL-1β possibly is a key player determining the severity of the disease in DCL patients. The analysis of polymorphisms in CXCL8 and IL-1RA showed no differences between patients with different disease severities or between patients and controls

    Comparison of vision with multifocal contact lenses and SimVis Gekko simulations in a clinical site

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    ARVO Annual Meeting Abstract, June 202

    A second update on mapping the human genetic architecture of COVID-19

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    Rhizobium Presence and Functions in Microbiomes of Non-leguminous Plants

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    The genus Rhizobium is well known in the context of its interaction with leguminous plants. The symbiosis Rhizobium-legume constitutes a significant source of ammonia in the biosphere. Rhizobium species have been studied and applied as biofertilizers for decades in legumes and nonlegumes, due to the potential as N-fixer and plant growth promoter. Since its discovery, conventional culture-dependent techniques were used to isolate Rhizobium members from their natural niche, the nodule, and their identification was routinely performed via 16S rRNA gene and different housekeeping genes. Biotechnological advances based on the use of omics-based technologies showed that species belonging to the genus Rhizobium are keystone taxa in several diverse environments, such as forests, agricultural land, Arctic, and Antarctic ecosystems, contaminated soils and plant-associated microbiota. In this chapter, we will summarize the advances in the study of the Rhizobium genus, from culturomics strategies to modern omics methodologies, mostly based on next-generation sequencing approaches. These cutting-edge molecular approaches are fundamental in the study of the behavior of Rhizobium species in their interaction with Non-leguminous plants, supporting their potential as an ecological alternative to chemical fertilizers in the battle against Climatic Change
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