A Further Unique Chondroitin Sulfate from the shrimp Litopenaeus vannamei with Antithrombin Activity that Modulates Acute Inflammation

The detailed structure of a further Chondroitin Sulfate from Litopenaeus vannamei shrimp (sCS) is described. The backbone structure was established by 1H/13C NMR, which identified 3-O-sulfated GlcA, 4-O-sulfated GalNAc, 6-O-sulfated GalNAc, and 4,6-di-O-sulfated GalNAc residues. GlcA is linked to GalNAc 4,6 di S and GlcA 3S is linked to GalNAc 4S, GalNAc 4,6 di-S and GalNAc6S residues. The anticoagulant properties of this sCS were evaluated by activated partial thromboplastin time, anti-IIa, anti-Xa and anti-heparin cofactor II-mediated activities, and sCS failed to stabilise antithrombin in a fluoresence shift assay. The anti-inflammatory effect of sCS was explored using a model of acute peritonitis, followed by leukocyte count and measurement of the cytokines, IL-1β, IL-6 and TNF-α. The compound showed low clotting effects, but high anti-IIa activity and HCII-mediated thrombin inhibition. Its anti-inflammatory effect was shown by leukocyte recruitment inhibition and a decrease in pro-inflammatory cytokine levels. Although the biological role of sCS remains unknown, its properties indicate that it is suitable for studies of multi-potent molecules obtained from natural sources

Benznidazole biotransformation and multiple targets in <i>Trypanosoma</i> cruzi revealed by metabolomics

&lt;b&gt;Background&lt;/b&gt;&lt;p&gt;&lt;/p&gt; The first line treatment for Chagas disease, a neglected tropical disease caused by the protozoan parasite Trypanosoma cruzi, involves administration of benznidazole (Bzn). Bzn is a 2-nitroimidazole pro-drug which requires nitroreduction to become active, although its mode of action is not fully understood. In the present work we used a non-targeted MS-based metabolomics approach to study the metabolic response of T. cruzi to Bzn.&lt;p&gt;&lt;/p&gt; &lt;b&gt;Methodology/Principal findings&lt;/b&gt;&lt;p&gt;&lt;/p&gt; Parasites treated with Bzn were minimally altered compared to untreated trypanosomes, although the redox active thiols trypanothione, homotrypanothione and cysteine were significantly diminished in abundance post-treatment. In addition, multiple Bzn-derived metabolites were detected after treatment. These metabolites included reduction products, fragments and covalent adducts of reduced Bzn linked to each of the major low molecular weight thiols: trypanothione, glutathione, γ-glutamylcysteine, glutathionylspermidine, cysteine and ovothiol A. Bzn products known to be generated in vitro by the unusual trypanosomal nitroreductase, TcNTRI, were found within the parasites, but low molecular weight adducts of glyoxal, a proposed toxic end-product of NTRI Bzn metabolism, were not detected.&lt;p&gt;&lt;/p&gt; &lt;b&gt;Conclusions/significance&lt;/b&gt;&lt;p&gt;&lt;/p&gt; Our data is indicative of a major role of the thiol binding capacity of Bzn reduction products in the mechanism of Bzn toxicity against T. cruzi

Contribution of microscopy for understanding the mechanism of action against trypanosomatids

Transmission electron microscopy (TEM) has proved to be a useful tool to study the ultrastructural alterations and the target organelles of new antitrypanosomatid drugs. Thus, it has been observed that sesquiterpene lactones induce diverse ultrastructural alterations in both T. cruzi and Leishmania spp., such as cytoplasmic vacuolization, appearance of multilamellar structures, condensation of nuclear DNA, and, in some cases, an important accumulation of lipid vacuoles. This accumulation could be related to apoptotic events. Some of the sesquiterpene lactones (e.g., psilostachyin) have also been demonstrated to cause an intense mitochondrial swelling accompanied by a visible kinetoplast deformation as well as the appearance of multivesicular bodies. This mitochondrial swelling could be related to the generation of oxidative stress and associated to alterations in the ergosterol metabolism. The appearance of multilamellar structures and multiple kinetoplasts and flagella induced by the sesquiterpene lactone psilostachyin C indicates that this compound would act at the parasite cell cycle level, in an intermediate stage between kinetoplast segregation and nuclear division. In turn, the diterpene lactone icetexane has proved to induce the external membrane budding on T. cruzi together with an apparent disorganization of the pericellar cytoskeleton. Thus, ultrastructural TEM studies allow elucidating the possible mechanisms and the subsequent identification of molecular targets for the action of natural compounds on trypanosomatids.Fil: Lozano, Esteban Sebastián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Medicina y Biología Experimental de Cuyo; ArgentinaFil: Spina Zapata, Renata María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Barrera, Patricia Andrea. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Tonn, Carlos Eugenio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Investigaciones en Tecnología Química. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Investigaciones en Tecnología Química; ArgentinaFil: Sosa Escudero, Miguel Angel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentin

Use of five probiotic strains to determine sensitivity in vitro on pathogenic bacteria growth isolated from sick fishes

ABSTRACT Ornamental aquaculture is an activity in clear economic growth, both globally and in Mexico where the development is particularly relevant to freshwater species. Infectious diseases produced by fungus, bacteria and virus are considered one of the principal limitations during the productive process. Between implemented strategies for reduction of antibiotic use, which are &quot;living microorganisms that confer a health benefit to the host if they are given in adequate quantities&quot;; lactic acid bacteria and yeast are among the most common used microorganism in aquaculture. This investigation, prove the effect of isolated probiotic bacteria from the digestive tract of healthy fish, belonging to specie: Bacillus sp., Bacillus laterosporus, Bacillus subtilis, Lactobacillus sp, and Lactococcus lactis, at different dilutions (10 9 ,10 8 , 10 7 ,10 6 , 10 5 and 10 4 ) in vitro growth of pathogenic bacteria: Citrobacter freundii, Enterobacter sakasakii, Klebsiella oxytoca, Proteus vulgaris, and Vibrio fluvialis, isolated from kidney of sick fish, cultured and purified through successive inoculations and identificated by the amplification of gene 16S of rRNA (PCR) using universal primers 8 for. (5&apos;-AGACTTTGATCATGGCTCAG-3&apos;) and 1492 rev. (5&apos;-TACGGCTACCTTGTTACGACTT-3&apos;) and comparison with GENEBANK sequences base. Probiotic strains were previously isolated from the digestive tract of different healthy fish in the laboratory. In order to perform in vitro challenge tests, pathogenic strains were inoculated three times each in BHI agar boxes at a concentration of 1x10 7 CFU mL -1 and subsequently using the well diffusion method, 70 µL from a suspension with each of the probiotic strains were added. Agar boxes were incubated 24 h at 30ºC to observe the formation of inhibition halos. Obtained values from inhibition halos were transformed to qualitative data with the following premise: halo diameter &lt; 2.0 mm negative effect; halo diameter &gt; 2.0 mm positive effect. In this study, it was determined that probiotic strains B. subtilis was the one that gave better results to inhibit the growth of pathogenic bacteria P. vulgaris, E. sakazakii, V. fluvialis, K. oxytoca and C. freundii in most of used dilutions. Making it a strain with high potential in aquaculture. Key words: Growth, halos, probiotics, bacteria, sensibility. RESUMEN La acuicultura de especies ornamentales es una actividad económica en franco crecimiento, tanto a nivel mundial como en México, en donde tiene particular desarrollo lo correspondiente a especies dulceacuícolas. Las enfermedades infeccionas producidas por hongos, bacterias y virus, están consideradas una de las limitantes principales durante el proceso productivo. Entre las estrategias implementadas para disminuir el uso de antibióticos para el control de patógenos, se encuentra el control biológico mediante el uso de organismos probióticos, los cuales son &quot;microorganismos vivos los cuales, administrados en cantidades adecuadas, confieren un beneficio en la salud del hospedador&quot;; entre los de uso más común en acuicultura se encuentran las lactobacterias y las levaduras. En el presente trabajo, se probó el efecto de bacterias probióticas aisladas del tracto digestivo de peces sanos, pertenecientes a las especies: Bacillus sp., Bacillus laterosporus, Bacillus subtilis, Lactobacillus sp, y Lactococcus lactis, a diferentes diluciones (10 9 ,10 8 , 10 7 ,10 6 , 10 5 y 10 4 ) en el crecimiento in vitro de las bacterias patógenas: Citrobacter freundii, Enterobacter sakasakii, Klebsiella oxytoca, Proteus vulgaris y Vibrio fluvialis, aisladas del riñón de peces enfermos, cultivadas y purificadas a través de resiembras sucesivas e identificadas mediante la amplificación del gen 16S del ARNr (PCR) utilizando los primers universales 8 for. 24 AGACTTTGATCATGGCTCAG-3&apos;) y 1492 rev. (5&apos;-TACGGCTACCTTGTTACGACTT-3&apos;) y su comparación con la base de secuencias GENEBANK. Las cepas probióticos fueron aisladas previamente del tracto intestinal de diversos peces sanos en el laboratorio. Para llevar a cabo las pruebas de desafío in vitro, las cepas patógenas se sembraron por triplicado en cajas de agar BHI a una concentración de 1x10 7 UFC mL -1 y posteriormente, utilizando el método de difusión en pozos, se adicionaran 70 µL de una suspensión con cada una de las cepas probióticas Las placas se incubaron durante 24 h a 30ºC para observar la formación de halos de inhibición. Los valores obtenidos de los halos de inhibición fueron transformados a datos cualitativos con la siguiente premisa: diámetro halo &lt; 2.0 mm efecto negativo; diámetro de halo &gt; 2.0 mm efecto positivo. En este estudio, se determinó que la cepas probiótica B. subtilis fue la que dio mejores resultados al inhibir el crecimiento de las bacterias patógenas P. vulgaris, E. sakazakii, V. fluvialis, K. oxytoca y C. freundii en la mayoría de las diluciones utilizadas. Por lo que es una cepa con alto potencial en acuicultura

Silencing cytokeratin 18 gene inhibits intracellular replication of Trypanosoma cruzi in HeLa cells but not binding and invasion of trypanosomes

<p>Abstract</p> <p>Background</p> <p>As an obligatory intracellular parasite, <it>Trypanosoma cruzi</it>, the etiological agent of Chagas' disease, must invade and multiply within mammalian cells. Cytokeratin 18 (CK18) is among the host molecules that have been suggested as a mediator of important events during <it>T. cruzi</it>-host cell interaction. Based on that possibility, we addressed whether RNA interference (RNAi)-mediated down regulation of the CK18 gene could interfere with the parasite life cycle <it>in vitro</it>. HeLa cells transiently transfected with CK18-RNAi had negligible levels of CK18 transcripts, and significantly reduced levels of CK18 protein expression as determined by immunoblotting or immunofluorescence.</p> <p>Results</p> <p>CK18 negative or positive HeLa cells were invaded equally as well by trypomastigotes of different <it>T. cruzi </it>strains. Also, in CK18 negative or positive cells, parasites recruited host cells lysosomes and escaped from the parasitophorous vacuole equally as well. After that, the growth of amastigotes of the Y or CL-Brener strains, was drastically arrested in CK18 RNAi-treated cells. After 48 hours, the number of amastigotes was several times lower in CK18 RNAi-treated cells when compared to control cells. Simultaneous staining of parasites and CK18 showed that in HeLa cells infected with the Y strain both co-localize. Although the amastigote surface protein-2 contains the domain VTVXNVFLYNR previously described to bind to CK18, in several attempts, we failed to detect binding of a recombinant protein to CK-18.</p> <p>Conclusion</p> <p>The study demonstrates that silencing CK18 by transient RNAi, inhibits intracellular multiplication of the Y and CL strain of <it>T. cruzi </it>in HeLa cells, but not trypanosome binding and invasion.</p