Ocean warming and freshening effects on lipid metabolism in coastal Antarctic phytoplankton assemblages dominated by sub-Antarctic species.

Marine phytoplankton can utilize different strategies to cope with ocean warming and freshening from glacial melting in polar regions, which are disproportionally impacted by global warming. In the present study, we investigated the individual and combined effects of a 4 °C increase in seawater temperature (T+) and a 4 psu decrease in salinity (S-) from ambient values on biomass, nutrient use, fatty acid composition and lipid damage biochemistry of natural phytoplankton assemblages from Potter Cove (25 de Mayo/King George Island, Antarctica). Experiments were conducted by exposing the assemblages to four treatments during a 7-day incubation period using microcosm located along shore from January 23 to 31, 2016. The N:P ratio decreased in all treatments from day 4 onwards, but especially under high temperature (T+). Lipid damage was mainly detected under S0T+ and S-T+ conditions, and it decreased when the production of the antioxidant α-tocopherol increased. This antioxidant protection resulted in a build-up of phytoplankton biomass, especially at T+. Under the combined effect of both stressors (S-T+), the concentration of ω3 fatty acids increased, potentially leading to higher-quality FA composition. These results, which were related to the dominance of sub-Antarctic species in phytoplankton assemblages, contribute to the understanding of the potential consequences of ocean warming and increase seawater freshening on the trophic webs of the Southern Ocean.

Multicenter Diagnostic Accuracy Evaluation of the Luminex Aries Real-Time PCR Assay for Group B Streptococcus Detection in Lim Broth-Enriched Samples.

The vertical transmission of group B Streptococcus (GBS) strains causing neonatal sepsis is one of the leading reasons for neonatal mortality worldwide. The gold standard for GBS detection is enriched culture with or without the aid of chromogenic agars. Given the high risk for morbidity and mortality in this population, high assay sensitivity is required to prevent the personal and economic costs of GBS disease. Nucleic acid amplification tests (NAATs) allow for objective determination of GBS colonization with a sensitivity and a specificity higher than those of traditional culture methods. In this study, we determined the analytical and clinical performance of the Aries GBS assay compared to those of the enrichment culture method, biochemical identification, and the NAATs used at the study sites. Remnant Lim broth samples were used to perform the Aries assay and reference testing. Upon first testing using enriched culture as the reference standard, the Aries GBS assay identified GBS with a 96.1% sensitivity (95% confidence interval [CI], 91.2 to 98.7%) and a 91.4% specificity (95% CI, 88.8 to 93.6%). The test performed with 100% positive agreement (95% CI, 83.2 to 100%) compared to the results of the BD Max GBS assay and 98.0% positive agreement (95% CI, 89.2 to 99.9%) compared to the results of the Cepheid Xpert GBS LB test. Repeatability and reproducibility were maintained in intra- and interlaboratory testing, regardless of the instrument, module, or user who performed the test. The Aries GBS assay can be set up in less than 5 min and produces results in 2 h. The easy setup, with minimal hands-on time, and high assay sensitivity and specificity make this a useful testing option for GBS screening in prepartum women.

Fast Screening of Polycyclic Aromatic Hydrocarbons using Trapped Ion Mobility Spectrometry - Mass Spectrometry.

In the present paper, we showed the advantages of trapped ion mobility spectrometry coupled too mass spectrometry (TIMS-MS) combined with theoretical calculations for fast identification (millisecond timescale) of polycyclic aromatic hydrocarbons (PAH) compounds from complex mixtures. Accurate PAH collision cross sections (CCS, in nitrogen as a bath gas) are reported for the most commonly encountered PAH compounds and the ability to separate PAH geometric isomers is shown for three isobaric pairs with mobility resolution exceeding 150 (3-5 times higher than conventional IMS devices). Theoretical candidate structures (optimized at the DFT/B3LYP level) are proposed for the most commonly encountered PAH compounds showing good agreement with the experimental CCS values (<5%). The potential of TIMS-MS for the separation and identification of PAH compounds from complex mixtures without the need of lengthy pre-separation steps is illustrated for the case of a complex soil mixture.

Neuroendocrine system of the digestive tract in Rhamdia quelen juvenile: an immunohistochemical study.

In this work, an immunohistochemical study was performed to determine the distribution and relative frequencies of some neuromodulators of the digestive tract of silver catfish (Rhamdia quelen). The digestive tract of silver catfish was divided into six portions; the oesophagus, stomach, intestine (ascendant, descendant and convoluted segments), and rectum. Immunohistochemical method using a pool of specific antisera against-gastrin, -cholecystokinin-8, -leu-enkephalin, -neuropeptide Y, -calcitonin gene-related peptide (CGRP), and -vasoactive intestinal peptide (VIP) was employed. Immunoreactivity to all antisera was identified in neuroendocrine cells (NECs) localized in the gut epithelium, although no reaction was observed in the oesophagus or stomach. The morphology of NECs immunopositive to each antibody was similar. They were slender in shape, with basally located nucleus, and their main axis perpendicular to the basement membrane. The number of NECs immunoreactive to all antisera was higher in the ascendant and descendant intestine, exhibiting a decreasing trend toward distal segments of the gut. In addition, immunoreactivity to CGRP and VIP was observed in the myenteric plexus and nerve fibers distributed in the mucosal, submucosal and muscular layers. The higher number of immunopositive NECs in the ascendant and descendant intestine may indicate the primary role of these segments in the control of food intake by means of orexigenic and anorexigenic peripheral signals.

Morphology, histology and histochemistry of the digestive system of South American Catfish (Rhamdia quelen) / Morfología, histología e histoquímica del tubo digestivo del Bagre Sudamericano (Rhamdia quelen)

The purpose of the present work was the anatomical, histo logical and histochemical description oí Rhamdia quelen juvenile digestive system. Samples of gut were fixed, dehydrated and included in paraffin and then stained with haematoxylin and eosin. For the identification and differentiation of mucosubstances the preparations were treated with Periodic Acid Schiff, Alcian Blue pH 0,4 and 2,5 andPAS/AB pH 2,5. Anatomical details of the oesophagus were like a short tube with primary and secondary mucous folds. The stratified epithelium is composed of three cellular types: small cells, abundant goblet cells with acid and neutral mucosubstances (MS) and large acid cells. The stomach is J-shaped and its mucosa presents broad and deep folds in relaxing state. Histologically, the stomach shows three different regions: cardiac, fundic and pyloric region. The luminal surface of the epithelium consists of a layer of secretory columnar cells of neutral MS. Tubuloacinar glands were surrounded by connective and muscular smooth fibers bundle. The intestine extends from the stomach until the anus, and four different sections can be distinguished: ascending, descending, convoluta and terminal straight. It was identified a simple columnar epithelium mainly composed by two cellular types: absorptive cell and goblet cell neutral MS secretory. On the basis of the anatomical and histo logical study carried out, we conclude that R. quelen presents an alimentary canal compatible with species that possess omnivorous nutritious habits.

El propósito del presente trabajo fue realizar las descripciones anatómica, histológica e histoqufmica del sistema digestivo de Rhamdia quelen jóvenes. Las muestras de intestino fueron fijadas, deshidratadas e incluidas en parafina y posteriormente teñidas con hematoxilina y eosina. Para la identificación y diferenciación de muco substancias los preparados fueron tratados con ácido periódico de Schiff, Azul Alcian pH 0,4 y 2,5 y PAS/AB pH 2,5. Los detalles anatómicos del esófago mostraron un pequeño tubo con pliegues mucosos primarios y secundarios. El epitelio estratificado presentaba tres tipos celulares: células pequeñas, abundantes células caliciformes con muco substancia (MS) acida y neutra y células grandes acidas. El estómago tenía forma de J y su mucosa presenta pliegues amplios y profundos en estado de relajación. Histológicamente, el estómago mostraba tres diferentes regiones: cardiaca, fúndica y pilórica. La superficie luminal del epitelio constaba de una capa de células columnares secretoras de MS neutro. Glándulas tubuloacinares estaban rodeadas por tejido conjuntivo y fibras musculares lisas. El intestino se extendía desde el estómago hasta el ano, y cuatro diferentes secciones era posible distinguir: ascendente, descendente, convoluta y terminal recta. Se identificó un epitelio columnar simple, compuesto principalmente por dos tipos celulares: células de absorción y células caliciformes secretoras de MS neutra. Sobre la base de los estudios anatómico e histológico realizados, se concluye que R. quelen presenta un canal alimentario compatible con las especies que poseen hábitos nutritivos omnívoros.

CEBPG regulates ERCC5/XPG expression in human bronchial epithelial cells and this regulation is modified by E2F1/YY1 interactions.

Marked inter-individual variation in lung cancer risk cannot be accounted for solely by cigarette smoke and other environmental exposures. Evidence suggests that variation in bronchial epithelial cell expression of key DNA repair genes plays a role. Variation in these genes correlates with variation in expression of CEBPG and E2F1 transcription factors. Here, we investigated the mechanistic basis for correlation of the DNA repair gene ERCC5 (previously known as XPG) with CEBPG and E2F1. CEBPG expression vector transfected into H23 or H460 cell lines up-regulated endogenous ERCC5 and also luciferase from a reporter construct containing 589 bp of ERCC5 5' regulatory region. A recognition site for CEBPG and a region containing sites for YY1 on the sense strand and E2F1 on the anti-sense strand participated in CEBPG up-regulation of ERCC5. CEBPG, E2F1 and YY1 binding to their respective sites were confirmed by electrophoretic mobility shift assay. Thus, we conclude that CEBPG regulates ERCC5 expression and this regulation is modified by E2F1/YY1 interactions. Several polymorphisms have been identified in these regions and, based on the data presented here, it is reasonable to hypothesize that they may contribute to risk for bronchogenic carcinoma.