Estrategias de afrontamiento de padres con niños en condición de discapacidad

La presente investigación se realizó con el objetivo de describir las estrategias de afrontamiento utilizadas por los padres de niños y niñas en condición de discapacidad, con el fin de identificar los recursos cognitivos y comportamentales que emplean los padres para resolver situaciones relacionadas con la condición de sus hijos. La muestra utilizada fue de 47 padres. Los instrumentos manipulados para la medición de las variables fueron: Apgar Familiar, elaborado por Gabriel Smilkstein (1978), la escala de sobrecarga del cuidador Zarith, elaborado por (Zarith, Rever y Bach-Peterson) y la escala de afrontamiento elaborada por (Tobin, Holroyd, Reynolds y Kigal, 1989. Adaptación por Cano, Rodríguez y García, 2006). Los resultados encontrados fueron, la mayoría de los padres de niños y niñas en estado de discapacidad se distribuyen entre sobrecarga intensa y sobrecarga moderada, sin embargo, la mayoría de estos niños conviven con familias que según la prueba de Apgar familiar son funcionales. Con respecto a las estrategias de afrontamiento se encontró que la mayoría de los padres de niños y niñas con discapacidad presentan estilos adecuados de afrontamiento en las siguientes dimensiones, evitación del problema, reestructuración cognitiva, expresión emocional, la dimensión de resolución de los padres presentan dificulta

The B Subunit of PirABvp Toxin Secreted from Vibrio parahaemolyticus Causing AHPND Is an Amino Sugar Specific Lectin

Vibrio parahaemolyticus (Vp) is the etiological agent of the acute hepatopancreatic necrosis disease (AHPND) in Penaeus vannamei shrimp. Vp possesses a 63–70 kb conjugative plasmid that encodes the binary toxin PirAvp/PirBvp. The 250 kDa PirABvp complex was purified by affinity chromatography with galactose-sepharose 4B and on a stroma from glutaraldehyde-fixed rat erythrocytes column, as a heterotetramer of PirAvp and PirBvp subunits. In addition, recombinant pirB (rPirBvp) and pirA (rPirAvp) were obtained. The homogeneity of the purified protein was determined by SDS-PAGE analysis, and the yield of protein was 488 ng/100 μg of total protein of extracellular products. The PirABvp complex and the rPirBvp showed hemagglutinating activity toward rat erythrocytes. The rPirAvp showed no hemagglutinating capacity toward the animal red cells tested. Among different mono and disaccharides tested, only GalNH2 and GlcNH2 were able to inhibit hemagglutination of the PirABvp complex and the rPirBvp. Glycoproteins showed inhibitory specificity, and fetuin was the glycoprotein that showed the highest inhibition. Other glycoproteins, such as mucin, and glycosaminoglycans, such as heparin, also inhibited the activity. Desialylation of erythrocytes enhanced the hemagglutinating activity. This confirms that Gal or Gal (β1,4) GlcNAc are the main ligands for PirABvp. The agglutinating activity of the PirABvp complex and the rPirBvp is not dependent on cations, because addition of Mg2+ or Ca2+ showed no effect on the protein capacity. Our results strongly suggest that the PirBvp subunit is a lectin, which is part of the PirA/PirBvp complex, and it seems to participate in bacterial pathogenicity

Th17 cells in autoimmune and infectious diseases

The view of CD4 T-cell-mediated immunity as a balance between distinct lineages of Th1 and Th2 cells has changed dramatically. Identification of the IL-17 family of cytokines and of the fact that IL-23 mediates the expansion of IL-17-producing T cells uncovered a new subset of Th cells designated Th17 cells, which have emerged as a third independent T-cell subset that may play an essential role in protection against certain extracellular pathogens. Moreover, Th17 cells have been extensively analyzed because of their strong association with inflammatory disorders and autoimmune diseases. Also, they appear to be critical for controlling these disorders. Similar to Th1 and Th2 cells, Th17 cells require specific cytokines and transcription factors for their differentiation. Th17 cells have been characterized as one of the major pathogenic Th cell populations underlying the development of many autoimmune diseases, and they are enhanced and stabilized by IL-23. The characteristics of Th17 cells, cytokines, and their sources, as well as their role in infectious and autoimmune diseases, are discussed in this review

New Insights into the Mechanism of Action of PirAB from Vibrio Parahaemolyticus

PirAB toxins secreted by Vibrio parahaemolyticus (Vp) harbor the pVA1 virulence plasmid, which causes acute hepatopancreatic necrosis disease (AHPND), an emerging disease in Penaeid shrimp that can cause 70–100% mortality and that has resulted in great economic losses since its first appearance. The cytotoxic effect of PirABVp on the epithelial cells of the shrimp hepatopancreas (Hp) has been extensively documented. New insights into the biological role of the PirBVp subunit show that it has lectin-like activity and recognizes mucin-like O-glycosidic structures in the shrimp Hp. The search for toxin receptors can lead to a better understanding of the infection mechanisms of the pathogen and the prevention of the host disease by blocking toxin–receptor interactions using a mimetic antagonist. There is also evidence that Vp AHPND changes the community structure of the microbiota in the surrounding water, resulting in a significant reduction of several bacterial taxa, especially Neptuniibacter spp. Considering these findings, the PirABvp toxin could exhibit a dual role of damaging the shrimp Hp while killing the surrounding bacteria

New Insights into the Mechanism of Action of PirAB from Vibrio Parahaemolyticus

PirAB toxins secreted by Vibrio parahaemolyticus (Vp) harbor the pVA1 virulence plasmid, which causes acute hepatopancreatic necrosis disease (AHPND), an emerging disease in Penaeid shrimp that can cause 70–100% mortality and that has resulted in great economic losses since its first appearance. The cytotoxic effect of PirABVp on the epithelial cells of the shrimp hepatopancreas (Hp) has been extensively documented. New insights into the biological role of the PirBVp subunit show that it has lectin-like activity and recognizes mucin-like O-glycosidic structures in the shrimp Hp. The search for toxin receptors can lead to a better understanding of the infection mechanisms of the pathogen and the prevention of the host disease by blocking toxin–receptor interactions using a mimetic antagonist. There is also evidence that Vp AHPND changes the community structure of the microbiota in the surrounding water, resulting in a significant reduction of several bacterial taxa, especially Neptuniibacter spp. Considering these findings, the PirABvp toxin could exhibit a dual role of damaging the shrimp Hp while killing the surrounding bacteria

High frequency of the risk allele of rs4132601 and rs11978267 from the IKZF1

Abstract Background IKZF1 is a relevant gene associated with the pathogenesis of acute lymphoblastic leukemia, and the rs4132601 (T>G) and rs11978267 (A>G) polymorphisms have been associated with the development of this disease in several populations. The aim of this study was to determine the allelic and genotypic frequencies of the rs4132601 and rs11978267 polymorphisms in two indigenous Mexican groups (Cora and Huichol) and Mestizo populations from Nayarit, Mexico, and compare them with the frequencies of both polymorphisms in other populations of the world. Methods One hundred, 116, and 100 subjects from the Mestizo, Huichol, and Cora populations, respectively, all of them residents of the state of Nayarit, Mexico, were analyzed. The frequencies of rs4132601 and rs11978267 were determined by allelic discrimination using TaqMan assays. Results The allelic frequencies of rs4132601 were as follows: Mestizo group T = 0.74, G = 0.26; Cora T = 0.745, G = 0.255; and Huichol T = 0.47, G = 0.53. In the case of the rs11978267 polymorphism, the allelic frequencies were Mestizo A = 0.745, G = 0.255; Cora A = 0.735, G = 0.265; and Huichol A = 0.457, G = 0.543. For each population, both polymorphisms were in Hardy–Weinberg equilibrium. Conclusion The Huichol population from Nayarit presented the highest frequencies of the risk allele reported to date in the whole world for both rs4132601 and rs11978267 polymorphisms

Detection of white spot syndrome virus in filtered shrimp-farm water fractions and experimental evaluation of its infectivity in Penaeus (Litopenaeus) vannamei

White spot syndrome virus (WSSV) may spread through water to neighbor ponds or farms. Routine water exchange and wastewater released during white spot disease (WSD)-emergency harvests may preserve WSSV in shrimp farming areas. To test this hypothesis, on-site experiments were performed in a WSSV-affected farm in Guasave, Sinaloa, Mexico. Plankton and shrimp hemolymph were collected from 12 ponds during a WSD outbreak. PCR analyses showed that 72% of the hemolymph pools (26 out of 36) were WSSV-positive. In contrast, only 14% (4 of 28) plankton samples (filtered through 10 and 0.45 µm) from three ponds (2, 7 and 10) were WSSV-positive. Plankton from pond 9 was WSSV-negative, but 14 days later, shrimp began to die. At this point, a differential filtration experiment was performed in pond 9. WSSV-positive samples were only found in three fractions [particulate fraction (PF) 1 µm and liquid fractions (LF) 0.65 µm) became WSSV-positive. Results indicate that water fractions between 100 and 0.65 µm induced WSSV infection to shrimp. Results showed that pond water and/or particulate fractions are vehicles for WSSV dispersion via virus suspended in water, attached to microalgae, or carried by zooplankton

Infection of WSSV-negative Shrimp, Litopenaeus vannamei, Cultivated under Fluctuating Temperature Conditions

To test whether effluents released from white spot syndrome virus (WSSV)-infected farm ponds are a pathway for spreading WSSV, WSSV-negative Pacific whiteleg shrimp, Litopenaeus vannamei, were exposed to WSSV-containing water under conditions of fluctuating water temperatures. White spot disease outbreaks occurred at the shrimp ponds before and during the experiment. Two cages were placed inside each test pond, and one was placed at the outlet canal. Each cage was stocked with 30 shrimp. Hemolymph from stocked shrimp was collected at intervals of 24, 48, 72, 120, 168, and 360 h after exposure and analyzed for presence of WSSV DNA by nested polymerase chain reaction. At diurnal variation of water temperature from 28.0 to 33.4 C, WSSV was detected as early as 120 h (ca. 11% of shrimp hemolymph pools) and 168 h (ca. 18% of shrimp hemolymph pools). WSSV was detected by 360 h (ca. 33% of shrimp hemolymph pools) in all cages, when water temperature varied from 24.9 to 28.5 C during a 48-h period. Cumulative mortality in cages inside ponds was ≤50.0 and 86.7% at the outlet canal. These data show that grow-out operations during the summer–autumn transition are at risk of WSSV outbreaks. The experiment demonstrated that WSSV can be spread by shrimp farm water drainage