Immune Modulation Ability of Hepcidin from Teleost Fish.

Antimicrobial peptides (AMP) play an essential role in the innate immune system, modulating the defense response. In a previous study, we demonstrated the antimicrobial activity of synthetic hepcidin (hep20) from rainbow trout (Oncorhynchus mykiss), and its protective effect in European sea bass (Dicentrarchus labrax) challenged with Vibrio anguillarum. Additionally, we described the uptake and distribution of hep20 in different tissues and leukocyte cells. Interestingly, various AMPs characterized in high vertebrates, called host defense peptides (HDPs), also possess immunomodulation activity. For that reason, the present study explores the immunomodulatory abilities of hep20 through in vitro and in vivo studies. First, a monocyte/macrophage RTS-11 cell line from rainbow trout was used to evaluate hep20 effects on pro- and anti-inflammatory cytokines in fish leukocyte cells. Next, the European sea bass juveniles were used to determine if hep20 can regulate the expression of cytokines in fish immune tissues. The results show that hep20 was uptake inner to RTS-11 cells and was able to induce the expression of IL-10, IL-1ß, and TNFα at transcriptional and protein levels. Then, the European sea bass juveniles were given intraperitoneal injections of the peptide. At 1, 3, 7, 14, and 21 days post-injection (dpi), IL-10, IL -1ß, and TNFα mRNA were quantified in the anterior gut, spleen, and head kidney. The hep20 was able to up-regulate cytokine gene expression in these tissues, mainly in the head kidney. Furthermore, the evaluated cytokines showed a cyclical tendency of higher to lesser expression. Finally, a bioinformatics analysis showed that the structure adopted by hep20 is similar to the γ-core domain described for cysteine-stabilized AMP, defined as immunomodulatory and antimicrobial, which could explain the ability of hep20 to regulate the cytokine expression. This study provides new insights into immunomodulatory function complementary to the previously established antimicrobial activity of hep20, suggesting a role as an HDP in teleost fish. These facts are likely to be associated with molecular functions underpinning the protective effect of fish hepcidin against pathogens.

Dietary supplementation of Bacillus velezensis improves Vibrio anguillarum clearance in European sea bass by activating essential innate immune mechanisms.

Bacillus spp. supplementation as probiotics in cultured fish diets has a long history of safe and effective use. Specifically, B. velezensis show great promise in fine-tuning the European sea bass disease resistance against the pathogenicity caused by several members of the Vibrio family. However, the immunomodulatory mechanisms behind this response remain poorly understood. Here, to examine the inherent immune variations in sea bass, two equal groups were fed for 30 days with a steady diet, with one treatment supplemented with B. velezensis. The serum bactericidal capacity against live cells of Vibrio anguillarum strain 507 and the nitric oxide and lysozyme lytic activities were assayed. At the cellular level, the phagocytic response of peripheral blood leukocytes against inactivated Candida albicans was determined. Moreover, head-kidney (HK) total leukocytes were isolated from previously in vivo treated fish with LPS of V. anguillarum strain 507. Mechanistically, the expression of some essential proinflammatory genes (interleukin-1 (il1b), tumor necrosis factor-alpha (tnfa), and cyclooxygenase 2 (cox2) and the sea bass specific antimicrobial peptide (AMP) dicentracin (dic) expressions were assessed. Surprisingly, the probiotic supplementation significantly increased all humoral lytic and cellular activities assayed in the treated sea bass. In addition, time-dependent differences were observed between the control and probiotic treated groups for all the HK genes markers subjected to the sublethal LPS dose. Although the il1b was the fastest responding gene to a significant level at 48 h post-injection (hpi), all the other genes followed 72 h in the probiotic supplemented group. Finally, an in vivo bacteria challenge against live V. anguillarum was conducted. The probiotic fed fish observed a significantly higher survival. Overall, our results provide clear vertical evidence on the beneficial immune effects of B. velezensis and unveil some fundamental immune mechanisms behind its application as a probiotic agent in intensively cultured European sea bass.

Dietary Phytogenics and Galactomannan Oligosaccharides in Low Fish Meal and Fish Oil-Based Diets for European Sea Bass (Dicentrarchus labrax) Juveniles: Effects on Gill Structure and Health and Implications on Oxidative Stress Status.

An effective replacement for fish meal (FM) and fish oil (FO) based on plant-based raw materials in the feed of marine fish species is necessary for the sustainability of the aquaculture sector. However, the use of plant-based raw materials to replace FM and FO has been associated with several negative health effects, some of which are related to oxidative stress processes that can induce functional and morphological alterations in mucosal tissues. This study aimed to evaluate the effects of dietary oligosaccharides of plant origin (5,000 ppm; galactomannan oligosaccharides, GMOS) and a phytogenic feed additive (200 ppm; garlic oil and labiatae plant extract mixture, PHYTO) on the oxidative stress status and mucosal health of the gills of juvenile European sea bass (Dicentrarchus labrax). The experimental diets, low FM and FO diets (10%FM/6%FO) were supplemented with GMOS from plant origin and PHYTO for 63 days. GMOS and PHYTO did not significantly affect feed utilization, fish growth, and survival. GMOS and PHYTO downregulated the expression of ß-act, sod, gpx, cat, and gr in the gills of the fish compared with that in fish fed the control diet. The expression of hsp70 and ocln was upregulated and downregulated, respectively, in the GMOS group compared with that in the control group, whereas the expression of zo-1 was downregulated in the PHYTO group compared with that in the GMOS group. The morphological, histopathological, immunohistochemical, and biochemical parameters of the fish gills were mostly unaffected by GMOS and PHYTO. However, the PHYTO group had lower incidence of lamellar fusion than did the control group after 63 days. Although the tissular distribution of goblet cells was unaffected by GMOS and PHYTO, goblet cell size showed a decreasing trend (-11%) in the GMOS group. GMOS and PHYTO significantly reduced the concentration of PCNA+ in the epithelium of the gills. The above findings indicated that GMOS and PHYTO in low FM/FO-based diets protected the gill epithelia of D. labrax from oxidative stress by modulating the expression of oxidative enzyme-related genes and reducing the density of PCNA+ cells in the gills of the fish.

Dietary phytogenics and galactomannan oligosaccharides in low fish meal and fish oil-based diets for European sea bass (Dicentrarchus labrax) juveniles: Effects on gut health and implications on in vivo gut bacterial translocation.

European sea bass were fed four low FM/FO (10%/6%) diets containing galactomannan oligosaccharides (GMOS), a mixture of garlic oil and labiatae plants oils (PHYTO), or a combination of both functional products (GMOSPHYTO) for 63 days before exposing the fish to an intestinal Vibrio anguillarum infection combined with crowding stress. In order to evaluate functional diets efficacy in terms of gut health maintenance, structural, cellular, and immune intestinal status were evaluated by optical and electron microscopy and gene expression analyses. A semi-automated software was adapted to determine variations in goblet cell area and mucosal mucus coverage during the challenge test. Feeding with functional diets did not affect growth performance; however, PHYTO and GMOS dietary inclusion reduced European sea bass susceptibility to V. anguillarum after 7 days of challenge testing. Rectum (post-ileorectal valve) showed longer (p = 0.001) folds than posterior gut (pre-ileorectal valve), whereas posterior gut had thicker submucosa (p = 0.001) and higher mucus coverage as a result of an increased cell density than rectum. Functional diets did not affect mucosal fold length or the grade of granulocytes and lymphocytes infiltration in either intestinal segment. However, the posterior gut fold area covered by goblet cells was smaller in fish fed GMOS (F = 14.53; p = 0.001) and PHYTO (F = 5.52; p = 0.019) than for the other diets. PHYTO (F = 3.95; p = 0.049) reduced posterior gut goblet cell size and increased rodlet cell density (F = 3.604; p = 0.068). Dietary GMOS reduced submucosal thickness (F = 51.31; p = 0.001) and increased rodlet cell density (F = 3.604; p = 0.068) in rectum. Structural TEM analyses revealed a normal intestinal morphological pattern, but the use of GMOS increased rectum microvilli length, whereas the use of PHYTO increased (p≤0.10) Ocln, N-Cad and Cad-17 posterior gut gene expression. After bacterial intestinal inoculation, posterior gut of fish fed PHYTO responded in a more controlled and belated way in terms of goblet cell size and mucus coverage in comparison to other treatments. For rectum, the pattern of response was similar for all dietary treatments, however fish fed GMOS maintained goblet cell size along the challenge test.

Human neutrophils phagocytose and kill Acinetobacter baumannii and A. pittii.

Acinetobacter baumannii is a common cause of health care associated infections worldwide. A. pittii is an opportunistic pathogen also frequently isolated from Acinetobacter infections other than those from A. baumannii. Knowledge of Acinetobacter virulence factors and their role in pathogenesis is scarce. Also, there are no detailed published reports on the interactions between A. pittii and human phagocytic cells. Using confocal laser and scanning electron microscopy, immunofluorescence, and live-cell imaging, our study shows that immediately after bacteria-cell contact, neutrophils rapidly and continuously engulf and kill bacteria during at least 4 hours of infection in vitro. After 3 h of infection, neutrophils start to release neutrophil extracellular traps (NETs) against Acinetobacter. DNA in NETs colocalizes well with human histone H3 and with the specific neutrophil elastase. We have observed that human neutrophils use large filopodia as cellular tentacles to sense local environment but also to detect and retain bacteria during phagocytosis. Furthermore, co-cultivation of neutrophils with human differentiated macrophages before infections shows that human neutrophils, but not macrophages, are key immune cells to control Acinetobacter. Although macrophages were largely activated by both bacterial species, they lack the phagocytic activity demonstrated by neutrophils.

Acinetobacter baumannii and A. pittii clinical isolates lack adherence and cytotoxicity to lung epithelial cells in vitro.

The molecular and genetic basis of Acinetobacter baumannii and Acinetobacter pittii virulence remains poorly understood, and there is still lack of knowledge in host cell response to these bacteria. In this study, we have used eleven clinical Acinetobacter strains (A. baumannii n = 5; A. pittii n = 6) to unravel bacterial adherence, invasion and cytotoxicity to human lung epithelial cells. Our results showed that adherence to epithelial cells by Acinetobacter strains is scarce and cellular invasion was not truly detected. In addition, all Acinetobacter strains failed to induce any cytotoxic effect on A549 cells.

Experimental Lactococcus garvieae infection in zebrafish and first evidence of its ability to invade non-phagocytic cells.

Zebrafish has been used for studying infections and host-pathogen interactions in different bacterial fish pathogens. In the present study we evaluated the ability of Lactococcus garvieae to infect zebrafish when inoculated intraperitoneally with 2 × 10(7)UFC of this pathogen. L. garvieae can colonize and invade zebrafish at multiple anatomical sites causing a lethal acute septicemic infection with clinical signs and lesions consistent with those observed in lactococcosis outbreaks. Immunohistochemical studies showed the presence of L. garvieae into macrophages as well as into non-phagocytic zebrafish cells of liver (hepatocytes). The internalization capacity showed by L. garvieae in zebrafish cells was confirmed in the rainbow trout cell line RTG-2. Our results provide the first evidence that L. garvieae is able to invade non-phagocytic host cells.

Interaction of macrophages with a cytotoxic Serratia liquefaciens human isolate.

Macrophages play key roles in host defense by recognizing, engulfing, and killing microorganisms. Understanding the response of macrophages to pathogens may provide insights into host defenses and the tactics used by pathogens to circumvent these defenses. In the present study, we investigated the interaction between a clinical isolate of Serratia liquefaciens and macrophages. S. liquefaciens strain HUMV-3250 triggers a fast and potent cytotoxic effect upon infection. This process requires the presence of live bacteria, adherence, and protein synthesis but not phagocytosis/bacterial internalization. Moreover, cytotoxicity assays, analysis of DNA integrity, immunofluorescence, and confocal, scanning, and time-lapse microscopy revealed that macrophage viability decreased rapidly with time upon challenge, and depends on the MOI used. Treatment of macrophages with caspase-1 inhibitors, or with specific inhibitors of phagocytosis, did not alter the infection outcome. Moreover, human macrophages exhibited similar cytotoxic changes after infection with this strain. Macrophages responded to this cytotoxic strain with a robust pattern of pro-inflammatory gene expression. However, phagocytosis attempts to engulf live bacteria were unsuccessful, and the phagocytes were unable to kill the bacteria. We conclude that macrophage cell death occurs rapidly as a result of necrotic events after close contact with S. liquefaciens. These results likely have important implications for understanding Serratia pathogenesis and host response to infection.

Método gammagráfico simplificado para el estudio de pacientes pediátricos con estreñimiento crónico idiomático / Simplified gammagraphic method for the study of pediatric patients with chronic idiopathic constipation / Método gamagrafico simplificado para o estudo de doentes pediátricos com constipação crônica idiopática

Un importante reto para los cirujanos pediatras es el estreñimiento en la población infantil, que se presenta en cerca del 25% de los pacientes, sin que en la mayoría de los casos -hasta un 90%- no se especifique su causa orgánica. Este trabajo se realizó para mostrar, dentro del manejo de pacientes pediátricos con estreñimiento crónico idiopático, la viabilidad de replicar el método gammagráfico, un examen ampliamente divulgado en la literatura, para simplificar el que se ha descrito para tránsito intestinal y para justificar su uso en la orientación de un tratamiento efectivo para esta patología. El estudio mostró que el tránsito intestinal por gammagrafía es un método viable y preciso para la evaluación de pacientes con diagnóstico de estreñimiento crónico idiopático y que sus ventajas sobre otros estudios de tránsito intestinal con marcadores radio-opacos son muy evidentes, al tratarse de un método bien tolerado, no invasor y con mínima exposición radioactiva...

It is estimated that constipation is a common problem in children, accounting on the average as much as 25% of pediatric consultations. It has become a true challenge for the pediatric surgeon because no specific organic cause can be found in approximately 90% of the cases. Our study had two main objectives. First, to demonstrate the ability to replicate the method widely described in the literature and to simplify the gammagraphic exam described for the assessment of pediatric patients with chronic idiopathic constipation, and also to justify its use and value to provide enough information for the effective treatment of this pathology. This paper demonstrates that the gammagraphic colonic transit time is a viable and precise method for assessment of patients with chronic idiopathic constipation. The advantages of gammagraphic studies against other types, which use radio-opaque markers, are evident. It is a well-tolerated method, non-invasive and furthermore provides minimal radioactive exposure...

Um grande desafio para os cirurgiões pediátricos é a constipação em crianças, que acontece ao redor de um 25% dos doentes, e na maioria dos casos, - até um 90% - não se consiga especificar a causa orgânica. Este trabalho foi feito para mostrar, no manejo de pacientes pediátricos com constipação crônica idiopática, a viabilidade de replicar o método de cintilo grafia, um teste amplamente relatado na literatura, para simplificar o descrito para o trânsito intestinal e para justificar seu uso na orientação de um tratamento eficaz para esta condição. O estudo mostrou que a cintilografia de trânsito intestinal é um método viável e preciso para a avaliação de pacientes com constipação crônica idiopática e sua vantagem em relação a outros estudos de trânsito intestinal com marcadores radia - opacos são muito evidentes, sendo um método bem tolerado, não-invasivo e com a exposição à radiação mínima...

Obtención de un conjugado peroxidasa-antígeno de superficie del virus de la hepatitis B / Obtention of a peroxidase-hepatitis B virus surface antigen conjugate

Se preparó un conjugado para la determinación de anticuerpos contra el antígeno de superficie del virus de la hepatitis B por inmunoensayo enzimático tipo sandwich de doble Ag. Se utilizó la peroxidasa, el antígeno de la vacuna cubana contra la hepatitis B y el método de conjugación del periodato. Se evaluó la actividad enzimática, la actividad inmunológica y la actividad específica del conjugado. La enzima y el antígeno conservaron su actividad luego de la conjugación y se escogió la dilución óptima de trabajo 1/200. Se concluyó que el conjugado obtenido presentaba adecuada especificidad, detectabilidad y reactividad, y podía considerarse apto para su utilización.

A conjugate was prepared for the determination of antibodies against the surface antigen of hepatitis B virus by double Ag sandwich ELISA. Peroxidase, the antigen of the Cuban vaccine against hepatitis B, and the periodate-conjugation method were used. The enzymatic activity, the immunological activity and the specific conjugate activity were evaluated. The enzyme and the antigen conserved their activity after conjugation, and the optimal working dilution 1/200 was selected. It was concluded that the conjugate obtained had an adequate specificity, detectability and reactivity, and could be considered apt for its use.

Infectious pancreatic necrosis virus suppresses type I interferon signalling in rainbow trout gonad cell line but not in Atlantic salmon macrophages.

RTG-P1 cells are a rainbow trout fibroblastic cell line permanently transfected with the luciferase gene under the control of the Mx promoter. On exposure to interferon (IFN) or IFN inducing agents, the cells produce luciferase. IPNV did not induce luciferase production up to 24h post-infection but did not suppress constitutive luciferase production. Furthermore, IPNV suppressed luciferase production induced by poly I:C. RT-PCR analysis of IPNV infected cells showed IFN gene transcription from 6h post-infection with increasing expression up to 24h. Housekeeping genes beta-actin and GAPDH were also expressed along with upregulation of IRF1 and slight upregulation of STAT1. When RTG-P1 cells were stimulated with IFN, Mx transcripts, measured by qRT-PCR, peaked at 3-6h and thereafter fell to low levels, but in the presence of IPNV, Mx transcription at this time was significantly suppressed but continued to rise gradually. Luciferase production was lower in infected cells at 12h post-infection but not significantly after 24h. These results indicate that, in non-stimulated RTG-P1 cells, while IPNV induces IFN transcription, activation of Mx expression is suppressed. Furthermore, when stimulated by IFN, the rate of Mx transcription is significantly suppressed by the virus. This would probably give time for the virus to replicate rapidly in the early phases of infection. Contrary to the fibroblastic cell line, IPNV stimulated IFN production by salmon macrophages in vitro at least as strongly as poly I:C, with no suppression of the IFN response to poly I:C, and the virus persisted for up to 9 days without causing CPE.

Propuesta de la actividad enzimática como procedimiento analítico rector en la evaluación de conjugados / Proposal of the enzymatic activity as a ruling analytical procedure in the evaluation of conjugates

Se propuso el empleo de la determinación de la actividad enzimática sin mediación de la interacción antígeno-anticuerpo, como procedimiento analítico inicial en la evaluación de conjugados inmunoenzimáticos. Los conjugados empleados en los métodos inmunoenzimáticos deben ser evaluados una vez obtenidos y cada cierto tiempo. Como en estos procedimientos la señal que se obtiene depende del producto enzimático formado, sería ventajoso iniciar la evaluación determinando la actividad de la enzima independientemente de la del producto como conjugado. Se sugirió un método basado en la adición del conjugado de manera directa al soporte empleado para el inmunoensayo enzimático y seguidamente el sustrato de la enzima. Se incluyó la forma de interpretar los resultados y se concluyó que este es un proceder sencillo, que pudiera tener un papel rector en la evaluación de estos reactivos

Detección radioinmunoguiada de perforación del tracto gastrointestinal Estudio experimental / Radioimmunogided detection of perforation of the gastrointestinal tract

Se presenta un estudio experimental que tiene por objetivo evaluar la sensibilidad y especificidad de la detección de solución de continuidad del tracto gastrointestinal con la utilización de partículas pesadas marcadas con Tecnecio 99. Se diseñó un estudio experimental prospectivo triple ciego, con un cálculo de tamaño de muestra teniendo en cuenta una sensibilidad y especificidad superiores al 95 por ciento, con un error alfa del 0.05 y una precisión de 0.05. Inicialmente se evaluaron 4 conejos de la raza Nueva Zelanda para determinar: el anestésico y la dosis a utilizar, la capacidad del estómago en mililitros; los tiempos promedios de tránsito gastrointestinal, la capacidad de la cavidad abdominal en mililitros y la biodistribución del radiofármaco (absorción gastrointestinal, diseminación y distribución hemática y eliminación renal). Se utilizaron 40 conejos de la raza Nueva Zelanda y se analizaron en tres estaciones de trabajo independientes, asignando aleatoriamente 20 conejos en cada grupo de estudio (perforados y no perforados). El radiofármaco utilizado fue Tecnecio 99 sulfuro coloidal > 100 nm, 2.5 mCi a 140 –Kev de energía preparado en una dilución de solución salina al 0.9 por ciento quedando una concentración de 0.0025 mCi por mililitro. El rastreo se realizó con una sonda gamma a 10X. El análisis estadístico se realizó con el programa Episet V:1 aplicando la prueba de Chi Cuadrado.Todos los 20 conejos que tenían disrupción del estómago, presentaron una prueba positiva para detección de radioactividad en el líquido peritoneal analizado con un valor promedio de 467 y un rango de 37 a 1748. En los 20 conejos restantes que no tenían perforación de la pared gástrica la prueba fue negativa.La sensibilidad de la metodología diagnóstica fue de 0.98 y la especificidad de 0.98 con un intervalo...