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1.
Physiol Biochem Zool ; 88(3): 266-83, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25860826

RESUMEN

The nutritional condition of cultured Sagmariasus verreauxi juveniles over the molt and during starvation was investigated by studying their metabolism, bioenergetics of nutrient reserves, and hemolymph biochemistry. Juveniles were shown to downregulate standard metabolic rate by as much as 52% within 14 d during starvation. Hepatopancreas (HP) lipid was prioritized as a source of energy, but this reserve represented only between 1% and 13% of the total measured energy reserve and was used quickly during starvation, especially in the immediate postmolt period when as much as 60% was depleted within 3 d. Abdominal muscle (AM) protein represented between 74% and 90% of the total measured energy reserve in juvenile lobsters, and as much as 40% of available AM protein energy was used over 28 d of starvation after the molt. Carbohydrate reserves represented less than 2% of the measured total energy reserve in fed intermolt lobsters and provided negligible energy during starvation. Eighteen hemolymph parameters were measured to identify a nondestructive biomarker of condition that would reflect accurately the state of energy reserves of the lobster. Among these, the hemolymph Brix index was the most accurate and practical method to predict HP lipid and the total energy content of both the HP and the AM in juvenile S. verreauxi. The Brix index was strongly correlated with hemolymph proteins, triglyceride, cholesterol, calcium, and phosphorus concentrations, as well as lipase activity; all were useful in predicting condition. Electrolytes such as chloride, magnesium, and potassium and metabolites such as glucose and lactate were poor indicators of nutritional condition. Uric acid and the "albumin"-to-"globulin" ratio provided complementary information to the Brix index, which may assist in determining nutritional condition of wild juvenile lobsters of unknown intermolt development. This study will greatly assist future ecological studies examining the nutritional condition of juvenile lobsters in the wild, as well as the development of husbandry protocols and feeds for aquaculture.


Asunto(s)
Hemolinfa/metabolismo , Palinuridae/metabolismo , Animales , Acuicultura , Metabolismo Energético , Privación de Alimentos , Glucosa/metabolismo , Lípidos/análisis , Muda , Proteínas Musculares/metabolismo , Palinuridae/crecimiento & desarrollo , Triglicéridos/análisis
2.
Fish Shellfish Immunol ; 34(3): 778-88, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23291253

RESUMEN

A partial sequence of the recombination activating gene-1 (RAG-1) and several full length sequences of the immunoglobulin M (IgM) heavy chain mRNA were obtained from the striped trumpeter (Latris lineata). The RAG-1 fragment consisted of 205 aa and fell within the core region of the open reading frame. The complete IgM heavy chain sequences translated into peptides ranging between 581 and 591 aa. Both genes showed good homology to other vertebrate sequences. The expression of the two genes was assessed throughout the early developmental stages of striped trumpeter larvae (5-100 dph) and used as markers to follow the ontogeny of the adaptive immune response. Using RT-PCR, RAG-1 mRNA expression was detectable at 5 dph and remained so until 80 dph, before becoming undetectable at 100 dph. IgM expression was also detectable at 5 dph, and remained so throughout. These patterns of expression may suggest that the striped trumpeter possess mature B cells with surface IgM at 100 dph. However, complete immunological competence is likely not reached until some time later. The early detection of IgM mRNA at 5 dph led to the investigation of its presence in oocytes. Both RAG-1 and IgM mRNA transcripts were detected in unfertilized oocytes, suggesting that they are maternally transferred. The biological significance of such a phenomenon remains to be investigated.


Asunto(s)
Inmunidad Adaptativa , Proteínas de Peces/genética , Proteínas de Homeodominio/genética , Inmunoglobulina M/genética , Perciformes/genética , Perciformes/inmunología , Secuencia de Aminoácidos , Animales , Biomarcadores/metabolismo , Clonación Molecular , ADN Complementario/análisis , ADN Complementario/genética , Proteínas de Peces/química , Proteínas de Peces/metabolismo , Regulación de la Expresión Génica , Regulación del Desarrollo de la Expresión Génica , Proteínas de Homeodominio/química , Proteínas de Homeodominio/metabolismo , Inmunoglobulina M/química , Inmunoglobulina M/metabolismo , Larva/genética , Larva/crecimiento & desarrollo , Larva/inmunología , Larva/metabolismo , Datos de Secuencia Molecular , Especificidad de Órganos , Óvulo/crecimiento & desarrollo , Óvulo/inmunología , Óvulo/metabolismo , Perciformes/crecimiento & desarrollo , Perciformes/metabolismo , Filogenia , ARN Mensajero/análisis , ARN Mensajero/genética , Reacción en Cadena en Tiempo Real de la Polimerasa/veterinaria , Alineación de Secuencia/veterinaria , Análisis de Secuencia de ADN/veterinaria , Tasmania
6.
J Fish Dis ; 36(1): 57-65, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-22947107

RESUMEN

Myxozoan parasites are known pathogens of cultured finfish. Kudoa neurophila n. comb. (Grossel, Dyková, Handlinger & Munday) has historically infected hatchery-produced striped trumpeter, Latris lineata (Forster in Bloch and Schneider), a candidate species for seacage aquaculture in Australia. We examined the efficacy of four water treatment methods to prevent K. neurophila infection in post-larval (paperfish) and juvenile striped trumpeter. Treatments included dose-controlled ultraviolet irradiation [hydro-optic disinfection (HOD)], ozone with conventional UV (ozone), mechanical filtration at 25 µm and then foam fractionation (primary filtration), and 50-µm-filtered sea water (control). In post-larvae (initially 10.3 ± 2.7 g, mean ± SD, 259 days post-hatching, dph), the infection prevalence (PCR test) after 51 days was 93 ± 12% in the control, 100 ± 0% in primary filtration and 0 ± 0% in both ozone and HOD. Likewise, in juveniles (initially 114 ± 18 g, 428 dph), prevalence was 100 ± 0% in the control and primary filtration treatments with no infection detected in ozone and HOD. Concurrently, there was a 50-100% reduction in heterotrophic bacteria and 100% reduction in presumptive Vibrio sp. in sea water HOD and ozone treatments. HOD with a dose of ≥44 mJ cm(-2) UV was as effective as ozonation at >700 mV ORP for 10 min, in preventing K. neurophila infection.


Asunto(s)
Enfermedades de los Peces/prevención & control , Myxozoa/efectos de la radiación , Enfermedades Parasitarias en Animales/prevención & control , Perciformes/parasitología , Agua de Mar/parasitología , Rayos Ultravioleta , Purificación del Agua/métodos , Animales , Carga Bacteriana , Ozono , Perciformes/crecimiento & desarrollo , Vibrio/efectos de la radiación , Agua/química , Agua/parasitología , Microbiología del Agua , Purificación del Agua/normas
7.
Fish Shellfish Immunol ; 26(5): 773-86, 2009 May.
Artículo en Inglés | MEDLINE | ID: mdl-19332136

RESUMEN

This study reports the cloning and sequencing of three striped trumpeter (Latris lineata Forster) pro-inflammatory cytokines, TNF-alpha, IL-1beta and IL-8, as well as their differential expression in response to an infection by the ectoparasite Chondracanthus goldsmidi. The striped trumpeter TNF-alpha transcript consisted of 1093 bp, including a 759 bp ORF which translated into a 253 aa transmembrane peptide. The sequence contained a TACE cut site, that would produce a 167 aa soluble peptide containing the TNF ligand family signature. The IL-1beta sequence consisted of 963 bp, including a 774 bp ORF which translated into a 258 aa protein. The protein lacked both a signal peptide and an ICE cleavage site, but did contain the IL-1 family signature. The sequence for the chemokine IL-8 contained 906 bp, with an ORF of 297 bp, which translated into a 99 aa protein. The protein lacked an ELR motif as is common with many teleost IL-8 sequences. The differential expression of the three cytokine genes in parasitized fish was investigated via quantitative real-time PCR. A significant up-regulation of all three pro-inflammatory cytokines was found in the gills, which were the site of parasite attachment. Examination of head kidney cells revealed a significant up-regulation of TNF-alpha, but not IL-1beta or IL-8. Conversely, the spleen cells showed significant up-regulation of both IL-1beta and IL-8, but not TNF-alpha. These findings allow for more detailed investigations of the striped trumpeter immune response.


Asunto(s)
Copépodos/fisiología , Citocinas/genética , Infestaciones Ectoparasitarias/veterinaria , Enfermedades de los Peces , Regulación de la Expresión Génica/inmunología , Perciformes/genética , Perciformes/inmunología , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , Citocinas/química , Infestaciones Ectoparasitarias/inmunología , Enfermedades de los Peces/inmunología , Enfermedades de los Peces/parasitología , Perfilación de la Expresión Génica , Branquias/citología , Branquias/parasitología , Interleucina-1beta/genética , Interleucina-8/genética , Datos de Secuencia Molecular , Alineación de Secuencia , Homología de Secuencia de Aminoácido , Homología de Secuencia de Ácido Nucleico , Factor de Necrosis Tumoral alfa/genética
8.
Lipids ; 39(3): 215-22, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15233399

RESUMEN

We determined the effect of dietary long-chain (> or = C20) PUFA (LC-PUFA), 20:5n-3 and 22:6n-3, on larval striped trumpeter (Latris lineata) biochemistry through early development and during live feeding with rotifers (Brachionus plicatilis). Rotifers were enriched using seven experimental emulsions formulated with increasing concentrations of n-3 LC-PUFA, mainly 20:5n-3 and 22:6n-3. Enriched rotifer n-3 LC-PUFA concentrations ranged from 10-30 mg/g dry matter. Enriched rotifers were fed to striped trumpeter larvae from 5 to 18 d post-hatch (dph) in a short-term experiment to minimize gross deficiency symptoms such as poor survival that could confound results. No relationships were observed between larval growth or survival with dietary n-3 LC-PUFA at 18 dph. The larval FA profiles generally reflected those of the rotifer diet, and significant positive regressions were observed between most dietary and larval FA at 10, 14, and 18 dph. The major exception observed was an inverse relationship between dietary and larval 22:5n-3. The presence of 22:5n-3 in elevated amounts when dietary 22:6n-3 was depressed suggests that elongation of 20:5n-3 may be occurring in an attempt to raise body concentrations of 22:6n-3. We hypothesize that accumulation of 22:5n-3 might be an early indicator of 22:6n-3 deficiency in larval fish that precedes a reduction in growth or survival. A possible role of 22:5n-3 as a biochemical surrogate for 22:6n-3 is discussed.


Asunto(s)
Ácidos Grasos Omega-3/metabolismo , Ácidos Grasos Omega-3/farmacología , Perciformes/crecimiento & desarrollo , Perciformes/metabolismo , Animales , Emulsiones/química , Ácidos Grasos Omega-3/análisis , Larva/química , Larva/efectos de los fármacos , Océanos y Mares , Rotíferos/química , Distribución Tisular
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