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Substitution of live food by formulated diets in marine fish larvae

Identifieur interne : 001492 ( Istex/Corpus ); précédent : 001491; suivant : 001493

Substitution of live food by formulated diets in marine fish larvae

Auteurs : Chantal Cahu ; José Zambonino Infante

Source :

RBID : ISTEX:788ACAE13967AD72E4FC0633F52365F3B63ACCB5

Abstract

Until recently, it was considered impossible to feed newly hatched marine fish species with a compound diet. Substituting a compound diet for live prey was performed several weeks after hatching, depending on the species. Compound diets were well ingested at the early stage but larvae died with a gut full of food, suggesting that larvae were unable to digest the compound diet. The hypothesis was that younger larvae have insufficient digestive enzymes to thrive on compound diets, and that exogenous enzymes, provided from live prey, are necessary for early stages. The organogenesis of marine fish larvae is not completely achieved at hatching and histological studies have revealed that the anatomy of the digestive tract undergoes developmental changes over some weeks. Nevertheless, biochemical studies over 20 years have shown that most of the digestive enzymes are present in young larvae. Recent studies have provided better understanding of digestion mechanisms in larvae and have led to proposed dietary compositions meeting larvae nutritional requirements. Pancreatic digestive enzymes are detected before mouth opening. Their synthesis is not induced by diet ingestion, but secretory mechanisms in the pancreas, and so enzymatic action, become efficient chronologically after those of synthesis. Inadequate diets can delay the onset of secretion mechanisms. The ratio of secreted enzymes to total enzymes indicates the nutritional value of the diet ingested by the larvae. At the intestinal level, cytosolic enzymes, which are peptidases, exhibit high activity in the early stages, suggesting a high capacity in larvae to digest protein hydrolysate. Indeed, larvae growth and survival is improved by the incorporation of a moderate concentration of peptide or hydrolysate in the diet. Peptidase activity abruptly decreases around day 25 in sea bass, concurrent with an increase in enzymes of the brush border membranes. This corresponds to a normal maturation process of enterocytes. Compound diets can slightly delay the onset of this maturation process, and inadequate diet can prevent it, leading to near death of the larvae. A proper onset of the maturation process has been associated with high larvae survival. The early developmental stage larvae exhibit high hydrolytic capacity, related to their weight. Enzyme activity pattern is age-dependent, but can be modulated by diet composition. Thus, larvae have the ability to digest and thrive on compound diet, if this diet is well adapted. Larvae have different specificities in digestion and nutritional requirements when compared to juveniles. Taking these specificities into consideration, recent research has led to the formulation of a compound diet that was well adapted for larvae from mouth opening, and could totally replace live prey.

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DOI: 10.1016/S0044-8486(01)00699-8

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<div type="abstract" xml:lang="en">Until recently, it was considered impossible to feed newly hatched marine fish species with a compound diet. Substituting a compound diet for live prey was performed several weeks after hatching, depending on the species. Compound diets were well ingested at the early stage but larvae died with a gut full of food, suggesting that larvae were unable to digest the compound diet. The hypothesis was that younger larvae have insufficient digestive enzymes to thrive on compound diets, and that exogenous enzymes, provided from live prey, are necessary for early stages. The organogenesis of marine fish larvae is not completely achieved at hatching and histological studies have revealed that the anatomy of the digestive tract undergoes developmental changes over some weeks. Nevertheless, biochemical studies over 20 years have shown that most of the digestive enzymes are present in young larvae. Recent studies have provided better understanding of digestion mechanisms in larvae and have led to proposed dietary compositions meeting larvae nutritional requirements. Pancreatic digestive enzymes are detected before mouth opening. Their synthesis is not induced by diet ingestion, but secretory mechanisms in the pancreas, and so enzymatic action, become efficient chronologically after those of synthesis. Inadequate diets can delay the onset of secretion mechanisms. The ratio of secreted enzymes to total enzymes indicates the nutritional value of the diet ingested by the larvae. At the intestinal level, cytosolic enzymes, which are peptidases, exhibit high activity in the early stages, suggesting a high capacity in larvae to digest protein hydrolysate. Indeed, larvae growth and survival is improved by the incorporation of a moderate concentration of peptide or hydrolysate in the diet. Peptidase activity abruptly decreases around day 25 in sea bass, concurrent with an increase in enzymes of the brush border membranes. This corresponds to a normal maturation process of enterocytes. Compound diets can slightly delay the onset of this maturation process, and inadequate diet can prevent it, leading to near death of the larvae. A proper onset of the maturation process has been associated with high larvae survival. The early developmental stage larvae exhibit high hydrolytic capacity, related to their weight. Enzyme activity pattern is age-dependent, but can be modulated by diet composition. Thus, larvae have the ability to digest and thrive on compound diet, if this diet is well adapted. Larvae have different specificities in digestion and nutritional requirements when compared to juveniles. Taking these specificities into consideration, recent research has led to the formulation of a compound diet that was well adapted for larvae from mouth opening, and could totally replace live prey.</div>
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<note type="content">Fig. 1: Variation of specific activity and mRNA level of amylase during sea bass (D. labrax) development.</note>
<note type="content">Fig. 2: Specific activity and mRNA level of amylase in 29-day-old sea bass (D. labrax) fed diets containing 5% (S5) or 25% (S25) starch. Means±S.E.M. (n=4) with different superscripts, independently for RNA and activity, are significantly different (p<0.05).</note>
<note type="content">Fig. 3: Variation in specific activity of enterocyte enzymes during fish larvae (D. labrax) development: increase in a brush border membrane enzyme (AP: alkaline phosphatase) and decrease in a cytosolic enzyme (leu ala: leucine alanine peptidase) in larvae fed live preys (filled line) or weaned with a conventional diet (dotted line).</note>
<note type="content">Fig. 4: Growth (wet weight) of sea bass (D. labrax) larvae fed from day 14 isonitrogenous compound diet containing 10%, 15% 20%, 25% or 30% lipids. Survival rate, from hatching to day 39, is in brackets (from Zambonino Infante and Cahu, 1999). Means±S.E.M. (n=4) with different superscripts are significantly different (p<0.05).</note>
<note type="content">Fig. 5: Growth of P. olivaceus larvae fed different levels fed eicosapentaenoic acid (EPA) and docohexaenoic acid (DHA) (from Kanazawa et al., 1981 in Watanabe and Kiron, 1994).</note>
<note type="content">Fig. 6: Growth (wet weight) of sea bass larvae (D. labrax) fed from day 14 with isoenergetic compound diets incorporating 30%, 40%, 50% or 60% proteins. Survival rate, from hatching to day 36, is in brackets (from Péres et al., 1996). Means±S.E.M. (n=4) with different superscripts are significantly different (p<0.05).</note>
<note type="content">Fig. 7: Growth (wet weight) of fish larvae fed diets incorporating different protein hydrolysate level in replacement of protein. (A) Goldfish (Carassius auratus) larvae fed diets incorporating 0% (H0), 50% (H50) and 100% (H100) hydrolysate (from Szlaminska et al., 1993). (B) Sea bass (D. labrax) larvae fed diets incorporating 0% (H0), 20% (H20) and 40% (H40) di- and tripeptides. Survival rate, from hatching to day 39, is in brackets (from Zambonino Infante et al., 1997).</note>
<note type="content">Table 1: Composition of experimental microparticles (g/100 g dry diet) for marine fish larvae: I, microbound diet (Person Le Ruyet, in Guillaume et al., 1999); II, crumbles (Zambonino Infante and Cahu, 1999); III, microcapsulated diet (Yufera et al., 1999)</note>
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<ce:surname>Cahu</ce:surname>
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<ce:e-address>Chantal.Cahu@ifremer.fr</ce:e-address>
</ce:author>
<ce:author>
<ce:given-name>José</ce:given-name>
<ce:surname>Zambonino Infante</ce:surname>
</ce:author>
<ce:affiliation>
<ce:textfn>Unité Mixte INRA IFREMER de Nutrition des Poissons, BP 70, 29280 Plouzané, France</ce:textfn>
</ce:affiliation>
<ce:correspondence id="COR1">
<ce:label>*</ce:label>
<ce:text>Corresponding author. Tel.: +33-02-9822-4403, fax: +33-02-9822-4653</ce:text>
</ce:correspondence>
</ce:author-group>
<ce:abstract>
<ce:section-title>Abstract</ce:section-title>
<ce:abstract-sec>
<ce:simple-para>Until recently, it was considered impossible to feed newly hatched marine fish species with a compound diet. Substituting a compound diet for live prey was performed several weeks after hatching, depending on the species. Compound diets were well ingested at the early stage but larvae died with a gut full of food, suggesting that larvae were unable to digest the compound diet. The hypothesis was that younger larvae have insufficient digestive enzymes to thrive on compound diets, and that exogenous enzymes, provided from live prey, are necessary for early stages.</ce:simple-para>
<ce:simple-para>The organogenesis of marine fish larvae is not completely achieved at hatching and histological studies have revealed that the anatomy of the digestive tract undergoes developmental changes over some weeks. Nevertheless, biochemical studies over 20 years have shown that most of the digestive enzymes are present in young larvae. Recent studies have provided better understanding of digestion mechanisms in larvae and have led to proposed dietary compositions meeting larvae nutritional requirements. Pancreatic digestive enzymes are detected before mouth opening. Their synthesis is not induced by diet ingestion, but secretory mechanisms in the pancreas, and so enzymatic action, become efficient chronologically after those of synthesis. Inadequate diets can delay the onset of secretion mechanisms. The ratio of secreted enzymes to total enzymes indicates the nutritional value of the diet ingested by the larvae.</ce:simple-para>
<ce:simple-para>At the intestinal level, cytosolic enzymes, which are peptidases, exhibit high activity in the early stages, suggesting a high capacity in larvae to digest protein hydrolysate. Indeed, larvae growth and survival is improved by the incorporation of a moderate concentration of peptide or hydrolysate in the diet. Peptidase activity abruptly decreases around day 25 in sea bass, concurrent with an increase in enzymes of the brush border membranes. This corresponds to a normal maturation process of enterocytes. Compound diets can slightly delay the onset of this maturation process, and inadequate diet can prevent it, leading to near death of the larvae. A proper onset of the maturation process has been associated with high larvae survival.</ce:simple-para>
<ce:simple-para>The early developmental stage larvae exhibit high hydrolytic capacity, related to their weight. Enzyme activity pattern is age-dependent, but can be modulated by diet composition. Thus, larvae have the ability to digest and thrive on compound diet, if this diet is well adapted. Larvae have different specificities in digestion and nutritional requirements when compared to juveniles. Taking these specificities into consideration, recent research has led to the formulation of a compound diet that was well adapted for larvae from mouth opening, and could totally replace live prey.</ce:simple-para>
</ce:abstract-sec>
</ce:abstract>
<ce:keywords class="keyword">
<ce:section-title>Keywords</ce:section-title>
<ce:keyword>
<ce:text>Fish larvae</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Gut maturation</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Protein hydrolysate</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Intestinal enzymes</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Microparticulate diet</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Pancreatic enzymes</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Phospholipid</ce:text>
</ce:keyword>
<ce:keyword>
<ce:text>Protein</ce:text>
</ce:keyword>
</ce:keywords>
</head>
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<title>Substitution of live food by formulated diets in marine fish larvae</title>
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<title>Substitution of live food by formulated diets in marine fish larvae</title>
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<name type="personal">
<namePart type="given">Chantal</namePart>
<namePart type="family">Cahu</namePart>
<affiliation>Unité Mixte INRA IFREMER de Nutrition des Poissons, BP 70, 29280 Plouzané, France</affiliation>
<affiliation>E-mail: Chantal.Cahu@ifremer.fr</affiliation>
<description>Corresponding author. Tel.: +33-02-9822-4403, fax: +33-02-9822-4653</description>
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<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">José</namePart>
<namePart type="family">Zambonino Infante</namePart>
<affiliation>Unité Mixte INRA IFREMER de Nutrition des Poissons, BP 70, 29280 Plouzané, France</affiliation>
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<abstract lang="en">Until recently, it was considered impossible to feed newly hatched marine fish species with a compound diet. Substituting a compound diet for live prey was performed several weeks after hatching, depending on the species. Compound diets were well ingested at the early stage but larvae died with a gut full of food, suggesting that larvae were unable to digest the compound diet. The hypothesis was that younger larvae have insufficient digestive enzymes to thrive on compound diets, and that exogenous enzymes, provided from live prey, are necessary for early stages. The organogenesis of marine fish larvae is not completely achieved at hatching and histological studies have revealed that the anatomy of the digestive tract undergoes developmental changes over some weeks. Nevertheless, biochemical studies over 20 years have shown that most of the digestive enzymes are present in young larvae. Recent studies have provided better understanding of digestion mechanisms in larvae and have led to proposed dietary compositions meeting larvae nutritional requirements. Pancreatic digestive enzymes are detected before mouth opening. Their synthesis is not induced by diet ingestion, but secretory mechanisms in the pancreas, and so enzymatic action, become efficient chronologically after those of synthesis. Inadequate diets can delay the onset of secretion mechanisms. The ratio of secreted enzymes to total enzymes indicates the nutritional value of the diet ingested by the larvae. At the intestinal level, cytosolic enzymes, which are peptidases, exhibit high activity in the early stages, suggesting a high capacity in larvae to digest protein hydrolysate. Indeed, larvae growth and survival is improved by the incorporation of a moderate concentration of peptide or hydrolysate in the diet. Peptidase activity abruptly decreases around day 25 in sea bass, concurrent with an increase in enzymes of the brush border membranes. This corresponds to a normal maturation process of enterocytes. Compound diets can slightly delay the onset of this maturation process, and inadequate diet can prevent it, leading to near death of the larvae. A proper onset of the maturation process has been associated with high larvae survival. The early developmental stage larvae exhibit high hydrolytic capacity, related to their weight. Enzyme activity pattern is age-dependent, but can be modulated by diet composition. Thus, larvae have the ability to digest and thrive on compound diet, if this diet is well adapted. Larvae have different specificities in digestion and nutritional requirements when compared to juveniles. Taking these specificities into consideration, recent research has led to the formulation of a compound diet that was well adapted for larvae from mouth opening, and could totally replace live prey.</abstract>
<note type="content">Fig. 1: Variation of specific activity and mRNA level of amylase during sea bass (D. labrax) development.</note>
<note type="content">Fig. 2: Specific activity and mRNA level of amylase in 29-day-old sea bass (D. labrax) fed diets containing 5% (S5) or 25% (S25) starch. Means±S.E.M. (n=4) with different superscripts, independently for RNA and activity, are significantly different (p<0.05).</note>
<note type="content">Fig. 3: Variation in specific activity of enterocyte enzymes during fish larvae (D. labrax) development: increase in a brush border membrane enzyme (AP: alkaline phosphatase) and decrease in a cytosolic enzyme (leu ala: leucine alanine peptidase) in larvae fed live preys (filled line) or weaned with a conventional diet (dotted line).</note>
<note type="content">Fig. 4: Growth (wet weight) of sea bass (D. labrax) larvae fed from day 14 isonitrogenous compound diet containing 10%, 15% 20%, 25% or 30% lipids. Survival rate, from hatching to day 39, is in brackets (from Zambonino Infante and Cahu, 1999). Means±S.E.M. (n=4) with different superscripts are significantly different (p<0.05).</note>
<note type="content">Fig. 5: Growth of P. olivaceus larvae fed different levels fed eicosapentaenoic acid (EPA) and docohexaenoic acid (DHA) (from Kanazawa et al., 1981 in Watanabe and Kiron, 1994).</note>
<note type="content">Fig. 6: Growth (wet weight) of sea bass larvae (D. labrax) fed from day 14 with isoenergetic compound diets incorporating 30%, 40%, 50% or 60% proteins. Survival rate, from hatching to day 36, is in brackets (from Péres et al., 1996). Means±S.E.M. (n=4) with different superscripts are significantly different (p<0.05).</note>
<note type="content">Fig. 7: Growth (wet weight) of fish larvae fed diets incorporating different protein hydrolysate level in replacement of protein. (A) Goldfish (Carassius auratus) larvae fed diets incorporating 0% (H0), 50% (H50) and 100% (H100) hydrolysate (from Szlaminska et al., 1993). (B) Sea bass (D. labrax) larvae fed diets incorporating 0% (H0), 20% (H20) and 40% (H40) di- and tripeptides. Survival rate, from hatching to day 39, is in brackets (from Zambonino Infante et al., 1997).</note>
<note type="content">Table 1: Composition of experimental microparticles (g/100 g dry diet) for marine fish larvae: I, microbound diet (Person Le Ruyet, in Guillaume et al., 1999); II, crumbles (Zambonino Infante and Cahu, 1999); III, microcapsulated diet (Yufera et al., 1999)</note>
<subject>
<genre>Keywords</genre>
<topic>Fish larvae</topic>
<topic>Gut maturation</topic>
<topic>Protein hydrolysate</topic>
<topic>Intestinal enzymes</topic>
<topic>Microparticulate diet</topic>
<topic>Pancreatic enzymes</topic>
<topic>Phospholipid</topic>
<topic>Protein</topic>
</subject>
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<title>Aquaculture</title>
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<title>AQUA</title>
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<name type="conference">
<namePart>Advanced Biotechnology in Hatchery Production, Honolulu, Hawaii</namePart>
<namePart type="date">19991206</namePart>
<namePart type="date">19991209</namePart>
</name>
<name type="personal">
<namePart>C.-S. Lee</namePart>
<role>
<roleTerm type="text">editor</roleTerm>
</role>
</name>
<name type="personal">
<namePart>P.J. O'Bryen</namePart>
<role>
<roleTerm type="text">editor</roleTerm>
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<genre type="journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">20010815</dateIssued>
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<identifier type="ISSN">0044-8486</identifier>
<identifier type="PII">S0044-8486(00)X0135-4</identifier>
<part>
<date>20010815</date>
<detail type="issue">
<title>Advanced Biotechnology in Hatchery Production, Honolulu, Hawaii</title>
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<detail type="volume">
<number>200</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>1–2</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>1</start>
<end>250</end>
</extent>
<extent unit="pages">
<start>161</start>
<end>180</end>
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</part>
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<identifier type="DOI">10.1016/S0044-8486(01)00699-8</identifier>
<identifier type="PII">S0044-8486(01)00699-8</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©2001 Elsevier Science B.V.</accessCondition>
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