Effects of autochthonous strains mixture on gut microbiota and metabolic profile in cobia (Rachycentron canadum)

Sci Rep. 2022 Oct 18;12(1):17410. doi: 10.1038/s41598-022-19663-x.

Abstract

The fish immune system is a topic or subject that offers a unique understanding of defensive system evolution in vertebrate heredity. While gut microbiota plays several roles in fish: well-being, promoting health and growth, resistance to bacterial invasion, regulation of energy absorption, and lipid metabolism. However, studies on fish gut microbiota face practical challenges due to the large number of fish varieties, fluctuating environmental conditions, and differences in feeding habits. This study was carried out to evaluate the impacts of supplemented three autochthonous strains, Bacillus sp. RCS1, Pantoea agglomerans RCS2, and Bacillus cereus RCS3 mixture diet on cobia fish (Rachycentron canadum). Also, chromatography, mass spectrometry and high throughput sequencing were combined to explore composition and metabolite profile of gut microbiota in juvenile cobia fed with supplemented diet. In the trial group, juvenile cobia received diets supplemented with 1 × 1012 CFU mL-1 autochthonous strains for ten weeks and a control diet without supplementation. Juvenile cobia receiving diets supplementation exhibited significantly improved growth than those without additives (control). Haematological indices, such as red blood cells, white blood cells, corpuscular haemoglobin concentration, mean corpuscular volume, haemoglobin, and mean corpuscular haemoglobin, were higher in the supplemented group. Similarly, digestive enzymes (trypsin, lipase, amylase, pepsin and cellulose, activities) activities were higher in supplemented diet with an indigenous isolates mixture. Serum biochemical parameters albumin, globulin, and total protein were significantly higher, while triglyceride, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and cholesterol showed no significant difference. On the other hand, glucose was significantly (P < 0.05) higher in the group without supplementation. On gene expression in the midgut, Immunoglobulin, Colony-stimulating factor receptor 1, major histocompatibility complex 1 were up-regulated by native isolates while T cell receptor beta, and Major histocompatibility complex 2 showed no significant difference. Gut bacterial composition was altered in fish receiving supplemented diet with autochthonous strains. Metabolomics also revealed that some metabolic pathways were considerably enriched in fish fed with supplemented diet; pathway analysis based on Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment revealed that differentially expressed metabolites were involved in galactose metabolism, tryptophan metabolism, carbohydrate digestion and absorption, purine metabolism, and ABC transporters. Functional analysis of bacterial community showed that differences in enriched metabolic pathways generally comprised carbohydrate and its metabolites, nucleotide and its metabolites, amino acid and its metabolites, heterocyclic compounds, and tryptamines, cholines, pigments. The current investigation results showed that autochthonous strains mixture has significantly enhanced the growth, survival, and innate and adaptive immunities of juvenile cobia.

Publication types

  • Randomized Controlled Trial, Veterinary
  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters / metabolism
  • Alanine / metabolism
  • Albumins / metabolism
  • Alkaline Phosphatase / metabolism
  • Amino Acids / metabolism
  • Amylases / metabolism
  • Animal Feed / analysis
  • Animals
  • Aspartate Aminotransferases / metabolism
  • Cellulose / metabolism
  • Cholesterol / metabolism
  • Diet
  • Fishes / metabolism
  • Galactose / metabolism
  • Gastrointestinal Microbiome*
  • Glucose / metabolism
  • Lipase / metabolism
  • Metabolome
  • Nucleotides / metabolism
  • Pepsin A / metabolism
  • Perciformes* / physiology
  • Purines / metabolism
  • Receptors, Antigen, T-Cell / metabolism
  • Receptors, Colony-Stimulating Factor / metabolism
  • Triglycerides / metabolism
  • Trypsin / metabolism
  • Tryptamines
  • Tryptophan / metabolism

Substances

  • Alanine
  • Albumins
  • Alkaline Phosphatase
  • Amino Acids
  • Amylases
  • Aspartate Aminotransferases
  • ATP-Binding Cassette Transporters
  • Cellulose
  • Cholesterol
  • Galactose
  • Glucose
  • Lipase
  • Nucleotides
  • Pepsin A
  • Purines
  • Receptors, Antigen, T-Cell
  • Receptors, Colony-Stimulating Factor
  • Triglycerides
  • Trypsin
  • Tryptamines
  • Tryptophan