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1.
Front Immunol ; 11: 610934, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33363546

RESUMO

Grape seed is rich in vitamin E, flavonoids, and proanthocyanidins and has the potential to be used as an antibiotic substitute in broilers. We investigated the effects of grape seed proanthocyanidin extract (GSPE) on growth performance, immune responses, cecal microflora, and serum metabolism in early stage broilers. Data indicated that GSPE improved broiler growth performance by strengthening antioxidant capacity, enhancing immune responses, and increasing cecal short chain fatty acids. 16S rRNA sequencing indicated that GSPE changed the predominant cecal microflora and induced the metabolism of amino acids, lipids, and carbohydrates. An UPLC-Q-TOF/MS-based metabolomics analysis identified 23 serum metabolites (mainly related to lipid, amino acid, and alkaloid) were extremely changed by GSPE treatment. The correlations between the changes of cecal microflora and serum metabolites in birds fed with GSPE were analyzed. Hence, GSPE potentially provides active ingredients that may be used as antibiotic substitute and reduces environmental pollution by grape by-products.


Assuntos
Bactérias/crescimento & desenvolvimento , Ceco/microbiologia , Galinhas/sangue , Galinhas/microbiologia , Suplementos Nutricionais , Microbioma Gastrointestinal , Extrato de Sementes de Uva/administração & dosagem , Metaboloma , Proantocianidinas/administração & dosagem , Ração Animal , Criação de Animais Domésticos , Animais , Bactérias/genética , Biomarcadores/sangue , Galinhas/crescimento & desenvolvimento , Metabolômica , Ribotipagem
2.
Mol Biol Rep ; 39(2): 1869-76, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21660473

RESUMO

The study was conducted to evaluate the effects of different starch sources on Bacillus spp. in intestinal tract and expression of intestinal development related genes of weanling piglets. Twenty-eight PIC male piglets were divided into four homogeneous groups according to initial body weight (similar birth and parity, weaned at 21 ± 1.5 days). Diets for the four treatments consisted of corn starch, wheat starch, tapioca starch and pea starch with the determined ratio for amylose to amylopectin of 0.21, 0.24, 0.12 and 0.52 respectively. Real-time quantitative polymerase chain reaction was applied to: (1) detect genomic DNA of Bacillus and to quantify the number of Bacillus in the intestinal tract chyme of piglets with the primers and probe which designed based on the 16S rRNA sequences of maximum species of Bacillus on GenBank; (2) measure the mRNA level of glucagon-like peptide 2 (GLP-2), insulin-like growth factors 1 (IGF-1) and epidermal growth factor (EGF) in duodenum, jejunum and ileum. Results showed that the number of Baciilus and the percentage based on all bacteria in the whole intestinal content of piglets fed pea starch was highest in all groups (P < 0.05). There was no significant differance on copy numbers for all bacteria and Bacillus in the whole intestinal tract of piglets between the corn starch group and wheat starch group (P > 0.05). In addition, the expression level of GLP-2, IGF-1 mRNA in jejunum and ileum of pea starch treatment (the high amylose/amylopectin ratio) were increased while the tapioca starch decreased their mRNA level significantly compared to other three treatments (P < 0.05). There was no significant difference for the mRNA level of EGF in each group. The present study revealed that high amylose/amylopectin ratio of starches significantly enhanced the numbers of Bacillus in all segments of intestine and the mRNA level of intestinal development related genes.


Assuntos
Bacillus/efeitos dos fármacos , Carboidratos da Dieta/farmacologia , Regulação da Expressão Gênica no Desenvolvimento/efeitos dos fármacos , Intestinos/microbiologia , Amido/farmacologia , Sus scrofa/genética , Sus scrofa/microbiologia , Análise de Variância , Animais , Bacillus/genética , Primers do DNA/genética , Fator de Crescimento Epidérmico/metabolismo , Peptídeo 2 Semelhante ao Glucagon/metabolismo , Fator de Crescimento Insulin-Like I/metabolismo , Mucosa Intestinal/metabolismo , Masculino , Reação em Cadeia da Polimerase em Tempo Real
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