13 research outputs found

    Applications of Metabolomics in Reproductive Biology

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    Metabolomics can be performed associated with other omics approaches such as genomics, transcriptomics, and proteomics. For example, a recent study showed interesting results using an Integrative Personal Omics Profile (iPOP) to identify markers for possible diseases affecting an individual. This chapter suggests that such a method leads to an early diagnosis and facilitates prevention of certain diseases, such as type 2 diabetes, aplastic anemia, human rhinovirus infection, and respiratory syncytial virus infection. For assisted reproductive technologies (ART), metabolomics methods have been chosen as noninvasive approaches to improve the assessment of embryo quality. Metabolic profiling analysis of follicular fluids (FF) from lactating cows and heifers by gas chromatography-mass spectrometry (GC-MS) identified the presence of greater concentrations of saturated fatty acids in follicles from cows than those from heifers. Large animals have been used as models for research of human disease and physiology due to their specific physiological characteristics, sometimes similar to the human

    Metabolomic markers of fertility in bull seminal plasma

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    Metabolites play essential roles in biological systems, but detailed identities and significance of the seminal plasma metabolome related to bull fertility are still unknown. The objectives of this study were to determine the comprehensive metabolome of seminal plasma from Holstein bulls and to ascertain the potential of metabolites as biomarkers of bull fertility. The seminal plasma metabolome from 16 Holstein bulls with two fertility rates were determined by gas chromatography-mass spectrometry (GC-MS). Multivariate and univariate analyses of the data were performed, and the pathways associated with the seminal plasma metabolome were identified using bioinformatics approaches. Sixty-three metabolites were identified in the seminal plasma of all bulls. Fructose was the most abundant metabolite in the seminal fluid, followed for citric acid, lactic acid, urea and phosphoric acid. Androstenedione, 4-ketoglucose, D-xylofuranose, 2-oxoglutaric acid and erythronic acid represented the least predominant metabolites. Partial-Least Squares Discriminant Analysis (PLSDA) revealed a distinct separation between high and low fertility bulls. The metabolites with the greatest Variable Importance in Projection score (VIP \u3e 2) were 2-oxoglutaric acid and fructose. Heat-map analysis, based on VIP score, and univariate analysis indicated that 2-oxoglutaric acid was less (P = 0.02); whereas fructose was greater (P = 0.02) in high fertility than in low fertility bulls. The current study is the first to describe the metabolome of bull seminal plasma using GC-MS and presented metabolites such as 2-oxoglutaric acid and fructose as potential biomarkers of bull fertility

    Seminal plasma proteins and metabolites: Effects on sperm function and potential as fertility markers

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    Molecular components of sperm and in the media surrounding them influence male fertility. In this regard, seminal plasma proteins and metabolites modulate various reproductive events, including sperm motility and capacitation, cell protection, acrosome reaction, fertilization and embryonic development. Empirical associations between seminal proteins and metabolites and fertility indicate that these molecules are potential molecular markers of male reproductive status in cattle and other species

    Metabolomic markers of fertility in bull seminal plasma

    No full text
    <div><p>Metabolites play essential roles in biological systems, but detailed identities and significance of the seminal plasma metabolome related to bull fertility are still unknown. The objectives of this study were to determine the comprehensive metabolome of seminal plasma from Holstein bulls and to ascertain the potential of metabolites as biomarkers of bull fertility. The seminal plasma metabolome from 16 Holstein bulls with two fertility rates were determined by gas chromatography-mass spectrometry (GC-MS). Multivariate and univariate analyses of the data were performed, and the pathways associated with the seminal plasma metabolome were identified using bioinformatics approaches. Sixty-three metabolites were identified in the seminal plasma of all bulls. Fructose was the most abundant metabolite in the seminal fluid, followed for citric acid, lactic acid, urea and phosphoric acid. Androstenedione, 4-ketoglucose, D-xylofuranose, 2-oxoglutaric acid and erythronic acid represented the least predominant metabolites. Partial-Least Squares Discriminant Analysis (PLSDA) revealed a distinct separation between high and low fertility bulls. The metabolites with the greatest Variable Importance in Projection score (VIP > 2) were 2-oxoglutaric acid and fructose. Heat-map analysis, based on VIP score, and univariate analysis indicated that 2-oxoglutaric acid was less (<i>P</i> = 0.02); whereas fructose was greater (<i>P</i> = 0.02) in high fertility than in low fertility bulls. The current study is the first to describe the metabolome of bull seminal plasma using GC-MS and presented metabolites such as 2-oxoglutaric acid and fructose as potential biomarkers of bull fertility.</p></div

    VIP scores of seminal plasma metabolites in high (HF) and low fertility (LF) bulls.

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    <p>The selected metabolites were those with VIP score of greater than 1.5. Heat map with red or green boxes on the right indicates high and low abundance ratio, respectively, of the corresponding metabolite in HF and LF bulls. VIP score was based on the PLS-DA model.</p

    Number of metabolites per chemical class.

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    <p>Metabolites identified were categorized according to their chemical classes, defined as amino acids, peptides and analogues; carbohydrates and carbohydrate conjugates; fatty acids and conjugates; steroids and steroid derivatives; nucleosides, nucleotides, and analogues; others organic compounds and inorganic compounds.</p

    PLS-DA score plot of seminal plasma from high (HF) and low fertility (LF) bulls.

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    <p>The plots indicate that a separation could be observed between HF and LF bulls. Supervised PLS-DA was obtained with 2 components. The explained variances are shown in parentheses.</p

    Representative GC-MS chromatogram of bull seminal plasma.

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    <p>Peaks of lactic acid, glycerol, phosphoric acid, citric acid, fructose, heptadecanoic acid (internal standard) and cholesterol are indicated.</p
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