Mukhethwa Micheal Mphephu’s research while affiliated with Sefako Makgatho Health Sciences University and other places

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Publications (1)


A scatter plot illustrating the 37 metabolites that are insignificant and significant based on one-way ANOVA from the (A) stomach content and (B) colon content of different seals of A. pusillus pusillus, L. carcinophaga, O. rossii, A. tropicalis 1 and 2 species.
A heatmap illustrating the 37 metabolites clearly segregated in samples of A. pusillus pusillus, L. carcinophaga, O. rossii and A. tropicalis 1 and 2 species for stomach contents
(A) Each colored cell on the map represents the correlation value of metabolites in the data table. (B) Each colored cell on the map corresponds to a concentration value in the data table, where samples are in columns and metabolites are in rows. The heatmap was employed to identify metabolites with high or low concentrations.
A heatmap illustrating the 37 metabolites clearly segregated in samples of A. pusillus pusillus, L. carcinophaga, O. rossii and A. tropicalis 1 and 2 species for colon contents
(A) Each colored cell on the map represents a correlation value of metabolites in the data table. (B) Each colored cell on the map corresponds to a concentration value in the data table, with samples in columns and metabolites in rows. The heatmap was employed to identify metabolites with high or low concentrations.
Summaries the correlation of stomach content between species of A. pusillus pusillus, L. carcinophaga, O. rossii and A. tropicalis 1 and 2
A scatter plot illustrating the metabolites that are insignificant and significantly downregulated and upregulated in the stomachs of different seals
(A) Metabolites in A. tropicalis 1 versus O. rossii. (B) Metabolites in A. tropicalis 1 versus L. carcinophaga. (C) Metabolites in A. tropicalis 1 versus A. pusillus pusillus (D) Metabolites in A. tropicalis 1 versus A. tropicalis 2.

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Metabolomics approach for predicting stomach and colon contents in dead Arctocephalus pusillus pusillus, Arctocephalus tropicalis, Lobodon carcinophaga and Ommatophoca rossii from sub-Antarctic region
  • Article
  • Full-text available

April 2024

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Mukhethwa Micheal Mphephu

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The dietary habits of seals play a pivotal role in shaping management and administration policies, especially in regions with potential interactions with fisheries. Previous studies have utilized various methods, including traditional approaches, to predict seal diets by retrieving indigestible prey parts, such as calcified structures, from intestines, feces, and stomach contents. Additionally, methods evaluating nitrogen and stable isotopes of carbon have been employed. The metabolomics approach, capable of quantifying small-scale molecules in biofluids, holds promise for specifying dietary exposures and estimating disease risk. This study aimed to assess the diet composition of five seal species—Arctocephalus pusillus pusillus, Lobodon carcinophaga, Ommatophoca rossii, and Arctocephalus tropicalis 1 and 2—by analyzing stomach and colon contents collected from stranded dead seals at various locations. Metabolite concentrations in the seal stomach and colon contents were determined using Nuclear Magnetic Resonance Spectroscopy. Among the colon and stomach contents, 29 known and 8 unknown metabolites were identified. Four metabolites (alanine, fumarate, lactate, and proline) from stomach contents and one metabolite (alanine) from colon contents showed no significant differences between seal species (p>0.05). This suggests that traces of these metabolites in the stomach and colon contents may be produced by the seals’ gut microbiome or derived from other animals, possibly indicating reliance on fish caught at sea. Despite this insight, the cause of death for stranded seals remains unclear. The study highlights the need for specific and reliable biomarkers to precisely indicate dietary exposures across seal populations. Additionally, there is a call for the development of relevant metabolite and disease interaction networks to explore disease-related metabolites in seals. Ultimately, the metabolomic method employed in this study reveals potential metabolites in the stomach and colon contents of these seal species.

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