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Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources
Published on: January 22, 2018
Trophic dynamics and metabolic pathways in host parasite interactions revealed by nitrogen isotope analysis of amino
Shaista Khaliq1,2, Milen Nachev3,2, Philip M Riekenberg4,5
1Instrumental Analytical Chemistry, University of Duisburg-Essen, Universitätsstr. 5, 45141, Essen, Germany.
Abstract:
Trophic interactions are crucial for understanding food web complexity and energy flow in ecosystems. Including parasites in these analyses can alter dynamics and challenge ecological assumptions. Compound-specific isotope analysis offers greater precision than bulk stable isotope analysis by analyzing individual amino acids, providing deeper insights into nutrient exchange and metabolism in host-parasite systems. In this study, we conducted a 120-day controlled feeding experiment to investigate parasite metabolic pathways, host-parasite trophic dynamics, and trophic fractionation between infected and uninfected sticklebacks. Nitrogen isotope composition (δ15N) was measured in host Gasterosteus aculeatus liver and muscle tissues, and its 'cestode' parasite (Schistocephalus solidus). Parasite serine δ15N values were higher by 4.4 ± 2.4‰ compared to host liver, indicating a strong metabolic link. Lower proline concentrations and increased alanine δ15N values (5‰) indicate support of parasite growth through conversion to hydroxyproline and increased gluconeogenesis. The trophic position difference between parasite and host tissues was < 0.5, suggesting direct assimilation of host-derived products. Infected host tissues exhibited ~ 5‰ increase in glycine δ15N over time compared to control tissues, likely reflecting the host's increased metabolic demand for immune support during infection. This study highlights the complex metabolic interactions in host-parasite systems.
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