A new technique to study nutrient flow in host-parasite systems by carbon stable isotope analysis of amino acids and glucose

[1]  B. Sures,et al.  Insights into amino acid fractionation and incorporation by compound-specific carbon isotope analysis of three-spined sticklebacks , 2022, Scientific reports.

[2]  T. Larsen,et al.  Tracing the Trophic Fate of Aquafeed Macronutrients With Carbon Isotope Ratios of Amino Acids , 2022, Frontiers in Marine Science.

[3]  W. Brand,et al.  How to Couple LC-IRMS with HRMS─A Proof-of-Concept Study. , 2022, Analytical chemistry.

[4]  C. Agnisola,et al.  A theoretical evaluation of the respiration rate partition in the Gasterosteus aculeatus-Schistocephalus solidus host-parasite system , 2021 .

[5]  L. IJsseldijk,et al.  Stable nitrogen isotope analysis of amino acids as a new tool to clarify complex parasite–host interactions within food webs , 2021, Oikos.

[6]  E. Borvinskaya,et al.  Zone of Interaction Between the Parasite and the Host: Protein Profile of the Body Cavity Fluid of Gasterosteus aculeatus L. Infected with the Cestode Schistocephalus solidus (Muller, 1776) , 2021, Acta parasitologica.

[7]  Andrew D. Moore,et al.  Climate change facilitates a parasite’s host exploitation via temperature‐mediated immunometabolic processes , 2020, Global change biology.

[8]  Y. Takano,et al.  A new insight into isotopic fractionation associated with decarboxylation in organisms: implications for amino acid isotope approaches in biogeoscience , 2020, Progress in Earth and Planetary Science.

[9]  Brian D. Slaughter,et al.  Adaptation to low parasite abundance affects immune investment and immunopathological responses of cavefish , 2020, Nature Ecology & Evolution.

[10]  Y. Takano,et al.  A method for stable carbon isotope measurement of underivatized individual amino acids by multi-dimensional high-performance liquid chromatography and elemental analyzer/isotope ratio mass spectrometry. , 2020, Rapid communications in mass spectrometry : RCM.

[11]  R. Poulin,et al.  Why ignoring parasites in fish ecology is a mistake. , 2020, International journal for parasitology.

[12]  C. Micheloni,et al.  Bulk and compound-specific stable isotope ratio analysis for authenticity testing of organically grown tomatoes. , 2020, Food chemistry.

[13]  B. Sures,et al.  You are how you eat: differences in trophic position of two parasite species infecting a single host according to stable isotopes , 2020, Parasitology Research.

[14]  C. Landry,et al.  The parasite Schistocephalus solidus secretes proteins with putative host manipulation functions , 2020, Parasites & Vectors.

[15]  B. Sures,et al.  Stable isotope analysis spills the beans about spatial variance in trophic structure in a fish host – parasite system from the Vaal River System, South Africa , 2019, International journal for parasitology. Parasites and wildlife.

[16]  Iain D. Couzin,et al.  Schistocephalus parasite infection alters sticklebacks’ movement ability and thereby shapes social interactions , 2019, Scientific Reports.

[17]  R. Heintz,et al.  Assessment of two feeds on survival, proximate composition, and amino acid carbon isotope discrimination in hatchery-reared Chinook salmon , 2019, Fisheries Research.

[18]  T. Larsen,et al.  13C values of glycolytic amino acids as indicators of carbohydrate utilization in carnivorous fish , 2019, PeerJ.

[19]  J. Rabinowitz,et al.  T Cell Activation Depends on Extracellular Alanine. , 2019, Cell reports.

[20]  A. Senior,et al.  Parasites and stable isotopes: a comparative analysis of isotopic discrimination in parasitic trophic interactions , 2019, Oikos.

[21]  W. Brand,et al.  New Concepts for the Determination of Oxidation Efficiencies in Liquid Chromatography-Isotope Ratio Mass Spectrometry. , 2019, Analytical chemistry.

[22]  S. Shikano,et al.  Application of stable isotopic analyses for fish host–parasite systems: an evaluation tool for parasite-mediated material flow in aquatic ecosystems , 2019, Aquatic Ecology.

[23]  Glen P. Jackson,et al.  Analysis of the 13C isotope ratios of amino acids in the larvae, pupae and adult stages of Calliphora vicina blow flies and their carrion food sources , 2018, Analytical and Bioanalytical Chemistry.

[24]  Sora L. Kim,et al.  Amino acid isotope discrimination factors for a carnivore: physiological insights from leopard sharks and their diet , 2018, Oecologia.

[25]  T. Larsen,et al.  Know your fish: A novel compound-specific isotope approach for tracing wild and farmed salmon. , 2018, Food chemistry.

[26]  Keita Yamada,et al.  Position‐specific 13C/12C analysis of amino acid carboxyl groups – automated flow‐injection analysis based on reaction with ninhydrin , 2018, Rapid communications in mass spectrometry : RCM.

[27]  C. MacLeod,et al.  Stable-isotope analysis: a neglected tool for placing parasites in food webs , 2018, Journal of Helminthology.

[28]  H. W. van der Veer,et al.  Trophic relationship between the invasive parasitic copepod Mytilicola orientalis and its native blue mussel (Mytilus edulis) host , 2017, Parasitology.

[29]  T. O’Connell.  ‘Trophic’ and ‘source’ amino acids in trophic estimation: a likely metabolic explanation , 2017, Oecologia.

[30]  B. T. Fuller,et al.  The dietary protein paradox and threonine 15 N-depletion: Pyridoxal-5'-phosphate enzyme activity as a mechanism for the δ15 N trophic level effect. , 2017, Rapid communications in mass spectrometry : RCM.

[31]  Cristina E. Valdiosera,et al.  High-resolution palaeodietary reconstruction: Amino acid δ13C analysis of keratin from single hairs of mummified human individuals , 2017 .

[32]  B. Sures,et al.  Understanding trophic interactions in host-parasite associations using stable isotopes of carbon and nitrogen , 2017, Parasites & Vectors.

[33]  C. Landry,et al.  Major host transitions are modulated through transcriptome‐wide reprogramming events in Schistocephalus solidus, a threespine stickleback parasite , 2017, Molecular ecology.

[34]  D. Bolnick,et al.  Recent evolution of extreme cestode growth suppression by a vertebrate host , 2016, Proceedings of the National Academy of Sciences.

[35]  Jian-ying Zhang,et al.  Live Edwardsiella tarda vaccine enhances innate immunity by metabolic modulation in zebrafish. , 2015, Fish & shellfish immunology.

[36]  K. McMahon,et al.  Carbon and nitrogen isotope fractionation of amino acids in an avian marine predator, the gentoo penguin (Pygoscelis papua) , 2015, Ecology and evolution.

[37]  K. Lafferty,et al.  Parasites as prey in aquatic food webs: implications for predator infection and parasite transmission , 2013 .

[38]  T. Larsen,et al.  Tracing Carbon Sources through Aquatic and Terrestrial Food Webs Using Amino Acid Stable Isotope Fingerprinting , 2013, PloS one.

[39]  J. Locasale.  Serine, glycine and one-carbon units: cancer metabolism in full circle , 2013, Nature Reviews Cancer.

[40]  Guoyao Wu,et al.  Glycine metabolism in animals and humans: implications for nutrition and health , 2013, Amino Acids.

[41]  R. Hedges,et al.  Variation of bone collagen amino acid δ13C values in archaeological humans and fauna with different dietary regimes: developing frameworks of dietary discrimination. , 2012, American journal of physical anthropology.

[42]  D. Post,et al.  Applying stable isotopes to examine food‐web structure: an overview of analytical tools , 2012, Biological reviews of the Cambridge Philosophical Society.

[43]  Richard W. Hanson,et al.  Resurgence of Serine: An Often Neglected but Indispensable Amino Acid* , 2012, The Journal of Biological Chemistry.

[44]  R. Evershed,et al.  Comparison of liquid chromatography-isotope ratio mass spectrometry (LC/IRMS) and gas chromatography-combustion-isotope ratio mass spectrometry (GC/C/IRMS) for the determination of collagen amino acid δ13C values for palaeodietary and palaeoecological reconstruction. , 2011, Rapid communications in mass spectrometry : RCM.

[45]  M. Fogel,et al.  Contributions of direct incorporation from diet and microbial amino acids to protein synthesis in Nile tilapia , 2011 .

[46]  J. McCullagh,et al.  The effect of dietary amino acid abundance and isotopic composition on the growth rate, metabolism and tissue δ13C of rainbow trout , 2011, British Journal of Nutrition.

[47]  D. Mathis,et al.  Immunometabolism: an emerging frontier , 2011, Nature Reviews Immunology.

[48]  M. Richards,et al.  Investigation of amino acid d13C signatures in bone collagen to reconstruct human palaeodiets using liquid chromatography–isotope ratio mass spectrometry , 2010 .

[49]  T. Elsdon,et al.  Carbon isotope fractionation of amino acids in fish muscle reflects biosynthesis and isotopic routing from dietary protein. , 2010, The Journal of animal ecology.

[50]  S. Carleton,et al.  Growth and catabolism in isotopic incorporation: a new formulation and experimental data , 2010 .

[51]  Paul L. Koch,et al.  Using stable isotope biogeochemistry to study marine mammal ecology , 2010 .

[52]  J. McCullagh,et al.  Mixed-mode chromatography/isotope ratio mass spectrometry. , 2010, Rapid communications in mass spectrometry : RCM.

[53]  M. Raghavan,et al.  Amino acid delta13C analysis of hair proteins and bone collagen using liquid chromatography/isotope ratio mass spectrometry: paleodietary implications from intra-individual comparisons. , 2010, Rapid communications in mass spectrometry : RCM.

[54]  J. Cooper,et al.  Structure and function of the l-threonine dehydrogenase (TkTDH) from the hyperthermophilic archaeon Thermococcus kodakaraensis. , 2009, Journal of structural biology.

[55]  I. Barber,et al.  The three-spined stickleback-Schistocephalus solidus system: an experimental model for investigating host-parasite interactions in fish , 2009, Parasitology.

[56]  K. Lafferty,et al.  Food web topology and parasites in the pelagic zone of a subarctic lake. , 2009, The Journal of animal ecology.

[57]  J. Middelburg,et al.  A versatile method for stable carbon isotope analysis of carbohydrates by high-performance liquid chromatography/isotope ratio mass spectrometry. , 2008, Rapid communications in mass spectrometry : RCM.

[58]  Walter Jetz,et al.  Homage to Linnaeus: How many parasites? How many hosts? , 2008, Proceedings of the National Academy of Sciences.

[59]  K. Hiraga,et al.  Glycine cleavage system: reaction mechanism, physiological significance, and hyperglycinemia. , 2008, Proceedings of the Japan Academy. Series B, Physical and biological sciences.

[60]  Eleca J. Dunham,et al.  Ecosystem energetic implications of parasite and free-living biomass in three estuaries , 2008, Nature.

[61]  K. Hammerschmidt,et al.  Who is in control of the stickleback immune system: interactions between Schistocephalus solidus and its specific vertebrate host , 2007, Proceedings of the Royal Society B: Biological Sciences.

[62]  A. Dobson,et al.  Parasites dominate food web links. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[63]  S. Jennings,et al.  Effects of chemical lipid extraction and arithmetic lipid correction on stable isotope ratios of fish tissues. , 2006, Rapid communications in mass spectrometry : RCM.

[64]  H. Boeing,et al.  Carbon and nitrogen stable isotopic composition of hair protein and amino acids can be used as biomarkers for animal-derived dietary protein intake in humans. , 2005, The Journal of nutrition.

[65]  M. Perga,et al.  ‘Are fish what they eat’ all year round? , 2005, Oecologia.

[66]  I. Barber,et al.  Effects of experimental Schistocephalus solidus infections on growth, morphology and sexual development of female three-spined sticklebacks, Gasterosteus aculeatus , 2003, Parasitology.

[67]  Kevin D. Lafferty,et al.  Trophic strategies, animal diversity and body size , 2002 .

[68]  D. Post.  USING STABLE ISOTOPES TO ESTIMATE TROPHIC POSITION: MODELS, METHODS, AND ASSUMPTIONS , 2002 .

[69]  W. Brand,et al.  Referencing strategies and techniques in stable isotope ratio analysis. , 2001, Rapid communications in mass spectrometry : RCM.

[70]  J. Grey.  Trophic fractionation and the effects of diet switch on the carbon stable isotopic ‘signatures’ of pelagic consumers , 2000 .

[71]  C. Wedekind,et al.  Lifetime reproductive output in a hermaphrodite cestode when reproducing alone or in pairs: a time cost of pairing , 1999, Evolutionary Ecology.

[72]  A. Danfær.  Nutrient metabolism and utilization in the liver , 1994 .

[73]  J. Hayes.  Factors controlling 13C contents of sedimentary organic compounds: Principles and evidence , 1993 .

[74]  P. E. Hare,et al.  The isotopic composition of carbon and nitrogen in individual amino acids isolated from modern and fossil proteins , 1991 .

[75]  R. A. Dale.  Catabolism of threonine in mammals by coupling of L-threonine 3-dehydrogenase with 2-amino-3-oxobutyrate-CoA ligase. , 1978, Biochimica et biophysica acta.

[76]  J. Barrett,et al.  Carbohydrate catabolism in the plerocercoids of Schistocephalus solidus (Cestoda: Pseudophyllidea) , 1977 .

[77]  G. Cross,et al.  Threonine catabolism in Trypanosoma brucei. , 1977, Journal of general microbiology.

[78]  P. Felig.  The glucose-alanine cycle. , 1973, Metabolism: clinical and experimental.

[79]  J. Simmons,et al.  Biochemistry and physiology of tapeworms. , 1963, Physiological reviews.

[80]  C. A. Hopkins.  Studies on cestode metabolism. I. Glycogen metabolism in Schistocephalus solidus in vivo. , 1950, The Journal of parasitology.

[81]  D. Cai,et al.  Stable carbon isotopic analysis of amino acids in a simplified food chain consisting of the green alga Chlorella spp., the calanoid copepod Calanus sinicus, and the Japanese anchovy (Engraulis japonicus) , 2018 .

[82]  K. Lafferty,et al.  Nematomorph parasites drive energy flow through a riparian ecosystem. , 2011, Ecology.

[83]  Robert Poulin,et al.  Importance of parasites and their life cycle characteristics in determining the structure of a large marine food web , 2005 .

[84]  P. Jordan,et al.  The mechanism of action of serine transhydroxymethylase. , 1970, The Biochemical journal.

[85]  J. D. Smyth.  Studies on tapeworm physiology. VII. Fertilization of Schistocephalus solidus in vitro. , 1954, Experimental parasitology.