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Immunometabolic checkpoints are often exploited by kinetoplastid and protozoan parasites to establish chronic infection, which can significantly impair host metabolic homeostasis. The recent growth of tools to analyze metabolism is expanding our understanding of these questions. Here, we review and contrast host metabolic alterations that occur\n                    <jats:italic>in vivo<\/jats:italic>\n                    during infection with\n                    <jats:italic>Leishmania<\/jats:italic>\n                    , trypanosomes,\n                    <jats:italic>Toxoplasma<\/jats:italic>\n                    ,\n                    <jats:italic>Plasmodium,<\/jats:italic>\n                    and\n                    <jats:italic>Cryptosporidium<\/jats:italic>\n                    . Although genetically divergent, there are commonalities among these pathogens in terms of metabolic needs, induction of the type I immune responses required for clearance, and the potential for sustained host metabolic dysbiosis. Comparing these pathogens provides an opportunity to explore how transmission strategy, nutritional demand, and host cell and tissue tropism drive similarities and unique aspects in host response and infection outcome and to design new strategies to treat disease.\n                  <\/jats:p>","DOI":"10.1128\/mmbr.00164-22","type":"journal-article","created":{"date-parts":[[2024,2,1]],"date-time":"2024-02-01T09:01:11Z","timestamp":1706778071000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":14,"title":["The intersection of host\n                    <i>in vivo<\/i>\n                    metabolism and immune responses to infection with kinetoplastid and apicomplexan parasites"],"prefix":"10.1128","volume":"88","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-5327-7578","authenticated-orcid":true,"given":"Sarah","family":"Ewald","sequence":"first","affiliation":[{"name":"Department of Microbiology, Immunology, and 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