{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T20:07:40Z","timestamp":1792181260946,"version":"4.4.0"},"reference-count":48,"publisher":"Rockefeller University Press","issue":"7","content-domain":{"domain":["rupress.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2011,7,4]]},"abstract":"<jats:p>Apicomplexa are important pathogens that include the causative agents of malaria, toxoplasmosis, and cryptosporidiosis. Apicomplexan parasites contain a relict chloroplast, the apicoplast. The apicoplast is indispensable and an attractive drug target. The apicoplast is home to a 1-deoxy-d-xylulose-5-phosphate (DOXP) pathway for the synthesis of isoprenoid precursors. This pathway is believed to be the most conserved function of the apicoplast, and fosmidomycin, a specific inhibitor of the pathway, is an effective antimalarial. Surprisingly, fosmidomycin has no effect on most other apicomplexans. Using Toxoplasma gondii, we establish that the pathway is essential in parasites that are highly fosmidomycin resistant. We define the molecular basis of resistance and susceptibility, experimentally testing various host and parasite contributions in T. gondii and Plasmodium. We demonstrate that in T. gondii the parasite plasma membrane is a critical barrier to drug uptake. In strong support of this hypothesis, we engineer de novo drug-sensitive T. gondii parasites by heterologous expression of a bacterial transporter protein. Mice infected with these transgenic parasites can now be cured from a lethal challenge with fosmidomycin. We propose that the varied extent of metabolite exchange between host and parasite is a crucial determinator of drug susceptibility and a predictor of future resistance.<\/jats:p>","DOI":"10.1084\/jem.20110039","type":"journal-article","created":{"date-parts":[[2011,6,21]],"date-time":"2011-06-21T01:13:00Z","timestamp":1308618780000},"page":"1547-1559","update-policy":"https:\/\/doi.org\/10.1084\/jem.crossmarkpolicy","source":"Crossref","is-referenced-by-count":165,"title":["Apicoplast isoprenoid precursor synthesis and the molecular basis of fosmidomycin resistance in\n                    <i>Toxoplasma gondii<\/i>"],"prefix":"10.1084","volume":"208","author":[{"given":"Sethu C.","family":"Nair","sequence":"first","affiliation":[{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Carrie F.","family":"Brooks","sequence":"additional","affiliation":[{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christopher D.","family":"Goodman","sequence":"additional","affiliation":[{"name":"School of Botany University of Melbourne, Melbourne VIC 3010, Australia 3"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Angelika","family":"Strurm","sequence":"additional","affiliation":[{"name":"School of Botany University of Melbourne, Melbourne VIC 3010, Australia 3"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Geoffrey I.","family":"McFadden","sequence":"additional","affiliation":[{"name":"School of Botany University of Melbourne, Melbourne VIC 3010, Australia 3"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandeep","family":"Sundriyal","sequence":"additional","affiliation":[{"name":"Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030 4"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Justin L.","family":"Anglin","sequence":"additional","affiliation":[{"name":"Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030 4"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yongcheng","family":"Song","sequence":"additional","affiliation":[{"name":"Department of Pharmacology, Baylor College of Medicine, Houston, TX 77030 4"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Silvia N.J.","family":"Moreno","sequence":"additional","affiliation":[{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"},{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Boris","family":"Striepen","sequence":"additional","affiliation":[{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"},{"name":"Department of Cellular Biology 1 and 2"},{"name":"Center for Tropical and Emerging Global Diseases, University of Georgia, Athens, GA, 30602 1 and 2"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"291","published-online":{"date-parts":[[2011,6,20]]},"reference":[{"key":"2023072600500549900_bib1","doi-asserted-by":"publisher","first-page":"851","DOI":"10.1111\/j.1462-5822.2006.00834.x","article-title":"Babesia and plasmodia increase host erythrocyte permeability through distinct mechanisms","volume":"9","author":"Alkhalil","year":"2007","journal-title":"Cell. 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