Experimental Genetics of <i>Plasmodium berghei</i> NFU in the Apicoplast Iron-Sulfur Cluster Biogenesis Pathway

<div><p>Eukaryotic pathogens of the phylum <i>Apicomplexa</i> contain a non-photosynthetic plastid, termed apicoplast. Within this organelle distinct iron-sulfur [Fe-S] cluster proteins are likely central to biosynthesis pathways, including generation of isoprenoids and lipoic acid. Here, we targeted a nuclear-encoded component of the apicoplast [Fe-S] cluster biosynthesis pathway by experimental genetics in the murine malaria parasite <i>Plasmodium berghei</i>. We show that ablation of the gene encoding a nitrogen fixation factor U (NifU)-like domain containing protein (<i>NFUapi</i>) resulted in parasites that were able to complete the entire life cycle indicating redundant or non-essential functions. <i>nfu</i>^– parasites displayed reduced merosome formation <i>in vitro</i>, suggesting that apicoplast NFUapi plays an auxiliary role in establishing a blood stage infection. NFUapi fused to a combined fluorescent protein-epitope tag delineates the <i>Plasmodium</i> apicoplast and was tested to revisit inhibition of liver stage development by azithromycin and fosmidomycin. We show that the branched apicoplast signal is entirely abolished by azithromycin treatment, while fosmidomycin had no effect on apicoplast morphology. In conclusion, our experimental genetics analysis supports specialized and/or redundant role(s) for NFUapi in the [Fe-S] cluster biosynthesis pathway in the apicoplast of a malarial parasite.</p>