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A\n            <jats:italic>plaC<\/jats:italic>\n            mutant showed even higher levels of\n            <jats:italic>lapA<\/jats:italic>\n            and\n            <jats:italic>lapB<\/jats:italic>\n            transcripts, and a\n            <jats:italic>lapA lapB<\/jats:italic>\n            mutant showed heightening of\n            <jats:italic>plaC<\/jats:italic>\n            mRNA levels, suggesting that the role of the LapA\/B aminopeptidase is compensatory with respect to that of the PlaC acyltransferase. Hence, we made double mutants and found that\n            <jats:italic>lapA plaC<\/jats:italic>\n            mutants have an ~50-fold defect during infection of\n            <jats:named-content content-type=\"genus-species\">A.\u00a0castellanii<\/jats:named-content>\n            . These data revealed, for the first time, the importance of LapA in any sort of infection; thus, we purified LapA and defined its crystal structure, activation by another T2S-dependent protease (ProA), and broad substrate specificity. When the amoebal infection medium was supplemented with amino acids, the defect of the\n            <jats:italic>lapA plaC<\/jats:italic>\n            mutant was reversed, implying that LapA generates amino acids for nutrition. Since the LapA and PlaC data did not fully explain the role of T2S in infection, we identified, via proteomic analysis, a novel secreted protein (NttD) that promotes infection of\n            <jats:named-content content-type=\"genus-species\">A.\u00a0castellanii<\/jats:named-content>\n            . A\n            <jats:italic>lapA plaC nttD<\/jats:italic>\n            mutant displayed an even greater (100-fold) defect, demonstrating that the LapA, PlaC, and NttD data explain, to a significant degree, the importance of T2S. LapA-, PlaC-, and NttD-like proteins had distinct distribution patterns within and outside the\n            <jats:italic>Legionella<\/jats:italic>\n            genus. LapA was notable for having as its closest homologue an\n            <jats:named-content content-type=\"genus-species\">A.\u00a0castellanii<\/jats:named-content>\n            protein.\n          <\/jats:p>\n          <jats:p>\n            <jats:bold>IMPORTANCE<\/jats:bold>\n            Transmission of\n            <jats:named-content content-type=\"genus-species\">L.\u00a0pneumophila<\/jats:named-content>\n            to humans is facilitated by its ability to grow in\n            <jats:italic>Acanthamoeba<\/jats:italic>\n            species. We previously documented that type II secretion (T2S) promotes\n            <jats:named-content content-type=\"genus-species\">L.\u00a0pneumophila<\/jats:named-content>\n            infection of\n            <jats:named-content content-type=\"genus-species\">A.\u00a0castellanii<\/jats:named-content>\n            . Utilizing transcriptional analysis and proteomics, double and triple mutants, and crystal structures, we defined three secreted substrates\/effectors that largely clarify the role of T2S during infection of\n            <jats:named-content content-type=\"genus-species\">A.\u00a0castellanii<\/jats:named-content>\n            . Particularly interesting are the unique functional overlap between an acyltransferase (PlaC) and aminopeptidase (LapA), the broad substrate specificity and eukaryotic-protein-like character of LapA, and the novelty of NttD. Linking LapA to amino acid acquisition, we defined, for the first time, the importance of secreted aminopeptidases in intracellular infection. Bioinformatic investigation, not previously applied to T2S, revealed that effectors originate from diverse sources and distribute within the\n            <jats:italic>Legionella<\/jats:italic>\n            genus in unique ways. The results of this study represent a major advance in understanding\n            <jats:italic>Legionella<\/jats:italic>\n            ecology and pathogenesis, bacterial secretion, and the evolution of intracellular parasitism.\n          <\/jats:p>","DOI":"10.1128\/mbio.00528-18","type":"journal-article","created":{"date-parts":[[2018,4,16]],"date-time":"2018-04-16T08:42:35Z","timestamp":1523868155000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":38,"title":["Type II Secretion-Dependent Aminopeptidase LapA and Acyltransferase PlaC Are Redundant for Nutrient Acquisition during\n            <i>Legionella pneumophila<\/i>\n            Intracellular Infection of Amoebas"],"prefix":"10.1128","volume":"9","author":[{"given":"Richard C.","family":"White","sequence":"first","affiliation":[{"name":"Department of Microbiology and Immunology, Northwestern University Medical School, Chicago, Illinois, 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