Essential roles of HGT-derived sterol biosynthesis in trypanosomatid growth and parasitism

Horizontal gene transfer (HGT) has played a major role in the evolution of kinetoplastids, but its scope and functional significance remain incompletely understood. We performed a comparative genomic analysis of 12 trypanosomatid parasites together with the free-living kinetoplastid Bodo saltans as an outgroup, using the DarkHorse algorithm to identify putative HGT candidates. B. saltans encoded the largest number of HGT-derived genes (980; 5.2% of coding sequences), whereas parasitic Leishmania species retained the fewest (67-71; 0.8-0.9%), consistent with extensive gene loss accompanying the transition to parasitism. Dollo parsimony reconstruction indicated that the kinetoplastid ancestor acquired numerous horizontally transferred genes, many of which were subsequently lost, but several functionally important families were retained in trypanosomatids. Among these, we identified a bacterial-derived aspartate ammonia ligase that, together with aspartate ammonia lyase, likely supports redox balance and succinate fermentation under anaerobic conditions in the insect gut. Phylogenetic analyses also revealed bacterial or archaeal origins of multiple enzymes in ergosterol biosynthesis, an essential pathway in trypanosomatids. Functional characterization in Lotmaria passim demonstrated that sterol C-8 isomerase is indispensable, whereas sterol C-5 desaturase is nonessential in vitro but critical for parasite growth at low temperature, amphotericin B sensitivity, and successful colonization of the honey bee hindgut. These findings illustrate the dual evolutionary trajectory of HGT in kinetoplastids: extensive gene loss during the transition to parasitism, coupled with the retention of lineage-specific innovations essential for survival in host environments.