Silva Francisco J, Domínguez-Santos Rebeca, Latorre Amparo, García-Ferris Carlos
Institute for Integrative Systems Biology (I2SysBio), University of Valencia and Spanish Research Council, 46980 Paterna, Spain.
Genomics and Health Area, Foundation for the Promotion of Sanitary and Biomedical Research of the Valencia Region, 46020 Valencia, Spain.
Int J Mol Sci. 2024 Apr 11;25(8):4228. doi: 10.3390/ijms25084228.
We explored the metabolic integration of and its obligate endosymbiont by the transcriptomic analysis of the fat body of quasi-aposymbiotic cockroaches, where the endosymbionts were almost entirely removed with rifampicin. Fat bodies from quasi-aposymbiotic insects displayed large differences in gene expression compared to controls. In quasi-aposymbionts, the metabolism of phenylalanine and tyrosine involved in cuticle sclerotization and pigmentation increased drastically to compensate for the deficiency in the biosynthesis of these amino acids by the endosymbionts. On the other hand, the uricolytic pathway and the biosynthesis of uric acid were severely decreased, probably because the reduced population of endosymbionts was unable to metabolize urea to ammonia. Metabolite transporters that could be involved in the endosymbiosis process were identified. Immune system and antimicrobial peptide (AMP) gene expression was also reduced in quasi-aposymbionts, genes encoding peptidoglycan-recognition proteins, which may provide clues for the maintenance of the symbiotic relationship, as well as three AMP genes whose involvement in the symbiotic relationship will require additional analysis. Finally, a search for AMP-like factors that could be involved in controlling the endosymbiont identified two orphan genes encoding proteins smaller than 200 amino acids underexpressed in quasi-aposymbionts, suggesting a role in the host-endosymbiont relationship.
我们通过对拟aposymbiotic蟑螂脂肪体的转录组分析,探索了[物种名称]及其专性内共生菌的代谢整合情况,在这些蟑螂中,用利福平几乎完全去除了内共生菌。与对照组相比,拟aposymbiotic昆虫的脂肪体在基因表达上表现出很大差异。在拟aposymbionts中,参与表皮硬化和色素沉着的苯丙氨酸和酪氨酸代谢急剧增加,以补偿内共生菌在这些氨基酸生物合成方面的不足。另一方面,尿酸分解途径和尿酸的生物合成严重减少,可能是因为内共生菌数量减少无法将尿素代谢为氨。鉴定出了可能参与内共生过程的代谢物转运蛋白。拟aposymbionts中的免疫系统和抗菌肽(AMP)基因表达也降低了,编码肽聚糖识别蛋白的基因,这可能为共生关系的维持提供线索,还有三个AMP基因,其在共生关系中的作用需要进一步分析。最后,对可能参与控制内共生菌的AMP样因子的搜索,鉴定出两个孤儿基因,它们编码的蛋白质小于200个氨基酸,在拟aposymbionts中表达下调,表明其在宿主-内共生菌关系中发挥作用。