Duwor Seth, Brites Daniela, Mäser Pascal
Swiss Tropical and Public Health Institute, 4123 Allschwil, Switzerland.
Faculty of Science, University of Basel, 4001 Basel, Switzerland.
Biology (Basel). 2024 Mar 9;13(3):178. doi: 10.3390/biology13030178.
The present frontrunners in the chemotherapy of infections caused by protozoa are nitro-based prodrugs that are selectively activated by PFOR-mediated redox reactions. This study seeks to analyze the distribution of PFOR in selected protozoa and bacteria by applying comparative genomics to test the hypothesis that PFOR in eukaryotes was acquired through horizontal gene transfer (HGT) from bacteria. Furthermore, to identify other putatively acquired genes, proteome-wide and gene enrichment analyses were used. A plausible explanation for the patchy occurrence of PFOR in protozoa is based on the hypothesis that bacteria are potential sources of genes that enhance the adaptation of protozoa in hostile environments. Comparative genomics of and the putative gene donor, , identified eleven candidate genes for HGT involved in intermediary metabolism. If these results can be reproduced in other PFOR-possessing protozoa, it would provide more validated evidence to support the horizontal transfer of from bacteria.
目前,用于治疗原生动物感染的化疗药物中,领先的是硝基前体药物,它们通过丙酮酸铁氧化还原酶(PFOR)介导的氧化还原反应被选择性激活。本研究旨在通过应用比较基因组学来分析PFOR在选定原生动物和细菌中的分布,以检验真核生物中的PFOR是通过水平基因转移(HGT)从细菌获得的这一假设。此外,为了识别其他可能获得的基因,还进行了全蛋白质组和基因富集分析。原生动物中PFOR分布不均的一个合理的解释基于这样的假设:细菌是增强原生动物在恶劣环境中适应性的基因的潜在来源。对[具体物种1]和假定的基因供体[具体物种2]进行比较基因组学分析,确定了11个参与中间代谢的HGT候选基因。如果这些结果能够在其他含有PFOR的原生动物中得到重现,将为支持PFOR从细菌的水平转移提供更多经过验证的证据。