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丙酮酸-铁氧化还原蛋白氧化还原酶的系统发育分析,一种参与细菌和原生动物中硝基前药药理活化的氧化还原酶。

Phylogenetic Analysis of Pyruvate-Ferredoxin Oxidoreductase, a Redox Enzyme Involved in the Pharmacological Activation of Nitro-Based Prodrugs in Bacteria and Protozoa.

作者信息

Duwor Seth, Brites Daniela, Mäser Pascal

机构信息

Swiss Tropical and Public Health Institute, 4123 Allschwil, Switzerland.

Faculty of Science, University of Basel, 4001 Basel, Switzerland.

出版信息

Biology (Basel). 2024 Mar 9;13(3):178. doi: 10.3390/biology13030178.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/950e/10968658/16cf383ccedf/biology-13-00178-g001.jpg

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本文引用的文献

1
The Gene Ontology knowledgebase in 2023.
Genetics. 2023 May 4;224(1). doi: 10.1093/genetics/iyad031.
2
From Magic Bullet to Magic Bomb: Reductive Bioactivation of Antiparasitic Agents.
ACS Infect Dis. 2021 Oct 8;7(10):2777-2786. doi: 10.1021/acsinfecdis.1c00118. Epub 2021 Sep 2.
4
Horizontal Gene Transfer in Eukaryotes: Not if, but How Much?
Trends Genet. 2020 Dec;36(12):915-925. doi: 10.1016/j.tig.2020.08.006. Epub 2020 Oct 1.
5
Lateral Gene Transfer Mechanisms and Pan-genomes in Eukaryotes.
Trends Parasitol. 2020 Nov;36(11):927-941. doi: 10.1016/j.pt.2020.07.014. Epub 2020 Aug 19.
8
Distinct evolutionary dynamics of horizontal gene transfer in drug resistant and virulent clones of Klebsiella pneumoniae.
PLoS Genet. 2019 Apr 15;15(4):e1008114. doi: 10.1371/journal.pgen.1008114. eCollection 2019 Apr.
9
Resistance formation to nitro drugs in Giardia lamblia: No common markers identified by comparative proteomics.
Int J Parasitol Drugs Drug Resist. 2019 Apr;9:112-119. doi: 10.1016/j.ijpddr.2019.03.002. Epub 2019 Mar 15.
10
MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.
Mol Biol Evol. 2018 Jun 1;35(6):1547-1549. doi: 10.1093/molbev/msy096.

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