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捻转血矛线虫及其他寄生线虫的生物化学

The Biochemistry of Haemonchus contortus and Other Parasitic Nematodes.

作者信息

Harder A

机构信息

WE Biology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.

出版信息

Adv Parasitol. 2016;93:69-94. doi: 10.1016/bs.apar.2016.02.010. Epub 2016 Mar 17.

DOI:10.1016/bs.apar.2016.02.010
PMID:27238003
Abstract

Different life cycle stages of Haemonchus contortus adapt to different ecosystems. This adaptation is accompanied by alterations in gene transcription and expression associated with the energy, amino acid, nitrogen, lipid and/or nucleic acid metabolism of the respective stages. For example, the aerobic metabolism of larvae depends on an efficient citric acid cycle, whereas the anaerobic metabolism of adults requires glycolysis, resulting in the production of volatile fatty acids, such as acetic acid and propionic acid. There are only few anthelmintics targeting nematode energy metabolism. In addition, H. contortus has reduced pathways for amino acid metabolism, polyamine metabolism and nitrogen excretion pathways. Moreover, nucleic acid metabolism comprising purine and pyrimidine salvage pathways as well as lipid metabolism are reduced. In addition, nematodes possess a particular composition of their cuticle. Energy production of adult worms is mainly linked to egg production and complex regulation of the neuromuscular system in both females and males. In this context, microtubules consisting of α- and β-tubulin heterodimers play a crucial role in the presynaptic vesicle transport. Due to the significant distinction of its quarternary structure in nematodes in comparison to other organisms, β-tubulin was identified as a major target for benzimidazoles used for anthelmintic treatment. Concerning the function of the neuromuscular system, acetylcholine, a ligand of the nicotinic acetylcholine receptor (nAChR), is the major excitatory neurotransmitter in H. contortus. In contrast, glutamate-gated chloride channels, calcium- and voltage-dependent potassium channels as well as γ-aminobutyric acid (GABA)A and its receptors act as inhibitory neurotransmitters and thus opponents to nAChR. For example, the calcium- and voltage-dependent potassium channel SLO-1 is an important target of emodepside, which is involved in the sensitive regulation of activatory and inhibitory receptors of the nervous system. Most of the modern anthelmintics target these different neuromuscular receptors. The mechanisms of resistance to anthelmintics, either specific or non-specific, are associated with changes in the molecular targets of the drugs, changes in metabolism of the drug (inactivation, removal or prevention of its activation) and/or increased efflux systems. The biochemical and molecular analyses of key developmental, metabolic and structural process of H. contortus still require substantial efforts. The nAChR, glutamate-gated chloride channel and calcium- and voltage-dependent potassium channel SLO-1 have long been known as being essential for nematode survival. Therefore, future research should be intensified to fully resolve the three-dimensional structures of these receptors, as has already been started for glutamate-gated chloride channel. With this knowledge, it should be possible to design new anthelmintics, which possess improved binding capacities to corresponding receptors.

摘要

捻转血矛线虫的不同生命周期阶段适应不同的生态系统。这种适应伴随着与各阶段能量、氨基酸、氮、脂质和/或核酸代谢相关的基因转录和表达的改变。例如,幼虫的有氧代谢依赖于高效的柠檬酸循环,而成虫的无氧代谢则需要糖酵解,从而产生挥发性脂肪酸,如乙酸和丙酸。针对线虫能量代谢的驱虫药很少。此外,捻转血矛线虫的氨基酸代谢、多胺代谢和氮排泄途径有所减少。此外,包括嘌呤和嘧啶补救途径的核酸代谢以及脂质代谢也有所减少。此外,线虫的角质层具有特殊的组成。成虫的能量产生主要与产卵以及雌雄两性神经肌肉系统的复杂调节有关。在这种情况下,由α-和β-微管蛋白异二聚体组成的微管在突触前囊泡运输中起关键作用。由于线虫中其四级结构与其他生物体相比有显著差异,β-微管蛋白被确定为用于驱虫治疗的苯并咪唑类药物的主要靶点。关于神经肌肉系统的功能,烟碱型乙酰胆碱受体(nAChR)的配体乙酰胆碱是捻转血矛线虫中的主要兴奋性神经递质。相比之下,谷氨酸门控氯离子通道、钙和电压依赖性钾通道以及γ-氨基丁酸(GABA)A及其受体作为抑制性神经递质,因此是nAChR的拮抗剂。例如,钙和电压依赖性钾通道SLO-1是埃莫昔丁的重要靶点,它参与神经系统激活和抑制受体的敏感调节。大多数现代驱虫药靶向这些不同的神经肌肉受体。驱虫药抗性机制,无论是特异性还是非特异性的,都与药物分子靶点的变化、药物代谢的变化(失活、清除或防止其激活)和/或外排系统增加有关。对捻转血矛线虫关键发育、代谢和结构过程的生化和分子分析仍需要大量努力。nAChR、谷氨酸门控氯离子通道和钙和电压依赖性钾通道SLO-1长期以来一直被认为对线虫生存至关重要。因此,应加强未来研究以全面解析这些受体的三维结构,就像已经针对谷氨酸门控氯离子通道开展的研究那样。有了这些知识,应该有可能设计出对相应受体具有更好结合能力的新型驱虫药。

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