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巨蟒血中的 BoaγPLI 是一种广谱的蛇毒 PLA 病理生理作用抑制剂。

BoaγPLI from Boa constrictor Blood is a Broad-Spectrum Inhibitor of Venom PLA Pathophysiological Actions.

机构信息

Venom Evolution Lab, School of Biological Sciences, The University of Queensland, St. Lucia, QLD, 4072, Australia.

Laboratório de Herpetologia, Instituto Butantan, São Paulo, Brazil.

出版信息

J Chem Ecol. 2021 Nov;47(10-11):907-914. doi: 10.1007/s10886-021-01289-4. Epub 2021 Jun 24.

Abstract

The use of venom in predation exerts a corresponding selection pressure for the evolution of venom resistance. One of the mechanisms related to venom resistance in animals (predators or prey of snakes) is the presence of molecules in the blood that can bind venom toxins, and inhibit their pharmacological effects. One such toxin type are venom phospholipase As (PLAs), which have diverse effects including anticoagulant, myotoxic, and neurotoxic activities. BoaγPLI isolated from the blood of Boa constrictor has been previously shown to inhibit venom PLAs that induced myotoxic and edematogenic activities. Recently, in addition to its previously described and very potent neurotoxic effect, the venoms of American coral snakes (Micrurus species) have been shown to have anticoagulant activity via PLA toxins. As coral snakes eat other snakes as a major part of their diet, neonate Boas could be susceptible to predation by this sympatric species. Thus, this work aimed to ascertain if BoaγPLI provided a protective effect against the anticoagulant toxicity of venom from the model species Micrurus laticollaris in addition to its ability shown previously against other toxin types. Using a STA R Max coagulation analyser robot to measure the effect upon clotting time, and TEG5000 thromboelastographers to measure the effect upon clot strength, we evaluated the ability of BoaγPLI to inhibit M. laticollaris venom. Our results indicate that BoaγPLI is efficient at inhibiting the M. laticollaris anticoagulant effect, reducing the time of coagulation (restoring them closer to non-venom control values) and increasing the clot strength (restoring them closer to non-venom control values). These findings demonstrate that endogenous PLA inhibitors in the blood of non-venomous snakes are multi-functional and provide broad resistance against a myriad of venom PLA-driven toxic effects including coagulotoxicity, myotoxicity, and neurotoxicity. This novel form of resistance could be evidence of selective pressures caused by predation from venomous snakes and stresses the need for field-based research aimed to expand our understanding of the evolutionary dynamics of such chemical arms race.

摘要

在捕食过程中使用毒液会对毒液抗性的进化施加相应的选择压力。动物(蛇的捕食者或猎物)中与毒液抗性相关的机制之一是血液中存在可以结合毒液毒素并抑制其药理作用的分子。蛇毒磷脂酶 A(PLA)就是这样一种毒素类型,它具有抗凝、肌毒性和神经毒性等多种作用。以前从巨蟒的血液中分离出的 BoaγPLI 已被证明可以抑制引起肌毒性和水肿活性的蛇毒 PLA。最近,除了以前描述的非常有效的神经毒性作用外,还发现美洲珊瑚蛇(Micrurus 种)的毒液通过 PLA 毒素具有抗凝活性。由于珊瑚蛇将其他蛇作为其主要食物来源的一部分,新生的巨蟒可能容易受到这种同域物种的捕食。因此,这项工作旨在确定 BoaγPLI 是否除了以前显示的对其他毒素类型的能力之外,还能提供针对模型物种 Micrurus laticollaris 毒液的抗凝毒性的保护作用。使用 STA R Max 凝血分析仪机器人测量对凝血时间的影响,以及 TEG5000 血栓弹性描记仪测量对凝血强度的影响,我们评估了 BoaγPLI 抑制 M. laticollaris 毒液的能力。我们的结果表明,BoaγPLI 能有效地抑制 M. laticollaris 的抗凝作用,缩短凝血时间(使它们更接近非毒液对照值)并增加血凝块强度(使它们更接近非毒液对照值)。这些发现表明,无毒蛇血液中的内源性 PLA 抑制剂具有多功能性,能广泛抵抗包括凝血毒性、肌毒性和神经毒性在内的多种由蛇毒 PLA 驱动的毒性作用。这种新形式的抗性可能是由来自毒蛇的捕食造成的选择压力的证据,并强调需要进行基于野外的研究,以扩大我们对这种化学军备竞赛进化动态的理解。

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