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热激蛋白和抗氧化酶在温度、饥饿和寄生反应中的差异表达,以栗实象甲幼虫,Ectomyelois ceratoniae(鳞翅目:Pyralidae)为例。

Differential expression of heat shock proteins and antioxidant enzymes in response to temperature, starvation, and parasitism in the Carob moth larvae, Ectomyelois ceratoniae (Lepidoptera: Pyralidae).

机构信息

Plant Protection Department, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran.

Department of Agronomy and Plant Breeding, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran.

出版信息

PLoS One. 2020 Jan 29;15(1):e0228104. doi: 10.1371/journal.pone.0228104. eCollection 2020.

DOI:10.1371/journal.pone.0228104
PMID:31995629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6988935/
Abstract

Insects face diverse biotic and abiotic stresses that can affect their survival. Many of these stressors impact cellular metabolism, often resulting in increased accumulation of reactive oxygen species (ROS). Consequently, insects will respond to these stressors by increasing antioxidant activity and increased production of heat shock proteins (HSPs). In this study, the effect of heat, cold, starvation, and parasitism by Habroacon hebetor wasps was examined in the carob moth, Ectomyelois ceratoniae, to determine which responses were common to different stresses. For all stressors, malondialdehyde levels increased, indicative of oxidative stress in the insects. The activity of two antioxidant enzymes, superoxide dismutase (SOD) and catalase (CAT), increased with each stress, suggesting that these enzymes were serving a protective role for the insects. Heat (46°C for 100 min) and cold (-15°C for 30 min) treatments caused significant mortalities to all developmental stages, but pretreatments of moderate heat (37°C for 10 min) or cold (10°C for 10 min) induced thermotolerance and reduced the mortality rates when insects were subsequently exposed to lethal temperatures. Quantitative RT-PCR confirmed that heat and cold tolerance were associated with up-regulation of two HSPs, HSP70 and HSP90. Interestingly, HSP70 transcripts increased to a greater extent with cold treatment, while HSP90 transcripts increased more in response to high temperatures. RNA interference (RNAi)-mediated knockdown of either HSP70 or HSP90 transcripts was achieved by injecting larvae with dsRNA targeting each gene's transcripts, and resulted in a loss of acquired thermotolerance in insects subjected to the heat or cold pretreatments. These observations provide convincing evidence that both HSP70 and HSP90 are important mediators of the acquired thermotolerance. Starvation and parasitism by wasps caused differential expression of the HSP genes. In response to starvation, HSP90 transcripts increased to a greater extent than HSP70, while in contrast, HSP70 transcripts increased to a greater extent than those of HSP90 during the first 48 h of wasp parasitism. These results showed the differential induction of the two HSPs' transcripts with variable stresses. As well as, heat, cold, starvation, and parasitism induce oxidative stress, and antioxidant enzymes likely play an important role in reducing oxidative damage in E. ceratoniae.

摘要

昆虫面临着各种生物和非生物压力,这些压力会影响它们的生存。这些胁迫因素中的许多都会影响细胞代谢,通常会导致活性氧物质 (ROS) 的积累增加。因此,昆虫会通过增加抗氧化活性和热休克蛋白 (HSPs) 的产生来应对这些胁迫因素。在这项研究中,研究了高温、低温、饥饿和Habroacon hebetor 黄蜂寄生对角豆蛾(Ectomyelois ceratoniae)的影响,以确定哪些反应是不同胁迫因素共有的。对于所有的胁迫因素,丙二醛水平的增加表明昆虫受到了氧化应激。两种抗氧化酶,超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的活性随着每种胁迫因素的增加而增加,这表明这些酶对昆虫起到了保护作用。高温(46°C 持续 100 分钟)和低温(-15°C 持续 30 分钟)处理对所有发育阶段的昆虫都有显著的致死作用,但适度的高温(37°C 持续 10 分钟)或低温(10°C 持续 10 分钟)预处理会诱导耐热性,并降低随后暴露于致死温度时的死亡率。定量 RT-PCR 证实,耐热性和耐寒性与两种 HSPs(HSP70 和 HSP90)的上调有关。有趣的是,冷处理时 HSP70 转录物的增加幅度更大,而高温时 HSP90 转录物的增加幅度更大。通过向幼虫注射靶向每个基因转录物的 dsRNA,实现了 HSP70 或 HSP90 转录物的 RNAi 介导敲低,这导致了经高温或低温预处理的昆虫丧失了获得的耐热性。这些观察结果提供了令人信服的证据,证明 HSP70 和 HSP90 都是获得耐热性的重要介导物。饥饿和黄蜂寄生会导致 HSP 基因的差异表达。对饥饿的反应中,HSP90 的转录物增加幅度大于 HSP70,而相反,在黄蜂寄生的前 48 小时内,HSP70 的转录物增加幅度大于 HSP90。这些结果表明,两种 HSPs 的转录物对不同的胁迫因素有不同的诱导。除了高温、低温、饥饿和寄生会引起氧化应激外,抗氧化酶可能在降低角豆蛾 E. ceratoniae 的氧化损伤方面发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/6988935/ef323fb7b2e9/pone.0228104.g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/6988935/6b4384dabb72/pone.0228104.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/6988935/f30ea4cedac9/pone.0228104.g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b595/6988935/ef323fb7b2e9/pone.0228104.g005.jpg

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