Selective protein self-deprivation by Mormon crickets following fungal attack

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY Journal of insect physiology Pub Date : 2023-09-01 DOI:10.1016/j.jinsphys.2023.104555
Robert B. Srygley
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引用次数: 1

Abstract

Immune responses to infection result in behavioral changes that affect resource acquisition, such as general starvation and compensatory feeding to offset changes in resource allocation. Mormon crickets aggregate and march in bands containing millions of insects. Some bands are comprised of insects seeking proteins. They are also low in circulating phenoloxidase (PO) and more susceptible to fungal attack, as we have demonstrated in the lab. Here, we ask: Do Mormon crickets elevate PO and consume protein in response to infection by the pathogenic fungus Beauveria bassiana? B. bassiana was applied topically (day 0), and mortality began on day 5. Total protein, PO, and prophenoloxidase (proPO) were assayed in hemolymph on day 1 and 4. On day 1, PO titers were not different between inoculated and control insects, whereas by day 4, PO was greater in the inoculated group. proPO activity was unchanged. Circulating protein declined in inoculated insects relative to controls. As predicted, PO titers were elevated as a result of fungal infection, and hemolymph protein was reduced, but the insects did not compensate behaviorally. Indeed, during the first three days post-infection, infected insects reduced protein consumption while maintaining carbohydrate consumption similar to the controls. Following day 3, a more general reduction in protein and carbohydrate intake was evident in infected insects. Survivorship to infection was associated with the amount of protein consumed and unrelated to carbohydrate consumption. Selective protein deprivation by the host seems counterintuitive, but it might limit growth and toxin production by the invading fungus. Alternatively, the fungus might control the host diet to compromise host immunity to infection. Abrupt changes in allocation resulting from an infection can lead to changes in acquisition that are not always intuitive. Because protein acquisition drives aggression between members of the migratory band, B. bassiana application may reduce cannibalism and slow band movement.

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摩门教徒蟋蟀在真菌攻击后选择性蛋白质自我剥夺
对感染的免疫反应会导致影响资源获取的行为变化,如普遍饥饿和补偿喂养,以抵消资源分配的变化。摩门教徒蟋蟀聚集在一起,组成包含数百万只昆虫的队伍行进。有些条带是由寻找蛋白质的昆虫组成的。正如我们在实验室中所证明的那样,它们的循环酚氧化酶(PO)含量也很低,更容易受到真菌攻击。在这里,我们要问:摩门蟋蟀是否会在感染病原真菌白僵菌时提高PO并消耗蛋白质?局部施用B.bassiana(第0天),第5天开始死亡。在第1天和第4天测定血淋巴中的总蛋白、PO和proPO。在第1天,接种昆虫和对照昆虫之间的PO滴度没有差异,而到第4天,接种组的PO更高。proPO活性没有变化。与对照组相比,接种疫苗的昆虫的循环蛋白下降。正如预测的那样,由于真菌感染,PO滴度升高,血淋巴蛋白降低,但昆虫的行为没有补偿。事实上,在感染后的前三天,受感染的昆虫减少了蛋白质的消耗,同时保持了与对照组相似的碳水化合物消耗。第3天之后,受感染昆虫的蛋白质和碳水化合物摄入量普遍减少。感染的存活率与蛋白质的消耗量有关,与碳水化合物的消耗无关。宿主选择性剥夺蛋白质似乎违反直觉,但这可能会限制入侵真菌的生长和毒素产生。或者,真菌可能会控制宿主的饮食,从而损害宿主对感染的免疫力。感染导致分配的突然变化可能导致获取的变化,而这些变化并不总是直观的。由于蛋白质的获取驱动迁移带成员之间的攻击性,应用球孢菌可以减少同类相残和减缓迁移带的移动。
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来源期刊
Journal of insect physiology
Journal of insect physiology 生物-昆虫学
CiteScore
4.50
自引率
4.50%
发文量
77
审稿时长
57 days
期刊介绍: All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.
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