Buchnera aphidicola 中必需氨基酸生物合成对补充寄主营养不足的动态响应。

IF 2.3 2区 农林科学 Q1 ENTOMOLOGY
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引用次数: 0

摘要

内共生细菌 Buchnera aphidicola 通过提供必需氨基酸(EAAs),使其宿主 Acyrthosiphon pisum 能够利用营养有限的韧皮部汁液而不会大量死亡。先前的研究报告了蚜虫如何利用宿主提供的非必需氨基酸(NEAAs),以及生物合成途径中的基因如何对氨基酸缺乏做出反应。尽管已经报道了从 A. pisum 的食物中移除单一 EAA 和多种 NEAAs 对 B. aphidicola 基因表达的影响,但对同时完全移除多种 EAA,尤其是支链氨基酸(BCAAs)的影响却知之甚少。为了探究这一问题,我们为 A. pisum 提供了氨基酸缺乏的日粮 ilv-(缺乏异亮氨酸、亮氨酸和缬氨酸)或 thra-(缺乏苏氨酸、蛋氨酸和赖氨酸)。由于它们参与多种氨基酸的生产,因此分析了基因 ilvC、ilvD(均参与异亮氨酸、亮氨酸和缬氨酸的生物合成)和 thrA(参与苏氨酸、蛋氨酸和赖氨酸的生物合成)的表达情况,并以基因 trpC(参与色氨酸的生物合成)的表达情况作为对照。与最适人工饲料相比,用 ilv- 或 thra- 饲养 A. pisum 的存活率明显降低(分别为 P < 0.001 和 P = 0.000),用 ilv- 饲养的存活率明显低于用 thra- 饲养的存活率(P < 0.001)。这可能是因为ilv-中缺乏的EAAs比thra-中缺乏的EAAs在蚜虫生长过程中需要更高浓度的EAAs。当 A. pisum 在 ilv- 和 thra- 上饲养时,ilvC 和 ilvD 的表达分别上调了 2.49 倍和 2.08 倍,thrA 的表达分别增加了 2.35 倍和 2.12 倍。在 ilv- 上饲养时,thrA 的表达出人意料地大幅上调,这可能是因为苏氨酸是异亮氨酸生物合成的中间体。使用两种氨基酸缺乏的日粮饲养都不会影响 trpC 的表达。据我们所知,这项研究首次显示了内共生体生物合成途径中的基因如何对宿主食物中同时完全缺乏多种 EAA 以及全部三种 BCAA(亮氨酸、异亮氨酸和缬氨酸)做出反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dynamic response of essential amino acid biosynthesis in Buchnera aphidicola to supplement sub-optimal host nutrition

Dynamic response of essential amino acid biosynthesis in Buchnera aphidicola to supplement sub-optimal host nutrition

The endosymbiotic bacterium Buchnera aphidicola allows its host Acyrthosiphon pisum to utilise a nutritionally limited phloem sap diet without significant mortality by providing essential amino acids (EAAs), which it biosynthesises de novo via complex pathways consisting of multiple enzymes. Previous studies have reported how non-essential amino acids (NEAAs) provided by the host are utilised by B. aphidicola, along with how genes within the biosynthetic pathways respond to amino acid deficiency. Although the effect on B. aphidicola gene expression upon the removal of a single EAA and multiple NEAAs from the A. pisum diet has been reported, little is known about the effects of the complete simultaneous removal of multiple EAAs, especially branched-chain amino acids (BCAAs). To investigate this, A. pisum was provided with amino acid deficient diets ilv- (lacking isoleucine, leucine, valine) or thra- (lacking threonine, methionine, lysine). Due to their involvement in the production of several amino acids, the expression of genes ilvC, ilvD (both involved in isoleucine, leucine and valine biosynthesis) and thrA (involved in threonine, methionine and lysine biosynthesis) was analysed and the expression of trpC (involved in tryptophan biosynthesis) was used as a control. Survival was reduced significantly when A. pisum was reared on ilv- or thra- (P < 0.001 and P = 0.000 respectively) compared to optimal artificial diet and was significantly lower on ilv- (P < 0.001) than thra-. This is likely attributed to the EAAs absent from ilv- being required at higher concentrations for aphid growth, than those EAAs absent from thra-. Expression of ilvC and ilvD were upregulated 2.49- and 2.08-fold (respectively) and thrA expression increased 2.35- and 2.12-fold when A. pisum was reared on ilv- and thra- (respectively). The surprisingly large upregulation of thrA when reared on ilv- is likely due to threonine being an intermediate in isoleucine biosynthesis. Expression of trpC was not affected by rearing on either of the two amino acid deficient diets. To our knowledge this study has shown, for the first time, how genes within the biosynthetic pathways of an endosymbiont respond to the simultaneous complete omission of multiple EAAs as well as all three BCAAs (leucine, isoleucine, valine), from the host diet.

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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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