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感染白垩病真菌的蜜蜂幼虫的转录反应。

Transcriptional responses in honey bee larvae infected with chalkbrood fungus.

机构信息

Honey Bee Research Unit, USDA-ARS, Weslaco, TX 78596, USA.

出版信息

BMC Genomics. 2010 Jun 21;11:391. doi: 10.1186/1471-2164-11-391.

Abstract

BACKGROUND

Diseases and other stress factors working synergistically weaken honey bee health and may play a major role in the losses of bee populations in recent years. Among a large number of bee diseases, chalkbrood has been on the rise. We present here the experimental identification of honey bee genes that are differentially expressed in response to infection of honey bee larvae with the chalkbrood fungus, Ascosphaera apis.

RESULTS

We used cDNA-AFLP Technology to profile transcripts in infected and uninfected bee larvae. From 64 primer combinations, over 7,400 transcriptionally-derived fragments were obtained A total of 98 reproducible polymorphic cDNA-AFLP fragments were excised and sequenced, followed by quantitative real-time RT-PCR (qRT-PCR) analysis of these and additional samples.We have identified a number of differentially-regulated transcripts that are implicated in general mechanisms of stress adaptation, including energy metabolism and protein transport. One of the most interesting differentially-regulated transcripts is for a chitinase-like enzyme that may be linked to anti-fungal activities in the honey bee larvae, similarly to gut and fat-body specific chitinases found in mosquitoes and the red flour beetle. Surprisingly, we did not find many components of the well-characterized NF-kappaB intracellular signaling pathways to be differentially-regulated using the cDNA-AFLP approach. Therefore, utilizing qRT-PCR, we probed some of the immune related genes to determine whether the lack of up-regulation of their transcripts in our analysis can be attributed to lack of immune activation or to limitations of the cDNA-AFLP approach.

CONCLUSIONS

Using a combination of cDNA-AFLP and qRT-PCR analyses, we were able to determine several key transcriptional events that constitute the overall effort in the honey bee larvae to fight natural fungal infection. Honey bee transcripts identified in this study are involved in critical functions related to transcriptional regulation, apoptotic degradation of ubiquitinated proteins, nutritional regulation, and RNA processing. We found that immune regulation of the anti-fungal responses in honey bee involves highly coordinated activation of both NF-kappaB signaling pathways, leading to production of anti-microbial peptides. Significantly, activation of immune responses in the infected bee larvae was associated with down-regulation of major storage proteins, leading to depletion of nutritional resources.

摘要

背景

协同作用的疾病和其他应激因素削弱了蜜蜂的健康,可能在近年来蜜蜂种群减少中起主要作用。在大量蜜蜂疾病中,蜂曲霉病呈上升趋势。我们在此介绍了实验鉴定的蜜蜂基因,这些基因在感染蜜蜂幼虫的蜂曲霉时表现出差异表达。

结果

我们使用 cDNA-AFLP 技术来描绘感染和未感染的蜜蜂幼虫中的转录物。在 64 个引物组合中,获得了超过 7400 个转录衍生片段。总共获得了 98 个可重复的多态性 cDNA-AFLP 片段,并对这些和其他样本进行了测序,随后对这些和其他样本进行了定量实时 RT-PCR(qRT-PCR)分析。我们已经鉴定出一些差异调节的转录物,这些转录物与一般的应激适应机制有关,包括能量代谢和蛋白质运输。最有趣的差异调节转录物之一是一种几丁质酶样酶,它可能与蜜蜂幼虫的抗真菌活性有关,类似于在蚊子和红粉甲虫中发现的肠道和脂肪体特异性几丁质酶。令人惊讶的是,我们没有发现许多特征明确的 NF-kappaB 细胞内信号通路的组成部分在使用 cDNA-AFLP 方法时被差异调节。因此,我们利用 qRT-PCR 来探测一些免疫相关基因,以确定它们的转录物在我们的分析中缺乏上调是否归因于免疫激活的缺乏或 cDNA-AFLP 方法的限制。

结论

我们使用 cDNA-AFLP 和 qRT-PCR 分析的组合,能够确定构成蜜蜂幼虫对抗天然真菌感染的整体努力的几个关键转录事件。在这项研究中鉴定的蜜蜂转录物参与与转录调节、泛素化蛋白的凋亡降解、营养调节和 RNA 处理相关的关键功能。我们发现,蜜蜂中抗真菌反应的免疫调节涉及 NF-kappaB 信号通路的高度协调激活,导致抗菌肽的产生。显著的是,感染蜜蜂幼虫中免疫反应的激活与主要储存蛋白的下调有关,导致营养资源的耗尽。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/2996924/2e4a9240a941/1471-2164-11-391-1.jpg

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