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花园里还有更多“杂草”:切叶蚁巢穴中的真菌新物种。

Yet more "weeds" in the garden: fungal novelties from nests of leaf-cutting ants.

作者信息

Augustin Juliana O, Groenewald Johannes Z, Nascimento Robson J, Mizubuti Eduardo S G, Barreto Robert W, Elliot Simon L, Evans Harry C

机构信息

Departamento de Entomologia, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.

Centraalbureau voor Schimmelcultures-Fungal Biodiversity Centre, Utrecht, The Netherlands.

出版信息

PLoS One. 2013 Dec 20;8(12):e82265. doi: 10.1371/journal.pone.0082265. eCollection 2013.

Abstract

BACKGROUND

Symbiotic relationships modulate the evolution of living organisms in all levels of biological organization. A notable example of symbiosis is that of attine ants (Attini; Formicidae: Hymenoptera) and their fungal cultivars (Lepiotaceae and Pterulaceae; Agaricales: Basidiomycota). In recent years, this mutualism has emerged as a model system for studying coevolution, speciation, and multitrophic interactions. Ubiquitous in this ant-fungal symbiosis is the "weedy" fungus Escovopsis (Hypocreales: Ascomycota), known only as a mycoparasite of attine fungal gardens. Despite interest in its biology, ecology and molecular phylogeny--noting, especially, the high genetic diversity encountered--which has led to a steady flow of publications over the past decade, only two species of Escovopsis have formally been described.

METHODS AND RESULTS

We sampled from fungal gardens and garden waste (middens) of nests of the leaf-cutting ant genus Acromyrmex in a remnant of subtropical Atlantic rainforest in Minas Gerais, Brazil. In culture, distinct morphotypes of Escovopsis sensu lato were recognized. Using both morphological and molecular analyses, three new species of Escovopsis were identified. These are described and illustrated herein--E. lentecrescens, E. microspora, and E. moelleri--together with a re-description of the genus and the type species, E. weberi. The new genus Escovopsioides is erected for a fourth morphotype. We identify, for the first time, a mechanism for horizontal transmission via middens.

CONCLUSIONS

The present study makes a start at assigning names and formal descriptions to these specific fungal parasites of attine nests. Based on the results of this exploratory and geographically-restricted survey, we expect there to be many more species of the genus Escovopsis and its relatives associated with nests of both the lower and higher Attini throughout their neotropical range, as suggested in previous studies.

摘要

背景

共生关系在生物组织的各个层面调节着生物的进化。共生的一个显著例子是切叶蚁(切叶蚁亚科;蚁科:膜翅目)与其真菌培养物(白鬼伞科和皱孔菌科;伞菌目:担子菌门)之间的关系。近年来,这种共生关系已成为研究协同进化、物种形成和多营养级相互作用的模型系统。在这种蚂蚁 - 真菌共生关系中普遍存在的是“杂草性”真菌埃斯科沃普氏菌(肉座菌目:子囊菌门),它仅作为切叶蚁真菌园的真菌寄生物为人所知。尽管人们对其生物学、生态学和分子系统发育感兴趣——尤其是注意到所遇到的高遗传多样性——这导致在过去十年中有源源不断的出版物,但正式描述的埃斯科沃普氏菌只有两个物种。

方法与结果

我们从巴西米纳斯吉拉斯州一片亚热带大西洋雨林残余地中切叶蚁属顶切叶蚁巢穴的真菌园和园垃圾(蚁冢)中进行采样。在培养过程中,识别出了广义埃斯科沃普氏菌的不同形态型。通过形态学和分子分析,鉴定出了三种新的埃斯科沃普氏菌物种。本文对它们进行了描述和图示——缓生埃斯科沃普氏菌、小孢埃斯科沃普氏菌和莫氏埃斯科沃普氏菌——同时对该属及其模式种韦伯氏埃斯科沃普氏菌进行了重新描述。为第四种形态型建立了新属埃斯科沃普氏菌属。我们首次确定了一种通过蚁冢进行水平传播的机制。

结论

本研究开始为这些切叶蚁巢穴的特定真菌寄生物命名并进行正式描述。基于这项探索性且地域受限的调查结果,正如之前研究所暗示的,我们预计在新热带地区,整个切叶蚁亚科中,无论是低级还是高级切叶蚁的巢穴,都与更多的埃斯科沃普氏菌属及其近缘物种相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aec0/3869688/a93eda3fd7b5/pone.0082265.g001.jpg

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