The genus Entomophthora: bringing the insect destroyers into the twenty-first century.

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Carolyn Elya, Henrik H De Fine Licht
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引用次数: 19

Abstract

The fungal genus Entomophthora consists of highly host-specific pathogens that cause deadly epizootics in their various insect hosts. The most well-known among these is the "zombie fly" fungus E. muscae, which, like other Entomophthora species, elicits a series of dramatic behaviors in infected hosts to promote optimal spore dispersal. Despite having been first described more than 160 years ago, there are still many open questions about Entomophthora biology, including the molecular underpinnings of host behavior manipulation and host specificity. This review provides a comprehensive overview of our current understanding of the biology of Entomophthora fungi and enumerates the most pressing outstanding questions that should be addressed in the field. We briefly review the discovery of Entomophthora and provide a summary of the 21 recognized Entomophthora species, including their type hosts, methods of transmission (ejection of spores after or before host death), and for which molecular data are available. Further, we argue that this genus is globally distributed, based on a compilation of Entomophthora records in the literature and in online naturalist databases, and likely to contain additional species. Evidence for strain-level specificity of hosts is summarized and directly compared to phylogenies of Entomophthora and the class Insecta. A detailed description of Entomophthora's life-cycle and observed manipulated behaviors is provided and used to summarize a consensus for ideal growth conditions. We discuss evidence for Entomophthora's adaptation to growth exclusively inside insects, such as producing wall-less hyphal bodies and a unique set of subtilisin-like proteases to penetrate the insect cuticle. However, we are only starting to understand the functions of unusual molecular and genomic characteristics, such as having large > 1 Gb genomes full of repetitive elements and potential functional diploidy. We argue that the high host-specificity and obligate life-style of most Entomophthora species provides ample scope for having been shaped by close coevolution with insects despite the current general lack of such evidence. Finally, we propose six major directions for future Entomophthora research and in doing so hope to provide a foundation for future studies of these fungi and their interaction with insects.

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疫霉属:将昆虫杀手带入二十一世纪。
虫霉属真菌由高度宿主特异性病原体组成,可在其各种昆虫宿主中引起致命的动物传染病。其中最著名的是“僵尸蝇”真菌E. muscae,它和其他昆虫疫霉物种一样,在被感染的宿主中引发一系列戏剧性的行为,以促进最佳的孢子传播。尽管早在160多年前就已被首次描述,但关于虫霉生物学仍有许多悬而未决的问题,包括宿主行为操纵的分子基础和宿主特异性。这篇综述提供了一个全面的概述,我们目前的理解昆虫疫霉的生物学和列举了最紧迫的突出问题,应在该领域予以解决。我们简要回顾了虫疫霉的发现,并对21种已发现的虫疫霉进行了综述,包括它们的寄主类型、传播方式(寄主死亡后或死亡前的孢子喷射)以及可获得的分子数据。此外,根据文献和在线自然学家数据库中的昆虫疫霉记录汇编,我们认为该属是全球分布的,并且可能包含其他物种。总结了宿主菌株水平特异性的证据,并直接与疫霉和虫纲的系统发育进行了比较。详细描述了虫霉的生命周期和观察到的操纵行为,并用于总结理想生长条件的共识。我们讨论了虫霉适应只在昆虫体内生长的证据,例如产生无壁菌丝体和一套独特的枯草杆菌样蛋白酶来穿透昆虫角质层。然而,我们才刚刚开始了解不寻常的分子和基因组特征的功能,例如拥有大于1gb的基因组,充满重复元素和潜在的功能性二倍体。我们认为,尽管目前普遍缺乏这样的证据,但大多数虫疫霉菌物种的高宿主特异性和专性生活方式为它们与昆虫的密切共同进化提供了充足的空间。最后,我们提出了今后疫霉研究的六个主要方向,希望为今后研究疫霉及其与昆虫的相互作用提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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