The burrower bug Macroscytus japonensis (Hemiptera: Cydnidae) acquires obligate symbiotic bacteria from the environment.

IF 1.7 3区 生物学 Q2 ZOOLOGY Zoological Letters Pub Date : 2024-08-02 DOI:10.1186/s40851-024-00238-9
Takuma Nakawaki, Shuto Watanabe, Takahiro Hosokawa
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Abstract

Many plant-feeding stinkbugs belonging to the infraorder Pentatomomorpha possess a specialized symbiotic organ at the posterior end of the midgut, in which mutualistic bacterial symbionts are harbored extracellularly. In species of the superfamily Pentatomoidea, these symbionts typically are verticallytransmitted from host mothers to offspring, whereas in species of the superfamilies Coreoidea and Lygaeoidea they are acquired from the environment. In the pentatomoid family Cydnidae, vertical symbiont transmission has been reported in several species. Here, we report the first case of environmental symbiont acquisition in Cydnidae, observed in the burrower bug Macroscytus japonensis. A comprehensive survey of 72 insect samples from 23 sites across the Japanese archipelago revealed that (1) symbionts exhibit remarkably high diversity, forming six distinct phylogenetic groups within the Enterobacteriaceae of the γ-Proteobacteria, (2) most symbionts are cultivable and closely related to free-living Pantoea-allied bacteria, and (3) symbiont phylogenetic groups do not reflect the host phylogeny. Microbial inspection of eggs revealed the absence of bacteria on the egg surface. These results strongly suggest that symbionts are acquired from the environment, not vertical transmission. Rearing experiments confirmed environmental symbiont acquisition. When environmental symbiont sources were experimentally withheld, nymphs became aposymbiotic and died before molting to the second instar, indicating that nymphs environmentally acquire symbionts during the first-instar stage and that symbionts are essential for nymphal growth and survival. This study highlights Cydnidae as the only pentatomoid family that includes species that environmentally acquire symbionts and those that vertically transmit symbionts, providing an ideal platform for comparative studies of the ecological and environmental factors that influence the evolution of symbiont transmission modes.

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穴居蝽(Macroscytus japonensis)(半翅目:穴居蝽科)从环境中获取强制性共生细菌。
五目蝽亚目中的许多以植物为食的蝽类在中肠的后端都有一个专门的共生器官,在这个器官中,细胞外藏有互生的细菌共生体。在五膜虫超科的物种中,这些共生体通常从宿主母体垂直传播给后代,而在核心虫超科和Lygaeoidea超科的物种中,这些共生体是从环境中获得的。据报道,在五触角虫科(Cydnidae)的多个物种中,共生体都是垂直传播的。在这里,我们报告了在穴居昆虫日本穴居蝇(Macroscytus japonensis)中观察到的第一个穴居昆虫环境共生体获取案例。我们对日本列岛 23 个地点的 72 个昆虫样本进行了全面调查,结果发现:(1)共生体表现出极高的多样性,在γ-蛋白质细菌的肠杆菌科中形成了六个不同的系统发育群;(2)大多数共生体是可培养的,与自由生活的泛变形菌密切相关;(3)共生体系统发育群并不反映宿主的系统发育。对卵进行微生物检查后发现,卵表面没有细菌。这些结果有力地表明,共生体是从环境中获得的,而不是垂直传播。饲养实验证实了共生体是从环境中获得的。当实验性地切断环境共生体来源时,若虫在蜕皮至第二龄期之前变得无共生能力并死亡,这表明若虫在第一龄期从环境中获得共生体,共生体对若虫的生长和生存至关重要。这项研究表明,蝶形花科是唯一一个包括从环境中获得共生体的物种和垂直传播共生体的物种的五蠹科,为比较研究影响共生体传播模式演化的生态和环境因素提供了一个理想的平台。
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来源期刊
Zoological Letters
Zoological Letters Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
3.60
自引率
0.00%
发文量
12
审稿时长
10 weeks
期刊介绍: Zoological Letters is an open access journal that publishes new and important findings in the zoological sciences. As a sister journal to Zoological Science, Zoological Letters covers a wide range of basic fields of zoology, from taxonomy to bioinformatics. We also welcome submissions of paleontology reports as part of our effort to contribute to the development of new perspectives in evolutionary zoology. Our goal is to serve as a global publishing forum for fundamental researchers in all fields of zoology.
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