伴侣之间垂直传播肠道微生物群的一致性降低了牛蛙的繁殖能力

IF 1.6 4区 农林科学 Q2 ENTOMOLOGY
Anna L. M. Macagno, Armin P. Moczek
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引用次数: 1

摘要

在这项研究中,我们以牛蒡(Schreber,1759)及其姊妹种O.illyricus(Scopoli,1763)为模型系统(鞘翅目:Scarabaidae:Scarabainae:Onhophagini),探索了肠道微生物组对隧道粪甲虫繁殖隔离的潜在贡献。肠道微生物群在这些甲虫的正常发育中发挥着关键作用,并通过一种称为基座的母体粪便颗粒垂直遗传。我们首先比较了用来自同一物种或姐妹物种的基座饲养的个体的发育结果(分别为自身和交叉接种处理)。然后,我们以三种组合(自雌性X自雄性;自雌性X交叉雄性;交叉雌性X自男性)杂交得到的成年牛头怪。我们预测,如果垂直传播的肠道微生物组通过促进物种识别在生殖隔离中发挥作用,那么与伴侣肠道微生物组不匹配的系相比,Self-XSelf系将改善生殖结果。相反,我们发现,伴侣之间母体传播的肠道微生物群的一致性导致后代减少,而这种减少是由于交配前的部分隔离,Self-X-Self系的精子转移减少就是明证。这种模式与微生物组介导的熟悉度/亲属识别一致,或者与微生物组不匹配的杂交中没有配偶选择一致。我们根据最近关于细胞外微生物共生体对昆虫交配偏好的影响的研究来讨论我们的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Between-partner concordance of vertically transmitted gut microbiota diminishes reproductive output in the dung beetle Onthophagus taurus

Between-partner concordance of vertically transmitted gut microbiota diminishes reproductive output in the dung beetle Onthophagus taurus

In this study, we explored the potential contribution of the gut microbiome to reproductive isolation in tunnelling dung beetles, using Onthophagus taurus (Schreber, 1759) and its sister species O. illyricus (Scopoli, 1763) as a model system (Coleoptera: Scarabaeidae: Scarabaeinae: Onthophagini). Gut microbiota play critical roles in normative development of these beetles, and are vertically inherited via a maternally derived faecal pellet called the pedestal. We first compared the developmental outcomes of individuals reared with pedestals derived from either the same or the sister species (Self and Cross inoculation treatments, respectively). We then crossed the resulting adult O. taurus in three combinations (Self female X Self male; Self female X Cross male; Cross female X Self male). We predicted that if the vertically transmitted gut microbiome plays a role in reproductive isolation by facilitating species recognition, the Self X Self line would have improved reproductive outcomes compared to the lines in which partners had mismatched gut microbiomes. Instead, we found that between-partner concordance of maternally transmitted gut microbiota resulted in fewer offspring, and that this reduction was due to partial pre-copulatory isolation as evidenced by reduced sperm transfer in the Self X Self line. This pattern is consistent either with microbiome-mediated familiarity/kin recognition, or with absence of mate choice in crosses with mismatched microbiomes. We discuss our results in the light of recent research on the influence of extracellular microbial symbionts over insects' mating preferences.

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来源期刊
Physiological Entomology
Physiological Entomology 生物-昆虫学
CiteScore
2.80
自引率
6.70%
发文量
21
审稿时长
>12 weeks
期刊介绍: Physiological Entomology broadly considers “how insects work” and how they are adapted to their environments at all levels from genes and molecules, anatomy and structure, to behaviour and interactions of whole organisms. We publish high quality experiment based papers reporting research on insects and other arthropods as well as occasional reviews. The journal thus has a focus on physiological and experimental approaches to understanding how insects function. The broad subject coverage of the Journal includes, but is not limited to: -experimental analysis of behaviour- behavioural physiology and biochemistry- neurobiology and sensory physiology- general physiology- circadian rhythms and photoperiodism- chemical ecology
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