Intraspecies variation in cytoplasmic incompatibility intensity in the bean beetle Callosobruchus analis

IF 1.8 3区 环境科学与生态学 Q3 ECOLOGY
Yuko Numajiri, Natsuko Ito Kondo, Yukihiko Toquenaga, Daisuke Kageyama
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Abstract

Wolbachia, a prevalent endosymbiont amongst arthropods, can effectively invade the host population by inducing cytoplasmic incompatibility (CI). CI occurs when a female parent lacks the Wolbachia strain that is possessed by its male mate, resulting in embryonic death. In the bean beetle, Callosobruchus analis, two distinct Wolbachia strains have been identified: the non-CI-inducing wCana1 and the CI-inducing wCana2. Field-collected C. analis individuals were either singly infected with wCana1 or doubly infected with wCana1 and wCana2. The higher prevalence of wCana1 over wCana2 in C. analis raises the question of why CI-inducing wCana2 is not more widespread. To address this, we measured the egg hatch rates in all the cross combinations between seven C. analis lines differing in Wolbachia infection status. We found that the intensity of CI was highly variable between combinations, which can be attributed to either the host genetic background or intra-strain genetic variation of wCana2. These findings may suggest that CI is susceptible to change and emphasize the need to consider the adaptive nature of host manipulation. Understanding the genetic and environmental factors underlying the CI variation is crucial for predicting the long-term stability of Wolbachia-host associations.

Abstract Image

豆甲虫细胞质不相容强度的种内变异
沃尔巴克氏体(Wolbachia)是节肢动物中普遍存在的内共生体,它可以通过诱导细胞质不相容(CI)来有效入侵宿主种群。当雌性亲本缺乏雄性配偶所拥有的 Wolbachia 菌株时,就会发生 CI,导致胚胎死亡。在豆甲虫(Callosobruchus analis)中,已经发现了两种不同的沃尔巴克氏体菌株:不诱导 CI 的 wCana1 和诱导 CI 的 wCana2。野外采集的肛裂茧蜂个体要么单一感染了 wCana1,要么双重感染了 wCana1 和 wCana2。在 C. analis 中,wCana1 的流行率高于 wCana2,这就提出了一个问题:为什么 CI 诱导的 wCana2 没有更广泛地流行?为了解决这个问题,我们测量了七个不同沃尔巴克氏体感染状况的 C. analis 品系之间所有杂交组合的卵孵化率。我们发现,不同杂交组合的 CI 强度差异很大,这可能是宿主遗传背景或 wCana2 株系内遗传变异造成的。这些发现可能表明,CI容易发生变化,并强调需要考虑宿主操纵的适应性。了解CI变异的遗传和环境因素对于预测沃尔巴奇-宿主关系的长期稳定性至关重要。
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来源期刊
Evolutionary Ecology
Evolutionary Ecology 环境科学-进化生物学
CiteScore
3.00
自引率
5.30%
发文量
70
审稿时长
3 months
期刊介绍: Evolutionary Ecology is a concept-oriented journal of biological research at the interface of ecology and evolution. We publish papers that therefore integrate both fields of research: research that seeks to explain the ecology of organisms in the context of evolution, or patterns of evolution as explained by ecological processes. The journal publishes original research and discussion concerning the evolutionary ecology of organisms. These may include papers addressing evolutionary aspects of population ecology, organismal interactions and coevolution, behaviour, life histories, communication, morphology, host-parasite interactions and disease ecology, as well as ecological aspects of genetic processes. The objective is to promote the conceptual, theoretical and empirical development of ecology and evolutionary biology; the scope extends to any organism or system. In additional to Original Research articles, we publish Review articles that survey recent developments in the field of evolutionary ecology; Ideas & Perspectives articles which present new points of view and novel hypotheses; and Comments on articles recently published in Evolutionary Ecology or elsewhere. We also welcome New Tests of Existing Ideas - testing well-established hypotheses but with broader data or more methodologically rigorous approaches; - and shorter Natural History Notes, which aim to present new observations of organismal biology in the wild that may provide inspiration for future research. As of 2018, we now also invite Methods papers, to present or review new theoretical, practical or analytical methods used in evolutionary ecology. Students & Early Career Researchers: We particularly encourage, and offer incentives for, submission of Reviews, Ideas & Perspectives, and Methods papers by students and early-career researchers (defined as being within one year of award of a PhD degree) – see Students & Early Career Researchers
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