转座子测序揭示了昆虫共生体Caballeronia insecticola肠道共生的基本基因组和基因。

IF 5.1 Q1 ECOLOGY
ISME communications Pub Date : 2024-01-10 eCollection Date: 2024-01-01 DOI:10.1093/ismeco/ycad001
Romain Jouan, Gaëlle Lextrait, Joy Lachat, Aya Yokota, Raynald Cossard, Delphine Naquin, Tatiana Timchenko, Yoshitomo Kikuchi, Tsubasa Ohbayashi, Peter Mergaert
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引用次数: 0

摘要

Caballeronia insecticola是一种属于伯克霍尔德氏菌属的细菌,能够在土壤和豆虫Riptortus pedestris的肠道等多种环境中定植。我们构建了一个饱和的 Himar1 mariner 转座子文库,并通过转座子测序发现,498 个蛋白编码基因构成了 Caballeronia insecticola 在自由生活条件下生长所必需的基因组。通过比较Caballeronia insecticola和7个相关伯克霍尔德氏菌(Burkholderia s.l.)菌株的基本基因组,只发现了120个共同基因,这表明基本基因组的很大一部分具有菌株特异性。为了重现Riptortus pedestris肠道中存在的特定营养条件,我们在补充了候选肠道营养物质的最小培养基中培养突变体文库,并通过转座子测序鉴定了几个依赖于条件的适存缺陷基因。为了验证该方法的稳健性,我们构建了六个适性基因的插入突变体,并确认了它们在补充了相应营养物质的培养基中的生长缺陷。我们还进一步检测了这些突变体在 Riptortus pedestris 肠道定殖中的效率,证实葡萄糖酸碳源、牛磺酸和肌醇是共生体在肠道中消耗的营养物质。因此,我们的研究有助于了解昆虫宿主对细菌共生体的具体贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transposon sequencing reveals the essential gene set and genes enabling gut symbiosis in the insect symbiont Caballeronia insecticola.

Caballeronia insecticola is a bacterium belonging to the Burkholderia genus sensu lato, which is able to colonize multiple environments like soils and the gut of the bean bug Riptortus pedestris. We constructed a saturated Himar1 mariner transposon library and revealed by transposon-sequencing that 498 protein-coding genes constitute the essential genome of Caballeronia insecticola for growth in free-living conditions. By comparing essential gene sets of Caballeronia insecticola and seven related Burkholderia s.l. strains, only 120 common genes were identified, indicating that a large part of the essential genome is strain-specific. In order to reproduce specific nutritional conditions that are present in the gut of Riptortus pedestris, we grew the mutant library in minimal media supplemented with candidate gut nutrients and identified several condition-dependent fitness-defect genes by transposon-sequencing. To validate the robustness of the approach, insertion mutants in six fitness genes were constructed and their growth deficiency in media supplemented with the corresponding nutrient was confirmed. The mutants were further tested for their efficiency in Riptortus pedestris gut colonization, confirming that gluconeogenic carbon sources, taurine and inositol, are nutrients consumed by the symbiont in the gut. Thus, our study provides insights about specific contributions provided by the insect host to the bacterial symbiont.

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