Impact of Iron Deficiency on the Growth and Bioelectrical Profile of Different Gut Bacteria

IF 3.9 3区 生物学 Q2 MICROBIOLOGY
Elisa Quarta, Marwane Bourqqia-Ramzi, David Muñoz-Rodriguez, María Teresa García-Esteban, Antonio Murciano-Cespedosa, Álvaro Mateos González, Francisco José Conejero-Meca, Juan Lombardo-Hernandez, Jesús Mansilla-Guardiola, Simona Baroni, Simonetta Geninatti Crich, Stefano Geuna, Luca Munaron, Deborah Chiabrando, Celia Herrera-Rincon
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引用次数: 0

Abstract

Scope: Iron deficiency (ID) is the most common nutritional deficiency worldwide, impacting gut bacteria's metabolism and cellular biochemistry, but its effects on the microbiota-gut-brain axis (MGB) are poorly understood. Early-life ID-related dysbiosis is linked to neurodevelopmental impairments like autism and attention deficit hyperactivity disorder. Studying ID's impact on bacterial signaling can guide interventions to target MGB in iron-deficient populations. This study examined the responses of Escherichia coli (E. coli) and Limosilactobacillus reuteri (L. reuteri) to in-vitro ID conditions using the iron chelator 2,2’-Bipyridyl (BP). Methods and Results: We assessed and modeled their growth and cultivability and explored their bioelectric profiles using the voltage-sensitive dye DiBAC4(3). Results showed differential responses: L. reuteri's growth and cultivability were unaffected by BP, while E. coli's growth rate and cultivability decreased under ID. Additionally, we created a deterministic mathematical model that demonstrated a decrease in the population's average reproduction rate in E. coli under ID. Only E. coli exhibited an altered bioelectric profile, marked by increased cell depolarization in ID conditions, which was largely rescued upon the addition of a saturating concentration of iron. Conclusion: These findings highlight specific bioelectrical responses in gut bacteria to ID. Understanding this variability is crucial for deciphering the microbiota's role in health and disease, particularly concerning nutritional iron imbalance and bacterial signaling in the MGB.

缺铁对不同肠道细菌生长和生物电特性的影响
范围:铁缺乏症(ID)是世界范围内最常见的营养缺乏症,影响肠道细菌的代谢和细胞生物化学,但其对微生物-肠-脑轴(MGB)的影响知之甚少。早期与id相关的生态失调与自闭症和注意力缺陷多动障碍等神经发育障碍有关。研究ID对细菌信号传导的影响可以指导干预措施针对缺铁人群的MGB。本研究利用铁螯合剂2,2′-联吡啶(BP)检测了大肠杆菌(E. coli)和罗伊氏乳酸杆菌(L. reuteri)对体外ID条件的反应。方法和结果:我们使用电压敏感染料DiBAC4(3)评估和模拟了它们的生长和可培养性,并探索了它们的生物电谱。结果表明:BP对罗伊氏乳杆菌的生长和可培养性没有影响,而ID对大肠杆菌的生长和可培养性有抑制作用。此外,我们创建了一个确定性的数学模型,证明了在ID下大肠杆菌种群的平均繁殖率下降。只有大肠杆菌表现出改变的生物电谱,其特征是在ID条件下细胞去极化增加,这在很大程度上是在添加饱和浓度的铁后恢复的。结论:这些发现突出了肠道细菌对ID的特异性生物电反应。理解这种可变性对于解读微生物群在健康和疾病中的作用至关重要,特别是关于营养铁失衡和MGB中的细菌信号。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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