Auxotrophy from bioenergetic demand: the case of proline addiction in Clostridioides difficile.

IF 4 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2026-07-28 Epub Date: 2026-06-26 DOI:10.1128/msphere.00246-26
Michael A Johnstone, William T Self
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引用次数: 0

Abstract

Many microbial growth requirements are interpreted as auxotrophy arising from loss of biosynthetic capacity. Clostridioides difficile is widely considered to be proline auxotrophic because it fails to grow in defined media lacking proline, yet it harbors proline biosynthesis genes. Because C. difficile preferentially uses proline as an electron acceptor via D-proline reductase (Prd), we argue that this phenotype arises from a bioenergetic constraint rather than an inability to make proline. Consistent with this view, mutants lacking Prd gain the ability to grow without proline. Moreover, conditions that adapt the organism to Prd-independent redox metabolism, such as Wood-Ljungdahl-linked acetobutyrogenesis, also enable proline-independent growth. We propose a model for "proline addiction" in which sustained Prd flux depletes the intracellular proline pool faster than biosynthesis can replenish it, making growth dependent on environmental proline. This bioenergetic addiction model may help explain cryptic auxotrophies that genome-based cultivation approaches would otherwise miss.

生物能需求引起的营养缺陷:艰难梭菌脯氨酸成瘾的案例。
许多微生物的生长需求被解释为由于生物合成能力的丧失而引起的营养不良。艰难梭菌被广泛认为是脯氨酸营养不良,因为它不能在缺乏脯氨酸的培养基中生长,但它含有脯氨酸生物合成基因。由于艰难梭菌通过d -脯氨酸还原酶(Prd)优先使用脯氨酸作为电子受体,我们认为这种表型是由于生物能量限制而不是无法产生脯氨酸。与这一观点一致的是,缺乏Prd的突变体在没有脯氨酸的情况下也能生长。此外,使生物体适应不依赖于脯氨酸的氧化还原代谢的条件,如Wood-Ljungdahl-linked acetobutyrogenesis,也能实现不依赖脯氨酸的生长。我们提出了一个“脯氨酸成瘾”模型,其中持续的Prd通量消耗细胞内脯氨酸库的速度比生物合成补充脯氨酸的速度快,使生长依赖于环境脯氨酸。这种生物能量成瘾模型可能有助于解释基于基因组的培养方法无法解释的隐性缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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