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根际细菌获得分解代谢途径能够轻易地利用根系分泌物成分实现生长,但不会影响其在根际的定殖。

Catabolic pathway acquisition by rhizosphere bacteria readily enables growth with a root exudate component but does not affect root colonization.

作者信息

Christel Stephan, Carrell Alyssa A, Hochanadel Leah H, Villalobos Solis Manuel I, Abraham Paul E, Jawdy Sara S, Chaves Julie E, Engle Nancy L, Berhane Timkhite-Kulu, Yao Tao, Chen Jin-Gui, Muchero Wellington, Tschaplinski Timothy J, Cregger Melissa A, Michener Joshua K

机构信息

Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee, USA.

出版信息

mBio. 2025 Jan 8;16(1):e0301624. doi: 10.1128/mbio.03016-24. Epub 2024 Dec 11.

DOI:10.1128/mbio.03016-24
PMID:39660924
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11708038/
Abstract

Horizontal gene transfer (HGT) is a fundamental evolutionary process that plays a key role in bacterial evolution. The likelihood of a successful transfer event is expected to depend on the precise balance of costs and benefits resulting from pathway acquisition. Most experimental analyses of HGT have focused on phenotypes that have large fitness benefits under appropriate selective conditions, such as antibiotic resistance. However, many examples of HGT involve phenotypes that are predicted to provide smaller benefits, such as the ability to catabolize additional carbon sources. We have experimentally simulated the consequences of one such HGT event in the laboratory, studying the effects of transferring a pathway for catabolism of the plant-derived aromatic compound salicyl alcohol between rhizosphere isolates from the genus. We find that pathway acquisition enables rapid catabolism of salicyl alcohol with only minor disruptions to the existing metabolic and regulatory networks of the new host. However, this new catabolic potential does not confer a measurable fitness advantage during competitive growth in the rhizosphere. We conclude that the phenotype of salicyl alcohol catabolism is readily transferable but is selectively neutral under environmentally relevant conditions. We propose that this condition is common and that HGT of many pathways will be self-limiting because the selective benefits are small.IMPORTANCEHorizontal gene transfer (HGT) is a key process in microbial evolution, but the factors limiting HGT are poorly understood. Aside from the rather unique scenario of antibiotic resistance, the evolutionary benefits of pathway acquisition are still unclear. To experimentally test the effects of pathway acquisition, we transferred a pathway for catabolism of a plant-derived aromatic compound between soil bacteria isolated from the roots of poplar trees and determined the resulting phenotypic and fitness effects. We found that pathway acquisition allowed bacteria to grow using the plant-derived compound in the laboratory, but that this new phenotype did not provide an advantage when the bacteria were reinoculated onto plant roots. These results suggest that the benefits of pathway acquisition may be small when measured under ecologically-relevant conditions. From an engineering perspective, efforts to alter microbial community composition by manipulating catabolic pathways or nutrient availability will be challenging when gaining access to a new niche does not provide a benefit.

摘要

水平基因转移(HGT)是一种基本的进化过程,在细菌进化中起着关键作用。成功转移事件的可能性预计取决于因获得途径而产生的成本和收益的精确平衡。大多数关于HGT的实验分析都集中在那些在适当选择条件下具有巨大适应性益处的表型上,比如抗生素抗性。然而,许多HGT的例子涉及的表型预计能提供较小的益处,例如分解代谢额外碳源的能力。我们在实验室中通过实验模拟了这样一个HGT事件的后果,研究了在来自该属根际分离物之间转移植物衍生芳香化合物水杨醇分解代谢途径的影响。我们发现获得该途径能够使水杨醇快速分解代谢,同时对新宿主现有的代谢和调控网络只有轻微干扰。然而,在根际的竞争性生长过程中,这种新的分解代谢潜力并未赋予可测量的适应性优势。我们得出结论,水杨醇分解代谢的表型很容易转移,但在与环境相关的条件下是选择性中性的。我们提出这种情况很常见,并且许多途径的HGT将是自我限制的,因为选择性益处很小。

重要性

水平基因转移(HGT)是微生物进化中的一个关键过程,但限制HGT的因素却知之甚少。除了抗生素抗性这种相当独特的情况外,获得途径的进化益处仍不明确。为了通过实验测试获得途径的影响,我们在从杨树根部分离的土壤细菌之间转移了一种植物衍生芳香化合物的分解代谢途径,并确定了由此产生的表型和适应性影响。我们发现获得该途径使细菌能够在实验室中利用植物衍生化合物生长,但当这些细菌重新接种到植物根部时,这种新表型并未提供优势。这些结果表明,在与生态相关的条件下衡量时,获得途径的益处可能很小。从工程学角度来看,当进入新生态位没有益处时,通过操纵分解代谢途径或养分可用性来改变微生物群落组成的努力将具有挑战性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/6d29f9b15177/mbio.03016-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/814241bb3334/mbio.03016-24.f001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/6d29f9b15177/mbio.03016-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/814241bb3334/mbio.03016-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/9ff10eed12f3/mbio.03016-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad28/11708038/35e163f4aa97/mbio.03016-24.f003.jpg
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