Yanping Zhu, Yanhong Zeng, Meng Liu, Ting Lu, Xiuhua Pang
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Using physical barriers to separate the strains on culture plates, we determined that volatile compounds produced by wild-type <i>S. venezuelae</i> could rescue the phenotype of strain MU-1, and pH analysis of the growth medium indicated that these volatile compounds were alkaline. Ultra-high-performance liquid chromatography, combined with mass spectrometry analysis, showed that wild-type <i>S. venezuelae</i> produced abundant levels of the alkaline volatile trimethylamine (TMA) and the oxide form TMAO; however, the levels of these compounds were much lower in strain MU-1. Notably, exposure to TMA alone could rescue the phenotype of this mutant strain, restoring the production of aerial mycelia and spores. We also showed that the rescue effect by alkaline volatiles is mostly species-specific, suggesting that the volatiles may aid particular mutants or other less-fit variants of closely related species to resume normal physiological status and to compete more effectively in complex communities such as soil. Our study reveals a new and intriguing role for bacterial volatiles, including volatiles that may have toxic effects on other species.</p><p><strong>Importance: </strong>Bacterial volatiles have a wide range of biological roles at intra- or inter-kingdom levels. The impact of volatiles has mainly been observed between producing bacteria and recipient bacteria, mostly of different species. In this study, we report that the wild-type, soil-dwelling bacterium <i>Streptomyces venezuelae</i>, which forms aerial hypha and spores as part of its normal developmental cycle, also produces the alkaline volatile compound trimethylamine (TMA) under multiple growth conditions. We showed that the environmental dispersion of TMA produced by <i>S. venezuelae</i> promotes the growth and differentiation of growth-deficient mutants of the same species or other slowly growing <i>Streptomyces</i> bacteria, and thus aids in their survival and their ability to compete in complex environmental communities such as soil. 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引用次数: 0
摘要
微生物可产生种类繁多的不同化学类别的挥发性有机化合物,这些化合物能够介导生物界内部和生物界之间的相互作用。在本研究中,我们通过对 S. venezuelae 突变菌株 MU-1 的研究发现,生活在土壤中的 Streptomyces venezuelae 细菌能在多种生长条件下产生碱性挥发性物质。经扫描电子显微镜证实,菌株 MU-1 形态有缺陷,由于缺乏气生菌丝和孢子而表现出秃头表型。利用物理屏障将菌株在培养板上分开,我们确定野生型 S. venezuelae 产生的挥发性化合物可以挽救菌株 MU-1 的表型,生长培养基的 pH 值分析表明这些挥发性化合物呈碱性。超高效液相色谱法结合质谱分析表明,野生型 S. venezuelae 产生了大量的碱性挥发性物质三甲胺(TMA)及其氧化形式 TMAO;然而,这些化合物在菌株 MU-1 中的含量要低得多。值得注意的是,仅接触 TMA 就能挽救该突变株的表型,恢复气生菌丝和孢子的产生。我们还发现,碱性挥发物的拯救作用主要是针对特定物种的,这表明挥发物可能有助于特定突变体或其他密切相关物种的不太适合变体恢复正常生理状态,并在土壤等复杂群落中更有效地竞争。我们的研究揭示了细菌挥发物新的有趣作用,包括可能对其他物种产生毒性作用的挥发物:重要性:细菌挥发物在生物界内部或生物界之间具有广泛的生物学作用。挥发性物质的影响主要是在产生细菌和接受细菌(大多为不同物种)之间观察到的。在本研究中,我们报告了野生型、生活在土壤中的委内瑞拉链霉菌(Streptomyces venezuelae)在其正常发育周期中会形成气生菌丝和孢子,在多种生长条件下也会产生碱性挥发性化合物三甲胺(TMA)。我们的研究表明,委内瑞拉链霉菌产生的三甲胺在环境中的扩散能促进同种链霉菌或其他生长缓慢的链霉菌生长缺陷突变体的生长和分化,从而帮助它们在复杂的环境群落(如土壤)中生存和竞争。我们的新发现表明,挥发性化合物在产生挥发性物质的链霉菌群落的生长和生存过程中可能起着深远的生物学作用。
Rescue of morphological defects in Streptomyces venezuelae by the alkaline volatile compound trimethylamine.
Microorganisms can produce a vast diversity of volatile organic compounds of different chemical classes that are capable of mediating intra- and inter-kingdom interactions. In this study, we showed that the soil-dwelling bacterium Streptomyces venezuelae can produce alkaline volatiles under multiple growth conditions, which we discovered through investigation of the S. venezuelae mutant strain MU-1. Strain MU-1 has a defective morphology and exhibits a bald phenotype due to the lack of aerial mycelia and spores, as confirmed by scanning electron microscopy. Using physical barriers to separate the strains on culture plates, we determined that volatile compounds produced by wild-type S. venezuelae could rescue the phenotype of strain MU-1, and pH analysis of the growth medium indicated that these volatile compounds were alkaline. Ultra-high-performance liquid chromatography, combined with mass spectrometry analysis, showed that wild-type S. venezuelae produced abundant levels of the alkaline volatile trimethylamine (TMA) and the oxide form TMAO; however, the levels of these compounds were much lower in strain MU-1. Notably, exposure to TMA alone could rescue the phenotype of this mutant strain, restoring the production of aerial mycelia and spores. We also showed that the rescue effect by alkaline volatiles is mostly species-specific, suggesting that the volatiles may aid particular mutants or other less-fit variants of closely related species to resume normal physiological status and to compete more effectively in complex communities such as soil. Our study reveals a new and intriguing role for bacterial volatiles, including volatiles that may have toxic effects on other species.
Importance: Bacterial volatiles have a wide range of biological roles at intra- or inter-kingdom levels. The impact of volatiles has mainly been observed between producing bacteria and recipient bacteria, mostly of different species. In this study, we report that the wild-type, soil-dwelling bacterium Streptomyces venezuelae, which forms aerial hypha and spores as part of its normal developmental cycle, also produces the alkaline volatile compound trimethylamine (TMA) under multiple growth conditions. We showed that the environmental dispersion of TMA produced by S. venezuelae promotes the growth and differentiation of growth-deficient mutants of the same species or other slowly growing Streptomyces bacteria, and thus aids in their survival and their ability to compete in complex environmental communities such as soil. Our novel findings suggest a potentially profound biological role for volatile compounds in the growth and survival of communities of volatile-producing Streptomyces species.
期刊介绍:
Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.