Shawn M Christensen, Ivan Munkres, Rachel L Vannette
{"title":"花蜜细菌刺激花粉萌发和破裂,以提高微生物的适应性。","authors":"Shawn M Christensen, Ivan Munkres, Rachel L Vannette","doi":"10.1016/j.cub.2021.07.016","DOIUrl":null,"url":null,"abstract":"<p><p>Many organisms consume pollen, yet mechanisms of its digestion remain a fundamental enigma in pollination biology,<sup>1-3</sup> as pollen is protected by a recalcitrant outer shell.<sup>4-8</sup> Pollen is commonly found in floral nectar,<sup>9</sup><sup>,</sup><sup>10</sup> as are nectar microbes, which are nearly ubiquitous among flowers.<sup>11-13</sup> Nectar specialist bacteria, like Acinetobacter, can reach high densities (up to 10<sup>9</sup> cells/mL), despite the fact that floral nectar is nitrogen poor.<sup>14-17</sup> Here, we show evidence that the genus Acinetobacter, prevalent nectar- and bee-associated bacteria,<sup>12</sup><sup>,</sup><sup>18-20</sup> can induce pollen germination and bursting, gain access to protoplasm nutrients, and thereby grow to higher densities. Although induced germination had been suggested as a potential method in macroscopic pollen consumers,<sup>2</sup><sup>,</sup><sup>21-23</sup> and fungal inhibition of pollen germination has been shown,<sup>24-27</sup> direct biological induction of germination has not been empirically documented outside of plants.<sup>28-32</sup>Acinetobacter pollinis SCC477<sup>19</sup> induced over 5× greater pollen germination and 20× greater pollen bursting than that of uninoculated pollen by 45 min. When provided with germinable pollen, A. pollinis stimulates protein release and grows to nearly twice the density compared to growth with ungerminable pollen, indicating that stimulation of germination benefits bacterial fitness. In contrast, a common nectar-inhabiting yeast (Metschnikowia)<sup>33</sup> neither induced nor benefited from pollen germination. We conclude that Acinetobacter both specifically causes and benefits from inducing pollen germination and bursting. Further study of microbe-pollen interactions may inform many aspects of pollination ecology, including floral microbial ecology,<sup>34</sup><sup>,</sup><sup>35</sup> pollinator nutrient acquisition from pollen,<sup>2</sup><sup>,</sup><sup>3</sup><sup>,</sup><sup>21</sup><sup>,</sup><sup>36</sup> and cues of pollen germination for plant reproduction.<sup>37-39</sup>.</p>","PeriodicalId":11359,"journal":{"name":"Current Biology","volume":null,"pages":null},"PeriodicalIF":8.1000,"publicationDate":"2021-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.cub.2021.07.016","citationCount":"22","resultStr":"{\"title\":\"Nectar bacteria stimulate pollen germination and bursting to enhance microbial fitness.\",\"authors\":\"Shawn M Christensen, Ivan Munkres, Rachel L Vannette\",\"doi\":\"10.1016/j.cub.2021.07.016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Many organisms consume pollen, yet mechanisms of its digestion remain a fundamental enigma in pollination biology,<sup>1-3</sup> as pollen is protected by a recalcitrant outer shell.<sup>4-8</sup> Pollen is commonly found in floral nectar,<sup>9</sup><sup>,</sup><sup>10</sup> as are nectar microbes, which are nearly ubiquitous among flowers.<sup>11-13</sup> Nectar specialist bacteria, like Acinetobacter, can reach high densities (up to 10<sup>9</sup> cells/mL), despite the fact that floral nectar is nitrogen poor.<sup>14-17</sup> Here, we show evidence that the genus Acinetobacter, prevalent nectar- and bee-associated bacteria,<sup>12</sup><sup>,</sup><sup>18-20</sup> can induce pollen germination and bursting, gain access to protoplasm nutrients, and thereby grow to higher densities. Although induced germination had been suggested as a potential method in macroscopic pollen consumers,<sup>2</sup><sup>,</sup><sup>21-23</sup> and fungal inhibition of pollen germination has been shown,<sup>24-27</sup> direct biological induction of germination has not been empirically documented outside of plants.<sup>28-32</sup>Acinetobacter pollinis SCC477<sup>19</sup> induced over 5× greater pollen germination and 20× greater pollen bursting than that of uninoculated pollen by 45 min. When provided with germinable pollen, A. pollinis stimulates protein release and grows to nearly twice the density compared to growth with ungerminable pollen, indicating that stimulation of germination benefits bacterial fitness. In contrast, a common nectar-inhabiting yeast (Metschnikowia)<sup>33</sup> neither induced nor benefited from pollen germination. We conclude that Acinetobacter both specifically causes and benefits from inducing pollen germination and bursting. Further study of microbe-pollen interactions may inform many aspects of pollination ecology, including floral microbial ecology,<sup>34</sup><sup>,</sup><sup>35</sup> pollinator nutrient acquisition from pollen,<sup>2</sup><sup>,</sup><sup>3</sup><sup>,</sup><sup>21</sup><sup>,</sup><sup>36</sup> and cues of pollen germination for plant reproduction.<sup>37-39</sup>.</p>\",\"PeriodicalId\":11359,\"journal\":{\"name\":\"Current Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2021-10-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.cub.2021.07.016\",\"citationCount\":\"22\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cub.2021.07.016\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/7/28 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cub.2021.07.016","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/7/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Nectar bacteria stimulate pollen germination and bursting to enhance microbial fitness.
Many organisms consume pollen, yet mechanisms of its digestion remain a fundamental enigma in pollination biology,1-3 as pollen is protected by a recalcitrant outer shell.4-8 Pollen is commonly found in floral nectar,9,10 as are nectar microbes, which are nearly ubiquitous among flowers.11-13 Nectar specialist bacteria, like Acinetobacter, can reach high densities (up to 109 cells/mL), despite the fact that floral nectar is nitrogen poor.14-17 Here, we show evidence that the genus Acinetobacter, prevalent nectar- and bee-associated bacteria,12,18-20 can induce pollen germination and bursting, gain access to protoplasm nutrients, and thereby grow to higher densities. Although induced germination had been suggested as a potential method in macroscopic pollen consumers,2,21-23 and fungal inhibition of pollen germination has been shown,24-27 direct biological induction of germination has not been empirically documented outside of plants.28-32Acinetobacter pollinis SCC47719 induced over 5× greater pollen germination and 20× greater pollen bursting than that of uninoculated pollen by 45 min. When provided with germinable pollen, A. pollinis stimulates protein release and grows to nearly twice the density compared to growth with ungerminable pollen, indicating that stimulation of germination benefits bacterial fitness. In contrast, a common nectar-inhabiting yeast (Metschnikowia)33 neither induced nor benefited from pollen germination. We conclude that Acinetobacter both specifically causes and benefits from inducing pollen germination and bursting. Further study of microbe-pollen interactions may inform many aspects of pollination ecology, including floral microbial ecology,34,35 pollinator nutrient acquisition from pollen,2,3,21,36 and cues of pollen germination for plant reproduction.37-39.
期刊介绍:
Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.