{"title":"硝酸盐通过促进谷氨酸和天门冬氨酸的分解,促进共生厌氧菌 Veillonella dispar 在乳酸盐缺乏环境中的生长以及短链脂肪酸和色氨酸的产生。","authors":"Jia-He Hung, Shi-Min Zhang, Shir-Ly Huang","doi":"10.1128/aem.01148-24","DOIUrl":null,"url":null,"abstract":"<p><p><i>Veillonella</i> spp. are nitrate-reducing bacteria with anaerobic respiratory activity that reduce nitrate to nitrite. They are obligate anaerobic, Gram-negative cocci that ferment lactate as the main carbon source and produce short-chain fatty acids (SCFAs). Commensal <i>Veillonella</i> reside in the human body site where lactate level is, however, limited for <i>Veillonella</i> growth. In this study, nitrate was shown to promote the anaerobic growth of <i>Veillonella</i> in the lactate-deficient media. We aimed to investigate the underlying mechanisms and the metabolism involved in nitrate respiration. Nitrate (15 mM) was demonstrated to promote <i>Veillonella dispar</i> growth and viability in the tryptone-yeast extract medium containing 0.5 mM L-lactate. Metabolite and transcriptomic analyses revealed nitrate enabled <i>V. dispar</i> to actively utilize glutamate and aspartate from the medium and secrete tryptophan. Glutamate or aspartate was further supplemented to a medium to investigate individual catabolism during nitrate respiration. Notably, nitrate was demonstrated to elevate SCFA production in the glutamate-supplemented medium, and further increase tryptophan production in the aspartate-supplemented medium. We proposed that the increased consumption of glutamate provided reducing power for nitrate respiration and aspartate served as a substrate for fumarate formation. Both glutamate and aspartate were incorporated into the central metabolic pathways <i>via</i> reverse tricarboxylic acid cycle and were linked with the increased production of acetate, propionate, and tryptophan. This study provides further understanding of the promoted growth and metabolic mechanisms by commensal <i>V. dispar</i> utilizing nitrate and specific amino acids to adapt to the lactate-deficient environment.IMPORTANCENitrate is a pivotal ecological factor influencing microbial community and metabolism. Dietary nitrate provides health benefits including anti-diabetic and anti-hypertensive effects <i>via</i> microbial-derived metabolites such as nitrite. Unraveling the impacts of nitrate on the growth and metabolism of human commensal bacteria is imperative to comprehend the intricate roles of nitrate in regulating microbial metabolism, community, and human health. <i>Veillonella</i> are lactate-utilizing, nitrate-reducing bacteria that are frequently found in the human body site where lactate levels are low and nitrate is at millimolar levels. Here, we comprehensively described the metabolic strategies employed by <i>V. dispar</i> to thrive in the lactate-deficient environment using nitrate respiration and catabolism of specific amino acids. The elevated production of SCFAs and tryptophan from amino acids during nitrate respiration of <i>V. dispar</i> further suggested the potential roles of nitrate and <i>Veillonella</i> in the promotion of human health.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337843/pdf/","citationCount":"0","resultStr":"{\"title\":\"Nitrate promotes the growth and the production of short-chain fatty acids and tryptophan from commensal anaerobe <i>Veillonella dispar</i> in the lactate-deficient environment by facilitating the catabolism of glutamate and aspartate.\",\"authors\":\"Jia-He Hung, Shi-Min Zhang, Shir-Ly Huang\",\"doi\":\"10.1128/aem.01148-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Veillonella</i> spp. are nitrate-reducing bacteria with anaerobic respiratory activity that reduce nitrate to nitrite. They are obligate anaerobic, Gram-negative cocci that ferment lactate as the main carbon source and produce short-chain fatty acids (SCFAs). Commensal <i>Veillonella</i> reside in the human body site where lactate level is, however, limited for <i>Veillonella</i> growth. In this study, nitrate was shown to promote the anaerobic growth of <i>Veillonella</i> in the lactate-deficient media. We aimed to investigate the underlying mechanisms and the metabolism involved in nitrate respiration. Nitrate (15 mM) was demonstrated to promote <i>Veillonella dispar</i> growth and viability in the tryptone-yeast extract medium containing 0.5 mM L-lactate. Metabolite and transcriptomic analyses revealed nitrate enabled <i>V. dispar</i> to actively utilize glutamate and aspartate from the medium and secrete tryptophan. Glutamate or aspartate was further supplemented to a medium to investigate individual catabolism during nitrate respiration. Notably, nitrate was demonstrated to elevate SCFA production in the glutamate-supplemented medium, and further increase tryptophan production in the aspartate-supplemented medium. We proposed that the increased consumption of glutamate provided reducing power for nitrate respiration and aspartate served as a substrate for fumarate formation. Both glutamate and aspartate were incorporated into the central metabolic pathways <i>via</i> reverse tricarboxylic acid cycle and were linked with the increased production of acetate, propionate, and tryptophan. This study provides further understanding of the promoted growth and metabolic mechanisms by commensal <i>V. dispar</i> utilizing nitrate and specific amino acids to adapt to the lactate-deficient environment.IMPORTANCENitrate is a pivotal ecological factor influencing microbial community and metabolism. Dietary nitrate provides health benefits including anti-diabetic and anti-hypertensive effects <i>via</i> microbial-derived metabolites such as nitrite. Unraveling the impacts of nitrate on the growth and metabolism of human commensal bacteria is imperative to comprehend the intricate roles of nitrate in regulating microbial metabolism, community, and human health. <i>Veillonella</i> are lactate-utilizing, nitrate-reducing bacteria that are frequently found in the human body site where lactate levels are low and nitrate is at millimolar levels. Here, we comprehensively described the metabolic strategies employed by <i>V. dispar</i> to thrive in the lactate-deficient environment using nitrate respiration and catabolism of specific amino acids. The elevated production of SCFAs and tryptophan from amino acids during nitrate respiration of <i>V. dispar</i> further suggested the potential roles of nitrate and <i>Veillonella</i> in the promotion of human health.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337843/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.01148-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/7/31 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.01148-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/31 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
Veillonella 菌属是硝酸盐还原菌,具有厌氧呼吸活性,可将硝酸盐还原为亚硝酸盐。它们是必须厌氧的革兰氏阴性球菌,以乳酸盐为主要碳源进行发酵,并产生短链脂肪酸(SCFAs)。维氏菌寄生在人体部位,但人体部位的乳酸盐水平限制了维氏菌的生长。在本研究中,硝酸盐被证明能促进维氏菌在乳酸盐缺乏的培养基中厌氧生长。我们的目的是研究硝酸盐呼吸所涉及的基本机制和新陈代谢。在含有 0.5 mM L-乳酸盐的胰蛋白酶-酵母提取物培养基中,硝酸盐(15 mM)被证明能促进 Veillonella 的生长和存活。代谢物和转录组分析表明,硝酸盐能使Veillonella dispar积极利用培养基中的谷氨酸和天冬氨酸,并分泌色氨酸。进一步向培养基中添加谷氨酸或天门冬氨酸,以研究硝酸盐呼吸过程中的个体分解代谢。值得注意的是,在补充谷氨酸的培养基中,硝酸盐被证明能提高 SCFA 的产生,而在补充天门冬氨酸的培养基中,色氨酸的产生进一步增加。我们认为,谷氨酸消耗的增加为硝酸盐呼吸提供了还原力,而天冬氨酸则成为富马酸形成的底物。谷氨酸和天门冬氨酸都通过反向三羧酸循环进入中央代谢途径,并与乙酸盐、丙酸盐和色氨酸产量的增加有关。这项研究让人们进一步了解了共生菌 V. dispar 利用硝酸盐和特定氨基酸适应乳酸盐缺乏环境的促进生长和代谢机制。重要意义硝酸盐是影响微生物群落和代谢的关键生态因子。膳食硝酸盐通过微生物衍生的代谢物(如亚硝酸盐)提供健康益处,包括抗糖尿病和抗高血压作用。要理解硝酸盐在调节微生物代谢、群落和人类健康方面的复杂作用,就必须揭示硝酸盐对人类共生细菌的生长和代谢的影响。Veillonella是一种利用乳酸盐的硝酸盐还原菌,经常出现在乳酸盐水平较低而硝酸盐处于毫摩尔水平的人体部位。在这里,我们全面描述了V. dispar利用硝酸盐呼吸和特定氨基酸的分解代谢在乳酸盐缺乏的环境中茁壮成长的代谢策略。在V. dispar的硝酸盐呼吸过程中,氨基酸产生的SCFAs和色氨酸增加,这进一步说明了硝酸盐和Veillonella在促进人类健康方面的潜在作用。
Nitrate promotes the growth and the production of short-chain fatty acids and tryptophan from commensal anaerobe Veillonella dispar in the lactate-deficient environment by facilitating the catabolism of glutamate and aspartate.
Veillonella spp. are nitrate-reducing bacteria with anaerobic respiratory activity that reduce nitrate to nitrite. They are obligate anaerobic, Gram-negative cocci that ferment lactate as the main carbon source and produce short-chain fatty acids (SCFAs). Commensal Veillonella reside in the human body site where lactate level is, however, limited for Veillonella growth. In this study, nitrate was shown to promote the anaerobic growth of Veillonella in the lactate-deficient media. We aimed to investigate the underlying mechanisms and the metabolism involved in nitrate respiration. Nitrate (15 mM) was demonstrated to promote Veillonella dispar growth and viability in the tryptone-yeast extract medium containing 0.5 mM L-lactate. Metabolite and transcriptomic analyses revealed nitrate enabled V. dispar to actively utilize glutamate and aspartate from the medium and secrete tryptophan. Glutamate or aspartate was further supplemented to a medium to investigate individual catabolism during nitrate respiration. Notably, nitrate was demonstrated to elevate SCFA production in the glutamate-supplemented medium, and further increase tryptophan production in the aspartate-supplemented medium. We proposed that the increased consumption of glutamate provided reducing power for nitrate respiration and aspartate served as a substrate for fumarate formation. Both glutamate and aspartate were incorporated into the central metabolic pathways via reverse tricarboxylic acid cycle and were linked with the increased production of acetate, propionate, and tryptophan. This study provides further understanding of the promoted growth and metabolic mechanisms by commensal V. dispar utilizing nitrate and specific amino acids to adapt to the lactate-deficient environment.IMPORTANCENitrate is a pivotal ecological factor influencing microbial community and metabolism. Dietary nitrate provides health benefits including anti-diabetic and anti-hypertensive effects via microbial-derived metabolites such as nitrite. Unraveling the impacts of nitrate on the growth and metabolism of human commensal bacteria is imperative to comprehend the intricate roles of nitrate in regulating microbial metabolism, community, and human health. Veillonella are lactate-utilizing, nitrate-reducing bacteria that are frequently found in the human body site where lactate levels are low and nitrate is at millimolar levels. Here, we comprehensively described the metabolic strategies employed by V. dispar to thrive in the lactate-deficient environment using nitrate respiration and catabolism of specific amino acids. The elevated production of SCFAs and tryptophan from amino acids during nitrate respiration of V. dispar further suggested the potential roles of nitrate and Veillonella in the promotion of human health.
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.