Selma María V, Beltrán David, Luna María C, Romo-Vaquero María, García-Villalba Rocío, Mira Alex, Espín Juan C, Tomás-Barberán Francisco A
Laboratory of Food and Health, Research Group on Quality, Safety and Bioactivity of Plant Foods, Department of Food Science and Technology, Centre for Applied Soil Science and Biology of the Segura - Spanish National Research CouncilMurcia, Spain.
Department of Health and Genomics, Center for Advanced Research in Public Health, FISABIO FoundationValencia, Spain.
Front Microbiol. 2017 Aug 7;8:1521. doi: 10.3389/fmicb.2017.01521. eCollection 2017.
Urolithins are intestinal microbial metabolites produced from ellagitannin- and ellagic acid-containing foods such as walnuts, strawberries, and pomegranates. These metabolites, better absorbed than their precursors, can contribute significantly to the beneficial properties attributed to the polyphenols ellagitannins and ellagic acid (EA). However, both the ability of producing the final metabolites in this catabolism (urolithins A, B and isourolithin A) and the health benefits associated with ellagitannin consumption differ considerably among individuals depending on their gut microbiota composition. Three human urolithin metabotypes have been previously described, i.e., metabotype 0 (urolithin non-producers), metabotype A (production of urolithin A as unique final urolithin) and metabotype B (urolithin B and/or isourolithin A are produced besides urolithin A). Although production of some intermediary urolithins has been recently attributed to intestinal species from family named and , the identification of the microorganisms responsible for the complete transformation of EA into the final urolithins, especially those related to metabotype B, are still unknown. In the present research we illustrate the isolation of urolithin-producing strains from human feces of a healthy adult and their ability to transform EA into different urolithin metabolites, including isourolithin A. The isolates belong to a new genus from family. EA transformation and urolithin production arisen during the stationary phase of the growth of the bacteria under anaerobic conditions. The HPLC-DAD-MS analyses demonstrated the sequential appearance of 3,8,9,10-tetrahydroxy-urolithin (urolithin M6), 3,8,9-trihydroxy-urolithin (urolithin C) and 3,9-dihydroxy-urolithin (isourolithin A) while 3,8-dihydroxy-urolithin (urolithin A) and 3-hydroxy-urolithin (urolithin B) were not detected. For the first time isourolithin A production capacity of pure strains has been described. The biological activity attributed to urolithins A and B and isourolithin A (anti-inflammatory, anti-carcinogenic, cardioprotective, and neuroprotective properties) explains the relevance of identifying these urolithin-producing bacteria as potential novel probiotics with applications in the development of functional foods and nutraceuticals. Their human administration could improve the health benefits upon ellagitannin consumption, especially in metabotype 0 individuals. However, further research is necessary to probe well-established beneficial effects on the host and safety requirements before being considered among the next-generation probiotics.
尿石素是肠道微生物对含鞣花单宁和鞣花酸的食物(如核桃、草莓和石榴)进行代谢产生的产物。这些代谢产物比其前体更易吸收,能显著增强归因于多酚类鞣花单宁和鞣花酸(EA)的有益特性。然而,个体在这种分解代谢中产生最终代谢产物(尿石素A、B和异尿石素A)的能力以及与食用鞣花单宁相关的健康益处,因肠道微生物群组成的不同而有很大差异。此前已描述了三种人类尿石素代谢型,即代谢型0(不产生尿石素)、代谢型A(仅产生尿石素A作为唯一的最终尿石素)和代谢型B(除尿石素A外还产生尿石素B和/或异尿石素A)。尽管最近已将一些中间尿石素的产生归因于[某科]的肠道菌种,但负责将EA完全转化为最终尿石素的微生物,尤其是与代谢型B相关的微生物,仍不明确。在本研究中,我们阐述了从一名健康成年人的粪便中分离出产生尿石素的菌株,以及它们将EA转化为不同尿石素代谢产物(包括异尿石素A)的能力。这些分离菌株属于[某科]的一个新属。EA的转化和尿石素的产生发生在细菌在厌氧条件下生长的稳定期。HPLC-DAD-MS分析表明,依次出现了3,8,9,10-四羟基尿石素(尿石素M6)、3,8,9-三羟基尿石素(尿石素C)和3,9-二羟基尿石素(异尿石素A),而未检测到3,8-二羟基尿石素(尿石素A)和3-羟基尿石素(尿石素B)。首次描述了纯菌株产生异尿石素A的能力。尿石素A、B和异尿石素A所具有的生物活性(抗炎、抗癌、心脏保护和神经保护特性)解释了鉴定这些产生尿石素的细菌作为潜在新型益生菌在功能性食品和营养保健品开发中的应用的相关性。对它们进行人体施用可以提高食用鞣花单宁后的健康益处,尤其是对代谢型0个体。然而,在被视为下一代益生菌之前,还需要进一步研究以探究其对宿主的确立的有益作用和安全性要求。