从生牛奶奶酪到肠道:研究蒙氏双歧杆菌的定植策略。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-09-18 Epub Date: 2024-08-16 DOI:10.1128/aem.01244-24
Giulia Longhi, Gabriele Andrea Lugli, Chiara Tarracchini, Federico Fontana, Massimiliano Giovanni Bianchi, Elisa Carli, Ovidio Bussolati, Douwe van Sinderen, Francesca Turroni, Marco Ventura
{"title":"从生牛奶奶酪到肠道:研究蒙氏双歧杆菌的定植策略。","authors":"Giulia Longhi, Gabriele Andrea Lugli, Chiara Tarracchini, Federico Fontana, Massimiliano Giovanni Bianchi, Elisa Carli, Ovidio Bussolati, Douwe van Sinderen, Francesca Turroni, Marco Ventura","doi":"10.1128/aem.01244-24","DOIUrl":null,"url":null,"abstract":"<p><p>The microbial ecology of raw milk cheeses is determined by bacteria originating from milk and milk-producing animals. Recently, it has been shown that members of the <i>Bifidobacterium mongoliense</i> species may become transmitted along the Parmigiano Reggiano cheese production chain and ultimately may colonize the consumer intestine. However, there is a lack of knowledge regarding the molecular mechanisms that mediate the interaction between <i>B. mongoliense</i> and the human gut. Based on 128 raw milk cheeses collected from different Italian regions, we isolated and characterized 10 <i>B. mongoliense</i> strains. Comparative genomics allowed us to unveil the presence of enzymes required for the degradation of sialylated host-glycans in <i>B. mongoliense</i>, corroborating the appreciable growth on de Man-Rogosa-Sharpe (MRS) medium supplemented with 3'-sialyllactose (3'-SL) or 6'-sialyllactose (6'-SL). The <i>B. mongoliense</i> BMONG18 was chosen, due to its superior ability to utilize 3'-SL and mucin as representative strain, to investigate its behavior when co-inoculated with other bifidobacterial species. Conversely, members of other bifidobacterial species did not appear to benefit from the presence of BMONG18, highlighting a competitive scenario for nutrient acquisition. Transcriptomic data of BMONG18 reveal no significant differences in gene expression when cultivated in a gut simulating medium (GSM), regardless of whether cheese was included or not. Furthermore, BMONG18 was shown to exhibit high adhesion capabilities to HT29-MTX human cells, in line with its colonization ability of a human host.IMPORTANCEFermented foods are nourishments produced through controlled microbial growth that play an essential role in worldwide human nutrition. Research interest in fermented foods has increased since the 80s, driven by growing awareness of their potential health benefits beyond mere nutritional content. <i>Bifidobacterium mongoliense</i>, previously identified throughout the production process of Parmigiano Reggiano cheese, was found to be capable of establishing itself in the intestines of its consumers. Our study underscores molecular mechanisms through which this bifidobacterial species, derived from food, interacts with the host and other gut microbiota members.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11409640/pdf/","citationCount":"0","resultStr":"{\"title\":\"From raw milk cheese to the gut: investigating the colonization strategies of <i>Bifidobacterium mongoliense</i>.\",\"authors\":\"Giulia Longhi, Gabriele Andrea Lugli, Chiara Tarracchini, Federico Fontana, Massimiliano Giovanni Bianchi, Elisa Carli, Ovidio Bussolati, Douwe van Sinderen, Francesca Turroni, Marco Ventura\",\"doi\":\"10.1128/aem.01244-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The microbial ecology of raw milk cheeses is determined by bacteria originating from milk and milk-producing animals. Recently, it has been shown that members of the <i>Bifidobacterium mongoliense</i> species may become transmitted along the Parmigiano Reggiano cheese production chain and ultimately may colonize the consumer intestine. However, there is a lack of knowledge regarding the molecular mechanisms that mediate the interaction between <i>B. mongoliense</i> and the human gut. Based on 128 raw milk cheeses collected from different Italian regions, we isolated and characterized 10 <i>B. mongoliense</i> strains. Comparative genomics allowed us to unveil the presence of enzymes required for the degradation of sialylated host-glycans in <i>B. mongoliense</i>, corroborating the appreciable growth on de Man-Rogosa-Sharpe (MRS) medium supplemented with 3'-sialyllactose (3'-SL) or 6'-sialyllactose (6'-SL). The <i>B. mongoliense</i> BMONG18 was chosen, due to its superior ability to utilize 3'-SL and mucin as representative strain, to investigate its behavior when co-inoculated with other bifidobacterial species. Conversely, members of other bifidobacterial species did not appear to benefit from the presence of BMONG18, highlighting a competitive scenario for nutrient acquisition. Transcriptomic data of BMONG18 reveal no significant differences in gene expression when cultivated in a gut simulating medium (GSM), regardless of whether cheese was included or not. Furthermore, BMONG18 was shown to exhibit high adhesion capabilities to HT29-MTX human cells, in line with its colonization ability of a human host.IMPORTANCEFermented foods are nourishments produced through controlled microbial growth that play an essential role in worldwide human nutrition. Research interest in fermented foods has increased since the 80s, driven by growing awareness of their potential health benefits beyond mere nutritional content. <i>Bifidobacterium mongoliense</i>, previously identified throughout the production process of Parmigiano Reggiano cheese, was found to be capable of establishing itself in the intestines of its consumers. Our study underscores molecular mechanisms through which this bifidobacterial species, derived from food, interacts with the host and other gut microbiota members.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11409640/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.01244-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/16 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.01244-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/16 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

生乳奶酪的微生物生态由源自牛奶和产乳动物的细菌决定。最近的研究表明,双歧杆菌(Bifidobacterium mongoliense)的成员可能会沿着 Parmigiano Reggiano 奶酪的生产链传播,并最终在消费者的肠道中定植。然而,人们对介导 B. mongoliense 与人体肠道之间相互作用的分子机制还缺乏了解。基于从意大利不同地区收集的 128 种生奶奶酪,我们分离并鉴定了 10 株 B. mongoliense 菌株。通过比较基因组学,我们发现了蒙戈菌中存在降解寄主聚糖所需的酶,并证实了其在添加了 3'-sialyllactose (3'-SL) 或 6'-sialyllactose (6'-SL) 的 de Man-Rogosa-Sharpe (MRS) 培养基上的显著生长。由于 B. mongoliense BMONG18 利用 3'-SL 和粘蛋白的能力较强,因此被选为代表菌株,以研究其与其他双歧杆菌共同接种时的行为。相反,其他双歧杆菌成员似乎并没有从 BMONG18 的存在中获益,这凸显了营养物质获取的竞争情况。BMONG18 的转录组数据显示,在肠道模拟培养基(GSM)中培养时,无论是否加入奶酪,基因表达均无明显差异。此外,研究表明 BMONG18 对 HT29-MTX 人体细胞具有很强的粘附能力,这与其在人类宿主中的定植能力是一致的。 重要意义发酵食品是通过控制微生物生长而产生的营养品,在全球人类营养中发挥着重要作用。自上世纪 80 年代以来,人们对发酵食品的研究兴趣与日俱增,因为人们越来越意识到发酵食品不仅具有营养成分,还具有潜在的健康益处。之前在 Parmigiano Reggiano 奶酪的整个生产过程中发现的双歧杆菌(Bifidobacterium mongoliense)能够在消费者的肠道中生长。我们的研究强调了这种从食物中提取的双歧杆菌与宿主和其他肠道微生物群成员相互作用的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
From raw milk cheese to the gut: investigating the colonization strategies of Bifidobacterium mongoliense.

The microbial ecology of raw milk cheeses is determined by bacteria originating from milk and milk-producing animals. Recently, it has been shown that members of the Bifidobacterium mongoliense species may become transmitted along the Parmigiano Reggiano cheese production chain and ultimately may colonize the consumer intestine. However, there is a lack of knowledge regarding the molecular mechanisms that mediate the interaction between B. mongoliense and the human gut. Based on 128 raw milk cheeses collected from different Italian regions, we isolated and characterized 10 B. mongoliense strains. Comparative genomics allowed us to unveil the presence of enzymes required for the degradation of sialylated host-glycans in B. mongoliense, corroborating the appreciable growth on de Man-Rogosa-Sharpe (MRS) medium supplemented with 3'-sialyllactose (3'-SL) or 6'-sialyllactose (6'-SL). The B. mongoliense BMONG18 was chosen, due to its superior ability to utilize 3'-SL and mucin as representative strain, to investigate its behavior when co-inoculated with other bifidobacterial species. Conversely, members of other bifidobacterial species did not appear to benefit from the presence of BMONG18, highlighting a competitive scenario for nutrient acquisition. Transcriptomic data of BMONG18 reveal no significant differences in gene expression when cultivated in a gut simulating medium (GSM), regardless of whether cheese was included or not. Furthermore, BMONG18 was shown to exhibit high adhesion capabilities to HT29-MTX human cells, in line with its colonization ability of a human host.IMPORTANCEFermented foods are nourishments produced through controlled microbial growth that play an essential role in worldwide human nutrition. Research interest in fermented foods has increased since the 80s, driven by growing awareness of their potential health benefits beyond mere nutritional content. Bifidobacterium mongoliense, previously identified throughout the production process of Parmigiano Reggiano cheese, was found to be capable of establishing itself in the intestines of its consumers. Our study underscores molecular mechanisms through which this bifidobacterial species, derived from food, interacts with the host and other gut microbiota members.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
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.
期刊最新文献
Acidification-based mineral weathering mechanism involves a glucose/methanol/choline oxidoreductase in Caballeronia mineralivorans PML1(12). Adaptive immunity in Mus musculus influences the acquisition and abundance of Borrelia burgdorferi in Ixodes scapularis ticks. Does strain-level persistence of lactobacilli in long-term back-slopped sourdoughs inform on domestication of food-fermenting lactic acid bacteria? Rhizosphere microbiomes are closely linked to seagrass species: a comparative study of three coastal seagrasses. Assessing horizontal gene transfer in the rhizosphere of Brachypodium distachyon using fabricated ecosystems (EcoFABs).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1