韦氏芽孢杆菌 HBXN2020 可通过改善肠道屏障完整性和减轻炎症缓解小鼠感染鼠伤寒沙门氏菌的症状。

IF 6.4 1区 生物学 Q1 BIOLOGY eLife Pub Date : 2024-11-19 DOI:10.7554/eLife.93423
Linkang Wang, Haiyan Wang, Xinxin Li, Mengyuan Zhu, Dongyang Gao, Dayue Hu, Zhixuan Xiong, Xiangmin Li, Ping Qian
{"title":"韦氏芽孢杆菌 HBXN2020 可通过改善肠道屏障完整性和减轻炎症缓解小鼠感染鼠伤寒沙门氏菌的症状。","authors":"Linkang Wang, Haiyan Wang, Xinxin Li, Mengyuan Zhu, Dongyang Gao, Dayue Hu, Zhixuan Xiong, Xiangmin Li, Ping Qian","doi":"10.7554/eLife.93423","DOIUrl":null,"url":null,"abstract":"<p><p><i>Bacillus velezensis</i> is a species of <i>Bacillus</i> that has been widely investigated because of its broad-spectrum antimicrobial activity. However, most studies on <i>B. velezensis</i> have focused on the biocontrol of plant diseases, with few reports on antagonizing <i>Salmonella</i> Typhimurium infections. In this investigation, it was discovered that <i>B. velezensis</i> HBXN2020, which was isolated from healthy black pigs, possessed strong anti-stress and broad-spectrum antibacterial activity. Importantly, <i>B. velezensis</i> HBXN2020 did not cause any adverse side effects in mice when administered at various doses (1×10<sup>7</sup>, 1×10<sup>8</sup>, and 1×10<sup>9</sup> CFU) for 14 days. Supplementing <i>B. velezensis</i> HBXN2020 spores, either as a curative or preventive measure, dramatically reduced the levels of <i>S.</i> Typhimurium ATCC14028 in the mice's feces, ileum, cecum, and colon, as well as the disease activity index (DAI), in a model of infection caused by this pathogen in mice. Additionally, supplementing <i>B. velezensis</i> HBXN2020 spores significantly regulated cytokine levels (<i>Tnfa</i>, <i>Il1b</i>, <i>Il6</i>, and <i>Il10</i>) and maintained the expression of tight junction proteins and mucin protein. Most importantly, adding <i>B. velezensis</i> HBXN2020 spores to the colonic microbiota improved its stability and increased the amount of beneficial bacteria (<i>Lactobacillus</i> and <i>Akkermansia</i>). All together, <i>B. velezensis</i> HBXN2020 can improve intestinal microbiota stability and barrier integrity and reduce inflammation to help treat infection by <i>S.</i> Typhimurium.</p>","PeriodicalId":11640,"journal":{"name":"eLife","volume":"13 ","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Bacillus velezensis</i> HBXN2020 alleviates <i>Salmonella</i> Typhimurium infection in mice by improving intestinal barrier integrity and reducing inflammation.\",\"authors\":\"Linkang Wang, Haiyan Wang, Xinxin Li, Mengyuan Zhu, Dongyang Gao, Dayue Hu, Zhixuan Xiong, Xiangmin Li, Ping Qian\",\"doi\":\"10.7554/eLife.93423\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Bacillus velezensis</i> is a species of <i>Bacillus</i> that has been widely investigated because of its broad-spectrum antimicrobial activity. However, most studies on <i>B. velezensis</i> have focused on the biocontrol of plant diseases, with few reports on antagonizing <i>Salmonella</i> Typhimurium infections. In this investigation, it was discovered that <i>B. velezensis</i> HBXN2020, which was isolated from healthy black pigs, possessed strong anti-stress and broad-spectrum antibacterial activity. Importantly, <i>B. velezensis</i> HBXN2020 did not cause any adverse side effects in mice when administered at various doses (1×10<sup>7</sup>, 1×10<sup>8</sup>, and 1×10<sup>9</sup> CFU) for 14 days. Supplementing <i>B. velezensis</i> HBXN2020 spores, either as a curative or preventive measure, dramatically reduced the levels of <i>S.</i> Typhimurium ATCC14028 in the mice's feces, ileum, cecum, and colon, as well as the disease activity index (DAI), in a model of infection caused by this pathogen in mice. Additionally, supplementing <i>B. velezensis</i> HBXN2020 spores significantly regulated cytokine levels (<i>Tnfa</i>, <i>Il1b</i>, <i>Il6</i>, and <i>Il10</i>) and maintained the expression of tight junction proteins and mucin protein. Most importantly, adding <i>B. velezensis</i> HBXN2020 spores to the colonic microbiota improved its stability and increased the amount of beneficial bacteria (<i>Lactobacillus</i> and <i>Akkermansia</i>). All together, <i>B. velezensis</i> HBXN2020 can improve intestinal microbiota stability and barrier integrity and reduce inflammation to help treat infection by <i>S.</i> Typhimurium.</p>\",\"PeriodicalId\":11640,\"journal\":{\"name\":\"eLife\",\"volume\":\"13 \",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2024-11-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eLife\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.7554/eLife.93423\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.7554/eLife.93423","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

韦氏芽孢杆菌(Bacillus velezensis)是芽孢杆菌中的一种,因其具有广谱抗菌活性而被广泛研究。然而,关于 B. velezensis 的研究大多集中在植物病害的生物防治方面,很少有关于拮抗伤寒沙门氏菌感染的报道。本次研究发现,从健康黑猪体内分离出的 B. velezensis HBXN2020 具有很强的抗应激和广谱抗菌活性。重要的是,以不同剂量(1×107、1×108 和 1×109 CFU)连续给药 14 天,B. velezensis HBXN2020 不会对小鼠造成任何不良副作用。在由该病原体引起的小鼠感染模型中,作为治疗或预防措施补充 B. velezensis HBXN2020 孢子可显著降低小鼠粪便、回肠、盲肠和结肠中的鼠伤寒杆菌 ATCC14028 的含量以及疾病活动指数(DAI)。此外,补充 B. velezensis HBXN2020 孢子可显著调节细胞因子水平(Tnfa、Il1b、Il6 和 Il10),并维持紧密连接蛋白和粘蛋白的表达。最重要的是,在结肠微生物群中添加 B. velezensis HBXN2020 孢子能提高其稳定性,并增加有益菌(乳酸杆菌和 Akkermansia)的数量。总之,B. velezensis HBXN2020 可以提高肠道微生物区系的稳定性和屏障完整性,减少炎症,从而帮助治疗伤寒杆菌感染。
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
Bacillus velezensis HBXN2020 alleviates Salmonella Typhimurium infection in mice by improving intestinal barrier integrity and reducing inflammation.

Bacillus velezensis is a species of Bacillus that has been widely investigated because of its broad-spectrum antimicrobial activity. However, most studies on B. velezensis have focused on the biocontrol of plant diseases, with few reports on antagonizing Salmonella Typhimurium infections. In this investigation, it was discovered that B. velezensis HBXN2020, which was isolated from healthy black pigs, possessed strong anti-stress and broad-spectrum antibacterial activity. Importantly, B. velezensis HBXN2020 did not cause any adverse side effects in mice when administered at various doses (1×107, 1×108, and 1×109 CFU) for 14 days. Supplementing B. velezensis HBXN2020 spores, either as a curative or preventive measure, dramatically reduced the levels of S. Typhimurium ATCC14028 in the mice's feces, ileum, cecum, and colon, as well as the disease activity index (DAI), in a model of infection caused by this pathogen in mice. Additionally, supplementing B. velezensis HBXN2020 spores significantly regulated cytokine levels (Tnfa, Il1b, Il6, and Il10) and maintained the expression of tight junction proteins and mucin protein. Most importantly, adding B. velezensis HBXN2020 spores to the colonic microbiota improved its stability and increased the amount of beneficial bacteria (Lactobacillus and Akkermansia). All together, B. velezensis HBXN2020 can improve intestinal microbiota stability and barrier integrity and reduce inflammation to help treat infection by S. Typhimurium.

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
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
期刊最新文献
NE contribution to rebooting unconsciousness caused by midazolam. Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity. The gamma rhythm as a guardian of brain health. Zika virus remodels and hijacks IGF2BP2 ribonucleoprotein complex to promote viral replication organelle biogenesis. Extramacrochaetae regulates Notch signaling in the Drosophila eye through non-apoptotic caspase activity.
×
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