与宿主相适应的辅助营养性肠道共生菌诱导粘膜免疫缺陷

IF 44.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Science Pub Date : 2024-09-27 DOI:10.1126/science.adk2536
Qiuhe Lu, Thomas C. A. Hitch, Julie Y. Zhou, Mohammed Dwidar, Naseer Sangwan, Dylan Lawrence, Lila S. Nolan, Scott T. Espenschied, Kevin P. Newhall, Yi Han, Paul E. Karell, Vanessa Salazar, Megan T. Baldridge, Thomas Clavel, Thaddeus S. Stappenbeck
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引用次数: 0

摘要

要利用微生物群造福人类健康,首先需要确定影响宿主特定生理功能的致病微生物的身份和功能。我们对肠道免疫球蛋白 A(IgA)水平较低的小鼠的细菌微生物群进行了功能筛选;我们发现了一种革兰氏阴性细菌,被认为是嗜免疫托马西菌,它能诱导和降解小鼠肠道中的 IgA。携带免疫嗜酸乳杆菌的小鼠易受感染,粘膜修复能力差。嗜免疫球菌对细菌细胞壁氨基酸糖 N-乙酰氨基氨酸具有辅助营养作用。它能将免疫球蛋白降解蛋白酶输送到外膜囊泡中,这种蛋白酶能优先降解啮齿类动物的卡帕轻链抗体,而不能降解λ轻链抗体。这项研究表明了共生体在免疫缺陷中的作用,这可能适用于人类疾病。
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A host-adapted auxotrophic gut symbiont induces mucosal immunodeficiency
Harnessing the microbiome to benefit human health requires an initial step in determining the identity and function of causative microorganisms that affect specific host physiological functions. We show a functional screen of the bacterial microbiota from mice with low intestinal immunoglobulin A (IgA) levels; we identified a Gram-negative bacterium, proposed as Tomasiella immunophila, that induces and degrades IgA in the mouse intestine. Mice harboring T. immunophila are susceptible to infections and show poor mucosal repair. T. immunophila is auxotrophic for the bacterial cell wall amino sugar N-acetylmuramic acid. It delivers immunoglobulin-degrading proteases into outer membrane vesicles that preferentially degrade rodent antibodies with kappa but not lambda light chains. This work indicates a role for symbionts in immunodeficiency, which might be applicable to human disease.
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来源期刊
Science
Science 综合性期刊-综合性期刊
CiteScore
61.10
自引率
0.90%
发文量
0
审稿时长
2.1 months
期刊介绍: Science is a leading outlet for scientific news, commentary, and cutting-edge research. Through its print and online incarnations, Science reaches an estimated worldwide readership of more than one million. Science’s authorship is global too, and its articles consistently rank among the world's most cited research. Science serves as a forum for discussion of important issues related to the advancement of science by publishing material on which a consensus has been reached as well as including the presentation of minority or conflicting points of view. Accordingly, all articles published in Science—including editorials, news and comment, and book reviews—are signed and reflect the individual views of the authors and not official points of view adopted by AAAS or the institutions with which the authors are affiliated. Science seeks to publish those papers that are most influential in their fields or across fields and that will significantly advance scientific understanding. Selected papers should present novel and broadly important data, syntheses, or concepts. They should merit recognition by the wider scientific community and general public provided by publication in Science, beyond that provided by specialty journals. Science welcomes submissions from all fields of science and from any source. The editors are committed to the prompt evaluation and publication of submitted papers while upholding high standards that support reproducibility of published research. Science is published weekly; selected papers are published online ahead of print.
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