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病原体介导的节肢动物微生物群操纵以促进感染。

Pathogen-mediated manipulation of arthropod microbiota to promote infection.

作者信息

Abraham Nabil M, Liu Lei, Jutras Brandon Lyon, Yadav Akhilesh K, Narasimhan Sukanya, Gopalakrishnan Vissagan, Ansari Juliana M, Jefferson Kimberly K, Cava Felipe, Jacobs-Wagner Christine, Fikrig Erol

机构信息

Section of Infectious Disease, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510.

Howard Hughes Medical Institute, Chevy Chase, MD 20815.

出版信息

Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):E781-E790. doi: 10.1073/pnas.1613422114. Epub 2017 Jan 17.

Abstract

Arthropods transmit diverse infectious agents; however, the ways microbes influence their vector to enhance colonization are poorly understood. Ixodes scapularis ticks harbor numerous human pathogens, including Anaplasma phagocytophilum, the agent of human granulocytic anaplasmosis. We now demonstrate that A. phagocytophilum modifies the I. scapularis microbiota to more efficiently infect the tick. A. phagocytophilum induces ticks to express Ixodes scapularis antifreeze glycoprotein (iafgp), which encodes a protein with several properties, including the ability to alter bacterial biofilm formation. IAFGP thereby perturbs the tick gut microbiota, which influences the integrity of the peritrophic matrix and gut barrier-critical obstacles for Anaplasma colonization. Mechanistically, IAFGP binds the terminal d-alanine residue of the pentapeptide chain of bacterial peptidoglycan, resulting in altered permeability and the capacity of bacteria to form biofilms. These data elucidate the molecular mechanisms by which a human pathogen appropriates an arthropod antibacterial protein to alter the gut microbiota and more effectively colonize the vector.

摘要

节肢动物传播多种感染因子;然而,微生物影响其载体以增强定殖的方式却知之甚少。肩突硬蜱携带众多人类病原体,包括嗜吞噬细胞无形体,即人类粒细胞无形体病的病原体。我们现在证明,嗜吞噬细胞无形体会改变肩突硬蜱的微生物群,从而更有效地感染蜱虫。嗜吞噬细胞无形体诱导蜱虫表达肩突硬蜱抗冻糖蛋白(iafgp),该蛋白编码一种具有多种特性的蛋白质,包括改变细菌生物膜形成的能力。IAFGP进而扰乱蜱虫肠道微生物群,这会影响围食膜和肠道屏障的完整性,而围食膜和肠道屏障是无形体定殖的关键障碍。从机制上讲,IAFGP与细菌肽聚糖五肽链的末端d - 丙氨酸残基结合,导致通透性改变以及细菌形成生物膜的能力改变。这些数据阐明了一种人类病原体利用节肢动物抗菌蛋白改变肠道微生物群并更有效地定殖于载体的分子机制。

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