| Literature DB >> 28096373 |
Nabil M Abraham1,2, Lei Liu3, Brandon Lyon Jutras2,4,5, Akhilesh K Yadav6, Sukanya Narasimhan1, Vissagan Gopalakrishnan1,2,7, Juliana M Ansari8, Kimberly K Jefferson9, Felipe Cava6, Christine Jacobs-Wagner2,4,5,10, Erol Fikrig3,2,10.
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.Entities:
Keywords: Anaplasma; Ixodes scapularis; antifreeze protein; biofilm; microbiome
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Year: 2017 PMID: 28096373 PMCID: PMC5293115 DOI: 10.1073/pnas.1613422114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205