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      Gut microbiota of the tick vector Ixodes scapularis modulate colonization of the Lyme disease spirochete.

      Cell Host & Microbe
      Animals, Arachnid Vectors, microbiology, Borrelia burgdorferi, growth & development, pathogenicity, Carrier Proteins, antagonists & inhibitors, genetics, metabolism, Dysbiosis, Gene Expression Regulation, Host-Pathogen Interactions, Humans, Intestinal Mucosa, Ixodes, Larva, Microbiota, RNA, Small Interfering, STAT Transcription Factors, Signal Transduction

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          Abstract

          Arthopods such as Ixodes scapularis ticks serve as vectors for many human pathogens. The arthropod gut presents a pivotal microbial entry point and determines pathogen colonization and survival. We show that the gut microbiota of I. scapularis, a major vector of the Lyme disease spirochete Borrelia burgdorferi, influence spirochete colonization of ticks. Perturbing the gut microbiota of larval ticks reduced Borrelia colonization, and dysbiosed larvae displayed decreased expression of the transcription factor signal transducer and activator of transcription (STAT). Diminished STAT expression corresponded to lower expression of peritrophin, a key glycoprotein scaffold of the glycan-rich mucus-like peritrophic matrix (PM) that separates the gut lumen from the epithelium. The integrity of the I. scapularis PM was essential for B. burgdorferi to efficiently colonize the gut epithelium. These data elucidate a functional link between the gut microbiota, STAT-signaling, and pathogen colonization in the context of the gut epithelial barrier of an arthropod vector. Copyright © 2014 Elsevier Inc. All rights reserved.

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