<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY accession="ERP120010" alias="ena-STUDY-CGS-GL-13-02-2020-18:42:54:541-337" center_name="Gordon Lab at The Washington University School of Medicine, Center for Genome Sciences and Systems Biology">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP120010</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB36780</EXTERNAL_ID>
      <SUBMITTER_ID namespace="CGS-GL">ena-STUDY-CGS-GL-13-02-2020-18:42:54:541-337</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Gordon Lab at The Washington University School of Medicine, Center for Genome Sciences and Systems Biology">ena-STUDY-CGS-GL-13-02-2020-18:42:54:541-337</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Airway Microbiota-Host Interactions Regulate Secreted Leukocyte Proteinase Inhibitor Levels and Influence Allergic Airway Inflammation</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Homeostatic mucosal immune responses are fine-tuned by naturally evolved interactions with native microbes and integrating these relationships into experimental models can provide new insights into human diseases. Here, we leverage a recently discovered murine-adapted airway microbe, Bordetella pseudohinzii (Bph), to investigate how chronic colonization impacts mucosal immunity and the development of allergic airway inflammation (AAI). Colonization with Bph induced the differentiation of IL-17A secreting T-helper cells that aid in controlling bacterial abundance. Bph colonization protected from AAI and was associated with increased Secreted Leukocyte Proteinase Inhibitor (SLPI), an antimicrobial peptide with anti-inflammatory properties. These findings were additionally supported by clinical data showing that higher levels of upper respiratory SLPI correlate both to improved asthma control and the presence of Haemophilus, a bacterial genus associated with allergic airway inflammation. We propose that SLPI could be used as a biomarker of beneficial host-commensal relationships in the airway.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Bordetella pseudohinzii airway colonization</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>Homeostatic mucosal immune responses are fine-tuned by naturally evolved interactions with native microbes and integrating these relationships into experimental models can provide new insights into human diseases. Here, we leverage a recently discovered murine-adapted airway microbe, Bordetella pseudohinzii (Bph), to investigate how chronic colonization impacts mucosal immunity and the development of allergic airway inflammation (AAI). Colonization with Bph induced the differentiation of IL-17A secreting T-helper cells that aid in controlling bacterial abundance. Bph colonization protected from AAI and was associated with increased Secreted Leukocyte Proteinase Inhibitor (SLPI), an antimicrobial peptide with anti-inflammatory properties. These findings were additionally supported by clinical data showing that higher levels of upper respiratory SLPI correlate both to improved asthma control and the presence of Haemophilus, a bacterial genus associated with allergic airway inflammation. We propose that SLPI could be used as a biomarker of beneficial host-commensal relationships in the airway.</STUDY_DESCRIPTION>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2020-04-14</VALUE>
      </STUDY_ATTRIBUTE>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2020-02-13</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
