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<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
    <responseDate>2026-10-15T12:41:11Z</responseDate>
    <request verb="GetRecord" identifier="oai:data.mendeley.com/brsgf8h6dc.1" metadataPrefix="oai_dc">https://data.mendeley.com/oai</request>
    <GetRecord>
        <record>
            <header>
                <identifier>oai:data.mendeley.com/brsgf8h6dc.1</identifier>
                <datestamp>2024-12-13T14:22:30Z</datestamp>
            </header>
            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Bakaletz, Lauren</dc:creator>
    <dc:title>Human PMNs exhibit greater phagocytosis, NETosis, and enhanced migration towards nontypeable Haemophilus influenzae newly released from biofilms Wilbanks et al.</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Biofilms exhibit diverse evasion mechanisms, thus releasing bacteria from biofilm residence affords both antibiotics and immune effectors greater access. A monoclonal antibody against an essential biofilm matrix protein induces rapid biofilm collapse with release of bacteria into a highly vulnerable phenotype. Newly released (‘NRel’) bacteria are significantly more sensitive to antibiotic-, PMN-, or antimicrobial peptide-mediated killing in vitro, and are rapidly eradicated in four animal models without antibiotic treatment, highlighting the role of innate immune effectors. Here, we characterize PMN-mediated activity against three clinical isolates of nontypeable Haemophilus influenzae NRel. Indeed, NTHI was most sensitive in the NRel state to both  PMN-mediated phagocytosis and NETosis elimination. Moreover, PMNs incubated with NTHI NRel released significantly more IL-8 to recruit additional PMNs. These data provide the mechanism and treatment regimen to facilitate host mediated biofilm eradication in our pre-clinical models where biofilm bacteria were induced into the highly vulnerable NRel state.</dc:description>
    <dc:subject>Immunology</dc:subject>
    <dc:subject>Microbiology</dc:subject>
    <dc:subject>Biofilm</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/brsgf8h6dc.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/brsgf8h6dc.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/brsgf8h6dc</dc:relation>
    <dc:date>2024-12-13T14:22:30Z</dc:date>
</oai_dc:dc></metadata>
        </record>
    </GetRecord>
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