{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T04:36:48Z","timestamp":1791175008738,"version":"4.1.0"},"reference-count":75,"publisher":"Oxford University Press (OUP)","issue":"7","license":[{"start":{"date-parts":[[2008,10,1]],"date-time":"2008-10-01T00:00:00Z","timestamp":1222819200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2008,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Cathelicidins are a family of cationic peptides expressed in mammals that possess numerous bactericidal and immunomodulatory properties. In vitro analyses showed that human, mouse, and pig cathelicidins inhibited Bacillus anthracis bacterial growth at micromolar concentrations in the presence or absence of capsule. Combined in vitro analyses of the effects of each peptide on spore germination and vegetative outgrowth by time lapse phase contrast microscopy, transmission electron microscopy, and flow cytometric analysis showed that only the pig cathelicidin was capable of directly arresting vegetative outgrowth and killing the developing bacilli within the confines of the exosporium. C57BL\/6 mice were protected from spore-induced death by each cathelicidin in a time- and dose-dependent manner. Protection afforded by the porcine cathelicidin was due to its bactericidal effects, whereas the human and mouse cathelicidins appeared to mediate protection through increased recruitment of neutrophils to the site of infection. These findings suggest that cathelicidins might be utilized to augment the initial innate immune response to B. anthracis spore exposure and prevent the development of anthrax.<\/jats:p>","DOI":"10.4049\/jimmunol.181.7.4989","type":"journal-article","created":{"date-parts":[[2014,4,18]],"date-time":"2014-04-18T19:07:10Z","timestamp":1397848030000},"page":"4989-5000","source":"Crossref","is-referenced-by-count":31,"title":["Cathelicidin Administration Protects Mice from\n                    <i>Bacillus anthracis<\/i>\n                    Spore Challenge"],"prefix":"10.1093","volume":"181","author":[{"given":"Mark W","family":"Lisanby","sequence":"first","affiliation":[{"name":"Department of Microbiology, University of Alabama at Birmingham , Birmingham, AL 35294"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa K","family":"Swiecki","sequence":"additional","affiliation":[{"name":"Department of Microbiology, University of Alabama at Birmingham , Birmingham, AL 35294"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brian L P","family":"Dizon","sequence":"additional","affiliation":[{"name":"Department of Microbiology, University of Alabama at Birmingham , Birmingham, AL 35294"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kathryn J","family":"Pflughoeft","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Molecular Genetics, University of Texas-Houston Medical School , Houston, TX 77030"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Theresa M","family":"Koehler","sequence":"additional","affiliation":[{"name":"Department of Microbiology and Molecular Genetics, University of Texas-Houston Medical School , Houston, TX 77030"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John F","family":"Kearney","sequence":"additional","affiliation":[{"name":"Department of Microbiology, University of Alabama at Birmingham , Birmingham, AL 35294"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2008,10,1]]},"reference":[{"key":"2026012807114701500_R1","first-page":"710","article-title":"Defensins: antimicrobial peptides of innate immunity","volume-title":"Nat. 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