Inflammatory bowel disease-associated adherent-invasive Escherichia coli have elevated host-defense peptide resistance

التفاصيل البيبلوغرافية
العنوان: Inflammatory bowel disease-associated adherent-invasive Escherichia coli have elevated host-defense peptide resistance
المؤلفون: Youn Hee Cho, Michael J Renouf, Oluwafikemi Omotoso, Joseph B McPhee
المصدر: FEMS microbiology letters. 369(1)
سنة النشر: 2022
مصطلحات موضوعية: Crohn Disease, Genetics, Escherichia coli, Humans, Colitis, Ulcerative, Intestinal Mucosa, Inflammatory Bowel Diseases, Molecular Biology, Microbiology, Escherichia coli Infections, Bacterial Adhesion, Antimicrobial Cationic Peptides, Peptide Hydrolases
الوصف: Adherent-invasive Escherichia coli (AIEC) are isolated from inflammatory bowel disease (IBD) patients at a higher rate than from control patients. Using a collection of E. coli strains collected from Crohn's disease (CD), ulcerative colitis (UC), or non-IBD control patients, antibiotic and resistance to the antimicrobial peptides HBD-3 and LL-37 was assessed. Carriage of bacterial-encoded omptin protease genes was assessed by PCR and omptin protease activity was measured using a whole-cell based fluorescence assay. Elevated resistance to antibiotics and host defense peptides in IBD-associated AIEC were observed. IBD-associated strains showed increased (but statistically non-significant) antibiotic resistance. CD-associated strains showed greater (but statistically non-significant) resistance to HBD3-mediated killing while UC-associated strains showed statistically greater resistance to LL-37 mediated killing. High-level resistance to LL-37 was associated with carriage of omptin protease genes and with increased omptin protease activity. Antimicrobial host defense peptide resistance may be an adaptive feature of AIEC leading to enhanced pathogenesis during the initiation or progression of IBD.
تدمد: 1574-6968
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5fe162b203ac981f4f611bbc048b1a0
https://pubmed.ncbi.nlm.nih.gov/36208952
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....b5fe162b203ac981f4f611bbc048b1a0
قاعدة البيانات: OpenAIRE