{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,21]],"date-time":"2026-01-21T07:22:53Z","timestamp":1768980173961,"version":"3.49.0"},"reference-count":42,"publisher":"American Society for Microbiology","issue":"23","license":[{"start":{"date-parts":[[2007,12,1]],"date-time":"2007-12-01T00:00:00Z","timestamp":1196467200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Bacteriol"],"published-print":{"date-parts":[[2007,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n          <jats:p>\n            Chronic granulomatous disease (CGD) is an inherited immune deficiency characterized by increased susceptibility to infection with\n            <jats:italic>Staphylococcus<\/jats:italic>\n            , certain gram-negative bacteria, and fungi.\n            <jats:italic>Granulibacter bethesdensis<\/jats:italic>\n            , a newly described genus and species within the family\n            <jats:italic>Acetobacteraceae<\/jats:italic>\n            , was recently isolated from four CGD patients residing in geographically distinct locales who presented with fever and lymphadenitis. We sequenced the genome of the reference strain of\n            <jats:italic>Granulibacter bethesdensis<\/jats:italic>\n            , which was isolated from lymph nodes of the original patient. The genome contains 2,708,355 base pairs in a single circular chromosome, in which 2,437 putative open reading frames (ORFs) were identified, 1,470 of which share sequence similarity with ORFs in the nonpathogenic but related\n            <jats:italic>Gluconobacter oxydans<\/jats:italic>\n            genome. Included in the 967 ORFs that are unique to\n            <jats:italic>G. bethesdensis<\/jats:italic>\n            are ORFs potentially important for virulence, adherence, DNA uptake, and methanol utilization. GC% values and best BLAST analysis suggested that some of these unique ORFs were recently acquired. Comparison of\n            <jats:italic>G. bethesdensis<\/jats:italic>\n            to other known CGD pathogens demonstrated conservation of some putative virulence factors, suggesting possible common mechanisms involved in pathogenesis in CGD. Genotyping of the four patient isolates by use of a custom microarray demonstrated genome-wide variations in regions encoding DNA uptake systems and transcriptional regulators and in hypothetical ORFs.\n            <jats:italic>G. bethesdensis<\/jats:italic>\n            is a genetically diverse emerging human pathogen that may have recently acquired virulence factors new to this family of organisms.\n          <\/jats:p>","DOI":"10.1128\/jb.00793-07","type":"journal-article","created":{"date-parts":[[2007,9,8]],"date-time":"2007-09-08T00:40:10Z","timestamp":1189212010000},"page":"8727-8736","update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":43,"title":["Genome Sequence Analysis of the Emerging Human Pathogenic Acetic Acid Bacterium\n            <i>Granulibacter bethesdensis<\/i>"],"prefix":"10.1128","volume":"189","author":[{"given":"David E.","family":"Greenberg","sequence":"first","affiliation":[{"name":"Immunopathogenesis Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, U.S. Department of Health and Human Services, Bethesda, Maryland 20892"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Stephen F.","family":"Porcella","sequence":"additional","affiliation":[{"name":"Research Technologies Section, Genomics Unit, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, U.S. Department of Health and Human Services, Hamilton, Montana 59840"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Adrian M.","family":"Zelazny","sequence":"additional","affiliation":[{"name":"Immunopathogenesis Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, U.S. Department of Health 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