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Journal of Clinical Microbiology, June 1998, p. 1674-1678, Vol. 36, No. 6
Division of Bacterial and Mycotic
Diseases1 and
Hospital Infections
Program,2 National Center for Infectious
Diseases, Centers for Disease Control and Prevention, Public Health
Service, U.S. Department of Health and Human Services, Atlanta,
Georgia 30333
Received 17 November 1997/Returned for modification 22 December
1997/Accepted 17 March 1998
Between 1983 and 1994, 13 phenotypically similar unidentified
clinical isolates were received by the Special Bacteriology Reference
Laboratory, Centers for Disease Control and Prevention (CDC). Sources
included blood (four strains), lung (three strains), knee fluid and
duodenal tissue (one strain each), bone, and lymph node tissue (two
strains each). All were aerobic glucose-oxidizing, slender, long,
curved gram-negative rods that utilized xylose, sucrose, and maltose;
did not grow on MacConkey agar in 1 to 2 days; were oxidase positive;
hydrolyzed esculin; and grew on Campylobacter selective
medium. All were negative for urease, indole, nitrate reduction, and
gelatin hydrolysis. All were motile by means of a single polar
flagellum with a noticeably short wavelength; however, motility was
sometimes difficult to demonstrate. The cellular fatty acid
compositions of these strains, as analyzed by gas-liquid chromatography, were unique, characterized by relatively large amounts
of 16:1
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
CDC Group O-3: Phenotypic Characteristics, Fatty
Acid Composition, Isoprenoid Quinone Content, and In Vitro Antimicrobic
Susceptibilities of an Unusual Gram-Negative Bacterium Isolated from
Clinical Specimens
7c, 16:0, and 18:1
7c with smaller amounts of 12:0,
3-OH-12:1, 14:0, 15:0, 18:0, Br-19:1, and 19:0cyc11-12.
High-performance liquid chromatography and mass spectrometry of the
quinone extracts of three representative strains showed ubiquinone-10
as the major component. Based on the breakpoints for the family
Enterobacteriaceae, all the strains were susceptible in
vitro to aminoglycosides, sulfamethoxazole-trimethoprim, and chloramphenicol but were resistant to most beta-lactams except imipenem. The MICs of amoxicillin-clavulanate and ciprofloxacin for
these strains clustered around the breakpoints, which makes it
difficult to predict the strains' response in vivo to these agents.
This group has been designated CDC oxidizer group 3 (O-3).
*
Corresponding author. Mailing address: Analytical
Chemistry Laboratory, Centers for Disease Control and Prevention,
Mailstop G06, Atlanta, GA 30333. Phone: (404) 639-3861. Fax: (404)
639-4421. E-mail: MID2{at}CDC.GOV.
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