Literature DB >> 9620398

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.

M I Daneshvar1, B Hill, D G Hollis, C W Moss, J G Jordan, J P Macgregor, F Tenover, R S Weyant.   

Abstract

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 16:1omega7c, 16:0, and 18:1omega7c 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).

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Year:  1998        PMID: 9620398      PMCID: PMC104898     

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  14 in total

1.  Isoprenoid quinones of "Afipia" spp.

Authors:  C W Moss; M I Daneshvar; D G Hollis; K A Birkness
Journal:  J Clin Microbiol       Date:  1991-12       Impact factor: 5.948

2.  Capnocytophaga canimorsus sp. nov. (formerly CDC group DF-2), a cause of septicemia following dog bite, and C. cynodegmi sp. nov., a cause of localized wound infection following dog bite.

Authors:  D J Brenner; D G Hollis; G R Fanning; R E Weaver
Journal:  J Clin Microbiol       Date:  1989-02       Impact factor: 5.948

3.  Practical procedure for demonstrating bacterial flagella.

Authors:  H Kodaka; A Y Armfield; G L Lombard; V R Dowell
Journal:  J Clin Microbiol       Date:  1982-11       Impact factor: 5.948

4.  "Agrobacterium yellow group" and Pseudomonas paucimobilis causing peritonitis in patients receiving continuous ambulatory peritoneal dialysis.

Authors:  R A Swann; S J Foulkes; B Holmes; J B Young; R G Mitchell; S T Reeders
Journal:  J Clin Pathol       Date:  1985-11       Impact factor: 3.411

5.  Biochemical and chemical characterization of pink-pigmented oxidative bacteria.

Authors:  P L Wallace; D G Hollis; R E Weaver; C W Moss
Journal:  J Clin Microbiol       Date:  1990-04       Impact factor: 5.948

6.  Rochalimaea henselae sp. nov., a cause of septicemia, bacillary angiomatosis, and parenchymal bacillary peliosis.

Authors:  D F Welch; D A Pickett; L N Slater; A G Steigerwalt; D J Brenner
Journal:  J Clin Microbiol       Date:  1992-02       Impact factor: 5.948

7.  Chemical and cultural characterization of CDC group WO-1, a weakly oxidative gram-negative group of organisms isolated from clinical sources.

Authors:  D G Hollis; R E Weaver; C W Moss; M I Daneshvar; P L Wallace
Journal:  J Clin Microbiol       Date:  1992-02       Impact factor: 5.948

8.  Separation of bacterial ubiquinones by reverse-phase high-pressure liquid chromatography.

Authors:  C W Moss; G O Guerrant
Journal:  J Clin Microbiol       Date:  1983-07       Impact factor: 5.948

9.  Proposal of Afipia gen. nov., with Afipia felis sp. nov. (formerly the cat scratch disease bacillus), Afipia clevelandensis sp. nov. (formerly the Cleveland Clinic Foundation strain), Afipia broomeae sp. nov., and three unnamed genospecies.

Authors:  D J Brenner; D G Hollis; C W Moss; C K English; G S Hall; J Vincent; J Radosevic; K A Birkness; W F Bibb; F D Quinn
Journal:  J Clin Microbiol       Date:  1991-11       Impact factor: 5.948

10.  Isoprenoid quinone content and cellular fatty acid composition of Campylobacter species.

Authors:  C W Moss; A Kai; M A Lambert; C Patton
Journal:  J Clin Microbiol       Date:  1984-06       Impact factor: 5.948

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  1 in total

1.  Assignment of CDC weak oxidizer group 2 (WO-2) to the genus Pandoraea and characterization of three new Pandoraea genomospecies.

Authors:  M I Daneshvar; D G Hollis; A G Steigerwalt; A M Whitney; L Spangler; M P Douglas; J G Jordan; J P MacGregor; B C Hill; F C Tenover; D J Brenner; R S Weyant
Journal:  J Clin Microbiol       Date:  2001-05       Impact factor: 5.948

  1 in total

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