Abstract
The in vitro activity of minocycline against Acinetobacter calcoaceticus var. anitratus (Herellea vaginicola) was examined. All strains of A. anitratus were inhibited by minocycline at concentrations of 0.4 μg/ml or less. The strains studied were considerably more susceptible to minocycline than tetracycline. No difference between the susceptibility to minocycline and tetracycline was seen with Escherichia coli, Klebsiella pneumoniae, Enterobacter and Proteus sp. A regression line of the log minimal inhibitory concentration (MIC) values and the diameter of the zone of inhibition, determined by the Kirby-Bauer technique, showed good linear correlation for minocycline. Comparison of the disk diffusion results and MICs indicated that an inhibitory zone size of 19 mm produced by a 30-μg minocycline disk was equivalent to a MIC of 3.1 μg/ml, a serum concentration achieved by oral administration of the drug. When the zone of inhibition was greater than 19 mm, however, there was poor correlation with the MIC for Enterobacteriaceae.
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Selected References
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- Bauer A. W., Kirby W. M., Sherris J. C., Turck M. Antibiotic susceptibility testing by a standardized single disk method. Am J Clin Pathol. 1966 Apr;45(4):493–496. [PubMed] [Google Scholar]
- DALY A. K., POSTIC B., KASS E. H. Infections due to organisms of the genus Herellea. B5W and B. anitratum. Arch Intern Med. 1962 Nov;110:580–591. doi: 10.1001/archinte.1962.03620230026006. [DOI] [PubMed] [Google Scholar]
- Elston H. R., Hoffman K. C. Identification and clinical significance of Achromobacter (Herellea) anitratus in urinary tract infections. Am J Med Sci. 1966 Jan;251(1):75–80. doi: 10.1097/00000441-196601000-00013. [DOI] [PubMed] [Google Scholar]
- Maderazo E. G., Quintiliani R., Tilton R. C., Bartlett R., Joyce N. C., Andriole V. T. Activity of minocycline against Acinetobacter calcoaceticus var. anitratus (syn. Herellea vaginicola) and Serratia marcescens. Antimicrob Agents Chemother. 1975 Jul;8(1):54–57. doi: 10.1128/aac.8.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pedersen M. M., Marso E., Pickett M. J. Nonfermentative bacilli associated with man. 3. Pathogenicity and antibiotic susceptibility. Am J Clin Pathol. 1970 Aug;54(2):178–192. doi: 10.1093/ajcp/54.2.178. [DOI] [PubMed] [Google Scholar]
- Pickett M. J., Manclark C. R. Nonfermentative bacilli associated with man. I. Nomenclature. Am J Clin Pathol. 1970 Aug;54(2):155–163. doi: 10.1093/ajcp/54.2.155. [DOI] [PubMed] [Google Scholar]
- Steigbigel N. H., Reed C. W., Finland M. Absorption and excretion of five tetracycline analogues in normal young men. Am J Med Sci. 1968 May;255:296–312. doi: 10.1097/00000441-196805000-00005. [DOI] [PubMed] [Google Scholar]
- Steigbigel N. H., Reed C. W., Finland M. Susceptibility of common pathogenic bacteria to seven tetracycline antibiotics in vitro. Am J Med Sci. 1968 Mar;255:179–195. doi: 10.1097/00000441-196803000-00005. [DOI] [PubMed] [Google Scholar]
- Washington J. A., 2nd, Yu P. K., Martin W. J. In vitro antibacterial activity of minocycline and effect of agar medium utilized in its susceptibility testing. Appl Microbiol. 1970 Feb;19(2):259–263. doi: 10.1128/am.19.2.259-263.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
