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ANTIMICROBIAL RESISTANCE |

Department of Veterinary Microbiology, The Royal Veterinary and Agricultural University, 1870 Frederiksberg C., Denmark; *Department of Infectious Diseases, Leiden University Medical Centre, 2300 RC Leiden, Netherlands; and
Section of Biosafety and Biotechnology, Scientific Institute Public Health-Louis Pasteur, B-1050 Brussels, Belgium.
Corresponding author: Dr. L. Guardabassi (e-mail: lg{at}kvl.dk).
Received 25 August 1999; revised version received 22 February 2000; accepted 29 March 2000.
Abstract
Following characterisation by phenotypic tests and amplified ribosomal DNA restriction analysis (ARDRA), 50 tetracycline-resistant (MIC
165mumg/L) Acinetobacter strains from clinical (n=35) and aquatic (n=15) samples were analysed by PCR for tetracycline resistance (Tet) determinants of classes AE. All the clinical strains were A. baumannii; most (33 of 35) had Tet A (n=16) or B (n=17) determinants, and only two did not yield amplicons with primers for any of the five tetracycline resistance determinants. The aquatic strains belonged to genomic species other than A. baumannii, and most (12 of 15) did not contain determinants Tet AE. Strains negative for Tet AE were also negative for Tet G and M; further analysis of two aquatic strains with specific primers for Tet O and Tet Y and degenerate primers for Tet M-S-O-P(B)-Q also showed negative results. Transfer of tetracycline resistance was tested for 20 strains with three aquatic Acinetobacter strains and Escherichia coli K-12 as recipients. Transfer of resistance was demonstrated between aquatic strains from distinct ecological niches, but not from clinical to aquatic strains, nor from any Acinetobacter strain to E. coli K-12. Most transconjugants acquired multiple relatively small plasmids (<36 kb). Transfer did not occur when DNA from the donor strains was added to the recipient cultures and was not affected by deoxyribonuclease I, suggesting a conjugative mechanism. It is concluded that Tet A and B are widespread among tetracycline-resistant A. baumannii strains of clinical origin, but unknown genetic determinants are responsible for most tetracycline resistance among aquatic Acinetobacter spp. These differences, together with the inability of clinical strains to transfer tetracycline resistance in vitro to aquatic strains, contra-indicate any important flow of tetracycline resistance genes between clinical and aquatic acinetobacter populations.
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