Origin in Acinetobacter gyllenbergii and dissemination of aminoglycoside-modifying enzyme AAC(6')-Ih
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
HHSN272200900018C
NIAID NIH HHS - United States
HHSN272200900018C
NIAID NIH HHS - United States
PubMed
26645270
PubMed Central
PMC4743700
DOI
10.1093/jac/dkv390
PII: dkv390
Knihovny.cz E-resources
- MeSH
- Acetyltransferases genetics metabolism MeSH
- Acinetobacter baumannii classification drug effects enzymology genetics MeSH
- Aminoglycosides metabolism pharmacology MeSH
- Anti-Bacterial Agents metabolism pharmacology MeSH
- Drug Resistance, Bacterial * MeSH
- Gene Dosage MeSH
- Acinetobacter Infections microbiology MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Humans MeSH
- Microbial Sensitivity Tests MeSH
- Plasmids analysis MeSH
- Gene Transfer, Horizontal MeSH
- Promoter Regions, Genetic MeSH
- DNA Transposable Elements MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Acetyltransferases MeSH
- aminoglycoside N(6')-acetyltransferase MeSH Browser
- Aminoglycosides MeSH
- Anti-Bacterial Agents MeSH
- DNA Transposable Elements MeSH
OBJECTIVES: The aac(6')-Ih gene encoding aminoglycoside 6'-N-acetyltransferase type I subtype h [AAC(6')-Ih] is plasmid-borne in Acinetobacter baumannii where it confers high-level amikacin resistance, but its origin remains unknown. We searched for the gene in the genomes of a collection of 133 Acinetobacter spp. and studied its species specificity, expression and dissemination. METHODS: Gene copy number was determined by quantitative PCR, expression by quantitative RT-PCR, MIC by microdilution and transfer by plasmid mobilization. RESULTS: The aac(6')-Ih gene was present in the chromosome of the two Acinetobacter gyllenbergii of the collection and was detected in all seven A. gyllenbergii clinical isolates. They had indistinguishable flanking regions indicating that the gene was intrinsic to this species. A. baumannii PIS Aba23 promoters were provided by insertion of ISAba23, which disrupted the Pnative promoter in A. gyllenbergii. Both types of promoters were similarly potent in Escherichia coli and A. baumannii. Aminoglycoside MICs for A. baumannii harbouring pIP1858 were higher than for A. gyllenbergii due to gene dosage. The non-self-transferable plasmid could be mobilized to other A. baumannii cells by the broad host range plasmid RP4. CONCLUSIONS: We have found the origin of aac(6')-Ih in A. gyllenbergii, a species isolated, although rarely, in humans, and documented that dissemination of this gene is restricted to the Acinetobacter genus.
EA4043 Faculté de Pharmacie Université Paris Sud Châtenay Malabry France
Institut Pasteur Unité des Agents Antibactériens Paris France
Laboratory of Bacterial Genetics National Institute of Public Health Prague Czech Republic
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