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Origin in Acinetobacter gyllenbergii and dissemination of aminoglycoside-modifying enzyme AAC(6')-Ih
EJ. Yoon, S. Goussard, A. Nemec, T. Lambert, P. Courvalin, C. Grillot-Courvalin,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
NT14466
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Free Medical Journals
od 1996 do Před 1 rokem
Open Access Digital Library
od 1996-01-01
PubMed
26645270
DOI
10.1093/jac/dkv390
Knihovny.cz E-zdroje
- MeSH
- acetyltransferasy genetika metabolismus MeSH
- Acinetobacter baumannii klasifikace účinky léků enzymologie genetika MeSH
- aminoglykosidy metabolismus farmakologie MeSH
- antibakteriální látky metabolismus farmakologie MeSH
- bakteriální léková rezistence * MeSH
- genová dávka MeSH
- infekce bakteriemi rodu Acinetobacter mikrobiologie MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- plazmidy analýza MeSH
- přenos genů horizontální MeSH
- promotorové oblasti (genetika) MeSH
- transpozibilní elementy DNA MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural 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
Citace poskytuje Crossref.org
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