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Understanding the dynamics of imipenem-resistant Acinetobacter baumannii lineages within Portugal

Title
Understanding the dynamics of imipenem-resistant Acinetobacter baumannii lineages within Portugal
Type
Article in International Scientific Journal
Year
2011
Authors
Grosso, F
(Author)
Other
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Quinteira, S
(Author)
Other
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Peixe, L
(Author)
FFUP
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Journal
Vol. 17 No. 8
Pages: 1275-1279
ISSN: 1198-743X
Publisher: Elsevier
Indexing
Publicação em ISI Web of Science ISI Web of Science
Pubmed / Medline
Scientific classification
FOS: Medical and Health sciences > Health sciences
Other information
Authenticus ID: P-002-PAK
Resumo (PT): Clin Microbiol Infect 2011; 17: 1275-1279 Abstract A recent collection of 213 imipenem-resistant Acinetobacter baumannii (IRAB) clinical isolates was characterized for the presence of acquired carbapenem-hydrolysing class D β-lactamases (CHDLs) and clonality. A population structure analysis of IRAB was also conducted, with five molecular typing methods. Three main clusters, each one associated with a specific CHDL, were observed with multilocus sequence typing. Overall, our results suggest a switch in the dominant clone, with sequence type (ST) 92, carrying blaOXA-23 (63.4%), replacing the closely related ST98, carrying blaOXA-24/40 (22%). In addition, ST103, an independent lineage, was associated with blaOXA-58-carrying isolates (14.6%). <br> <br> Keywords: ACINETOBACTER *PATHOGENIC bacteria *CLONE cells *BETA lactamases. <br> <a target="_blank" href="http://web.ebscohost.com/ehost/detail?vid=7&hid=113&sid=a797790d-a87d-4eb5-bfc5-936e5299decf%40sessionmgr112&bdata=Jmxhbmc9cHQtYnImc2l0ZT1laG9zdC1saXZl#db=a9h&AN=63069458"> texto integral </a> <br> <br>
Abstract (EN): A recent collection of 213 imipenem-resistant Acinetobacter baumannii (IRAB) clinical isolates was characterized for the presence of acquired carbapenem-hydrolysing class D beta-lactamases (CHDLs) and clonality. A population structure analysis of IRAB was also conducted, with five molecular typing methods. Three main clusters, each one associated with a specific CHDL, were observed with multilocus sequence typing. Overall, our results suggest a switch in the dominant clone, with sequence type (ST) 92, carrying bla(OXA-23) (63.4%), replacing the closely related ST98, carrying bla(OXA-24/40) (22%). In addition, ST103, an independent lineage, was associated with bla(OXA-58)-carrying isolates (14.6%).
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 6
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