Local acquisition of methicillin-resistance in predominant Staphylococcus aureus clones of western Switzerland.
Details
Serval ID
serval:BIB_8CAD31126671
Type
Inproceedings: an article in a conference proceedings.
Publication sub-type
Poster: Summary – with images – on one page of the results of a researche project. The summaries of the poster must be entered in "Abstract" and not "Poster".
Collection
Publications
Institution
Title
Local acquisition of methicillin-resistance in predominant Staphylococcus aureus clones of western Switzerland.
Title of the conference
20th European Congress of Clinical Microbiology and Infectious (ECCMID)
Address
Vienna, Austria, April 10-13, 2010
ISBN
1469-0691
Publication state
Published
Issued date
2010
Peer-reviewed
Oui
Volume
16
Series
Clinical Microbiology and Infection
Pages
S290
Language
english
Abstract
Objectives: Recent population genetic studies suggest that the Staphylococcal
Chromosome Cassettes mec (SCCmec) was acquired at a global
scale much more frequently than previously thought. We hypothesized
that such acquisitions can also be observed at a local level. In the present
study, we aimed at investigating the diversity of SCCmec in a local
MRSA population, where the dissemination of four MRSA clones has
been observed (JCM 2007, 45: 3729).
Methods: All the MRSA isolates (one per patient) recovered in the
Vaud canton of Switzerland from January 2005 to December 2008 were
analyzed in this study. We used the Double Locus Sequence Typing
(DLST) method, based on clfB and spa loci, and the e-BURST algorithm
to group the types with one allele in common (i.e. clone). To increase the
discriminatory power of the DLST method, a third polymorphic marker
(clfA) was further analyzed on a sub-sample of isolates. The SCCmec
type of each isolate was determined with the first two PCRs of the Kondo
scheme.
Results: DLST analysis indicated that 1884/2036 isolates (92.5%)
belong to the four predominant clones. A majority of isolates in each
clone harboured an identical SCCmec type: 61/64 (95%) isolates to
DLST clone 1−1 SCCmec IV, 1282/1323 (97%) to clone 2−2 SCCmec
II, 237/288 (82%) to clone 3−3 SCCmec IV, and 192/209 (92%) to clone
4−4 SCCmec I.
Unexpectedly, different SCCmec types were present in a single
predominant DLST clone: SCCmec V plus one unusual type in 3 isolates
of clone 1−1; SCCmec I, IV, V, VI plus two unusual types in 41 isolates
of clone 2−2; SCCmec I, II, VI plus three unusual types in 51 isolates of
clone 3−3; and SCCmec II, IV, V plus one unusual type in 17 isolates of
clone 4−4. Interestingly, adding a third locus generally did not change
the classification of incongruent SCCmec types, suggesting that these
SCCmec elements have been acquired locally during the dissemination
of the clones.
Conclusion: Although the SCCmec diversity within clones was
relatively low at a local level, a significant proportion of isolates with
different SCCmec have been identified in the four major clones. This
suggests that the local acquisition of SCCmec elements is not a rare
event and illustrates the great capacity of S. aureus to quickly adapt to
its environment by acquiring new genetic elements.
Chromosome Cassettes mec (SCCmec) was acquired at a global
scale much more frequently than previously thought. We hypothesized
that such acquisitions can also be observed at a local level. In the present
study, we aimed at investigating the diversity of SCCmec in a local
MRSA population, where the dissemination of four MRSA clones has
been observed (JCM 2007, 45: 3729).
Methods: All the MRSA isolates (one per patient) recovered in the
Vaud canton of Switzerland from January 2005 to December 2008 were
analyzed in this study. We used the Double Locus Sequence Typing
(DLST) method, based on clfB and spa loci, and the e-BURST algorithm
to group the types with one allele in common (i.e. clone). To increase the
discriminatory power of the DLST method, a third polymorphic marker
(clfA) was further analyzed on a sub-sample of isolates. The SCCmec
type of each isolate was determined with the first two PCRs of the Kondo
scheme.
Results: DLST analysis indicated that 1884/2036 isolates (92.5%)
belong to the four predominant clones. A majority of isolates in each
clone harboured an identical SCCmec type: 61/64 (95%) isolates to
DLST clone 1−1 SCCmec IV, 1282/1323 (97%) to clone 2−2 SCCmec
II, 237/288 (82%) to clone 3−3 SCCmec IV, and 192/209 (92%) to clone
4−4 SCCmec I.
Unexpectedly, different SCCmec types were present in a single
predominant DLST clone: SCCmec V plus one unusual type in 3 isolates
of clone 1−1; SCCmec I, IV, V, VI plus two unusual types in 41 isolates
of clone 2−2; SCCmec I, II, VI plus three unusual types in 51 isolates of
clone 3−3; and SCCmec II, IV, V plus one unusual type in 17 isolates of
clone 4−4. Interestingly, adding a third locus generally did not change
the classification of incongruent SCCmec types, suggesting that these
SCCmec elements have been acquired locally during the dissemination
of the clones.
Conclusion: Although the SCCmec diversity within clones was
relatively low at a local level, a significant proportion of isolates with
different SCCmec have been identified in the four major clones. This
suggests that the local acquisition of SCCmec elements is not a rare
event and illustrates the great capacity of S. aureus to quickly adapt to
its environment by acquiring new genetic elements.
Create date
10/03/2011 13:42
Last modification date
20/08/2019 14:51