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Journal of Clinical Microbiology, January 2006, p. 287, Vol. 44, No. 1
0095-1137/06/$08.00+0 doi:10.1128/JCM.44.1.287.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Panton-Valentine Leukocidin Genes in a Laboratory Quality Control Strain of Staphylococcus aureus

LETTER
Until rather recently, our total awareness of the
Staphylococcus aureus-associated exotoxin known as Panton-Valentine leukocidin
(PVL) was limited to a few historic publications (
2). Interest
in PVL was renewed in the 1990s with the recognition of two
distinct yet soon-to-be-linked observations: infections caused
by strains of methicillin-resistant
Staphylococcus aureus (MRSA)
were finding their way into the community (
4), and strains of
S. aureus-producing PVL were being found with increasing frequency
in patients with localized soft tissue infections (
1,
3) and
hemorrhagic pneumonia (
3). These initial reports were followed
by a profusion of publications describing cases, outbreaks,
and the epidemiology of infection caused by community-acquired
MRSA (CA-MRSA), by PVL-producing
S. aureus, and ultimately by
PVL-producing CA-MRSA (for an excellent and succinct review,
see the commentary of Jerome Etienne [
2]). To keep up with the
times, and to better understand the significance of PVL production
by strains of
S. aureus in our institution and community, an
in-house PCR assay was evaluated based on the method of Lina
et al. (
3). It was soon obvious after running this assay with
DNA extracted from a number of CA- and hospital-acquired (HA)-MRSA
strains that the former generated a number of positive strains
while the latter appeared to be uniformly negative for the appropriate
amplicon. To formalize the protocol, a PVL-positive CA-MRSA
strain was selected for routine use until an appropriate positive
control (
S. aureus ATCC 49775) (
3) could be ordered. Rather
than using one of the PCR-negative HA-MRSA strains evaluated
initially, I opted to use DNA from a strain of
S. aureus that
is routinely used in the clinical microbiology laboratory for
quality control of antimicrobial susceptibility testing (ATCC
25923). This strain had also been used in our laboratory for
quality control of an in-house molecular typing assay. Much
to my surprise, this putative negative control turned out to
be PCR positive for the PVL genes
lukS-PV and
lukF-PV. Repeat
extraction of DNA from a fresh isolate produced the same result.
As a consequence, I was forced to return to my collection of
HA-MRSA strains for the elusive PVL-negative control strain
and was left to ponder how many other domesticated laboratory
quality control strains are currently packing concealed weapons.

REFERENCES
1 - Cribier, B., G. Prevost, P. Couppie, V. Finck-Barbancon, E. Frosshans, and Y. Piemont. 1992. Staphylococcus aureus leukocidin: a new virulence vactor in cutaneous infections? An epidemiological and experimental study. Dermatology 185:175-180.[Medline]
2 - Etienne, J. 2005. Panton-Valentine leukocidin: a marker of severity for Staphylococcus aureus infection? Clin. Infect. Dis. 41:591-593.[CrossRef][Medline]
3 - Lina, G., Y. Piemont, F. Godail-Gamot, M. Bes, M.-O. Peter, V. Gauduchon, F. Vandenesch, and J. Etienne. 1999. Involvement of Panton-Valentine leukocidin-producing Staphylococcus aureus in primary skin infections and pneumonia. Clin. Infect. Dis. 29:1128-1132.[CrossRef][Medline]
4 - Lindenmayer, J. M., S. Schoenfeld, R. O'Grady, and J. K. Carney. 1998. Methicillin-resistant Staphylococcus aureus in a high school wrestling team and the surrounding community. Arch. Intern. Med. 158:895-899.[Abstract/Free Full Text]
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W. Michael Dunne Jr.*
Department of Pathology and Immunology Washington University School of Medicine St. Louis, Missouri 63110
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* Phone: (314) 362-1547, Fax: (314) 362-1461, E-mail: dunne{at}wustl.edu |
Journal of Clinical Microbiology, January 2006, p. 287, Vol. 44, No. 1
0095-1137/06/$08.00+0 doi:10.1128/JCM.44.1.287.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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