By Teruyo Ito
ESI Special Topics,
October 2005
Citing URL - http://www.esi-topics.com/fbp/2005/october05-TeruyoIto.html
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Teruyo Ito answers a
few questions about this month's fast breaking paper in the field of
Microbiology.
From
•>>October 2005
Field:
Microbiology
Article Title: Novel type v staphylococcal cassette chromosome mec driven by a novel cassette chromosome
recombinase, ccrC
Authors: Ito,
T;Ma, XX;Takeuchi, F;Okuma, K;Yuzawa,
H;Hiramatsu, K
Journal: ANTIMICROB AGENTS CHEMOTHER
Volume: 48
Page: 2637-2651
Year: JUL 2004
* Juntendo Univ, Sch Med, Fac Med, Dept Bacteriol, Bunkyo Ku, 2-1-1
Hongo, Tokyo 113, Japan.
* Juntendo Univ, Sch Med, Fac Med, Dept Bacteriol, Bunkyo Ku, Tokyo 113, Japan.
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November
1, 2005:
This paper has also been named the New Hot Paper in
Microbiology for November
2005. |
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Why
do you think your paper is highly cited?
MRSA, which has been a dominant hospital-associated pathogen
because of its resistance to antibiotics, is emerging in the
community. Genetically, MRSA is produced when MSSA acquires a
mobile genetic element staphylococcal cassette chromosome mec (SCCmec).
There is considerable current interest in MRSA strains isolated
from community exposure, and it has been reported that
community-associated MRSA (C-MRSA) strains carry mostly type-IV
SCCmec elements which are different from those carried by
hospital-associated MRSA. The paper describes a novel SCCmec
element (type-V SCCmec) carried by a C-MRSA strain, and
anticipates a particular concern of researchers in this field by
describing the characteristic features of the type-V SCCmec
element in comparison with the other four types of SCCmec.
Does
it describe a new discovery or a new methodology that’s useful
to others?
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“I think the most major contribution of our research is that a new methodology for the epidemiology of MRSA has been established.”
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This paper describes the fifth allotype of SCCmec (type-V
SCCmec), which carried class C2 mec gene complex composed of
IS431-ΔmecR1-mecA-IS431 and type-5 ccr gene complex
composed of ccrC gene and surrounding orfs. In addition, the
paper describes the function of the ccrC gene as a new
site-specific recombinase responsible for the mobility of the
type-V SCCmec element. The ccrC was proven to catalyze the
precise excision as well as site- and orientation-specific
integration of the type-V SCCmec element, whereas a set of ccrA
and ccrB genes in other types of SCCmec elements was found to be
required for those functions.
Could
you summarize the significance of your paper in laymen’s term?
The finding of SCCmec elements leads to the notion that MRSA
clones could be defined by the combination of types of SCCmec
element and genotypes of MSSA strains into which the SCCmec
element was integrated. SCCmec typing is now essential for the
epidemiology of MRSA. By determining SCCmec types, it has been
reported that MRSA clones isolated within a community were
distinct from H-MRSA clones, since the former carried mostly
type-IV SCCmec elements, whereas the latter carried type-I, II,
and III SCCmec elements. The identification of type-V SCCmec
types which does not carry any antibiotic resistance gene other
than mecA in C-MRSA strains further supports the proposal that
C-MRSA strains have been generated de novo from S.
aureus.
How
did you become involved in this research?
I began studying the genetic bases of methicillin resistance
in 1992. At first, we determined the entire nucleotide sequence
of SCCmec element of N315, which was called mecDNA at that time.
We found two site-specific recombinase genes in mecDNA. By
cloning two genes, we have shown two genes catalyzed by precise
excision and site- and orientation-specific integration of
mecDNA, and designated mecDNA as SCCmec, which signifies a kind
of mobile genetic element specifically found in staphylococci
and an element encoding methicillin resistance, and two enzymes
as cassette chromosome recombinase (ccr) A and B. Furthermore,
we found allotypic differences in SCCmec, and reported type-I,
II, and III SCCmec elements carried by MRSA strains isolated in
hospitals. In 2002, we reported on a type-IV SCCmec element
carried by C-MRSA strain as part of a collaborative project with
Dr. Robert S. Daum, a Professor of Medicine at the University of
Chicago’s Children’s Hospital. The strain used in this
paper, WIS [WBG3813], is one of the C-MRSA strains sent to our
lab as part of a collaborative work undertaken with Dr. Warren
B. Grubb
a professor of the School of Biomedical Sciences, Curtin University
of Technology, Australia.
What are the social or political implications of your research?
I think the most important contribution of our research is
that a new methodology for the epidemiology of MRSA has been
established. Prior to the discovery of SCCmec elements, MRSA
strains were regarded as S. aureus strains carrying mecA.
However, by introducing SCCmec typing, MRSA clones could be
discriminated by the other types of SCCmec elements besides
genotypes. By applying this system, many studies have been
reported from other countries. We have noted that well-defined
C-MRSA strains carried type-IV and type-V SCCmec elements, and
that large outbreaks of C-MRSA carrying type-IV SCCmec and
Panton-Valentine Leukocidin genes had occurred in Uruguay.
Teruyo Ito
Department of Bacteriology, School of Medicine
Juntendo University
Tokyo, Japan
One
of Teruyo Ito’s papers was identified as part of this Fast
Moving Front map from May, 2004.
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ESI Special Topics,
October 2005
Citing URL - http://www.esi-topics.com/fbp/2005/october05-TeruyoIto.html
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