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Fast Breaking Comments

By Teruyo Ito

ESI Special Topics, October 2005
Citing URL - http://www.esi-topics.com/fbp/2005/october05-TeruyoIto.html

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.

  November 1, 2005: This paper has also been named the New Hot Paper in Microbiology for November 2005.

ST:  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.

ST:  Does it describe a new discovery or a new methodology that’s useful to others?

Left to right: Xiao Xue Ma; Research associate, Department of Bacteriology, Juntendo University. Keiichi Hiramatsu; Professor, Department of Bacteriology, Juntendo University, Professor, Department of Infection Control Science, Graduate School of Medicine, Juntendo University. Teruyo Ito. Fumihiko Takeuchi; Lecturer on Infection Control Science, Graduate School of Medicine, Juntendo University.
“I think the most major contribution of our research is that a new methodology for the epidemiology of MRSA has been established.”

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.

ST:  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.

ST:  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.End

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.

ESI Special Topics, October 2005
Citing URL - http://www.esi-topics.com/fbp/2005/october05-TeruyoIto.html

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