2008Zhongguo kangganran hualiao zazhiRequires access

Prevalence of Panton-Valentine leukocidin gene in Staphylococcus aureus and its molecular epidemiology in 18 teaching hospitals of China

Chen Min-ju

Open publisher page 1 citations

Abstract

Objective To investigate the distribution of Panton-Valentine leukocidin(PVL) gene in S.aureus,and the clinical implication of PVL gene.Methods PVL gene was detected by PCR in 809 strains of S.aureus isolated from 18 teaching hospitals.Methicillin-resistant S.aureus(MRSA) carrying PVL gene phenotype was determined by K-B method,and were confirmed by mecA-femB double PCR.SCCmec typing was confirmed by multiplex PCR.Pulsed-field gel electrophoresis(PFGE) with SmaI digestion of chromosomal DNA was used for the genotyping analysis.Results We identified PVL gene in 58 isolates.The average prevalence of PVL was 7.2% in S.aureus isolates.The prevalence of PVL gene in MRSA(15/407,3.5%) was lower than in MSSA(43/402,11.1%).The difference was not statistically significant(P0.05).The prevalence of PVL gene was significantly higher in the isolates from outpatients than that from inpatients(P0.05).SCCmec typing was conducted for 15 PVL-positive MRSA isolates.The prevalence of SCCmec II,SCCmec III and nontypable strains accounted for 3.8%,4.7%,and 1.0% respectively(P0.05).PVL-positive MRSA isolates were further typed by PFGE.The most common PFGE type was type A and its related subtypes(73.3%),followed by type B(13.3%),C(6.7%),and D(6.7%).Conclusions PVL toxin can result in serous diseases.It is necessary to identify the genotype timely for adequate control of PVL-positive MRSA outbreak in hospital.

About this research paper

What this paper is about

Objective To investigate the distribution of Panton-Valentine leukocidin(PVL) gene in S.aureus,and the clinical implication of PVL gene.Methods PVL gene was detected by PCR in 809 strains of S.aureus isolated from 18 teaching hospitals.Methicillin-resistant S.aureus(MRSA) carrying PVL gene phenotype was determined by K-B method,and were confirmed by mecA-femB double PCR.SCCmec typing was confirmed by multiplex PCR.Pulsed-field gel electrophoresis(PFGE) with SmaI digestion of chromosomal DNA was used for the genotyping analysis.Results We identified PVL gene in 58 isolates.The average prevalence of PVL was 7.2% in S.aureus isolates.The prevalence of PVL gene in MRSA(15/407,3.5%) was lower than in MSSA(43/402,11.1%).The difference was not statistically significant(P0.05).The prevalence of PVL gene was significantly higher in the isolates from outpatients than that from inpatients(P0.05).SCCmec typing was conducted for 15 PVL-positive MRSA isolates.The prevalence of SCCmec II,SCCmec III and nontypable strains accounted for 3.8%,4.7%,and 1.0% respectively(P0.05).PVL-positive MRSA isolates were further typed by PFGE.The most common PFGE type was type A and its related subtypes(73.3%),followed by type B(13.3%),C(6.7%),and D(6.7%).Conclusions PVL toxin can result in serous diseases.It is necessary to identify the genotype timely for adequate control of PVL-positive MRSA outbreak in hospital.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the distribution of Panton-Valentine leukocidin(PVL) gene in S.aureus,and the clinical implication of PVL gene.Methods PVL gene was detected by PCR in 809 strains of S.aureus isolated from 18 teaching hospitals.Methicillin-resistant S.aureus(MRSA) carrying PVL gene phenotype was determined by K-B method,and were confirmed by mecA-femB double PCR.SCCmec typing was confirmed by multiplex PCR.Pulsed-field gel electrophoresis(PFGE) with SmaI digestion of chromosomal DNA was used for the genotyping analysis.Results We identified PVL gene in 58 isolates.The average prevalence of PVL was 7.2% in S.aureus isolates.The prevalence of PVL gene in MRSA(15/407,3.5%) was lower than in MSSA(43/402,11.1%).The difference was not statistically significant(P0.05).The prevalence of PVL gene was significantly higher in the isolates from outpatients than that from inpatients(P0.05).SCCmec typing was conducted for 15 PVL-positive MRSA isolates.The prevalence of SCCmec II,SCCmec III and nontypable strains accounted for 3.8%,4.7%,and 1.0% respectively(P0.05).PVL-positive MRSA isolates were further typed by PFGE.The most common PFGE type was type A and its related subtypes(73.3%),followed by type B(13.3%),C(6.7%),and D(6.7%).Conclusions PVL toxin can result in serous diseases.It is necessary to identify the genotype timely for adequate control of PVL-positive MRSA outbreak in hospital.

Key concepts: SCCmec, Pulsed-field gel electrophoresis, Panton–Valentine leukocidin, Microbiology, Staphylococcus aureus, Leukocidin, Genotyping, Typing

Related papers

Back to paper searchBrowse research topicsOriginal source
Prevalence of Panton-Valentine leukocidin gene in Staphylococcus aureus and its molecular epidemiology in 18 teaching hospitals of China — Research Paper | ScholarLens