中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2009年
4期
302-306
,共5页
表皮葡萄球菌%细菌物被膜%icaA基因
錶皮葡萄毬菌%細菌物被膜%icaA基因
표피포도구균%세균물피막%icaA기인
Staphylococccas epidermidis%Bacterial biofitm%icaA gene
目的 检测表皮葡萄球菌临床株生物被膜的形成能力,了解icaA基因及其表达与生物被膜形成的关系.方法 收集205株临床分离表皮葡萄球菌,刚果红平板试验检测其黏附性,半定量黏附试验检测其生物被膜的形成能力,扫描电镜观察生物被膜形态,PCR方法 扩增icaA基因片段,RT-PCR方法 分析icaA基因表达情况.结果 205株表皮葡萄球菌中刚果红平板试验阳性24株,半定量黏附试验阳性22株,28株枪测到icaA基因.半定量黏附试验阳性菌株的icaA基因表达水平呈现高于半定量黏附试验阴性菌株的趋势.结论 表皮葡萄球菌临床株具有一定的形成生物被膜的能力,icaA基因的存在及其正常表达是表皮葡萄球菌形成生物被膜的重要分子生物学基础,icaA基因表达尚有其他因索调控.
目的 檢測錶皮葡萄毬菌臨床株生物被膜的形成能力,瞭解icaA基因及其錶達與生物被膜形成的關繫.方法 收集205株臨床分離錶皮葡萄毬菌,剛果紅平闆試驗檢測其黏附性,半定量黏附試驗檢測其生物被膜的形成能力,掃描電鏡觀察生物被膜形態,PCR方法 擴增icaA基因片段,RT-PCR方法 分析icaA基因錶達情況.結果 205株錶皮葡萄毬菌中剛果紅平闆試驗暘性24株,半定量黏附試驗暘性22株,28株鎗測到icaA基因.半定量黏附試驗暘性菌株的icaA基因錶達水平呈現高于半定量黏附試驗陰性菌株的趨勢.結論 錶皮葡萄毬菌臨床株具有一定的形成生物被膜的能力,icaA基因的存在及其正常錶達是錶皮葡萄毬菌形成生物被膜的重要分子生物學基礎,icaA基因錶達尚有其他因索調控.
목적 검측표피포도구균림상주생물피막적형성능력,료해icaA기인급기표체여생물피막형성적관계.방법 수집205주림상분리표피포도구균,강과홍평판시험검측기점부성,반정량점부시험검측기생물피막적형성능력,소묘전경관찰생물피막형태,PCR방법 확증icaA기인편단,RT-PCR방법 분석icaA기인표체정황.결과 205주표피포도구균중강과홍평판시험양성24주,반정량점부시험양성22주,28주창측도icaA기인.반정량점부시험양성균주적icaA기인표체수평정현고우반정량점부시험음성균주적추세.결론 표피포도구균림상주구유일정적형성생물피막적능력,icaA기인적존재급기정상표체시표피포도구균형성생물피막적중요분자생물학기출,icaA기인표체상유기타인색조공.
Objective To determine the ability of biofilm formation of Staphylococcus ephtermidis isolates and analyze the correlation between the icaA gene and its expression and biofilm formation. Methods Collecting 205 Staphylococcus epidermidis isolates identified with normal laboratory tests (coagulase-negative, biochemical identification, polymyxin-resistant and novobiocin-sensitive ), the suspected isolates were con-formed with API-Staph. Biofilm production was assessed by incubating the strains on Congo Red Agar (CRA) plates and quantitative biofilm production determined by a 96-well tissue culture plate and biofilm morphous were detected by scanning electron microscope ( SEM ) ; Amplifying partial fragments of icaA genes with PCR; Analyzing the expression levels of icaA gene with RT-PCR through Bio-Rad system and Quantity One software. Results 24 isolates showed positive in CRA tests, 22 isolates were positive in semiquantita- tive adhesion assays and 28 isolates existed icaA gene among 205 isolates of Staphylococcus epidermidis. The icaA-positive strains demonstrated biofilm formation (microcolonies on silica films ) while icaA-negative strains only adhered as individual cells under scanning electron microscope. All 22 strains which showed positive in semiquantitative adhesion assays harbored the icaA gene. The expression levels of icaA gene with RT-PCR in 6 Staphylococcus epidermidis isolates showed a higher tendency in 4 strains which demonstrated positive in semiquantitative adhesion assays than 2 negative strains in semiquantitative adhesion assays. Conclusion The isolations of Staphylococcus epidermidis have the abilities of forming biofilm, and the icaA gene and its normal expression is the important molecular biology foundation of biofilm formation. Other fac-tors maybe involve in the expression of icaA gene in Staphylococcus epidermidis isolates.