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<i>vicK</i>Gene as Potential Identification Marker for <i>Staphylococcus aureus</i>
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作者 Nurmusfirah Morad Suzana Misbah 《Journal of Biosciences and Medicines》 2018年第11期98-110,共13页
Staphylococcus aureus is an important human pathogen frequently detected in hospital community and has emerged as an important health concern in human medicine. Identification of S. aureus from clinical specimens by p... Staphylococcus aureus is an important human pathogen frequently detected in hospital community and has emerged as an important health concern in human medicine. Identification of S. aureus from clinical specimens by phenotypic methods may produce variable characteristics leading to ambiguity. Hence, a rapid and reliable method for identification of S. aureus is required which could expedite appropriate antibiotic therapy. This study aimed to evaluate the specificity of polymerase chain reaction (PCR) targeting a signal transduction gene, vicK, among S. aureus isolates of Hospital Sultanah Nur Zahirah, Kuala Terengganu, Malaysia. A total of 118 bacterial isolates were screened, which consisted of one hundred S. aureus isolates, ten Staphylococcus spp. and eight non-Staphylococci. Results indicated that PCR targeting vicK was able to identify 98% of S. aureus isolates with high sensitivity and specificity, while the remaining isolates of Staphylococcus spp. and non-Staphylococci did not yield any amplification of the gene. vicK thus, is highly specific within interspecies and intraspecies, which is potential to be used as a molecular identification marker for S. aureus. 展开更多
关键词 vick gene STAPHYLOCOCCUS aureus IDENTIFICATION MARKER Rapid Diagnostic Two-Component Signal Transduction
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vicK基因ATP结合位点对变异链球菌生物学功能的影响
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作者 黄珊珊 宋秀宇 +2 位作者 徐巧丽 饶慧华 张加勤 《中国人兽共患病学报》 CAS CSCD 北大核心 2021年第5期435-443,共9页
目的构建变异链球菌UA159 vicK ATP缺失突变株,研究vicK基因ATP结合位点对变异链球菌生长、产酸耐酸、细胞外多糖(exopolysaccharides,EPS)和生物膜形成等生物学功能的影响。方法quick change法构建vicK ATP缺失突变质粒,同时引入Sma lI... 目的构建变异链球菌UA159 vicK ATP缺失突变株,研究vicK基因ATP结合位点对变异链球菌生长、产酸耐酸、细胞外多糖(exopolysaccharides,EPS)和生物膜形成等生物学功能的影响。方法quick change法构建vicK ATP缺失突变质粒,同时引入Sma lI,Sma lI插入kan基因盒(lox71-kan-lox66),建立vicK ATP缺失同源重组载体。所获载体转化变异链球菌,卡那霉素筛选阳性菌。pCrePA质粒转化阳性菌,30℃移除kan基因,37℃去除pCrePA,同源重组法获得无标记基因组vicK ATP缺失突变株。表达纯化VicK ATP缺失蛋白,并验证其ATP激酶活性。结果成功构建UA159 vicK ATP缺失突变株和补偿株。vicK ATP突变株生长速率和pH值下降均较野生株缓慢;实验株随致死性酸处理时间延长,生存率呈下降趋势,但突变株生存率较野生株高,即耐酸性增强;突变株EPS和生物膜形成较野生株明显减少。结论vicK基因ATP结合位点对变异链球菌的生长、产酸、酸耐受、EPS和生物膜形成起着重要调控作用。 展开更多
关键词 变异链球菌 vick基因 ATP结合位点 Cre/lox P系统 双组分信号传导系统
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变异链球菌vicK基因调控vicR反义RNA影响胞外多糖代谢 被引量:1
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作者 卓妮娅 邓雅兰 +2 位作者 雷蕾 杨英明 胡涛 《临床口腔医学杂志》 2021年第4期195-200,共6页
目的:探讨vicK调控反义RNA ASvicR(Antisense vicR)及gtfB/C/D表达水平,影响变异链球菌胞外多糖代谢的机制。方法:同源重组法构建vicK缺失株及vicK补偿株,通过RT-qPCR检测与变异链球菌UA159标准株比较ASvicR及gtfB/C/D的表达水平差异。... 目的:探讨vicK调控反义RNA ASvicR(Antisense vicR)及gtfB/C/D表达水平,影响变异链球菌胞外多糖代谢的机制。方法:同源重组法构建vicK缺失株及vicK补偿株,通过RT-qPCR检测与变异链球菌UA159标准株比较ASvicR及gtfB/C/D的表达水平差异。通过Western Blot来确定葡糖基转移酶GtfB/C/D的变化;激光共聚焦显微镜及扫描电镜下观测生物膜的结构和致密性。结果:相比UA159,当vicK基因缺失,变异链球菌的ASvicR表达升高,gtfB/C/D表达降低,GtfB/C/D水平降低,生物膜结构松散,致密性降低;而vicK补偿株对于GtfB/C/D亦有调控作用。结论:基因vicK调控GtfB/C/D蛋白表达,vicK缺失使ASvicR表达增高,胞外多糖合成减少,从而降低变异链球菌的致龋性。 展开更多
关键词 变异链球菌 龋病 生物膜 vick基因 反义RNA 葡糖基转移酶
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