Tulsiani S M, Craig S B, Graham G C, Cobbold R C, Dohnt M F, Burns M-A, Leung L K-P, Field H E, Smythe L D
The University of Queensland, School of Veterinary Science, St Lucia, Queensland, Australia.
Ann Trop Med Parasitol. 2010 Mar;104(2):151-61. doi: 10.1179/136485910X12607012374037.
A new test for pathogenic Leptospira isolates, based on RAPD-PCR and high-resolution melt (HRM) analysis (which measures the melting temperature of amplicons in real time, using a fluorescent DNA-binding dye), has recently been developed. A characteristic profile of the amplicons can be used to define serovars or detect genotypes. Ten serovars, of leptospires from the species Leptospira interrogans (serovars Australis, Robinsoni, Hardjo, Pomona, Zanoni, Copenhageni and Szwajizak), L. borgpetersenii (serovar Arborea), L. kirschneri (serovar Cynopteri) and L. weilii (serovar Celledoni), were typed against 13 previously published RAPD primers, using a real-time cycler (the Corbett Life Science RotorGene 6000) and the optimised reagents from a commercial kit (Quantace SensiMix). RAPD-HRM at specific temperatures generated defining amplicon melt profiles for each of the tested serovars. These profiles were evaluated as difference-curve graphs generated using the RotorGene software package, with a cut-off of at least 8 'U' (plus or minus). The results demonstrated that RAPD-HRM can be used to measure serovar diversity and establish identity, with a high degree of stability. The characterisation of Leptospira serotypes using a DNA-based methodology is now possible. As an objective and relatively inexpensive and rapid method of serovar identification, at least for cultured isolates, RAPD-HRM assays show convincing potential.
最近开发了一种针对致病性钩端螺旋体分离株的新检测方法,该方法基于随机扩增多态性DNA聚合酶链反应(RAPD-PCR)和高分辨率熔解曲线分析(HRM)(使用荧光DNA结合染料实时测量扩增子的熔解温度)。扩增子的特征图谱可用于定义血清型或检测基因型。使用实时循环仪(Corbett生命科学公司的RotorGene 6000)和商业试剂盒(Quantace SensiMix)中的优化试剂,针对13种先前发表的RAPD引物,对问号钩端螺旋体(血清型澳大利亚型、罗宾逊型、哈德乔型、波莫纳型、扎诺尼型、哥本哈根型和斯瓦伊扎克型)、博氏钩端螺旋体(血清型阿尔博雷亚型)、克氏钩端螺旋体(血清型犬蝠型)和魏氏钩端螺旋体(血清型塞莱多尼型)的10种血清型进行分型。在特定温度下的RAPD-HRM产生了每种测试血清型的定义扩增子熔解图谱。这些图谱作为使用RotorGene软件包生成的差异曲线图进行评估,截断值为至少8个“U”(正负)。结果表明,RAPD-HRM可用于测量血清型多样性并确定身份,具有高度稳定性。现在可以使用基于DNA的方法对钩端螺旋体血清型进行鉴定。作为一种客观、相对廉价且快速的血清型鉴定方法,至少对于培养的分离株而言,RAPD-HRM分析显示出令人信服的潜力。