Duplex Real-Time Fluorescent Quantitative PCR Assays for the Detection of Toxigenic Microcystis Genotypes Based on SNP/InDel Variation in mcy Gene Cluster
文献类型： 外文期刊
作者： Bi, Xiangdong 1 ; Wei, Peng 1 ; Wang, Qian 2 ; Duan, Lijin 2 ; Dai, Wei 1 ; Chen, Rui 2 ; Zhang, Dajuan 1 ;
作者机构： 1.Tianjin Agr Univ, Coll Fishery, Key Lab Aquat Ecol & Aquaculture Tianjin, Tianjin, Peoples R China
2.Tianjin Acad Agr Sci, Inst Crop Germplasm & Biotechnol, Tianjin, Peoples R China
期刊名称：CURRENT MICROBIOLOGY （ 影响因子：2.3； 五年影响因子：2.4 ）
ISSN： 0343-8651
年卷期： 2024 年 81 卷 9 期
页码：
收录情况： SCI
摘要： In this study, the toxigenic characteristics of 14 strains of Microcystis were analyzed, and single nucleotide polymorphism (SNP) and insertion/deletion (InDel) loci in microcystin synthetase (mcy) gene clusters were screened. Based on SNP and InDel loci associated with the toxigenic characteristics, primers and TaqMan or Cycling fluorescent probes were designed to develop duplex real-time fluorescent quantitative PCR (FQ-PCR) assays. After evaluating specificity and sensitivity, these assays were applied to detect the toxigenic Microcystis genotypes in a shrimp pond where Microcystis blooms occurred. The results showed a total of 2155 SNP loci and 66 InDel loci were obtained, of which 12 SNP loci and 5 InDel loci were associated with the toxigenic characteristics. Three duplex real-time FQ-PCR assays were developed, each of which could quantify two genotypes of toxigenic Microcystis. These FQ-PCR assays were highly specific, and two Cycling assays were more sensitive than TaqMan assay. In the shrimp pond, six genotypes of toxigenic Microcystis were detected using the developed FQ-PCR assays, indicating that above genotyping assays have the potential for quantitative analysis of the toxigenic Microcystis genotypes in natural water.
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