Scholin C A, Villac M C, Buck K R, Krupp J M, Powers D A, Fryxell G A, Chavez F P
Monterey Bay Aquarium Research Institute, Pacific Grove, CA 93950.
Nat Toxins. 1994;2(4):152-65. doi: 10.1002/nt.2620020403.
Cultured isolates of Pseudonitzschia australis Frenguelli, P. delicatissima (Cleve) Heiden, P. americana (Hasle) Fryxell, P. pungens (Grunow) Hasle, and P. pungens f. multiseries (Hasle) Hasle from Monterey Bay, California, were compared on the basis of their large-subunit ribosomal RNA gene (LsrDNA). Pseudonitzschia australis, P. pungens f. multiseries, and P. delicatissima were previously shown to produce the neurotoxin domoic acid; the remaining isolates are considered non-toxic. For each isolate approximately 800 base pairs of LsrDNA, encompassing both evolutionarily conserved and evolutionarily variable regions of the molecule, were amplified using the polymerase chain reaction (PCR) and sequenced. Phylogenetic trees generated by parsimony analysis of aligned sequences afford a preliminary view of the organisms genetic relationships. Species defined by morphological criteria are also distinguishable by LsrDNA sequence. Organisms known or suspected to produce domoic acid cluster at different termini on the phylogenetic tree. Two genetically distinct strains of P. australis and P. pungens were identified. Development of a restriction fragment length polymorphism (RFLP) assay of the LsrDNA is described. The RFLP assay discriminates each species, including distinguished strains of P. australis and P. pungens. The restriction test provides a rapid and convenient method for screening isolates' LsrDNA, facilitating further tests of the apparent positive correlation between Pseudonitzschia species' ribosomal gene signatures, morphology, and capacity to produce domoic acid.
对从加利福尼亚州蒙特雷湾分离培养的澳洲伪菱形藻(Pseudonitzschia australis Frenguelli)、柔弱伪菱形藻(P. delicatissima (Cleve) Heiden)、美洲伪菱形藻(P. americana (Hasle) Fryxell)、尖刺伪菱形藻(P. pungens (Grunow) Hasle)以及尖刺伪菱形藻多列变型(P. pungens f. multiseries (Hasle) Hasle),基于其大亚基核糖体RNA基因(LsrDNA)进行了比较。先前已表明,澳洲伪菱形藻、尖刺伪菱形藻多列变型和柔弱伪菱形藻可产生神经毒素软骨藻酸;其余分离株被认为无毒。对于每个分离株,使用聚合酶链反应(PCR)扩增了约800个碱基对的LsrDNA,该区域涵盖了该分子的进化保守区和进化可变区,并进行了测序。通过对排列好的序列进行简约分析生成的系统发育树,初步展示了这些生物的遗传关系。根据形态学标准定义的物种,也可通过LsrDNA序列区分开来。已知或疑似产生软骨藻酸的生物在系统发育树的不同末端聚类。鉴定出了两种基因上不同的澳洲伪菱形藻和尖刺伪菱形藻菌株。描述了一种针对LsrDNA的限制性片段长度多态性(RFLP)分析方法。该RFLP分析可区分每个物种,包括不同的澳洲伪菱形藻和尖刺伪菱形藻菌株。限制性测试为筛选分离株的LsrDNA提供了一种快速便捷的方法,有助于进一步测试伪菱形藻物种的核糖体基因特征、形态与产生软骨藻酸能力之间明显的正相关性。