Tillmann Urban, Wietkamp Stephan, Gu Haifeng, Krock Bernd, Salas Rafael, Clarke Dave
Helmholtz Center for Polar and Marine Research, Alfred Wegener Institute, Am Handelshafen 12, D-27570 Bremerhaven, Germany.
Third Institute of Oceanography, Ministry of Natural Resources, Xiamen 361005, China.
Microorganisms. 2021 Jan 8;9(1):134. doi: 10.3390/microorganisms9010134.
Azaspiracids (AZA) are a group of lipophilic toxins, which are produced by a few species of the marine nanoplanktonic dinoflagellates and (Amphidomataceae). A survey was conducted in 2018 to increase knowledge on the diversity and distribution of amphidomatacean species and their toxins in Irish and North Sea waters (North Atlantic). We here present a detailed morphological, phylogenetic, and toxinological characterization of 82 new strains representing the potential AZA producers and . A total of ten new strains of were obtained from the North Sea, and all conformed in terms of morphology and toxin profile (AZA-38 and-39) with previous records from the area. Within 72 strains assigned to there were strains of two distinct ribotypes (A and B) which consistently differed in their toxin profile (dominated by AZA-1 and -2 in ribotype A, and by AZA-11 and -51 in ribotype B strains). Five strains conformed in morphology with but no AZA could be detected in these strains. Moreover, they revealed significant nucleotide differences compared to known sequences and clustered apart from all other strains within the phylogenetic tree, and therefore were provisionally designated as cf. . These . cf. strains without detectable AZA were shown not to cause amplification in the species-specific qPCR assay developed to detect and quantify . As shown here for the first time, AZA profiles differed between strains of ribotype A in the presence/absence of AZA-1, AZA-2, and/or AZA-33, with the majority of strains having all three AZA congeners, and others having only AZA-1, AZA-1 and AZA-2, or AZA-1 and AZA-33. In contrast, no AZA profile variability was observed in ribotype B strains. Multiple AZA analyses of a period of up to 18 months showed that toxin profiles (including absence of AZA for cf. strains) were consistent and stable over time. Total AZA cell quotas were highly variable both among and within strains, with quotas ranging from 0.1 to 63 fg AZA cell. Cell quota variability of single AZA compounds for strains could be as high as 330-fold, but the underlying causes for the extraordinary large variability of AZA cell quota is poorly understood.
azaspiracids(AZA)是一类亲脂性毒素,由少数海洋微型浮游甲藻(双鞭甲藻科)产生。2018年开展了一项调查,以增加对爱尔兰和北海海域(北大西洋)双鞭甲藻科物种及其毒素的多样性和分布的了解。我们在此展示了代表潜在AZA产生菌的82个新菌株的详细形态学、系统发育学和毒素学特征。总共从北海获得了10个新的[具体名称未提及]菌株,所有菌株在形态和毒素谱(AZA - 38和 - 39)方面均与该地区先前的记录相符。在归为[具体名称未提及]的72个菌株中,有两种不同的核糖体型(A和B)的菌株,它们的毒素谱始终不同(核糖体型A以AZA - 1和 - 2为主,核糖体型B菌株以AZA - 11和 - 51为主)。有5个菌株在形态上与[具体名称未提及]相符,但在这些菌株中未检测到AZA。此外,与已知的[具体名称未提及]序列相比,它们显示出显著的核苷酸差异,并且在系统发育树中与所有其他[具体名称未提及]菌株聚类分开,因此被暂时指定为[具体名称未提及]cf。[具体名称未提及]。这些未检测到AZA的[具体名称未提及]cf。[具体名称未提及]菌株在用于检测和定量[具体名称未提及]的物种特异性qPCR检测中未显示出扩增。如首次在此所示,在核糖体型A的菌株中,AZA谱在是否存在AZA - 1、AZA - 2和/或AZA - 33方面存在差异,大多数菌株具有所有三种AZA同系物,而其他菌株仅具有AZA - 1、AZA - 1和AZA - 2或AZA - 1和AZA - 33。相比之下,在核糖体型B菌株中未观察到AZA谱的变异性。长达18个月的多次AZA分析表明,毒素谱(包括[具体名称未提及]cf。[具体名称未提及]菌株中不存在AZA)随时间一致且稳定。总AZA细胞配额在菌株之间和菌株内部都高度可变,配额范围为0.1至63 fg AZA/细胞。[具体名称未提及]菌株单个AZA化合物的细胞配额变异性可能高达330倍,但AZA细胞配额异常大的变异性的根本原因尚不清楚。