Collection of Cyanobacteria, Institut Pasteur, Université Paris Cité, Paris, France.
Department of Biological Sciences, Ramniranjan Jhunjhunwala College of Arts, Science and Commerce, Mumbai, India.
J Phycol. 2024 Oct;60(5):1139-1160. doi: 10.1111/jpy.13488. Epub 2024 Aug 8.
Two new species of Dulcicalothrix, D. adhikaryi sp. nov. and D. iyengarii sp. nov., were discovered in India and are characterized and described in accordance with the rules of the International Code of Nomenclature for algae, fungi, and plants (ICN). As a result of phylogenetic analysis, Calothrix elsteri is reassigned to Brunnivagina gen. nov. During comparison with all Dulcicalothrix for which sequence data were available, we observed that the genus has six ribosomal operons in three orthologous types. Each of the three orthologs could be identified based upon indels occurring in the D1-D1' helix sequence in the ITS rRNA region between the 16S and 23S rRNA genes, and in these three types, there were operons containing ITS rRNA regions with and without tRNA genes. Examination of complete genomes in Dulcicalothrix revealed that, at least in the three strains for which complete genomes are available, there are five ribosomal operons, two with tRNA genes and three with no tRNA genes in the ITS rRNA region. Internal transcribed spacer rRNA regions have been consistently used to differentiate species, both on the basis of secondary structure and percent dissimilarity. Our findings call into question the use of ITS rRNA regions to differentiate species in the absence of efforts to obtain multiple operons of the ITS rRNA region through cloning or targeted PCR amplicons. The ITS rRNA region data for Dulcicalothrix is woefully incomplete, but we provide herein a means for dealing with incomplete data using the polyphasic approach to analyze diverse molecular character sets. Caution is urged in using ITS rRNA data, but a way forward through the complexity is also proposed.
两种新的 Dulcicalothrix 物种,即 D. adhikaryi sp. nov. 和 D. iyengarii sp. nov.,在印度被发现,并根据藻类、真菌和植物国际命名法规(ICN)的规则进行了特征描述和命名。通过系统发育分析,将 Calothrix elsteri 重新分配到 Brunnivagina 属。在与所有可获得序列数据的 Dulcicalothrix 进行比较时,我们观察到该属在三个同源类型中有六个核糖体操纵子。通过在 16S 和 23S rRNA 基因之间的 ITS rRNA 区域中 D1-D1' 螺旋序列中的插入/缺失,可识别出这三个同源类型中的每一个,并且在这三种类型中,存在含有 ITS rRNA 区域的操纵子,这些区域含有或不含有 tRNA 基因。对 Dulcicalothrix 的完整基因组进行检查,结果表明,至少在三个可获得完整基因组的菌株中,在 ITS rRNA 区域中,有五个核糖体操纵子,其中两个具有 tRNA 基因,三个没有 tRNA 基因。内部转录间隔区 rRNA 区域一直被用于区分物种,无论是基于二级结构还是相似性百分比。我们的发现质疑了在不努力通过克隆或靶向 PCR 扩增子获得多个 ITS rRNA 区域操纵子的情况下,使用 ITS rRNA 区域来区分物种的做法。 Dulcicalothrix 的 ITS rRNA 区域数据非常不完整,但我们在此提供了一种使用多相方法分析多种分子特征集来处理不完整数据的方法。在使用 ITS rRNA 数据时需要谨慎,但也提出了一种解决复杂性的方法。