Raphidiopsis and Cylindrospermopsis are planktic, freshwater bloom-forming cyanobacteria of great concern to human health due to the production of potent cyanotoxins. The presence (in Cylindrospermopsis) or absence (in Raphidiopsis) of heterocytes is the traditional character used to distinguish them. This has led to misidentifications and to questions about the validity of the genus Raphidiopsis. We studied two strains of R. mediterranea isolated from Argentinean shallow lakes using a polyphasic approach that included the morphological description of the natural populations and their ultrastructural, physiological and molecular characterisation. Heterocyte differentiation was not observed in the field or in cultures of R. mediterranea submitted to nitrogen deprivation. These results support the occurrence of stable native populations of R. mediterranea without heterocytes, which would not be a part of the Cylindrospermopsis complex life cycle. Based on 16S rRNA, 16S-23S ITS, and cpcBA-IGS sequences, these two genera are virtually identical. Thus, strains of Raphidiopsis and Cylindrospermopsis make up a monophyletic lineage in all phylogenetic reconstructions. Furthermore, the 16S-23S ITS secondary structure provided further evidence that these two genera cannot be separated. The intermixed position in the trees points to several losses of heterocytes during the evolution of these cyanobacteria. We conclude that these two genera should not be regarded as separate and distinct generic units and propose their unification under the name Raphidiopsis, respecting the principle of priority. Accordingly, we revisited and emended the description of Raphidiopsis.
Cyanobacteria are globally widespread photosynthetic prokaryotes and are major contributors to global biogeochemical cycles. One of the most critical processes determining cyanobacterial eco-physiology is cellular death. Evidence supports the existence of controlled cellular demise in cyanobacteria, and various forms of cell death have been described as a response to biotic and abiotic stresses. However, cell death research in this phylogenetic group is a relatively young field and understanding of the underlying mechanisms and molecular machinery underpinning this fundamental process remains largely elusive. Furthermore, no systematic classification of modes of cell death has yet been established for cyanobacteria. In this work, we analyzed the state of knowledge in the field of cyanobacterial cell death. Based on that, we propose unified criterion for the definition of accidental, regulated, and programmed forms of cell death in cyanobacteria based on molecular, biochemical, and morphologic aspects following the directions of the Nomenclature Committee on Cell Death (NCCD). With this, we aim to provide a guide to standardize the nomenclature related to this topic in a precise and consistent manner, which will facilitate further ecological, evolutionary, and applied research in the field of cyanobacterial cell death.
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