Unlike most rotifers (Rotifera), which are planktonic and direct developers, many gnesiotrochan rotifers (Monogononta: Gnesiotrocha) are sessile and have indirect development. Few details exist on larval metamorphosis in most gnesiotrochans, and considering the drastic transformation that takes place at metamorphosis-the replacement of the ciliated corona with a new head that bears ciliated tentacles (the infundibulum)-it is perhaps surprising that there are limited data on the process. Here, we document part of this metamorphosis by examining the presence and distribution of neurons with serotonin immunoreactivity in the nervous system of both planktonic larvae and sessile adult females. Using antibodies against serotonin combined with confocal laser-scanning microscopy (CLSM) and 3D reconstruction software, we mapped the immunoreactive cell bodies and neurites in both life stages and found that relatively few changes occurred during metamorphosis. The larvae possessed a total of eight perikarya with serotonergic immunoreactivity (5HT-IR) in the brain, with at least two pairs of perikarya outside the brain in the region of the corona. Cells with 5HT-IR in the brain innervated the larval corona and also sent neurites to the trunk via the nerve cords. During metamorphosis, the corona was replaced by the infundibulum, which emerged from the larval mouth to become the new functional head. This change led to a posterior displacement of the brain and also involved the loss of 5HT-IR in the lateral brain perikarya and the gain of two perikarya with 5HT-IR in the anterior brain region. The innervation of the anterior end was retained in the adult; neurites that extended anteriorly to the mouth of the larva formed a distinct neural ring that encircled the infundibulum after metamorphosis. Significantly, there was no innervation of the infundibular tentacles by neurites with 5HT-IR, which suggests that ciliary control is unlikely to be modulated by serotonin within the tentacles themselves.
The rotifer integument is a well-described syncytium that contains an apical intracytoplasmic lamina (ICL) that functions for both skeletal support and muscle insertion. To date, there is limited information on the structure of the integument in species of Gnesiotrocha, a diverse subclade of Monogononta that consists of solitary, colonial, sessile, and planktonic species. In this study, we examined the ultrastructure of the integument in the colonial rotifer Sinantherina socialis to determine how it corresponds to that of other monogononts. The integument of S. socialis was broadly similar to that of other rotifers, consisting of a thickened glycocalyx, multilaminate ICL, and syncytial epidermis. However, it was different in several regards. The ICL consisted of three distinct layers from apical to basal: layer 1 consisted of at least two electron-dense laminae; layer 2 was a thickened matrix of amorphous, electron-dense material or was fibrous; and layer 3 was an electrondense lamina of varying thickness that covered the underlying syncytium. Significantly, layers 1 and 2 formed a ridge-and-groove like system of finger-like projections across the trunk surface that has not been observed in other rotifers. A voluminous syncytial cytoplasm (up to 3 lm thick) was present beneath the ICL and was mostly electron lucent and with few organelles. Bundles of potential microtubules were scattered throughout the syncytium. We hypothesize that the voluminous cytoplasm with microtubules serves as skeletal support for the rotifer's sessile lifestyle, while the external ridges may function as a texturebased deterrent to predators, or serves to trap secretions from the species' defensive glands. Basally, the epidermis was highly folded and bordered by a thin basal lamina that separated the plasmalemma from the blastocoel. Membrane-bound vesicles were present throughout the integument's cytoplasm and are hypothesized to function in the secretion of extracellular matrix and in the maintenance of the ICL.
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