A chemical view of the most ancient metazoa--biomarker chemotaxonomy of hexactinellid sponges

Hexactinellid sponges are often considered to be the most ancient metazoans. Lipid biomarkers from 23 species were studied for information on their phylogenetic properties, particularly their disputed relation to the two other sponge classes (Demospongiae, Calcarea). The most prominent lipid compounds in the Hexactinellida comprise C28 to C32 polyenoic fatty acids. Their structures parallel the unique patterns found in demosponge membrane fatty acids ('demospongic acids') and strongly support a close phylogenetic association of the Demospongiae and the Hexactinellida. Both taxa also show unusual mid-chain methylated fatty acids (C15-C25) and irregular C25- and C40-isoprenoid hydrocarbons, tracers for specific eubacteria and Archaea, respectively. These biomarkers indicate a similar, highly conservative symbiont community, although some shift in the abundance of the associated microbiota was observed. The lack of these features in calcareous sponges further contradicts the still common view that Calcarea and Demospongiae are more closely related to each other than either is to the Hexactinellida.     

The steroids of hexactinellid sponges

The Hexactinellida ('glass sponges') are commonly considered to be the most basic metazoans. Steroids of 20 species from different taxa were studied for chemotaxonomy and biosynthetic implications. All Hexactinellida contain cholest-5-en-3#-ol (cholesterol) and/or its saturated derivative 5!(H)-cholestan-3#-ol, along with their C-24-alkylated homologues. Where 5!(H)-stanols are present, they regularly co-occur with their 3-keto analogues. The steroid concentrations generally decrease with increasing carbon numbers, similar to sterol distributions typically found in marine sediments. These features argue against de novo sterol biosynthesis operating in hexactinellid sponges. Rather, we suggest a dietary uptake of (⁵-stenols and their stereoselective transformation via 3-keto intermediates to 5!(H)-stanols.     

Prenatal demonstration of a cervical myelocystocele

Myelocystocele is a rare spinal cord disorder and has not been described prenatally. We report a case in which prenatal ultrasound and magnetic resonance imaging (MRI) demonstrated a posterior cervical mass which was initially thought to be a meningocele or an atypical cystic hygroma. Surgery performed at 1 day of age showed this to be a myelocystocele. Therefore, the differential diagnosis of an extracranial cystic mass in the posterior cervical region should be expanded to include myelocystoceles.