Metal composition of arrow squid (Nototodarus sloanii [Gray 1849]) from the Chatham Rise, New Zealand: implications for human consumption.

Cephalopods are important in the diets of humans and many other apex predators, and can play an important role in the bioaccumulation of metals. In this study, metal concentrations were analysed in the commercially and ecologically important southern arrow squid, Nototodarus sloanii (Gray 1849), from a heavily targeted fisheries area on New Zealand's Chatham Rise. A variety of tissue types were compared in order to assess the bioaccumulation in edible tissues (mantle and arms) and other organs (digestive gland, kidney, and hearts). Although metal concentrations varied among tissue types, the highest concentrations were found in the digestive gland (for Cd, Cu, Fe, Ni, Zn) and branchial hearts (for Cr, U). We report the first Cd concentrations for N. sloanii from the Chatham Rise, with mean values of 3.11 µg. g-1 in the mantle and 102.53 µg. g-1 in the digestive gland. Our data suggest that concentrations observed in the mantle tissue (which forms the majority of the muscle tissue) and digestive gland (the primary organ for metal accumulation) can be used to estimate the animal's total body burden for all metals analysed. The toxicological and dietary consequences for predators (including humans) feeding on arrow squid can be inferred from measurements of mass and metal concentration in these tissues. Arrow squid represent an important vector for Cd transfer within the pelagic Chatham Rise food web. These are the first recorded baseline data for metal concentrations for any squid in this oceanic region.

A mitochondrial phylogeny of the family Onychoteuthidae (Cephalopoda: Oegopsida).

The oegopsid squid family Onychoteuthidae was recently revised based on morphology, but sufficient material for a complementary molecular analysis has not been available until now. In the present study, over 250 sequences of cytochrome c oxidase subunit I (COI) and 16S rRNA for 222 individuals were analysed to create a combined phylogeny for the family. Results support monophyly for the family and all seven onychoteuthid genera (including Moroteuthopsis, established herein as the senior genus name for species formerly attributed to Kondakovia); 29 genetically distinct species were recovered, with the BIN (Barcode Index Number) analysis for COI showing good congruence overall with morphological species groupings. No sequences were available for five additional known species, making the total family diversity likely to exceed 34 species. Seven of the BINs formed in this study appear to represent undescribed taxa, suggesting that even in this relatively well-studied family, much additional work remains before a comprehensive understanding of the diversity and evolutionary relationships for the Onychoteuthidae can be achieved.

Blood dendritic cells in systemic lupus erythematosus exhibit altered activation state and chemokine receptor function.

BACKGROUND: Dendritic cells (DCs) have a pivotal role in the pathogenesis of systemic lupus erythematosus (SLE). Reduced numbers of blood DCs and the accumulation of DCs at inflammatory sites have been observed in SLE. One crucial feature of DCs is their ability to migrate. OBJECTIVE: To analyse the maturation/activation state and the migratory capacity of different DC precursor subsets in SLE to further elucidate their role in autoimmunity. METHODS: Plasmacytoid DCs (pDCs), myeloid DCs (mDCs) and monocytes from patients with SLE, healthy volunteers and healthy volunteers immunised with tetanus/diphtheria were examined by flow cytometry for expression of subset-specific antigens (BDCA-2, CD11c, CD14, HLA-DR), activation/maturation markers (CD83, CD86, CD40, BLyS) and chemokine receptors (CCR1, CCR5, CCR7, ChemR23). Additionally, migratory capacity to chemokine receptors was investigated in vitro using the chemokines RANTES, CCL19 and chemerin. RESULTS: SLE monocytes and mDCs had higher CD86 and B-lymphocyte stimulatory factor (BLyS) expression levels. ChemR23 expression was lower in SLE pDCs and mDCs. Basal and CCL19-specific migration levels were higher in SLE pDCs. Altered DC function in SLE had no correlative changes in chemokine receptor expression, whereas immunisation-induced blood DC migration patterns in healthy donors were accompanied by changes in chemokine receptor expression. CONCLUSIONS: The phenotypic and migratory disturbances observed in SLE blood DCs could result in altered distribution of DCs in peripheral tissues, contributing to dysregulated immune responses and autoimmunity.