Pollen analysis reveals the effects of uncovered interactions, pollen-carrying structures, and pollinator sex on the structure of wild bee-plant networks.

Pollination networks are increasingly used to model the complexity of interactions between pollinators and flowering plants in communities. Different methods exist to sample these interactions, with direct observations of plant-pollinator contacts in the field being by far the most common. Although the identification of pollen carried by pollinators allows uncovering interactions and increasing sample sizes, the methods used to build pollen-transport networks are variable and their effect on network structure remains unclear. To understand how interaction sampling influences the structure of networks, we analyzed the pollen found on wild bees from eight communities across Mallorca Island and investigated the differences in pollen loads between bee body parts (scopa vs. body) and sexes. We then assessed how these differences, as well as the uncovered interactions not detected in the field, influenced the structure of wild bee-plant networks. We identified a higher quantity and diversity of pollen in the scopa than in the rest of the female body, but these differences did not lead to differences in structure between plant-pollination (excluding scopa pollen) and bee-feeding interaction (including scopa pollen) networks. However, networks built with pollen data were richer in plant species and interactions and showed lower modularity and specialization (H2 '), and higher nestedness than visitation networks based on field observations. Female interactions with plants were stronger compared to those of males, although not richer. Accordingly, females were more generalist (low d') and tended to be more central in interaction networks, indicating their more key role structuring pollination networks in comparison to males. Our study highlights the importance of palynological data to increase the resolution of networks, as well as to understand important ecological questions such as the differences between plant-pollination and bee-feeding interaction networks, and the role of sexes in pollination.

Extra-criteria antiphospholipid antibodies in patients with small vessel brain lesions and clinical manifestations associated with antiphospholipid syndrome.

OBJECTIVES: Neurological manifestations compatible with small vessel brain lesions (SVBL), such as migraine, cognitive impairment, seizures, and transverse myelitis, may be related to antiphospholipid syndrome (APS) and patients could need APS therapies even though they do not fit into thrombosis or obstetric morbidity. Furthermore, extra-criteria antiphospholipid antibodies (aPL) provide an increase in sensitivity in patients with clinical manifestations related to APS but negative for IgG/IgM anticardiolipin (aCL), anti-ß2 glycoprotein I (aß2GPI), and lupus anticoagulant, which are the antibodies included in the classification criteria for APS. METHODS: We determined extra-criteria aPL in 65 SVBL patients with neurological traits and Magnetic Resonance Imaging suggestive of APS but negative for APS classification criteria, 47 of whom were prospectively followed and tested over three years. A group of 95 patients with autoimmune diseases (AD) but without clinical traits of APS was also studied. RESULTS: A persistent presence of extra-criteria aPL was detected in 27.7% of patients: 12.77% IgM anti- prothrombin (PT), 6.38% IgG anti-PT, 6.38% IgM anti-phosphatidylethanolamine (PE), 4.26% IgA aß2GPI, 2.13% IgG anti-phosphatidylserine/prothrombin (PS/PT) and 2.13% IgM anti-PS/PT. There was a tendency towards a higher prevalence of these aPL in SVBL patients than in AD - especially for IgA aß2GPI - and a lack of IgG aPS/PT positivity in the AD group. We found no SVBL patient positive for IgA aCL, IgG anti-PE, annexin V, or aß2GPI domain I. CONCLUSIONS: Extra-criteria aPL can improve sensitivity for APS diagnosis in patients with SVBL, especially IgA aß2GPI and IgG anti-PS/PT antibodies.

In vitro differentiation of murine hematopoietic progenitor cells toward the myeloid lineage occurs in response to Staphylococcus aureus and yeast species.

We have studied the effect of inactivated microbial stimuli (Candida albicans, Candida glabrata, Saccharomyces boulardii, and Staphylococcus aureus) on the in vitro differentiation of lineage negative (Lin(-)) hematopoietic progenitor mouse cells. Purified Lin(-) progenitors were co-cultured for 7 days with the stimuli, and cell differentiation was determined by flow cytometry analysis. All the stimuli assayed caused differentiation toward the myeloid lineage. S. boulardii and particularly C. glabrata were the stimuli that induced in a minor extent differentiation of Lin(-) cells, as the major population of differentiated cells corresponded to monocytes, whereas C. albicans and S. aureus induced differentiation beyond monocytes: to monocyte-derived dendritic cells and macrophages, respectively. Interestingly, signaling through TLR2 by its pure ligand Pam3CSK4 directed differentiation of Lin(-) cells almost exclusively to macrophages. These data support the notion that hematopoiesis can be modulated in response to microbial stimuli in a pathogen-dependent manner, being determined by the pathogen-associated molecular patterns and the pattern-recognition receptors involved, in order to generate the populations of mature cells required to deal with the pathogen.