Habitat requirements and local persistence of three damselfly species (odonata: coenagrionidae)

Habitat requirements and population persistence were investigated in three damselfly species, all coastal plain pond specialists: Enallagma recurvatum, E. laterale, and E. pictum. Because of geographic restriction, two are of special concern to conservation, E. recurvatum and E. laterale. We surveyed more than 70 ponds on Cape Cod, Massachusetts, and collected adult presence-absence data during the summers of 1999 and 2000. We achieved a detection rate approaching 100% for each species by visiting each pond up to three times. We looked for relationships between the presence of each damselfly species and presence of specific aquatic vegetation, the presence of the other Enallagma species, and the number of ponds within various distances of the 72 surveyed ponds. Using stepwise logistic regression, we found the following significant associations: E. recurvatum with the rush Juncus militaris; E. laterale with water lilies (Nuphar variegatum and Brasenia schreberi) the damselfly E. pictum, and the number of ponds within 2 km; and E. pictum with the water lily Nymphaea odorata, the damselfly E. laterale, and the number of ponds within 1.5 km and 2.5 km. Presence-absence data were used to calculate turnover and local extinction rates for each species between the two years. E. recurvatum's turnover and local extinction rates (33.3% and 41% respectively) were much higher than either E. laterale (9.8%, 11.5%) or E. pictum (7.7%, 10%). These results suggest that E. recurvatum occurs in a metapopulation, and that patch colonization rates might be important to local population persistence.     

Differential effects of extracellular calcium removal and nonspecific effects of Ca2+ antagonists on acid secretory activity in isolated gastric glands

The role of extracellular calcium in the action of the secretagogues, carbachol, histamine and forskolin, on parietal cell HCl secretion was investigated using glands isolated from rabbit gastric mucosa. Omission of calcium from the cellular incubation medium and chelation of a major portion of contaminating calcium with EGTA resulted in a disappearance of the initial transient response to carbachol (as measured by uptake of the weak base, amino[14C]pyrine), but the sustained response to carbachol persisted. Neither histamine nor forskolin-stimulated increase in amino[14C]pyrine uptake were affected by omission of extracellular calcium. Furthermore, the potentiating interactions between histamine and carbachol and between forskolin and carbachol appeared to occur independent of extracellular calcium. Attempts to assess the contribution of intracellular calcium to secretory activity using the Ca2+ antagonists, verapamil, nifedipine, nicardipine and lanthanum, and the putative intracellular Ca2+ antogonist, TMB-8 (3,4,5-trimethyloxybenzoic acid 8-(diethyl-amino)-octyl ester) were unsuccessful. Nifedipine had no effect on secretagogue stimulated amino[14C]pyrine accumulation even at concentration well above the pA2 reported for excitable tissues. Verapamil, nicardipine, lanthanum and TMB-8 all appeared to have nonspecific inhibitory effects on amino [14C]pyrine uptake. From these results we conclude that: (1) parietal cell HCl secretion can occur independent of extracellular Ca2+; (2) influx of extracellular Ca2+ enhances the response to carbachol but has little influence on the secretory response initiated by cAMP-dependent secretagogues; and (3) parietal cell Ca2+ channels have a different molecular configuration than Ca2+ channels in excitable cells.     

Genome Sequence of Multidrug-Resistant Escherichia coli EC302/04, Isolated from a Human Tracheal Aspirate

Escherichia coli is an important etiologic agent of lower respiratory tract infections (LRTI). Multidrug-resistant E. coli EC302/04 was isolated from a tracheal aspirate, and its genome sequence is expected to provide insights into antimicrobial resistance as well as adaptive and virulence mechanisms of E. coli involved in LRTI.     

Bifidobacteria-mediated immune system imprinting early in life

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HIV glycoprotein gp120 enhances mesenchymal stem cell migration by upregulating CXCR4 expression

Background

HIV infection and/or the direct pathogenic effects of circulating HIV proteins impairs the physiological function of mesenchymal stem cells (MSCs), and contribute to the pathogenesis of age-related clinical comorbidities in people living with HIV. The SDF-1/CXCR4 pathway is vital for modulating MSC proliferation, migration and differentiation. HIV glycoprotein gp120 inhibits SDF-1 induced chemotaxis by downregulating the expression and function of CXCR4 in monocytes, B and T cells. The influence of gp120 on CXCR4 expression and migration in MSCs is unknown.