Isolation and characterization of human pathogenic multidrug resistant bacteria associated with plastic litter collected in Zanzibar.

Plastic pollution is a growing problem, not at least in areas where poor waste management results in direct pollution of coastal zones, such as South Asia and regions in Africa. In addition to the effect on ecosystems and their related services, plastic pollution may also affect human health indirectly as vectors for infectious disease. As plastic offers a suitable surface for the attachment of biofilm forming bacteria, it may contribute to disease outbreaks and antimicrobial resistance. To investigate the role of plastic litter as potential vectors for pathogenic bacteria, we collected plastic litter from four rural sites in Zanzibar, and isolated adhered bacteria. Isolates were short-read sequenced for further molecular analysis. This revealed that collected plastic litter was associated with diverse bacterial species, including human pathogens Citrobacter freundii, Klebsiella pneumoniae and Vibrio cholerae. Furthermore, most isolates were found to be multidrug resistant. Our findings confirm that plastic litter, serve as novel reservoir for human multidrug resistant pathogenic bacteria that combined with poor sanitation and waste handling, may lead to transmission of infectious diseases and antimicrobial resistance. These findings add a new level to the environmental challenges with plastic pollution; the potential health risk associated with exposure to plastic litter.

Design and fabrication of memory devices based on nanoscale polyoxometalate clusters.

Flash memory devices--that is, non-volatile computer storage media that can be electrically erased and reprogrammed--are vital for portable electronics, but the scaling down of metal-oxide-semiconductor (MOS) flash memory to sizes of below ten nanometres per data cell presents challenges. Molecules have been proposed to replace MOS flash memory, but they suffer from low electrical conductivity, high resistance, low device yield, and finite thermal stability, limiting their integration into current MOS technologies. Although great advances have been made in the pursuit of molecule-based flash memory, there are a number of significant barriers to the realization of devices using conventional MOS technologies. Here we show that core-shell polyoxometalate (POM) molecules can act as candidate storage nodes for MOS flash memory. Realistic, industry-standard device simulations validate our approach at the nanometre scale, where the device performance is determined mainly by the number of molecules in the storage media and not by their position. To exploit the nature of the core-shell POM clusters, we show, at both the molecular and device level, that embedding [(Se(IV)O3)2](4-) as an oxidizable dopant in the cluster core allows the oxidation of the molecule to a [Se(v)2O6](2-) moiety containing a {Se(V)-Se(V)} bond (where curly brackets indicate a moiety, not a molecule) and reveals a new 5+ oxidation state for selenium. This new oxidation state can be observed at the device level, resulting in a new type of memory, which we call 'write-once-erase'. Taken together, these results show that POMs have the potential to be used as a realistic nanoscale flash memory. Also, the configuration of the doped POM core may lead to new types of electrical behaviour. This work suggests a route to the practical integration of configurable molecules in MOS technologies as the lithographic scales approach the molecular limit.

Label-free segmentation of Co-cultured cells on a nanotopographical gradient.

The function and fate of cells is influenced by many different factors, one of which is surface topography of the support culture substrate. Systematic studies of nanotopography and cell response have typically been limited to single cell types and a small set of topographical variations. Here, we show a radical expansion of experimental throughput using automated detection, measurement, and classification of co-cultured cells on a nanopillar array where feature height changes continuously from planar to 250 nm over 9 mm. Individual cells are identified and characterized by more than 200 descriptors, which are used to construct a set of rules for label-free segmentation into individual cell types. Using this approach we can achieve label-free segmentation with 84% confidence across large image data sets and suggest optimized surface parameters for nanostructuring of implant devices such as vascular stents.

A dual gradient assay for the parametric analysis of cell-surface interactions.

Cellular response to microgrooves is addressed using a new assay format, comprising orthogonal gradients of continuously varied groove pitch and depth. Dual layer etch masks are created using a combination of micropatterning and plasma polymer deposition. A silicon substrate with a constant groove width of 8 µm and with ridge width increasing from 8 µm in 0.5 µm steps across 10 mm is fabricated by photolithography. A plasma-polymerized hexane film which is 120 nm thick at one end of these grooves, and 10 nm at the other, is deposited under a diffusion mask. Reactive etching of the patterned sample transfers a gradient of groove pitch and groove depth into the silicon substrate. A silicon master with a gradient of groove depth spanning more than two orders of magnitude (less than 10 nm to over 1000 nm) is used to create an injection molding inlay for mass replication of the screening topography. Polycarbonate replicas are molded for use in cell culture studies, and the functionality of the topography as a high-throughput screening platform is investigated. The response of MDCK, h-TERT fibroblasts, and LE2 endothelial cells is examined, in terms of attachment and morphological response to the variation in topographical cues, with the aim of pinpointing the optimal combination of groove pitch and depth to elicit a tailored response from each cell type. When the range of topographical features screened on a single substrate is considered, this new assay represents a significant step forward in the parametric design and analysis of topographical cues at the biomaterial interface.

Near-field excitation of nanoantenna resonance.

An array of paired elliptic nanoparticles designed to enhance local fields around the particle pair is fabricated with gold embedded in quartz. Light excites a coupled plasmon resonance in the particle pair and the system acts like a plasmonic nanoantenna providing an enhanced electromagnetic field. Near-field scanning optical microscopy and finite element modeling are used to study the local field effects of the nanoantenna system. Local illumination shows similar resonant properties as plane wave illumination: a strong, localized optical resonance for light polarized parallel to the main, center-to-center axis.