Institution
University of Salford
Education•Salford, Manchester, United Kingdom•
About: University of Salford is a education organization based out in Salford, Manchester, United Kingdom. It is known for research contribution in the topics: Population & Thin film. The organization has 13049 authors who have published 22957 publications receiving 537330 citations. The organization is also known as: University of Salford Manchester & The University of Salford Manchester.
Topics: Population, Thin film, Health care, Poison control, Sputtering
Papers published on a yearly basis
Papers
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TL;DR: This work quantifies the in silico performance of twelve primer pairs from four mitochondrial loci – COI, cytochrome b, 12S and 16S – in terms of reference library coverage, taxonomic discriminatory power and primer universality, and test in vitro four primer pairs – three COI and one 12S – for their specificity, reproducibility, and congruence with independent datasets derived from traditional survey methods.
Abstract: 1.Metabarcoding extra‐organismal DNA from environmental samples is now a key technique in aquatic biomonitoring and ecosystem health assessment. Of critical consideration when designing experiments, and especially so when developing community standards and legislative frameworks, is the choice of genetic marker and primer set. Mitochondrial cytochrome c oxidase subunit I (COI), the standard DNA barcode marker for animals, with its extensive reference library, taxonomic discriminatory power, and predictable sequence variation, is the natural choice for many metabarcoding applications. However, for targeting specific taxonomic groups in environmental samples, the utility of COI has yet to be fully scrutinised.
2.Here, by using a case study of marine and freshwater fishes from the British Isles, we quantify the in silico performance of twelve primer pairs from four mitochondrial loci—COI, cytochrome b, 12S and 16S—in terms of reference library coverage, taxonomic discriminatory power and primer universality. We subsequently test in vitro four primer pairs—three COI and one 12S—for their specificity, reproducibility, and congruence with independent datasets derived from traditional survey methods at five estuarine and coastal sites around the English Channel and North Sea.
3.Our results show that for aqueous extra‐organismal DNA at low template concentrations, both metazoan‐targeted and fish‐targeted COI primers perform poorly in comparison to 12S, exhibiting low levels of reproducibility due to non‐specific amplification of prokaryotic and non‐target eukaryotic DNAs.
4.An ideal metabarcode would have an extensive reference library upon which custom primers could be designed, either for broad assessments of biodiversity, or taxon specific surveys. Such a database is available for COI, but low primer specificity hinders practical application, while conversely, 12S primers offer high specificity, but lack adequate references. The latter, however, can be mitigated by expanding the concept of DNA barcodes to include whole mitochondrial genomes generated by genome‐skimming existing tissue collections.
166 citations
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TL;DR: In this article, the residual stress profiles in aluminum and steel welds, and in shot peened aluminium, obtained via synchrotron and neutron diffraction at the ESRF-ILL in Grenoble, were presented.
165 citations
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TL;DR: An 8-week program of high-intensity IMT resulted in significant benefits for CF patients, which included increased IMF and thickness of the diaphragm (during contraction), improved lung volumes, increased PWC, and improved psychosocial status.
165 citations
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TL;DR: The techniques of genetic algorithms are proposed as an alternative means of tuning digital PID controllers for complex multivariable plants with highly interactive dynamics.
Abstract: The techniques of genetic algorithms are proposed as an alternative means of tuning digital PID controllers. This use of genetic algorithms is particularly attractive because the same basic approach can always be readily used, even in the case of digital PID controllers for complex multivariable plants with highly interactive dynamics.
164 citations
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TL;DR: Recombinant onchocystatin has the potential to contribute to a state of cellular hyporesponsiveness and is a possible pathogenicity factor essential for the persistence of O. volvulus within its human host.
Abstract: Immune responses of individuals infected with filarial nematodes are characterized by a marked cellular hyporesponsiveness and a shift of the cytokine balance toward a Th2/Th3 response. This modulation of cellular immune responses is considered as an important mechanism to avoid inflammatory immune responses that could eliminate the parasites. We investigated the immunomodulatory potential of a secreted cysteine protease inhibitor (onchocystatin) of the human pathogenic filaria Onchocerca volvulus. Recombinant onchocystatin (rOv17), a biologically active cysteine protease inhibitor that inhibited among others the human cysteine proteases cathepsins L and S, suppressed the polyclonally stimulated and the Ag-driven proliferation of human PBMC. Stimulated as well as unstimulated PBMC in the presence of rOv17 produced significantly more IL-10, which was paralleled in some situations by a decrease of IL-12p40 and preceded by an increase of TNF-alpha. At the same time, rOv17 reduced the expression of HLA-DR proteins and of the costimulatory molecule CD86 on human monocytes. Neutralization of IL-10 by specific Abs restored the expression of HLA-DR and CD86, whereas the proliferative block remained unaffected. Depletion of monocytes from the PBMC reversed the rOv17-induced cellular hyporeactivity, indicating monocytes to be the target cells of immunomodulation. Therefore, onchocystatin has the potential to contribute to a state of cellular hyporesponsiveness and is a possible pathogenicity factor essential for the persistence of O. volvulus within its human host.
163 citations
Authors
Showing all 13134 results
Name | H-index | Papers | Citations |
---|---|---|---|
Hongjie Dai | 197 | 570 | 182579 |
Michael P. Lisanti | 151 | 631 | 85150 |
Matthew Jones | 125 | 1161 | 96909 |
David W. Denning | 113 | 736 | 66604 |
Wayne Hall | 111 | 1260 | 75606 |
Richard Gray | 109 | 808 | 78580 |
Christopher E.M. Griffiths | 108 | 671 | 47675 |
Thomas P. Davis | 107 | 724 | 41495 |
Nicholas Tarrier | 92 | 326 | 25881 |
David M. A. Mann | 88 | 338 | 43292 |
Ajith Abraham | 86 | 1113 | 31834 |
Federica Sotgia | 85 | 247 | 28751 |
Mike Hulme | 84 | 300 | 35436 |
Robert N. Foley | 84 | 260 | 31580 |
Richard Baker | 83 | 514 | 22970 |