Microarrays Research Today is a free monthly online journal that collates and summarizes the latest research about Microarrays, including details on experiments, designs, statistics, analysis, software. | ||||||
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Metabolic capacity of Sinorhizobium (Ensifer) meliloti strains detected by phenotype microarray.Biondi EG, Tatti E, Comparini D, Giuntini E, Mocali S, Giovannetti L, Bazzicalupo M, Mengoni A, Viti C Department of Evolutionary Biology, University of Florence, via Romana, 17, Florence, Italy; Department of Agricultural Biotechnology, Section of Microbiology, University of Florence, Piazzale delle Cascine 24, I-50144, Florence, Italy; Department of Biology (Area 3), University of York, PO Box 373, York YO10 5YW, UK; C.R.A. - Centro di Ricerca per lo Studio delle Relazioni tra Pianta e Suolo, Via della Navicella, 2-4, 00184, Rome, Italy. Sinorhizobium meliloti is a soil bacterium that fixes atmospheric nitrogen in plant roots. The high genetic diversity of its natural populations has been the subject of extensive analysis. Recent genomic studies on several isolates revealed a high content of variable genes suggesting a corresponding large phenotypic differentiation among strains of S. meliloti species. Here, using the Phenotype Microarray (PM) technique, hundreds of different growth conditions were tested in order to compare the metabolic capabilities of the laboratory reference strain Rm1021 with four natural S. meliloti isolates, previously analyzed by comparative genomic hybridization (CHG). Results of PM analysis showed that most phenotypic differences involved carbon source utilization and tolerance to osmolytes and pH, while fewer differences were scored for nitrogen, phosphorus and sulfur source utilization. Only the variability of the tested strain in tolerance to sodium nitrite and ammonium sulfate pH 8 was hypothesized to be associated with the genetic polymorphisms detected by CGH analysis. Also colony and cell morphology and ability to nodulate Medicago truncatula plants were compared revealing further phenotypic diversity. Overall, our results suggest that the study of functional (phenotypic) variability of S. meliloti populations is an important and complementary step in the investigation of genetic polymorphism of rhizobia, and may help to elucidate rhizobial evolutionary dynamics, including adaptation to diverse environments. Published 29 June 2009 in Appl Environ Microbiol. Articles on Microarrays published 29 June 2009: Serological microarray for detection of HSV-1, HSV-2, VZV, and CMV antibodies. J Virol Methods, 160(1): 167-71. The seroprevalence of human herpesviruses is high and reactivations occur frequently. A microarray was designed and tested for the detection of IgG and IgM antibodies for Puumala hantavirus (PUUV) and IgG antibodies against four herpesviruses. Initially, a microarray platform was set up using an unrelated in-house antigen, PUUV recombinant nucleocapsid protein, to optimize the protocol for the detection of antibodies. Detection of the four herpesviruses was set up in a microarray using the ... [Abstract] [Full-text] Sample size calculation for microarray experiments with blocked one-way design. BMC Bioinformatics, 10: 164. ABSTRACT: BACKGROUND: One of the main objectives of microarray analysis is to identify differentially expressed genes for different types of cells or treatments. Many statistical methods have been proposed to assess the treatment effects in microarray experiments. RESULTS: In this paper, we consider discovery of the genes that are differentially expressed among K (> 2) treatments when each set of K arrays consists of a block. In this case, the array data among K treatments tend to be ... [Abstract] [Full-text] Rapid haemagglutinin subtyping and pathotyping of avian influenza viruses by a DNA microarray. J Virol Methods, 160(1): 200-5. Rapid and reliable methods are fundamental for the comprehensive characterization of emerging and evolving avian influenza viruses. Although microarrays provide new possibilities with their parallel approach, their use in diagnostic laboratories is still limited due to economical and practical factors. An easy-to-use, low-cost microarray-based assay for haemagglutinin subtyping and pathotyping of avian influenza viruses and specific detection of highly pathogenic H5N1/Asia clade 2.2 is ... [Abstract] [Full-text] MicroRNAs (miRNAs) are very important regulators of biological processes such as development, cellular differentiation, and tumor generation. MiRNA microarray has been found to be a high throughput global analysis tool for detecting miRNA expression profiling, and miRNA expression profiling will facilitate the study of the biological function of miRNAs. In this report, we describe the miRNA expression level in rat cerebral cortex after traumatic brain injury using microarray method. We choose ... [Abstract] [Full-text] Best practices for hybridization design in two-colour microarray analysis. Trends Biotechnol, 27(7): 406-14. Two-colour microarrays are a popular platform of choice in gene expression studies. Because two different samples are hybridized on a single microarray, and several microarrays are usually needed in a given experiment, there are many possible ways to combine samples on different microarrays. The actual combination employed is commonly referred to as the 'hybridization design'. Different types of hybridization designs have been developed, all aimed at optimizing the experimental setup for the ... [Abstract] [Full-text] Error control variability in pathway-based microarray analysis. Bioinformatics. MOTIVATION: The decision to commit some or many false positives in practice rests with the investigator. Unfortunately, not all error control procedures perform the same. Our problem is to choose an error control procedure to determine a p-value threshold for identifying differentially expressed pathways in high-throughput gene expression studies. Pathway analysis involves fewer tests than differential gene expression analysis, on the order of a few hundred. We discuss and compare methods for ... [Abstract] [Full-text] Construction and evaluation of an ORFeome-based Brucella whole-genome DNA microarray. Microb Pathog. The genus Brucella contains bacteria producing a zoonosis of large sanitary and economical impact. The complete nucleotide sequence of eight Brucella isolates is currently available. This information can be used for high throughput approaches to the biology of this genus such as the construction of comprehensive collections of ORF clones or ORFeomes. The ORFeome of Brucella melitensis was a first contribution to this goal. Using the Brucella ORFeome as starting material we have amplified each ... [Abstract] [Full-text] Comparative DNA microarray analysis of human monocyte derived dendritic cells and MUTZ-3 cells exposed to the moderate skin sensitizer cinnamaldehyde. Toxicol Appl Pharmacol. The number of studies involved in the development of in vitro skin sensitization tests has increased since the adoption of the EU 7th amendment to the cosmetics directive proposing to ban animal testing for cosmetic ingredients by 2013. Several studies have recently demonstrated that sensitizers induce a relevant up-regulation of activation markers such as CD86, CD54, IL-8 or IL-1beta in human myeloid cell lines (e.g., U937, MUTZ-3, THP-1) or in human peripheral blood monocyte-derived dendritic ... [Abstract] [Full-text] © 2004-2009 Microarrays Research Today. All Rights Reserved. |
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