Visions of Performance in Exile: The Book, the Exhibition, and the Digital Archive

This article adopts the trope of exile in order to investigate the visual and spatial displacement experienced by the artwork of certain female artists when, in the passage from one technology to the next, disappear and re-appear technically and poetically, ‘surviving’ in new critical forms of reception and understanding. The photographs that Emily Jacir collected in Where We Come From (2001-2003) re-appear on the pages of the ‘book’ devoted to Seeking Palestine (2012); Shilpa Gupta’s digital installation I Have Many Dreams (2008) travels from Mumbai to Europe where it reaches the art exhibition DigitaLife-2012 held in Rome; Latifa Laâbissi’s choreography Loredreamsong (2011) transforms the ephemerality of its live event into its virtual documentation within the digital archive of re.act.feminism # 2 (2008-2013). The ‘book’, the ‘exhibition’ and the ‘digital archive’ become the new ‘homelands’, the new contexts of ‘survival’, of the artists’ originary performances. The Palestinian photographer Jacir, the Indian artist Gupta, and the Arab choreographer Laâbissi come from various geographical, political and cultural spaces, displaying, in their uses of languages and technologies, a critical art which proves the ability of women to survive beyond the difficulties of their ‘exiled’ existences by hoping, dreaming and resisting creatively

Speaking with...Nelisiwe Xaba. Re-Dancing a Body, Re-Imagining a Continent

In July 2010, Annalisa Piccirillo met the South African dancer and choreographer Nelisiwe Xaba at the 4th edition of Teatro Civile Festival in Monte Sant’Angelo (Foggia), where she was presenting one of her recent productions, The Venus, in its first Italian performance. The production combined two solo pieces inspired by the figure of Sarah Baartman, the “Hottentot Venus”. Piccirillo sees Xaba’s work as a choreographic and historical re-vision of the dark “body-continent”. Her conversation with Xaba includes reflections on the connection between the female dancing body and the African continent as a single entity, concealed, fixed and essentialized on the Eurocentric stage by the colonial gaze. In the provocative and political act of re-dancing the Venus’s body, Xaba’s artistic and personal experience intersects with and participates in the performative act of re-imagining Africa

Assessing the occurrence and transfer dynamics of ESBL/pAmpC-producing Escherichia coli across the broiler production pyramid

Extended-spectrum \u3b2-lactamase (ESBL)- and plasmid mediated AmpC-type cephalosporinase (pAmpC)-producing Escherichia coli (ESBL/pAmpC E. coli) in food-producing animals is a major public health concern. This study aimed at quantifying ESBL/pAmpC-E. coli occurrence and transfer in Italy's broiler production pyramid. Three production chains of an integrated broiler company were investigated. Cloacal swabs were taken from parent stock chickens and offspring broiler flocks in four fattening farms per chain. Carcasses from sampled broiler flocks were collected at slaughterhouse. Samples were processed on selective media, and E. coli colonies were screened for ESBL/pAmpC production. ESBL/pAmpC genes and E. coli phylogroups were determined by PCR and sequencing. Average pairwise overlap of ESBL/pAmpC E. coli gene and phylogroup occurrences between subsequent production stages was estimated using the proportional similarity index, modelling uncertainty in a Monte Carlo simulation setting. In total, 820 samples were processed, from which 513 ESBL/pAmpC E. coli isolates were obtained. We found a high prevalence (92.5%, 95%CI 72.1-98.3%) in day-old parent stock chicks, in which blaCMY-2 predominated; prevalence then dropped to 20% (12.9-29.6%) at laying phase. In fattening broilers, prevalence was 69.2% (53.6-81.3%) at the start of production, 54.2% (38.9-68.6%) at slaughter time, and 61.3% (48.1-72.9%) in carcasses. Significantly decreasing and increasing trends for respectively blaCMY-2 and blaCTX-M-1 gene occurrences were found across subsequent production stages. ESBL/pAmpC E. coli genetic background appeared complex and bla-gene/phylogroup associations indicated clonal and horizontal transmission. Modelling revealed that the average transfer of ESBL/pAmpC E. coli genes between subsequent production stages was 47.7% (42.3-53.4%). We concluded that ESBL/pAmpC E. coli in the broiler production pyramid is prevalent, with substantial transfer between subsequent production levels

Imipenem resistance in clinical Escherichia coli from Qom, Iran

OBJECTIVE: The emergence of metallo-\u3b2-lactamase-producing Enterobacteriaceae is a worldwide health concern. In this study, the first evaluation of MBL genes, bla IMP and bla VIM , in Escherichia coli resistant to imipenem isolated from urine and blood specimens in Qom, Iran is described. Three hundred urine and blood specimens were analysed to detect the presence of E. coli. Resistance to imipenem and other antimicrobials was determined by disk diffusion and MIC. MBL production was screened using CDDT. PCR was also carried out to determine the presence of bla IMP and bla VIM genes in imipenem-resistant isolates. RESULTS: In total, 160 E. coli isolates were collected from March to May 2016. According to disk diffusion, high-level of resistance (20%) to cefotaxime was observed, whereas the lowest (1%) was detected for tetracycline. In addition, five isolates showed resistance to imipenem with a MIC\u2009 65\u20094 \ub5g/mL. CDDT test confirmed that five isolates were MBL-producing strains, but no bla IMP and bla VIM genes were detected. Results of this study show a very low level of resistance to imipenem in our geographical area

Effects of the feeding system on performance and myopathy occurrence in two broiler chicken genotypes

To evaluate whether performance and myopathy occurrence differed according to genotype (Cobb 500 vs. Ross 308) and feeding system (AL: ad libitum vs. ER: early restricted from 13 to 23 d of age, vs. LR: late restricted from 27 to 37 d; restriction rate: 80% of ad libitum), 828 day- old male chicks were assigned to 6 groups (2 x 3 arrangement), housed in 36 pens, and controlled for: individual live weight (weekly) and pen feed intake (daily) until slaughter (48 d); white striping and wooden breast occurrence at slaughter. Individual data were analysed by PROC MIXED of SAS (fixed effects: feeding system, genotype, and interaction; random effect: pen); pen feed intake and myopathy occurrence were analysed by PROC GLM and CATMOD, respectively. The feeding system affected performance: at the end of the first period (1-22 d), ER chickens showed lower weight gain (40.5 g/d vs. 47.8 g/d and 48.0 g/d), feed intake (50.8 g/d vs 61.0 g/d and 60.2 g/d) and weight (903 g vs 1056 g and 1059 g) than AL and LR broilers (P<0.001); at the end of the second period (23-48 d), ER chickens showed higher weight gain (98.3 g/d vs 93.6 g/d and 90.2 g/d) and feed intake (182 g/d vs. 177 g/d and 171 g/d) compared to AL and LR chickens (P<0.001). Final live weight was the highest in AL group, intermediate in ER group, and the lowest in the LR one (3482 g, 3454 g, and 3399 g; P<0.01). Feed conversion in the whole period did not change with the feeding system. At gross examination, white striping occurrence changed from 77.8% to 67.1%, and 81.7% in AL, ER and LR broilers (p<0.10). Differences between genotypes were evident from the first day and, at the end of the trial, weight gain (74.3 g/d vs 70.1 g/d), feed intake (126 g/d vs 114 g/d), feed conversion (1.69 vs 1.64), and live weight (3548 g vs. 3342 g) were higher in the Ross than in the Cobb chickens (P<0.001). At slaughter, the rate of white-striped breasts was similar (on average 75.5%), but the occurrence of severely white-striped breasts was higher in the Ross than in the Cobb chickens (25.9% vs. 7.41%; P<0.001). Wooden breast occurrence (on average 5.1%) did not change with the feeding system or the genotype. In conclusion, under our conditions, a late feed restriction did not permit to recover performance at the end of the trial nor to control white striping occurrence. Moreover, the genotype affected growth rate and white striping degree: the highest the growth rate, the highest the severity of white striping

Functional crosstalk between dendritic cells and Foxp3+ regulatory T cells in the maintenance of immune tolerance

Peripheral immune tolerance requires a controlled balance between the maintenance of self-tolerance and the capacity to engage protective immune responses against pathogens. Dendritic cells (DCs) serve as sentinels of the immune system by sensing environmental and inflammatory signals, and play an essential role in the maintenance of immune tolerance. To achieve this, DC play a key role in dictating the outcome of immune responses by influencing the balance between inflammatory or Foxp3+ regulatory T (Treg) cell responses. At the heart of this immunological balance is a finely regulated DC and Treg cell crosstalk whereby Treg cells modulate DC phenotype and function, and DC drive the differentiation of Foxp3+ Treg cells in order to control immune responses. This review will focus on recent advances, which highlight the importance of this bidirectional DC and Treg cell crosstalk during the induction of tolerance and organ-specific autoimmunity. More specifically, we will discuss how Treg cells modulate DC function for the suppression of inflammatory responses and how DC subsets employ diverse mechanisms to drive differentiation of Treg cells. Finally, we will discuss the therapeutic potential of tolerogenic DCs for the induction of tolerance in autoimmune diseases

Post-Transcriptional and Translational Mechanisms of Regulation of Gene Expression in T Cell Subsets

The immune system is under strict regulatory control to ensure homeostasis of inflammatory responses, lying dormant when not needed but quick to act when called upon. Small changes in gene expression can lead to drastic changes in lineage commitment, cellular function, and immunity. Conventional assessment of these changes centered on the analysis of mRNA levels through a variety of methodologies, including microarrays. However, mRNA synthesis does not always correlate directly to protein synthesis and downstream functional activity. Work conducted in recent years has begun to shed light on the various post-transcriptional changes that occur in response to a dynamic external environment in which a given immune cell type encounters. In this chapter, we provide a critical review of key post-transcriptional and translational mechanisms of regulation of gene expression in the immune system, with an emphasis of these regulatory processes in various CD4+ T cell subsets and their related effector functions

A Radio Determination of the Time of the New Moon

The detection of the New Moon at sunset is of importance to communities based on the lunar calendar. This is traditionally undertaken with visual observations. We propose a radio method which allows a higher visibility of the Moon relative to the Sun and consequently gives us the ability to detect the Moon much closer to the Sun than is the case of visual observation. We first compare the relative brightness of the Moon and Sun over a range of possible frequencies and find the range 5--100\,GHz to be suitable. The next consideration is the atmospheric absorption/emission due to water vapour and oxygen as a function of frequency. This is particularly important since the relevant observations are near the horizon. We show that a frequency of $\sim 10$ GHz is optimal for this programme. We have designed and constructed a telescope with a FWHM resolution of 0$^\circ{}\!\!$.6 and low sidelobes to demonstrate the potential of this approach. At the time of the 21 May 2012 New Moon the Sun/Moon brightness temperature ratio was $72.7 \pm 2.2$ in agreement with predictions from the literature when combined with the observed sunspot numbers for the day. The Moon would have been readily detectable at $\sim 2^{\circ}$ from the Sun. Our observations at 16\,hr\,36\,min UT indicated that the Moon would have been at closest approach to the Sun 16\,hr\,25\,min earlier; this was the annular solar eclipse of 00\,hr\,00\,min\,UT on 21 May 2012.Comment: 11 pages, 15 figures, accepted for publication in MNRA

IL-2 as a therapeutic target for the restoration of Foxp3+ regulatory T cell function in organ-specific autoimmunity: implications in pathophysiology and translation to human disease

Peripheral immune tolerance requires a finely controlled balance between tolerance to self-antigens and protective immunity against enteric and invading pathogens. Self-reactive T cells sometimes escape thymic clonal deletion, and can subsequently provoke autoimmune diseases such as type 1 diabetes (T1D) unless they are controlled by a network of tolerance mechanisms in the periphery, including CD4+ regulatory T cells (Treg) cells. CD4+ Treg cells are characterized by the constitutive expression of the IL-2Rα chain (CD25) and preferentially express the forkhead winged helix transcriptional regulator Foxp3. These cells have been shown to possess immunosuppressive properties towards various immune cell subsets and their defects are thought to contribute to many autoimmune disorders. Strong evidence shows that IL-2 is one of the important stimulatory signals for the development, function and fitness of Treg cells. The non-obese diabetic (NOD) mouse model, a prototypic model of spontaneous autoimmunity, mimics many features of human T1 D. Using this model, the contribution of the IL-2-IL-2R pathway to the development of T1 D and other autoimmune disorders has been extensively studied. In the past years, strong genetic and molecular evidence has indicated an essential role for the IL-2/IL-2R pathway in autoimmune disorders. Thus, the major role of IL-2 is to maintain immune tolerance by promoting Treg cell development, functional fitness and stability. Here we first summarize the genetic and experimental evidence demonstrating a role for IL-2 in autoimmunity, mainly through the study of the NOD mouse model, and analyze the cellular and molecular mechanisms of its action on Treg cells. We then move on to describe how this data can be translated to applications for human autoimmune diseases by using IL-2 as a therapeutic agent to restore Treg cell fitness, numbers and functions