128 research outputs found
The circumburst environment of a FRED GRB: study of the prompt emission and X-ray/optical afterglow of GRB 051111
We report a multi-wavelength analysis of the prompt emission and early
afterglow of GRB051111 and discuss its properties in the context of current
fireball models. The detection of GRB051111 by the Burst Alert Telescope
on-board Swift triggered early BVRi' observations with the 2-m robotic Faulkes
Telescope North in Hawaii, as well as X-ray observations with the Swift X-Ray
Telescope. The prompt gamma-ray emission shows a classical FRED profile. The
optical afterglow light curves are fitted with a broken power law, with
alpha_1=0.35 to alpha_2=1.35 and a break time around 12 minutes after the GRB.
Although contemporaneous X-ray observations were not taken, a power law
connection between the gamma-ray tail of the FRED temporal profile and the late
XRT flux decay is feasible. Alternatively, if the X-ray afterglow tracks the
optical decay, this would represent one of the first GRBs for which the
canonical steep-shallow-normal decay typical of early X-ray afterglows has been
monitored optically. We present a detailed analysis of the intrinsic
extinction, elemental abundances and spectral energy distribution. From the
absorption measured in the low X-ray band we find possible evidence for an
overabundance of some alpha elements such as oxygen, [O/Zn]=0.7+/-0.3, or,
alternatively, for a significant presence of molecular gas. The IR-to-X-ray
Spectral Energy Distribution measured at 80 minutes after the burst is
consistent with the cooling break lying between the optical and X-ray bands.
Extensive modelling of the intrinsic extinction suggests dust with big grains
or grey extinction profiles. The early optical break is due either to an energy
injection episode or, less probably, to a stratified wind environment for the
circumburst medium.Comment: accepted to A&A on Nov. 10 (14 pages, 8 figures
Silver sulfadiazine eradicates antibiotic-tolerant Staphylococcus aureus and Pseudomonas aeruginosa biofilms in patients with infected diabetic foot ulcers
Infections are among the most frequent and challenging events in diabetic foot ulcers (DFUs). Pathogenic bacteria growing in biofilms within host tissue are highly tolerant to environmental and chemical agents, including antibiotics. The present study was aimed at assessing the use of silver sulfadiazine (SSD) for wound healing and infection control in 16 patients with DFUs harboring biofilm-growing Staphylococcus aureus and Pseudomonas aeruginosa. All patients received a treatment based on a dressing protocol including disinfection, cleansing, application of SSD, and application of nonadherent gauze, followed by sterile gauze and tibio-breech bandage, in preparation for toilet surgery after 30 days of treatment. Clinical parameters were analyzed by the T.I.M.E. classification system. In addition, the activity of SSD against biofilm-growing S. aureus and P. aeruginosa isolates was assessed in vitro. A total of 16 patients with S. aureus and P. aeruginosa infected DFUs were included in the study. Clinical data showed a statistically significant (p < 0.002) improvement of patients’ DFUs after 30 days of treatment with SSD with significant amelioration of all the parameters analyzed. Notably, after 30 days of treatment, resolution of infection was observed in all DFUs. In vitro analysis showed that both S. aureus and P. aeruginosa isolates developed complex and highly structured biofilms. Antibiotic susceptibility profiles indicated that biofilm cultures were significantly (p ≤ 0.002) more tolerant to all tested antimicrobials than their planktonic counterparts. However, SSD was found to be effective against fully developed biofilms of both S. aureus and P. aeruginosa at concentrations below those normally used in clinical preparations (10 mg/mL). These results strongly suggest that the topical administration of SSD may represent an effective alternative to conventional antibiotics for the successful treatment of DFUs infected by biofilm-growing S. aureus and P. aeruginosa
Paraoxonase-1 is related to inflammation, fibrosis and PPAR delta in experimental liver disease
<p>Abstract</p> <p>Background</p> <p>Paraoxonase-1 (PON1) is an antioxidant enzyme synthesized by the liver. It protects against liver impairment and attenuates the production of the pro-inflammatory monocyte chemoattractant protein-1 (MCP-1). We investigated the relationships between hepatic PON1 and MCP-1 expression in rats with liver disease and explored the possible molecular mechanisms involved.</p> <p>Methods</p> <p>CCl<sub>4 </sub>was administered for up to 12 weeks to induce liver damage. Serum and hepatic levels of PON1 and MCP-1, their gene and protein expression, nuclear transcription factors, and histological and biochemical markers of liver impairment were measured.</p> <p>Results</p> <p>High levels of PON1 and MCP-1 expression were observed at 12<sup>th </sup>week in the hepatocytes surrounding the fibrous septa and inflammatory areas. CCl<sub>4</sub>-administered rats had an increased hepatic PON1 concentration that was related to decreased gene transcription and inhibited protein degradation. Decreased PON1 gene transcription was associated with PPARδ expression. These changes were accompanied by increased hepatic MCP-1 concentration and gene expression. There were significant direct relationships between hepatic PON1 and MCP-1 concentrations (P = 0.005) and between PON1 and the amount of activated stellate cells (P = 0.001).</p> <p>Conclusion</p> <p>Our results from this experimental model suggest a hepato-protective role for PON1 against inflammation, fibrosis and liver disease mediated by MCP-1.</p
GRB 070724B: the first gamma ray burst localized by SuperAGILE and its Swift X-ray afterglow
GRB 070724B is the first gamma ray burst localized by SuperAGILE, the hard X-ray monitor aboard the AGILE satellite. The coordinates of the event were published similar to 19 h after the trigger. The Swift X-Ray Telescope pointed at the SuperAGILE location and detected the X-ray afterglow inside the SuperAGILE error circle. The AGILE gamma-ray Tracker and Minicalorimeter did not detect any significant gamma ray emission associated with GRB 070724B in the MeV and GeV range, neither prompt nor delayed. Searches for the optical afterglow were performed by the Swift UVOT and the Palomar automated 60-inch telescopes, resulting in no significant detection. Similarly, the Very Large Array did not detect any radio afterglow. This is the first GRB event associated with an X-ray afterglow with a firm upper limit in the 100 MeV-30 GeV energy range
A Novel Obligate Intracellular Gamma-Proteobacterium Associated with Ixodid Ticks, Diplorickettsia massiliensis, Gen. Nov., Sp. Nov
Background: Obligate intracellular bacteria of arthropods often exhibit a significant role in either human health or arthropod ecology. Methodology/Principal Findings: An obligate intracellular gamma-proteobacterium was isolated from the actively questing hard tick Ixodes ricinus using mammalian and amphibian cell lines. Transmission electron microscopy revealed a unique morphology of the bacterium, including intravacuolar localization of bacteria grouped predominantly in pairs and internal structures composed of electron-dense crystal-like structures and regular multilayer sheath-like structures. The isolate 20B was characterized to determine its taxonomic position using a polyphasic approach. Comparative 16S rRNA gene sequence analysis showed that this strain belongs to the family Coxiellaceae, order Legionellales of Gamma-proteobacteria, and the closest relatives are different Rickettsiella spp. The level of 16S rRNA gene sequence similarity between strain 20B and other recognized species of the family was below 94.5%. Partial sequences of the rpoB, parC and ftsY genes confirmed the phylogenetic position of the new isolate. The G+C content estimated on the basis of whole genome analysis of strain 20B was 37.88%. On the basis of its phenotypic and genotypic properties, together with phylogenetic distinctiveness, we propose that strain 20B to be classified in the new genus Diplorickettsia as the type strain of a novel species named Diplorickettsia massiliensis sp. nov. Conclusions/Significance: Considering the source of its isolation (hard tick, often biting humans) the role of this bacterium in the pathology of humans, animals and ticks should be further investigated
Variations of Plasmid Content in Rickettsia felis
Background: Since its first detection, characterization of R. felis has been a matter of debate, mostly due to the contamination of an initial R. felis culture by R. typhi. However, the first stable culture of R. felis allowed its precise phenotypic and genotypic characterization, and demonstrated that this species belonged to the spotted fever group rickettsiae. Later, its genome sequence revealed the presence of two forms of the same plasmid, physically confirmed by biological data. In a recent article, Gillespie et al. ( PLoS One. 2007; 2( 3): e266.) used a bioinformatic approach to refute the presence of the second plasmid form, and proposed the creation of a specific phylogenetic group for R. felis. Methodology/ Principal Findings: In the present report, we, and five independent international laboratories confirmed unambiguously by PCR the presence of two plasmid forms in R. felis strain URRWXCal(2)(T), but observed that the plasmid content of this species, from none to 2 plasmid forms, may depend on the culture passage history of the studied strain. We also demonstrated that R. felis does not cultivate in Vero cells at 37 degrees C but generates plaques at 30 degrees C. Finally, using a phylogenetic study based on 667 concatenated core genes, we demonstrated the position of R. felis within the spotted fever group. Significance: We demonstrated that R. felis, which unambiguously belongs to the spotted fever group rickettsiae, may contain up to two plasmid forms but this plasmid content is unstable
Metagenomic Profile of the Bacterial Communities Associated with Ixodes ricinus Ticks
Assessment of the microbial diversity residing in arthropod vectors of medical importance is crucial for monitoring endemic infections, for surveillance of newly emerging zoonotic pathogens, and for unraveling the associated bacteria within its host. The tick Ixodes ricinus is recognized as the primary European vector of disease-causing bacteria in humans. Despite I. ricinus being of great public health relevance, its microbial communities remain largely unexplored to date. Here we evaluate the pathogen-load and the microbiome in single adult I. ricinus by using 454- and Illumina-based metagenomic approaches. Genomic DNA-derived sequences were taxonomically profiled using a computational approach based on the BWA algorithm, allowing for the identification of known tick-borne pathogens at the strain level and the putative tick core microbiome. Additionally, we assessed and compared the bacterial taxonomic profile in nymphal and adult I. ricinus pools collected from two distinct geographic regions in Northern Italy by means of V6-16S rRNA amplicon pyrosequencing and community based ecological analysis. A total of 108 genera belonging to representatives of all bacterial phyla were detected and a rapid qualitative assessment for pathogenic bacteria, such as Borrelia, Rickettsia and Candidatus Neoehrlichia, and for other bacteria with mutualistic relationship or undetermined function, such as Wolbachia and Rickettsiella, was possible. Interestingly, the ecological analysis revealed that the bacterial community structure differed between the examined geographic regions and tick life stages. This finding suggests that the environmental context (abiotic and biotic factors) and host-selection behaviors affect their microbiome
Swift observations of the prompt X-ray emission and afterglow from GRB050126 and GRB050219A
We report on the temporal and spectral characteristics of the early X-ray
emission from the Gamma Ray Bursts GRB050126 and GRB050219A as observed by
Swift. The X-ray light-curves of these 2 bursts both show remarkably steep
early decays (F(t)\propto t^{-3}), breaking to flatter slopes on timescales of
a few hundred seconds. For GRB050126 the burst shows no evidence of spectral
evolution in the 20-150 keV band, and the spectral index of the gamma-ray and
X-ray afterglows are significantly different suggesting a separate origin. By
contrast the BAT spectrum of GRB050219A displays significant spectral
evolution, becoming softer at later times, with Gamma evolving toward the XRT
photon index seen in the early X-ray afterglow phase. For both bursts, the
0.2-10 keV spectral index pre- and post-break in the X-ray decay light-curve
are consistent with no spectral evolution. We suggest that the steep early
decline in the X-ray decay light-curve is either the curvature tail of the
prompt emission; X-ray flaring activity; or external forward shock emission
from a jet with high density regions of small angular size (> Gamma^{-1}). The
late slope we associate with the forward external shock.Comment: 13 pages, 12 figures, accepted for publication in Astronomy &
Astrophysic
Revolutionizing Clinical Microbiology Laboratory Organization in Hospitals with In Situ Point-of-Care
BACKGROUND: Clinical microbiology may direct decisions regarding hospitalization, isolation and anti-infective therapy, but it is not effective at the time of early care. Point-of-care (POC) tests have been developed for this purpose. METHODS AND FINDINGS: One pilot POC-lab was located close to the core laboratory and emergency ward to test the proof of concept. A second POC-lab was located inside the emergency ward of a distant hospital without a microbiology laboratory. Twenty-three molecular and immuno-detection tests, which were technically undemanding, were progressively implemented, with results obtained in less than four hours. From 2008 to 2010, 51,179 tests yielded 6,244 diagnoses. The second POC-lab detected contagious pathogens in 982 patients who benefited from targeted isolation measures, including those undertaken during the influenza outbreak. POC tests prevented unnecessary treatment of patients with non-streptococcal tonsillitis (n = 1,844) and pregnant women negative for Streptococcus agalactiae carriage (n = 763). The cerebrospinal fluid culture remained sterile in 50% of the 49 patients with bacterial meningitis, therefore antibiotic treatment was guided by the molecular tests performed in the POC-labs. With regard to enterovirus meningitis, the mean length-of-stay of infected patients over 15 years old significantly decreased from 2008 to 2010 compared with 2005 when the POC was not in place (1.43±1.09 versus 2.91±2.31 days; p = 0.0009). Altogether, patients who received POC tests were immediately discharged nearly thrice as often as patients who underwent a conventional diagnostic procedure. CONCLUSIONS: The on-site POC-lab met physicians' needs and influenced the management of 8% of the patients that presented to emergency wards. This strategy might represent a major evolution of decision-making regarding the management of infectious diseases and patient care
IL-1β, IL-6, and RANTES as Biomarkers of Chikungunya Severity
Little is known about the immunopathogenesis of Chikungunya virus. Circulating levels of immune mediators and growth factors were analyzed from patients infected during the first Singaporean Chikungunya fever outbreak in early 2008 to establish biomarkers associated with infection and/or disease severity.Adult patients with laboratory-confirmed Chikungunya fever infection, who were referred to the Communicable Disease Centre/Tan Tock Seng Hospital during the period from January to February 2008, were included in this retrospective study. Plasma fractions were analyzed using a multiplex-microbead immunoassay. Among the patients, the most common clinical features were fever (100%), arthralgia (90%), rash (50%) and conjunctivitis (40%). Profiles of 30 cytokines, chemokines, and growth factors were able to discriminate the clinical forms of Chikungunya from healthy controls, with patients classified as non-severe and severe disease. Levels of 8 plasma cytokines and 4 growth factors were significantly elevated. Statistical analysis showed that an increase in IL-1beta, IL-6 and a decrease in RANTES were associated with disease severity.This is the first comprehensive report on the production of cytokines, chemokines, and growth factors during acute Chikungunya virus infection. Using these biomarkers, we were able to distinguish between mild disease and more severe forms of Chikungunya fever, thus enabling the identification of patients with poor prognosis and monitoring of the disease
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