ABSTRACT
Etruria contained one of the great early urban civilisations in the Italian peninsula during the first millennium BC, much studied from a cultural, humanities-based, perspective, but relatively little with scientific data, and rarely in combination. We have addressed the unusual location of twenty inhumations found in the sacred heart of the Etruscan city of Tarquinia, focusing on six of these as illustrative, contrasting with the typical contemporary cremations found in cemeteries on the edge of the city. The cultural evidence suggests that the six skeletons were also distinctive in their ritualization and memorialisation. Focusing on the six, as a representative sample, the scientific evidence of osteoarchaeology, isotopic compositions, and ancient DNA has established that these appear to show mobility, diversity and violence through an integrated bioarchaeological approach. The combination of multiple lines of evidence makes major strides towards a deeper understanding of the role of these extraordinary individuals in the life of the early city of Etruria.
Subject(s)
Archaeology , Italy , Humans , History, Ancient , Male , DNA, Ancient/analysis , FemaleABSTRACT
In this study, blood and plasma of grey partridges (Perdix perdix) were analyzed to assess their potential contamination by plant protection products (PPP) and especially pesticide compounds. The group of pesticides selected is composed of a huge variety of compounds. Therefore, in this study, two methods were optimized and validated to analyze 104 compounds including herbicides, insecticides, fungicides and photoprotectors or synergists. Various extraction methods found in the literature were compared and adapted for the extraction of pesticides from blood and plasma. After extraction, samples were concentrated then injected for quantification simultaneously in LC-MS/MS and ATD-GC-MS/MS with an automatic thermal desorption step (ATD). Both LC-MS/MS and ATD-GC-MS/MS analyses were performed using the MRM mode with 2 mass transitions for each compound.The two analytical methods achieved a good linearity for the calibration responses in plasma and blood. Methods allowed sensitive detection and quantification in complex biological matrices such as plasma and blood in both LC and GC. For plasma samples and considering all 104 compounds of the study, the average LOD was 0.005 ng mg-1 in LC-MS/MS and 0.035 ng mg-1 in ATD-GC-MS/MS and the average LOQ was 0.017 ng mg-1 and 0.116 ng mg-1 in LC-MS/MS and ATD-GC-MS/MS respectively. Accordingly, the average LOD for blood samples was 0.011 ng mg-1 in LC and 0.028 ng mg-1 in GC whereas the average LOQ was 0.038 ng mg-1 and 0.094 ng mg-1 in LC-MS/MS and ATD-GC-MS/MS respectively. Those analytical methods were then successfully applied to 70 blood samples and 35 plasma samples.
Subject(s)
Galliformes , Pesticide Residues , Pesticides , Animals , Pesticides/analysis , Tandem Mass Spectrometry/methods , Chromatography, Liquid/methods , Pesticide Residues/analysisABSTRACT
Although Glyphosate-based herbicides are often marketed as environmentally friendly and easily biodegradable, its bioavailability and risks to wildlife raise significant concerns. Among non-target organisms, earthworms which live in close contact with the soil can be directly exposed to pesticides and harmed. We investigated soil contamination and the exposure of earthworms to glyphosate, its metabolite AMPA, and glufosinate in an arable landscape in France, both in treated (i.e. temporary grasslands and cereal fields under conventional farming), and nontreated habitats (i.e. hedgerows, permanent grasslands and cereal fields under organic farming) (n = 120 sampling sites in total). Glyphosate, AMPA and glufosinate were detected in 88%, 58% and 35% of the soil samples, and in 74%, 38% and 12% of the earthworm samples, respectively. For both glyphosate and AMPA, concentrations in soils were at least 10 times lower than predicted environmental concentrations. However, the maximum glyphosate soil concentration measured (i.e., 0.598 mg kg-1) was only 2 to 3 times lower than the concentrations revealed to affect earthworms (survival and avoidance) in the literature. These compounds were found both in conventional and organic farming fields, thus supporting a recent study, and for the first time they were detected in hedgerows and grasslands. However, glyphosate and AMPA were more frequently detected in soils from cereal fields and hedgerows than in grasslands, and median concentrations measured in soils from cereal fields were significantly higher than in the two other habitats. Bioaccumulation of glyphosate and AMPA in earthworms was higher than expected according to the properties of the molecules. Our findings raised issues about the high occurrence of glyphosate and AMPA in soils from cropped and more natural areas in arable landscapes. They also highlight the potential for transfer of these molecules in terrestrial food webs as earthworms are prey for numerous animals.
Subject(s)
Herbicides , Oligochaeta , Soil Pollutants , Aminobutyrates , Animals , Glycine/analogs & derivatives , Herbicides/analysis , Herbicides/toxicity , Soil , Soil Pollutants/analysis , alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid , GlyphosateABSTRACT
More than 35% of lung adenocarcinoma patients have bone metastases at diagnosis and have a poor survival. Periostin, a carboxylated matrix protein, mediates lung cancer cell dissemination by promoting epithelial-mesenchymal transition, and is involved in bone response to mechanical stress and bone formation regulation. This suggests that periostin may be used as a biomarker to predict survival in lung cancer patients. Serum periostin was assessed at diagnosis in a prospective cohort of 133 patients with lung adenocarcinoma of all stages. Patients were divided into localized and bone metastatic groups. Both groups were matched to healthy controls. Survival analysis and Cox proportional hazards models were conducted in the total population and in bone metastatic group. The median serum periostin level was higher in bone metastatic (nâ¯=â¯67; median: 1752â¯pmol/L) than in the localized group (nâ¯=â¯66; 861â¯pmol/L; pâ¯<â¯0.0001). Patients with high periostin (>median) had a poorer overall survival in the whole population (33.3â¯weeks vs. NR; pâ¯<â¯0.0001) and the bone metastatic group (24.4 vs. 66.1â¯weeks; pâ¯<â¯0.001). In multivariate analysis, patients with high periostin had increased risk of death (HRâ¯=â¯2.09, 95%CI [1.06-4.13]; pâ¯=â¯0.03). This was also found in the bone metastatic group (HRâ¯=â¯3.62, 95%CI [1.74-7.52]; pâ¯=â¯0.0005). Immunohistochemistry on bone metastasis biopsies showed periostin expression in the bone matrix and nuclear and cytoplasmic staining in cancer cells. Serum periostin was an independent survival biomarker in all-stage and in bone metastatic lung adenocarcinoma patients. IHC data suggest that periostin might be induced in cancer cells in bone metastatic niche in addition to bone microenvironment expression.
ABSTRACT
A number of in vitro test methods using Reconstructed human Tissues (RhT) are regulatory accepted for evaluation of skin corrosion/irritation. In such methods, test chemical corrosion/irritation potential is determined by measuring tissue viability using the photometric MTT-reduction assay. A known limitation of this assay is possible interference of strongly coloured test chemicals with measurement of formazan by absorbance (OD). To address this, Cosmetics Europe evaluated use of HPLC/UPLC-spectrophotometry as an alternative formazan measurement system. Using the approach recommended by the FDA guidance for validation of bio-analytical methods, three independent laboratories established and qualified their HPLC/UPLC-spectrophotometry systems to reproducibly measure formazan from tissue extracts. Up to 26 chemicals were then tested in RhT test systems for eye/skin irritation and skin corrosion. Results support that: (1) HPLC/UPLC-spectrophotometry formazan measurement is highly reproducible; (2) formazan measurement by HPLC/UPLC-spectrophotometry and OD gave almost identical tissue viabilities for test chemicals not exhibiting colour interference nor direct MTT reduction; (3) independent of the test system used, HPLC/UPLC-spectrophotometry can measure formazan for strongly coloured test chemicals when this is not possible by absorbance only. It is therefore recommended that HPLC/UPLC-spectrophotometry to measure formazan be included in the procedures of in vitro RhT-based test methods, irrespective of the test system used and the toxicity endpoint evaluated to extend the applicability of these test methods to strongly coloured chemicals.
Subject(s)
Coloring Agents/toxicity , Formazans/toxicity , Skin Irritancy Tests/methods , Animal Testing Alternatives , Chromatography, High Pressure Liquid , Cosmetics/toxicity , Eye Diseases/chemically induced , Humans , Irritants/toxicity , Reproducibility of Results , Skin Diseases/chemically induced , Skin Diseases/pathology , Spectrophotometry, Ultraviolet , Tetrazolium Salts/chemistry , Thiazoles/chemistryABSTRACT
OBJECTIVE: To evaluate the validity of the common tangent and conventional tibial plateau angle methods for measuring the patellar tendon angle (PTA) in dogs. METHODS: Radiographs of cadaveric stifles (n = 20) placed at 135° in true lateral position were obtained to measure the PTA with both methods. A Kirschner wire was inserted perpendicularly to the patellar tendon at its insertion on the tibia and the stifle was dissected. Two Kirschner wires were then used to identify the anatomical landmarks of the tibial plateau. A digital image was obtained of the proximal tibia in true lateral position. Six blinded observers measured each PTA digitally while the anatomical PTA was determined by an independent blinded observer from the angle between the line representing the tibial plateau and the Kirschner wire representing the perpendicular to the patellar tendon. The agreement between the methods was determined statistically from an intraclass correlation coefficient (ICC). RESULTS: The global ICC for the common tangent method (0.44) and for the conventional method (0.4) indicated that their overall validity is poor. The measurements obtained by common tangentmethod and conventional method were respectively below and above the anatomical measurements. The reproducibility of the PTA measurements based on images of the dissected stifles was very good. CLINICAL SIGNIFICANCE: Both the common tangent and conventional methods show poor concordance with the anatomical measurement of PTA. Further studies are needed to determine if errors in measurements affect the clinical outcome.
Subject(s)
Dogs , Patellar Ligament/diagnostic imaging , Stifle/anatomy & histology , Animals , Cadaver , Radiography , Stifle/diagnostic imaging , Tibia/diagnostic imagingABSTRACT
This study aimed at: (a) providing information on the occurrence and concentration ranges in urban stormwater for a wide array of pollutants (n = 77); (b) assessing whether despite the differences between various catchments (land use, climatic conditions, etc.), the trends in terms of contamination level are similar; and (c) analyzing the contribution of total atmospheric fallout (TAF) with respect to sources endogenous to this contamination. The studied contaminants include conventional stormwater contaminants (polycyclic aromatic hydrocarbons (PAHs), Zn, Cu, Pb, etc.), in addition to poorly or undocumented pollutants such as nonylphenol and octylphenol ethoxylates (NPnEO and OPnEO), bisphenol A (BPA), polybrominated diphenyl ethers (PBDEs), a wide variety of pesticides, and various metals of relevance (As, Ti, Sr, V). Sampling and analysis were performed using homogeneous methods on three urban catchments with different land use patterns located in three distinct French towns. For many of these pollutants, the results do not allow highlighting a significant difference in stormwater quality at the scale of the three urban catchments considered. Significant differences were, however, observed for several metals (As, Cr, Cu, Ni, Sr and Zn), PAHs, and PBDEs, though this assessment would need to be confirmed by further experiments. The pollutant distributions between dissolved and particulate phases were found to be similar across the three experimental sites, thus suggesting no site dependence. Lastly, the contributions of TAF to stormwater contamination for micropollutants were quite low. This finding held true not only for PAHs, as previously demonstrated in the literature, but also for a broader range of molecules such as BPA, NPnEO, OPnEO, and PBDEs, whose high local production is correlated with the leaching of urban surfaces, buildings, and vehicles.
Subject(s)
Water Pollutants, Chemical/analysis , Atmosphere/chemistry , Benzhydryl Compounds/analysis , Cities , Environmental Monitoring/methods , France , Metals/analysis , Phenols/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Rain/chemistry , Water Pollution, Chemical/statistics & numerical dataABSTRACT
OBJECTIVES: To (i) compare agreement of the common tangent (CT) and tibial plateau angle (TP) methods in terms of measuring the patellar tendon angle (PTA) and required advancement and (ii) determine the intra- and inter-observer reliability of observers who measured PTA and the advancement. METHODS: Six observers were divided into three groups based on their level of experience. They measured the PTA and the required advancement on 43 radiographic images of the tibiae of dogs affected by cranial cruciate ligament rupture. Each observer repeated the measurements three times with each method. The inter-technique (interT), intra-observer (intraO), and interobserver (interO) reliabilities were evaluated, assessed by calculating the intraclass correlation coefficient (ICC), and represented by Jones plots. RESULTS: The agreement between PTA-CT and PTA-TP was low (the ICC interT values ranged from 0.11 to 0.4). The PTA-CT was associated with moderate intra-observer reliability (ICC intraO, CT = 0.61) and poor interobserver reliability (ICC interO, CT = 0.33). The PTA-TP was associated with good intra-observer reliability (ICC intraO, TP = 0.75) and moderate interobserver reliability (ICC interO, TP = 0.59). Interobserver reliability did not depend on the level of experience. The advancement measurements were associated with reliability results similar to those obtained for PTA. Jones' plots showed that the CT method consistently yielded lower PTA and advancement values than the TP method. CONCLUSION: Given its poor reliability, the CT method is not recommended.
Subject(s)
Anterior Cruciate Ligament/diagnostic imaging , Dogs , Patellar Ligament/diagnostic imaging , Rupture/veterinary , Tibia/diagnostic imaging , Animals , Anterior Cruciate Ligament/pathology , Female , Male , Observer Variation , Patella , Patellar Ligament/anatomy & histology , Radiography , Rupture/pathology , Stifle/diagnostic imaging , Tibia/anatomy & histologyABSTRACT
OBJECTIVE: To determine association between computed tomography measurements of spinal cord compression and postoperative outcome. METHODS: A retrospective review of medical records of dogs presenting with intervertebral disease. Data were collected with a minimum of 2 years follow-up period. Computed tomography morphometric indices, particularly the ratio of spinal cord or herniated disc to vertebral canal dimensions, were obtained from survey and myelogram computed tomographic images. The pattern of disc disease was scored as single or continuous (multiple herniated discs), and was compared to postoperative outcome. RESULTS: Fifty-two dogs were included. There was no significant correlation between the degree of spinal cord compression and postoperative outcome. However, postoperative outcome differed significantly between dogs with single or continuous patterns of disc disease (P=0·001). Of those with single patterns, 75% had a postoperative outcome score greater than 75% while 75% of continuous pattern cases had scores lower than 83%. CLINICAL SIGNIFICANCE: Simple observation of the pattern of disc disease as revealed by computed tomography could be used as a prognostic indicator. The outcome tends to be better for single patterns of disc disease, whereas the outcome was poor for most cases with continuous patterns.
Subject(s)
Dog Diseases/diagnostic imaging , Intervertebral Disc Displacement/veterinary , Myelography/veterinary , Animals , Dog Diseases/diagnosis , Dog Diseases/surgery , Dogs , Female , Intervertebral Disc Displacement/diagnosis , Intervertebral Disc Displacement/diagnostic imaging , Intervertebral Disc Displacement/surgery , Lumbar Vertebrae/diagnostic imaging , Male , Thoracic Vertebrae/diagnostic imaging , Tomography, X-Ray Computed , Treatment OutcomeABSTRACT
Acute and different chronic ecotoxic effects of deltamethrin have been investigated on two strains (coming from two different laboratories) of Daphnia magna. The effective concentrations immobilizing 50% of daphnids (EC50s) after 24 h and 48 h were 9.40 and 0.32 µg L(-1), 8.86 and 0.63 µg L(-1) for first strain (strain 1) and second strain (strain 2), respectively. Thus, there was an increase of deltamethrin ecotoxicity with time of exposure as confirmed by chronic studies. After 21 days of exposure to deltamethrin, daphnids have showed significant effects on survival at deltamethrin concentrations of 0.16 µg L(-1) and 0.31 µg L(-1) for strains 1 and 2, respectively. Eleven other endpoints were examined: body length, population growth rate and various reproductive parameters (days to first brood, number of broods, number of cumulative molts and number of neonates), embryotoxicity and appearance of males. IC10 values related to the number of juveniles per live adult were 11 and 46 ng L(-1) for strains 1 and 2, respectively. Furthermore, an increase in embryo deformities was observed at the highest concentrations tested for both strains. Following deltamethrin exposure, undeveloped second antennae, curved or unextended shell spines, and curved post abdomen spines were observed in live neonates. The production of male juveniles was only registered with strain 1 at 0.16 µg L(-1). Results suggest that deltamethrin could act as an endocrine disruptor in D. magna as it interferes with sex determination and development abnormality but there is a difference in sensitivity between the two tested strains.
Subject(s)
Daphnia/drug effects , Daphnia/growth & development , Embryonic Development/drug effects , Insecticides/toxicity , Nitriles/toxicity , Pyrethrins/toxicity , Sex Differentiation/drug effects , Animals , Body Size/drug effects , Female , Inhibitory Concentration 50 , Male , Reproduction/drug effects , Sex Ratio , Species Specificity , Survival Analysis , Time FactorsABSTRACT
Surface runoff and spray drift represent a primary mode of pesticide mobilisation from agricultural land to ecosystem. Though pesticide drift has mainly been studied at small scale (<1 ha), pesticide transports by drift and runoff have rarely been compared in the same agricultural catchment. Here kresoxim methyl (KM) drift during foliar application was evaluated in a vineyard catchment (Rouffach, Alsace, France), and KM deposition on non-target surfaces was compared to KM runoff. KM was detected on 55% of the collectors and concentration reached 18% of the applied dose (i.e. 1.5 mg m(-2)). Our results indicated that KM soil deposition greatly varied in space and time. The total KM soil deposition in the vineyard plots was estimated by four different interpolation methods (arithmetic mean, Thiessen method, inverse weighting distance and ordinary kriging) and ranged between 53 g and 61 g (5.8 and 6.6% of the total mass applied). The amount of KM drifted on roads was 50 times larger than that in runoff water collected at the outlet of the catchment. Although KM application was carried out under regular operational and climatic conditions, its deposition on non-target surfaces may be significant and lead to pesticide runoff. These results can be anticipated as a starting point for assessing pesticide deposition during spray application and corresponding pesticide runoff in agricultural catchments.
Subject(s)
Environmental Monitoring , Pesticides/analysis , Phenylacetates/analysis , Soil/analysis , Vitis/growth & development , Water Pollutants, Chemical/analysis , Agriculture , Environmental Monitoring/methods , France , Methacrylates/analysis , Methacrylates/chemistry , Molecular Structure , Phenylacetates/chemistry , Strobilurins , Water Movements , Water Pollutants, Chemical/chemistry , WineABSTRACT
BACKGROUND: Liver and lung metastases are the predominant cause of colorectal cancer (CRC)-related mortality. Chemokine-receptor pairs have a critical role in determining the metastatic progression of tumours. Our hypothesis was that disruption of CXCR7/CXCR7 ligands axis could lead to a decrease in CRC metastases. METHODS: Primary tumours and metastatic tissues from patients with CRC were tested for the expression of CXCR7 and its ligands. Relevance of CXCR7/CXCR7 ligands for CRC metastasis was then investigated in mice using small pharmacological CXCR7 antagonists and CRC cell lines of human and murine origins, which - injected into mice - enable the development of lung and liver metastases. RESULTS: Following injection of CRC cells, mice treated daily with CXCR7 antagonists exhibited a significant reduction in lung metastases. However, CXCR7 antagonists failed to reduce the extent of liver metastasis. Moreover, there were subtle differences in the expression of CXCR7 and its ligands between lung and liver metastases. CONCLUSION: Our study suggests that the activation of CXCR7 on tumour blood vessels by its ligands may facilitate the progression of CRC within lung but not within liver. Moreover, we provide evidence that targeting the CXCR7 axis may be beneficial to limit metastasis from colon cancer within the lungs.
Subject(s)
Carcinoma/metabolism , Carcinoma/secondary , Colonic Neoplasms/metabolism , Colonic Neoplasms/pathology , Lung Neoplasms/metabolism , Lung Neoplasms/secondary , Receptors, CXCR/metabolism , Animals , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Chemokine CXCL12/metabolism , Disease Models, Animal , Disease Progression , Female , Gene Expression Regulation, Neoplastic , Humans , Immunohistochemistry , Interleukin-8/metabolism , Liver Neoplasms/metabolism , Liver Neoplasms/secondary , Mice , Mice, Inbred BALB C , Mice, SCID , Real-Time Polymerase Chain Reaction , Receptors, CXCR/antagonists & inhibitors , Vascular Endothelial Growth Factor A/metabolismABSTRACT
Liver and lung metastases are the predominant cause of colorectal cancer (CRC)-related mortality. Recent research has indicated that CXCR3/chemokines interactions that orchestrate haematopoetic cell movement are implicated in the metastatic process of malignant tumours, including that of CRC cells to lymph nodes. To date, however, the contribution of CXCR3 to liver and lung metastasis in CRC has not been addressed. To determine whether CXCR3 receptors regulate malignancy-related properties of CRC cells, we have used CXCR3-expressing CRC cell lines of human (HT29 cells) and murine (C26 cells) origins that enable the development of liver and lung metastases when injected into immunodeficient and immunocompetent mice, respectively, and assessed the effect of CXCR3 blockade using AMG487, a small molecular weight antagonist. In vitro, activation of CXCR3 on human and mouse CRC cells by its cognate ligands induced migratory and growth responses, both activities being abrogated by AMG487. In vivo, systemic CXCR3 antagonism by preventive or curative treatments with AMG487 markedly inhibited the implantation and the growth of human and mouse CRC cells within lung without affecting that in the liver. In addition, we measured increased levels of CXCR3 and ligands expression within lung nodules compared with liver tumours. Altogether, our findings indicate that activation of CXCR3 receptors by its cognate ligands facilitates the implantation and the progression of CRC cells within lung tissues and that inhibition of this axis decreases pulmonary metastasis of CRC in two murine tumour models.
Subject(s)
Colonic Neoplasms/metabolism , Colonic Neoplasms/pathology , Receptors, CXCR3/antagonists & inhibitors , Animals , Antineoplastic Agents/therapeutic use , Cell Line, Tumor , Cell Movement , Colonic Neoplasms/drug therapy , Humans , Ligands , Liver Neoplasms/drug therapy , Liver Neoplasms/metabolism , Liver Neoplasms/secondary , Lung Neoplasms/drug therapy , Lung Neoplasms/metabolism , Lung Neoplasms/secondary , Mice , Neoplasm Transplantation , Organ Specificity , Receptors, CXCR3/metabolism , Survival RateABSTRACT
UNLABELLED: Little information is available about the health risks associated with time spent in underground parking garages. The objective of this study was to determine whether it is possible to quantify the health risks associated with these garages without epidemiologic data on the subject. We followed the standard procedure for health risk assessment. We searched the literature for pollutant concentrations in the air samples of underground parking garages, the hazards associated with their inhalation, and their toxicological reference values. Conditions of occupational and user exposure were estimated by scenarios and taken into account to discuss toxicological reference values by modifying (with Haber's law) the adjustment factors for exposure frequency and duration. Risk quantification was possible for 39 pollutants. Acute exposures to CO and NO2 exceed toxicological reference values, as does chronic exposure to benzene for threshold effects. The risk of a carcinogenic effect associated with benzene may be greater than 10(-5). Excess exposure to air pollution indicators (PM and NO2) is also elevated, judging by the WHO Air Quality Guidelines, and also when comparing to levels with reported effects in epidemiologic studies. The risk associated with underground parking garages can be evaluated only in part. The information available is nonetheless sufficient to justify actions to reduce exposure. PRACTICAL IMPLICATIONS: The risks associated with exposure in underground parking garages cannot be thoroughly evaluated because of inadequate knowledge of exposures and of the toxicity of pollutants. The available knowledge is nonetheless sufficient to advise that risk management measures should be taken to reduce both acute and chronic exposures.
Subject(s)
Air Pollution, Indoor , Occupational Exposure/analysis , Parking Facilities , Humans , Risk AssessmentABSTRACT
A comprehensive Pb-Sr-Nd isotope and REE tracer study of atmospheric trace metal pollution by a steel plant situated to the north of the urban communities of Strasbourg (France) and Kehl (Germany) has been performed using tree barks as biomonitors. The 206Pb/207Pb and 208Pb/207Pb isotopic ratios of the steel plant's filter dust are similar to values found in dust of waste incinerators. The 87Sr/86Sr ratio is similar to present-day ratios of Phanerozoic or Precambrian granitic rocks. The 143Nd/144Nd isotopic composition is very low and corresponds to an (Nd) value of -17.5. Such a low value is characteristic of old Precambrian granitic rocks and banded iron formations. Thus, this low (Nd) value might point to the origin of the iron necessary for the steel production. The fact, that this isotopic composition does not occur in crustal rocks of Western Central Europe makes the Nd isotope ratio a powerful tool to trace steel plants atmospheric emissions. The rare earth element (REE) distribution pattern of the steel plant's filter dust shows very specific fractionations like La and Nd enrichments which are traceable in tree barks over a distance of 4 km. The Pb, Sr and Nd isotope ratios not only enable the steel plant's emissions to be traced in a north-easterly direction, along the principal wind pathway but also enables the interference of this emission at 4 km NE from the steel plant with another atmospheric component originating from the Strasbourg Rhine harbour to be identified.
Subject(s)
Air Pollutants/analysis , Dust/analysis , Environmental Monitoring/methods , Plant Bark/chemistry , Steel , Fagus , Fraxinus , Industrial Waste , Isotopes , Lead/analysis , Neodymium/analysis , Populus , Quercus , Radioisotopes/analysis , Strontium/analysisABSTRACT
The production of most factors involved in Bordetella pertussis virulence is controlled by a two-component regulatory system termed BvgA/S. In the Bvg+ phase virulence-activated genes (vags) are expressed, and virulence-repressed genes (vrgs) are down-regulated. The expression of these genes can also be modulated by MgSO(4) or nicotinic acid. In this study we used microarrays to analyse the influence of BvgA/S or modulation on the expression of nearly 200 selected genes. With the exception of one vrg, all previously known vags and vrgs were correctly assigned as such, and the microarray analyses identified several new vags and vrgs, including genes coding for putative autotransporters, two-component systems, extracellular sigma factors, the adenylate cyclase accessory genes cyaBDE, and two genes coding for components of a type III secretion system. For most of the new vrgs and vags the results of the microarray analyses were confirmed by RT-PCR analysis and/or lacZfusions. The degree of regulation and modulation varied between genes, and showed a continuum from strongly BvgA/S-activated genes to strongly BvgA/S-repressed genes. The microarray analyses also led to the identification of a subset of vags and vrgs that are differentially regulated and modulated by MgSO(4) or nicotinic acid, indicating that these genes may be targets for multiple regulatory circuits. For example, the expression of bilA, a gene predicted to encode an intimin-like protein, was found to be activated by BvgA/S and up-modulated by nicotinic acid. Furthermore, surprisingly, in the strain analysed here, which produces only type 2 fimbriae, the fim3 gene was identified as a vrg, while fim2 was confirmed to be a vag.
Subject(s)
Bordetella pertussis/pathogenicity , Virulence/genetics , Bordetella pertussis/genetics , Gene Expression Regulation, Bacterial , Kinetics , Oligonucleotide Array Sequence Analysis , RNA, Messenger/metabolism , Recombinant Fusion Proteins/metabolism , Reverse Transcriptase Polymerase Chain ReactionSubject(s)
Bacteremia/microbiology , Enterobacteriaceae Infections/microbiology , Providencia/pathogenicity , Adult , Bacteremia/drug therapy , Bacteremia/etiology , Ciprofloxacin/therapeutic use , Disease Susceptibility , Drug Resistance, Microbial , Drug Therapy, Combination/therapeutic use , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae Infections/etiology , Gentamicins/therapeutic use , Humans , Male , Multiple Sclerosis/complications , Ofloxacin/therapeutic use , Providencia/drug effects , Providencia/isolation & purification , Urinary Incontinence/etiology , Urinary Tract Infections/drug therapy , Urinary Tract Infections/etiologyABSTRACT
Despite increasing knowledge on the biology of Helicobacter pylori, little is known about the expression pattern of its genome during infection. While mouse models of infection have been widely used for the screening of protective antigens, the reliability of the mouse model for gene expression analysis has not been assessed. In an attempt to address this question, we have developed a quantitative reverse transcriptase PCR (RT-PCR) that allowed the detection of minute amounts of mRNA within the gastric mucosa. The expression of four genes, 16S rRNA, ureA (encoding urease A subunit), katA (catalase), and alpA (an adhesin), was monitored during the course of a 6-month infection of mice and in biopsy samples from of 15 infected humans. We found that the selected genes were all expressed within both mouse and human infected mucosae. Moreover, the relative abundance of transcripts was the same (16S rRNA > ureA > katA > alpA), in the two models. Finally, results obtained with the mouse model suggest a negative effect of bacterial burden on the number of transcripts of each gene expressed per CFU (P < 0.05 for 16S rRNA, alpA, and katA). Overall, this study demonstrates that real-time RT-PCR is a powerful tool for the detection and quantification of H. pylori gene expression within the gastric mucosa and strongly indicates that mice experimentally infected with H. pylori provide a valuable model for the analysis of bacterial gene expression during infection.
Subject(s)
Escherichia coli Proteins , Gastric Mucosa/microbiology , Gene Expression , Genes, Bacterial , Helicobacter Infections/microbiology , Helicobacter pylori/genetics , Animals , Bacterial Proteins/genetics , Catalase/genetics , Female , Gastric Mucosa/pathology , Gene Expression Profiling , Helicobacter Infections/pathology , Humans , Mice , RNA, Ribosomal, 16S , Reverse Transcriptase Polymerase Chain Reaction , Stomach/pathology , Time Factors , Transcription Factors/genetics , Transcription, GeneticABSTRACT
Fractalkine displays features that distinguishes it from the other chemokines. In particular, besides its chemoattractant action it promotes, under physiologic flow, the rapid capture and the firm adhesion of a subset of leukocytes or intervenes in the neuron/microglia interaction. This study verified that indeed the human monocytic MonoMac6 cell line adheres to fibronectin-coated filters in response to soluble fractalkine (s-FKN). s-FKN stimulates, with distinct time courses, extracellular signal-related kinases (ERK1 and ERK2) and stress-activated protein kinases (SAPK1/JNK1 and SAPK2/p38). Both p60 Src and p72 Syk were activated under s-FKN stimulation with a rapid kinetic profile compatible with a downstream regulation on the mitogen-activated protein kinase (MAPK) congeners. The use of specific tyrosine kinase inhibitors revealed that the ERK pathway is strictly controlled by Syk, whereas c-Src up-regulated the downstream SAPK2/p38. In contrast, the SAPK1/JNK1 pathway was not regulated by any of these nonreceptor tyrosine kinases. The s-FKN-mediated increased adherence of MonoMac6 cells was partially inhibited by SB202190, a broad SAPKs inhibitor, PD98059, an MEK inhibitor, LY294002, a phosphatidyl inositol 3-kinase inhibitor, and a pertussis toxin-sensitive G protein. These data highlight that the integration of a complex array of signal transduction pathways is necessary to complete the full s-FNK-dependent adherence of human monocytic cells to fibronectin. (Blood. 2001;97:2031-2037)
Subject(s)
Chemokines, CX3C , Chemokines, CXC/physiology , Membrane Proteins/physiology , Monocytes/drug effects , Receptors, Cytokine/physiology , Receptors, HIV/physiology , Signal Transduction/physiology , CX3C Chemokine Receptor 1 , Cell Adhesion/drug effects , Chemokine CX3CL1 , Cholera Toxin/pharmacology , Chromones/pharmacology , Enzyme Inhibitors/pharmacology , Enzyme Precursors/physiology , Fibronectins/metabolism , Flavonoids/pharmacology , GTP-Binding Proteins/drug effects , GTP-Binding Proteins/physiology , Humans , Imidazoles/pharmacology , Intracellular Signaling Peptides and Proteins , Mitogen-Activated Protein Kinase 1/physiology , Mitogen-Activated Protein Kinase 3 , Mitogen-Activated Protein Kinase 8 , Mitogen-Activated Protein Kinases/physiology , Monocytes/cytology , Morpholines/pharmacology , Pertussis Toxin , Phosphatidylinositol 3-Kinases/physiology , Phosphoinositide-3 Kinase Inhibitors , Protein-Tyrosine Kinases/physiology , Proto-Oncogene Proteins pp60(c-src)/physiology , Pyridines/pharmacology , Receptors, Cytokine/drug effects , Receptors, HIV/drug effects , Syk Kinase , Virulence Factors, Bordetella/pharmacology , p38 Mitogen-Activated Protein KinasesABSTRACT
Monocyte chemoattractant protein-1 (MCP-1) is a major chemoattractant for monocytes and T lymphocytes. The MonoMac6 cell line was used to examine MCP-1 receptor-mediated signal transduction events in relation to MCP-1-mediated monocytic transendothelial migration. MCP-1 stimulates, with distinct time courses, extracellular signal-related kinases (ERK1 and ERK2) and stress-activated protein kinases (SAPK1/JNK1 and SAPK2/p38). SAPK1/JNK1 activation was blocked by piceatannol, indicating that it is regulated by Syk kinase, whereas SAPK2/p38 activation was inhibited by PP2, revealing an upstream regulation by Src-like kinases. In contrast, ERK activation was insensitive to PP2 and piceatannol. Pertussis toxin, a blocker of Go/Gi proteins, abrogated MCP-1-induced ERK activation, but was without any effect on SAPK1/JNK1 and SAPK2/p38 activation. These results underscore the major implication of Go/Gi proteins and nonreceptor tyrosine kinases in the early MCP-1 signaling. Furthermore, MCP-1-mediated chemotaxis and transendothelial migration were significantly diminished by a high concentration of SB202190, a broad SAPK inhibitor, or by SB203580, a specific inhibitor of SAPK2/p38, and abolished by pertussis toxin treatment. Altogether, these data suggest that coordinated action of distinct signal pathways is required to produce a full response to MCP-1 in terms of monocytic locomotion.