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1.
Histopathology ; 85(4): 614-626, 2024 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-38859768

RESUMEN

AIMS: Molecular classification according to The Cancer Genome Atlas (TCGA) improves endometrial endometrioid carcinoma (EEC) prognostication and has specific treatment implications; however, original data were skewed towards low-grade and low-stage tumours. Herein, we molecularly classify EECs metastatic at the time of diagnosis or with subsequently documented recurrent/metastatic disease to examine correlation with clinical outcomes. METHODS: TCGA categories include POLE-mutated, microsatellite instability (MSI), p53 abnormal (p53 abnl) and no specific molecular profile (NSMP). POLE targeted sequencing at exons 9, 11, 13 and 14 and immunohistochemistry (IHC) for PMS2, MSH6 and p53 were performed to establish molecular classification. RESULTS: The distribution in our cohort of 141 EECs was similar to that generally reported in EEC, with nine POLE-mutated (6%), 45 MSI (32%), 16 p53 abnl (11%) and 71 NSMP (50%), with similar distributions between low- and high-stage cohorts. We demonstrate that when stratified by molecular subtype, disease-specific survival from the time of high-stage (stages III-IV) presentation or time of recurrence in low-stage (stages I-II) disease among metastatic and/or recurrent EEC is strongly associated with TCGA classification (high-stage P = 0.02, low-stage P = 0.017). Discordant molecular classification between primary and metastatic/recurrent tumours occurred in four of 105 (3.8%) patients, two related to PMS2/MSH6 IHC and two related to p53 IHC. CONCLUSIONS: We demonstrate that molecular classification is prognostically relevant not only at the time of diagnosis, but also at the time of recurrence and in the metastatic setting. Rare subclonal alterations occur and suggest a role for confirming TCGA classification in recurrent/metastatic tumours.


Asunto(s)
Carcinoma Endometrioide , Neoplasias Endometriales , Inestabilidad de Microsatélites , Recurrencia Local de Neoplasia , Humanos , Femenino , Neoplasias Endometriales/patología , Neoplasias Endometriales/genética , Neoplasias Endometriales/clasificación , Carcinoma Endometrioide/patología , Carcinoma Endometrioide/genética , Persona de Mediana Edad , Recurrencia Local de Neoplasia/patología , Pronóstico , Anciano , Biomarcadores de Tumor/genética , Biomarcadores de Tumor/metabolismo , Adulto , Anciano de 80 o más Años , Proteínas de Unión a Poli-ADP-Ribosa/genética , Mutación , Inmunohistoquímica , Estadificación de Neoplasias
2.
Stem Cells ; 40(8): 778-790, 2022 08 25.
Artículo en Inglés | MEDLINE | ID: mdl-35639980

RESUMEN

Cartilaginous airways of larger mammals and the mouse trachea contain at least 3 well-established stem cell compartments, including basal cells of the surface airway epithelium (SAE) and ductal and myoepithelial cells of the submucosal glands (SMG). Here we demonstrate that glandular Sox9-expressing progenitors capable of SAE repair decline with age in mice. Notably, Sox9-lineage glandular progenitors produced basal and ciliated cells in the SAE, but failed to produce secretory cells. Lef1 was required for glandular Sox9 lineage contribution to SAE repair, and its deletion significantly reduced proliferation following injury. By contrast, in vivo deletion of Sox9 enhanced proliferation of progenitors in both the SAE and SMG shortly following injury, but these progenitors failed to proliferate in vitro in the absence of Sox9, similar to that previously shown for Lef1 deletion. In cystic fibrosis ferret airways, Sox9 expression inversely correlated with Ki67 proliferative marker expression in SMG and the SAE. Using in vitro and ex vivo models, we demonstrate that Sox9 is extinguished as glandular progenitors exit ducts and proliferate on the airway surface and that Sox9 is required for migration and proper differentiation of SMG, but not surface airway, progenitors. We propose a model whereby Wnt/Lef1 and Sox9 signals differentially regulate the proliferative and migratory behavior of glandular progenitors, respectively.


Asunto(s)
Hurones , Factor de Unión 1 al Potenciador Linfoide/metabolismo , Sistema Respiratorio , Factor de Transcripción SOX9/metabolismo , Animales , Diferenciación Celular , Células Epiteliales/metabolismo , Ratones , Células Madre/metabolismo
3.
Tob Control ; 32(6): 795-798, 2023 11.
Artículo en Inglés | MEDLINE | ID: mdl-35803674

RESUMEN

OBJECTIVE: Nicotine pouch products are an emerging and rapidly growing smokeless tobacco (ST) category in the USA. Little is known about the promotional strategies and media channels used to advertise this ST category or the extent to which the marketing strategies differ from strategies used to promote 'conventional' smokeless products (eg, snuff). We describe the nature, timing of and expenditures related to conventional, snus and newer ST product advertising on print, broadcast and internet media. METHODS: Advertising expenditures were collected using Kantar Media's 'Stradegy' tool, which provides advertising data including dollars spent promoting specific products across various media channels, including print magazines and newspapers, broadcast television and radio, outdoor posters and billboards, and internet. We identified 306 smokeless products within Kantar database and collected ad expenditures retrospectively for January 2018-April 2020. Promotional expenditures were aggregated by product category, by month and by designated market area (DMA). RESULTS: Kantar data analysis returned 28 conventional ST, 22 oral nicotine and 3 snus products (53 total) advertised during the period of observation, with over $71 million spent collectively on ST promotion. Across categories, more advertising dollars were spent on conventional ST products (63%) than newer oral nicotine products (25%) or snus (12%). However, during the later 9-month period from August 2019 to April 2020, oral nicotine products accounted for the majority of monthly ad spending. Most ad spending was placed in the national market ($66.5 million), with Atlanta ($1.1 million), Houston ($1 million) and Las Vegas ($0.8 million) as the top three local DMAs for expenditures. DISCUSSION: Advertising expenditures for nicotine pouches have recently exceeded conventional ST product advertising and nicotine pouches are being promoted nationally. Marketing surveillance as well as understanding consumer appeal, perceptions and consumption are critical next steps in tracking potential uptake of these new products.


Asunto(s)
Productos de Tabaco , Tabaco sin Humo , Humanos , Publicidad , Nicotina , Gastos en Salud , Estudios Retrospectivos
4.
J Sports Sci ; 40(8): 934-949, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-35220909

RESUMEN

In the research concerning rational emotive behaviour therapy (REBT) in sport and exercise, irrational beliefs are proposed as a risk factor for health. Concurrent to this, researchers have also indicated that autonomous and controlled motivation, as proposed in organismic integration theory could, together with irrational beliefs, determine individual health. However, research is yet to align irrational beliefs and motivation, and explore how this alignment relates to mental health. The present two study paper identifies individual subgroups, drawn from data concerning irrational beliefs, motivation, and health (psychological distress, and physical health), in a sample of exercisers (study 1) and student athletes (study 2). We examined the latent profile structure of irrational beliefs and motivation, and how these latent profiles relate to psychological distress (studies 1 and 2), and physical health (study 2). Results indicate a two class profile whereby class 1 is characterised by high irrational beliefs, low self-determined motivation, and poor health outcomes. Class 2 is characterised by low irrational beliefs, high self-determined motivation, and better health outcomes. The findings are discussed in relation to the theoretical implications for REBT and organismic integration theory, and the practical implications for key stakeholders in the health of exercise participants and athletes.


Asunto(s)
Motivación , Distrés Psicológico , Atletas/psicología , Humanos , Salud Mental , Autonomía Personal
5.
BMC Vet Res ; 17(1): 215, 2021 Jun 10.
Artículo en Inglés | MEDLINE | ID: mdl-34112165

RESUMEN

BACKGROUND: The popularity of new world camelids, particularly alpacas, is growing rapidly in Ireland, presenting a clinical challenge to veterinary practitioners who may not have worked with these species previously. To the authors' knowledge, the clinical course of a case of acute fasciolosis in an alpaca has not previously been reported, and fasciolosis has not been reported at all in alpacas in Ireland, making this case report a valuable addition to the current literature. CASE PRESENTATION: A three-year-old male castrated huacaya alpaca was admitted to UCD Veterinary Hospital with a two-day history of colic and tenesmus. He had been treated with albendazole, dexamethasone and potentiated amoxycillin by the referring veterinary practitioner with no response. On initial clinical exam, sensitivity to abdominal palpation was the only abnormality. However, the alpaca proceeded to show abnormal lying positions, tenesmus and reduced faecal output over the next 24 h. A general blood panel demonstrated moderate anaemia, marked hyperglobulinaemia and moderately increased hepatocellular and hepatobiliary enzyme activity. Abdominal radiography revealed enlargement of the first forestomach compartment without evidence of gastrointestinal obstruction or peritonitis. An abdominal ultrasound exam revealed an elongated, heterogenous mass in the caudoventral abdomen that appeared to be contiguous with the liver. FNA of this mass revealed that it was in fact a liver lobe with biliary stasis and inflammation. Faecal sedimentation demonstrated Fasciola hepatica eggs. In spite of treatment with triclabendazole and supportive treatment including blood transfusion, the alpaca's condition continued to deteriorate and he was euthanised. On post-mortem exam, acute fasciolosis was diagnosed. CONCLUSIONS: The clinical presentation and course of a case of acute fasciolosis in an individual alpaca is described, including the results of a range of diagnostic tests that were carried out. The final diagnosis is supported by a description of post-mortem findings. This information will serve as a resource for veterinary practitioners involved in the diagnosis and treatment of similar cases.


Asunto(s)
Camélidos del Nuevo Mundo , Fascioliasis/veterinaria , Enfermedad Aguda , Amoxicilina/uso terapéutico , Animales , Antibacterianos/uso terapéutico , Antiplatelmínticos/uso terapéutico , Cólico/parasitología , Cólico/veterinaria , Fascioliasis/diagnóstico , Fascioliasis/tratamiento farmacológico , Irlanda , Masculino , Resultado del Tratamiento , Triclabendazol/uso terapéutico
6.
Emerg Infect Dis ; 26(12): 2989-2993, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-33219658

RESUMEN

The Onchocerca lupi nematode infects dogs, cats, and humans, but whether it can be spread by coyotes has been unknown. We conducted surveillance for O. lupi nematode infection in coyotes in the southwestern United States. We identified multiple coyote populations in Arizona and New Mexico as probable reservoirs for this species.


Asunto(s)
Coyotes , Enfermedades de los Perros , Oncocercosis , Animales , Arizona/epidemiología , Reservorios de Enfermedades , Enfermedades de los Perros/epidemiología , Perros , New Mexico , Onchocerca/genética , Oncocercosis/epidemiología , Oncocercosis/veterinaria , Sudoeste de Estados Unidos , Estados Unidos/epidemiología , Zoonosis
7.
Emerg Infect Dis ; 26(5): 937-944, 2020 05.
Artículo en Inglés | MEDLINE | ID: mdl-32310081

RESUMEN

Rhizopus spp. fungi are ubiquitous in the environment and a rare but substantial cause of infection in immunosuppressed persons and surgery patients. During 2005-2017, an abnormally high number of Rhizopus infections in surgery patients, with no apparent epidemiologic links, were reported in Argentina. To determine the likelihood of a common source of the cluster, we performed whole-genome sequencing on samples collected during 2006-2014. Most isolates were separated by >60 single-nucleotide polymorphisms, and we found no evidence for recombination or nonneutral mutation accumulation; these findings do not support common source or patient-to-patient transmission. Assembled genomes of most isolates were ≈25 Mbp, and multiple isolates had substantially larger assembled genomes (43-51 Mbp), indicative of infections with strain types that underwent genome expansion. Whole-genome sequencing has become an essential tool for studying epidemiology of fungal infections. Less discriminatory techniques may miss true relationships, possibly resulting in inappropriate attribution of point source.


Asunto(s)
Mucormicosis , Rhizopus , Argentina/epidemiología , Humanos , Mucormicosis/epidemiología , Rhizopus/genética
8.
Emerg Infect Dis ; 25(3): 501-506, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30789132

RESUMEN

Coccidioidomycosis is an emerging fungal infection in Washington, USA, and the epidemiology of the disease in this state is poorly understood. We used whole-genome sequencing to differentiate locally acquired cases in Washington on the basis of the previously identified phylogeographic population structure of Coccidioides spp. Clinical isolates from coccidioidomycosis cases involving possible Washington soil exposure were included. Of 17 human infections with epidemiologic evidence of possible local acquisition, 4 were likely locally acquired infections and 13 were likely acquired outside Washington. Isolates from locally acquired cases clustered within the previously established Washington clade of C. immitis. Genetic differences among these strains suggest multiple environmental reservoirs of C. immitis in the state.


Asunto(s)
Coccidioides/genética , Coccidioidomicosis/epidemiología , Coccidioidomicosis/microbiología , Genoma Bacteriano , Secuenciación Completa del Genoma , Coccidioides/clasificación , Coccidioides/aislamiento & purificación , Biología Computacional/métodos , Genómica/métodos , Humanos , Filogenia , Polimorfismo de Nucleótido Simple , Vigilancia en Salud Pública , Washingtón/epidemiología
9.
Med Mycol ; 57(Supplement_1): S30-S40, 2019 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-30690599

RESUMEN

The incidence of reported coccidioidomycosis in the past two decades has increased greatly; monitoring its changing epidemiology is essential for understanding its burden on patients and the healthcare system and for identifying opportunities for prevention and education. We provide an update on recent coccidioidomycosis trends and public health efforts nationally and in Arizona, California, and Washington State. In Arizona, enhanced surveillance shows that coccidioidomycosis continues to be associated with substantial morbidity. California reported its highest yearly number of cases ever in 2016 and has implemented interventions to reduce coccidioidomycosis in the prison population by excluding certain inmates from residing in prisons in high-risk areas. Coccidioidomycosis is emerging in Washington State, where phylogenetic analyses confirm the existence of a unique Coccidioides clade. Additional studies of the molecular epidemiology of Coccidioides will improve understanding its expanding endemic range. Ongoing public health collaborations and future research priorities are focused on characterizing geographic risk, particularly in the context of environmental change; identifying further risk reduction strategies for high-risk groups; and improving reporting of cases to public health agencies.


Asunto(s)
Coccidioides/aislamiento & purificación , Coccidioidomicosis/epidemiología , Coccidioidomicosis/prevención & control , Arizona/epidemiología , California/epidemiología , Coccidioides/genética , Humanos , Incidencia , Filogenia , Prisioneros , Salud Pública , Factores de Riesgo , Estados Unidos/epidemiología , Washingtón/epidemiología
10.
Emerg Infect Dis ; 24(11): 2095-2097, 2018 11.
Artículo en Inglés | MEDLINE | ID: mdl-30334716

RESUMEN

We conducted molecular clock analysis of whole-genome sequences from a set of autochthonous isolates of Cryptococcus gattii sensu stricto from the southeastern United States. Our analysis indicates that C. gattii arrived in the southeastern United States approximately 9,000-19,000 years ago, long before its arrival in the Pacific Northwest.


Asunto(s)
Criptococosis/microbiología , Cryptococcus gattii/genética , Genoma Fúngico/genética , Teorema de Bayes , Criptococosis/epidemiología , Cryptococcus gattii/aislamiento & purificación , Humanos , Noroeste de Estados Unidos/epidemiología , Filogenia , Polimorfismo de Nucleótido Simple/genética , Programas Informáticos , Sudeste de Estados Unidos/epidemiología , Secuenciación Completa del Genoma
11.
J Anat ; 232(5): 721-728, 2018 05.
Artículo en Inglés | MEDLINE | ID: mdl-29430649

RESUMEN

The Anatomical Society has developed a series of learning outcomes in consultation with nursing educators delivering anatomical content to undergraduate (preregistration) nursing students. A Delphi panel methodology was adopted to select experts within the field that would recommend core anatomical content in undergraduate nursing programmes throughout the UK. Using the Anatomical Society's Core Gross Anatomy Syllabus for Medical Students as a foundation, a modified Delphi technique was used to develop discipline-specific outcomes to nursing graduates. The Delphi panel consisted of 48 individuals (n = 48) with a minimum of 3 years' experience teaching anatomy to nursing students, representing a broad spectrum of UK Higher Education Institutions. The output from this study was 64 nursing specific learning outcomes in anatomy that are applicable to all undergraduate (preregistration) programmes in the UK. The new core anatomy syllabus for Undergraduate Nursing offers a basic anatomical framework upon which nurse educators, clinical mentors and nursing students can underpin their clinical practice and knowledge. The learning outcomes presented may be used to develop anatomy teaching within an integrated nursing curriculum.


Asunto(s)
Anatomía/educación , Curriculum/normas , Educación en Enfermería/normas
13.
Med Mycol ; 56(7): 857-867, 2018 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-29554336

RESUMEN

Cryptococcosis is an opportunistic fungal infection caused by members of the two sibling species complexes: Cryptococcus neoformans and Cryptococcus gattii. Flucytosine (5FC) is one of the most widely used antifungals against Cryptococcus spp., yet very few studies have looked at the molecular mechanisms responsible for 5FC resistance in this pathogen. In this study, we examined 11 C. gattii clinical isolates of the major molecular type VGIII based on differential 5FC susceptibility and asked whether there were genomic changes in the key genes involved in flucytosine metabolism. Susceptibility assays and sequencing analysis revealed an association between a point mutation in the cytosine deaminase gene (FCY1) and 5FC resistance in two of the studied 5FC resistant C. gattii VGIII clinical isolates, B9322 and JS5. This mutation results in the replacement of arginine for histidine at position 29 and occurs within a variable stretch of amino acids. Heterologous expression of FCY1 and spot sensitivity assays, however, demonstrated that this point mutation did not have any effect on FCY1 activities and was not responsible for 5FC resistance. Comparative sequence analysis further showed that no changes in the amino acid sequence and no genomic alterations were observed within 1 kb of the upstream and downstream sequences of either cytosine permeases (FCY2-4) or uracil phosphoribosyltransferase (FUR1) genes in 5FC resistant and 5FC susceptible C. gattii VGIII isolates. The herein obtained results suggest that the observed 5FC resistance in the isolates B9322 and JS5 is due to changes in unknown protein(s) or pathway(s) that regulate flucytosine metabolism.


Asunto(s)
Antifúngicos/farmacología , Cryptococcus gattii/efectos de los fármacos , Flucitosina/farmacología , Proteínas Fúngicas/metabolismo , Mapas de Interacción de Proteínas , Criptococosis/microbiología , Cryptococcus gattii/genética , Cryptococcus gattii/aislamiento & purificación , Cryptococcus gattii/metabolismo , Citosina Desaminasa/genética , Citosina Desaminasa/metabolismo , Análisis Mutacional de ADN , Proteínas Fúngicas/genética , Humanos , Masculino , Proteínas de Transporte de Membrana/genética , Proteínas de Transporte de Membrana/metabolismo , Pruebas de Sensibilidad Microbiana , Pentosiltransferasa/genética , Pentosiltransferasa/metabolismo , Análisis de Secuencia de ADN
15.
Emerg Infect Dis ; 22(6): 1098-101, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27191335

RESUMEN

Cryptococcus gattii is a recognized pathogenic fungus along the Pacific coast of the United States from California to Washington. Here we report that C. gattii may also be endemic to the southeastern United States and has probably been present there longer than in the Pacific Northwest.


Asunto(s)
Criptococosis/epidemiología , Criptococosis/microbiología , Cryptococcus gattii/genética , Genoma Fúngico , Secuenciación Completa del Genoma , Cryptococcus gattii/clasificación , Genotipo , Humanos , Tipificación de Secuencias Multilocus , Polimorfismo de Nucleótido Simple , Vigilancia de la Población , Sudeste de Estados Unidos/epidemiología
16.
Emerg Infect Dis ; 22(3): 476-81, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26891230

RESUMEN

We used whole-genome sequence typing (WGST) to investigate an outbreak of Sarocladium kiliense bloodstream infections (BSI) associated with receipt of contaminated antinausea medication among oncology patients in Colombia and Chile during 2013-2014. Twenty-five outbreak isolates (18 from patients and 7 from medication vials) and 11 control isolates unrelated to this outbreak were subjected to WGST to elucidate a source of infection. All outbreak isolates were nearly indistinguishable (<5 single-nucleotide polymorphisms), and >21,000 single-nucleotide polymorphisms were identified from unrelated control isolates, suggesting a point source for this outbreak. S. kiliense has been previously implicated in healthcare-related infections; however, the lack of available typing methods has precluded the ability to substantiate point sources. WGST for outbreak investigation caused by eukaryotic pathogens without reference genomes or existing genotyping methods enables accurate source identification to guide implementation of appropriate control and prevention measures.


Asunto(s)
Antieméticos/efectos adversos , Brotes de Enfermedades , Contaminación de Medicamentos , Fungemia/etiología , Hypocreales , Chile , Colombia , ADN de Hongos , Fungemia/diagnóstico , Fungemia/microbiología , Humanos , Hypocreales/genética , Hypocreales/aislamiento & purificación , Polimorfismo de Nucleótido Simple , Análisis de Secuencia de ADN
17.
Hereditas ; 153: 11, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-28096773

RESUMEN

BACKGROUND: Prevention of nosocomial transmission of infections is a central responsibility in the healthcare environment, and accurate identification of transmission events presents the first challenge. Phylogenetic analysis based on whole genome sequencing provides a high-resolution approach for accurately relating isolates to one another, allowing precise identification or exclusion of transmission events and sources for nearly all cases. We sequenced 24 methicillin-resistant Staphylococcus aureus (MRSA) genomes to retrospectively investigate a suspected point source of three surgical site infections (SSIs) that occurred over a one-year period. The source of transmission was believed to be a surgical team member colonized with MRSA, involved in all surgeries preceding the SSI cases, who was subsequently decolonized. Genetic relatedness among isolates was determined using whole genome single nucleotide polymorphism (SNP) data. RESULTS: Whole genome SNP typing (WGST) revealed 283 informative SNPs between the surgical team member's isolate and the closest SSI isolate. The second isolate was 286 and the third was thousands of SNPs different, indicating the nasal carriage strain from the surgical team member was not the source of the SSIs. Given the mutation rates estimated for S. aureus, none of the SSI isolates share a common ancestor within the past 16 years, further discounting any common point source for these infections. The decolonization procedures and resources spent on the point source infection control could have been prevented if WGST was performed at the time of the suspected transmission, instead of retrospectively. CONCLUSIONS: Whole genome sequence analysis is an ideal method to exclude isolates involved in transmission events and nosocomial outbreaks, and coupling this method with epidemiological data can determine if a transmission event occurred. These methods promise to direct infection control resources more appropriately.


Asunto(s)
Portador Sano/microbiología , Personal de Salud , Staphylococcus aureus Resistente a Meticilina/genética , Polimorfismo de Nucleótido Simple , Infecciones Estafilocócicas/microbiología , Infección de la Herida Quirúrgica/microbiología , Técnicas de Tipificación Bacteriana , Infección Hospitalaria/microbiología , ADN Bacteriano/genética , Genoma Bacteriano , Humanos , Staphylococcus aureus Resistente a Meticilina/clasificación , Filogenia , Estudios Retrospectivos , Análisis de Secuencia de ADN
18.
J Clin Microbiol ; 53(1): 212-8, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25378576

RESUMEN

A retrospective investigation was performed to evaluate whole-genome sequencing as a benchmark for comparing molecular subtyping methods for Salmonella enterica serotype Enteritidis and survey the population structure of commonly encountered S. enterica serotype Enteritidis outbreak isolates in the United States. A total of 52 S. enterica serotype Enteritidis isolates representing 16 major outbreaks and three sporadic cases collected between 2001 and 2012 were sequenced and subjected to subtyping by four different methods: (i) whole-genome single-nucleotide-polymorphism typing (WGST), (ii) multiple-locus variable-number tandem-repeat (VNTR) analysis (MLVA), (iii) clustered regularly interspaced short palindromic repeats combined with multi-virulence-locus sequence typing (CRISPR-MVLST), and (iv) pulsed-field gel electrophoresis (PFGE). WGST resolved all outbreak clusters and provided useful robust phylogenetic inference results with high epidemiological correlation. While both MLVA and CRISPR-MVLST yielded higher discriminatory power than PFGE, MLVA outperformed the other methods in delineating outbreak clusters whereas CRISPR-MVLST showed the potential to trace major lineages and ecological origins of S. enterica serotype Enteritidis. Our results suggested that whole-genome sequencing makes a viable platform for the evaluation and benchmarking of molecular subtyping methods.


Asunto(s)
Genoma Bacteriano , Genotipo , Infecciones por Salmonella/epidemiología , Infecciones por Salmonella/microbiología , Salmonella enteritidis/clasificación , Salmonella enteritidis/genética , Serogrupo , Repeticiones Palindrómicas Cortas Agrupadas y Regularmente Espaciadas , Brotes de Enfermedades , Electroforesis en Gel de Campo Pulsado , Humanos , Repeticiones de Microsatélite , Tipificación de Secuencias Multilocus , Filogenia
19.
MMWR Morb Mortal Wkly Rep ; 63(20): 450, 2014 May 23.
Artículo en Inglés | MEDLINE | ID: mdl-24848217

RESUMEN

Coccidioidomycosis ("valley fever") is caused by inhaling spores of the soil-dwelling fungi Coccidioides immitis or Coccidioides posadasii. Most infections are subclinical. When clinical manifestations do occur (typically 1-4 weeks after exposure), they are similar to those associated with influenza or community-acquired pneumonia. Disseminated disease is rare. Residual pulmonary nodules can lead to chronic lung disease. Fluconazole or other triazoles often are used for treatment, but mild cases often resolve without specific therapy. A total of 17,802 cases were reported in the United States in 2012.


Asunto(s)
Coccidioides/clasificación , Coccidioides/aislamiento & purificación , Microbiología del Suelo , Coccidioidomicosis/epidemiología , Humanos , Washingtón/epidemiología
20.
Ultraschall Med ; 35(3): 273-8, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24327470

RESUMEN

PURPOSE: 2800 renal transplants are carried out annually in the UK and it is standard practice to perform a Tc-DTPA renogram examination after surgery to check perfusion. This provides some functional information but suffers from low spatial resolution, is lengthy, immobile and costly and uses ionizing radiation. We surmised that contrast-enhanced ultrasound (CEUS) would provide an accurate alternative with increased speed, resolution (temporal and spatial), cost efficiency and safety. MATERIALS AND METHODS: 97 renal transplant patients underwent both Tc-DTPA and CEUS after surgery to assess the perfusion of the graft. Tc-DTPA was performed in the nuclear medicine department with at least 10 minutes of continuous screening and a standard dose of 150 mBq Tc-DTPA. CEUS consisted of I. V. 2.4 ml Sonovue contrast agent, 60 seconds continuous capture and a 3 D acquisition of the organ. 3 D CEUS was assessed using QLab analysis software. RESULTS: Tc-DTPA detected 9 perfusion defects of varying size. CEUS detected all these defects plus 14 further defects (0.2 - 17 % of total renal volume) not detected on DTPA. These results demonstrate a statistically significant divergence (p < 0.0001). Retrospective clinical correlation showed ligated polar arteries in 8 of these 14 cases. CONCLUSION: CEUS will detect perfusion defects seen with Tc-DTPA and due to increased spatial and temporal resolution and multiple scanning angles, will detect further perfusion defects not seen on Tc-DTPA. 3 D CEUS is useful in the quantification of perfusion defects. CEUS is an accurate examination for detecting renal transplant perfusion defects and will detect significantly more defects than DTPA.


Asunto(s)
Aumento de la Imagen , Imagenología Tridimensional , Isquemia/diagnóstico , Trasplante de Riñón , Riñón/irrigación sanguínea , Complicaciones Posoperatorias/diagnóstico , Cintigrafía , Pentetato de Tecnecio Tc 99m , Ultrasonografía , Adulto , Femenino , Humanos , Interpretación de Imagen Asistida por Computador , Masculino , Persona de Mediana Edad , Fosfolípidos , Sensibilidad y Especificidad , Hexafluoruro de Azufre , Ultrasonografía Doppler en Color
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