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1.
Clin Toxicol (Phila) ; 59(2): 169-171, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-32475191

RESUMEN

Abrin is a toxin of public health concern due to its lethality, lack of antidote, and potential for use as a bioterrorism agent. Possible routes of exposure include ingestion, inhalation, and injection. Onset of symptoms is often delayed, even in severe cases. In fatal cases, death occurs from multi-organ failure. We describe the clinical course, laboratory, and pathologic findings in a case of fatal human poisoning associated with abrin injection. The Abrus precatorius seeds in this case were obtained via the internet. The Centers for Disease Control and Prevention's Laboratory Response Network detected abrine in the urine confirming abrin exposure in this fatal poisoning.


Asunto(s)
Abrina/envenenamiento , Adulto , Resultado Fatal , Humanos , Inyecciones , Masculino
2.
mBio ; 11(5)2020 09 04.
Artículo en Inglés | MEDLINE | ID: mdl-32887735

RESUMEN

In December of 2019, a novel coronavirus, SARS-CoV-2, emerged in the city of Wuhan, China, causing severe morbidity and mortality. Since then, the virus has swept across the globe, causing millions of confirmed infections and hundreds of thousands of deaths. To better understand the nature of the pandemic and the introduction and spread of the virus in Arizona, we sequenced viral genomes from clinical samples tested at the TGen North Clinical Laboratory, the Arizona Department of Health Services, and those collected as part of community surveillance projects at Arizona State University and the University of Arizona. Phylogenetic analysis of 84 genomes from across Arizona revealed a minimum of 11 distinct introductions inferred to have occurred during February and March. We show that >80% of our sequences descend from strains that were initially circulating widely in Europe but have since dominated the outbreak in the United States. In addition, we show that the first reported case of community transmission in Arizona descended from the Washington state outbreak that was discovered in late February. Notably, none of the observed transmission clusters are epidemiologically linked to the original travel-related case in the state, suggesting successful early isolation and quarantine. Finally, we use molecular clock analyses to demonstrate a lack of identifiable, widespread cryptic transmission in Arizona prior to the middle of February 2020.IMPORTANCE As the COVID-19 pandemic swept across the United States, there was great differential impact on local and regional communities. One of the earliest and hardest hit regions was in New York, while at the same time Arizona (for example) had low incidence. That situation has changed dramatically, with Arizona now having the highest rate of disease increase in the country. Understanding the roots of the pandemic during the initial months is essential as the pandemic continues and reaches new heights. Genomic analysis and phylogenetic modeling of SARS-COV-2 in Arizona can help to reconstruct population composition and predict the earliest undetected introductions. This foundational work represents the basis for future analysis and understanding as the pandemic continues.


Asunto(s)
Betacoronavirus/genética , Infecciones por Coronavirus/epidemiología , Infecciones por Coronavirus/transmisión , Neumonía Viral/epidemiología , Neumonía Viral/transmisión , Arizona/epidemiología , Betacoronavirus/clasificación , Betacoronavirus/aislamiento & purificación , COVID-19 , Infecciones por Coronavirus/virología , Evolución Molecular , Genoma Viral/genética , Humanos , Incidencia , Mutación , Pandemias , Filogenia , Neumonía Viral/virología , SARS-CoV-2 , Proteínas Virales/genética
3.
Med Mycol ; 58(4): 552-559, 2020 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-31506673

RESUMEN

Coccidioidomycosis is a debilitating fungal disease caused by inhalation of arthroconidia. We developed a novel approach for detection of airborne Coccidioides and used it to investigate the distribution of arthroconidia across the Phoenix, Arizona, metropolitan area. Air filters were collected daily from 21 stationary air-sampling units across the area: the first set collected before, during and after a large dust storm on August 25, 2015, and the second over the 45-day period September 25-November 8, 2016. Analysis of DNA extracted from the filters demonstrated that the day of the dust storm was not associated with increase of Coccidioides in air samples, although evidence of the low-level polymerase chain reaction (PCR) inhibition was observed in DNA extracted from samples collected on the day of the dust storm. Testing over 45 days identified uneven geographic distribution suggesting Coccidioides hot spots. In 2016, highest daily concentration of arthroconidia was observed between September 25-October 20, and only sporadic low levels were detected after that. These results provide evidence of seasonality and uneven spatial distribution of Coccidioides in the air. Our results demonstrate that routine air monitoring for arthroconidia is possible and provides an important tool for Coccidioides surveillance, which can address important questions about environmental exposure and human infection.


Asunto(s)
Microbiología del Aire , Coccidioides/genética , Estaciones del Año , Arizona , Ciudades , Coccidioides/aislamiento & purificación , ADN de Hongos/genética , Esporas Fúngicas/genética
4.
mBio ; 7(2): e00550-16, 2016 Apr 26.
Artículo en Inglés | MEDLINE | ID: mdl-27118594

RESUMEN

UNLABELLED: Coccidioidomycosis (or valley fever) is a fungal disease with high morbidity and mortality that affects tens of thousands of people each year. This infection is caused by two sibling species, Coccidioides immitis and C. posadasii, which are endemic to specific arid locales throughout the Western Hemisphere, particularly the desert southwest of the United States. Recent epidemiological and population genetic data suggest that the geographic range of coccidioidomycosis is expanding, as new endemic clusters have been identified in the state of Washington, well outside the established endemic range. The genetic mechanisms and epidemiological consequences of this expansion are unknown and require better understanding of the population structure and evolutionary history of these pathogens. Here we performed multiple phylogenetic inference and population genomics analyses of 68 new and 18 previously published genomes. The results provide evidence of substantial population structure in C. posadasii and demonstrate the presence of distinct geographic clades in central and southern Arizona as well as dispersed populations in Texas, Mexico, South America, and Central America. Although a smaller number of C. immitis strains were included in the analyses, some evidence of phylogeographic structure was also detected in this species, which has been historically limited to California and Baja, Mexico. Bayesian analyses indicated that C. posadasii is the more ancient of the two species and that Arizona contains the most diverse subpopulations. We propose a southern Arizona-northern Mexico origin for C. posadasii and describe a pathway for dispersal and distribution out of this region. IMPORTANCE: Coccidioidomycosis, or valley fever, is caused by the pathogenic fungi Coccidioides posadasii and C. immitis The fungal species and disease are primarily found in the American desert southwest, with spotted distribution throughout the Western Hemisphere. Initial molecular studies suggested a likely anthropogenic movement of C. posadasii from North America to South America. Here we comparatively analyze eighty-six genomes of the two Coccidioides species and establish local and species-wide population structures to not only clarify the earlier dispersal hypothesis but also provide evidence of likely ancestral populations and patterns of dispersal for the known subpopulations of C. posadasii.


Asunto(s)
Coccidioides/aislamiento & purificación , Coccidioidomicosis/microbiología , América Central/epidemiología , Coccidioides/clasificación , Coccidioides/genética , Coccidioidomicosis/epidemiología , Filogenia , América del Sur/epidemiología , Sudoeste de Estados Unidos/epidemiología
5.
Emerg Infect Dis ; 22(4): 734-8, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26982330
7.
Public Health Rep ; 128 Suppl 2: 20-33, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23997300

RESUMEN

Beginning in early 2011, the Centers for Disease Control and Prevention and the Association of Public Health Laboratories launched the Laboratory Efficiencies Initiative (LEI) to help public health laboratories (PHLs) and the nation's entire PHL system achieve and maintain sustainability to continue to conduct vital services in the face of unprecedented financial and other pressures. The LEI focuses on stimulating substantial gains in laboratories' operating efficiency and cost efficiency through the adoption of proven and promising management practices. In its first year, the LEI generated a strategic plan and a number of resources that PHL directors can use toward achieving LEI goals. Additionally, the first year saw the formation of a dynamic community of practitioners committed to implementing the LEI strategic plan in coordination with state and local public health executives, program officials, foundations, and other key partners.


Asunto(s)
Laboratorios/organización & administración , Salud Pública/métodos , Centers for Disease Control and Prevention, U.S. , Sistemas de Información en Laboratorio Clínico/organización & administración , Sistemas de Información en Laboratorio Clínico/normas , Ahorro de Costo , Análisis Costo-Beneficio , Eficiencia Organizacional , Planificación en Salud , Humanos , Relaciones Interinstitucionales , Laboratorios/economía , Laboratorios/normas , Salud Pública/economía , Salud Pública/normas , Administración en Salud Pública , Estados Unidos , Recursos Humanos
8.
J Med Microbiol ; 62(Pt 9): 1295-1300, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23741021

RESUMEN

Acinetobacter spp. are a diverse group of Gram-negative bacteria frequently implicated in nosocomial infections. Genotypic methods have been instrumental in studying Acinetobacter, but few offer high resolution, rapid turnaround time, technical ease and high inter-laboratory reproducibility, which has hampered understanding of disease incidence, transmission patterns and diversity within this genus. Here, we further evaluated multilocus PCR electrospray ionization/mass spectrometry (PCR/ESI-MS), a method that is simple and robust, and provides both species characterization and strain-level resolution of Acinetobacter spp. on a single platform. We examined 125 Acinetobacter isolates from 21 hospitals, laboratories and medical centres spanning four counties in Arizona, USA, using PCR/ESI-MS. We compared PCR/ESI-MS with an in-house amplified fragment length polymorphism (AFLP) genotyping scheme. PCR/ESI-MS demonstrated that Acinetobacter spp. from Arizonan hospitals had similar species and strain distributions to other US civilian hospitals. Furthermore, we showed that the PCR/ESI-MS and AFLP genotypes were highly congruent, with the former having the advantages of robust inter-laboratory reproducibility, rapid turnaround time and simple experimental set-up and data analysis. PCR/ESI-MS is an effective and high-throughput platform for strain typing of Acinetobacter baumannii and for identification of other Acinetobacter spp., including the emerging nosocomial pathogens Acinetobacter pittii and Acinetobacter nosocomialis.


Asunto(s)
Acinetobacter/clasificación , Tipificación de Secuencias Multilocus/métodos , Reacción en Cadena de la Polimerasa/métodos , Espectrometría de Masa por Ionización de Electrospray/métodos , Acinetobacter/genética , Acinetobacter/aislamiento & purificación , Análisis del Polimorfismo de Longitud de Fragmentos Amplificados , Arizona , Técnicas de Tipificación Bacteriana/métodos , Genes Bacterianos , Genotipo , Humanos , Filogenia , ARN Bacteriano/genética , ARN Ribosómico 16S/genética , Reproducibilidad de los Resultados
9.
PLoS One ; 8(1): e54287, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23365658

RESUMEN

Acinetobacter baumannii is an emergent and global nosocomial pathogen. In addition to A. baumannii, other Acinetobacter species, especially those in the Acinetobacter calcoaceticus-baumannii (Acb) complex, have also been associated with serious human infection. Although mechanisms of attachment, persistence on abiotic surfaces, and pathogenesis in A. baumannii have been identified, the genetic mechanisms that explain the emergence of A. baumannii as the most widespread and virulent Acinetobacter species are not fully understood. Recent whole genome sequencing has provided insight into the phylogenetic structure of the genus Acinetobacter. However, a global comparison of genomic features between Acinetobacter spp. has not been described in the literature. In this study, 136 Acinetobacter genomes, including 67 sequenced in this study, were compared to identify the acquisition and loss of genes in the expansion of the Acinetobacter genus. A whole genome phylogeny confirmed that A. baumannii is a monophyletic clade and that the larger Acb complex is also a well-supported monophyletic group. The whole genome phylogeny provided the framework for a global genomic comparison based on a blast score ratio (BSR) analysis. The BSR analysis demonstrated that specific genes have been both lost and acquired in the evolution of A. baumannii. In addition, several genes associated with A. baumannii pathogenesis were found to be more conserved in the Acb complex, and especially in A. baumannii, than in other Acinetobacter genomes; until recently, a global analysis of the distribution and conservation of virulence factors across the genus was not possible. The results demonstrate that the acquisition of specific virulence factors has likely contributed to the widespread persistence and virulence of A. baumannii. The identification of novel features associated with transcriptional regulation and acquired by clades in the Acb complex presents targets for better understanding the evolution of pathogenesis and virulence in the expansion of the genus.


Asunto(s)
Acinetobacter baumannii/patogenicidad , Acinetobacter/patogenicidad , Proteínas Bacterianas/genética , Genoma Bacteriano , ARN Ribosómico 16S/genética , Factores de Virulencia/genética , Acinetobacter/clasificación , Acinetobacter/genética , Acinetobacter/aislamiento & purificación , Infecciones por Acinetobacter/microbiología , Acinetobacter baumannii/clasificación , Acinetobacter baumannii/genética , Acinetobacter baumannii/aislamiento & purificación , Proteínas Bacterianas/clasificación , Secuencia de Bases , Evolución Biológica , Mapeo Cromosómico , Cromosomas Bacterianos/genética , Genómica , Humanos , Tipificación de Secuencias Multilocus , Filogenia , ARN Ribosómico 16S/clasificación , Virulencia , Factores de Virulencia/clasificación
10.
PLoS Negl Trop Dis ; 5(10): e1347, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22028940

RESUMEN

Melioidosis is caused by Burkholderia pseudomallei, a Gram-negative bacillus, primarily found in soils in Southeast Asia and northern Australia. A recent case of melioidosis in non-endemic Arizona was determined to be the result of locally acquired infection, as the patient had no travel history to endemic regions and no previous history of disease. Diagnosis of the case was confirmed through multiple microbiologic and molecular techniques. To enhance the epidemiological analysis, we conducted several molecular genotyping procedures, including multi-locus sequence typing, SNP-profiling, and whole genome sequence typing. Each technique has different molecular epidemiologic advantages, all of which provided evidence that the infecting strain was most similar to those found in Southeast Asia, possibly originating in, or around, Malaysia. Advancements in new typing technologies provide genotyping resolution not previously available to public health investigators, allowing for more accurate source identification.


Asunto(s)
Burkholderia pseudomallei/clasificación , Burkholderia pseudomallei/genética , Melioidosis/diagnóstico , Melioidosis/microbiología , Tipificación Molecular , Arizona/epidemiología , Burkholderia pseudomallei/aislamiento & purificación , Análisis por Conglomerados , Genotipo , Humanos , Epidemiología Molecular , Filogenia
11.
Med Mycol ; 48(3): 466-9, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-20370360

RESUMEN

Coccidioidomycosis is an infection caused by Coccidioides immitis or C. posadasii. We developed a TaqMan real-time PCR assay that rapidly and accurately differentiates the species. This assay can be used as a tool to improve disease surveillance, increase understanding of the natural history of the infection, and assist in clinical differentiation studies.


Asunto(s)
Coccidioides/clasificación , Coccidioides/aislamiento & purificación , Coccidioidomicosis/diagnóstico , Reacción en Cadena de la Polimerasa/métodos , Coccidioides/genética , Coccidioidomicosis/microbiología , Humanos , Reacción en Cadena de la Polimerasa/economía , Factores de Tiempo
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