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2.
Elife ; 82019 08 06.
Artículo en Inglés | MEDLINE | ID: mdl-31385805

RESUMEN

Dengue virus (DENV) exists as four genetically distinct serotypes, each of which is historically assumed to be antigenically uniform. Recent analyses suggest that antigenic heterogeneity may exist within each serotype, but its source, extent and impact remain unclear. Here, we construct a sequence-based model to directly map antigenic change to underlying genetic divergence. We identify 49 specific substitutions and four colinear substitution clusters that robustly predict dengue antigenic relationships. We report moderate antigenic diversity within each serotype, resulting in genotype-specific patterns of heterotypic cross-neutralization. We also quantify the impact of antigenic variation on real-world DENV population dynamics, and find that serotype-level antigenic fitness is a dominant driver of dengue clade turnover. These results provide a more nuanced understanding of the relationship between dengue genetic and antigenic evolution, and quantify the effect of antigenic fitness on dengue evolutionary dynamics.


Asunto(s)
Variación Antigénica , Virus del Dengue/clasificación , Virus del Dengue/genética , Dengue/virología , Evolución Molecular , Genotipo , Serogrupo , Análisis por Conglomerados , Variación Genética , Pruebas de Neutralización , Homología de Secuencia
3.
Viruses ; 10(9)2018 09 18.
Artículo en Inglés | MEDLINE | ID: mdl-30231576

RESUMEN

Vaccination could be an evolutionary pressure on seasonal influenza if vaccines reduce the transmission rates of some ("targeted") strains more than others. In theory, more vaccinated populations should have a lower prevalence of targeted strains compared to less vaccinated populations. We tested for vaccine-induced selection in influenza by comparing strain frequencies between more and less vaccinated human populations. We defined strains in three ways: first as influenza types and subtypes, next as lineages of type B, and finally as clades of influenza A/H3N2. We detected spatial differences partially consistent with vaccine use in the frequencies of subtypes and types and between the lineages of influenza B, suggesting that vaccines do not select strongly among all these phylogenetic groups at regional scales. We did detect a significantly greater frequency of an H3N2 clade with known vaccine escape mutations in more vaccinated countries during the 2014⁻2015 season, which is consistent with vaccine-driven selection within the H3N2 subtype. Overall, we find more support for vaccine-driven selection when large differences in vaccine effectiveness suggest a strong effect size. Variation in surveillance practices across countries could obscure signals of selection, especially when strain-specific differences in vaccine effectiveness are small. Further examination of the influenza vaccine's evolutionary effects would benefit from improvements in epidemiological surveillance and reporting.


Asunto(s)
Virus de la Influenza A/inmunología , Vacunas contra la Influenza/inmunología , Gripe Humana/inmunología , Gripe Humana/virología , Estaciones del Año , Selección Genética/inmunología , Algoritmos , Variación Antigénica , Humanos , Inmunogenicidad Vacunal , Incidencia , Subtipo H3N2 del Virus de la Influenza A/inmunología , Virus de la Influenza A/clasificación , Gripe Humana/prevención & control , Modelos Estadísticos , Vacunación , Cobertura de Vacunación
4.
Bioinformatics ; 34(23): 4121-4123, 2018 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-29790939

RESUMEN

Summary: Understanding the spread and evolution of pathogens is important for effective public health measures and surveillance. Nextstrain consists of a database of viral genomes, a bioinformatics pipeline for phylodynamics analysis, and an interactive visualization platform. Together these present a real-time view into the evolution and spread of a range of viral pathogens of high public health importance. The visualization integrates sequence data with other data types such as geographic information, serology, or host species. Nextstrain compiles our current understanding into a single accessible location, open to health professionals, epidemiologists, virologists and the public alike. Availability and implementation: All code (predominantly JavaScript and Python) is freely available from github.com/nextstrain and the web-application is available at nextstrain.org.


Asunto(s)
Biología Computacional , Evolución Molecular , Genoma Viral , Programas Informáticos , Virus/patogenicidad , Bases de Datos Genéticas
5.
PLoS Pathog ; 13(7): e1006466, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28672035

RESUMEN

Cross-species transmission (CST) has led to many devastating epidemics, but is still a poorly understood phenomenon. HIV-1 and HIV-2 (human immunodeficiency virus 1 and 2), which have collectively caused over 35 million deaths, are the result of multiple CSTs from chimpanzees, gorillas, and sooty mangabeys. While the immediate history of HIV is known, there are over 45 lentiviruses that infect specific species of primates, and patterns of host switching are not well characterized. We thus took a phylogenetic approach to better understand the natural history of SIV recombination and CST. We modeled host species as a discrete character trait on the viral phylogeny and inferred historical host switches and the pairwise transmission rates between each pair of 24 primate hosts. We identify 14 novel, well-supported, ancient cross-species transmission events. We also find that lentiviral lineages vary widely in their ability to infect new host species: SIVcol (from colobus monkeys) is evolutionarily isolated, while SIVagms (from African green monkeys) frequently move between host subspecies. We also examine the origins of SIVcpz (the predecessor of HIV-1) in greater detail than previous studies, and find that there are still large portions of the genome with unknown origins. Observed patterns of CST are likely driven by a combination of ecological circumstance and innate immune factors.


Asunto(s)
Primates/virología , Recombinación Genética , Síndrome de Inmunodeficiencia Adquirida del Simio/virología , Virus de la Inmunodeficiencia de los Simios/genética , Animales , Variación Genética , Genoma Viral , Especificidad del Huésped , Humanos , Filogenia , Primates/clasificación , Síndrome de Inmunodeficiencia Adquirida del Simio/transmisión , Virus de la Inmunodeficiencia de los Simios/clasificación , Virus de la Inmunodeficiencia de los Simios/aislamiento & purificación , Virus de la Inmunodeficiencia de los Simios/fisiología
6.
Biochem Mol Biol Educ ; 41(2): 87-94, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23401174

RESUMEN

In this laboratory module, introductory biochemistry students are exposed to two-dimensional (1) H-nuclear magnetic resonance of glycerophospholipids (GPLs). Working in groups of three, students enzymatically synthesized and purified a variety of 2-acyl lyso GPLs. The structure of the 2-acyl lyso GPL was verified using (1) H-correlation spectroscopy. Students scored significantly higher on an assessment of NMR knowledge after having participated in this lab module and in comparison to a similar cohort who did not participate. Inaddition, student confidence in their NMR knowledge and abilities increased 62% following the module and correlated with their ability to apply their NMR knowledge. Based on these results, the laboratory module was very effective at providing students with a more extensive understanding of the underlying concepts of NMR as a tool for structural determination.


Asunto(s)
Bioquímica/educación , Glicerofosfolípidos/química , Glicerofosfolípidos/síntesis química , Lisofosfolípidos/química , Lisofosfolípidos/síntesis química , Espectroscopía de Resonancia Magnética/métodos , Acilación , Cromatografía en Capa Delgada , Glicerofosfolípidos/aislamiento & purificación , Humanos , Lisofosfolípidos/aislamiento & purificación , Protones
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