Publications by authors named "Timothy Stockwell"

Avian influenza A virus (IAV) surveillance in Northern California, USA, revealed unique IAV hemagglutinin (HA) genome sequences in cloacal swabs from lesser scaups. We found two closely related HA sequences in the same duck species in 2010 and 2013. Phylogenetic analyses suggest that both sequences belong to the recently discovered H19 subtype, which thus far has remained uncharacterized.

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Excessive alcohol use is a leading cause of preventable death in the United States (1) and costs associated with it, such as those from losses in workplace productivity, health care expenditures, and criminal justice, were $249 billion in 2010 (2). CDC used the Alcohol-Related Disease Impact (ARDI) application* to estimate national and state average annual alcohol-attributable deaths and years of potential life lost (YPLL) during 2011-2015, including deaths from one's own excessive drinking (e.g.

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Excessive alcohol use is a leading cause of preventable death in the United States (1) and costs associated with it, such as those from losses in workplace productivity, health care expenditures, and criminal justice, were $249 billion in 2010 (2). CDC used the Alcohol-Related Disease Impact (ARDI) application* to estimate national and state average annual alcohol-attributable deaths and years of potential life lost (YPLL) during 2011-2015, including deaths from one's own excessive drinking (e.g.

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Background: Alcohol warning labels are a promising, well-targeted strategy to increase public awareness of alcohol-related health risks and support more informed and safer use. However, evidence of their effectiveness in real-world settings remains limited and inconclusive.

Objective: This paper presents a protocol for a real-world study examining the population-level impact of enhanced alcohol warning labels with a cancer message; national drinking guidelines; and standard drink information on attention, processing, and alcohol-related behaviors among consumers in Canada.

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Development of antiviral drug resistance is a continuous concern for viruses with high mutation rates such as influenza. The use of antiviral drugs targeting host proteins required for viral replication is less likely to result in the selection of resistant viruses than treating with direct-acting antivirals. The iminosugar UV-4B is a host-targeted glucomimetic that inhibits endoplasmic reticulum α-glucosidase I and II enzymes resulting in improper glycosylation and misfolding of viral glycoproteins.

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The original publication of this article [1] was missing the below author that made contributions to the research and the published article.

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  • Wild ducks and gulls serve as primary reservoirs for avian influenza A viruses (AIVs), with their evolution influenced by environmental factors where various species interact.
  • The Republic of Georgia, situated at a crucial migratory crossroads, was studied from 2010 to 2016, revealing diverse subtypes of AIV, including both low-pathogenic and highly pathogenic ones.
  • Genetic analyses showed that AIVs exhibited host-specific lineages and varying rates of gene reassortment, highlighting both local maintenance of certain virus strains and connections to broader Eurasian and African virus populations.
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  • * The draft genome assembly is mostly complete but is missing some repetitive sequences and has separated haplotypes at various locations.
  • * Short-read DNA data validated the assembly by showing a higher mapping rate to the ISE6 genome compared to a reference genome, suggesting this assembly could help filter out host DNA when studying pathogen-infected cells.
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Eastern equine encephalitis virus (EEEV) has a high case-fatality rate in horses and humans, and Florida has been hypothesized to be the source of EEEV epidemics for the northeastern United States. To test this hypothesis, we sequenced complete genomes of 433 EEEV strains collected within the United States from 1934 to 2014. Phylogenetic analysis suggested EEEV evolves relatively slowly and that transmission is enzootic in Florida, characterized by higher genetic diversity and long-term local persistence.

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High throughput sequencing (HTS) has been used for a number of years in the field of paleogenomics to facilitate the recovery of small DNA fragments from ancient specimens. Recently, these techniques have also been applied in forensics, where they have been used for the recovery of mitochondrial DNA sequences from samples where traditional PCR-based assays fail because of the very short length of endogenous DNA molecules. Here, we describe the biological sexing of a ~4000-year-old Egyptian mummy using shotgun sequencing and two established methods of biological sex determination (R and R), by way of mitochondrial genome analysis as a means of sequence data authentication.

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Background: Influenza vaccination aims to prevent infection by influenza virus and reduce associated morbidity and mortality; however, vaccine effectiveness (VE) can be modest, especially for subtype A(H3N2). Low VE has been attributed to mismatches between the vaccine and circulating influenza strains and to the vaccine's elicitation of protective immunity in only a subset of the population. The low H3N2 VE in the 2012-2013 season was attributed to egg-adaptive mutations that created antigenic mismatch between the actual vaccine strain (IVR-165) and both the intended vaccine strain (A/Victoria/361/2011) and the predominant circulating strains (clades 3C.

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Human adenoviruses (HAdVs) are uniquely important "model organisms" as they have been used to elucidate fundamental biological processes, are recognized as complex pathogens, and are used as remedies for human health. As pathogens, HAdVs may effect asymptomatic or mild and severe symptomatic disease upon their infection of respiratory, ocular, gastrointestinal, and genitourinary systems. High-resolution genomic data have enhanced the understanding of HAdV epidemiology, with recombination recognized as an important and major pathway in the molecular evolution and genesis of emergent HAdV pathogens.

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  • Foot-and-mouth disease (FMD) is a serious viral infection in livestock, with persistent infections in animals like Asian buffalo providing insight into the virus's evolution within hosts.
  • A study collected genetic data from 12 buffalo over a year, revealing minimal genetic changes in FMDV despite long-term infections, and finding specific mutations compared to earlier virus samples from 2008-2009.
  • The results suggest that understanding the genetic dynamics of FMDV in persistent infections can inform better vaccination strategies and disease control measures in affected regions.
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  • Human cell lines HepG2, HuH-7, and Jurkat are used to amplify RNA viruses from environmental samples.
  • Researchers sequenced these cell lines and created a subtraction database to filter out sequences commonly found in uninfected cells.
  • Analyzing RNAseq data from cell lines infected with Sendai virus allowed for mapping against the subtraction database, significantly reducing non-viral reads and enabling more efficient data analysis.
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  • The C6/36 cell line, derived from Aedes albopictus mosquitoes, is crucial for studying viruses like Zika, dengue, and chikungunya, and now has an annotated genomic assembly.
  • This new genome assembly features the largest contig N50 seen in mosquitoes, includes complete haplotypes, and reveals important genetic mutations and expressions that could inform research.
  • The enhanced genome data allows researchers to better analyze virus-host interactions and develop strategies to combat mosquito-borne diseases.
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  • Current methods for genetic engineering of cytomegalovirus (CMV) are inefficient, leading to mutations and difficulties in manipulating multiple genome locations simultaneously due to the use of bacterial artificial chromosomes (BACs).
  • The researchers adapted synthetic biology tools to clone the entire CMV genome by using transformation-associated recombination (TAR), successfully reconstituting the parental strain from overlapping fragments in yeast.
  • This new strategy not only allows for more efficient genome manipulation of CMV but also facilitates the creation of viral genomes derived from synthetic DNA, improving the experimental capabilities in studying large DNA viruses.
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Influenza A and B viruses are the causative agents of annual influenza epidemics that can be severe, and influenza A viruses intermittently cause pandemics. Sequence information from influenza virus genomes is instrumental in determining mechanisms underpinning antigenic evolution and antiviral resistance. However, due to sequence diversity and the dynamics of influenza virus evolution, rapid and high-throughput sequencing of influenza viruses remains a challenge.

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Venezuelan equine encephalitis (VEE) complex alphaviruses are important re-emerging arboviruses that cause life-threatening disease in equids during epizootics as well as spillover human infections. We conducted a comprehensive analysis of VEE complex alphaviruses by sequencing the genomes of 94 strains and performing phylogenetic analyses of 130 isolates using complete open reading frames for the nonstructural and structural polyproteins. Our analyses confirmed purifying selection as a major mechanism influencing the evolution of these viruses as well as a confounding factor in molecular clock dating of ancestors.

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  • The study details the complete genome of a newly isolated Dezidougou virus (DEZV) from a Zika virus culture.
  • The DEZV sequence shows a 99% nucleotide similarity to a previously reported strain (accession no. JQ675604.1).
  • The new sequence includes extra repeat regions and a deleted region that were confirmed through Sanger sequencing as missing from the original report.
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  • The CP 96-1252 cultivar is an important hybrid type of sugarcane used in agriculture.
  • Researchers extracted DNA from lab-grown leaves and sequenced it for analysis.
  • The sequencing produced 101 gigabases of data, which is accessible online for further study.
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  • Ebola and Marburg viruses, known for causing fatal hemorrhagic fever, utilize the VP35 protein to inhibit the body's antiviral response by blocking RIG-I-like receptor pathways.
  • The VP35 protein binds to both viral immunostimulatory RNA (isRNA) and specific host RNAs, effectively preventing the immune system from detecting and responding to the infection.
  • Research identified the virus's interaction with SeV copy-back defective interfering (DI) RNA as a significant factor in VP35's ability to prevent antiviral activation while highlighting differences in RNA binding between wild-type and mutant VP35 proteins.
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We characterise the evolutionary dynamics of influenza infection described by viral sequence data collected from two challenge studies conducted in human hosts. Viral sequence data were collected at regular intervals from infected hosts. Changes in the sequence data observed across time show that the within-host evolution of the virus was driven by the reversion of variants acquired during previous passaging of the virus.

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