Publications by authors named "Jennifer L Havens"

Background: Congregate living provides an ideal setting for SARS-CoV-2 transmission in which many outbreaks and superspreading events occurred. To avoid large outbreaks, universities turned to remote operations during the initial COVID-19 pandemic waves in 2020 and 2021. In late-2021, the University of California San Diego (UC San Diego) facilitated the return of students to campus with comprehensive testing, vaccination, masking, wastewater surveillance, and isolation policies.

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The emergence of SARS-CoV in 2002 and SARS-CoV-2 in 2019 led to increased sampling of sarbecoviruses circulating in horseshoe bats. Employing phylogenetic inference while accounting for recombination of bat sarbecoviruses, we find that the closest-inferred bat virus ancestors of SARS-CoV and SARS-CoV-2 existed less than a decade prior to their emergence in humans. Phylogeographic analyses show bat sarbecoviruses traveled at rates approximating their horseshoe bat hosts and circulated in Asia for millennia.

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Using a phylogenetic framework to characterize natural selection, we investigate the hypothesis that zoonotic viruses require adaptation prior to zoonosis to sustain human-to-human transmission. Examining the zoonotic emergence of Ebola virus, Marburg virus, influenza A virus, SARS-CoV, and SARS-CoV-2, we find no evidence of a change in the intensity of natural selection immediately prior to a host switch, compared with typical selection within reservoir hosts. We conclude that extensive pre-zoonotic adaptation is not necessary for human-to-human transmission of zoonotic viruses.

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Socio-economic disparities were associated with disproportionate viral incidence between neighborhoods of New York City (NYC) during the first wave of SARS-CoV-2. We investigated how these disparities affected the co-circulation of SARS-CoV-2 variants during the second wave in NYC. We tested for correlation between the prevalence, in late 2020/early 2021, of Alpha, Iota, Iota with E484K mutation (Iota-E484K), and B.

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Article Synopsis
  • The emergence of SARS-CoV and SARS-CoV-2 has led to more research on related viruses in horseshoe bats, showing they frequently recombine and have distinct patterns across Asia.
  • The closest known bat virus ancestors to these coronaviruses existed only 1-3 years before they infected humans, suggesting a recent link to their emergence.
  • The study indicates that these bat ancestors circulated far from the emergence sites, implying that other factors, beyond just bat transmission, contributed to the emergence of these viruses in humans.
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The eukaryotic protozoan parasite Trypanosoma brucei is transmitted by the tsetse fly to both humans and animals, where it causes a fatal disease called African trypanosomiasis. While the parasite lacks canonical DNA sequence-specific transcription factors, it does possess histones, histone modifications, and proteins that write, erase, and read histone marks. Chemical inhibition of chromatin-interacting bromodomain proteins has previously been shown to perturb bloodstream specific trypanosome processes, including silencing of the variant surface glycoprotein (VSG) genes and immune evasion.

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  • HSV-2 is a common DNA virus with two main lineages: one in West and Central Africa and another present globally.
  • Competing theories exist about its migration out of Africa, either following early human migrations 50-100,000 years ago or spreading through the trans-Atlantic slave trade 150-500 years ago.
  • Analysis of newly sequenced HSV-2 genomes indicates that the virus likely originated in East Africa and spread globally about 22-29,000 years ago, coinciding with human migrations after the Last Glacial Maximum.
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Regional connectivity and land travel have been identified as important drivers of SARS-CoV-2 transmission. However, the generalizability of this finding is understudied outside of well-sampled, highly connected regions. In this study, we investigated the relative contributions of regional and intercontinental connectivity to the source-sink dynamics of SARS-CoV-2 for Jordan and the Middle East.

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Understanding the circumstances that lead to pandemics is important for their prevention. We analyzed the genomic diversity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) early in the coronavirus disease 2019 (COVID-19) pandemic. We show that SARS-CoV-2 genomic diversity before February 2020 likely comprised only two distinct viral lineages, denoted "A" and "B.

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Background: Monitoring the emergence and spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants is an important public health objective. We investigated how the Gamma variant was established in New York City (NYC) in early 2021 in the presence of travel restrictions that aimed to prevent viral spread from Brazil, the country where the variant was first identified.

Methods: We performed phylogeographic analysis on 15 967 Gamma sequences sampled between 10 March and 1 May 2021, to identify geographic sources of Gamma lineages introduced into NYC.

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Article Synopsis
  • * In this case, an individual was superinfected with two SARS-CoV-2 variants, Alpha (B.1.1.7) and Epsilon (B.1.429), which led to unexpected genomic characteristics in the Alpha variant.
  • * Full genome sequencing indicated that the Alpha variant made up about 75% of the viral presence, with the Epsilon variant at around 20%, and revealed multiple recombinant forms that could influence the virus's evolution.
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  • Wide-scale genome sequencing of SARS-CoV-2 is essential for tracking how the virus evolves during the pandemic.
  • A new software tool called Variant Database (VDB) has been developed to analyze changes in spike mutations, leading to the identification of a new lineage, B.1.526, in New York.
  • The B.1.526 lineage has mutations that may weaken the effectiveness of vaccines and natural immunity, which potentially impacted the duration of the second wave of COVID-19 cases.
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Article Synopsis
  • Wide-scale genome sequencing of SARS-CoV-2 is crucial for tracking viral changes, especially as new variants from places like the UK, South Africa, and Brazil spread globally.
  • Researchers developed a software tool called Variant Database (VDB) to quickly analyze mutations in the virus's spike protein, which is key for its entry into cells.
  • They identified a new lineage, B.1.526, in New York that showed a significant increase from <1% in late November 2020 to ~32% by February 2021, and this lineage's spike mutations may reduce the effectiveness of vaccines and convalescent plasma.
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