Publications by authors named "Kee Johnson"

We investigated the impact of antiviral treatment on the emergence of SARS-CoV-2 resistance during persistent infections in immunocompromised patients (n = 15). All patients received remdesivir and some also received nirmatrelvir-ritonavir (n = 3) or therapeutic monoclonal antibodies (n = 4). Sequence analysis showed that nine patients carried viruses with mutations in the nsp12 (RNA dependent RNA polymerase), while four had viruses with nsp5 (3C protease) mutations.

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Unlabelled: Split-virion-inactivated influenza vaccines are formulated based on viral hemagglutinin content. These vaccines also contain the viral neuraminidase (NA) protein, but NA content is not standardized and varies between manufacturers. In clinical studies and animal models, antibodies directed toward NA reduced disease severity and viral load; however, the impact of vaccine-induced NA immunity on airborne transmission of influenza A viruses is not well characterized.

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SARS-CoV-2 infection induces the generation of virus-specific CD4 and CD8 effector and memory T cells. However, the contribution of T cells in controlling SARS-CoV-2 during infection is not well understood. Following infection of C57BL/6 mice, SARS-CoV-2-specific CD4 and CD8 T cells are recruited to the respiratory tract, and a vast proportion secrete the cytotoxic molecule granzyme B.

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We investigated the impact of antiviral treatment on the emergence of SARS-CoV-2 resistance during persistent infections in immunocompromised patients (n=15). All patients received remdesivir and some also received nirmatrelvir-ritonavir or monoclonal antibodies. Sequence analysis showed that nine patients carried viruses with mutations in the nsp12 (RNA dependent RNA polymerase), while four had viruses with nsp5 (3C protease) mutations.

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Obesity is well established as a risk factor for many noncommunicable diseases; however, its consequences for infectious disease are poorly understood. Here, we investigated the impact of host obesity on influenza A virus (IAV) genetic variation using a diet-induced obesity ferret model and the A/Hong Kong/1073/1999 (H9N2) strain. Using a co-caging study design, we investigated the maintenance, generation, and transmission of intrahost IAV genetic variation by sequencing viral genomic RNA obtained from nasal wash samples over multiple days of infection.

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Article Synopsis
  • SARS-CoV-2, the virus causing COVID-19, triggers the quick production of T cells in the body, which help in fighting the infection and forming a memory against it.
  • A study using mice showed that while T cells are recruited to the respiratory tract, they have different roles in the upper (nose) and lower (lungs) parts; specifically, they are less crucial for clearing the virus from the lungs.
  • The research found that both CD4+ and CD8+ T cells are essential for controlling viral replication in the nasal region, suggesting that T cells play a significant role in managing the infection within the respiratory tract.
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High error rates of viral RNA-dependent RNA polymerases lead to diverse intra-host viral populations during infection. Errors made during replication that are not strongly deleterious to the virus can lead to the generation of minority variants. However, accurate detection of minority variants in viral sequence data is complicated by errors introduced during sample preparation and data analysis.

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Unlabelled: High error rates of viral RNA-dependent RNA polymerases lead to diverse intra-host viral populations during infection. Errors made during replication that are not strongly deleterious to the virus can lead to the generation of minority variants. However, accurate detection of minority variants in viral sequence data is complicated by errors introduced during sample preparation and data analysis.

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Airborne transmission in ferrets is a key component of pandemic risk assessment. However, some emerging avian influenza viruses transmit between ferrets but do not spread in humans. Therefore, we evaluated sequential rounds of airborne transmission as an approach to enhance the predictive accuracy of the ferret model.

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Article Synopsis
  • Alphaviruses and flaviviruses have similar class II fusion glycoproteins crucial for their assembly and infectivity, specifically noting conservation in the tip of domain II among both virus families.
  • Research on Zika virus identified a novel envelope glycoprotein variant that, while minimally affecting infection in mosquitoes, reduced viral replication in human cells and mice and heightened sensitivity to ammonium chloride.
  • The study further explored mutations in the flavivirus E β-strand c and ij loop, revealing that certain alterations can inhibit the production of infectious Zika and yellow fever viruses, suggesting that structural similarities in these glycoproteins play significant roles in viral infection and could inform antiviral strategies.
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Article Synopsis
  • Researchers created a system using immunocompromised mice to study how Zika virus (ZIKV) evolves during infection, focusing on its transmission and characteristics.
  • They found that the way ZIKV is transmitted and the specific environments in different organs affect the virus's diversity and the types of defective genomes produced.
  • The study also discovered ZIKV mutants that aligned with strains circulating in Asia and America, as well as unique mutations from the mouse model, enhancing our understanding of arbovirus evolution and the factors that influence it.
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The error-prone replication and life cycle of influenza virus generate a diverse set of genetic variants. Transmission between hosts strictly limits both the number of virus particles and the genetic diversity of virus variants that reach a new host and establish an infection. This sharp reduction in the virus population at transmission--the transmission bottleneck--is significant to the evolution of influenza virus and to its epidemic and pandemic potential.

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