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Multistate foodborne outbreaks pose significant public health risks and require meticulous investigation to identify sources and implement control measures. The Centers for Disease Control and Prevention (CDC) utilizes a dynamic seven-step process for these investigations, integrating data from laboratories, interviews, and environmental assessments to protect public health.Outbreak Detection: The detection of multistate outbreaks typically begins with PulseNet, the CDC's national laboratory...

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Methods for Rapid Transfer and Localization of Lyme Disease Pathogens Within the Tick Gut
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Virus Isolation from Field-Collected Ticks: In Vivo.

Jessica Crooker1,2,3, Dakota N Paine1,2,3, Saravanan Thangamani4,5

  • 1Department of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, NY, USA.

Methods in Molecular Biology (Clifton, N.J.)
|June 13, 2025
PubMed
Summary
This summary is machine-generated.

Powassan virus (POWV) and Deer tick virus (DTV) are emerging North American tick-borne viruses. This study presents a new protocol for isolating these viruses from field-collected ticks using an in vivo system.

Keywords:
Deer tick virusPowassan virusTick-borne diseaseTick-borne virusViral isolation

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Area of Science:

  • Virology
  • Epidemiology
  • Public Health

Background:

  • Tick-borne viruses like Powassan virus (POWV) and Deer tick virus (DTV) are increasing in prevalence.
  • These viruses are genetically similar but distinct emerging threats in North America, causing severe encephalitis.
  • Current research often relies on lab strains, potentially not reflecting circulating viral populations.

Purpose of the Study:

  • To develop and present a reliable protocol for isolating circulating strains of POWV and DTV from field-collected ticks.
  • To facilitate better understanding of viral evolution and more accurate human health risk assessments.
  • To enhance the translational potential of research on these emerging tick-borne viruses.

Main Methods:

  • The study outlines a protocol for isolating POWV and DTV.
  • The methodology utilizes an in vivo system for virus isolation.
  • Field-collected ticks are the source material for isolating circulating viral strains.

Main Results:

  • The protocol enables reliable isolation of POWV and DTV from field-collected ticks.
  • This method allows for the study of circulating viral strains, not just laboratory prototypes.
  • The findings support improved understanding of viral diversity and epidemiology.

Conclusions:

  • The presented in vivo protocol offers a reliable method for isolating emerging tick-borne viruses like POWV and DTV.
  • This approach is crucial for studying viral evolution and assessing public health risks associated with these pathogens.
  • The methodology advances translational research for tick-borne encephalitis viruses.