Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Identification of Arcobacter isolates by PCR

K M Harmon1, I V Wesley

  • 1Enteric Diseases and Food Safety Research, USDA, Agricultural Research Service, National Animal Disease Center, Ames, IA, USA.

Letters in Applied Microbiology
|October 1, 1996
PubMed
Summary

A new polymerase chain reaction (PCR) assay allows for rapid identification of three Arcobacter species (Arcobacter butzleri, Arcobacter skirrowii, and Arcobacter cryaerophilus) found in humans and livestock. This method significantly speeds upArcobacter strain identification.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Detection of Arcobacter spp. in Ground Pork by Modified Plating Methods.

Journal of food protection·2019
Same author

Detection and genetic characterization of porcine pegivirus in pigs in the United States.

Transboundary and emerging diseases·2018
Same author

Risk of exposure to Coxiella burnetii from ruminant livestock exhibited at Iowa agricultural fairs.

Zoonoses and public health·2017
Same author

Pathogenesis of porcine epidemic diarrhea virus isolate (US/Iowa/18984/2013) in 3-week-old weaned pigs.

Veterinary microbiology·2014
Same author

Cumulative trauma disorders among hand therapists.

Work (Reading, Mass.)·2014
Same author

Response of restraint stress-selected lines of Japanese quail to heat stress and Escherichia coli challenge.

Poultry science·2013

Area of Science:

  • Microbiology
  • Molecular Biology
  • Veterinary Science

Background:

  • Arcobacter species are increasingly recognized as potential pathogens in both humans and animals.
  • Accurate and rapid identification of Arcobacter is crucial for effective diagnosis and control.
  • Current identification methods can be time-consuming.

Purpose of the Study:

  • To develop a novel polymerase chain reaction (PCR) assay for the identification of three key Arcobacter species.
  • To target specific genetic markers for enhanced diagnostic accuracy.
  • To reduce the time required for Arcobacter species identification.

Main Methods:

  • Development of a PCR assay using primers specific to the 16S rRNA genes of Arcobacter spp.
  • Testing the assay's efficacy in identifying Arcobacter butzleri, Arcobacter skirrowii, and Arcobacter cryaerophilus.

Related Experiment Videos

  • Validation of the assay for clinical and livestock samples.
  • Main Results:

    • A specific and sensitive PCR assay was successfully developed.
    • The assay accurately identified the three target Arcobacter species.
    • The developed PCR assay significantly reduced the time for Arcobacter identification compared to conventional methods.

    Conclusions:

    • The novel PCR assay provides a rapid and reliable method for identifying clinically relevant Arcobacter species.
    • This assay has the potential to improve diagnostic workflows in human and veterinary medicine.
    • Faster identification of Arcobacter can aid in timely treatment and epidemiological investigations.