Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes
Protocol Name
DOI:10.17504/protocols.io.bbh9ij96 RRID Copied  
PDF Report How to cite
Peter Kuhnert, Tobias Hidber 2020. Detection of viable Dichelobacter nodosus by real-time PCR using PMAxx™. protocols.io dx.doi.org/10.17504/protocols.io.bbh9ij96
Copy Citation Copied
Protocol Information

URL: https://dx.doi.org/10.17504/protocols.io.bbh9ij96

Authors: Peter Kuhnert, Tobias Hidber

Summary: Dichelobacter nodosus is a gram-negative fastidious anaerobic bacterium and the causative agent of ovine footrot. The disease has a global presence and is endemic in many countries. Clinical symptoms range from mild interdigital dermatitis in benign footrot to severe underrunning and separation of the hoof horn from the underlying tissue in virulent footrot. Clinical symptoms start as early as 2 weeks after first contact and the disease leads to pain, lameness, decreased meat and wool production as well as animal welfare issues. Diagnosis has improved significantly by the development of a real-time PCR to detect and discriminate virulent (aprV2-positive) and benign (aprB2-positive) D. nodosus strains. However, the real-time PCR also detects dead cells making its use for testing e.g. disinfecting agents limited. A PMA (propidium monoazid) real-time PCR using the improved dye PMAxx™ was therefore developed for virulent D. nodosus that allows discrimination of viable and dead bacteria. The distinction between viable and non-viable cells is possible, based on membrane integrity. For that purpose, the samples containing D. nodosus are treated with the improved nucleic acid intercalating PMA dye PMAxx™ that selectively enters cells with compromised cell membranes, whereas the intact cell membrane presents a natural barrier for this molecule. After exposure to strong light, it covalently binds to the DNA, preventing DNA from being amplified by PCR, thereby enabling differentiation of viable from non-viable cells. The PMA-qPCR proved to be a valid method for comparison of antimicrobial efficiency in ex vivo experiments.

Associated Publications: Hidber T, Pauli U, Steiner A, Kuhnert P (2020) In vitro and ex vivo testing of alternative disinfectants to currently used more harmful substances in footbaths against Dichelobacter nodosus. PLoS ONE 15(2): e0229066. doi: 10.1371/journal.pone.0229066

Affiliations: Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Switzerland, Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Switzerland

External URL: https://doi.org/10.1371/journal.pone.0229066

Version: 1

Publication Date: 2020

Expand All
Usage and Citation Metrics

Coming soon.

Checkfor all resource mentions.

Collaborator Network

Coming soon.

Data and Source Information

Source: Protocols.io