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.n4sdgwe RRID Copied  
PDF Report How to cite
Crystal M. Gigante, Rene Edgar Condori, Lillian Orciari, Todd G. Smith, Yu Li 2018. Collection of brain stem for post-mortem diagnosis of rabies in animals by the LN34 pan-lyssavirus real-time RT-PCR assay. protocols.io dx.doi.org/10.17504/protocols.io.n4sdgwe
Copy Citation Copied
Protocol Information

URL: https://dx.doi.org/10.17504/protocols.io.n4sdgwe

Authors: Crystal M. Gigante, Rene Edgar Condori, Lillian Orciari, Todd G. Smith, Yu Li

Summary: Patterns of rabies virus spread within the central nervous system suggest that a thorough examination of the brain stem is critical for rabies diagnosis. Viral RNA is widespread in the brain of most animals positive for rabies. However, because virus spread may be unilateral, especially in larger animals, a negative finding for rabies can be made only if a complete cross section of the brain stem is examined. Examination may be made at the level of the pons, medulla, or midbrain of the brain stem.While a negative finding for rabies can be made only if a full cross section of brain stem tissue is examined, incomplete or suboptimal specimens should be tested, if possible. Identification of rabies virus RNA in any tissue is diagnostic of rabies infection [1, 2]. Examples of samples that may be tested for rabies virus RNA to rule-in (but not rule-out) rabies infection are hippocampus, cerebellum, cortex, saliva, and nuchal skin biopsy.

Associated Publications:

Gigante CM, Dettinger L, Powell JW, Seiders M, Condori REC, Griesser R, et al. (2018) Multi-site evaluation of the LN34 pan-lyssavirus real-time RT-PCR assay for post-mortem rabies diagnostics. PLoS ONE 13(5): e0197074. https://doi.org/10.1371/journal.pone.0197074

Affiliations: Poxvirus and Rabies Branch, Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA, Poxvirus and Rabies Branch, Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA, Poxvirus and Rabies Branch, Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA, Poxvirus and Rabies Branch, Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA, Poxvirus and Rabies Branch, Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Version: 1

Publication Date: 2018

Expand All
Usage and Citation Metrics

Coming soon.

Checkfor all resource mentions.

Collaborator Network

Coming soon.

Data and Source Information

Source: Protocols.io