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Zoologix performs rodent tests for...

Bordetella

Campylobacter

Clostridium piliforme (Tyzzer's disease)

EDIM (mouse rotavirus)

Encephalomyocarditis

Helicobacter

Mouse hepatitis virus (MHV)

Mouse minute virus (MMV) & mouse parvovirus (MPV)

Mouse polyoma virus (POLY)

Mouse rotavirus (EDIM)

Mycoplasma pulmonis

Mycoplasma screen

Pasteurella

Pneumocystis carinii

Reovirus screen

Reovirus type 3 (REO3)

Salmonella

Sendai virus (SEND)

Shigella and enteroinvasive E. coli

Theiler's murine encephalomyelitis virus (TMEV)

Tularemia

Yersinia pseudotuberculosis

...and more -- see our assay menu for a complete listing of rodent assays.


Theilers disease PCR test
rodent and rabbit assay data sheet

Theiler's murine encephalomyelitis virus (TMEV)

Test code: S0102 - Ultrasensitive qualitative detection of TMEV by reverse transcription real time PCR

Theiler’s murine encephalomyelitis virus (TMEV) is a single-stranded RNA picornavirus that persistently infects the murine central nervous system. The virus has recently been reclassified into the cardiovirus group. Mice are the natural host of this virus. In the wild it produces a gastrointestinal infection that may be complicated by concomitant infection of the nervous system.

There are two main groups of TMEV. One includes the GDVII and FA viruses, which produce an acute fulminant encephalomyelitis, which is fatal in about a week. The other, called Theiler’s original group, includes the DA, BeAn, and WW viruses. These produce a chronic persistent central nervous system infection, accompanied by inflammatory demyelinating lesions of the spinal cord with features very similar to those of demyelinating plaques seen in human multiple sclerosis. The demyelination induced by TMEV infection is mediated by the immune system rather than as a consequence of viral infection of oligodendrocytes, the myelin forming cells.

A classic study (Theiler, 1937) showed that mice infected with the virus may not show prominent symptoms and become carriers of the virus. The virus can be transmitted easily through soiled bedding.

Serological detection of the virus is inadequate, especially in nude or immunocompromised mice. Furthermore, neonatal mice infected with the virus may not be readily identified due to residual maternal antibodies. Molecular detection by PCR can overcome all these problems and is highly sensitive and specific for TMEV.

Utilities:

  • Confirm the disease causing agent
  • Shorten the time required to confirm a clinical diagnosis of TMEV
  • Ensure that vivariums are free of TMEV
  • Early prevention of spread of this virus among a vivarium
  • Minimize personnel exposure to this virus
  • Safety monitoring of biological products that derive from mice

References:
Theiler, M. (1937) Spontaneous encephalomyelitis of mice, a new virus disease, J. Exp. Med. 65: 705–719.

Specimen requirements: 0.1 ml whole blood in EDTA (purple top) or ACD (yellow top) tube, or CSF, or fresh or paraffin-embedded tissue, shipped overnight at room temperature; or tissue shipped frozen.

For specimen types other than those listed here, please call to confirm specimen acceptability and shipping instructions.

For all specimen types, if there will be a delay in shipping, or during very warm weather, refrigerate specimens until shipped and ship with a cold pack unless more stringent shipping requirements are specified. Frozen specimens should be shipped so as to remain frozen in transit. See shipping instructions for more information.

Turnaround time: 2 business days

Methodology: Ultrasensitive qualitative reverse transcription real time polymerase chain reaction

Normal range: Nondetected

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