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From: TSS ()
Subject: Canada’s Protocols for BSE Surveillance DOES NOT MANDATE WB CONFIRMATION
Date: August 4, 2005 at 1:16 pm PST

Canadian Food Inspection Agency
Factsheet

Canada’s Protocols for BSE Surveillance
Printer-Friendly PDF version

BSE testing in Canada is in full accordance with the guidelines recommended by the World Organisation for Animal Health (OIE).

The samples collected target the highest risk cattle. This includes animals over 30 months of age that are dead, down, dying or diseased. In addition, any cattle that are exhibiting symptoms consistent with BSE must be reported to the Canadian Food Inspection Agency. This targeted surveillance program is crucial to defining the level of BSE in Canada and to confirming the effectiveness of the measures in place to protect human and animal health from the disease. A robust surveillance program, with strong producer participation, gives domestic and international consumers confidence that Canada is taking responsible actions to monitor the health of the national herd.

In June 2005, Canada exceeded its minimum testing target of 30,000 animals for the year and, as of August 1, more than 36,000 cattle had been tested. The Government of Canada continues to work with provincial governments to support and encourage the participation of Canadian cattle producers in the surveillance program.

Preliminary Testing Procedures
In Canada, two rapid BSE screening tests are used for routine surveillance - the Prionics®- Check Western and the Bio-Rad TeSeE®.

Evaluations conducted by the CFIA and agencies in other governments have found the tests to be 100% accurate for detecting BSE in cattle in later stages of the incubation period. Due to the high sensitivity of the tests, there are rare instances in which samples not infected with BSE may produce an initial reaction, thus necessitating re-testing.

Second Round of Testing
Initially reactive samples are referred to as “non-negatives”and require that the same test be repeated in duplicate by the screening laboratory.

If the repeat tests are reactive, the sample is considered “inconclusive” for BSE, and the tissue from the animal is forwarded to the National BSE Reference Laboratory, National Centre for Foreign Animal Disease (NCFAD) in Winnipeg for confirmatory testing.

The rapid test on an inconclusive sample is repeated at the National BSE Reference Laboratory and if the test is again reactive, the sample is considered to be a BSE “suspect” and is subject to confirmatory testing. Even if this third rapid test is negative, a confirmatory test (immunohistochemistry or OIE Western Blot) is run for quality assurance purposes.

Confirmatory Testing
The immunohistochemistry (IHC) and the OIE Western Blot, also called the SAF Immunoblot, are internationally recognized confirmatory tests for BSE. The IHC is the principle confirmatory test used at NCFAD.

The OIE Western Blot test may be performed on the sample in addition to, or as an alternative to, the IHC test. It is always used on poor quality tissue samples when it may not be possible to conduct the IHC test, or on suspect samples where the IHC is negative.

http://www.inspection.gc.ca/english/anima/heasan/disemala/bseesb/bseesbsurve.shtml

THIS protocol has a flaw, the word ''or'' should be changed to ''and'';

(immunohistochemistry or OIE Western Blot)

should read ;

(immunohistochemistry AND OIE Western Blot)

WHY ASK for the blunders and the risks by not using WB, as been documented by the USDA et al in the USA???

WHY even go there???

IF the WB picks up detection where the IHC does not, then why are we even discussing this, IF they were truly trying to find and eradicate BSE/TSE$$$

IHC AND WB should be used for confirmation of any inconclusive.


anything less is not a confirmation, it's a guess.


still disgusted in Sunny Bacliff, Texas USA...TSS




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