| Genetic Information
Genetic makeup has been determined
to be a significant factor in a sheep's susceptibility
to infection with scrapie. At this time,
a correlation between specific genetics and
related scrapie susceptibility has not been
determined for goats. Current experimental
evidence indicates that there are different
forms of the sheep
prion proteins. Some forms are highly
susceptible to the structural transformation
to the abnormal form associated with scrapie
while others demonstrate resistance to this
change. As in all mammals, sheep are diploid
organisms, so that all cells contain two copies
of each chromosome and thus two copies of the
gene that codes for the prion protein.
Genes are made up of codons. A codon is
a stretch of DNA that determines which particular
amino acid will be included at a particular
location of a protein (in this case the prion
protein). The prion protein is composed
of 256 amino acids; therefore there are 256
codons determining these amino acids.
In the literature concerning susceptibility
to various strains of scrapie three codons are
discussed: 171, 154 and 136. In North
America (NA), 171 and 136 are given primary
importance. The presence of arginine
(R) at codon 171 of the prion protein confers
resistance to the prion protein undergoing the
structural change associated with NA scrapie.
The presence of glutamine (Q) or histidine at
codon 171 results in the prion protein being
susceptible to the structural change associated
with NA scrapie. Histidine at site 171
is considered to have the same susceptibility
as Q and is therefore represented as Q in all
further discussion. The coding for alanine
(A) by codon 136 confers resistance to the prion
protein undergoing the structural change associated
with scrapie. The coding for valine (V)
by codon 136 can produce susceptibility to structural
change associated with scrapie. V at site
136 is linked with Q at site 171 such that R
cannot be found at site 171 in combination with
V at site 136.
The majority of cases of scrapie,
worldwide have been in sheep homozygous for
glutamine (QQ) at 171. There have been
a small number of cases of scrapie reported
in QR (171) sheep. In these cases, the
amino acids coded for by codon 136 are examined
and coding for valine appears to indicate greater
susceptibility among the QR population. There
are currently two theories as to when the QR
(171) population becomes infected. One
is that these sheep are susceptible only to
certain strains of scrapie. The other
theory is that when the prevalence of infection
with the QQ (171) population of a flock builds
to very high levels, there is a spillover of
infection into the next most susceptible subpopulation
within the flock. During 2003, a very small
number of cases of scrapie were reported in
RR (171) sheep in Europe. The profile
of sheep's prion genotype varies between breeds,
between countries and between flocks.
Probability of a sheep
with that particular genotype being susceptible
to scrapie:
Genotype
(136, 171) |
Susceptibility
to Scrapie |
AARR |
Negligible |
AAQR |
Very
low |
AVQR |
Intermediate |
AAQQ |
|
AVQQ |
|
VVQQ |
High |
It is still not known definitively
whether animals with less susceptible genotypes
do not become infected with the scrapie agent
or whether they are merely protected from
developing the clinical signs of scrapie.
Recent science indicates that the genotype
of the fetus influences the migration and
accumulation of abnormal prion in the placenta
of an infected ewe. A QQ (171) infected
ewe carrying a QQ (171) fetus results in the
accumulation of large quantities of abnormal
prion, which is then shed during birth or
abortion. Theoretically, in a fetus
with a genotype QR (171) or RR (171), the
abnormal prion does not accumulate to a significant
degree in the placenta and associated fluids.
This means that use of a RR (171) ram can
prevent the shed of abnormal prion at lambing
even from infected ewes. Heavy promotion
of the use of RR (171) rams across Canada
might be effective in minimizing the spread
of scrapie, but it may result in a significant
change in the genotypic profile of sheep in
Canada. There might be impacts on secondary
characteristics, such as carcass quality,
or the unveiling of previously unidentified
congenital problems. As in other countries,
preliminary investigation of the demographics
of the Canadian sheep population have clearly
indicated that there is considerable genetic
variation in the presence of resistance for
scrapie between breeds and flocks. It
may be impossible or impractical for certain
sheep producers to select and breed for genetic
resistance for scrapie.
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