Llama Health Issues
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is to build up a database of articles
on health issues faced by llama owners in New Zealand
Ringworm
Tuberculosis
Feeding Ruminant Protein to
Ruminants is Banned
Guidelines for Llama
Vaccinations
Ig’s and the Immune System,
A
Short Primer by Stephen Mulholland
In most discussions of animal immunity and
vaccinations, you will come across references to "Ig". This is an
abbreviation for "immunoglobulin." An immunoglobulin, or Ig, is a protein
molecule that is produced by the immune system to help recognize invading
organisms (bacterial, viral, fungal, and parasitic worms) and mark them
for elimination by other cells of the immune system. Ig’s are more
commonly known as “antibodies.” Measuring the Ig level, or quantity of
antibodies, in the blood therefore provides a good indication of the
health and capabilities of the immune system.
When a baby mammal is born, it has no
antibodies at all, and is therefore very vulnerable to infection. The
mother's colostrum contains a large number of antibodies produced by the
mother to be passed on to the young. These antibodies provide protection
in the weeks and months after birth while the baby's own immune system is
developing. The stronger the mother's immune system, the better the
protection that the baby receives via the colostrum: this is why it is
recommended to give the mother a vaccine booster shot a few weeks before
birth, as it boosts her antibody levels against common paddock diseases,
and this improved protection is passed on to the cria. If the baby does
not get any colostrum, it is very vulnerable to infection and is much more
likely to die. A plasma infusion can save such an at-risk cria by
providing it with the antibodies of an adult animal.
Vaccination presents the immune system with
a sample of what some of the common and deadly infectious organisms look
like. Vaccinating an animal in the first few days after its birth is
pointless as there are not enough immune cells in the blood stream to
effectively respond – it has its mother's antibodies, but no means yet of
producing its own. To give a cria's own immune system enough time to
develop, its first vaccination should be given six weeks after birth, with
a second dose four to six weeks later. The repetition induces the immune
system to create “memory cells,” which are antibody (Ig) producing cells
that circulate in the blood and watch for more invaders. The memory cells
can last for months or years. By giving periodic booster vaccinations, we
refresh the population of memory cells, keeping the immune
system primed to fight off those invaders.
The primary components of the immune system
are the leukocytes, or “white blood cells”, manufactured in the bone
marrow and released into the blood stream. Leukocytes come in many
different varieties, but they are all designed to work together to
identify foreign invaders and destroy them. The combined mass of cells of
the immune system is about the same as the liver, making the leukocytes,
as a group, one of the largest “organs” in the body.
A subtype of the leukocyte is the
lymphocyte. Broadly speaking, there are two different classes of
lymphocytes, the T-lymphocytes (T-cells) and B-lymphocytes (B-cells). The
T-cells are involved in what are known as “cell mediated responses”: these
respond to cells which have foreign bodies displayed on their surface and
can eliminate virus-infected and cancerous cells. T-cells can also respond
to chemical signals to activate and search for invading bacteria. The
B-cells are involved in the production, presentation, and retention of
antibodies.
Immunoglobulins are the primary tools of
the B-cells. Specialized B-cells wander the body looking for cells or
particles that are foreign. Finding an invader is only the first step. The
rest of the immune system must be notified and mobilized. Almost any large
molecule (protein, carbohydrate, fat) can induce an immune response. These
molecules are known as antigens, which stands for “antibody generators”,
and a single bacterium or virus may be covered by thousands of them. The
antigens are chopped up into small pieces, and those pieces are then
presented to the antibody-producing cells.
Every day the body produces millions of
different antibody-producing cells in the bone marrow. Each of these cells
produces a different, unique antibody. The end-tips of the antibodies have
what is known as a “variable region” that is different for every antibody
and forms a unique three-dimensional shape. If that antibody finds an
antigen that has the mirror inverse of the shape at the variable-tip, then
the antibody and antigen will bind to on another like a key fitting into a
lock. When that happens the B-cell that makes that particular antibody
knows it has a “winner” and starts to mass-produce that antibody. An
invader coated in antibodies can be easily identified and eliminated. The
antibodies coating the surface of invading bacteria or virus often have an
additional effect of preventing them from attacking the body or
reproducing, speeding their elimination. A single infectious organism can
trigger the production of dozens or even hundreds of different antibodies
against it, as there will be lots of different “fits” -- since each
organism has many different antigens on its surface. These first
antibodies vary in their efficiency for targeting the foreign invader, but
as time goes on the response will “mature” as the immune system adapts and
produces antibodies better able to target the invading antigens.
Vaccines are mixtures of antigens that can
activate the immune system without causing an infection. One common tool
for making a vaccine is to use heat-killed bacteria or viruses. The immune
system is thus presented with the shell of the invader, and can start
producing antibodies against those antigens.
Because we are exposed to millions of
different antigens, the immune system has a method to distinguish
occasional threats from persistent threats. If it wasted all its efforts
mass-producing antibodies against infections you will never experience
again, it could not be ready for the more dangerous diseases. For this
reason there are memory cells. When an infection runs for a long time, or
if a creature gets infected by the same disease again and again, some of
the best antibody-producing cells will convert into memory cells. These
are antibody-producing cells that are effectively in storage. They drift
through the bloodstream, often for years, waiting and watching for the
invader for which they optimized to reappear. If that invader comes back,
the memory cell immediately kicks into gear: it makes thousands of copies
of itself, starts cranking out antibodies, and mobilizes the rest of the
immune system against the attacker. This speeds the response time of the
immune system from weeks to days, or even hours.
Vaccinations are typically given in two
doses four to six weeks apart because this is the best method to activate
the immune system (first dose), and then cause a maturation of the
response and the production of memory cells (second dose). Booster shots
cause the memory cells to activate and reproduce, increasing their numbers
in the bloodstream. This is necessary because the memory cells do
eventually die, so without periodic boosters the immunity would gradually
fade. For most human vaccines we know how long the memory cells against
various antigens last, and thus doctors prescribe different periods for
booster shots (3 years, 10 years, etc.). In camelids, the lifespan of the
memory cells is not known, but as the common vaccines are known to only
provide about 12 months of protection in cattle and sheep it is
recommended that booster shots be given at least once and preferably twice
per year to ensure protection.
If you ever give a new type of vaccine (such
as switching from 5 in 1 to 10 in 1) you need to give the two doses, about
six weeks apart, to trigger the production of the memory cells.
Recommendations for vaccinations:
Many
different vaccines are available.
Ask
your vet about what is best for you.
Newborn cria
1 ml of
vaccine at 6 weeks, subcutaneous injection
1 ml of
vaccine at 10-12 weeks, subcutaneous injection
Adults
2 ml of
vaccine every 6-12 months, subcutaneous injection.
Adult animals should be given a booster shot
every 6 to 12 months. Once a year may be enough, twice a year provides
additional security. Most animals in NZ need some selenium
supplementation, and the vaccine is a good time to do so. Selenated
vaccines should not be given to newborn animals, as it can result in a
selenium overdose. If you are unsure of the selenium levels in local feed,
consult your vet.
Adult animals can be switched from one
vaccine to another (for example from 5 in1 to 10 in 1). If switching over,
remember to give 2
injections about 6 weeks apart to induce the formation of memory cells,
after which 1-2 boosters per year should be given.