BVD (Bovine Viral Diarrhea) virus is
a sneaky pathogen that can affect cattle in many different ways.
It can cause abortion, mummification of a fetus, birth defects,
stillborn full-term calves, normal looking calves with immune
deficiencies, acute or chronic illness, and is an indirect cause
of many other types of disease because it has adverse affects on
the immune system. An estimate a few years ago stated that 80
percent of cattle in the U.S. have been exposed to BVDV and that
70 to 90 percent of infections go undetected, without visible
symptoms. The only clue that you might have BVDV in your herd
may be poor reproductive rate due to pregnancy losses, or a
higher than normal rate of sickness in calves.
The first descriptions of this disease in North America were
reported more than 60 years ago—describing outbreaks of highly
fatal diarrhea (hence the name), digestive tract ulcers, nasal
discharge and abortions. Many veterinarians feel that this
disease should be renamed, since diarrhea as a symptom is due to
just one aspect of the disease. In most herds you won’t find an
animal with diarrhea, but you might still find BVDV.
The virus is an elusive villain
because there are 2 different biotypes that have different
effects within body cells. These effects are called cyptopathic
(making obvious changes in the cells and killing them) and
noncytopathic. The latter category of virus does not destroy or
change the shape of the cells. The main difference is that the
cytopathic virus infects cells in the lymph tissues of the gut,
while the noncytopathic virus infects a wider range of body
cells—including respiratory tract and blood cells as well as
lymphoid tissue—and also persists longer in the animal.
The confusing thing is that there
are also 2 basic genetic types (Type I and Type II) of the
virus, and both can be present in the same animal. They can also
change their genetic composition during multiplication. This
explains why there can be such variation in disease symptoms and
differences in how an animal’s immune system deals with the
virus. Each type also has both cytopathic and noncytopathic
versions. Thus there are several forms of the disease, ranging
from sub-clinical infections in which the animal shows no
obvious signs, to a severe and highly fatal form called mucosal
disease, characterized by diarrhea.
BVDV can affect digestive,
respiratory, nervous, reproductive and immune systems. Non-cytopathic
viruses cause more than 90 percent of BVD outbreaks and are
always the cause of persistently infected cattle. BVDV can
mutate or change and since there are several strains, the
infected animal may or may not be able to mount a protective
immune response or be protected by vaccination. Type I and Type
II viruses can produce different disease signs.
The cytopathic biotype generally
causes acute rather than chronic infection. The illness may be
mild or severe, but it’s temporary. The animal sheds the virus
for up to 15 days after infection, then clears it from the body.
These animals are not a big a threat to herd health because they
don’t continue to shed the virus. By contrast, persistently
infected (PI) animals--infected before birth when the pregnant
cow is exposed to the virus--shed larger numbers of virus
particles in body secretions, and continue to do so throughout
their lives.
Mucosal Disease
The most serious form of BVD was first called mucosal disease
and the main symptom is diarrhea. This is a highly fatal
impairment of the small intestine. The virus has a cytopathic
effect, destroying the cells. Mucosal disease occurs only in
cattle that were infected before birth with a noncytopathic
version of the virus. These calves may seem normal at birth but
have no immunity to the virus and are persistently infected
(PI). If at some point they come into contact with a cyptopathic
version of BVDV they cannot build immunity. They can’t develop
immunity from vaccination, either. So they are vulnerable to
severe effects of the cell-killing version of the virus if it’s
a strain closely related to the persistently infecting virus.
But not every combination of noncytopathic and cytopathic BVDV
in a PI animal results in mucosal disase.
Cattle 6 months to 2 years of age
are most likely to develop mucosal disease. Though only a small
percentage of a herd may be affected, nearly all affected
animals die. Most of these were persistently infected before
birth with a strain of noncytopathic virus and then became
exposed to an animal shedding a cytopathic BVD virus of the same
strain. Mucosal disease often causes profuse watery diarrhea
which may contain blood and intestinal lining. The diarrhea
usually develops 2 to 3 days after the animal shows symptoms of
illness (goes off feed and becomes weak and depressed, with
fever). There are often lesions in the mouth (lips, tongue) or
insides of the nostrils. Due to dehydration and emaciation,
acute cases usually die in a few days or weeks. A few become
chronic and may survive many months, becoming more and more
emaciated.
Diarrhea in chronic cases may be
continuous or intermittent and some animals develop chronic
bloat. Lesions in the mouth are slow to heal. The animal may
also be lame. Treatment is not recommended because even if
there’s a slight chance for recovery, the animal will be
infected for life. Most veterinarians recommend humane
destruction. It’s important to work with your vet for proper
diagnosis, to know whether it’s worth trying to treat the sick
animal or not. Diarrhea from acute and temporary BVD infection
caused by a cytopathic biotype of the virus is usually mild and
followed by rapid recovery. But mucosal disease (which may be
acute or chronic) is the result of dual infection with both
cytopathic and noncytopathic biotypes and generally causes death
in PI animals.
The Problem of Persistent Infections
If a cow is infected while pregnant, the virus usually crosses
through the placenta to her unborn calf, even if the dam does
not show signs of illness. Outcome of fetal infection depends on
the age of the fetus at the time it’s infected. If infection
occurs prior to 100 days of gestation, BVDV may cause birth
defects or death of the fetus (absorption, mummification or
abortion). The dead fetus may be aborted at the time of
infection or up to several months later.
Calves infected during the third
trimester (after 150 days) may be normal at birth, having
developed immunity. If a blood test is taken, they have a titer
to BVDV. Their immune systems were mature enough at the time of
infection to create antibodies to protect themselves and fight
off the virus.
The biggest problem is when
fetuses are infected by a non-cytopathic virus before they’ve
developed a competent immune system (before 140-150 days of
gestation). These calves may end up persistently infected with
BVDV because their immune systems do not recognize the virus as
anything other than a part of their own body. The calf’s body
therefore tolerates it as something normal rather than foreign
and does not produce any immune response against it. The virus
continues to multiply, infecting more cells, and being excreted
from the animal. These calves may appear normal and healthy at
birth, but continue to shed BVDV throughout their lives. They
continually act as a source of infection for other cattle. These
carriers of BVDV are the biggest threat to herd health, and the
main source of spread within and between farms/ranches or in a
feedlot.
The PI animal sheds high numbers
of virus particles in nasal discharges, saliva, semen, milk,
urine and tears. Feces contain virus particles, but in lesser
numbers. Acute BVD infections, by contrast, are less likely to
spread the virus because even though the animal is ill the usual
shedding period is only 7 to 10 days. Then the sick animal
mounts an immune defense, clears the virus, and is no longer a
source of infection.
If you keep a PI heifer in your
herd, however, she sheds BVDV for the rest of her life, and all
her calves become infected during her pregnancies. This is one
of the main ways BVDV persists within a herd, and these PI
cattle are always at risk for mucosal disease if they encounter
a cytopathic form of the virus.
PI cattle are also at risk for
other diseases, since BVDV in their bodies hinders the immune
system. PI calves have higher incidence of scours and pneumonia,
and higher mortality rate. They may be unthrifty and won’t gain
well. Heifers may not be selected as replacements just because
they don’t grow as well as the other calves.
Diagnosis and Testing for BVDV
To determine if your herd has a BVD problem or a risk for
problems, look at your current pregnancy rates and death loss
and also whether you’ve added new animals that might have
brought the virus to your herd. Tests can be done, to find and
remove any PI animals before the next breeding season, so no
females will be exposed during breeding and pregnancy. This will
eliminate the risk of having any PI calves born in your herd.
The point to remember is that PI
animals are created before birth, when the dam encounters BVDV
between 40 and 125 days of gestation. Once a calf is PI it will
always be PI. If a calf is not PI at birth, it can never become
PI. After any animal has tested negative for BVDV, it never
needs to be tested again for PI status. The key to eliminating
PI animals is to protect the cow herd from BVDV during
pregnancy, so no fetuses ever become exposed.
If BVDV is present, it can
usually be isolated from a blood sample, from tissue of an
aborted fetus, or from an infected weak or unthrifty calf. You
might decide to test a cow because she aborted or gave birth to
a weak or abnormal calf. To screen a herd, most testing programs
focus first on finding any PI calves in the new calf crop,
before the next breeding season—before an infected calf can
spread the virus to a pregnant cow. If a calf is found to be PI,
its dam can be checked, too.
A small skin sample can be
checked for presence of the virus. Since PI cattle have high
levels of virus in their bodies, it can be readily detected. An
ear notch is easy to collect as a sample. A ¼ inch square piece
(about the size of a pencil eraser) is taken from an ear, using
a pig ear notcher or a large diameter hole punch. The sample is
placed in a labeled container such as a sandwich bag or blood
vial and sent to a diagnostic lab. Your vet can collect the ear
notches if you wish. Samples must be kept cool but don’t need to
be frozen. Any animal that tests positive should be checked
again 4 weeks later to see if it had an acute infection at the
time of testing or is persistently infected. Virus level will be
dropping by the second test if the animal had an acute infection
(and the animal will recover and get rid of the virus) but virus
level will remain at a high level if the animal is PI. All PI
animals should be culled—making sure they go to slaughter rather
than ending up in someone else’s herd.
The first year of testing, all
calves, heifers and bulls should be tested before breeding
season (and any cow that may have lost a calf). If tissue
samples are taken from suckling calves before the cows are
rebred, you can then test the dam of any calf of any calf that
tests positive. If a calf tests negative, the dam is ok. All PI
calves and their dams should be removed from the herd before
they come into contact with any pregnant animals. This
eliminates the risk of passing the virus to a fetus. If you can
keep BVDV from reaching a fetus, there will be no more PI calves
produced. In subsequent years, only the young calves in a herd
and any newly purchased animals need to be tested. An individual
only needs to be tested once. If it is negative, it will never
become PI.
In addition to testing live
animals, it pays to necropsy any calves that die of scours,
pneumonia or any other cause, along with any stillborn calves or
aborted fetuses. If a calf is PI, this means the dam was
infected. The best way to eliminate BVDV is to check all animals
in the herd at the beginning of an eradication program, cull any
shown to be PI, then keep the herd on a good vaccination
program. If you can keep the virus from reaching a fetus—making
sure all pregnant cows have strong immunity so they don’t get
BVD while pregnant—your herd will never produce a PI calf. No
new animals should be added unless they are tested to make sure
they are free of BVDV.
Vaccination
There are several different killed and modified live virus
vaccines containing various strains and concentrations of BVD
virus. Health programs using vaccination are aimed at preventing
infection of the fetus, and this goal is harder to achieve that
just protecting an animal against acute BVD infection. Calfhood
vaccination (if properly boostered to stimulate adequate
immunity, then boostered annually with modified live virus
vaccine or semi-annually with killed vaccine) will usually
protect the animal itself from BVDV unless it was born
persistently infected.
It’s harder to obtain 100 percent
protection for the fetus if the dam is exposed to the virus. She
may have enough immunity from previous exposure or vaccination
that she won’t get sick, but the virus can still, in some cases,
infect the fetus. If the cow is exposed to BVDV in early
pregnancy, the damage is done. Annual fall vaccination of
pregnant cows (using a killed vaccine that’s safe for pregnant
cows) will not correct a problem that’s already occurred. The
best protection against BVDV is to eliminate all sources of
infection within a herd, keep up a regular vaccination program
using modified live virus vaccine ahead of breeding or an
oil-based killed virus vaccine (so cows have strongest possible
protection in early pregnancy) and never let cattle become
exposed to infected animals.
In a herd that’s already
experienced BVD problems, starting a vaccination program may not
show immediate results unless you also test for and eliminate PI
animals. Those individuals can’t produce immune response to
vaccination and continue to carry and shed the virus. Without
testing, it may take 3 years of vaccinating and culling
(removing any cows that are late breeders or those that produce
unthrifty calves) to rid a herd of BVDV.
Modified live virus (MLV) vaccine
contains the virus itself but it has been altered so it won’t
cause disease. It retains some of its original characteristics,
however, so the animal’s body will recognize it and mount a
strong immune defense, just as it would do if confronted with
the actual disease. It thus produces a stronger and
longer-lasting immunity that some of the killed vaccines. Oil
based killed vaccines give good results, however, and according
to Dr. Ron Skinner (a veterinarian and seedstock producer near
Hall, Montana, who has done extensive research on BVDV during
the past 30 years), the oil based killed vaccines produce better
vaccine titers than either the modified live vaccines or the
aluminum hydroxide based killed vaccine—and are also safer than
modified live virus. He has seen several “wrecks” with modified
live vaccines in which the vaccines were flawed and actually
gave the cattle BVD.
In many herds, an annual booster (after the initial series of
shots in a young animal) with modified live vaccine is enough to
keep cows protected. Because the modified live vaccine is so
potent, however, it should only be given to non-pregnant cows.
Otherwise there’s risk that giving it to a pregnant cow may
infect her fetus, unless you are vaccinating her during the last
trimester. You’d have to be sure of the cow’s stage of pregnancy
(such as by rectal palpation) to be safe using this vaccine, and
only do it on the advice of your vet because this would be
off-label use. There’s no reason to use it in pregnant cows now,
however, since today there are better killed virus vaccines (oil
based) that some vets feel are just as effective as modified
live virus vaccines.
Label directions for MLV vaccines
state that they be given only to non-pregnant animals and to
calves not nursing pregnant dams. There’s always some risk that
a vaccinated calf still nursing its dam (vaccinated pre-weaning)
might pass the virus to the cow and infect her fetus. If you
vaccinate your calves pre-weaning, most vets recommend using
killed vaccines, even though they require a booster later.
MLV vaccines are commonly given
to young animals (after weaning) and once a year to the cow herd
after calving and before rebreeding—preferably at least 3 weeks
before breeding—to ensure that strong immunity has developed
before pregnancy begins. MLV vaccine given at the time of
breeding or soon after (to cows with no prior immunity) may
result in death of the embryo. And there are a few cows that
when vaccinated with MLV vaccine pre-breeding will carry the
virus in their ovarian tissue (around the ovary) for 60 to 90
days, and this may hinder their ability to become pregnant. Some
veterinarians recommend use of killed vaccines, instead, for
these reasons.
A killed vaccine cannot
replicate; the virus can’t reproduce in body tissues and there’s
no chance for it to cause disease. It’s safe for pregnant cows
or for calves nursing pregnant dams. But some types of killed
vaccine don’t give as strong nor as long-lasting protection
(because they don’t stimulate the immune system as much). Most
vets recommend giving killed vaccine twice a year to cows.
Calfhood vaccinations also require more boosters. Most killed
vaccines need 2 doses at least 2 weeks apart to confer immunity.
Some veterinarians feel that the
most protection can be gained by giving MLV vaccine to cows
after calving (and at least 3 weeks before rebreeding), and then
using a killed vaccine in the fall on pregnant cows as a
booster. This may give more immunity through winter, and better
levels of antibodies in colostrum at the next calving.
Calfhood Vaccination for BVD
Many stockmen vaccinate calves pre-weaning with BVD-IBR vaccines
to develop immunity before calves are stressed. Killed vaccine
is generally used pre-weaning so dams are not at risk, even
though the IBR portion of the vaccine doesn’t give calves as
much (nor as long lasting) protection as the BVD portion and
must be boostered. Some stockmen use MLV vaccines for calves
pre-weaning even though it’s not recommended on the label.
Working with their vets on a total herd health program, they’ve
found that if the herd has strong immunity (due to annual
vaccinations kept up to date) there’s little risk of cows being
affected by their calves’ vaccinations. Thus some ranchers, on
the advice of their vets, use MLV vaccine in pre-weaning
programs for calves, without need for an additional booster. If
immune status of the herd is in question, however, MLV vaccine
should not be given to calves until after they are weaned. Keep
in mind, however, that even though combination IBR-BVD vaccines
generally give calves good protection against BVD they may be
inadequate to protect against IBR. There can still be latent
carriers, and neither the modified live nor killed products can
solve that problem.
Best protection against BVDV for
young heifers or bulls going into the herd requires 3
vaccinations (preferably MLV or oil based killed products)
before breeding age. The first injection can be given at 1 to 2
months of age before the dam is bred again (such as at branding
time), the second at weaning age, and another booster just
before the animal’s first breeding season. This gives a heifer
the strongest protection against becoming infected in early
pregnancy. After that, annual pre-breeding vaccination with MLV
is usually adequate for the rest of her life.
A 1992 study showed that use of
killed IBR-BVD vaccine at 1 to 3 months of age resulted in good
immunity to BVD when boostered just before weaning. First dose
of a killed vaccine generally gives no protection, but
boostering an oil-based vaccine 30 days later (optimal time for
a booster, for best immunity) stimulates the calf to build
immunity. Stockmen who use MLV vaccine on young calves instead
of killed vaccine found that calves develop immunity after only
one dose—and have less calfhood illness (such as scours,
pneumonia, diphtheria, pinkeye, ruptured stomachs from abomasal
ulcers, etc.)
If calves are not vaccinated
until after bulls have been put with the cows, killed vaccine is
much safer, but water based or aluminum hydroxide based
adjuvants won’t give the calves any protection until they
receive a booster at or before weaning. You do get some
protection with one shot, using an oil-based killed product,
according to Dr. Skinner. Even if you use MLV vaccine in young
calves, a booster at weaning time is essential because immunity
in the young calf may last only a few months.
Note, much of this material will appear in my upcoming book on
Cattle Health Care, to be published by Storey in late 2008, and
was checked for accuracy by Ron Skinner, DVM, at Hall, Montana.
WAYS TO PREVENT INTRODUCTION OF BVDV INTO YOUR HERD
Any cattle coming to your place or added to your herd (even
home-raised heifers) should be tested to see if they are PI, and
kept away from the breeding herd until test results are
received. One of the primary ways BVDV is introduced or
perpetuated on farms is by bringing in new animals (purchased
bulls, cows, heifers, pairs, stocker cattle, calves to graft
onto cows that lost calves) without testing them. PI cattle can
be hard to recognize because they rarely show visible signs, yet
continually shed the virus.
Any cow or heifer that conceived
a calf somewhere else (bred on the range or in a communal
pasture, or purchased as a bred animal) should be isolated until
her calf is born and tested. Purchased pregnant animals can be
PI negative themselves and still carry a PI fetus if the dam was
infected during pregnancy; she may have recovered from the
infection that affected her fetus and she’ll test negative. But
her calf will be PI and can expose your cattle to BVDV after
it’s born.
Avoid using communal pastures and
try to minimize or eliminate fenceline contact between your herd
and other cattle during the time of year your cows are in early
to mid pregnancy. Make sure your females are adequately
vaccinated to provide a high degree of protection in case they
do become exposed to BVDV during pregnancy.
BVDV CAN BE SPREAD BY BREEDING, AND BY PREG-CHECKING
Semen from infected bulls may contain the virus. Reduced
conception rates may occur in otherwise healthy cows that were
bred to (or inseminated with semen from) PI bulls. Bulls
affected with acute BVD (as opposed to being PI) may shed the
virus in their semen for a while after being infected. Infection
at the time of breeding may result in reduced pregnancy rates
due to embryo or fetal loss.
BVDV can also be spread from
infected females to susceptible females via rectal palpation. A
veterinarian using the same obstetrical glove on multiple
animals when preg-checking rectally may spread the virus from
one animal to another. Some stockmen are now using a blood test
to check for pregnancy rather than using rectal palpation, not
only because pregnancy can usually be determined sooner, but
also because it’s safer for the cow and her fetus and has no
risk for spreading disease from animal to animal.
BIRTH DEFECTS DUE TO BVDV
Infection at any stage of gestation may retard fetal growth,
resulting in poor bone growth and low birth weight. Infection
between 50 and 150 days (roughly the second trimester) may
result in birth defects rather than killing the fetus. Lung
development may be incomplete. Skeletal defects that may occur
include a jaw too short or fused joints. Another defect
sometimes seen is no hair, or less than normal amount of hair,
or curly hair. Between 100 and 150 days is the stage when the
fetus’ nervous system is in final stages of development; defects
involving the nervous system include incomplete brain
development (calves may be incoordinated and have trouble
standing up), water on the brain, and other brain problems.
Defects involving the eyes include cataracts, opaque cornea,
inflammation of the optic nerve, atrophy or abnormality of the
retina, and varying degrees of blindness in the newborn calf. |