Bovine viral diarrhea virus outbreak in a beef cow herd in South Dakota
Journal of the American Veterinary Medical Association, June 15, 2015 (Vol. 246, No. 12)
Susan E. Kane, PhD; Larry D. Holler, DVM, PhD; Lyle J. Braun, MS; John D. Neill, PhD;
Douglas B. Young, BA; Julia F. Ridpath, PhD; Christopher C. L. Chase, DVM, PhD
Case Description
136 pregnant beef cows were purchased in the fall of 2003. The following spring, 128 cows calved as expected; 8 cows were believed to have aborted with the fetuses unavailable for evaluation. Of the 128 calves born, 8 died within 2 weeks after birth and 9 were born with congenital abnormalities.
Clinical Findings
Cows and their calves were evaluated for bovine viral diarrhea virus (BVDV) infection. Forty-four of 120 calves, but 0 cows, tested positive for BVDV antigen by immunohistochemical staining of ear notch specimens.
Treatment and Outcome
Five BVDV test-positive calves died shortly after weaning, and the remaining 39 BVDV test-positive calves were moved to an isolated feedlot and retested for BVDV at 5 to 6 months of age; 36 had positive results, which indicated that they were persistently infected (PI) with BVDV, whereas 3 had negative results, which indicated that they were transiently infected with BVDV at the time of the first test. All PI calves were infected with the same BVDV type 2a strain. As yearlings, 17 of the 36 PI calves died peracutely with lesions consistent with mucosal disease, 6 died without gross lesions, and 2 were euthanized because of chronic ill thrift. The remaining 11 PI calves appeared healthy and were sold for slaughter. Screening of the following year’s calf crop for BVDV by use of immunohistochemical staining of ear-notch specimens yielded negative results for all calves.
Clinical Relevance
Introduction of BVDV into a naïve cow herd resulted in a loss of 44% of the calf crop subsequent to reproductive loss, poor thrift, and mucosal disease.
One hundred thirty-six 3-year-old pregnant Angus and Angus-cross beef cows with unknown vaccination histories were purchased by the South Dakota State University Antelope Range and Livestock Research Station from a producer in western South Dakota in the fall of 2003. The cows were bred to Angus bulls and were confirmed pregnant by transrectal palpation prior to purchase. Following purchase, the cows were transported to the research station in northwestern South Dakota where they were maintained on pasture and fed a ration that was formulated to meet or exceed
National Research Council requirements.1 Water was available ad libitum at all times.
One hundred twenty-eight of the 136 cows calved between March 25 and May 27, 2004, resulting in 128 live calves; 8 cows did not calve as expected and were assumed to have aborted, and the aborted fetuses were unavailable for evaluation. The cows and their calves were maintained on pasture until the calves were weaned. Eight calves died within 2 weeks after birth and were not submitted for diagnostic testing. An additional 9 calves were born with congenital abnormalities such as corneal opacity, alopecia, and red hair, which raised concerns about a potential BVDV outbreak.
In June, ear notch specimens were obtained from all calves and their dams and submitted for immunohistochemical staining for BVDV antigen as described.2 Bovine viral diarrhea virus antigen was not detected in any of the ear notch specimens obtained from the cows but was detected in the ear notch specimens of 44 of the 120 (37%) surviving calves, including 5 of the 9 calves with congenital abnormalities. Further genetic analysis of the BVDV antigen detected in positive earnotch specimens performed by the National Animal Disease Laboratory in Ames, Iowa, revealed that all calves were infected with the same BVDV type 2a strain.
The calves were weaned in August, and 5 of the 44 BVDV test–positive calves died shortly thereafter. On October 6, 2004, the remaining 39 BVDV test– positive calves were transported to a university feedlot facility in Brookings, SD, where they were isolated as a group from other cattle and retested for BVDV. From each calf, a blood sample (approx 10 mL) was collected by jugular venipuncture into an evacuated blood collection tube containing EDTA. The buffy coat fraction was recovered from each sample and submitted for BVDV isolation, which was performed by the tube method,3,4 and for a BVDV antigen capture ELISA.a Thirty-six calves had positive results for BVDV as determined by both virus isolation and the antigen capture ELISA and were considered PI with BVDV (PI calves), whereas the remaining 3 calves had negative results and were considered to have been TI with BVDV (TI calves) at the time the ear notch specimen was obtained in June.
From each of the 39 isolated calves, a blood sample (approx 10 mL) was collected by jugular venipuncture into evacuated blood collection tubes on December 8, 2004 (approx age, 9 months); February 15, 2005 (approx age, 11 months); and March 31, 2005 (approx age, 13 months)
to obtain serum for determination of neutralizing antibody titers against BVDV types 1 (BVDV1) and 2 (BVDV2). The serum neutralization assays were performed in accordance with methods recommended by the World Organisation for Animal Health4 with a cytopathic Singer strain used as the reference strain for BVDV1 and a cytopathic A125 strain used as the reference strain for BVDV2. All 3 TI calves had antibodies against
both BVDV1 and BVDV2 during the testing period. Of the 36 PI calves, only 1 had serum neutralizing antibody titers against both BVDV1 and BVDV2, whereas 3 calves had antibody titers against BVDV1 but not BVDV2 and 5 calves had antibody titers against BVDV2 but not BVDV1. The geometric mean antibody titers against both BVDV1 and BVDV2 for the TI calves were higher than those for the PI calves on each test date. For all 3 TI calves, the anti-BVDV1 antibody titer was < 1:2 and 1:512 on December 8, 2004, and February 15, 2005, respectively. On March 31, 2005, the anti-BVDV1 antibody titer was 1:256 for 1 calf, 1:512 for 1 calf, and 1:1,024 for the remaining calf. The anti-BVDV2 antibody titer was 1:4,096 for 2 of the TI calves and 1:8,192 for the remaining TI calf on December 8, 2004. On February 15, 2005, the anti-BVDV2 antibody titer was 1:512 for 1 TI calf and 1:1,024 for the remaining 2 TI calves. On March 31, 2005, the anti-BVDV2 antibody titer was 1:2,048 for all 3 TI calves.
For the 4 PI calves that tested positive for anti-BVDV1 antibodies, 1 calf had a titer of 1:8 on December 8, 2004; 2 calves a titer of 1:8 and 2 others had a
titer of 1:16 on February 15, 2005; and none of the calves had an anti-BVDV1 antibody titer on March 31, 2005. For
the 6 PI calves that tested positive for anti-BVDV2 antibodies, all 6 had detectable titers (range, 1:8 to 1:256) on December 8, 2004, whereas 2 had detectable titers (1:8) on February 15, 2005, and only 1 had a detectable titer (1:32) on March 31, 2005. During a 110-day period between May 5 and August 22, 2005, 23 of the 36 PI calves (approx age, 13 to 15 months; approx weight, 400 kg [880 lb]) died. Fifteen
of those calves died peracutely without any clinical signs of disease. The other 8 calves were found laterally recumbent without any other clinical signs of disease and were unable to attain a sternal or standing position. Those calves failed to respond to palliative treatment (NSAID and oral and IV fluid administration) and died or were euthanized within 6 to 12 hours. Many of those calves died during or following days when the ambient temperature was greater than the seasonal mean temperature for Brookings, SD. Two other PI calves (approx weight, 160 kg [352 lb]) were euthanized because of poor weight gain and chronic ill thrift. The remaining 11 PI calves that appeared clinically normal with body weights ranging
from 400 to 500 kg (880 to 1,100 lb) were sold for slaughter at the end of June 2005. The clinical outcomes for the calves born from the 136 purchased cows were summarized (Figure 1). Necropsy was performed on each of the 23 PI calves that died between May 5 and August 22, 2005. Results indicated
that 17 of the 23 (74%) calves had lesions consistent with BVDV mucosal disease (extensive erosions and ulcerations throughout the gastrointestinal tract), whereas the remaining 6 (26%) calves did not have any gross lesions.
Because calves were observed only 2 to 3 times/d and many died when the ambient temperature was abnormally high, some of the bodies had severe postmortem autolysis, which prevented histologic evaluation. However, when nonautolyzed tissues were available for histologic evaluation,
the results invariably indicated extensive necrosis of lymphoid tissues, especially the gut-associated lymphoid
tissues. Noncytopathic and cytopathic BVDV were isolated from the tissues of 12 of the 17 calves with lesions and 2 of the 6 calves without lesions. Only noncytopathic BVDV was isolated from the tissues of 3 calves with lesions and 4 calves without lesions. Bovine viral diarrhea virus was not isolated from the tissues of the remaining 2 calves with lesions; however, failure to detect BVDV in those 2 calves was likely caused by severe postmortem autolysis. Review of the calving records indicated that BVDV test–positive calves were born throughout the entire calving season, rather than in separate clusters early or late in the season (Figure 2). Most of the BVDV test–positive calves were born during the first half of the calving season, which corresponded to the period during which most of the cows calved. The mean birth weight for the 44 calves that tested positive for BVDV antigen by immunohistochemical staining of ear notch specimens (35 kg [77 lb]) was significantly less than the mean birth weight for the 76 BVDV test–negative calves (42.4 kg [93.3 lb]). The mean body weight for the BVDV test–positive calves remained less than that for the BVDV test–negative calves at 7 and 14 weeks of age; however, the mean percentage of body weight increase from birth, which accounted for differences in birth weight among calves, did not differ significantly between the BVDV test– positive and BVDV test–negative calves at either 7 or 14 weeks old (Table 1). This indicated that the growth rate of the BVDV test–positive calves was similar to that of the BVDV–test negative calves through 14 weeks of age.
BVDV strains are classified into 1 of 2 genotypes (BVDV1 or BVDV2), each of which is further subdivided into 2 biotypes (cytopathic and noncytopathic) on the basis of whether a given strain causes lytic changes in cultured cells.8,9 Infection of a pregnant cow with a noncytopathic strain of BVDV prior to 40 days of gestation can result in early embryonic death, whereas infection between 40 and 150 days of gestation can result in a fetus that is PI with BVDV, and infection during the latter stages of the second and third trimesters can cause abortion or congenital abnormalities in the fetus or less severe outcomes such as the birth of calves with poor vigor or no clinically apparent abnormalities.6,10 Cattle PI with BVDV (PI cattle) are the major reservoir for the virus,11,12 and current recommendations for BVDV control focus on the detection and removal of PI cattle.11–17 Persistently infected cattle that survive the first year of life often die from mucosal disease, which results when an animal becomes infected with a cytopathic strain of BVDV that is substantially similar
to the noncytopathic strain with which it is PI (the cytopathic strain frequently emerges from a mutation of the noncytopathic strain).18,19 Information regarding the mortality rate of PI calves within 1 year after birth and the percentage of PI cattle that die as a result of mucosal disease or appear clinically normal is lacking. The present report provided additional information
about the clinical outcomes associated with the
apparent introduction of a single strain of BVDV2 into
a herd of 3-year-old pregnant beef cows.
The BVDV outbreak described in the present report
was particularly notable because of the substantial
impact that BVDV infection had on the 2004 calf
crop. We assumed that the 8 suspected abortions and
8 neonatal deaths were related to BVDV infection, and
44 calves subsequently tested positive for BVDV at least
once. Thus, 44% (60/136) of the 2004 calf crop for this
herd was lost or otherwise affected by BVDV. The source
of most BVDV outbreaks is generally traced back to the
introduction of a PI animal into a BVDV-naïve herd.
However, immunohistochemical staining of ear notch
specimens for BVDV antigen yielded negative results for
all 136 purchased cows; therefore, it is unlikely that there
was a PI cow among the purchased cows, and the exact
point source of BVDV entry into this herd is unknown.
The present report highlighted the risk producers
assume when they purchase pregnant cattle, a common
practice in the beef and dairy industries. Currently,
there is no affordable or safe method to determine
whether the fetus a pregnant cow is carrying is PI with
BVDV. The detection of maternal viremia is not a viable
option for identification of dams carrying PI calves
because viremia associated with BVDV infection has a
short duration (generally < 10 days) and must occur
during a particular time (40 to 150 days) of gestation
to result in a PI calf.6 Screening pregnant cows for
the presence of anti-BVDV antibody titers is also not
a useful method for identification of dams carrying PI
calves because currently available neutralization assays
cannot differentiate between anti-BVDV antibodies that
resulted from vaccination and those that resulted from
natural infection, and cattle are commonly vaccinated
against BVDV.20
Other reports21,22 of BVDV mucosal disease
outbreaks in beef herds were retrospectively evaluated.
In the present report, we described the effect of BVDV
on the growth and health of a group of PI calves and
the subsequent development of mucosal disease in
those calves in a prospective manner. Infection with
BVDV alters the growth of affected cattle.23 Although
the mean birth weight and body weights at 7 and 14
weeks of age for the BVDV test–positive calves of the
present report were less than those for their BVDV test–
negative herd mates, the actual amount and percentage
of weight increase between measurements did not
differ significantly between the 2 groups of calves. This
finding indicated that the growth rate for the BVDV
test–positive calves was similar to that of the BVDV
test–negative calves. It is generally believed that most
PI calves die within the first few months after birth,
but that notion was not upheld in the present outbreak
because all 36 PI calves were clinically normal for > 1
year until the first calf succumbed to mucosal disease.
Moreover, 11 of those 36 (31%) calves remained
healthy, achieved finished market weight, and were sold
for slaughter.
The serum neutralizing anti-BVDV antibody
titers for the BVDV test–positive calves are difficult to
interpret. The consistently high anti-BVDV2 antibody
titers of the 3 TI calves were likely the result of an active
infection and continuous exposure to calves PI with a
BVDV2a strain. The presence of anti-BVDV1 antibody
titers in all 3 TI calves in the absence of vaccination
against or natural exposure to BVDV1 was likely the
result of a cross-reaction between the BVDV1 reference
strain and the BVDV2 strain to which the calves were
exposed.20 Only 9 of the 36 PI calves had antibodies
against BVDV, and those titers were typically low and
tended to decrease over the 6-month observation period.
It is unlikely that the antibodies were indicative of an
acquired immunity against the persistent strain of BVDV
because immunotolerance of PI calves to the persistent
strain is documented.9 It is worth noting, however, that
PI calves are able to respond to BVDV strains other
than the persistent strain, and BVDV is an RNA virus
that can generate variants during replication.24,25 It is
possible that the anti-BVDV antibodies present in the PI
calves were the result of passive immunity. Anecdotally,
maternal antibodies have been reported to persist in
calves for 6 to 8 months after weaning. Admittedly,
this would be atypical and has not yet been established
under experimental settings; maternal antibody titers
are typically very high during the neonatal period and
then gradually decline over time. The decay of maternal
antibodies could have accounted for the decline in anti-
BVDV antibody titers observed in the PI calves over the
6-month observation period. Unfortunately, we cannot
confirm that the anti-BVDV antibody titers in the PI
calves were the result of maternal antibodies because
the titers were very low and were not determined for
the calves prior to 9 months of age. It also possible that
the kinetics of maternal antibody clearance in PI calves
is not the same as those in non–PI calves, and this has
not been evaluated.
Seventeen of the 23 PI calves that died had lesions
characteristic of mucosal disease. The other 6 calves died
without any gross lesions, and BVDV infection would not
have been suspected without knowledge that the calves
were PI. Thus, it is recommended that BVDV diagnostic
tests be routinely included in the necropsy workup for
cattle that die suddenly, even those without gross lesions.
Outbreaks of mucosal disease have been previously
reported in 2 beef herds in Saskatchewan, Canada.21,22 In
1 report, 28 of 105 (27%) yearling cattle were PI with
BVDV, and 20 (71%) of those cattle died from mucosal
disease. Interestingly, 1 PI calf was born in that herd
the year following the birth of the cattle that died from
mucosal disease.21 Five PI calves were born the second
year following the birth of the cattle that died from
mucosal disease, and 3 of those 5 PI calves were born to
cohorts of the PI cattle that died from mucosal disease.21
Hence, it is important to screen all cows and heifers
for BVDV for at least 2 years following an outbreak to
identify and remove PI cattle. Similar to the herd of the
present report, most of the PI cattle in that study21 were
> 1 year old when they died of mucosal disease. In the
other report,22 71 of 560 (13%) calves were suspected to
be PI with BVDV; 20 calves died before weaning and were
likely PI, and the remaining 51 calves were confirmed
to be PI with BVDV on the basis of virus isolation or
necropsy results. Of the 51 confirmed PI calves, 47 died
at < 1 year old, and 12 (26%) of those had no or only
mild lesions associated with mucosal disease.22
The presence of PI cattle is a threat to the health and
overall profit of any cattle operation.5,12,13 An increase in
producer awareness of BVDV and the use of appropriate
vaccination regimens, surveillance, and eradication efforts
have resulted in a decrease in the incidence of PI cattle.10,12,13,16
However, until an affordable and practical test to screen
fetuses for BVDV is developed, the risk of introducing BVDV
into a herd should be considered whenever pregnant cows
are purchased, and biosecurity practices (quarantine of
purchased cows and the calves from those cows) should be
implemented until appropriate testing can be performed.12,13
Additionally, all cattle that die suddenly with or without gross
lesions should be tested for BVDV.
The present report is a reminder that diligence in BVDV
prevention is vital for beef operations because a BVDV
outbreak can have devastating effects on productivity. Also,
although it is often recommended that any animal with a
positive result for BVDV antigen by immunohistochemical
staining of an ear notch specimen be culled,2,26 1 positive
result is insufficient to definitively identify an animal as
PI with BVDV. For the herd of the present report, 3 of the
44 (6.8%) calves that tested positive for BVDV antigen by
immunohistochemical staining of an ear notch specimen
subsequently tested negative for BVDV on virus isolation
and by antigen capture ELISA performed on buffy coat
samples and were determined to be only TI with BVDV at
the time of the positive test. This finding emphasizes the
importance of performing follow-up testing of BVDV test–
positive cattle to definitively determine whether they are
truly PI with BVDV. Proper biosecurity and vaccination
programs and the rapid identification and removal of
PI cattle are strongly recommended to minimize BVDVassociated
losses