Bovine Viral Diarrhea Virus in Camelids

Bovine Viral Diarrhea Virus in Camelids



Overview

The following tests are recommended by the Washington Animal Disease Diagnostic Laboratory (WADDL) and Washington State University Veterinary Teaching Hospital (WSU-VTH) for testing alpacas and llamas. These are based on the most current information available and may change as research is completed. Herds should be examined on a case-by-case basis as testing may not be warranted in some situations.

1. Herd Screening

Submit whole blood samples (purple top tube, PTT, whole blood in EDTA, and red top tube, RTT, serum) individually identified to WADDL on multiple animal ID form.

WADDL will test PTT sample for BVDV by PCR. Up to 12 samples can be pooled and tested, which may reduce testing costs. If needed, individual samples from positive pools would be retested to identify individual positive animals within the pool.

  • Negative results (BVDV not detected) = no BVD infection

  • Positive results (BVDV detected) = persistent OR transient BVD infection suspected

Definitive diagnosis of persistent infection requires submission of another blood sample (PTT) from an individual positive sample to be collected in 3-4 weeks and re-tested.

Serum samples (RTT) can be used to check for BVDV antibody to determine prior infection through serologic testing.

If unable to test entire herd, test all juveniles less than 2 years old and breeding males and females. Again diagnosis of BVDV persistent infection would require 2 whole blood samples collected 3-4 weeks apart.


2. New Arrivals to a Herd

Quarantine for minimum of 30 days. Quarantining is not only important to allow screening for BVDV, but also for other infections. Herd biosecurity is important to protect your herd from diseases that new animals may carry with them. For animals that will be remaining on your property a minimum 30-day quarantine is recommended before introducing new animals to your herd.

  • Negative results (BVDV not detected) = no BVD infection

  • Positive results (BVDV detected) = persistent OR transient BVD infection suspected
         Remain in quarantine until retested in 3-4 weeks
                 Negative re-test = most likely a transient infection
                 Positive re-test = persistent infection suspected

A negative-tested dam can be returned to the herd, but recommend quarantining just before delivery until newborn cria is tested with PCR and identified as BVD infected or not.


3. Other Recommended Tests

Necropsy and submit fixed and fresh tissues to test from all aborted and stillborn crias, and from crias or adults with unexplained deaths. Submit whole blood (PTT) and serum (RTT) from the dam as well. 

In addition to performing an abortion panel, it is a good opportunity to evaluate the herd’s trace mineral status, such as Selenium and Copper.


Additional Information

1. What is BVDV?

Bovine Viral Diarrhea Virus (BVDV) is one of several world-wide pestiviruses known to infect domestic and wild ruminants, camelids, and swine. For cattle producers the virus causes economic losses through decreased weight gains, decreased milk production, reproductive losses, and death. As with most viral infections, there is a wide range of signs, from inapparent infections, to diarrhea, respiratory tract disease, hemorrhage, abortions (pregnancy loss), birth defects, and death.

Acute Infection
Bovine viral diarrhea refers to a mild disease caused by a BVD virus infection in immunocompetent cattle. In general, animals develop acute BVD 10-12 days after initial infection. Since BVDV infects white blood cells, whole blood (buffy coat) is the sample of choice for isolation of BVDV from clinically ill animals.

Persistent Infection
BVDV can lead to a persistent infection in a calf infected during a certain time (40-120 days) in gestation. If infected prior to complete development of the fetal immune system, the virus will not be recognized as foreign  and tolerance occurs. After birth, the calf will shed virus, and infect other animals in the herd. Sometimes these calves look sick, but they can also look healthy, thereby making it impossible to visually identify these animals.


2. Why is BVDV important to my alpacas or llamas?

Research has shown that llamas and alpacas can be infected with BVDV and develop clinical signs. There have also been reports of persistent infections in crias. In cattle, persistent infected calves are one of the primary sources of transmitting the infection to other animals. Likewise, persistently infected crias are the primary source of herd infection in camelids. Since alpacas and llamas travel all over North America, for shows, breeding, etc., lapses in biosecurity could permit a persistent infected cria to infect other animals and herds. 


3. What are some possible clinical signs seen in alpacas and llamas?

Typical signs that a client may see include fever, oral ulcers, anorexia, diarrhea, abortion, ill-thrift, and birth defects.

4. How is BVDV transmitted?

The most efficient method of BVDV transmission in camelids is considered to be by aerosol. Transmission in cattle has been primarily by ingestion or inhalation of the virus. The virus can be detected in all body secretions and excretions(respiratory and oral secretions, urine, milk, semen, and feces). Transplacental (dam to fetus) transmission also occurs. Transmission is similar in other susceptible species including alpacas and llamas.

5. What species can transmit BVDV?

Virus can spread between domestic ruminants (cattle, sheep, goats), camelids, and wildlife (deer, elk, etc).

6. Is there a vaccine available for alpacas and llamas?

Currently there is no BVDV vaccine licensed for use in camelids. There are several vaccines available for use in cattle. The vaccines do not prevent infection but reduce the clinical disease effects. At this time, it is not recommended to vaccinate camelids until more is understood about the virus. Unwarranted vaccination can interfere with diagnostic testing and the capability to identify truly infected animals.

7. Can BVDV infections be prevented?

BVDV infections are dose related (virus challenge load) therefore, prevention is critical. Maintaining a closed herd, implementing strict biosecurity protocols for all incoming animals (recommended not just for reducing BVDV infections but others, like coronavirus), and periodic screening of open herds can reduce the occurrence. 


8. What diagnostic techniques are currently recommended for alpacas and llamas?

Types of Tests Available
  • Polymerase chain reaction (PCR) – nucleic acid detection, very sensitive. Will detect persistent as well as acute (transient) infections. Diagnostic method of choice because of good sensitivity.

  • Antigen-enzyme-linked immunosorbent assay (Ag-ELISA) – antigen detection; validation of this test has not been established in camelids but is being evaluated.

  • Serology (serum neutralization) – antibody detection, a single test indicates prior infection, but not active infection. Testing acute and convalescent samples and showing a 4-fold increase in antibody titer indicates active infection. False negatives may occur if sample taken soon after an infection (prior to development of an immune response), or in animals < 3 months of age when maternal, colostrum derived, antibodies interfere with the test.

  • Skin biopsy with immunohistochemistry (IHC) – antigen detection; results are not conclusive in camelids.

  • Virus isolation – Detects live virus in blood and tissues. May be required for virus typing.

Testing Strategies:
Acute Infection: BVDV acute infection can be diagnosed by virus isolation, polymerase chain reaction (PCR) or serology. Virus detection must be done in the first 3-10 days after infection. A whole blood sample is the best sample for BVDV detection by PCR or virus isolation. Paired acute and convalescent samples collected 3-4 weeks apart are required to identify four fold increase in serum antibody titers following recovery from clinical illness.

Persistent Infection: Definitive diagnosis of persistent infection in camelids cannot be based upon testing done at a single time point. Detection of BVDV persistent infection requires showing virus is present in a particular animal over time (the infection persists). Although the BVDV antigen ELISA test done at a single time point is used to detect BVDV persistent infection in cattle, whether or not similar interpretation of the test in camelids is accurate is not known. Therefore, persistent infections in camelids should be determined by detecting virus (by PCR or virus isolation) in sequential samples collected 3-4 weeks apart.

Contact the consulting Microbiologist at WADDL with any questions at: (509)335-9696


References:

  1. Broderson BW. Bovine viral Diarrhea Virus Infections: Manifestations of Infection and Recent Advances in Understanding Pathogenesis and Control. Vet Pathology 5: 453-464, 2014

  2. Belknap EB, Collins JK, Larsen RS, Conrad KP. Bovine viral diarrhea virus in New World camelids. J Vet Diagn Invest. 2000;12:568-570.

   3. Carman S, Carr N et al. BVD in alpaca: abortion and PI. J Vet Diag Invest 17:589-593, 2005.

   4. Evermann JF. Pestiviral infections of llamas and alpacas. Small Ruminant Res 61:201-206, 2006.

   5. Byers SR, Evermann JF, Bradway DS, et al. The effects of exposure of susceptible alpacas to alpacas persistently infected with    bovine viral diarrhea virus. Cand Vet J 52:263-27812, 2011

   6. Nelson DD, Duprau JL, Wolff PL, et al. Persistent bovine viral diarrhea virus infection in domestic and wild small ruminants and  camelids including the Mountain Goat (Oreamnos americanus) Frontiers Microbiology 5: 1-7, 2015