- Open Access
Persistent infections after natural transmission of bovine viral diarrhoea virus from cattle to goats and among goats
- Claudia Bachofen†1Email author,
- Hans-Rudolf Vogt†1,
- Hanspeter Stalder1,
- Tanja Mathys1,
- Reto Zanoni1,
- Monika Hilbe2,
- Matthias Schweizer1 and
- Ernst Peterhans1
© Bachofen et al.; licensee BioMed Central Ltd. 2013
- Received: 27 December 2012
- Accepted: 23 April 2013
- Published: 15 May 2013
Bovine viral diarrhoea virus (BVDV) is an economically important pathogen of cattle worldwide. Infection of a pregnant animal may lead to persistent infection of the foetus and birth of a persistently infected (PI) calf that sheds the virus throughout its life. However, BVD viruses are not strictly species specific. BVDV has been isolated from many domesticated and wild ruminants. This is of practical importance as virus reservoirs in non-bovine hosts may hamper BVDV control in cattle. A goat given as a social companion to a BVDV PI calf gave birth to a PI goat kid. In order to test if goat to goat infections were possible, seronegative pregnant goats were exposed to the PI goat. In parallel, seronegative pregnant goats were kept together with the PI calf. Only the goat to goat transmission resulted in the birth of a next generation of BVDV PI kids whereas all goats kept together with the PI calf aborted. To our knowledge, this is the first report which shows that a PI goat cannot only transmit BVD virus to other goats but that such transmission may indeed lead to the birth of a second generation of PI goats. Genetic analyses indicated that establishment in the new host species may be associated with step-wise adaptations in the viral genome. Thus, goats have the potential to be a reservoir for BVDV. However, the PI goats showed growth retardation and anaemia and their survival under natural conditions remains questionable.
- Persistently Infected
- Bovine Viral Diarrhoea Virus
- Bovine Viral Diarrhoea
- Border Disease Virus
- Bovine Viral Diarrhoea Virus Infection
Bovine viral diarrhoea (BVD) virus is one of the economically most important cattle pathogens world-wide. Together with border disease virus (BDV) of sheep and classical swine fever virus (CSFV) of pigs it forms the genus Pestivirus of the family Flaviviridae. The success of BVDV is due to its ability to cause two types of infection. Pregnant animals acutely infected between the second and fourth month of gestation may generate persistently infected (PI) offspring. Such PI animals are immunotolerant specifically to the infecting virus strain . They produce neither anti-BVDV antibodies nor BVD virus-specific T-cell responses; they do, however, spread the virus for life via saliva and other secretions and are the most important source of infection for other animals . Therefore, programmes to eradicate BVDV are primarily based on detection and removal of PI animals . However, the focus on bovines alone in BVD eradication programmes may be problematic because BVD virus is known to also infect other wild and domestic species of the artiodactyla, as shown by serological studies [5–7]. Besides cattle, evidence for persistent infection has been proven in at least seven species (sheep, pigs, alpaca, white-tailed deer, eland, mouse deer, and American mountain goat) [8–14].
Among these species, domestic small ruminants are of main interest as potential virus reservoir. Sheep PI with BVDV have been reported frequently, indicating that the virus is easily transmitted from cattle to sheep [8, 15–21]. By contrast, transmission of BVDV to goats is less clear. Prevalence of pestivirus antibodies in goats is reported to range from of 2–25%, with the majority of reports being between 10–16% [22–26]. Herd seroprevalences are highly variable. In Austria, the average flock prevalence was reported to be 31.3%  but may be as high as 83% . In several studies, the seroprevalence in goats was found to be significantly higher in herds that had contact to cattle [22, 24, 27]. Interestingly, compared to sheep where BDV antibodies are most prevalent, pestivirus antibodies in goats are more often not clearly specifiable or are rather directed against BVDV [25, 27].
Thus, observations from experimental or confirmed natural infections may be more informative for assessing the role and effects of BVDV infections in goats. In the majority of cases, infections of pregnant goats with BDV, BVDV-1 and BVDV-2 seem to result in abortions and stillbirths with an overall reproductive failure of up to 82% [28–31]. However, viable virus-positive offspring has also been reported, albeit rarely. Løken and Bjerkas  detected three virus-positive kids after experimental infection with BVDV of 21 pregnant goats. Virus was also isolated from 4 kids after 276 female goats were accidentally infected by BVDV via a contaminated Orf-vaccine . BVDV-2 has been isolated from one goat in India  and one goat in South Korea . A serological and virological survey in small ruminants in Austria revealed one BVDV-1 positive goat . However, due to a lack of repeated testing, in some cases it remained unclear if the infection was indeed persistent. Clinical signs of persistent infection with BVDV in goats may be quite diverse. In some cases goats remained apparently healthy but, more often, kids were weak and showed border disease-like symptoms and ill thrift [28, 29, 35]. Infection of neonatal kids with both BDV and BVDV resulted in growth retardation and histological changes in the CNS . Due to the low prevalence of PI goats and their poor survival rate, goats are not expected to play an important role in the epidemiology of BVDV .
In this work, we report on a PI goat kid born to a goat kept together with a BVDV PI calf. In order to analyse the potential of BVDV to establish a chain of infection within the goat population, we exposed seronegative pregnant goats to this initial PI goat. In addition, we repeated the cattle to goat transmission. However, only the goat to goat transmission resulted in the birth of a next generation of BVDV PI kids. Hence, a second round of persistent infection was initiated in a species which is generally considered to be a “dead end” for the spread of BVDV. Our results indicate that BVDV may have the potential to persist in the goat population even in the absence of contact to PI cattle and that establishment in the new host species may be associated with step-wise adaptations in the viral genome.
Generation of the initial PI goat
A female adult goat of the Saanen breed was housed as a social companion with a calf PI with BVDV. The PI animal was a female calf of the Swiss Rotfleck breed and three weeks of age when joined by the goat. Four months after the first exposure to the PI calf a small but healthy male goat kit was born. Therefore, infection of the dam must have occurred after day 37 of gestation. Blood samples were taken from the goat kid within 1–2 h after birth and 2 days later and tested for the presence of viral RNA by RT-PCR.
Experimentally exposed goats
All goats used for the experimental exposures were healthy adult females of the Saanen breed originating from a flock of experimental animals tested free of small ruminant lentiviruses and regularly treated against ecto- and endoparasites. They had been repeatedly tested negative of pestiviruses and antibodies to pestiviruses as analyzed by a pan-pesti RT-PCR and by antibody capture ELISA, respectively, as described below.
Set up for in vivo transmission experiments
Results of experimental exposure of pregnant, seronegative goats to BVDV
Possible sign of abortion
BVD status of kids/ foetuses
Aborted foetus not detected
Aborted foetus not detected
Aborted foetus (A3_1) BVDV positive
Aborted foetus not detected
Aborted foetus not detected
Three dead BVDV positive kids (B1_1, 2, 3)
Two living BVDV PI kids (B2_1, 2)
One healthy, BVDV negative kid
Group B: Three goats (B1-B3) were exposed to the PI goat that was 18 months old at the beginning of exposure. The three goats were housed together with the PI goat for 21 days in a stable some 10 km apart of group A. The barn was of about the same size as that of group A but due to the longer exposure time and for animal welfare reasons, access to an enclosed open-air paddock was allowed. After the exposure time the PI goat was removed from the group. Blood samples were taken on a weekly basis until day 42. The goats of group B were at days 42–63 (B1), 17–38 (B2) and 38–59 (B3) of gestation when they were exposed to the PI goat.
A graphical overview of the animal groups and individual animal numbers can be found in the Additional file 1. All animals were kept under traditional, agricultural conditions and in compliance with the Swiss Animal Protection Act (1978). All samplings and treatments were performed according to the principles of good veterinary practice which were considered non-regulated procedures by the ethics committee of the canton of Bern.
For RNA isolation from EDTA blood the QIAamp RNA Blood Mini Kit and for isolation from tissue samples the RNeasy Mini Kit were used (both from Qiagen, Hombrechtikon, Switzerland) according to the manufacturer’s instruction.
The real-time RT-PCR was applied as previously described, using primers and probes located in the 5’ untranslated region (5'utr) of the viral genome . Briefly, the TaqMan One-Step RT-PCR Master Mix Kit (Applied Biosystems, Life Technologies Europe BV, Zug, Switzerland) was used, the primers and probes as well as 5 μL of the isolated RNA added in a final volume of 25 μL and the reaction run in a ABI Prism 7700 Sequence Detection System using the following programme: 30 min 48°C (RT-step), 10 min 95°C (activating AmpliTaq Gold), and 45 cycles of 15 s 95°C and 1 min 60°C.
We used serum samples from the PI heifer and the initial PI goat taken two weeks prior to the beginning of the exposure experiment, and abdominal fluid from the aborted foetus (A3_1) for comparison of the deduced amino acid sequence of the viral envelope protein E2. Viral RNA from spleen samples of the stillborn goat kids (B1_1, 2, 3) and from uterus tissue samples of the dam (B1) was also sequenced. From the two living PI kids we used pre-colostral blood samples. In addition, in vitro passaged virus from the PI heifer and the PI goat was sequenced. Both sera had been passaged ten times in homologous and heterologous cells (bovine turbinate and goat synovial membrane cells) in parallel as described .
RNA isolation and conventional RT-PCR followed by sequencing of the viral genome in the 5’utr and the envelope protein E2 coding region was performed as previously described . Briefly, QIAGEN spin columns were used for the RNA isolations followed by one-step RT-PCR reactions using the One Step RT-PCR kit from QIAGEN. For the 5’utr sequencing we used the pan-pesti primer pair 324/326 . For the highly variable E2 coding region we designed the primer pair 232f/234r based on published full length sequences of BVDV 1 viruses. Their position in the BVDV NADL type strain is as follows: 232f (5’-GTYTAAGKCCYYARTGGTGGC-3’) 2244–2265, 234r (5’-RVTCRTCRCTRAGRAYDAGGTA-3’), 3671–3692. For sequence analysis and comparison, the SeqMan software from the Laser gene suite (DNASTAR Inc., Madison WI, USA) as well as the Clone Manager software (Scientific & Educational software, Cary NC, USA) were used.
The virus of the PI heifer has been described previously as strain “CH-Maria”  and has the Gen Bank accession numbers EU180028 (5’utr) and EU180048 (E2).
Antibody capture ELISA
A biphasic in-house ELISA was used as previously described  to detect antibodies against the conserved NS3 protein of pestiviruses in the goat sera. Briefly, ELISA microtitre plates (Maxisorp, A/S Nunc, Kamstrub, Denmark) were coated with antigen derived from bovine turbinate cells. For this purpose, cell cultures that were either infected with the cytopathic BVDV strain R1935/72 (Oregon C24V, subgenotype BVDV-1a) or that remained non-infected were freeze-thawed three times, centrifuged and the pellet re-suspended and incubated in phosphate buffered saline (PBS). In order to obtain mainly non-structural viral proteins, 2% Tween 20 was added. Columns were coated alternatively with antigen derived from infected and non-infected cell cultures to control for unspecific binding. Sera were diluted 1:10 in blocking buffer (PBS, 0.05% Tween 20 and 1% milk powder) before being added to the coat. As a conjugate, Protein-G-Peroxidase (Bioreba AG, Basel, Switzerland) was used for non-bovine species. To visualize bound antibodies, the substrate ABTS (2,2’-azino-di-(3-ethyl benzthiazoline-6- sulphonic acid); Roche Diagnostics, Rotkreuz, Switzerland) was added and the intensity of the staining was measured by an ELISA reader at 405nm.
Immunohistological analyses for BVDV antigen detection were performed as previously described . A snap frozen skin biopsy and paraffin embedded bone section (femur) were analysed using the C16 and 15c5 pan-pesti antibodies, respectively.
Goats exposed to the PI heifer (group A)
The clinical, serological and virological findings of the pregnant goats exposed to the PI heifer are summarised in Table 1. The health status of the five goats was analysed daily during the first 14 days. Animal A4 had a temperature of 39.9°C on day 8, goat A2 40.2°C on day 11 and 40.4°C on day 12. No loss of appetite or clinical signs such as diarrhoea, nasal discharge or coughing was observed. EDTA blood was tested by real-time RT-PCR to detect viremia. Two animals showed weak positive results with CT values above 35; one on day 11 (A3) and the other (A4) on days seven and nine after first exposure. The latter was the same animal that also had a fever at day eight. Serum samples analysed by antibody capture ELISA showed that four out of five animals of group A seroconverted between days 14 and 21 after initial exposure. All goats were seropositive by day 28 after first exposure, which indicated that they had been infected by the PI heifer. This had serious consequences for gestation: All animals aborted, most of them apparently in late gestation. All animals were still in gestation when being checked by ultrasound on day 55 of gestation, ten days after termination of the exposure. On day 66 of gestation, bloody vaginal secretion was observed from goat A1 and it returned to oestrus 12 days later. The other four goats remained clinically inconspicuous. However, no udder formation was observed by day 120 of gestation. In three cases bloody vaginal secretion was observed on days 146 (A3), 149 (A2) and 142 (A4) of gestation (with the normal duration of gestation in goats being on average 150 days). Only in one case the aborted foetus which showed signs of mummification was available for analysis (A3_1). It was detected on day 146 of gestation but the condition, size and development of the foetus indicated that it had died as early as around day 90 of gestation. We were able to detect BVD viral RNA in abdominal fluid and several organs of this foetus by RT-PCR. Bacteriological analyses for Brucella, Chlamydia, Coxiella and Neospora were negative. Sequencing in the BVDV 5’utr proved the virus to be identical to that of the PI calf and goat. No observations were made that pointed to the date of abortion in animal A5.
Goats exposed to the PI goat (group B)
No viremia was detected in the three goats exposed to the initial PI goat (Table 1). This is not unexpected as blood samples were taken only once a week and viremia during acute infection with BVDV is usually short-lived . The results of the antibody capture ELISA revealed that two goats had seroconverted; one between days 21 and 28 (B1), the other between days 35 and 42 after first exposure (B2). One goat (B3) remained antibody negative and gave birth to a healthy BVDV-free kid. Unfortunately, the goat B1 died shortly before the expected date of parturition. The post-mortem examination revealed a severe intestinal volvulus with haemorrhagic infarction as the most likely cause. It had carried three kids that however did not survive. They were well developed and RT-PCR showed that all of them were strongly BVDV positive in serum and all organs analysed. No antibodies against BVDV were detected. The goat B2 gave birth to two female kids (B2_1 and B2_2). Pre-colostral blood samples were taken and both were antibody negative but strongly BVDV positive by RT-PCR. Blood samples taken over the next few weeks were tested by conventional and real-time RT-PCR and were always positive.
Development of PI goats
The initial PI goat was undersized but stayed healthy until the age of 19 months when it developed severe untreatable anaemia and had to be euthanized at the age of 22 months.
Additional file 2: Video sequence of PI goat kids. The footage shows the BVDV PI goat kids B2_1 and B2_2 at the age of 3 hours and 3 weeks post partum. (MOV 5 MB)
Analysis of viral genomic sequences
Interestingly, three out of these four positions also showed up in sequences from an in vitro passaging experiment performed with serum from the PI heifer and the PI goat . After 10 passages in bovine turbinate (BT) or goat synovial membrane (GSM) cells, the virus from the initial PI goat revealed amino acid changes at positions 59 (in BT and GSM cells), 742 (GSM cells only) and 800 (BT cells only) as observed after goat to goat transmissions. By contrast, the virus from the PI heifer showed no amino acid changes after in vitro passaging in homologous (BT) and heterologous (GSM) cells (Figure 3).
BVDV is known to cross the species barrier with relative ease and the occurrence of BVDV positive offspring in small ruminants has been reported before [15, 16, 20, 32–34]. However, in order to estimate the role of these animals as a potential reservoir for BVDV it is essential to know if the virus can cause an independent chain of infection within the non-bovine species. The unintentional exposure of a pregnant goat to a PI heifer and the subsequent birth of a PI kid offered a unique opportunity to expose naive pregnant goats to a PI goat to gain evidence for i) the transmission of BVDV from goat to goat and ii) the generation of PI kids from this transmission. In addition, exposure of pregnant goats to the PI heifer permitted us to investigate the consequences of cattle to goat and the goat to goat transmissions for the viral genome.
As the seroconversions reveal, all animals in group A were infected within the 7 days exposure period (Table 1). However, all animals in this group lost their foetuses. It has been shown before that abortion is the most likely outcome when pregnant goats are exposed to BVDV [30, 31]. In case of foetus A3_1, other common causes of abortion in goats were excluded such as Chlamydia and Neospora. In addition, unexposed goats kept in the same premises as the exposed goats, did not abort. However, we cannot rule out that the stress of transport, change of environment and the unfamiliar presence of the heifer may have contributed to the abortions. In most cases, possible signs of abortions such as bloody vaginal secretions were observed between days 104 and 111 of gestation (Table 1). However, death of the conceptus may have occurred earlier, as shown in the case of goat A3 that discharged a small, mummified foetus shortly before the end of gestation. None of the other foetuses were found. Therefore, we conclude that they also died early and may have been lysed, resorbed or excreted, and over-seen. Abortions of small or mummified foetuses in late gestation have also been described by Broaddus et al.  after BVDV infection of pregnant goats. In contrast to abortions, reports of viable PI offspring generated by cattle to goat transmissions are rare and even though our initial PI goat was the result of such a transmission, we were unable to repeat this event although the pregnant goats were from the same flock and virus was transmitted from the same calf in the same pen.
Only two of the three goats exposed to the PI goat (group B) seroconverted after the 21 days of exposure (Table 1). The differences in experimental set-up and the small numbers of animal make a statistical comparison of the two groups impossible. However, it may well be that cattle spread pestiviruses more efficiently than small ruminants due to more saliva being spread during feed uptake. In an experimental exposure of naive cattle to two border disease PI sheep for 72 days, only six of the nine calves seroconverted which may point to PI small ruminants being relatively poor pestivirus shedders . Even though only two out of three animals in group B seroconverted, the generation of viable PI offspring was rather efficient as both animals generated BVDV positive kids. When newborn, the PI kids (B2_1 and 2) showed slight tremor and ataxia, symptoms that had not been observed in the initial PI goat. Border disease-like symptoms, difficulties to stand, ataxia and general weakness have been described previously in goat kids after BVDV infection during gestation [28, 29, 33, 46]. However, in most cases, the animals died within 24 h after birth. In our case the animals recovered without medical intervention except for being given an infrared lamp. However, similar to the findings in the Austrian PI goat , all our PI goats showed growth retardation. Also, ectoparasites were more of a problem than they are in normal goats. A striking sign was the massive anaemia that affected all PI goats at different ages. Anaemia was probably caused by a reduced erythropoiesis, but the exact pathogenesis and the way it is modulated by BVD virus remains unclear. A severe case of anaemia has previously been described in a BVDV PI cow , but seems to have been caused by haemolysis rather than by reduced erythropoiesis. Even though two of the three PI goats (the initial PI goat and B1_2) reached the age of 22 and 15 months, respectively, it should be taken into consideration that they were kept under controlled conditions. It remains questionable if, under field conditions, they would have survived long enough to pass the virus on. Recent reports indicate that cattle-independent BVDV infections can be sustained in white-tailed deer by PI fawns even though these PI animals show reduced performance [11, 48]. Furthermore, upon experimental transmissions, virus resulting from deer to deer transmission was infectious for cattle . We have not been able to analyse the BVDV transmission from PI goats back to cattle. However, an outbreak of BVDV in a goat herd in Norway that resulted from a contaminated vaccine led to seroconversions and one abortion in cattle kept in the same barn .
In vivo and in vitro experiments have shown that the highly variable viral envelope glycoprotein E2 of BVDV is a major determinant of its species tropism [19, 50]. Upon interspecies transmission, nucleotide changes in the E2 coding region of the viral genome may quickly become apparent , most likely as a result of selection of pre-existing viral variants rather than true adaptive mutations [51, 52]. Indeed, nucleotide ambiguities in the E2 sequence of the initial PI goat may point to changes in the composition of the quasispecies in this animal compared to the sequence obtained from the PI heifer, which might facilitate viral propagation in goats. In support of this interpretation, some of these ambiguities progressed to a complete switch of the amino acid in the consensus sequence in the second goat “passage”, i.e. the next generation of PI kids (Figure 3, Additional file 3). The initial PI goat that originated from cattle to goat transmission may thus represent an intermediate state of viral adaptation to the new host. A comparison of growth curves of virus from the PI heifer and the PI goat on caprine cells showed them to be nearly identical . While not excluding slight differences in viral growth as a contributing factor, adaptation to goats may involve mechanisms unrelated to the level of viral replication in goat cells in vitro. Among others, adaptation might involve interactions with the goats’ immune system. However, only the change at nucleotide position 59 falls into the known antigenic domain of the E2 protein and none of the four changes appears to affect any known epitope [53, 54]. Similarly, the “sheep-specific” nucleotide changes at positions 9 and 192 described by Paton et al.  upon consecutive cattle and sheep infections were unaffected. However, virus from the initial PI goat passaged in vitro showed amino acid changes at the same positions as those observed after goat to goat infection, which might indicate that they did not occur randomly (Figure 3). In contrast to the virus from the initial PI goat, the virus from the PI heifer did not show any changes in the consensus sequence even after 10 passages in bovine or caprine cells (“in vitro”, Figure 3 and Additional file 3), which indicates that a larger number of replication cycles is required to lead to a change in the consensus sequence of the viral quasispecies of this virus.
In summary, our results indicate that PI offspring are rarely generated in goats after contact with BVDV PI cattle. To our knowledge, this is the first report showing that a PI goat cannot only transmit BVD virus to other goats but that such a transmission may lead to the birth of a second generation of PI goats. The changes in the genome of BVD virus transmitted from a PI calf via transiently infected goats to first and second generation PI kids indicate that adaptation to the non-bovine species is correlated with changes in the quasispecies, leading to step-wise changes in the consensus sequence of the virus.
Thus, BVDV PI goats have the potential to initiate an independent chain of infection in their own species. However, even though second generation PI goats may be produced more easily than first generation PI goats, BVDV transmission from PI cattle to goats leads mainly to abortions and, provided that live PI animals are born, the fitness of these animals may be severely reduced. Hence, although BVDV may be able to infect goats transiently without causing serious disease, it is likely that, compared to infection in cattle, the host-pathogen interaction in goats is not sufficiently refined to enable permanent establishment in this species. It is not surprising, therefore, that BVD virus has not been detected as an “emerging goat pathogen” in serological and virological surveys . Although these arguments do not support the view that goats may become a reservoir host for BVD virus that could jeopardise ongoing BVD eradications, small ruminants could nevertheless acquire an undesired role in such programmes. Goats and, even more importantly, sheep are main hosts for border disease virus and diagnostic tests suitable for mass-testing do not clearly differentiate between different pestiviruses or antibodies to pestiviruses. Hence, after eradication of BVDV in cattle, spill-over of BVDV or BDV from goats and sheep could interfere with the monitoring of freedom from BVDV by serological means. Further knowledge on the role of interspecies transmissions of pestiviruses is therefore important, particularly for BVDV eradication programmes.
We thank the staff of the diagnostic department of the Institute of Veterinary Virology for their help with sample processing and analysis and Prof. Peter Tschudi from the Laboratory for Veterinary Clinical Diagnostics of the University of Bern for the assistance with the bone marrow analysis. We thank Ruth Parham for her linguistic improvements of the manuscript.
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