Oral and Poster Abstracts
Oral and Poster Abstracts
Oral and Poster Abstracts
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vaccine, mainly live vaccine. Due to the lack of combined vaccine<br />
containing IBR marker, the use of IBR marker vaccine<br />
simultaneously or concurrently with other vaccines is applied,<br />
mainly in large dairy herds.During the period 2000-2007, the follow<br />
up of the eradication has been performed in 232 dairy herds. The<br />
herds applied vaccination with marker vaccines without culling of<br />
seropositive animals <strong>and</strong> a mean replacement ratio of 30%. On the<br />
whole 88 herds achieved the eradication. The mean time to reach the<br />
eradication ranged from 3 years <strong>and</strong> 8 months to 6 years <strong>and</strong> 10<br />
months depending from the herd size <strong>and</strong> the starting<br />
seroprevalence. During the period of observation, in 32 (14%) of 232<br />
herds we have detected seroconversion to gE but in only 1 case the<br />
seroconversion was associated to clinical signs related to BoHV-1<br />
infection.<br />
246 Epidemiology <strong>and</strong> Eradication of the BHV1-Infection by the<br />
Example of Selected Farms in Lower Saxony<br />
J. Teuffert, K. Wiedl, F. Conraths<br />
Friedrich-Loeffler-Instutute, Department of Epizootiology, Berlin,<br />
Germany<br />
Objectives of study: A case-control study was conducted over two<br />
years (February 2004 - February 2006) in five selected administrative<br />
districts (L<strong>and</strong>kreise) in Lower Saxony to determine potential risk<br />
factors for the eradication of BHV1.<br />
Materials <strong>and</strong> Methods: Fourty-two control farms (cattle negative for<br />
BHV1) <strong>and</strong> 43 farms with an ongoing BHV1-eradication program<br />
(positive for BHV1; case farms) were chosen <strong>and</strong> studied on the basis<br />
of defined criteria. Information <strong>and</strong> data were collected regarding farm<br />
management, the BHV1 control <strong>and</strong>, if applicable, the BHV1<br />
immunisation strategy. Moreover, data on milk production <strong>and</strong> fertility<br />
were analysed for individual animals as well as herds. For this purpose,<br />
the BHV1 test protocols <strong>and</strong> vaccination lists that had been collected<br />
from various farms by the local veterinary authorities were compared.<br />
Finally, the farms were visited <strong>and</strong> the farmers interviewed using a<br />
st<strong>and</strong>ard questionnaire.<br />
Results: The statistical analysis revealed significant differences<br />
between the farm categories for 19 of the operational <strong>and</strong><br />
management variables. In the evaluation of the data collected on<br />
individual infected animals, the distribution of age classes at the<br />
time of the first positive test result <strong>and</strong> the duration the infected<br />
animals remained on the farms until slaughter proved to be<br />
significantly different between case <strong>and</strong> control farms. In particular,<br />
the analysis of the vaccination strategy showed that the following<br />
factors differed between BHV1-negative <strong>and</strong> positive farms: the<br />
number of animals with proper basic immunisation, the distribution<br />
of the number of vaccinations administered in given intervals, the<br />
proportion of infected but unvaccinated animals, <strong>and</strong> the time lapse<br />
between the date of the first BHV1-positive test results <strong>and</strong> the<br />
measures taken. The differences in milk production <strong>and</strong> fertility<br />
between case <strong>and</strong> control farms, however, were not significantly<br />
different. Also, no significant difference was found in the<br />
performance of BHV1-positive <strong>and</strong> BHV1-negative cattle.<br />
Conclusions: In summary, the results of this study lead to<br />
recommendations on vaccination, care <strong>and</strong> feeding, transportation,<br />
trade <strong>and</strong> documentation in cattle farms to improve BHV1 control.<br />
Key words: BHV-1, epidemiology, risk factors, case control study<br />
247 Evaluation of the Probability of Transmission of a Live<br />
BoHV-1 Marker Vaccine to Sentinels after Intranasal or<br />
Intramuscular Application<br />
B. Makoschey 1 , J. Patel 2 , M. Beer 3<br />
1<br />
Intervet-Schering-Plough, Int. Marketing, Boxmeer, Netherl<strong>and</strong>s<br />
2<br />
JAS Biologicals Ltd, Int. Marketing, Cambridge, United Kingdom<br />
3<br />
Friedrich-Loeffler-Institut, Institute of Diagnostic Virology, Insel<br />
Riems, Germany<br />
Objectives: Live marker vaccines against bovine herpesvirus type 1<br />
(BoHV-1) infections are widely applied. The probability of<br />
transmission vaccine virus to sentinels after intranasal or intramuscular<br />
application should be determined.<br />
Materials <strong>and</strong> Methods: Two studies have been performed to<br />
investigate the transmission of a live BoHV-1marker vaccine (Bovilis ®<br />
IBR marker live, Intervet) virus after combined intramuscular (IM) <strong>and</strong><br />
intranasal (IN) vaccination. A group of five (1 st study) or six (2 nd study)<br />
BoHV-1 negative calves was vaccinated with a 10x overdose of the<br />
vaccine IN <strong>and</strong> IM. The animals were housed together with 5 (1 st<br />
study) or 3 (2 nd study) unvaccinated calves during 2 weeks. Nasal swab<br />
samples were taken daily <strong>and</strong> tested for BoHV-1 vaccine virus. In a 3 rd<br />
study, it was established, whether animals vaccinated IM with the same<br />
vaccine become viremic <strong>and</strong> / or excrete vaccine virus with nasal<br />
discharge. Five animals were vaccinated once with an overdose via the<br />
IM route. Nasal swab samples were taken daily for 11 days. Blood<br />
samples were taken three times a week during the first two weeks <strong>and</strong><br />
then once a week until four weeks after vaccination. The nasal swab<br />
samples <strong>and</strong> the blood samples were tested for BoHV-1 in a virus<br />
infectivity assay. In addition, a polymerase chain reaction (PCR)<br />
specific for BoHV-1 DNA was performed on the blood samples.<br />
BoHV-1 neutralising antibody titers were determined in the sera taken<br />
prior to the vaccination <strong>and</strong> four weeks after immunisation.<br />
Results: In the 1 st study, 1/5 in contact animals excreted a minimal<br />
amount of vaccine virus during 1 day <strong>and</strong> developed a BoHV-1<br />
antibody response at very low titer. All remaining sentinels in the 1 st<br />
<strong>and</strong> 2 nd study did not excrete vaccine virus <strong>and</strong> remained seronegative.<br />
In the 3 rd study, all animals were successfully vaccinated as judged by<br />
the development of BoHV -1 neutralising antibodies. However, all<br />
nasal swab samples were tested negative for vaccine virus, <strong>and</strong> all<br />
blood samples were found negative for BoHV-1 virus <strong>and</strong> BoHV -1<br />
specific DNA.<br />
Conclusions: It can be concluded that transmission of the vaccine virus<br />
to sentinels is very limited after intranasal vaccination <strong>and</strong> that no<br />
vaccine virus was excreted with nasal discharge after IM vaccination,<br />
nor could viremia of vaccine virus be detected. It is recommended to<br />
apply the tested BoHV-1 marker live vaccine by the IM route in<br />
situations where excretion of vaccine virus is undesirable.<br />
248 Evolution of the Net Reproductive Ratio of Bovine Herpes<br />
Virus Type 1 Infection in Hyperimmunized Dairy Herds: a<br />
Longitudinal Study in the Field<br />
M. Dispas 1 , R. Soares Magalhaes 2 , M. Pearce 3 , A. Dupont 1 ,<br />
E. Thiry 4 , P. Kerkhofs 1<br />
1<br />
Veterinary & Agrochemical Research Centre, Virology, Brussels,<br />
Belgium<br />
2<br />
Royal Veterinary College, Epidemiology, London, United Kingdom<br />
3<br />
Pfizer Animal Health, R&D, S<strong>and</strong>wich, United Kingdom<br />
4<br />
Faculty of Veterinary Medecine-University of Liege, Virology,<br />
Liege, Belgium<br />
BoHV-1 control programmes have existed in Europe for 10 years.<br />
When seroprevalence is high, hyperimmunization of cattle is usually<br />
recommended to maximise virological protection. Marker vaccine<br />
usage has been promoted to allow discrimination of vaccinated cattle<br />
from cattle infected by a wild virus. Experimental studies show that<br />
effective immunity can be obtained by administration of live then<br />
inactivated vaccines (P1) but use of this protocol has in the field has<br />
not been reported. A 28-month longitudinal field study was<br />
conducted to compare the efficacy of protocol P1 with sole use of<br />
inactivated vaccine (P2), <strong>and</strong> the usual vaccination protocol defined<br />
as non intervention group (NIG). The study comprised 6 crosssectional<br />
serosurveys of all cattle on farms enrolled in P1 (n=10), P2<br />
(n=10) <strong>and</strong> NIG (n=16). New BoHV-1 infections were defined as gE<br />
seroconversion. Vaccinations <strong>and</strong> blood sampling followed the same<br />
schedule, providing 5 chronologically sequential time blocks: from<br />
winter 1, summer 1 <strong>and</strong> so on to winter 3. Mean net reproductive<br />
ratio (R) was calculated for each farm over the whole study <strong>and</strong><br />
within each time block to quantify transmission of BoHV-1 in partly<br />
susceptible populations. Two methods were used: martingale<br />
estimation (R mart) <strong>and</strong> a linear mixed model using a log link <strong>and</strong><br />
Poisson error distribution (R glm). Nine farms in P1, 8 in P2 <strong>and</strong> 13 in<br />
the NIG contributed to the calculation of R values. The mean R marts<br />
were, respectively, estimated to be 0.49, 0.61 <strong>and</strong> 0.70. Only the<br />
R marts for P1 <strong>and</strong> P2 did not include the value 1 in their confidence<br />
interval. In these groups BoHV-1 infection would fade out, but<br />
would persist in NIG. Mean R glms were smaller when infectiousness<br />
was presumed to be 3 days (respectively 0.23; 0.22 <strong>and</strong> 0.28 for P1,<br />
P2 <strong>and</strong> NIG) compared with 7 days (0.55; 0 .52 <strong>and</strong> 0.64) or 10 days<br />
(0.78; 0.74 <strong>and</strong> 0.92). In each group <strong>and</strong> respectively for the 5 time<br />
blocks, within each group, seasonal changes were observed: P1,<br />
0.64; 0.00; 0.37; 1.06 <strong>and</strong> 0.53; P2, 0.70; 0.77; 0.34; 0.73 <strong>and</strong> 0.41;<br />
NIG, 0.70; 0.61; 0.88; 0.49 <strong>and</strong> 0.93. Only P1 <strong>and</strong> P2 showed R mart<br />
values significantly smaller than 1, but not consistently. These<br />
IBR Workshop 325