- Research article
- Open Access
- Open Peer Review
Kinetics of maternal immunity against rabies in fox cubs (Vulpes vulpes)
© Müller et al; licensee BioMed Central Ltd. 2002
- Received: 8 March 2002
- Accepted: 11 June 2002
- Published: 11 June 2002
In previous experiments, it was demonstrated that maternal antibodies (maAb) against rabies in foxes (Vulpes vulpes) were transferred from the vixen to her offspring. However, data was lacking from cubs during the first three weeks post partum. Therefore, this complementary study was initiated.
Blood samples (n = 281) were collected from 64 cubs (3 to 43 days old) whelped by 19 rabies-immune captive-bred vixens. Sera was collected up to six times from each cub. The samples were analysed by a fluorescence focus inhibition technique (RFFIT), and antibody titres (nAb) were expressed in IU/ml. The obtained data was pooled with previous data sets. Subsequently, a total of 499 serum samples from 249 cubs whelped by 54 rabies-immune vixens were fitted to a non-linear regression model.
The disappearance rate of maAb was independent of the vixens' nAb-titre. The maAb-titre of the cubs decreased exponentially with age and the half-life of the maAb was estimated to be 9.34 days. However, maAb of offspring whelped by vixens with high nAb-titres can be detected for longer by RFFIT than that of offspring whelped by vixens with relatively low nAb-titres. At a mean critical age of about 23 days post partum, maAb could no longer be distinguished from unspecific reactions in RFFIT depending on the amount of maAb transferred by the mother.
The amount of maAb cubs receive is directly proportional to the titre of the vixen and decreases exponentially with age below detectable levels in seroneutralisation tests at a relatively early age.
- Rabies Virus
- Post Partum
- Vaccination Campaign
- Canine Distemper Virus
Campaigns of oral vaccination of foxes (Vulpes vulpes) against rabies have shown to be a powerful tool in vulpine rabies control [1, 2]. However, in some areas (temporarily) setbacks have been observed. Partially, these have been linked with a low vaccination coverage of the young fox population, which is possibly a result of maternally transferred immunity interfering with active oral immunization of fox cubs [3, 4]. However, until recently, no experimental evidence was available to support this hypothesis. Recently, after more than 20 years of oral vaccination campaigns, it was finally demonstrated that maternally transferred immunity in fox cubs does occur after oral immunization of vixens against rabies [5, 6]. During previous studies on maternal antibodies (maAb) against rabies in foxes, blood samples were taken only from animals aged 23 days or older [5, 6] hampering insights into the kinetics of rabies maAb. To overcome this shortcoming, in the present study blood samples from fox cubs were collected during the first six weeks after birth. By merging these results on rabies virus neutralising antibodies (nAb) with those obtained during previous experiments in 1998 and 1999 , it was possible to quantify the temporal decline of maAb against rabies in fox cubs in general. This decline was examined in relation to one of the most important parameters influencing the initial level of maAb: the rabies nAb-titre of the mother animal. Furthermore, we tried to answer the question at which age maAb are no longer distinguishable from unspecific reactions in the seroneutralisation test used.
In Spring 2000, 64 cubs whelped by 19 vixens at the Fur Animal Breeding station 'Gleinermühle' (Söllichau, Germany) were included in this study. The vixens were orally vaccinated with the attenuated rabies virus vaccine, SAD B19, shortly before mating or during early pregnancy. All vixens received 1.5 – 2.0 ml SAD B19 (106.7 FFU/ml) by direct oral instillation. The cubs and vixens were marked individually by electronic identification (Indexel® Iso Transponder, Rhone-Merieux GmbH, Laupheim, Germany). Blood samples (n = 281) were taken up to 6 times per cub at different ages ranging from day 3 to 43 days post partum. The study was performed according to the German Animal Welfare Act (Tierschutzgesetz) of 25 May 1998 and the experimental design was approved by the appropriate authorities.
For ethical reasons, depending on the general constitution of the new-born cubs, only a small number of cubs (n = 6) were bled between day 3 to 5 post partum. These six animals were euthanised using 1 ml of a 105 mg/ml barbiturate, Eunarcon® (Parke-Davis, Freiburg; Germany). From those animals, blood samples were taken from the heart during necropsy whilst from the others blood samples were taken by puncturing of the Vena safena. The serum samples were tested for the presence of nAb using the Rapid Fluorescence Focus Inhibition Test (RFFIT) as described by Smith et al. , with the modifications of that method as described by Cox & Schneider . Prior to testing, sera were heat inactivated for 30 minutes at 56°C. The nAb-titres were determined as described elsewhere  and were converted to International Units (IU) by comparison with an international standard immunoglobulin (2nd human rabies immunoglobulin preparation, National Institute for Standards and Control, Potters Bar, UK) adjusted to 0.5 IU/ml which served as a positive control .
The obtained data was pooled with the results obtained during 1998 and 1999. A Kruskal Wallis Test  was performed to test if these data sets could be merged. In accordance with Gooding & Robinson  and Krakowka et al. , we assumed an exponential decline of maAb of fox cubs (y) with time (i.e. age [days] of cubs [x]). We further assumed that maAb titres of newborn fox cubs depend on the nAb-titre of the mother animal (VT)) in a non-linear way. Thus:
y(VT,x) = VTae(b-nx). (1)
The pooled data sets were used to estimate the model parameters. Subsequently, model (1) was used to calculate the half-life of maAb in fox cubs which is given by ln(2)/n and the age of fox cubs (critical age) when maAb are below the threshold of 0.5 IU/ml. The critical age (x c ) when maAB equals 0.5 IU/ml is given by
The parameters of model (1) are estimated using SAS V8.1 Procedure NLIN (SAS-Institute, Cary, NC 27513, USA).
Detailed knowledge of the kinetics of maAb in fox cubs against rabies was missing, but is essential to optimise the timing of oral rabies vaccination campaigns in spring in order to achieve maximum vaccination coverage of the fox population . The study presented here completes previous experiments conducted in 1998 and 1999 [5, 6, 9, 15] by providing data on maternal antibodies in fox cubs during the first weeks post partum. Obtaining blood samples from cubs at such an early age is not without risks. It is known that vixens are very sensitive during the first days after birth and frequent manipulations during this period can lead to behavioural disorders, which often results in the loss of complete litters. However, during this study it was shown that blood samples can be taken from cubs aged 6 days or older without complications.
At first sight, the relatively low (<0.5 IU/ml) maAb titers observed during the first three weeks after birth were surprising. The great variance in individual maAb-titres during the first three weeks of cubs (Fig. 1) was similar to that observed in older fox cubs (Fig. 2). Large differences in maAb-titres were observed even among littermates; these could be a result of difference in suckling behaviour among the cubs . The initial level of maAb is influenced by many factors; e.g. quality and quantity of colostrum and milk-intake as well as body constitution (condition, birth-weight) [16–19]. In another canids species, the domestic dog (Canis familiaris), major transfer of maAb takes place during ingestion of colostrum and milk by the new-born [16, 17, 20]. In these animals, a limited transfer of maAb also occurs in utero [13, 16]. Additional studies have been initiated to clarify whether or not this also takes place in foxes. Unfortunately, these and other possible factors are, most of the time, extremely difficult to assess, mainly due to the previously-mentioned extreme susceptibility of the vixen to disturbance immediately prior and after parturition. Pollock & Carmichael  mentioned that increasing dog litter-size negatively influenced maAb-levels in puppies. This effect, however, could not be observed in foxes . The model presented here clearly identified another important parameter determining maAb-levels: the nAb-titre of the mother animal. A direct proportional relationship between the serum titre of the mother and her offspring has been identified in many studies on maternally derived immunity [18, 20–22]. Our results indicate that the subsequent disappearance rate of maAb in fox cubs was independent of the nAb-titre of the vixen. The exponential decline of maAb against rabies in foxes corresponded with the maAb-decline observed for other viruses in canine animal species, whereby maAb persist for up to 8–10 weeks on average [12, 13, 16]. The half-life of maAb against rabies in foxes was estimated to be 9.34 days, and is similar to that observed for maAb against canine distemper virus (8.4 days) and canine parvovirus (9.7 days) [13, 21]. However, the disappearance of maAb is also linked with the sensitivity of the serological techniques and the threshold to distinguish between positive and negative used (Fig. 4). At an international level nAb at concentrations < 0.5 U/ml representing an arbitrarily defined threshold are considered positive whilst such nAb below this threshold cannot be distinguished from unspecific reactions . Following rabies vaccination of female dogs, maAb in puppies could be detected up to 6–7 weeks post partum, on average . Taking an estimated mean time period of 23 days into account during which maAb can be distinguished from unspecific reactions in RFFIT (nAb-titre ≥ 0.5 IU/ml) after birth, there is evidence that maAb-titres in fox cubs are not as high as in puppies and therefore appear to decrease more quickly than in dogs. Further considering spring whelping activity, maternal immunity against rabies in young foxes is very difficult to detect under field conditions. Thus, the percentage of 9–20% of young foxes having nAb following spring vaccination campaigns [23–25], may result exclusively from active immunization by bait-uptake. It has been shown, however, that the detection of rabies maAb by immunoblotting is much more sensitive than the RFFIT, and consequently, by using the former method, maAb could be detected for a longer period of time (Müller, unpublished results). The relatively longevity of maAb at a low level results in an interference between passively and actively acquired immunity up to 8 weeks post partum which affected more severely the ability of fox cubs to resist a virus challenge . Taking this into account, concerning spring vaccination campaigns baits should not be distributed in previously baited areas before most cubs are more than 8 weeks of age. Therefore, to reach optimal immune response in young foxes, depending on the geographical region vaccination campaigns should be adjusted accordingly. In areas vaccinated for the first time, however, baits can be distributed earlier, while 5 weeks old cubs are already immunocompetent .
Number of fox cubs born to vaccinated vixens and the blood sampling scheme used in the years 1998–2000.
Blood sampling (days post partum)
The authors wish to thank Jeanette Burow, Astrid Schameitat, Elke Pommerening, Kathrin Teske and Doris Balan for their skilful technical assistance and patience during these long lasting experiments.
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