- Open Access
Schmallenberg virus challenge models in cattle: infectious serum or culture-grown virus?
© Wernike et al.; licensee BioMed Central Ltd. 2012
- Received: 18 September 2012
- Accepted: 14 November 2012
- Published: 11 December 2012
Schmallenberg virus (SBV), discovered in Europe in 2011, causes mild transient disease in adult ruminants, but fetal infection can lead to severe malformation in cattle, sheep and goats.
To elucidate the pathogenesis of this novel orthobunyavirus, considerable efforts are required. A reliable and standardized infection model is essential for in vivo studies. In the present study, two groups of four cattle were inoculated with either serum passaged in cattle only or cell culture-grown virus. The replication of culture-grown SBV in cattle was reduced compared to virus inoculated via infectious serum. In a second experiment, the infectious serum was titrated in calves; the tested batch contained 102.83 infectious doses per mL. Hence, serum-borne virus that was only passaged in the natural host is a suitable option for a standardized SBV infection model.
- Rift Valley Fever
- Rift Valley Fever Virus
- Baby Hamster Kidney Cell
- Undiluted Serum
- Epizootic Hemorrhagic Disease Virus
In 2011, Schmallenberg virus (SBV), an orthobunyavirus related to viruses of the Simbu serogroup, was discovered in Germany [1, 2]. In adult cattle, SBV infection is associated with mild transient disease, but it can lead to severe fetal malformations when pregnant cows and ewes are exposed in early to mid pregnancy . Currently, the knowledge about SBV is very limited; a reliable and highly standardized infection model is required to elucidate its pathogenesis and to test potential vaccines.
To this end, the present study compares the induction and progression of viremia in cattle for the two different inocula, (i) an SBV field strain that was only passaged in cattle (delivered as infectious serum) as well as (ii) virus grown in tissue culture for a maximum of 4 passages. In addition, the infectious serum was titrated in calves to quantify its infectivity.
All experimental protocols were reviewed by a state ethics commission and have been approved by the competent authority (State Office for Agriculture, Food Safety and Fisheries of Mecklenburg-Vorpommern, Rostock, Germany, ref. LALLF M-V TSD/7221.3-1.1-004/12). All animals were between 9 and 18 month of age.
Infectious serum as inoculum
In a previous study, a single calf had been subcutaneously inoculated with blood samples from four diseased cattle  of the same outbreak series that were positive in an SBV real-time quantitative reverse transcription PCR (RT-qPCR). EDTA-treated whole blood, taken from this calf 4 days after infection (dpi) was subcutaneously injected into two further calves (C01, C02). Both inoculated animals were PCR-positive for the first time at 2 dpi, and one developed diarrhea for several days. Half a liter of serum from each calf was collected at 3 dpi, divided into portions of 1 mL and stored at −70°C until it was used in the subsequent experiments.
The sera contained 2.0 × 103 and 1.3 × 103 50% tissue culture infectious doses per mL (TCID50/mL), respectively, as determined by end-point titration on baby hamster kidney (BHK) cells (cell line L0164, Collection of Cell Lines in Veterinary Medicine, Friedrich-Loeffler-Institut, Insel Riems, Germany). Both sera were tested free of any bacterial contamination. Using sensitive real-time PCR protocols, it could be shown that they did not contain detectable nucleic acids of bovine herpesvirus type 1 , pestiviruses , Rift Valley fever virus , bluetongue virus, foot-and-mouth disease virus or epizootic hemorrhagic disease virus (unpublished assays).
Cell culture supernatant as inoculum
SBV was isolated from the blood of an infected cow as previously described . After initial isolation on KC cells (cell line L1062; derived from Culicoides variipennis midges ) the virus was passaged in BHK cells, then in KC and again in BHK cells. The infectivity was determined by end-point titration on BHK cells.
Comparison between infectious serum and cell culture supernatant
Twelve SBV-naive calves were assigned to three groups of four animals each. Calves in group 1 (C03-C06) were subcutaneously injected with 1 mL of serum obtained from C01, while calves in group 2 (C07-C10) received 2 × 107 TCID50 of culture-grown virus. Animals in group 3 (C11-C14) were injected with phosphate-buffered saline (PBS) and kept as controls.
Following the inoculation, the animals were monitored for the presence of clinical signs every day, rectal body temperatures were measured daily and serum samples were taken daily during the first eight days and weekly thereafter. RNA was extracted using the MagNA Pure LC Total Nucleic Acid Isolation Kit for automated extraction (Roche Diagnostics Deutschland GmbH, Mannheim, Germany) according to the manufacturer’s recommendations. SBV genome load in the samples was determined by S segment-specific RT-qPCR as described previously  with an external standard based on the S genome segment; at its peak, the difference between the groups was statistically evaluated with a t-test. Serological data was collected at weekly intervals using a commercially available ELISA kit (ID Screen® Schmallenberg virus Indirect ELISA kit, IDvet, Montpellier, France). A diverse panel of tissue samples (e.g. lymphnodes, spleen) was taken at necropsy on days 24 or 25; they were homogenized and tested for the presence of SBV RNA by RT-qPCR.
In vivo titration of infectious serum
In a subsequent in vivo titration experiment two calves received the undiluted serum of C01 (group A, C15-C16), while groups of three calves each were given dilutions of 1/10 (group B, C17-C19), 1/100 (group C, C20-C22) and 1/1000 (group D, C23-C25) in sterile PBS, respectively. Serum samples were taken at days 1 to 7 and 21; they were tested for SBV RNA and SBV-specific antibodies as described above.
Comparison of cell culture supernatant and infectious serum as inoculum
SBV RNA was not detected in the control animals at any time. Fever was not observed in any animal, but C08 developed mild diarrhea for two days.
Necropsy of the animals did not reveal any significant gross pathomorphological lesions. The mesenteric lymph nodes of C03 and C06-C08 were positive in the RT-qPCR (average Cq value: 34.8 ± 5.2). In addition, SBV RNA was found in the mandibular lymph nodes of C04 and C06 (Cq values: 39.0, 37.8), and the spleens of C05 and C06 (Cq values: 44.5, 36.9).
All cattle in group 1 and 2 were positive in the ELISA two weeks after infection, while all in-contact animals remained negative until the end of the study (data not shown).
In vivo titration of the infectious serum
The reliable induction of viremia is an important feature of challenge models for vector-borne diseases . When viruses are passaged in cell culture, however, the positive selection of spontaneous mutations that promote replication in this environment can lead to changes in virus phenotype, including a reduced replication efficiency and virulence in the natural hosts. This has been demonstrated for several bunyaviruses [10, 11] and is commonly exploited for the production of AKAV vaccines . The genome stability of vector-borne viruses grown in culture can be promoted by switching between cell lines of mammalian and insect origin (mimicking natural host alternation) , but pertinent data for bunyaviruses are not available. In the present study, the replication of culture-grown SBV in cattle was reduced compared to a strain that had only been passaged in the natural host. While not statistically significant within the constraints of this experiment (small group size, high variability within groups), this difference provides a clear indication of the pitfalls of culture-based production of challenge inocula. The high level of infectivity in the tested serum batch offsets one of the major advantages of culture-grown viruses, namely the easier availability of large amounts of material. Based on our findings, cattle-derived infectious serum is a viable and robust option for a standardized SBV infection model, which is required for vaccine evaluation and pathogenesis studies.
Patrick Zitzow and Anja Landmesser rendered outstanding technical assistance. Dedicated animal care was provided by the staff of the isolation unit of the FLI. We are also grateful to Matthias Lenk from the cell culture collection for veterinary medicine of the FLI for his continuous support.
This work was financially supported by Boehringer Ingelheim Pharma GmbH & Co. KG.
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