- Research article
- Open Access
Familial occurrence of Danish and Dutch cases of the bovine brachyspina syndrome
© Agerholm and Peperkamp; licensee BioMed Central Ltd. 2007
- Received: 08 December 2006
- Accepted: 08 May 2007
- Published: 08 May 2007
The bovine brachyspina syndrome is a recently reported malformation in the Holstein breed. The aetiology of this syndrome is unknown, but its occurrence following breeding between genetically related and phenotypically normal cattle may indicate that it is an autosomal recessively inherited disorder. Three cases are reported and compared to the originally reported case.
Two Danish cases and a Dutch case are described. The calves were delivered following a slightly prolonged gestation period. Gross lesions consisted of growth retardation, significant shortening of the entire spine and long and slender limbs. Additionally, inferior brachygnatism and defects of several internal organs were recorded. The cases were diagnosed as having the brachyspina syndrome based on the presence of essential lesions. The parents of each case were genetically related and linked to the first reported case by a common ancestor.
The findings support the hypothesis that the brachyspina syndrome in Holstein cattle is inherited autosomal recessively and illustrate some of the assumed phenotypical variation of this syndrome. The brachyspina syndrome may be an emerging disease in the Holstein breed.
- Intervertebral Disc
- Bovine Virus Diarrhea Virus
- Bovine Virus Diarrhea Virus
- Appendicular Skeleton
Recently, a new congenital lethal syndrome was reported in a Danish Holstein calf (case DK1) . The syndrome was characterized by severely reduced body weight, widespread vertebral malformation causing significant shortening of the spine (brachyspina), and malformation of the heart, kidneys and testicles. The cause of the syndrome was not determined. But as the calf was the result of artificial breeding between genetically related and phenotypically normal animals and as it was the only affected calf occurring in a herd of 96 adult females, such an incident could be explained by transmission by descent of a defective recessive allele from a common ancestor. However, further cases were needed to evaluate the hypothesis of autosomal recessive inheritance.
Here, we report two additional cases from Denmark (cases DK2 and DK3) obtained through the Danish Bovine Genetic Disease Programme  and a case from the Netherlands (case NLD1) submitted for routine diagnostic.
The volume of the thoracic cavity was reduced and almost occupied by an enlarged heart. The ribs radiated from the spine with non-parallel intercostal spaces. The number of ribs was reduced to 11 in each side, but they were difficult to separate due to the presence of extensive synostoses. The lungs had congenital diffuse atelectasis, were of reduced size and compressed by the heart. Low-grade hydrothorax and hydropericardium was found. The heart had a round shape due to dilation of the right ventricle and hypertrophy of the corresponding myocardium. A high interventricular septal defect was present. Truncus pulmonalis and aorta arose separately from the right ventricle (dextroposition of the aorta). The basis of aorta was dilated.
The volume of the abdominal cavity was also reduced. The anterior part was occupied by an enlarged liver. Colon descendens had agenesia at the entrance to the pelvic cavity and a stenosis approximately 2 cm orally to the agenesia. The prestenotic segments were dilated due to accumulation of meconium, while the poststenotic segments only contained mucus. The kidneys had bilateral hypoplasia with a length of approximately 3 cm. The right uterine horn was hypoplastic. The adrenal glands and ovaries were present at their normal position.
The calf was tested negative for bovine virus diarrhea virus (BVDV) by cell culture and for antibodies against BVDV by an ELISA technique .
The calf was examined for BVDV and foetal antibodies with negative results. The calf was genotyped for the V180F mutation in the SLC35A3 gene, which causes the complex vertebral malformation syndrome (CVM) in Holsteins, and found homozygous normal.
The pedigree was compared to pedigrees of the two other Danish cases. The parents were genetically related to the other cases (Fig. 4).
Multiple tissues were taken for histopathology, processed by routine laboratory methods and stained by haematoxylin and eosin. Bone tissues were decalcified by Osteomoll® (Merck KGaA, Darmstadt, Germany) prior to processing. Vertebral lesions were characterized by widespread disturbed segmentation and organisation. Intervertebral disc development was mostly absent although protrusion of collagen from the periphery into the epiphyseal anlage was occasionally present. Consequently, adjacent vertebrae often share a common epiphysis with only one ossification centre. The growth zones were highly irregular towards the diaphyses with frequent abnormal arrangement of chondrocytes. The diaphyses were in some areas intersected by cartilaginous cores dividing the spongiosa into inlets of spongious bone. The appendicular skeleton was not examined. The kidneys were dysplastic with immature tubules, dilated tubules, intraluminal crystals and interstitial fibrosis.
The calf tested negative for BVDV by an antigen ELISA technique (HerdChek BVDV Antigen ELISA – Leukocyte, IDEXX Laboratories, Inc., Westbrook, ME, USA). Genotyping for the V180F mutation in the SLC35A3 gene was performed after retrieving DNA from formalin fixed and paraffin embedded liver and heart tissue . The calf was genotyped as homozygous normal.
Pedigree analysis demonstrated that the parents of the Dutch case were genetically related to the three Danish cases (Fig. 4).
The gross morphology of the three cases (DK2, DK3 and NLD1) was in many aspects similar to the lesions found in the original case (DK1)  and they were consequently considered to have the brachyspina syndrome. All cases were stillborn and were delivered after a slightly prolonged gestation period. The calves were severely growth retarded, had a significant shortening of the entire vertebral column, and the limbs appeared relatively long and slender (Figs. 1, 5 and 6). Additionally, multiple defects of the internal organs were found, i.e. renal dysplasia and intestinal atresia. However, discrepancies between the cases and the original case were also observed as they all had brachygnatism and one case had brain displacement – lesions that were absent in the first case. Histopathology was only performed in two cases (DK2 and NLD1). Bone lesions in these cases differed from the original case as the development of vertebrae was more disturbed and as the ossification process of the appendicular skeleton appeared normal in case DK2 compared to case DK1. The appendicular skeleton of case NLD1 was not examined. It could be objected that the four calves represented more than one syndrome, as the morphology was not completely identical. This point of view cannot be completely disproved, but it is not surprising that a certain variation is seen. Studies of CVM in Holstein cattle, which is due to a single base mutation , have demonstrated that phenotypical variation occurs. This variation is expressed in the severity of vertebral malformation as well as in the prevalence and type of internal organ defects [7, 8]. Phenotypical variation is also seen in other skeletal malformations due to single genes, i.e. syndactylism and chondrodysplasia [9, 10]. It is possible that a certain morphological variation of the brachyspina syndrome, which could explain the observed differences, could occur as well. At present, a diagnosis of the brachyspina syndrome should be based on the general appearance of abnormal calves (Figs. 1, 5 and 6). A detailed examination of future cases should be performed so that the variation of the syndrome can be determined and DNA should be stored to establish an exact diagnosis if a genotyping test becomes accessible.
The brachyspina syndrome and CVM are malformations occurring in the Holstein breed. Although these syndromes share several features as vertebral malformation, growth retardation and internal organ malformation, discrimination between these defects can be done morphologically. Calves suffering from the brachyspina syndrome have a mean body weight of 10.3 kg compared to a mean body weight of around 25 kg in CVM-affected calves . Vertebral lesions are more widespread and severe in the brachyspina syndrome than seen in CVM, where lesions mostly are restricted to the posterior cervical and the thoracic vertebrae. Consequently, the entire spine is reduced in length in the brachyspina syndrome compared to shortening of the cervical and thoracic spine in CVM. Renal dysplasia, which occurs in the brachyspina syndrome but not in CVM, also seems to be an important diagnostic mark. Finally, CVM-affected calves generally have a slightly reduced gestation period, while calves with the brachyspina syndrome seem to have a prolonged gestation period [7, 8]. Definitive discrimination between the defects can be done by genotyping. Genotyping of two cases included in this report and the original case DK1 (Agerholm, unpublished results) separated the two disorders without doubt.
The genealogical examination showed that the cases occurred in a familial pattern and that the parents of each calf were genetically related. A common ancestor to all parents (sire A) was found in generation VI (Fig. 4). The occurrence of the defective calves might therefore be explained by transmission of recessive alleles from this sire to the calves. Sire A and his son (sire B) are widely used US Holstein sires and it is therefore possible that they occur in the pedigree of the parents by chance. It has previously been reported that widely used sires may occur as common ancestors in the pedigree of malformed Holstein calves fortuitously [7, 8]. Consequently the observation cannot be regarded as a distinct proof for an inherited aetiology of the brachyspina syndrome and the sire cannot at present be regarded as a carrier of the defect. However, the observations support the hypothesis of a genetic basis of the brachyspina syndrome as the cases occurred in a familial pattern consistent with autosomal recessive inheritance. It is recommended to perform a breeding trial to determine the inheritance of this syndrome and veterinarians are encouraged to report additional cases. Evaluation of breeding data for heterozygous sires used for artificial insemination should be performed when sufficient data are available to evaluate if the brachyspina syndrome is associated with increased embryonic and foetal mortality as for CVM . The brachyspina syndrome may be an emerging disease in the Holstein breed worldwide, if the syndrome is inherited autosomal recessively.
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