BREEDING FOR RESISTANCE TO BOOPHILUS MICROPLUS IN AUSTRALIAN ILLAWARRA SHORTHORN AND BRAHMAN X AUSTRALIAN ILLAWARRA SHORTHORN CATTLE

SUMMARY Breeding for resistance to the cattle tick Boophilus microplus was undertaken in a herd of Australian Illawarra Shorthorn (AIS) cattle from 1961 to 1978 and in a herd of Braham x AIS cattle from 1970 to 1979. Breeder cows and their progeny were assessed for tick resistance during October to January. Resistance levels were determined as the average percentage mortality of female ticks from two artificial infestations with cohorts of c 20,000 larvae. Resistance increased from 89.2% to 99% in the AIS breeding herd, as a result of the yearly introductions of more resistant individuals and culling of less resistant ones. Concurrently resistance in the AIS progeny increased from 93.7% to 97.7%, thus demonstrating that the selection and breeding of the cows and bulls resulted in genetic improvement in the resistance of the progeny. Milk production tests on heifers from the selected AIS herd during 1975 to 79 indicated that selection for tick resistance did not select against milk production. Resistance of the Brahman x AIS increased from 98.4% to 99.3% in the breeding herd and from 97.6% to 99.6% in the progeny. Female calves of both breeds were more resistant than males.     

Hereditary parakeratosis in shorthorn beef calves

Parakeratosis was diagnosed in 9 Shorthorn beef calves over a 4-year period. When pedigrees of these calves were analyzed, familial associations were strong. Thirty-six coefficients of relationship among all possible combinations of the 9 affected calves ranged from 0.5 to 39.8% and averaged 15.6%. All affected calves were descendants of bull A. Of 9 affected calves, 6 had bull A in their paternal and maternal pedigrees. The 3 remaining affected calves had bull A in their sire's pedigree and were born to 2 full-sib dams. Seemingly, parakeratosis in this Shorthorn herd was hereditary with the mode of inheritance being that of a simple autosomal recessive.     

A genetic, pathological and virological study of congenital hypotrichosis and incisor anodontia in cattle

Two Friesian cows, half-sibs by a common dam, produced four bull calves with severe congenital hypotrichosis and incisor anodontia and three normal heifers by six unrelated Holstein, Friesian, Devon and Hereford bulls. The two dams, and their dam, had coats of a short, stubbly nature and the pigmented areas appeared rusty grey rather than black. Pathological examination of skin samples taken from multiple standardised sites from two of the affected calves showed a reduction in the number of large first-formed hair follicles. Smaller calibre hair follicles were present but, unlike those of normal neonatal calves, all were in the telogen (inactive) phase. Although the herd was infected with bovine virus diarrhoea virus there was no convincing evidence that the virus was implicated in the pathogenesis of these cases of congenital hypotrichosis with incisor anodontia. The family breeding information on the few severely affected and normal progeny and mildly affected and normal parents may be explained by the genetic hypothesis of an X-linked incompletely dominant gene.     

Prenatal occurrence and mode of inheritance of neuraxial oedema in Poll Hereford calves

Breeding experiments were conducted in 1981, 1982 and 1983 using bulls and cows that were obligatory heterozygotes for neuraxial oedema. Fifty-six calves were born in the herd, 14 of which were diagnosed as cases of neuraxial oedema. The mean gestation length for affected calves born in 1983 was nine days shorter than that for unaffected calves. Observations were made of the birth of three affected calves. In one calf spasms of the forelimbs were observed during an unassisted delivery, and in this and two others, typical clinical signs were observed within two minutes of birth. Radiological and, or, pathological examination of each of the eight affected calves born in 1983 revealed lesions in the coxae, some of which predated parturition. These observations are consistent with the calves being affected with neuraxial oedema while in utero.     

Growth patterns of Angus, Hereford and shorthorn cattle. II. Relationship of growth patterns of dams with progeny performance

Relationships between estimated growth curve parameters of dams and performance traits of their progeny were studied in Angus, Hereford and Shorthorn herds, each divided into four inbred and two noninbred lines. Growth curve parameters were calculated from the growth function Yt=A(1-Be-Kt), where Yt was weight at age t, A was estimated mature weight, B was an estimate related to early life weight changes and provided for a Y-intercept term and K was estimated general rate of maturing. Least-squares analyses of progeny variables were calculated separately for each breed and sex. Line differences did not influence any of the progeny variables except weaning type score of Shorthorn males (P less than .01). Birth year exerted a curvilinear effect on birth weights of Angus female progeny (P less than .01), a linear influence on 205-d weights of Shorthorn male progeny (P less than .05) and a curvilinear effect on weaning type scores of Angus and Shorthorn male progeny (P less than .01). Regression coefficients on weaning age indicated that calves born earlier in the calving season had lighter birth weights and that older calves at weaning received higher type scores. Inbreeding of the progeny negatively influenced (P less than .05) birth weights of Angus male and Hereford female progeny. Hereford male and Shorthorn female 205-d weights were negatively affected (P less than .05) by inbreeding, while weaning type scores of Shorthorn female progeny were negatively influenced (P less than .001) by inbreeding. Regression coefficients of all progeny variables on inbreeding in all analyses indicated negative trends.(ABSTRACT TRUNCATED AT 250 WORDS)     

Crossbreeding among British and continental European dual-purpose breeds in the coastal Pacific Northwest

From 1979 through 1987, British breed and crossbred cows were mated to Simmental, Pinzgauer or Tarentaise bulls or to Hereford-Angus crossbred bulls. Beginning in 1982, continental European crossbred females also entered the herd, to be mated for first calving to Hereford-Angus or Angus bulls and as cows to continental European or Hereford-Angus bulls. In progeny of British breed and crossbred cows, dam breed effects on birth and weaning weight were not important, but continental European crossbred calves were heavier than British crossbred contemporaries at birth and weaning. Pinzgauer- and Simmental-sired calves were heavier at birth than Tarentaise crosses, but calves sired by each of the continental breeds had similar weaning weights. Maternal heterosis was greater than direct heterosis effects on weaning weight (8% vs 5%), but only direct heterosis (13%) influenced birth weight. Within progeny of continental European crossbred cows, calves with a Tarentaise maternal grandsire were lighter at birth, with no significant difference among other maternal grandsire breeds. Maternal breed effects on weaning weight were not significant. Nevertheless, in contemporary years, continental European crossbred cows reared calves that were 10% heavier than calves reared by British crossbred cows. Pacific Northwestern cattle producers could achieve substantial increases in weaning weight from introducing inheritance from continental European dual-purpose breeds into cow herds and calf crops of British ancestry.     

Observations on spiral deviation of the penis in beef bulls

Premature spiral deviation of the penis was investigated in 1083 British breed beef bulls in 42 herds in Victoria (35) and Western Australia (7) by means of the serving capacity test. The herd prevalence was 60%. The prevalence of the defect at the initial test for all bulls was 10%. The prevalence in 635 polled bulls was 16% compared to a prevalence of 1 % in 448 horned bulls. The breed prevalence and the number of bulls tested per breed was Red Poll 27% (15), Murray Grey 25% (4), Poll Shorthorn 21 % (34), Angus 17% (415), Poll Hereford 10% (167) and Hereford 1 % (448). The difference between the last 2 breed types was highly significant (P<0.001). The prevalence of the defect increased from 0 to 30% over 9 years in one Victorian herd. The age of affected bulls varied from 2 to 11 years with most affected bulls aged from 3 to 6 years. Common ancestry was found between affected bulls in Western Australia, providing circumstantial evidence that it may be an inherited defect. None of the 103 affected bulls examined in this study had suffered obvious injury to the penis or prepuce. Eighty per cent of 56 affected bulls from Victoria had low serving capacity. Four bulls (2 from each state) with moderate to severe spiral deviation of the penis attained pregnancy rates of 43%, 33%, 3% and 3% respectively, in single sire mating trials. Recommendations for culling defective bulls are presented, based on the herd prevalence and severity of the defect in individual bulls.
It is concluded that bulls with moderate to severe spiral deviation of the penis have reduced fertility and remain permanently affected. The serving capacity test is a valuable diagnostic test for this serving defect in unhandled beef bulls. It is a common, although frequently undiagnosed disorder of polled beef breed bulls in Australia.     

Heterozygote detection for maple syrup urine disease in cattle

SUMMARY The clinical, pathological and biochemical manifestations of maple syrup urine disease (MSUD) are similar in Poll Hereford and Poll Shorthorn X Poll Hereford calves. No significant differences were observed in branched-chain amino acid concentrations in plasma, or of branched-chain keto acid dehydrogenase activity in fibroblasts, between Poll Herefords homozygous normal and heterozygous for the mutation responsible for MSUD. Haemopoietic chimerism resulted in incorrect diagnosis of the MSUD genotype in 30% of non-identical twins when blood DNA was analysed using allele-specific amplification. Hair roots are shown to be a suitable source of target DNA for genotyping Poll Hereford cattle for the MSUD mutation. Twelve of 203 (5.8%) aged Poll Hereford bulls, sampled at saleyards during the last 4 months of 1993, were found to be heterozygous for the mutation. In contrast, the mutant sequence was detected in only 1 of 150 (0.7%) 2- and 3-year-old Poll Hereford bulls offered for sale at 2 stud sales held during 1993, suggesting that the prevalence of the disease may decline over the next few years.     

DNA-based paternity analysis and genetic evaluation in a large, commercial cattle ranch setting

Deoxyribonucleic acid-based tests were used to assign paternity to 625 calves from a multiple-sire breeding pasture. There was a large variability in calf output and a large proportion of young bulls that did not sire any offspring. Five of 27 herd sires produced over 50% of the calves, whereas 10 sires produced no progeny and 9 of these were yearling bulls. A comparison was made between the paternity results obtained when using a DNA marker panel with a high (0.999), cumulative parentage exclusion probability (P(E)) and those obtained when using a marker panel with a lower P(E) (0.956). A large percentage (67%) of the calves had multiple qualifying sires when using the lower resolution panel. Assignment of the most probable sire using a likelihood-based method based on genotypic information resolved this problem in approximately 80% of the cases, resulting in 75% agreement between the 2 marker panels. The correlation between weaning weight, on-farm EPD based on pedigrees inferred from the 2 marker panels was 0.94 for the 24 bulls that sired progeny. Partial progeny assignments inferred from the lower resolution panel resulted in the generation of EPD for bulls that actually sired no progeny according to the high-P(E) panel, although the Beef Improvement Federation accuracies of EPD for these bulls were never greater than 0.14. Simulations were performed to model the effect of loci number, minor allele frequency, and the number of offspring per bull on the accuracy of genetic evaluations based on parentage determinations derived from SNP marker panels. The SNP marker panels of 36 and 40 loci produced EPD with accuracies nearly identical to those EPD resulting from use of the true pedigree. However, in field situations where factors including variable calf output per sire, large sire cohorts, relatedness among sires, low minor allele frequencies, and missing data can occur concurrently, the use of marker panels with a larger number of SNP loci will be required to obtain accurate on-farm EPD.     

Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.

The organisation of the E1alpha subunit of bovine branched-chain alpha-keto acid dehydrogenase gene was established. c DNA was cloned from Poll Shorthorn x Poll Hereford calves affected with Maple Syrup Urine Disease to identify the mutation responsible for the disease in Poll Shorthorns. Clones containing the c DNA sequences inherited from the Poll Shorthorn sire of the affected calves were identified. Paternal clones were sequenced and a cytidine to thymidine transition was found at nucleotide 1380. The mutation is predicted to substitute leucine in place of a highly conserved proline at codon 372. A polymerase chain reaction procedure was developed for detection of the 1380C-->T mutation in genomic DNA. Three Poll Shorthorn parents of affected calves and three affected Poll Shorthorn x Poll Hereford calves were heterozygous and an affected Poll Shorthorn calf was homozygous for this mutation. An improved polymerase chain reaction procedure was also devised to genotype Poll Herefords for the 248C-->T mutation. The procedures will facilitate disease prevention programs and assist in differential diagnosis of conditions in new-born calves that present with a rapid onset of progressive neurological disease and are characterised histologically by 'status spongiosus'. Maple Syrup Urine Disease (MSUD) is an autosomal recessive defect reported in humans (Danner and Elsas 1989), and in Poll Hereford (PH) and Poll Shorthorn (PS) calves (Harper et al 1986, Healy et al 1992). The clinical, biochemical and pathological manifestations of the disease are identical in the two breeds of cattle, and are characterised by the rapid onset of progressive neurological disease, leading to death within a few days of birth. The disease is caused by a deficiency of activity of the mitochondrial enzyme branched-chain alpha-keto acid dehydrogenase (BCKADH). This deficiency leads to elevated concentrations, in blood and tissues, of branched chain alpha-keto acids and their precursors, the branched chain amino acids, valine, leucine and isoleucine. BCKADH consists of four subunits E1alpha, E1beta, E2 and E3 that are encoded by separate genes, and MSUD may result from deficiency of any of the subunits. In PH s, the disease in caused by premature termination of translation, of the E1alpha subunit, that is induced by a cytidine to thymidine transition exon 2 (248C-->T), that converts the glutamine codon -6 to a stop codon (Q-6ST; Zhang et al 1990). We have shown that MSUD -affected PSxPH calves are heterozygous at the PH locus, illustrating molecular heterogeneity exists for bovine MSUD (Healy and Dennis 1994a). The fact that these crossbred calves are affected, indicates the PS, like the PH mutation, resides in the E1alpha subunit.     

CONGENITAL AND DEVELOPMENTAL ANOMALIES OF THE GENITALIA OF SLAUGHTERED BULLS

The genital tracts of 968 slaughtered bulls (46% of which were young post-puberal animals) were examined for defects of a congenital or developmental nature. The overall occurrence of such lesions was 7%. These comprised persistent penile frenulum (0.5%), hypospadias (0.3%), detached urethral process (0.4%), testicular hypoplasia (0.2%), cryptorchidism (0.6%), mesonephric duct abnormalities (1.1%) and bulbourethral cysts, fusion and aplasia (3.6%). Segmental aplasia of the mesonephric duct, not previously recorded in the study area, was found in 4 Shorthorn bulls (0.4%); 2 affected animals were from one herd. In 3 cases of hypospadias (2 from one herd), the urethra communicated with the ventral surface of the penis at the junction of the body and glans through a slit-like orifice. The occurrence of defects observed was generally comparable to that found in bull populations elsewhere but elevated occurrence of several defects in particular herds emphasized the need for further study.     

Phenotypic variation in bovine alpha-mannosidosis

Breeding experiments were conducted in 1984, 1985 and 1986, using Angus and Galloway bulls and cows that were obligatory heterozygotes for alpha-mannosidosis. Sixty-nine calves were born in the herd of which 16 were diagnosed as cases of alpha-mannosidosis. The clinical and pathological findings in eight Angus cross Angus, four Galloway cross Angus, and four Galloway cross Galloway calves affected with alpha-mannosidosis are reported. Thirteen calves displayed neurological signs in the early neonatal period. Three Galloway cross Galloway calves were stillborn. The severity of disease caused death or necessitated euthanasia within the first week of life of 10 affected calves. Three Angus cross Angus calves survived 40, 80 and 210 days. These findings illustrate significant variation in the phenotypic expression of alpha-mannosidosis both within and between the breeds.     

Reducing bias in the dairy cattle single‐step genomic evaluation by ignoring bulls without progeny

The number of genotyped animals has increased rapidly creating computational challenges for genomic evaluation. In animal model BLUP, candidate animals without progeny and phenotype do not contribute information to the evaluation and can be discarded. In theory, genotyped candidate animal without progeny can bring information into single‐step BLUP (ssGBLUP) and affect the estimation of other breeding values. We studied the effect of including or excluding genomic information of culled bull calves on genomic breeding values (GEBV) from ssGBLUP. In particular, GEBVs of genotyped bulls with daughters and GEBVs of young bulls selected into AI to be progeny tested (test bulls) were studied. The ssGBLUP evaluation was computed using Nordic test day (TD) model and TD data for the Nordic Red Dairy Cattle. The results indicate that genomic information of culled bull calves does not affect the GEBVs of progeny tested reference animals, but if genotypes of the culled bulls are used in the TD ssGBLUP, the genetic trend in the test bulls is considerably higher compared to the situation when genomic information of the culled bull calves is excluded. It seems that by discarding genomic information of culled bull calves without progeny, upward bias of GEBVs of test bulls is reduced.     

Inheritance of proportionate dwarfism in Angus cattle

OBJECTIVE: To determine the mode of inheritance of congenital proportionate dwarfism in Angus and Angus crossbred cattle, initially detected in two commercial beef herds in northern New South Wales. DESIGN: Matings of normal carrier sires to unrelated cows of diverse breeds, and of one carrier sire to his unaffected daughters. An unrelated Piedmontese bull was also mated to unaffected daughters of the carrier sires. PROCEDURE: Two carrier Angus bulls and nine unaffected daughters, all of whom were completely indistinguishable from normal animals, were purchased for controlled breeding studies under known nutritional and disease conditions. Affected and carrier individuals were examined for the presence of obvious chromosomal abnormalities. RESULTS: Angus dwarfism has been successfully reproduced under controlled experimental conditions over successive years using unrelated dams and is undoubtedly heritable. The high frequency of occurrence of affected individuals (23/61 = 0.38 +/- .06) among the progeny of matings of the Angus sires to unrelated females of diverse breeding is not compatible with recessive inheritance, because of the negligible frequency of proportionate dwarfism in the breeds of the dams. Both paternal and maternal transmission of the defect was demonstrated, so that imprinting in the strict sense of a gene that is only expressed when received from the male parent appears not to be involved. Tested individuals showed no evidence of gross chromosomal abnormality. Dominant autosomal inheritance with incomplete penetrance was indicated by the lack of expression of the defective gene in the two Angus sires and in three unaffected daughters who produced dwarf calves from matings to the Piedmontese bull. CONCLUSIONS: The mode of inheritance is that of a single autosomal dominant gene with a penetrance coefficient of 0.75 +/- 0.12, estimated from the observed incidence of 23/61 affected offspring of the two carrier Angus bulls mated to unrelated dams. Simple genetic models involving either (i) an unstable mutant which changes at high frequency to the expressed dominant dwarfing allele during gametogenesis, or (ii) a dominant allele with penetrance determined by an unlinked modifying locus, are shown to be compatible with the experimental data. Both models indicate that penetrance of the dwarfing gene may possibly be higher in matings involving carrier daughters of the two Angus bulls.     

奥系西门塔尔种公牛与母牛血液、被毛、乳和精液中几种微量元素含量的分析

从奥系西门塔尔牛群中选公母牛各3头,检测被毛、全血和乳中Fe、Cu、Co、Mn、Zn与Se的含量;还检测3种公牛(16头次)精液中Co、Mn、Zn和Se的含量。将测定值与日粮的微量元素含量进行综合分析看出,该牛群日粮中Mn含量明显不足,Cu、Zn略欠,Fe和Se足够。被毛中微量元素含量是衡量牛微量元素营养的较好指标。     

美系短角肉种牛繁殖性能研究

[目的]为了掌握短角肉种牛从美国引种到云南纯繁后的繁殖性能。[方法]通过对美系短角肉用种牛自2008年至2011年的参配母牛数、产犊数、成活数进行统计。[结果]四年的平均繁殖成活率69.18%,比驯化期间提高2%;其中以2008年最低(61.84%),2010年最高(72.26%)。[结论]美系短角肉种牛的繁殖性能逐年提高。     

Deficiency of uridine monophosphate synthase in Holstein cattle: inheritance and body measurements

Blood samples and body measurements were obtained from daughters of seven Holstein bulls previously shown to have a partial deficiency of uridine monophosphate (UMP) synthase and presumed to be heterozygous for the condition. Erythrocyte UMP synthase for 85 daughters showed a bimodal distribution with 42 having half the normal activity of 43 others. Furthermore, each bull had 50% of his daughters represented in each group, a finding fully consistent with the heterozygous designation of these bulls. Because UMP synthase is needed for pyrimidine biosynthesis and hence DNA and RNA metabolism, it was hypothesized that a partial deficiency could result in slower growth and smaller size for affected animals. Body measurements, as estimates of growth and size, included body length, wither height, hip height, hip width, rump length, pin width and taped body weight. Although measurements varied by age, differences between normal and heterozygous females were not found. One-half the normal activity of UMP synthase in cattle was adequate for near normal growth. Additionally, herd life was not significantly affected in heterozygous females.     

Inherited progressive spinal myelinopathy in Murray Grey cattle

In a breeding experiment conducted to determine the mode of inheritance of progressive spinal myelinopathy, semen from a Murray Grey bull which had previously sired affected calves was used to inseminate 120 cows. Female progeny were then inseminated with semen from the same bull. Of the 51 calves born, six (11.8%) had spinal cord lesions consistent with progressive spinal myelinopathy. From analysis of pedigrees and the results of the breeding experiment it was concluded that the condition was inherited as an autosomal recessive condition in Murray Grey cattle.     

Tibial hemimelia, meningocele, and abdominal hernia in Shorthorn cattle

Six genetically related Shorthorn calves were affected with the tibial hemimelia syndrome. The lesions included bilaterally malformed or absent tibia and abdominal hernia in all animals, a long shaggy haircoat, retained testicles in males, and meningocele in three animals. The malformations were similar to those described previously in Galloway calves. Pedigree analysis demonstrated a mechanism by which a recessive allele in a homozygous state could be responsible for the disorder. The condition in these calves was considered the result of a recurrence of a genetic mutation affecting a putative hemimelia locus.     

Status spongiosus of white matter in newborn Gelbvieh-cross calves.

Various forms of status spongiosus occur in neonatal cattle, the best characterized of which is due to mutations of the branched-chain alpha-keto acid dehydrogenase complex (BCKD), resulting in bovine maple syrup urine disease (MSUD, branched-chain ketoaciduria). A distinctive neurological syndrome was identified between 1998 and 2003 in 9 calves in a 250-cow stabilized Gelbvieh-Red Angus herd. Both sexes were affected (6 heifers, 3 bulls), with a low annual incidence (3 cases in 1998; no cases in 1999; 2 cases in 2000; 2 in 2001; 1 in 2002; 1 in 2003). Affected calves were born full-term, unable to stand, and had constant whole-body tremors when stimulated. Animals remained in lateral recumbency until death or euthanasia; the longest survival time was 10 days postpartum. The principal histological change in 2 affected calves was diffuse, moderately severe bilaterally symmetrical status spongiosus with Alzheimer type II cells throughout the white matter of the brain. Myelin deficits were not evident and vacuoles were due to cleaved myelin sheaths. Neither recognized mutation of MSUD was identified in the E1a subunit of BCKD in 2 affected calves, 8 dams that gave birth to affected calves, a grand-dam of 3 affected calves, or a sire of 1 calf. Amino acid analysis of serum from 1 affected calf revealed normal concentrations of branched-chain amino acids, indicating that this disease is distinct from MSUD. The genetic and biochemical basis for the disorder, provisionally named congenital status spongiosus of Gelbvieh-cross cattle, is undetermined. The pattern of inheritance was not established.