Abstract
Minimising health problems and increasing yield have always been the objectives in livestock agriculture. Hence, increases in incidences of reproductive conditions in cattle farming pose a great threat to productivity and impose undesirable economic implications. This study aimed to examine the concentrations of different biochemical compounds in cows with reproductive conditions. Seventy-seven blood samples were collected from cows at different rural areas around Mafikeng, following cases of downer cow syndrome, dystocia, retained placenta, vaginal prolapse and abortion. Means of serum metabolites across the different reproductive conditions were statistically compared using Pearson’s chi-square test to determine variations of serum metabolites in cows of different breeds. In mixed breed cows, higher than normal calcium concentrations were observed in downer cow syndrome (25.25 ± 8.47) and dystocia (85.50 ± 8.46) cases. It was also observed that cholesterol concentrations were significantly low in abortion (2.52 ± 0.79), retained placenta (3.18 ± 0.61) and vaginal prolapse (2.37 ± 0.97) cases in Afrikaner cows. The study showed that Brahman (43.1%) and Afrikaner (43.1%) breeds were mostly affected by downer cow syndrome. Additionally, the occurrences of downer cow syndrome (53.9%) and abortions (60%) were mostly observed in cows of 1–3 years, in second and first parities, respectively. This study proves that concentrations of calcium, urea or blood urea nitrogen (BUN), magnesium and cholesterol are significantly altered in incidences of reproductive conditions in cows of different breeds. It is also shown that serum biochemistry is affected by reproductive conditions in cows of different ages and parity. This data serves as a tool that could be used to enhance research in animal production and reproduction.
Keywords: animal health; cow; metabolic disorders; nutrition; reproductive performance; serum biochemistry.
Introduction
The use of serum metabolic profiling in veterinary medicine is a significant test in herd health assessment (Oetzel 2004). The physiological and nutritional status of cows can be evaluated using the analysis of blood biochemical parameters (Ashmawy 2015). Irregularities in numerous biochemical factors have been held liable for reproductive failures in cows (Bazzano et al. 2016). The cow’s immune capacity during the transition period greatly influences its susceptibility to reproductive and metabolic disorders (Azawi 2008). The incidences of reproductive conditions are normally elevated during the transition period (Santos, Rutigliano & Filho 2009).
Disturbances in the normal function of reproductive processes leading to dystocia can severely affect cattle production (Savc, Kenny & Beltman 2016). Associated risk factors and causes of dystocia include direct factors (e.g. uterine torsion and foetal mal-presentations), phenotypic factors (calf birth weight, multiple calving, prenatal mortality, cow pelvic area, cow body weight, body condition at calving and gestation length), non-genetic and genetic factors (Gaafar, El-Lateif & El-Hady 2011; Mee 2012; Zaborski et al. 2009). Dystocia is an undesirable condition because of its impact on cows’ subsequent reproductive performance and negative economic effects on farm production. The estimated cost of dystocia in any parity on average is approximately $24.24, which is approximately R323.78 (South African rand) as per case attendance (Dematawewa & Berger 1997).
Vaginal prolapse is another important reproductive health problem seen in cows. It is a condition of the reproductive tract frequently seen in 24-month-old cows, either pregnant or non-pregnant (Do Nascimento, Mello & Corrêa 2016). A study of Abuom et al. (2012) revealed that the incidences of vaginal prolapse increased during the dry season as a consequence of poor nutrition leading to loss of body condition as well as the peri-vaginal fat, which is important in supporting the uterus and vagina within the pelvic cavity. Also, foods containing oestrogenic substances such as subterranean clover pasture, soya-bean meal, mouldy maize and barley may result in a high incidence of vaginal prolapse (Noakes, Parkinson & England 2001).
Bovine abortions are complex reproductive conditions that occur between 42 and 280 days of pregnancy which may result from several pathogenic agents such as bacterial, viral, fungal, protozoal and non-infectious agents (Anka et al. 2014). The cost of production losses due to abortions is estimated to be about $640.00 (or R8548.64) per abortion case (Gädicke, Vidal & Monti 2010). Implementation of precautionary measures such as good health management, sufficient nutrition and other environmental factors affecting reproduction during pregnancy are important aspects to assure reduction in the high cost of animal losses through abortions.
The deficiency in secretions of oxytocin, prostaglandins (PGF2α) and serum calcium levels, dystocia and delay in the involution of the uterus may cause retained placenta (Akar & Yildiz 2005). Premature induction of parturition with glucocorticoids and/or prostaglandins, low plasma oestrogen concentration, deficiency in vitamin E and selenium, negative energy balance, hypocalcaemia hormonal disorders and others factors predispose cows to the incidences of retained placenta (Jemal 2016).
Downer cow syndrome is defined as lateral or sternal recumbency that persists longer than 24 hours whereby the animal is unable to rise to a standing position (Ménard & Thompson 2007:487). The aetiology of recumbency of the animal is not well understood; however, the association of energetic or electrolyte metabolism as well as infectious diseases and trauma may result in this syndrome (Guyot et al. 2017). The main causes of downer cow syndrome are hypocalcaemia and energy imbalance (Radostits et al. 2000). Other factors related to the incidences of downer cow syndrome include post-parturient disorders such as fatty liver, ketosis, metritis, nerve paralysis and mastitis (Kimura, Reinhardt & Goff 2006).
The association between nutrition, diseases and reproductive performance has been a subject of increasing interest to producers, veterinarians and nutritional researchers in recent years (Martinez et al. 2014; Pradhan & Nakagoshi 2008). The multifactorial nature of the reproductive conditions seriously limits the effectiveness of treatment methods and increases the risk of misdiagnoses. Note that it is difficult to monitor the level of impact reproductive conditions have on cattle production, mainly because of lack of data from diagnostics (Thornton 2010). Consequently, cattle production efficiency remains in a critically hindered status, as farmers still face challenges in their attempt to reduce reproductive health illnesses. Therefore it is necessary to conduct this study in order to bring about a guiding tool of variations in serum metabolites in cows of different breeds presenting with downer cow syndrome, dystocia, retained placenta, vaginal prolapse and abortion.
Materials and methods
Study design
The study was conducted in the Mafikeng area, found in the North-West Province in South Africa. The geographical coordinates of the study area are 25°51′S and 25°38′E. Blood samples were collected from communal farms around Mafikeng. Samples were collected when cases of reproductive conditions were reported to the North-West University Dale Beighle Centre for Animal Health Studies.
A total of 77 blood samples were collected from cows with cases of downer cow syndrome (n = 13), dystocia (n = 14), retained placenta (n = 13), vaginal prolapse (n = 9), and abortion (n = 28). Blood was collected from the jugular vein using an 18G double-pointed vacutainer needle into clot activator red stopped tubes (Greiner Bio-One, Kremsmunster, Austria; Germany). Samples were placed on ice and transported to the North-West University animal health laboratory for analysis. Serum was obtained by centrifugation (2500 revolutions per minute for 10 minutes) immediately after collection and was stored at -20 °C until assay. The IDEXX Catalyst Dx® Chemistry Analyzer was used for blood biochemistry testing of serum metabolites to determine concentrations of calcium, magnesium, total bilirubin, cholesterol (CHOL), ammonia, triglycerides, urea, uric acid and aspartate amino-transferase (AST) following the procedure of the manufacturer (IDEXX Laboratories Inc 2014, Westbrook, ME, United States [US]). Information about the age, parity and breed of the cows were also recorded.
Descriptive statistics (frequencies and percentages) were used to determine ages and parities of cows affected by reproductive conditions. The measure of association was performed using Pearson’s chi-square test to determine association between cow breeds (Afrikaner, Brahman, Charolaise, Mixed, Nguni, Drakensberger and Bonsmara) and blood chemistry (calcium, magnesium, total protein, creatinine kinase, lipase, triglycerides, urea or BUN, uric acid, AST, sodium, chloride, potassium, CHOL, total bilirubin and ammonia) in the different groups (cows experiencing downer cow syndrome, dystocia, retained placenta, vaginal prolapse and abortion) and different concentrations of serum metabolites, and the interaction (reproductive condition × cow breed) is indicated in the results. Data were analysed statistically in Statistical Analysis Software (version 20) using the analysis of variances techniques (ANOVA). The results for serum metabolites concentrations were expressed as means ± SE. Significance levels for all the tests were set at p < 0.05.
Ethical considerations
The study was approved by the Animal Ethics Committee at the North-West University (NWU-00409-18-S5).
Results
This study aimed to examine the concentrations of different biochemical compounds in different breeds of cows with reproductive conditions. The data in this section also shows the distribution of affected cows between ages and parities of affected cows.
This study showed significant (p < 0.05) variations regarding the reproductive condition × Cow breed interactions seen in concentrations of urea or BUN, calcium, AST, total bilirubin, lipase, potassium and total protein (Table 1). Additionally, the serum concentrations of triglyceride, creatinine kinase, sodium, chloride and total protein did not show a significant difference in association to the conditions (p > 0.05), as indicated in Table 1.
TABLE 1: p-Values obtained after statistical analysis of variance between average serum metabolites concentrations in cows affected by reproductive condition without the breed distinctions and within different breeds. |
The level of significance within a particular reproductive condition and breed is further elaborated in subsequent tables. In this section the tables indicate the mean variations of different serum metabolites in cows presented with reproductive conditions within a specific breed showing significant differences.
Table 2 shows significantly high serum mean concentrations of calcium in mixed breed cows which experienced downer cow syndrome (25.25 ± 8.47 mmol/L) and dystocia (85.50 ± 8.46 mmol/L). Significant difference in calcium concentrations was not observed in other reproductive conditions.
TABLE 2: Mean serum calcium (Ca) concentrations in different cow breeds experiencing reproductive conditions. |
The Table shows higher mean concentrations of urea in aborting Bonsmara cows (18.5 ± 3.04 mmol/L), Charolaise cows with downer cow syndrome (10.35 ± 3.04 mmol/L) and Afrikaner cows with vaginal prolapses (14.7 ± 2.15 mmol/L), while low mean urea (1.45 ± 3.04 mmol/L) concentrations were seen in Brahman cows with dystocia (Table 4).
TABLE 3: Mean serum magnesium concentrations in cows presenting abortion, downer cow syndrome and dystocia in different breeds. |
TABLE 4: Mean serum urea or blood urea nitrogen concentration in different cow breeds experiencing reproductive conditions. |
In aborting cows, CHOL mean concentrations were low in Afrikaner, Bonsmara, Brahman, Drakensberger and Nguni cows (Table 5). Moreover, cows presenting with downer cow syndrome showed low CHOL concentrations in Afrikaner, Brahman and mixed breed cows, as seen in Table 5. Low CHOL mean concentrations were also noted in retained placenta and vaginal prolapse in Afrikaner cows, as indicated in Table 5. Other findings revealed that Brahman, Afrikaner, mixed breed and Nguni cows with dystocia had significantly low CHOL mean concentrations, as shown in Table 5.
TABLE 5: Mean serum cholesterol concentrations in cows experiencing reproductive conditions in different breeds. |
The above graphical representation indicated abortion (46.15%), retained placenta (44.1%), dystocia (41.18%) and vaginal prolapse (43.5%) cases of cows in the first parities (Figure 1), whereas downer cow syndrome (46.15%) and vaginal prolapses (42.10%) mostly occurred in the second parity cows (Figure 1).
|
FIGURE 1: Parity distribution of cows affected by reproductive conditions parities. |
|
The histogram above shows that approximately 53.9% of downer cow syndrome and 60% of abortion cases were seen in cows of ages 3–4 years (Figure 2). Amongst other conditions, retained placenta (60%), dystocia (60%) and vaginal prolapses (41.2%) occurred in cows of ages 5–6 years. Additionally, the frequencies in 7–10 years old cows were very minimal showing low distribution amongst the occurring reproductive conditions (Figure 2).
|
FIGURE 2: Age association with the occurrence of reproductive conditions in cows. |
|
Discussion
Poor reproductive capacity in cow herds has negative implications on farm profitability as financial losses occur through high treatment and replacement costs, which consequently decreases farm income aptitudes (Gädicke et al. 2010). Constant herd health assessment can help reduce the impact of reproductive losses by minimising the costs of veterinary services. This study aimed to determine differences in the mean concentrations of serum metabolites in cows affected by reproductive conditions. In the current study, concentrations of calcium, urea or BUN, AST, total protein, total bilirubin, potassium and lipase significantly (p ≤ 0.05) varied in the breed and reproductive condition interactions (Table 1). Additionally, no significant differences were seen in concentrations of triglyceride, creatinine kinase, sodium and chloride and total protein did not show significant difference in relation to the incidences of reproductive conditions (p > 0.05).
In our study the mean concentrations of calcium indicated significantly high concentrations in cases of both downer cow syndrome (25.25 ± 8.47 mmol/L) and dystocia (85.50 ± 8.46 mmol/L) in mixed breed cows. On the contrary, the incidence of downer cow syndrome has been linked with low calcium levels (Benzaquen et al. 2015:186). However, such associations were not seen in this study, because the concentrations of calcium in most of the cows were within the normal ranges (2.0–2.8 mmol/L).
Similar observations were reported by McDougall (2001:60–67), where no relationship was established between low blood calcium, reproductive performance and dystocia. High levels of calcium in downer cow syndrome may be interpreted as a result of hormonal imbalance, for instance excessive secretion of parathyroid hormone (PTH) causing excessive bone resorption (Balamurugan et al. 2017:694), which could explain the increased calcium level in downer cows observed in this study. In downer cow syndrome, low mean concentration of calcium was observed in Brahman (1.98 ± 9.76 mmol/L) and Charolaise (0.78 ± 11.95 mmol/L) breed cows; however, no significant differences were indicated in the current study. This may be because of a lack of homogeneity in the number of cows within the different breeds, because low calcium is a known indicator for downer cow syndrome (Benzaquen et al. 2015:186).
A significantly different magnesium concentration below normal was seen in aborting Afrikaner cows in this experiment. Similar observations were reported by Musa, Lanyasunya & Mukisira (2016:117), indicating a magnesium deficiency in aborting cows. The results also indicated magnesium concentrations with no significant differences (p > 0.05) in aborting cows of Brahman and Nguni breeds. Magnesium mean concentrations in downer cow syndrome and dystocia were significantly high in mixed breed cows. These results agree with those recently reported by Adams, Ishler & Moore (2017:96), indicating that a rise in blood magnesium levels is usually observed in downer cow syndrome because of the decrease in calcium levels. Moreover, sufficient calcium levels are required to prevent dystocia and downer cow syndrome, because of its functional characteristics in muscle contraction and relation (Goff 2008:45).
The present study also showed significantly higher urea mean concentrations in aborting (18.5 ± 3.04 mmol/L) Bonsmara cows and downer cow syndrome (10.35 ± 3.04 mmol/L) Charolaise cows. Our findings agree with previous works reported, showing that high urea concentrations may lead to abortions in cows (Rhoads et al. 2009:1986). Other observed results indicated low urea levels in dystocia (1.45 ± 3.04 mmol/L) Bonsmara cows. Cholesterol mean concentrations of aborting cows were significantly low in different breeds experimented in the present study. Negative energy balance, poor body condition and low CHOL concentrations are usually indicators for postpartum health illnesses and poor nutrition status in cows (Sepúlveda-Varas et al. 2015:e0122317), which could explain the low level of CHOL in aborting cows.
In downer cow syndrome cows, significantly low CHOL concentrations were noted in Afrikaner (2.83 ± 1.12 mmol/L), Brahman (2.17 ± 1.12 mmol/L) and mixed breed cows (6.50 ± 0.97 mmol/L), as seen in Table 5. Civelek et al. (2011:341) reported similar results. These results imply that when calcium levels are decreased, the concentration of CHOL is likely to drop. Significantly low CHOL mean concentrations were also noted in retained placenta (3.18 ± 0.61 mmol/L) and vaginal prolapse (2.37 ± 0.97 mmol/L) in Afrikaner cows, as indicated in Table 5. The current results are in agreement with the study of Civelek et al. (2011:341) which reported lowered CHOL level in cows-retained placenta.
The results of this study showed that the incidences of dystocia were most frequent in cows of ages 5–6 years and in the first parity (Figures 1 and 2). Similar data indicating a direct relationship between dystocia, age and parity (more frequent in primiparous than high parity cows) have previously been presented (Abera 2017:1–9; McDougall 2001:60–67). The occurrence of dystocia have dire economic implications on production, as cows become more susceptible to post-partum illnesses, most likely to die soon after parturition and encounter increased calve mortalities (De Amicis et al. 2018:104).
According to Mee (2008:933–101), the cases of downer cow syndrome are mostly seen in older cows. However, in this study, the cases of downer cow syndrome were more prominent in cows of ages 3–4 than in those of 7–10 years (Figure 2). Similar results have been described, showing that age has an impact on the incidence of metabolic disorders as the level of susceptibility may vary according to age, and moreover, heifers are more susceptible to downer cow syndrome (Kutanaee et al. 2014:367).
The cases of retained placenta were observed (60%) in cows of ages 5–6 years in their first (44.1%) parity (Figures 1 and 2). The results agree with those of Sharma et al. (2017:3103) which indicated (40.22%) incidence in primiparous cows. Previous studies have also stated that incidences of retained placenta in most cases increase because of downer cow syndrome and dystocia (McDougall 2001:60–67). This study revealed that vaginal prolapses were most frequent in cows of ages 5–6 years in the first parity (44.1%), as seen in Figures 1 and 2. Similarly, prolapse of the vagina has been reported to be influenced by cow age and parity (Sarma, Das & Nath 2017:1067). These results therefore suggest that metabolic profile testing is a good indicator for bovine reproductive conditions.
Conclusion
The differences in serum metabolites concentrations were seen in cows of different breeds with reproductive conditions. Particularly, variations of serum calcium, magnesium, urea or BUN, AST and CHOL concentrations was observed in cows affected by dystocia, retained placenta, downer cow syndrome, vaginal prolapse and abortion. This study also showed that Nguni and Bonsmara breeds were the least affected by the reproductive conditions, suggesting that they are the most ideal to use in natural pasture rearing of cows. It is also indicated that age and parity could influence the change in blood chemistry as the cases of reproductive conditions were noted in cows of varying age groups and parities. The information obtained in this study serves as a useful tool for farmers as it can help them make informed decisions in determining the best animals to use for production.
Acknowledgements
The authors express their gratitude to all large animal clinic staff at the North-West University, particularly Mr V. Mjekula and Mr M.F. Ijane. The farmers from communal areas around Mafikeng are also acknowledged. The North-West University postgraduate bursary and the National Research Foundation (NRF) for their financial support are also acknowledged.
Competing interests
The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.
Authors’ contributions
K.M. collected and analysed samples and M.M. conceived and supervised the project. K.M. and M.M. conducted data analysis, interpreted the results and wrote the manuscript.
Funding information
This study was made possible by North-West University postgraduate bursary and the National Research Foundation.
Data availability statement
Data sharing is not applicable to this article as no new data were created or analysed in this study.
Disclaimer
The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of any affiliated agency of the authors.
References
Abera, D., 2017, ‘Management of dystocia cases in the cattle: A review’, Journal of Reproduction and Infertility 8(1), 1–9. https://doi.org/10.5829/idosi.jri.2017.01.09
Abuom, T.O., Njenga, M.J., Wabacha, J.K., Tsuma, V.T. & Gitau., G.K., 2012, ‘Incidence and risk factors of peri-parturient conditions in smallholder dairy cattle herds in Kikuyu Division of Kiambu District, Kenya’, Ethiopian Veterinary Journal 16(2), 85–102. https://doi.org/10.4314/evj.v16i2.8
Adams, R., Ishler, V. & Moore, D., 2017, ‘Trouble-shooting milk fever and downer cow problems’, in T.P.S. University (ed.), Penn State College of Agricultural Sciences research and extension programs are funded in part by Pennsylvania counties, the Commonwealth of Pennsylvania, and the U.S. Department of Agriculture (vol. DAS 96-27), Pennsylvania State University, Pennsylvania, United States.
Akar, Y. & Yildiz, H., 2005, ‘Concentrations of some minerals in cows with retained placenta and abortion’, Turkish Journal of Veterinary and Animal Sciences 29(5), 1157–1162.
Anka, M.S., Hassan, L., Khairani-Bejo, S., Zainal, M.A., Mohamad, R., Salleh, A. et al., 2014, ‘A case-control study of risk factors for Bovine Brucellosis Seropositivity in Peninsular Malaysia’, PLoS One 9(9), e108673. https://doi.org/10.1371/journal.pone.0108673
Ashmawy, N.A., 2015, ‘Blood metabolic profile and certain hormones concentrations in Egyptian buffalo during different physiological states’, Asian Journal Animal Veterinary Advances 10(6), 271–280. https://doi.org/10.3923/ajava.2015.271.280
Azawi, O.I., 2008, ‘Postpartum uterine infection in cattle’, Animal Reproduction Science 105(3–4), 187–208. https://doi.org/10.1016/j.anireprosci.2008.01.010
Balamurugan, B., Ramamoorthy, M., Mandal, R.S.K., Keerthana, J., Gopalakrishnan, G., Kavya, K. et al., 2017, ‘Mineral an important nutrient for efficient reproductive health in dairy cattle’, International Journal of Environmental Science and Technology 6(1), 694–701.
Bazzano, M., Giudice, E., Giannetto, C., Fazio, F., Scollo, C. & Piccione, G., 2016, ‘The peripartum period influenced the serum macro-mineral profile in mares’, Archives Animal Breeding 59(1), 65–70. https://doi.org/10.5194/aab-59-65-2016
Benzaquen, M., Galvão, K.N., Coleman, A.E., Santos, J.E.P., Goff, J.P., Risco, C.A., 2015, ‘Effect of oral mineral and energy supplementation on blood mineral concentrations, energetic and inflammatory profile, and milk yield in dairy cows affected with dystocia’, The Veterinary Journal 204(2), 186–191. https://doi.org/10.1016/j.tvjl.2015.03.001
Civelek, T., Aydin, I., Cingi, C.C., Yilmaz, O. & Kabu, M., 2011, ‘Serum non-esterified fatty acids and beta-hydroxybutyrate in dairy cows with retained placenta’, Pakistan Veterinary Journal 13(4), 341–344.
De Amicis, I., Veronesi, M.C., Robbe, D., Gloria, A. & Carluccio, A., 2018, ‘Prevalence, causes, resolution and consequences of bovine dystocia in Italy’, Theriogenology 107, 104–108. https://doi.org/10.1016/j.theriogenology.2017.11.001
Dematawewa, C.M.B. & Berger, P.J., 1997, ‘Effect of dystocia on yield, fertility, and cow losses and an economic evaluation of dystocia scores for Holsteins’, Journal of Dairy Science 80(4), 754–761.
Do Nascimento, G., Mello, I. & Corrêa, R., 2016, ‘Surgical treatment of partial prolapse of vaginal mucosa in Nelore cows submitted to follicular aspiration guided by ultrasound-technical report’, Animal Reproduction 13(3), 494.
Gaafar, H., El-Lateif, A. & El-Hady, S.B.A., 2011, ‘Effect of replacement of Berseem (Trifolium alexandrinum L.) hay by Berseem silage on performance of growing rabbits’, Archiva Zootechnica 14(4), 59–69.
Gädicke, P., Vidal, R. & Monti, G., 2010, ‘Economic effect of bovine abortion syndrome in commercial dairy herds in Southern Chile’, Preventive Veterinary Medicine 97(1), 9–19. https://doi.org/10.1016/j.prevetmed.2010.07.008
Goff, J.P., 2008, ‘Transition cow immune function and interaction with metabolic diseases’, in Tri-state dairy nutrition conference, 22–23 April 2008, pp. 45–57.
Guyot, H., Detilleux, J., Lebreton, P., Garnier, C., Bonvoisin, M. & Rollin, F., 2017, ‘Comparison of various indices of energy metabolism in recumbent and healthy dairy cows’, PLoS One 12(1), e0169716. https://doi.org/10.1371/journal.pone.0169716
IDEXX Laboratories Inc, 2014, IDEXX VetTest* chemistry analyzer operator’s manual, viewed 16 November 2017, from https://www.idexx.eu/globalassets/documents/chemistry/vettest_handbuch.pdf.
Jemal, J.Y., 2016, ‘A review on retention of placenta in dairy cattles’, International Journal of Veterinary Sciences 5(4), 200–207.
Kahn, C.M., Line, S. & Station, N.J., 2010, The Merck veterinary manual, Merck & Co, Whitehouse.
Kimura, K., Reinhardt, T.A. & Goff, J.P., 2006, ‘Parturition and hypocalcemia blunts calcium signals in immune cells of dairy cattle’, Journal of Dairy Science 89(7), 2588–2595. https://doi.org/10.3168/jds.S0022-0302(06)72335-9
Kutanaee, S.J., Sakha, M., Haghdoost, I.S. & Nadalian, G.M., 2014, ‘Measurement of cardiac troponin I in downer cows in dairy herds around Tehran’, Advances in Environmental Biology 8(17), 367–372. https://doi.org/10.1016/j.jvc.2015.02.003
Martinez, N., Sinedino, L., Bisinotto, R., Ribeiro, E., Gomes, G., Lima, F.S. et al., 2014, ‘Effect of induced subclinical hypocalcemia on physiological responses and neutrophil function in dairy cows’, Journal of Dairy Science 97(2), 874–887. https://doi.org/10.3168/jds.2013-7408
McDougall, S., 2001, ‘Effects of periparturient diseases and conditions on the reproductive performance of New Zealand dairy cows’, New Zealand Veterinary Journal 49(2), 60–67. https://doi.org/10.1080/00480169.2001.36204
Mee, J., 2008, ‘Prevalence and risk factors for dystocia in dairy cattle: A review’, The Veterinary Journal 176(1), 93–101. https://doi.org/10.1016/j.tvjl.2007.12.032
Mee, J., 2012, ‘Prevalence and risk factors for dystocia in dairy cattle – With emphasis on confinement systems’, Advances in Dairy Technology 24, 113–125.
Ménard, L. & Thompson, A., 2007, ‘Milk fever and alert downer cows: Does hypophosphatemia affect the treatment response?’ Canadian Veterinary Journal 48(5), 487–491.
Musa, H.H., Lanyasunya, T.P. & Mukisira, E. 2016, ‘Effects of poor nutrition on reproduction of dairy stock on smallholder farms in the tropics’, Pakistan Journal of Nutrition 4(2), 117–122. https://doi.org/10.3923/pjn.2005.117.122
Noakes, E.D., Parkinson, T.J. & England, G.C.W., 2001, ‘Post parturient prolapse of the uterus’, Arthur’s Veterinary Reproduction and Obstetrics 8th edn., 333–338.
Ode, S.A., Adamu, M. & Saror, D.I., 2017, ‘Haematology and some serum biochemistry of apparently healthy Muturu and Bunaji breeds of cattle in Benue State, Nigeria’, Comparative Clinical Pathology 26(1), 233–236. https://doi.org/10.1007/s00580-016-2375-1
Oetzel, G.R., 2004, ‘Monitoring and testing dairy herds for metabolic disease’, Veterinary Clinic of North America Food Animal Practice 20(3), 651–674. https://doi.org/10.1016/j.cvfa.2004.06.006
Pradhan, R. & Nakagoshi, N., 2008, ‘Reproductive disorders in cattle due to nutritional status’, Journal of International Development and Cooperation 14(1), 45–66.
Radostits, O.M., Arundel, J.H., Gay, C.C., Hinchcliff, F.F. & Blood, D.C., 2000, ‘Veterinary medicine: A textbook of the diseases of cattle, sheep, pigs and horses’, Bristol, SOM, United Kingdom, 9, 603–700.
Rhoads, M.L., Rhoads, R.P., VanBaale, M.J., Collier, R.J., Sanders, S.R., Weber, W.J. et al., 2009, ‘Effects of heat stress and plane of nutrition on lactating Holstein cows: I. Production, metabolism, and aspects of circulating somatotropin’, Journal of Dairy Science 92, 1986–1997. https://doi.org/10.3168/jds.2008-1641
Santos, J.E.P., Rutigliano, H.M. & Filho, M.F.S., 2009, ‘Risk factors for resumption of postpartum estrous cycles and embryonic survival in lactating dairy cows’, Animal Reproduction Science 110(3–4), 207–221. https://doi.org/10.1016/j.anireprosci.2008.01.014
Sarma, D.K., Das, A. & Nath, N., 2017, ‘Management of pre-partum vaginal prolapse in a crossbred cow with rope truss method’, International Journal of Current Microbiology and Applied Sciences 6(11), 1067–1070. https://doi.org/10.20546/ijcmas.2017.611.125
Savc, M., Kenny, D.A. & Beltman, M.E., 2016, ‘The effect of parturition induction treatment on interval to calving, calving ease, postpartum uterine health, and resumption of ovarian cyclicity in beef heifers’, Theriogenology 85(8), 1415–1420. https://doi.org/10.1016/j.theriogenology.2015.12.026
Sepúlveda-Varas, P., Weary, D.M., Noro, M. & Von Keyserlingk, M.A.G., 2015, ‘Transition diseases in grazing dairy cows are related to serum cholesterol and other analytes’, PLoS One 10(3), e0122317. https://doi.org/10.1371/journal.pone.0122317
Sharma, M., Bhat, Y., Sharma, N. & Rawat, S., 2017, ‘Effect of parity of animal and season of year on the rate of retention of placenta in dairy cattle’, International Journal of Current Microbiology and Applied Sciences 6(12), 3103–3108. https://doi.org/10.20546/ijcmas.2017.612.362
Thornton, P.K., 2010, ‘Livestock production: Recent trends, future prospects’, Philosophical Transactions B - Royal Society 365(1554), 2853–2867. https://doi.org/10.1098/rstb.2010.0134
Zaborski, D., Grzesiak, W., Szatkowsk, I., Dybus, A., Muszynska, M. & Jedrzejczak, M., 2009, ‘Factors affecting dystocia in cattle’, in Forsyth (ed.), International handbook of tourism economics, vol. 44, pp. 540–551, Edward Elgar, England.
|