Influence of environmental temperature on the physiological, endocrine, and immune responses in livestock exposed to a provocative immune challenge.

Although livestock experience many stressors throughout their life, one of the most commonly experienced, and most difficult to control, is stress caused by fluctuations in environmental temperatures that extend beyond the thermoneutral (TN) zone for an animal. In swine, cold stress has long been recognized as a main cause of neonatal morbidity and mortality. A possible explanation for this increased morbidity and mortality may be related to their inability to generate a febrile response. Previously, we reported that the acute phase immune response, including the generation of fever, after exposure to lipopolysaccharide (LPS; Escherichia coli O111: B4; Sigma-Aldrich, St Louis, MO, USA) is substantially altered in neonatal pigs maintained in a cold environment (ie, 18°C). Neonatal pigs that were maintained in a cold environment and administered LPS experienced a period of hypothermia coupled with altered endocrine and proinflammatory cytokine responses that could prove detrimental. In cattle, we previously reported differences in the acute phase immune response of two diverse breeds of Bos taurus cattle (Angus and Romosinuano) when maintained under TN conditions and exposed to LPS. More recently we have reported that differences in the stress and immune responses of Angus and Romosinuano heifers varies, depending on whether the cattle were housed at either TN or heat stress air temperatures. Our data clearly show that even intermittent periods of heat stress similar to that experienced in production environments can have significant effects on the stress and innate immune responses of cattle. Understanding the effect of thermal stress on livestock is critical to developing and implementing alternative management practices to improve their overall health and well-being.

Chromium supplementation alters the performance and health of feedlot cattle during the receiving period and enhances their metabolic response to a lipopolysaccharide challenge.

Crossbred steers (n = 180; 230 ± 6 kg) were fed during a 56-d receiving period to determine if supplementing chromium (Cr; KemTRACE Chromium Propionate 0.04%, Kemin Industries) would improve feedlot performance and health of newly-received cattle. A completely randomized block design (36 pens; 9 pens/treatment; 5 steers/pen) was used. Chromium premixes were supplemented to add 0 (Con), 0.1, 0.2, or 0.3 mg/kg of Cr to the total diet on a DM basis. No differences were detected on d 0 or after the first 14 d on feed. From d 0 to d 28, DMI (P = 0.07) and ADG increased linearly (P = 0.04) as Cr concentrations increased. From d 0 to d 56, BW (P = 0.08) displayed a tendency to increase linearly, and consequently ADG and G:F increased linearly (P ≤ 0.05) as Cr concentrations increased. The number of steers treated at least once for respiratory symptoms tended (P = 0.07) to linearly decrease as Cr concentrations increased. Twenty additional steers (235 ± 4 kg) were fed 56 d to determine if supplementing Cr (Con or 0.2 mg/kg Cr) would alter the metabolic response of newly-received cattle to a lipopolysaccharide (LPS) challenge. Cattle were fitted with jugular catheters on d 52. On d 55, blood samples were collected at 0.5-h intervals from -2 to 8 h, and again at 24 h relative to a LPS challenge (0.5 µg/kg BW) at 0 h. Serum glucose, insulin, and NEFA concentrations were determined from blood samples. Steer BW was also measured at cannulation, and 24 h and 8 d post-LPS. Steer BW did not differ at cannulation (P = 0.37), but 24 h post-LPS, Cr-supplemented steers had lost less BW (P = 0.03). Pre-LPS glucose concentration did not differ (P = 0.97). Post-LPS, there was a time × treatment interaction (P < 0.01) such that glucose concentration peaked earlier (0.5 h) and at a greater concentrations in Cr-supplemented steers (P < 0.01). Insulin concentration did not differ between treatments pre- or post-LPS (P > 0.13). Concentration of NEFA did not differ pre-LPS (P = 0.54); but 0.5 h post-LPS Cr-treated steers produced a greater peak NEFA concentration (P < 0.04). Results of this study indicate that supplementation of Cr to the basal diet can have beneficial effects on the performance and health of newly-received steers. These data also suggest that supplementation of Cr attenuated BW loss and allowed for a quicker recovery after a LPS challenge.

Chromium supplementation alters both glucose and lipid metabolism in feedlot cattle during the receiving period.

Crossbred steers (n = 20; 235 ± 4 kg) were fed for 53 d during a receiving period to determine if supplementing chromium (Cr; KemTRACE Chromium Propionate 0.04%, Kemin Industries, Des Moines, IA) would alter glucose or lipid metabolism of newly received cattle. Chromium premixes were supplemented to add 0 (Con) or 0.2 mg/kg of Cr to the total diet on a DM basis. Cattle were fitted with jugular catheters on d 52. A glucose tolerance test (GTT) and an insulin sensitivity test (IST) were conducted on d 53. Blood samples were collected from -60 to 150 min relative to each infusion. Serum was isolated to determine glucose, insulin, and NEFA concentrations. Throughout GTT, no differences were detected in glucose concentrations, glucose clearance rates (k), or preinfusion insulin concentrations (P > 0.50), but insulin concentrations postinfusion tended (P = 0.06) to be greater for the Cr-supplemented steers. This caused an increase in the insulin to glucose ratio (I:G) from 0 to 150 min postinfusion for the Cr-supplemented steers (P = 0.03). In addition, NEFA concentrations during GTT were lower (P ≤ 0.01) for Cr-supplemented steers both preinfusion and postinfusion. During IST, there was no treatment effect on glucose concentrations preinfusion (P = 0.38), but postinfusion glucose concentrations were greater (P< 0.01) in the Cr-supplemented steers. The k of Cr-supplemented steers tended (P = 0.06) to be faster than Con steers from 30 to 45 min postinfusion. During the same test, there was no treatment effect detected for insulin concentrations (P > 0.33). The I:G were not affected by treatment (P > 0.40).Concentrations of NEFA were reduced (P < 0.01) both preinfusion and postinfusion during IST for Cr-supplemented steers. Results of this study indicate that supplementation of Cr can significantly alter lipid metabolism. This suggests that these steers had less dependence on lipid metabolism for energy or sensitivity of adipose tissue to antilipolytic signals was reduced. Results of glucose and insulin metabolism were inconsistently modified after a GTT and an IST.

Differential acute phase immune responses by Angus and Romosinuano steers following an endotoxin challenge.

Our primary objective of this experiment was to evaluate potential genetic differences between two diverse Bos taurus breeds [Angus (AG) and Romosinuano (RO)] in response to an endotoxin challenge. Eighteen steers (n = 9 steers/breed; 299.4 ± 5.2 kg BW) were acclimated to environmentally controlled chambers maintained at thermoneutrality (19.7 °C) and then fitted with indwelling jugular catheters and rectal temperature (RT) recording devices 1 d before the endotoxin challenge. The next day, blood samples were collected at 30-min intervals from -2 to 8 h, and RT was measured continuously at 1-min intervals throughout the study. At time 0, all steers received an intravenous bolus injection of lipopolysaccharide (LPS; 2.5 µg/kg BW). Serum samples were stored at -80 °C until analyzed for cortisol, proinflammatory cytokines [tumor necrosis factor-alpha (TNF-α), interleukin-1 beta (IL-1ß), IL-6, and interferon gamma (IFN-γ)], and acute phase proteins (serum amyloid A, acid soluble protein, ceruloplasmin, and α-acid glycoprotein). Rectal temperatures increased in both breeds within 1 h after LPS, with RO producing a greater increase in RT than AG steers (P < 0.001). Serum cortisol and TNF-α increased (P < 0.01) in both breeds within 1 h after the LPS challenge. For cortisol, an overall breed effect (P < 0.02) was detected, such that AG steers had a higher cortisol response than RO steers. A breed × time interaction (P < 0.01) was observed for TNF-α, such that the response was delayed and extended in the RO steers compared with the AG steers. At 2 and 2.5 h after LPS, TNF-α concentrations were greater (P < 0.03) in RO steers than in AG steers. For IL-1ß, a breed × time interaction (P < 0.04) was also observed. At 3 h after LPS, IL-1ß concentrations were greater (P < 0.01) in RO steers than in AG steers. Serum IL-6 and IFN-γ increased (P < 0.01) in a similar manner in both groups after the LPS challenge. These data show differences in the innate immune response between two diverse Bos taurus breeds which may provide insight about differences observed in productivity, heat tolerance, disease resistance, and longevity among cattle breeds.

Technical note: Evolution of exit velocity in suckling Brahman calves.

The purpose of this study was to assess changes in exit velocity (EV) of Brahman calves from 21 d of age (DOA) to 56 d postweaning (231.30 ± 1.23 DOA). Spring-born calves (n = 308) from 2006 to 2008 were sired by 18 bulls. Exit velocity (m/s) was determined as the rate of speed of a calf traversing 1.83 m after being released from a working chute. Temperament score was determined as the average of EV and pen score 28 d before and at weaning (2006: 173 ± 2 DOA; 2007: 174 ± 2 DOA; 2008: 163 ± 2 DOA). Pen score was determined by separating calves into groups of 3 to 5 animals and scoring their reactivity to a human observer on a scale of 1 (calm, docile, approachable) to 5 (aggressive, volatile, crazy). The number of calves that switched temperament group was determined by ranking calves based on their EV at 21 to 24 DOA, 90 DOA, weaning, and at 56 d postweaning. The GLIMMIX procedure of SAS was used to analyze EV with DOA, birth year and sex as fixed effects, and sire and calf nested within sire included as random effects. Temperament classification (calm, intermediate, temperamental) was modeled as a fixed effect, and the linear regression of traits on DOA investigated. Spearman rank order correlations were determined between EV at 21 to 24 DOA, 90 DOA, weaning, and 56 d postweaning and correlations decreased as the number of days between EV measurements increased. Differences in EV were observed between the 2006 (2.23 ± 0.057 m/s) compared with the 2007 (1.90 ± 0.059 m/s) and 2008 (1.83 ± 0.057 m/s) calves (P < 0.001), but the 2007 and the 2008 calves did not differ (P = 0.75). The random effect of sire approached significance (P = 0.07) and accounted for some of the variation observed. Exit velocity increased as days of age increased (P < 0.001). Exit velocity of temperamental calves increased at a faster rate with age (P < 0.001; estimate of slope = 0.005 ± 0.0004 m/s daily) compared with intermediate (slope = 0.003 ± 0.0005 m/s daily; P < 0.001) and calm calves (slope = 0.0007 ± 0.0005 m/s daily; P < 0.001). Exit velocity is a useful and viable indicator of temperament classification. Results suggest that temperamental calves increase their EV at a faster rate and may be identified before weaning, which may enhance the ability of producers to select against temperamental animals.

Oral administration of dehydroepiandrosterone-sulfate (DHEAS) increases in vitro lymphocyte function and improves in vivo response of pigs to immunization against keyhole limpet hemocyanin (KLH) and ovalbumin.

The present study tested the hypothesis that the oral administration of DHEAS enhances the in vitro and the in vivo immune response of young pigs. Crossbred, female pigs (80 days of age; 49+/-2 kg) were separated into two treatment groups (n=4/treatment) receiving either 0mg/kg (control) or 1mg/kg DHEAS twice daily (DHEAS) for 5 weeks. On day 7 pigs were immunized against KLH and ovalbumin. Body weight increased weekly throughout the study but did not differ between treatment groups. While white blood cell counts increased in response to immunization but did not differ between treatments, the neutrophil:lymphocyte ratio was enhanced (P<0.05) in DHEAS-supplemented pigs. Concanavalin A (ConA) induced an in vitro dose-dependent increase (P<0.05) in lymphocyte proliferation, but treatment did not affect proliferation prior to immunization. However, lymphocytes isolated from DHEAS-supplemented pigs displayed a greater increase in proliferation following immunization relative to control pigs (P<0.05). Dexamethasone (DEX) attenuated ConA-induced lymphocyte proliferation, with DHEAS-supplemented pigs retaining a greater proliferative response relative to control pigs (P<0.05). Serum IgG concentrations and relative concentrations of antigen-specific IgG increased after immunization with maximum values attained at 21 and 28 days for control and DHEAS-supplemented pigs, respectively. The DHEAS-supplemented pigs had greater (P<0.05) concentrations of IgG and relative concentrations of antigen-specific IgG compared to control pigs. Collectively these data suggest DHEAS supplementation increases the responsiveness of young pigs to antigenic challenge, and may be beneficial for improving their immune function.

Interrelationships among growth, endocrine, immune, and temperament variables in neonatal Brahman calves.

Interrelationships among growth, endocrine, immune, and temperament variables were assessed in neonatal Brahman calves. The velocity upon exiting a working chute (exit velocity) of an animal was measured and used as an objective indicator of temperament to classify calves as calm, intermediate, or temperamental. Calves (n = 116) were weighed weekly between d 0 and 21 to 24, and blood samples were collected for plasma and serum on d 0, 1, 2, 7, 14, and 21 to 24 after birth to measure concentrations of immunoglobulins, cortisol, and epinephrine (EPI). Body weight increased from d 0 through d 21 to 24 (P < 0.001) with bulls (n = 60) having greater BW than heifers (n = 56; P = 0.02). Serum concentrations of cortisol were greatest on d 0 before declining (P < 0.001) over the ensuing 21 to 24 d and were not related to temperament (P = 0.89) or sex (P = 0.97). Concentrations of EPI were affected by time, with an increase in EPI concentrations in temperamental bulls between 2 and 14 d of age (P < 0.008). Concentrations of EPI were not affected by temperament (P = 0.44) or sex (P = 0.68). Serum immunoglobulin concentrations peaked on d 1 before declining (P < 0.01) but were not related to temperament (P = 0.40 to 0.68). Of the stress hormones measured (cortisol and EPI), only cortisol was associated with the early performance of the calf. Calf BW at d 21 to 24 and BW gain were positively associated with serum immunoglobulin concentrations, yet negatively associated with concentrations of cortisol. Serum immunoglobulin concentrations were negatively correlated with cortisol concentrations (r = -0.28; P = 0.003), yet positively associated with EPI concentrations (r = 0.51; P = 0.003). During the neonatal period in this study, there was no relationship of temperament with passive immunity or stress hormone concentrations; however, growth was positively associated with passive immunity and negatively associated with stress hormones. Measuring exit velocity as early in life as d 21 to 24 fails to accurately predict temperament at weaning in over 40% of Brahman calves. Our conclusion is that measurement of exit velocity should be done nearer to the time of weaning than to birth. These data can be beneficial in developing best management practices for young calves.