Physiological and psychological stressors have been associated with the attrition of telomeres, which are the protective caps of chromosomes. This study compares the telomere length (TL) in 4-year-old Brahman cows grouped by the first parity (n = 8) and the second parity (n = 11). The cows were bled via jugular venipuncture, weighed, and had their body condition scores recorded at Day −28 prior to calving and at Day + 7 and Day + 28 post-calving. The duration of labor (Dlabor) and parturition ease were recorded. The peripheral leukocytes were isolated, the leukocyte blood count with differential was recorded, and the genomic DNA was extracted. The relative quantity of telomere products, which is proportional to the average TL, was determined via multiplex quantitative PCR using the ratio (T/S ratio) of bovine telomere and β-globulin DNA. Standards of the bovine telomere (1012–107 dilution series) and β-globulin (109–104 dilution series) genes were utilized to produce relative copy numbers. The samples were assayed in triplicate and were included if the triplicate Cq difference was less than 0.25 cycles. The parity was the fixed effect, and the random effects included the sire and day repeated with the cow as the subject. Statistical significance was not observed in the leukocyte number or type (p > 0.1). A reduction in the TL of approximately 9225 telomeric copies was found between Parity 1 and Parity 2 (p = 0.02). A trend was found between the TL and Dlabor (p = 0.06). The stress of parturition and raising the first calf of a cow’s life may be responsible for TL attenuation. Parity may be considered a stressor of cow longevity.

The effects of escalating lipopolysaccharide (LPS) doses on vaginal temperature (VT) and complete blood count (CBC) were evaluated to develop a model of low-level inflammatory response in cattle. Brahman heifers (2-yr-old; 326 kg BW) paired by birthdate, sire, and weaning temperament score were fitted with self-contained, indwelling vaginal temperature probes 7 d before initiation of treatment (d 0) and randomly assigned to Control (n = 6) or LPS (n = 6) treatment. Heifers were maintained as a group with free choice access to Coastal bermudagrass hay and fed 3.6 kg of a 3:1 corn:corn gluten grain mix per head per day. Heifers were weighed, BCS recorded, and blood samples were collected weekly by jugular venapuncture before delivery of treatments. Treated heifers received LPS (from Escherichia coli) via subcutaneous injection in the neck (d 0: 0.25 μg / kg BW; d7: 0.50 μg /kg BW; d 14: 0.75 μg /kg BW) and Control heifers received saline. Sickness behavior score (SBS) was monitored at 30-min intervals for 12 hr after LPS. Treatment was the fixed effect of interest. Random effects included sire and day repeated with heifer as the subject. No dose-treatment interactions were detected. The SBS did not change after subcutaneous LPS or saline (P > 0.1). Neutrophil and lymphocyte numbers 7 d after each injection were not affected by LPS (P > 0.1). A febrile response began within 1 hr and persisted up to 14 hr after LPS injections. The febrile effect of the 0.25 μg LPS dose was less pronounced (P < 0.05) than that of the 0.50 μg and 0.75 μg LPS doses which were similar to one another. Lipopolysaccharide treatment increased maximum VT (P < 0.0001), hastened time to attain maximum VT (P = 0.0429), and increased the change in VT (P < 0.0001). Weekly subcutaneous injection of LPS facilitates the study of the effect of sub-clinical illness in beef cattle.

No abstract

Telomeres are comprised of G-rich nucleotide sequences (5’-TTAGGG-3’) at the chromosome termini that are responsible for protecting chromosomes; however, attrition of these sequences has been observed in conditions of physiological and psychological stress. The purpose of this study was to compare telomere length (TL) in 4-yr-old Brahman cows grouped by first parity (n = 8) and second parity (n = 11). Cows were bled by jugular venipuncture, weighed, and had BCS recorded d+28 prior to calving and d-7 and d-28 post calving. Cows were observed for duration of labor (Tlabor) and calving ease (CE) at the time of parturition. Calf birth weight (CBW) and gender (CG) were recorded. Peripheral leukocytes were isolated, complete blood counts (CBC) were recorded, and genomic DNA was extracted utilizing silicone membrane spin column kits. The relative quantity of telomere products, which is proportional to the average TL, was determined by multiplex quantitative PCR analysis using the ratio of bovine telomere and β-globulin DNA. An absolute standard of bovine telomere (1012–107 dilution series) and β-globulin (109-104 dilution series) genes was utilized to produce relative copy number. All samples were run in triplicate and samples were included if triplicate Cq difference was less than 0.25 cycles. Parity was the fixed effect of interest and random effects included sire and day repeated with cow as the subject. No differences in CBC were seen. Tlabor, CE, CG, and CBW did not impact TL (P &gt; 0.1). A trend was observed for day-parity interaction (P = 0.0918). TL between parity differed most on d-28 (P = 0.1046; parity one 127292 ± 6483; parity two 111045 ± 5376). The stress of parturition and raising the first calf of a cow’s life may be responsible for slight attenuation in TL.