Department of Animal and Food Sciences, Texas Tech University, Lubbock, TX 79409, USA.
Department of Diagnostic Medicine/Pathology, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506, USA.
J Anim Sci. 2023 Jan 3;101. doi: 10.1093/jas/skad242.
Holstein steers (n = 40; initial body weight [BW] = 96.0 ± 10.5 kg) were individually housed in a climate-controlled barn to evaluate potential models for the genesis of liver abscesses (LA). In this 2 × 2 factorial, steers were balanced by BW and randomly assigned to one of two treatments: 1) intravenous saline injection followed by intraruminal bacterial inoculation with Fusobacterium necrophorum subsp. necrophorum (1 × 109 colony forming unit [CFU]/mL) and Salmonella enterica serovar Lubbock (1 × 106 CFU/mL; CON; n = 20 steers); or 2) intravenous injection with 0.25 µg/kg BW of lipopolysaccharide (LPS; Escherichia coli O111:B4) followed by intraruminal bacterial inoculation of F. necrophorum subsp. necrophorum (1 × 109 CFU/mL) and S. enterica serovar Lubbock (1 × 106 CFU/mL; LBI; n = 20 steers) and 1 of 2 harvest dates (3 or 10 d post LPS infusion). Body weights were recorded on days -4, -1, 3, and 10, and blood was collected for hematology on days -4, 3, and 10, relative to LPS infusion on day 0. Intraruminal bacterial inoculation occurred on day 1. Steers from each treatment group were harvested at two different time points on day 3 or 10 to perform gross pathological examination of the lung, rumen, liver, LA (if present), and colon. Feed disappearance was less for LBI than CON (P < 0.01); however, BW did not differ (P = 0.33) between treatments. Neither treatment nor time differed for hematology (P ≥ 0.13), and no gross pathological differences were noted in the lung, liver, LA, or colon (P ≥ 0.25). A treatment × harvest date interaction was noted for ruminal pathology in which LBI had an increased percentage of abnormal rumen scores on day 3 (P < 0.01). These results suggest that an LPS challenge in combination with intraruminal bacterial inoculation of pathogens commonly isolated from LA was not sufficient to induce LA in steers within 3 or 10 d (P = 0.95) when compared to CON. Further evaluation is needed to produce a viable model to investigate the genesis and prevention of LA in cattle.
荷斯坦公牛(n = 40;初始体重[BW] = 96.0 ± 10.5 kg)单独饲养在气候可控的牛舍中,以评估肝脓肿(LA)发生的潜在模型。在这项 2×2 析因设计中,公牛按 BW 平衡,并随机分为两种处理之一:1)静脉注射生理盐水,然后经瘤胃接种坏死梭杆菌亚种坏死梭杆菌(1×109 菌落形成单位[CFU]/mL)和沙门氏菌 Lubbock 血清型(1×106 CFU/mL;CON;n = 20 头公牛);或 2)静脉注射 0.25 µg/kg BW 的脂多糖(LPS;大肠杆菌 O111:B4),然后经瘤胃接种坏死梭杆菌亚种坏死梭杆菌(1×109 CFU/mL)和沙门氏菌 Lubbock 血清型(1×106 CFU/mL;LBI;n = 20 头公牛),并在 LPS 输注后 1 天或 10 天进行 1 次收获。在 LPS 输注前 4 天、前 1 天、第 3 天和第 10 天记录体重,在 LPS 输注前 4 天、第 3 天和第 10 天采集血液进行血液学检查。瘤胃接种于第 1 天进行。每组公牛在第 3 天或第 10 天的两个不同时间点收获,以对肺、瘤胃、肝、LA(如果存在)和结肠进行大体病理检查。LBI 的采食量比 CON 少(P < 0.01);然而,处理之间的 BW 没有差异(P = 0.33)。血液学指标在处理或时间上均无差异(P≥0.13),肺、肝、LA 或结肠未见明显大体差异(P≥0.25)。瘤胃病理方面注意到处理×收获日期的相互作用,LBI 在第 3 天异常瘤胃评分的百分比增加(P < 0.01)。这些结果表明,与 CON 相比,LPS 挑战与常见的 LA 分离病原体的瘤胃接种相结合,在 3 或 10 天内不足以诱导公牛发生 LA(P = 0.95)。需要进一步评估以建立可行的模型来研究牛的 LA 发生和预防。