Sali Virpi, Veit Christina, Valros Anna, Junnikkala Sami, Heinonen Mari, Nordgreen Janicke
Department of Production Animal Medicine, University of Helsinki, Mäntsälä, Finland.
Department of Paraclinical Sciences, Norwegian University of Life Sciences, Oslo, Norway.
Front Vet Sci. 2021 Oct 14;8:698628. doi: 10.3389/fvets.2021.698628. eCollection 2021.
Infectious and inflammatory conditions are common especially in growing pigs. Lipopolysaccharide (LPS) is an important antigenic structure of Gram-negative bacteria and can be used to induce inflammation experimentally. As pigs are usually group-housed in commercial conditions, it is difficult to detect sick individuals, particularly at an early stage of illness. Acute phase proteins such as haptoglobin (Hp) are known indicators of an activated innate immune system whereas adenosine deaminase (ADA) is a relatively novel inflammatory biomarker in pigs. Both parameters can be measured in saliva and could be used as indicators of inflammation. Compared with blood sampling, saliva sampling is a less stressful procedure that is rapid, non-invasive and easy to perform both at group and at individual level. In this blinded randomized clinical trial, 32 female pigs at their post-weaning phase were allocated to one of four treatments comprising two injections of the following substance combinations: saline-saline (SS), ketoprofen-saline (KS), saline-LPS (SL), and ketoprofen-LPS (KL). First, ketoprofen or saline was administered intramuscularly on average 1 h before either LPS or saline was given through an ear vein catheter. In all groups, saliva was collected prior to injections (baseline) and at 4, 24, 48, and 72 h post-injection for determination of ADA, Hp, and cortisol concentrations. A multivariate model was applied to describe the dynamics of each biomarker. Pairwise relationships between ADA, Hp, and cortisol responses from baseline to 4 h post-injection within the SL group were studied with Spearman correlations. A significant increase in the SL group was seen in all biomarkers 4 h post-injection compared to baseline and other time points (pairwise comparisons, < 0.01 for all) and ketoprofen alleviated the LPS effect. We found a significant positive correlation between ADA and Hp within the SL group ( = 0.86, < 0.05). The primary and novel findings of the present study are the response of ADA to LPS, its time course and alleviation by ketoprofen. Our results support the evidence that ADA and Hp can be used as inflammatory biomarkers in pigs. We suggest further studies to be conducted in commercial settings with larger sample sizes.
感染性和炎症性疾病很常见,尤其是在生长猪中。脂多糖(LPS)是革兰氏阴性菌的一种重要抗原结构,可用于实验性诱导炎症。由于猪在商业环境中通常是群养的,很难检测出患病个体,尤其是在疾病早期。急性期蛋白如触珠蛋白(Hp)是已知的先天性免疫系统激活的指标,而腺苷脱氨酶(ADA)是猪中一种相对较新的炎症生物标志物。这两个参数都可以在唾液中测量,并可作为炎症指标。与采血相比,唾液采样压力较小,快速、无创,且在群体和个体水平上都易于操作。在这项双盲随机临床试验中,32头断奶后阶段的雌性猪被分配到四种处理之一,包括两次注射以下物质组合:生理盐水-生理盐水(SS)、酮洛芬-生理盐水(KS)、生理盐水-LPS(SL)和酮洛芬-LPS(KL)。首先,在通过耳静脉导管给予LPS或生理盐水之前平均1小时,肌肉注射酮洛芬或生理盐水。在所有组中,在注射前(基线)以及注射后4、24、48和72小时收集唾液,用于测定ADA、Hp和皮质醇浓度。应用多变量模型来描述每个生物标志物动力学。使用Spearman相关性研究SL组中从基线到注射后4小时ADA、Hp和皮质醇反应之间的成对关系。与基线和其他时间点相比,SL组在注射后4小时所有生物标志物均显著增加(成对比较,所有P<0.01),并且酮洛芬减轻了LPS的作用。我们发现SL组中ADA和Hp之间存在显著正相关(r = 0.86,P<0.05)。本研究的主要和新发现是ADA对LPS的反应、其时间进程以及酮洛芬的缓解作用。我们的结果支持ADA和Hp可作为猪炎症生物标志物的证据。我们建议在商业环境中进行更大样本量的进一步研究。