Repeat tuberculin skin testing leads to desensitisation in naturally infected tuberculous cattle which is associated with elevated interleukin-10 and decreased interleukin-1 beta responses

The principal surveillance tool used to control bovine tuberculosis in cattle is the removal of animals that provide a positive response to the tuberculin skin-test. In this study we performed a longitudinal investigation of the immunological and diagnostic consequences of repeated short-interval skin-tests in cattle naturally infected with Mycobacterium bovis. Tuberculin skin-test positive cattle were subjected to up to four further intradermal comparative cervical skin-tests at approximately 60-day intervals. A significant progressive reduction in the strength of the skin-test was observed after successive tests. In contrast, the magnitude of interferon-γ (IFN-γ) responses was not influenced by repeat skin-testing either transiently around the time of each skin-test or longitudinally following repeated tests. A significant boost in blood interleukin-10 (IL-10) production was observed within 3 days following each skin-test although the magnitude of this boosted response returned to lower levels by day 10 post-test. The application of a novel multiplex assay to simultaneously measure seven cytokines and chemokines also identified that skin-testing resulted in a significant and progressive reduction in antigen specific interleukin-1β (IL-1β) whilst confirming stable IFN-γ and elevated IL-10 responses in the blood. Therefore, we have demonstrated that in cattle naturally infected with M. bovis, repeat short-interval skin-testing can lead to a progressive reduction in skin-test responsiveness which has potential negative consequences for the detection of infected animals with marginal or inconclusive skin-test responses. The desensitising effect is associated with decreased IL-1β and elevated IL-10 responses, but importantly, does not influence antigen specific IFN-γ responses.     

盐胁迫对星星草幼苗保护酶系统的影响

在盐胁迫下,星星草幼苗过氧化氢酶活性随着胁迫时间的延长而增强,并与盐浓度呈显著正相关。超氧化物歧化酶活性随着胁迫浓度的增强而增强,当超过一定浓度(3.0%Na₂CO₃)时则趋减弱,尔后随着胁迫时间的延长而增强。过氧化物酶活性的变化规律与超氧化物歧化酶活性相似,但变化幅度较小。丙二醛含量随着胁迫时间的延长和胁迫强度的增强而增加。     

2型猪链球菌的血清学鉴定

本试验首次证实了２型猪链球菌在我国的存在，采用玻片凝集、琼脂扩散及毛细管沉淀等３项试验，对１９９０年以来广东某猪场断奶仔猪暴发流行的败血症、脑膜炎及关节炎病猪中分离的１５株链球菌进行了血清学鉴定。结果表明：１５株链球菌均为２型猪链球菌；用高压法提取抗原进行沉淀反应，其结果比酸热法提取抗原具有简便、敏感、特异性强的特点。     

CnAβ基因对大鼠RBL-2H3细胞脱颗粒的影响

过敏是人和养殖动物常见的疾病,而且发生的频率呈现逐渐增加的趋势.为了深入了解过敏反应的机制,本研究利用CRISPR/Cas9基因编辑技术,构建钙调磷酸酶A beta(calcineurin A beta,CnAβ)基因敲除的大鼠RBL-2H3细胞株,并探讨CnAβ基因对RBL-2H3细胞生长及脱颗粒的影响.选取大鼠Cn...     

Effects of N-methyl-D, L-aspartate on secretion of growth hormone-releasing hormone from the boar hypothalamic-preoptic area and median eminence in vitro

N-methyl-D, L-aspartate (NMA) elicited secretion of growth hormone (GH)-releasing hormone from both the hypothalamic-preoptic area and the median eminence that were collected from boars. We suggest that the previously described increase in GH secretion that follows peripheral treatment of swine with NMA is attributable, at least in part, to NMA-stimulated secretion of GH-releasing hormone from the central nervous system.     

Characterization of porcine circovirus type 2 (PCV2) infection in swine lymphocytes using mitogen-stimulated peripheral blood lymphocytes from healthy PCV2-carrier pigs

Information regarding the susceptibility of swine lymphocytes to PCV2 is rather limited. To further explore and characterize the PCV2 infection in swine lymphocytes, an in vitro model using concanavalin A (Con A)-stimulated peripheral blood lymphocytes (PBLs) obtained from clinically healthy PCV2-carrier pigs was introduced. It was found that the PCV2 antigen-containing rate was below 2% in PBLs from healthy PCV2-free pigs following treated simultaneously with Con A and PCV2. However, significantly higher PCV2 antigen- and nucleic acid-containing rates could be seen in Con A-stimulated PBLs from clinically healthy PCV2-carrier pigs. Prior to Con A treatment, both of the PCV2 antigen- and nucleic acid-containing rates in PBLs from healthy PCV2-carrier pigs were less than 1%; however, they reached 22.1+/-5.7% by flow cytometry and 27.1+/-6.5% by in situ hybridization, respectively, at 4-day post-incubation with Con A. Phenotyping of PCV2 antigen-containing cells revealed that PCV2-positive cells could be detected in both T and B lymphocyte populations within which IgM-positive B lymphocytes appeared to have a relatively higher positive rate. The Con A-stimulated PBLs also displayed a significantly higher viral load by the measurement of either PCV2 DNA copy number or viral titer when compared with the non-treated PBLs from healthy PCV2-carrier pigs. The results indicate that PBLs, especially IgM-bearing B lymphocytes, are indeed susceptible to PCV2 infection and PCV2 is capable of replicating in dividing lymphocytes. This activation-induced replication may explain in part the pathogenesis of lymphoid depletion in PMWS-affected pigs.     

小肽转运载体2及其在乳腺泌乳中的作用

作为一种潜在的重要的乳腺小肽转运系统,PepT2在乳腺氨基酸氮转运、降低乳汁药物分布以及乳腺疾病治疗方面都起到重要作用.对PepT2在乳腺中作用的深入研究在泌乳生理和临床治疗上都有着非常重要的意义.本文主要从PepT2的蛋白质结构与功能、底物转运特性、表达调控以及其在泌乳生理中的作用4个方面进行简要综述.     

不同蛋白源饲粮下断奶仔猪小肠中增食欲素受体2的表达特征

为探讨不同蛋白源饲粮对断奶仔猪小肠中增食欲素受体2（HCRTR2）的表达特征,研究采用实时荧光定量PCR方法检测HCRTR2的mRNA在断奶后分别饲喂动物蛋白替代30％总蛋白饲粮（处理1）及全植物性蛋白饲粮（处理2）0、3、7、14日龄大约克猪空肠中的表达特征。结果表明,不同蛋白源饲粮对日CR豫2基因mRNA的表达均有影响;与断奶0日龄相比．在处理1中,断奶3、7和14日龄时,HCRTR2的表达分别上升了4.30、6．60和4．12倍;处理2中,断奶3、7、14日龄HCRTR2基因mRNA的表达量分别为断奶0日龄时的0．71、1．44和4．50倍。结论：不同蛋白源饲粮对HCRTR2基因mRNA的表达均有影响。     

实验性雏鸡佝偻病的病理学研究——Ⅱ.形态学观察

4日龄 Aiboi Acies肉鸡健雏80只随机分为4组,分别喂给钙-磷缺乏(Ca 0.02％,P0.30％)、缺钙(Ca 0.02％,PO.71％)、缺磷(Ca 0.95％,PO.30％)和正常对照(Ca 0.95％PO.71％)日粮三周,进行了系统的病理形态学观察。缺磷组病变表现为肋骨头肿大,长骨骨骺生长板之肥大带明显增宽,骨小梁减少;缺钙组和钙-磷缺乏组病变表现为肋骨增粗弯曲,长骨骨骺生长板之增生带显著增宽,海绵骨类骨组织和结缔组织大量增生,成骨细胞和破骨细胞丰富。结果表明,钙缺乏和磷缺乏所致病变显著不同,为鉴别诊断提供了科学依据。     

Effect of dipeptide on intestinal peptide transporter 1 gene expression: An evaluation using primary cultured chicken intestinal epithelial cells

Peptide transporter 1 (PepT1) is a transporter responsible for absorbing dipeptide and tripeptide in enterocytes and is upregulated by dipeptide in mammals. It has not been certain whether intestinal PepT1 expression is responsive to dipeptides in chickens because of the lack of in vitro study using the cultured enterocytes. This study established a primary culture model of chicken intestinal epithelial cells (IECs) in two-dimensional monolayer culture using collagen gel by which the response of chicken PepT1 gene expression to dipeptide stimuli was evaluated. The cultured chicken IECs showed the epithelial-like morphology attached in a patch-manner and exhibited positive expression of cytokeratin and epithelial cadherin, specific marker proteins of epithelial cells. Moreover, the chicken IECs exhibited the gene expression of intestinal cell type-specific marker, villin1, mucin 2, and chromogranin A, suggesting that the cultured IECs were composed of enterocytes as well as goblet and enteroendocrine cells. PepT1 gene expression was significantly upregulated by synthetic dipeptide, glycyl-l-glutamine, in the cultured IECs. From the results, we herein suggested that dipeptide is a factor upregulating PepT1 gene expression in chicken IECs.