62 research outputs found
Pyelonephritis in slaughter pigs and sows: Morphological characterization and aspects of pathogenesis and aetiology
<p>Abstract</p> <p>Background</p> <p>Pyelonephritis is a serious disease in pig production that needs to be further studied. The purpose of this study was to describe the morphology, investigate the pathogenesis, and evaluate the aetiological role of <it>Escherichia coli </it>in pyelonephritis in slaughtered pigs by concurrent bacteriological, gross and histopathological examinations.</p> <p>Methods</p> <p>From Danish abattoirs, kidneys and corresponding lymph nodes from 22 slaughtered finishing pigs and 26 slaughtered sows with pyelonephritis were collected and evaluated by bacteriology and pathology. Based on gross lesions, each kidney (lesion) was grouped as acute, chronic, chronic active, or normal and their histological inflammatory stage was determined as normal (0), acute (1), sub-acute (2), chronic active (3), or chronic (4). Immunohistochemical identification of neutrophils, macrophages, T-lymphocytes, B-lymphocytes, plasma cells, <it>E. coli </it>and Tamm-Horsfall protein (THP) in renal sections was performed. The number of <it>E. coli </it>and the proportion of immunohistochemically visualized leukocytes out of the total number of infiltrating leukocytes were scored semi-quantitatively.</p> <p>Results</p> <p>Lesions in finishing pigs and sows were similar. Macroscopically, multiple unevenly distributed foci of inflammation mostly affecting the renal poles were observed. Histologically, tubulointerstitial infiltration with neutrophils and mononuclear cells and tubular destruction was the main findings. The significant highest scores of L1 antigen<sup>+ </sup>neutrophils were in inflammatory stage 1 while the significant highest scores of CD79αcy<sup>+ </sup>B-lymphocytes, IgG<sup>+ </sup>and IgA<sup>+ </sup>plasma cells were in stage 3 or 4. Neutrophils were the dominant leukocytes in stage 1 while CD3Δ<sup>+ </sup>T-lymphocytes dominated in stage 2, 3 and 4. Interstitially THP was seen in 82% and 98% of kidneys with pyelonephritis from finishing pigs and sows, respectively. <it>E. coli </it>was demonstrated in monoculture and/or identified by immunohistochemistry in relation to inflammation in four kidneys from finishing pigs and in 34 kidneys from sows.</p> <p>Conclusions</p> <p><it>E. coli </it>played a significant role in the aetiology of pyelonephritis. Neutrophils were involved in the first line of defence. CD3Δ<sup>+ </sup>T-lymphocytes were involved in both the acute and chronic inflammatory response while a humoral immune response was most pronounced in later inflammatory stages. The observed renal lesions correspond with an ascending bacterial infection with presence of intra-renal reflux.</p
Confusion and dependence in uses of history
Many people argue that history makes a special difference to the subjects of biology and psychology, and that history does not make this special difference to other parts of the world. This paper will show that historical properties make no more or less of a difference to biology or psychology than to chemistry, physics, or other sciences. Although historical properties indeed make a certain kind of difference to biology and psychology, this paper will show that historical properties make the same kind of difference to geology, sociology, astronomy, and other sciences. Similarly, many people argue that nonhistorical properties make a special difference to the nonbiological and the nonpsychological world. This paper will show that nonhistorical properties make the same difference to all things in the world when it comes to their causal behavior and that historical properties make the same difference to all things in the world when it comes to their distributions. Although history is special, it is special in the same way to all parts of the worl
The influence of recent social experience and physical environment on courtship and male aggression
Psychische Belastungen bei Angehörigen von Schlaganfallpatienten
Sustained psychosocial burdens as a consequence of stroke not only affect the stroke victim but frequently their spouses and significant others as well. The present study analyses the extent of emotional burden in spouses of stroke patients (Beck Depression Inventory, BDI and Beck Anxiety Inventory, BAI), examining the relationships of emotional burden in spouses with the medical assessment regarding stroke severity (Barthel Index, BI) and with the spouses' own perceptions of the stroke patients' impairment (Patient Competency Rating, PCR) as well as determining the factors that were independently associated with emotional burden in spouses. 82 spouses of stroke patients are examined in our study. The questioning was realised on admission into inpatient or partially inpatient rehabilitation centres. Initial results indicated that relatives of stroke victims have higher scores for anxiety compared to the general population. The assessment of disability in the stroke victims by their spouses correlates directly with the psychosocial burden of the spouses. By using this methodology, a high-risk group of spouses could be identified. The predictors of emotional burden in spouses (Anxiety and Depression) are gender of spouse and the spouse's subjective perception of disability in the stroke victim. The age of spouses and medical assessment of the severity of stroke on the other hand have no predictive value for the extent of emotional burden in spouses
Structural Basis for Aryl Hydrocarbon Receptor Mediated Gene Activation
The aryl hydrocarbon receptor (AHR) and the AHR nuclear translocator (ARNT) constitute a heterodimeric basic helix-loop-helix-Per-ARNT-Sim (bHLH-PAS) domain containing transcription factor with central functions in development and cellular homeostasis. AHR is activated by xenobiotics, notably dioxin, as well as by exogenous and endogenous metabolites. Modulation of AHR activity holds promise for the treatment of diseases featuring altered cellular homeostasis, such as cancer or autoimmune disorders. Here, we present the crystal structure of a heterodimeric AHR:ARNT complex containing the PAS A and bHLH domain bound to its target DNA. The structure provides insights into the DNA binding mode of AHR and elucidates how stable dimerization of AHR:ARNT is achieved through sophisticated domain interplay via three specific interfaces. Using mutational analyses, we prove the relevance of the observed interfaces for AHR-mediated gene activation. Thus, our work establishes the structural basis of AHR assembly and DNA interaction and provides a template for targeted drug design
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