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1.
Plasma concentrations of PAG‐1 are used for pregnancy diagnosis and as a marker of placental/foetal well‐being, while those of PAG‐2 may be an indicator of abortion risk in Neospora caninum‐infected cows. Studies have shown that N. caninum infection modifies PAG‐1 and PAG‐2 patterns in maternal blood plasma. However, no prior work has examined the effects of N. caninum infection on concentrations of PAGs in foetal fluids. In this study, PAG‐1, PAG‐2 and pH levels were determined in the amniotic and allantoic fluids of foetuses collected at 152 days of gestation from control uninfected dams and from dams experimentally infected with N. caninum on Day 110 of gestation. Foetal fluids from infected foetuses had significantly higher PAG‐2 concentrations (p = 0.026) and pH values (p = 0.02) than fluids from non‐infected foetuses. In infected foetuses, significantly higher concentrations of PAG‐1 (p < 0.001) and PAG‐2 (p < 0.001) were detected in fluid samples showing antibodies against N. caninum than those without antibodies. Moreover, pH values were significantly higher (p = 0.011) in foetal fluid samples with antibodies than in samples from non‐infected foetuses. In conclusion, this is the first report on the effect of N. caninum infection on PAG levels in foetal fluids. Our results indicate that following the experimental infection of dams with N. caninum on Day 110 of gestation, foetal fluids collected from the infected foetuses of these dams featured higher PAG‐1 and PAG‐2 levels and pH values than fluids from non‐infected controls, provided that the samples tested showed the presence of antibodies. The clinical implications of these findings are that following infection with N. caninum, most cows will experience some level of placental damage and that this injury correlates with foetal fluid PAG levels and pH.  相似文献   
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Pregnancy‐associated glycoproteins (PAGs) isolated from the placenta of various ruminant species are enzymatically inactive members of the aspartic proteinase family. The measurement of these proteins in the maternal blood can be a good indicator of the presence of a live embryo. As certain aspartic proteinases are present in biological fluids in physiological and pathological conditions at various concentrations, it was necessary to determine the specificity of three radioimmunoassay (RIA) systems currently used for the detection of PAG molecules. Commercially available members of the aspartic proteinase family like pepsinogen, pepsin, chymosin, rennet, cathepsin D and renin were tested in a wide concentration range (10 ng/ml – 1 mg/ml). Pepsinogen cross‐reacted in RIA 1, RIA 2 and RIA 3 over 1 mg/ml, 50 μg/ml and 500 μg/ml concentrations, respectively. In the presence of pepsin, cross‐reaction was observed in RIA 1, RIA 2 and RIA 3 over 1 mg/ml, 500 μg/ml and 1 mg/ml concentrations, respectively. Chymosin and rennet could cross‐react in RIA 2 and RIA 3, while renin and cathepsin D did not decrease the binding of the tracer to antisera more, than that of the minimal detection limit. As the plasma/serum concentrations of the examined aspartic proteinases reported in the literature were outside the concentration range where cross‐reaction was observed, it can be concluded that these RIA systems were specific for the detection of PAGs in biological fluids.  相似文献   
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Many studies across the central and southern Maya Lowlands of Belize, Guatemala, Honduras, and Mexico have produced records of land degradation, mostly sedimentation and soil erosion, during the ancient Maya period from before 1000 BC to the Maya Collapse of c. AD 900. This paper provides new data from two sites (Blue Creek and Cancuén), synthesizes more than a decade of the authors' research in Guatemala, Belize, and Mexico, and synthesizes other findings from this region. These research projects analyzed more than 100 excavations in upland and depression sites, cored lakes and wetland sediments, and studied sediments in the field and laboratory using radiocarbon dating, a battery of soil chemistry tests, stratigraphic analysis, magnetic susceptibility, elemental analyses, and artifact identification. Our objective was to date when sedimentation and soil erosion occurred, identify stable surfaces, and correlate them with the state of knowledge about past land use. These findings indicate three general epochs of accelerated soil erosion and identified two major paleosols. The three waves of soil erosion occurred in the Preclassic period (c. 1000 BC to AD 250), the Late Classic (AD 550 to 900), and in the last several decades. The major paleosol (‘Eklu'um’) in these sites is a well-developed Mollisol or Vertisol that started forming in the early Holocene and was buried in either the Preclassic or Classic periods (AD 250 to 900). At some sites the Eklu'um paleosol lies beneath sediments with a fainter paleosol, which in turn lies buried below Classic period and later sediments. This picture shows higher than expected soil erosion linked to the region's first pioneer farmers in the Preclassic and less than expected soil erosion in the Late Classic when population peaked and land use was the most intensive. In other regions like Cancuén, Guatemala, however, most soil erosion occurred during the Maya Late Classic (AD 550–830). Erosion here was intense but short-lived: depressions record 1–3 m of aggradation in two centuries. A third epoch of accelerated soil loss and aggradation arose with the rapid land use changes brought by new pioneers during the last several decades.  相似文献   
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Catalytic hydrolysis of vasoactive intestinal peptide by human autoantibody   总被引:11,自引:0,他引:11  
Vasoactive intestinal peptide (VIP) labeled with 125I, [Tyr10-125I]VIP, can be hydrolyzed by immunoglobulin G (IgG) purified from a human subject, as judged by trichloroacetic acid precipitation and reversed-phase high-performance liquid chromatography (HPLC). The hydrolytic activity was precipitated by antibody to human IgG, it was bound by immobilized protein G and showed a molecular mass close to 150 kilodaltons by gel filtration chromatography, properties similar to those of authentic IgG. The Fab fragment, prepared from IgG by papain treatment, retained the VIP hydrolytic activity of the IgG. Peptide fragments produced by treatment of VIP with the antibody fraction were purified by reversed-phase HPLC and identified by fast atom bombardment-mass spectrometry and peptide sequencing. The scissile bond in VIP deduced from these experiments was Gln16-Met17. The antibody concentration (73.4 fmol per milligram of IgG) and the Kd (0.4 nM) were computed from analysis of VIP binding under conditions that did not result in peptide hydrolysis. Analysis of the antibody-mediated VIP hydrolysis at varying concentrations of substrate suggested conformity with Michaelis-Menton kinetics (Km). The values for Km (37.9 X 10(-9) M) and the turnover number kcat (15.6 min-1) suggested relatively tight VIP binding and a moderate catalytic efficiency of the antibody.  相似文献   
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