Synthesis of optically pure chrysobactin and immunoassay development

Chrysobactin (-N-(2,3-dihydroxybenzoyl)-d-lysyl-l-serine), a siderophore that is essential for systemic virulence by plant pathogenic Erwinia chrysanthemi, was synthesized with high diastereomeric purity. Chrysobactin was prepared by coupling the N-hydroxysuccinimide ester of -N-(2,3-dibenzyloxybenzoyl)--N-Cbz-d-lysine with l-serine benzyl ester followed by deprotection via hydrogenolysis. Optically pure chrysobactin was obtained with 98% overall yield. A monoclonal antibody to ferric chrysobactin was developed and characterized as IgM. The antibody reacts with chrysobactin, ferric chrysobactin and less strongly with ferric dihydroxybenzoic acid. The antibody reacts weakly with the siderophores ferrichrome, A, ferric pseudobactin and ferric rhodotorulic acid. This antibody was used in a competitive immunoassay to detect ferric chrysobactin at 10^–8 to 10^–10 mol. This immunoassay may provide a useful method for the detection of chrysobactin in plant samples.     

pH-induced conformational changes in chromatin subunits measured by circular dichroism and immunochemical reactivity

Changes in the conformational state of chromatin core particles from chicken erythrocytes were studied by both immunochemical and biophysical methods as a function of pH and ionic strength. When the pH of core particles in a solution of ionic strength 3, 60 or 220 mM was lowered from pH 7.5, a sharp transition in the circular dichroism spectrum of DNA monitored between 320 and 260 nm was observed at pH 6.65. This change in DNA ellipticity was totally reversible. Binding to core particles of antibodies specific for histones H2B, H2A, H3 and for the IRGERA (synthetic C-terminal) peptide of H3 was used to follow changes in histone antigenicity. Binding was studied in the pH range 7.5-5.35, and at ionic strength of 60 and 220 mM. A change in reactivity of some histone epitopes was observed around pH 6.2–6.5. However, the changes observed by circular dichroism and antibody binding pertain to different components of chromatin subunits and they probably reflect independent phenomena. The alteration in accessibility of these determinants at the surface of core particles was completely reversible and was dependent on ionic strength. The conformation changes in core particles occurring near physiological ionic strength and pH may reflect dynamic changes in chromatin structure that possess functional significance.     

Some factors affecting the detection period of aphid remains in predators using ELISA

Quantitative enzyme-linked immunosorbent assay (ELSIA) was used to detect antigens of the aphid Sitobion averae (F.) in the guts of Linyphiidae, Carabidae and Staphylinidae. The effects of temperature, both constant and variable, and size of meal on the detection period and antigen decay rate were studied in the laboratory. Predators fed freshly-killed aphids were subsequently kept at one of several temperature regimes for a period from 0 to 13 days before being assayed for aphid remains. The proportion of prey remaining at intervals after feeding was measured. Curves were fitted to transformed data and the detection period estimated. The rate of decline in detectable remains was temperature-related, with the rate increasing as temperature increased. Prey remains in Staphylinidae declined much faster than in either Carabidae or Linyphiidae. In all but one case the decline was exponential with time. Variable temperature regimes produced results very similar to those obtained under conditions of constant temperature. Meal size produced a considerable difference in the amount of aphid remains detectable but little difference in the rate of decline or the estimated detection period. Data of the above types are a prerequisite for postmortem quantification of predator meals.

---

Influence de certains facteurs sur la détection par ELISA de vestiges de pucerons à l'intérieur des prédateurs

Résumé La recherche d'antigènes du puceron Sitobion avenae F. a été effectuée dans les tractus digestifs de Linyphiidae, Carabidae et Staphylinidae par ELISA (adsorption des antigènes sur l'anticorps fixé et dosage par l'anticorps enzymatiquement marqué). Les influences de la température, —soit constante, soit périodique —, de l'importance du repas, du moment de la détection et de la vitesse de disparition des antigènes ont été examinées au laboratoire. Des prédateurs alimentés en pucerons tués depuis peu ont été conservés de un à 13 jours à defférents régimes de températures avant la recherche de vestiges de pucerons. Une courbe d'atalonnage a été établie pour permettre la conversion de la valeur de la densité optique observée en mg de vestiges de pucerons en fonction du temps écoulé depuis le repas. Les données ont été soumises à une transformation angulaire et les courbes ajustées pour estimer la période de détection.La vitesse de disparition de vestiges détectables a augmenté avec la température. Les vestiges ont disparu beaucoup plus vite dans les Staphylinidae que dans les Carabidae ou les Linyphiidae. A l'exception d'un cas, la disparition était une expontentielle du temps. Les thermopériodes ont produit les mêmes effets que les températures constantes. La taille du repas a provoqué des différences considérables sur la quantité de pucerons décelable, mais peu sur la vitesse de la disparition ou la durée de la période où la détection est possible. L'obtention d'informations de ce type est une condition préalable à toute quantification post-mortem des repas de prédateurs.

     

Effects of hibernation on somatostatin-like immunoreactivity in the brain of the ground squirrel (Spermophilus richardsonii) and European hedgehog (Erinaceus europaeus)

Summary The localization of the somatostatin system in the brains of Richardson's ground squirrels (Spermophilus richardsonii) and European hedgehogs (Erinaceus europaeus) was described by use of immunocytochemical methods. In addition, (i) chemically differing types of somatostatin and (ii) different activity phases of the somatostatin system during the hibernation cycle were investigated in the ground squirrel by means of high pressure liquid chromatography (HPLC) and radioimmunoassay (RIA).In both species, the hypothalamic component of the somatostatin system (periventricular nuclei, fiber projections to the median eminence) is more prominent than the widespread extrahypothalamic representation of the system displaying mainly scattered perikarya and nerve fibers. The reactivity pattern of the somatostatin system varied among hibernating, aroused, and non-hibernating animals; moreover, the interspecific differences were pronounced. The activity of the hypothalamic somatostatin system in the hibernating ground squirrel appeared to be suppressed when compared to non-hibernating controls, whereas in the hibernating hedgehog this system showed signs of increased activity in comparison to non-hibernating controls. In contrast, in the present material the extrahypothalamic components of the somatostatin system did not exhibit significant changes in their activity.     

Detection of lactate dehydrogenase B4 in human hemolysate of patients deficient in lactate dehydrogenase B subunit activity using enzyme immunoassay

We developed a sensitive enzyme immunoassay system specific for human lactate dehydrogenase (LDH)- B₄ with antiacetylated LDH-B₄ Fab-horse-radish peroxidase conjugate. The enzyme immunoassay system was not interfered with by up to 0.3 mg/tube of hemoglobin. Thus, we measured LDH-B₄ concentrations in the hemolysate of seven heterozygous individuals deficient in LDH-B subunit activity and eight normal individuals. We could not find a significant difference between the LDH-B₄ concentrations in heterozygous and those in normal individuals. These results demonstrate that heterozygous individuals deficient in LDH-B subunit activity produce enzymatically inactive B subunits.This work was supported in part by grants in aid for Scientific Research from the Ministry of Education, Japan (59570998), and from the Clinical Pathology Research Foundation of Japan.     

测定呼吸道合胞病毒抗体方法敏感性的比较

用ELISA、间接免疫荧光和中和试验三种方法测定兔免疫血清的呼吸道合胞病毒抗体。结果中和试验测定的免疫血清几何平均抗体滴度为1:32;间接免疫荧光试验为1:508,比中和试验高16倍;ELISA测得的抗体滴度1:4,000～1:5,000,为中和试验的125～156倍。以ELISA敏感性最高,间接免疫荧光试验次之,中和试验景差。     

Developmental Changes in Distribution of Acidic Fibroblast Growth Factor in Rat Brain Evaluated by a Sensitive Two-Site Enzyme Immunoassay

We developed a sensitive two-site enzyme immunoassay (EIA) system for acidic fibroblast growth factor (aFGF), using a polyclonal antibody raised in rats. This assay is based on the sandwiching of the antigen between anti-aFGF antibody immunoglobulin G (IgG) coated on plates and biotinylated anti-aFGF antibody IgG; the detection of biotinylated IgG was performed by enzyme reaction of streptavidin-conjugated beta-D-galactosidase (beta-D-galactoside hydrolase; EC 3.2.1.23). Our system was specific for aFGF, because basic fibroblast growth factor, which shares a 55% homology of amino acid sequence with aFGF, hardly cross-reacted at all. The sensitivity of this system (0.2 ng/ml) enabled us to quantify endogenous immunoreactive aFGF in the CNS. Using this two-site EIA system, we examined the levels of aFGF in various regions of rat brain and their developmental changes. At the early stage of neonatal development, i.e., 2 days after birth, all brain regions registered low aFGF levels (less than 10 ng/g tissue). However, at the young adult stage (21- to 49-day-old animals), an extremely high level of aFGF (75-90 ng/g tissue) was found in the ponsmedulla; relatively high levels (30-40 ng/g tissue) were found in the diencephalon and mesencephalon; and comparatively low aFGF levels (5-15 ng/g tissue) were found in various other brain regions such as the frontal cortex, piriform cortex, hippocampus, olfactory bulb, cerebellum, and striatum. This marked change in the regional distribution of aFGF in the rat brain during postnatal development from 2 to 21 days after birth suggests that this factor plays a significant role in the brain during this period.     

Effect of temperature,gel concentration and cytokinins on vitrification of Olearia microdisca (J.M. Black) in vitro shoot cultures

The alkaloid content and profile of roots and aerial parts of diploid, haploid and hypohaploid plants of Nicotiana plumbaginifolia regenerated in vitro from leaf explants was determined by enzyme immunoassay and gas chromatography. Roots and buds separately neoformed in vitro were examined by the same methods. An interesting trait was found: buds, even without roots, contained alkaloids. Each of the tested hypohaploids exhibited a peculiar alkaloid content and profile compared to diploid and haploid genotypes, confirming the novel character of these hypohaploids. No correlation was observed between the degree of ploidy and the alkaloid content or profile.     

Detection of antibody responses and delayed dermal hypersensitivity with Blastomyces dermatitidis yeast and mycelial lysate antigens

Yeast cell lysate and mycelial lysate antigens prepared from one strain (T-58) of Blastomyces dermatitidis were evaluated with respect to the detection of antibodies and delayed dermal hypersensitivity. Comparable ELISA sensitivity values were evidenced with the two antigens when assayed against serum specimens from dogs with blastomycosis, sera from non-infected dogs residing in endemic and nonendemic areas for blastomycosis and sera from rabbits that were hyperimmunized with B. dermatitidis antigens. Specificity determinations with anti -Histoplasma capsulatum rabbit sera indicated that both reagents exhibited only minimal cross-reactivity; the mycelial antigen was slightly more specific than the yeast phase reagent. Similar sensitivity and specificity results were experienced when the two antigens were used to detect delayed dermal hypersensitivity in guinea pigs previously sensitized with B. dermatitidis or H. capsulatum.     

Antibody reactivities of Mycobacterium paratuberculosis infected sheep as analyzed by enzyme-linked immunosorbent assay and Western blotting

Antibody reactivities in sera from Mycobacterium paratuberculosis (M. ptb) infected and vaccinated sheep were analyzed by enzyme-linked immunosorbent assay (ELISA) and Western (immuno)blotting using a sonicate antigen from M. ptb. Both methods allowed good differentiation between infected/vaccinated animals and noninfected controls. Removal of nonspecific crossreactive antibodies by absorption with a M. phlei sonicate antigen coupled to Sepharose reduced ELISA reactivities of positive sera by 50% and those of noninfected serum by 85%. Immunoblotting analysis revealed that reduction by M. phlei absorption was due to lower reactivities of M. ptb antigens in the range of 30 to 45 kDa. However, one protein with a molecular mass of approx. 27 kDa seemed to be specific for M. ptb since it reacted similarly with nonabsorbed and absorbed serum but not with antibodies which were eluted from M. phlei-Sepharose after absorption. Our findings indicate that M. ptb and M. phlei share a number of common antigens of potential pathogenic importance and that only a smaller part of proteins (i.e. the 27 kDa protein) might be specific for M. ptb.