Assay of IgA to Shigella flexneri during shigellosis

Abstract An enzyme-linked immunosorbent assay (ELISA) to Shigella flexneri 2a whole bacterium was used to determine IgM, IgG and IgA serum titers in 50 acute-phase shigellosis patients and 37 controls, i.e., hospital patients without known recent infections. Compared to controls, the shigellosis patients displayed statistically raised average serum titers to S. flexneri in all 3 above immunoglobulin classes, most notably IgA, which displayed an average 42-fold increase. Specific IgM and IgG were 5- and 16-fold higher, respectively. All sera displayed statistically raised titers in at least one immunoglobulin class. A Widal agglutination detected a 7-fold increase in serum titers; this was comparable to the IgM ELISA. Statistical analysis showed that the intra-assay error of the ELISA varied from 5 to 14%, depending on the absorbance from which titers were calculated. A second ELISA was performed on the above shigellosis sera to determine titers to purified lipopolysaccharide (LPS): a statistical correlation was found between these and the above values for all 3 immunoglobulin classes. We conclude that the use of S. flexneri whole bacterium as an antigen in an IgA ELISA is a statistically valid and convenient parameter for monitoring shigellosis, comparable to the use of LPS as antigen, and more sensitive than IgM or IgG ELISAs or agglutinations.     

Indirect plaque-forming cells detected by use of normal mouse serum. I. Normal mouse serum plaque-forming cells are IgA producers.

The identity of indirect plaques developed upon addition of normal mouse serum (NMS) to Jerne test dishes was investigated. NMS plaques were significantly correlated with IgA, IgG_2A and IgG_2B plaques in decreasing order, but not with IgG₁ plaques. With protein A of Staphylococcus aureus as developer of IgG₂ plaques, the nonidentity of NMS plaque-forming cells (PFC) and IgG₂-producing cells could be demonstrated. The subsequent use in different orders of anti-α serum and NMS as developers of indirect plaques suggested that NMS PFC are IgA producers. Blocking experiments with purified myeloma IgA (MOPC 315) supplied further evidence for this idea. Using easily available protein A and NMS as developers of indirect plaques enables collection of more uniform data on the numbers of IgG₂ and IgA PFC than could be obtained with anti-heavy-chain sera.     

Quantifying the deposition of particulate matter on climber vegetation on living walls

The beneficial effect of vegetation on particle deposition is often stated in arboricultural literature but has rarely been researched in detail. To quantify these filtering effects of façade greening, it is necessary to study the accumulation properties of leaf surfaces on particle adsorption. In this paper attention will be given to a measure technique for particle adsorption on vegetation. The presented preliminary study aims to classify the total amount of particles by counting of particles on ESEM photographs. In the PhD research more attention will be given on the relation between particle reduction and the effect of vegetation on air quality improvements. Two locations were investigated, namely: leaves from near a traffic road and from a woodland. A difference in the particle amount was found at the underside and upper side of the leaves. For example, in a sampling at early autumn for the road location roughly 7000 particles (per 1275 × 950 μm) were counted for the upper side, and, roughly 3200 particles for the underside. Also a difference in particle amount was found between the two different locations, respectively roughly 7000 particles for the upper side of the leaf at the road location and roughly 3300 for the woodland location. The comparison must give more insight into the sink capacity of vegetation, but also between the environments. In the paper, results of counting particles on leaves from both locations are provided via a factorial design approach with four independent factors at two levels (height, leaf, time and environment). The outcome of the factorial design shows that there is a difference between the collecting capacity of the leaf (upper side/underside) and between the environments (road/woodland). Fine and ultra-fine particles (i.e., the fractions that are potentially the most harmful to human health) were more abundantly found on the leaves than coarser particles. Also some energy dispersive X-ray analysis (EDS) of the adhered particles is provided. As the main conclusion of this research, it can be said that counting particles instead of weighing particles on a specific leaf area seems to be a proper way to classify aerosol deposition on vegetation.     

Submicromolar free calcium modulates dexamethasone binding to the glucocorticoid receptor

The relative distribution of bound cis- and trans-(NH₃)₂PtCl₂ at specific sites in SV40 DNA is evaluated by monitoring the extent to which five restriction endonucleases, each of which cleave at a single, unique site, are inhibited as a result of the DNA modification. The order of cleavage inhibition is Bgl 1 ? Bam HI > Hpa II, Kpn I > Eco RI. Both isomers produce a comparable effect for any particular endonuclease. Inhibition correlates with the % (G+C) content within and about the recognition sequences. That modified sequences immediately adjacent to the recognition sequence influence cleavage is further supported by differential cleavage observed with the multicut Hind III endonuclease. The binding of cis-(NH₃)₂PtCl₂ at the hyper-reactive Bgl 1 site may well be directly responsible for inhibiting SV40 replication.