P‐15COMPARISON OF RESULTS FOR A NON‐GYNAECOLOGICAL CYTOLOGY EQA SCHEME

The problems encountered with a glass slide circulation are legion but timely circulation is a major problem and is an inherent deficiency of our Non‐gynaecological EQA scheme. This applies not only to consultants but also to specialist registrars (SpRs) and technical staff that are not formally included in the circulation list. In 2005 only 7 technical staff and 4 out of 47 SpRs took part on a formal basis, their participation being dependant on access to slides during their cytology attachment. The results for the 2005 circulation have been analysed and despite the small numbers of participating technical staff and SpRs their answers concur with the consultant body. To address the issues of timeliness and circulation problems a pilot teaching set has been developed by SlidePath into a virtual microscope web based circulation and sent to all SpRs in our region. They have recorded their answers and been given immediate access to the consensus consultant opinion with illustrations of follow up histology. A questionnaire was completed to evaluate the scheme. The facility of immediate feedback of consultant consensus is particularly pertinent to the educational element of the scheme and use of virtual microscopy addresses the issue of timely circulation. If further funding was made available technical staff could also be given the opportunity to try this web‐based circulation.     

STRUCTURE OF EXTRACELLULAR POLYSACCHARIDES PRODUCED BY A SOIL CRYPTOMONAS SP. (CRYPTOPHYCEAE)1

The Hindak strain of a Cryptomonas species (Cryptophyceae) produces extracellular polysaccharides. Because there is no information on the structure of these compounds in the Cryptophyceae we conducted structural studies. Gas–liquid chromatographic analyses showed that the polysaccharide is composed of fucose, rhamnose, xylose, mannose, glucose, galactose, galacturonic acid, glucuronic acid, and traces of 3-O-methyl galactose. The polysaccharide was separated into two subtractions by ion-exchange chromatography. Fraction A consisted mainly of 1,3-linked galactose units and 1,4-linked galacturonic acid. Unlike fraction B, fraction A did not have xylose, 3-O-methyl galactose, or glucuronic acid. Also, its degree of branching was low compared to that of fraction B. Only traces of sulfate were present infraction A, but fraction B was 10–15% sulfated. Protein was approximately 1% in both fractions. These polysaccharides appear to be a novel type of polymer in algae.     

Cellulose morphology and enzymatic reactivity: A modified solute exclusion technique

An expeditious and accurate simplification of Stone and Scallan's solute exclusion technique was developed, thereby avoiding several sources of experimental error coupled with the determination of cellulose pore volume. Using this method, it is shown that cellulolytic enzymes do not enter into the micropores of five studied celluloses. These results suggestes that hydrolysis occurs initially at the external surface of the fibers. This surface area was calculated with the help of adsorption isotherms of bovine serum albumin. The obtained values for the different samples agree with the microscopically observed cellulose morphology. The correlation obtained by several authors relating cellulose porosity and its digestibility is explained as a consequence of the lower crystallinity and easier fragmentation of the more porous celluloses during hydrolysis. (c) 1994 John Wiley & Sons, Inc.     

A rapid evaluation plate-test for the biodegradability of plastics

Solid-media agar-plate tests were investigated for their potential to evaluate the biodegradation of polymeric particles by certain strains of microorganisms. A reliable test was developed. Stable suspensions of 1-m globules of two poly(3-hydroxyalkanoates) were prepared. These were mixed with liquified agar-agar to form turbid plates. Inoculation was carried out by plate puncturing. Seven strains isolated from sewage sludge formed clear zones. These zones were distinct, circular, and reproducible in outlook and growth. The maximal duration of single experiments was 192 h. A growth rate was defined. It allowed the classification of the polymers, and of the microorganisms used. Poly(3-hydroxybutyrate-co-valerate) was degraded faster by all the strains used than was the homopolyester poly(3-hydroxybutyrate). Strains achieving high zone growth rates generally did so on both of the polymers. This led to the assumption of similar enzymatic processes being active. Zone formation was concluded to be dependent on the amount of enzyme production plus the enzyme activity. The technique provides a means of either distinguishing the degradation abilities of a microorganisms, or the degradability of materials. Correspondence to: R.-J. Müller     

Études histologiques et ultrastructurales des larves dePandemis heparana [Lep. Tortricidae] au cours des stades avancés d'une baculovirose due a un nouveau virus inducteur de diapause

Résumé Une polyédrose nucléaire de la tordeuse de la pelure,Pandemis heparana Denis & Schiffermuller (Lep.: Tortricidae) due à un baculovirus isolé dans un verger de pommiers en France est étudiée. Le baculovirus, uniquement actif sur les larves nouvelles nées, induit un arrêt de développement des larves au stade L3 et une mortalité ultérieue des larves aux stades L5 et L6. L'étude en microscopie optique et en microscopie électronique des larves L5 et L6 présentant des sympt?mes très prononcés de la viroise (début de paralysie et couleur blanchatre des segments abdominaux) montre que c'est essentiellement le tissu adipeux et accessoirement certains hémocytes et quelques cellules de l'hypoderme qui sont le siège de la multiplication virale. La morphogénèse virale dans les cellules du tissu adipeux est décrite en détail. Certains aspects de l'étude ultrastructurale liés à la forme en massue des virions, au processus de cristallisation des polyèdres et à l'accumulation de masses fibrillaires viro-induites sont discutés.

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Summary A nuclear polyhedrosis virus infecting the torticidPandemis heparana Denis & Schiffermuller, collected in an apple-orchard in France was isolated and studied. The baculovirus is active only in the newly hatched larvae. It induces a delayed arrest of development in the L3 larvae and subsequently the death of L5 and L6 larvae. Study by light and electron microscopy of L5 and L6 larvae exhibiting very marked symptoms of the virus disease (early stages of paralysis and whitish colour of abdominal segments) shows that the site of multiplication of the virus is mainly located in the fat body cells and occasionally in some hemocytes or hypoderm cells. Virus morphogenesis within the fat body cells is described in detail. Some aspects of the ultrastructure such as clubbed virions, process of crystallization of polyhedral bodies and clumps of fibrous material induced by the virus, are discussed.

     

Recent advances in microbial capture of hydrogen sulfide from sour gas via sulfur‐oxidizing bacteria

Biological desulfurization offers several remarkably environmental advantages of operation at ambient temperature and atmospheric pressure, no demand of toxic chemicals as well as the formation of biologically re‐usable sulfur (S⁰), which has attracted increasing attention compared to conventionally physicochemical approaches in removing hydrogen sulfide from sour gas. However, the low biomass of SOB, the acidification of process solution, the recovery of SOB, and the selectivity of bio‐S⁰ limit its industrial application. Therefore, more efforts should be made in the improvement of the BDS process for its industrial application via different research perspectives. This review summarized the recent research advances in the microbial capture of hydrogen sulfide from sour gas based on strain modification, absorption enhancement, and bioreactor modification. Several efficient solutions to limitations for the BDS process were proposed, which paved the way for the future development of BDS industrialization.     

A study of chemoreception based on membrane fluidity and circular dichroism of a membrane assembly model--role of protein penetrating into the lipid bilayer

We attempted to reconstitute a chemical sensing assembly by mimicking the natural constituents of cell membranes. This liposomal arrangement is able to recognize chemical stimulants by detecting perturbation of the ordered lipid bilayer due to penetration by protein molecules. It was ascertained by measuring membrane fluidity using ESR that this assembly may be able to detect individually added chemical stimulants such as short-chain-bearing odorants (isovaleric acid, isovaleraldehyde, and isoamyl alcohol etc) at a concentration of 3 x 10(-4) parts to 1 part water. This recognition mechanism may clarify both the affinity of chemical stimulants for the liposomal arrangement and the trigger action of conformational changes in poly-L-lysine (PLL) due to the penetration of the bilayer of the PLL and sodium octylsulfate complex.     

Distribution of domestic triatominae and stratification of Chagas Disease transmission in Oaxaca, Mexico

Mexico has 18 species of Triatomine bugs (Hemiptera: Reduviidae) reported to be vectors of Trypanosoma cruzi. Chagas Disease is widespread in Mexico, with up to 3.5% seropositivity of human transfusion blood. The State of Oaxaca has the longest history of endemic Chagas Disease, based on acute and chronic case reports, and of entomological surveys in the country. However, the State health care services need more information on current risks of vector transmission. In order to identify and characterize areas of transmission in Oaxaca and to stratify the vector potential, the distribution of domestic Triatominae was surveyed during 1996-98 in collaboration with the primary health care services and local communities. Villages were studied in 11% of 570 municipalities in Oaxaca. Eight triatomine species were found in domestic and peri-domestic habitats: Triatoma barberi Usinger, T. bolivari Carcavallo et al., T. dimidiata (Latreille), T. mazzottii Usinger, T. nitida Usinger, T. pallidipennis (Stal), T. phyllosoma (Burmeister) and Rhodnius prolixus Stal. For each triatomine species in Oaxaca, the range of distribution and habitat characteristics are described. Habitat partitioning, principally based on altitude and mean annual precipitation, limited the overlap of distribution between species. Relatively consistent altitude of human settlements facilitates the dispersion of individual species within microregions. Entomological indices of house infestation were used to estimate that approximately 50% of the human population (1,874,320 inhabitants) would be at risk of vector transmission, with a minimum of 134,320 infected people and 40,280 chronic cases of Chagas Disease currently in Oaxaca.     

Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice

Mice with a null mutation of the presenilin 1 gene (Psen1(-/-)) die during late intrauterine life or shortly after birth and exhibit multiple CNS and non-CNS abnormalities, including cerebral hemorrhages and altered cortical development. The cellular and molecular basis for the developmental effects of Psen1 remain incompletely understood. Psen1 is expressed in neural progenitors in developing brain, as well as in postmitotic neurons. We crossed transgenic mice with either neuron-specific or neural progenitor-specific expression of Psen1 onto the Psen1(-/-) background. We show that neither neuron-specific nor neural progenitor-specific expression of Psen1 can rescue the embryonic lethality of the Psen1(-/-) embryo. Indeed neuron-specific expression rescued none of the abnormalities in Psen1(-/-) mice. However, Psen1 expression in neural progenitors rescued the cortical lamination defects, as well as the cerebral hemorrhages, and restored a normal vascular pattern in Psen1(-/-) embryos. Collectively, these studies demonstrate that Psen1 expression in neural progenitor cells is crucial for cortical development and reveal a novel role for neuroectodermal expression of Psen1 in development of the brain vasculature.