Stimulatory effect of selected surface-active agents on the growth of pathogenic human fungi

Summary The growth ofCryptococcus neoformans andCandida albicans in Sabouraud's dextrose broth with added surface-active agents was measured by nephelometric methods. The surface-active agents was measured by nephelometric methods. The surface-active agents utilized were Polyethylene glycol 400 monolaurate, Pluronic L 64, and Mulsor 224. These three compounds definitely stimulated the growth of the above organisms as indicated in the accompanying tables. The nephelometric runs were corroborated with plate counts taken at suitable intervals.This project was supported by Research Grant E-1045(R) of the National Institute of Health, United States Public Health Service.     

Histochemical demonstration of acid mucopolysaccharide production by tissue cultured epithelial-like cells

Summary The production of mucopolysaccharides by human epithelial-like cells in vitro has been studied using histochemical techniques. Cells of the human amnion F/L line were grown for 12–14 days in Leighton tubes containing cover slips which were fixed and stained by the Hale, PAS, toluidine blue and alcian blue stains and techniques. Control slides were treated with active and heat inactivated solutions of testicular and bacterial hyaluronidase and chondroitinase prior to staining. Results indicated that material stainable by all the techniques employed was elaborated by the amnion cells and this was partially removable by various combinations of polysaccharases. It is concluded that epithelial-like cells can synthesize and elaborate the ground substance components, hyaluronic acid, chondroitin sulphates and unidentified polysaccharide complexes, in much the same manner as mesenchymal cells and thus contribute to the maintenance of epithelial integrity by de novo production of intercellular substances.Supported by USPHS Grants No. 991 and DE-01681, T01-DE00108 National Institute of Dental Research, National Institutes of Health and the National Health and Medical Research Council, Australia.     

A numerical method for renal models that represent tubules with abrupt changes in membrane properties

 The urine concentrating mechanism of mammals and birds depends on a counterflow configuration of thousands of nearly parallel tubules in the medulla of the kidney. Along the course of a renal tubule, cell type may change abruptly, resulting in abrupt changes in the physical characteristics and transmural transport properties of the tubule. A mathematical model that faithfully represents these abrupt changes will have jump discontinuities in model parameters. Without proper treatment, such discontinuities may cause unrealistic transmural fluxes and introduce suboptimal spatial convergence in the numerical solution to the model equations. In this study, we show how to treat discontinuous parameters in the context of a previously developed numerical method that is based on the semi-Lagrangian semi-implicit method and Newton's method. The numerical solutions have physically plausible fluxes at the discontinuities and the solutions converge at second order, as is appropriate for the method. Received: 13 November 2001 / Revised version: 28 June 2002 / Published online: 26 September 2002 This work was supported in part by the National Institutes of Health (National Institute of Diabetes and Digestive and Kidney Diseases, grant DK-42091.) Mathematics Subject Classification (2000): 65-04, 65M12, 65M25, 92-04, 92C35, 35-04, 35L45 Keywords or phrases: Mathematical models – Differential equations – Mathematical biology – Kidney – Renal medulla – Semi-Lagrangian semi-implicit     

Isozyme variability in species of the genus Drosophila. III. Qualitative comparison of the esterases of D. aldrichi and D. mulleri

Two closely related species, Drosophila aldrichi and D. mulleri, are compared on the basis of their esterase isozyme patterns after starch gel electrophoresis. Comparable esterases between the two species are identified by substrate specificity, inhibition, and enhancement of esterase activity by various agents. The extensive electrophoretic variability of most of the esterases in nature is described and data relating to the inheritance of the various enzyme forms are presented.This work was supported (in part) by a U.S. Public Health Service research grant (GM 11609 to W. S. Stone and M. R. Wheeler) and a training grant (2 T1-GM 337-07 to R. P. Wagner et al.) from the National Institutes of Health.     

Polymorphism and predictability at the α-glycerophosphate dehydrogenase locus in Colias butterflies: Gradients in allele frequency within single populations

Heterozygosity at the -glycerophosphate dehydrogenase locus of five species of Colias butterflies is widespread in montane populations; alpine and lowland populations are not heterozygous. Within a single demographically characterized population of C. meadii where the population extends from alpine down into montane habitats, a marked cline in allele frequency is seen. Such within-population clines suggest the involvement of strong selection across the marked ecological interface. Thermal factors are the most likely causative agents, but associative overdominance is not excluded.This work was supported by grants from Washington University, the National Institutes of Health, and the National Science Foundation.CIW-DPB Publication No. 562.     

The dissociation of insect embryos for cell culture

Summary Procedures and solutions were developed for dissociating embryos ofBlattella germanica in preparation for primary cell culture. Trypsin solutions were maximally effective at 0.01% for germ bands but higher concentrations, 0.05 to 0.1% were needed for embryos in later stages. This investigation was supported by U.S. Public Health Service Research Grant No. AI 09914 from the National Institute of Allergy and Infectious Diseases. This is paper No. 8855, Scientific Journal Series, Minnesota Agricultural Experiment Station. The work was selected from the dissertation of T. J. K. presented for the Ph. D. degree at the University of Minnesota.     

Period shortening and phase shifting effects of ethanol on theGonyaulax glow rhythm

Summary In a number of organisms which exhibit circadian rhythmicity, a continuous exposure to ethanol at moderate (0.1%) concentrations is known to cause period lengthening. In studies of the effects of ethanol on the circadian luminescence glow rhythm of the marine dinoflagellateGonyaulax, we observed that 0.1% ethanol causes instead a period shortening. We have also found that ethanol pulses cause phase shifts, with little or no after-effects on the period of the circadian rhythm which continues thereafter.Abbreviation CT circadian time This work has been supported in part by a grant from the National Institutes of Health GM-19536 to J.W. Hastings, and by a Rackham Block Grant to Walter Taylor from the University of Michigan     

Avian disease at the Salton Sea

A review of existing records and the scientific literature was conducted for occurrences of avian diseases affecting free-ranging avifauna within the Salton Sea ecosystem. The period for evaluation was 1907 through 1999. Records of the U.S. Department of Agriculture, Bureau of Biological Survey and the scientific literature were the data sources for the period of 1907–1939. The narrative reports of the U.S. Fish and Wildlife Service's Sonny Bono National Wildlife Refuge Complex and the epizootic database of the U.S. Geological Survey's National Wildlife Health Center were the primary data sources for the remainder of the evaluation. The pattern of avian disease at the Salton Sea has changed greatly over time. Relative to past decades, there was a greater frequency of major outbreaks of avian disease at the Salton Sea during the 1990s than in previous decades, a greater variety of disease agents causing epizootics, and apparent chronic increases in the attrition of birds from disease. Avian mortality was high for about a decade beginning during the mid-1920s, diminished substantially by the 1940s and was at low to moderate levels until the 1990s when it reached the highest levels reported. Avian botulism (Clostridium botulinum type C) was the only major cause of avian disease until 1979 when the first major epizootic of avian cholera (Pasteurella multocidia) was documented. Waterfowl and shorebirds were the primary species affected by avian botulism. A broader spectrum of species have been killed by avian cholera but waterfowl have suffered the greatest losses. Avian cholera reappeared in 1983 and has joined avian botulism as a recurring cause of avian mortality. In 1989, avian salmonellosis (Salmonella typhimurium) was first diagnosed as a major cause of avian disease within the Salton Sea ecosystem and has since reappeared several times, primarily among cattle egrets (Bubulcus ibis). The largest loss from a single epizootic occurred in 1992, when an estimated 155000 birds, primarily eared grebes (Podiceps nigricollis), died from an undiagnosed cause. Reoccurrences of that unknown malady have continued to kill substantial numbers of eared grebes throughout the 1990s. The first major epizootic of type C avian botulism in fish-eating birds occurred in 1996 and killed large numbers of pelicans (Pelecanus occidentalis & P. erythrorhynchos). Avian botulism has remained as a major annual cause of disease in pelicans. In contrast, the chronic on-Sea occurrence of avian botulism in waterfowl and shorebirds of previous decades was seldom seen during the 1990s. Newcastle disease became the first viral disease to cause major bird losses at the Salton Sea when it appeared in the Mullet Island cormorant (Phalacrocorax auritus) breeding colony during 1997 and again during 1998.     

Stimulation of trophoblastic giant cell differentiation in the homozygousYellow mouse embryo

Escape from pre-implantation lethality by homozygousyellow embryos depends on differentiation of trophoblastic cells. The evidence presented herein suggests that progesterone stimulated differentiation of trophoblastic giant cells in some homozygousyellow blastocysts and thereby increased the percentage ofA ^y/A^y “escaper” embryos. This work was supported in part by funds from research grant HDOOO36, National Institute of Child Health and Development, National Institutes of Health, U.S.A.     

Deficiency of dihydroxy acid dehydratase in the mito-chondria of the iv-1 mutants of Neurospora crassa

The isoleucine-valine requiring mutants of Neurospora crassa which map at the iv-1 locus lack, or have a very low level of activity for, the enzyme dihydroxy acid dehydratase in the mitochondrial fractions derived from them. This enzyme is, however, present in the soluble fractions of the mutant homogenates. The enzyme is present in both mitochondrial and soluble fractions from homogenates of wild-type and from homogenates of iv mutants blocked at other steps in the isoleucine-valine pathway.The work reported here was supported in part by grants GM 12323 and 5TO1-GM-00337-09 from the National Institutes of Health, United States Public Health Service, and by a grant from the Robert A. Welch Foundation.Recipient of Research Career Award 4-K-6-GM-18,383 from the National Institutes of Health, United States Public Health Service.     

Akute Vitamin A-Intoxikation der Maus

Summary Isolated fixed liver nuclei of Rana pipiens were stained at varied pH by the acid dye, fast green FCF. The amount of nuclear protein, as determined by cytophotometric measurement of the relative absorption of the stained nuclei, was found to increase in proportion to nuclear size when the pH of the dye solution was below 4.0. Relative absorption was found to be independent of nuclear size, but proportional to the pH of the staining solutions in the pH range between 5.0 and 7.0, These data suggest a change in composition and/or structure of the nuclear protein with increasing nuclear size.This investigation was supported by a grant from the U.S. Public Health Service, GM-10003-04.Post-Doctoral Trainee under U.S. Public Health Training Grant to the Department of Pathology, University of Florida, NIH-GM-1142-03.Supported by a Career Development Award from the National Institute of Child Health and Human Development, K3-HD-6176-04.     

Vibrio fluvialis andV. furnissii serotyping scheme for international use

A combination of two serotyping systems forVibrio fluvialis andV. furnissii, which were developed independently at the National Institute of Health (Tokyo) and Tokyo Metropolitan Research Laboratory of Public Health (Tokyo), was established as a single serotyping scheme comprising 35 O-antigen groups for international use.     

The development and evaluation of immunodiffusion,immunofluorescence and physiological tests for the differentiation of atypical trichophyton rubrum and T. mentagrophytes isolates

Five laboratory procedures: 1) immunodiffusion, 2) immunofluorescence, 3) in vitro hair perforation, 4) pigment stimulation, and 5) a urease test were compared for their ability to differentiateT. rubrum fromT. mentagrophytes. Of the physiological tests, thein vitro hair perforation technique was the most reliable for differentiating the two species. With the serological tests, the organisms were not differentiated by immunodiffusion, but if appropriate dilutions of the conjugates were used in immunofluorescence testing, most isolates could be differentiated.A portion of a Dissertation submitted by the senior author to the University of North Carolina in partial fulfillment of the requirements for the degree of Doctor of Public Health in the School of Public Health. Training was provided by the Laboratory Director's Program which is supported by Training Grant TO1 GM 00567-07 from the National Institute of General Medical Sciences, National Institutes of Health, United States Public Health Service. The laboratory research was performed at the Laboratory Division, Center for Disease Control, under the supervision of William Kaplan.     

新医改背景下委属委管医院绩效评价体系研究

目的 建立国家卫生计生委委属委管医院绩效评价指标体系。方法 通过文献查询梳理医院绩效评价指标、理论研究并设计结构化访谈提纲,对专家进行结构化访谈,设计问卷进行专家咨询。结果 根据新医改要求并结合国家卫生计生委委属委管医院职能定位,初步制定了评价指标体系。结论 指标体系的建立应充分考虑研究对象、本阶段政府的引导方向以及指标的内涵。     

The isolation and analysis of one functional type ofpyr-3 mutant inNeurospora

Twenty-seven pyrimidine-requiring mutants were isolated as suppressors of anarg-3 mutant. All 27 are deficient for ATCase activity and show linkage to thecol-4 marker located on linkage group IV. Analyses of prototroph frequencies resulting from crosses of the new mutants to previously mappedpyr-3 mutants indicate that this functional type ofpyr-3 mutant is restricted to one region of the genetic map. Complementation studies with 11 of the new mutants further extend and subdivide the complementation map of thepyr-3 locus.This work was supported in part by National Institutes of Health, Public Health Service Grant GM 15137-01 and by National Science Foundation Grant GB5998.     

The role of ribonucleoproteins in the production of mitotic abnormalities

Summary Immersion of growing roots of onion and lily in aerated solutions of ribonuclease affected their pattern of growth and altered the structure and mitotic distribution of the chromosomes. Action of the enzyme on meristematic cells caused enlargement of nucleoli, excessive contraction, stickiness, adhesion, and clumping of chromosomes, and production of aneuploid and polyploid chromosome complexes, tripolar and multipolar spindles, binucleate and multinucleate cells. Very few cases of chromosome fragmentation were observed.Accumulation of abnormalities accompanied the passage of ribonuclease across the root as determined by alterations in stainability of the cells with pyronin and fast green. There was no visible modification of stainability of the chromosomes with methyl green or the Feulgen reagent.These results, when compared with those produced by control solutions, indicate that ribonuclease enters the living cell and degrades ribonucleoproteins essential for maintenance of structural and functional integrity. The implications of these results, with respect to the production of aberrations by other agents, are discussed.This study was supported by a research grant (RG-149) from the National Institutes of Health, U.S. Public Health Service.     

Appetitive response of the nematodeCaenorhabditis elegans to oxygen

Summary Using a technique of recording the behavior of individual nematodes during exposure to various solutions, it was demonstrated thatC. elegans made more reversal behaviors after transfer to solutions of lower oxygen tension than higher. The response was stronger after the first hour in the apparatus than initially. This change was not dependent on reduced oxygen availability during the initial period. Starvation is the most likely cause of this change. A variety of mutant strains ofC. elegans that are defective in response to most known chemotactic stimuli, including two strains that have been shown to be severely abnormal in the ciliated endings of all sensory neurons of the worm's snout, all responded to changes in oxygen tension. This observation suggests that oxygen is sensed internally rather than by specialized peripheral receptor cells.I thank Deborah Higgins for technical assistance. This work was supported by a grant awarded by the Biomedical Research Support Grant Program of the National Institutes of Health.     

Species identity of insect cell lines

Summary Three mosquito cell cultures designated as Suitor's clone ofAedes aegypti, Culiseta inornata andAedes vexans were shown to be moth by immunological, karyological, and isozyme analyses. The cells reacted with rabbit antimoth serum but not rabbit antimosquito serum. Chromosome analyses indicated Lepidopteran rather than Dipteran morphology, and three isozyme systems were confirmative. Any one of these assays would be sufficient to indicate that contamination had occurred and could be used as a periodic check for identity of cell cultures. Morphology and growth characteristics are also valid criteria to distinguish between these particular orders of insect cells. These studies were supported by Grant CA-04953-12 from the National Cancer Institute; General Research Support Grant FR-5582 from the National Institues of Health; and Grant-in-Aid Contract M-43 from the State of New Jersey. Recipient of Research Career Award 5-K3-16,749. from the National Institutes of Health.     

Surfactant pollution,an emerging threat to ecosystem: Approaches for effective bacterial degradation

The use of surfactants in households and industries is inevitable and so is their discharge into the environment, especially into the water bodies as effluents. Being surface-active agents, their utilization is mostly seen in soaps, detergents, personal care products, emulsifiers, wetting agents, etc. Anionic surfactants are the most used class. These surfactants are responsible for the foam and froth in the water bodies and cause potential adverse effects to both biotic and abiotic components of the ecosystem. Surfactants are capable of penetrating the cell membrane and thus cause toxicity to living organisms. Accumulation of these compounds has been known to cause significant gill damage and loss of sight in fish. Alteration of physiological and biochemical parameters of water decreases the amount of dissolved oxygen and thus affecting the entire ecosystem. Microbes utilizing surfactants as substrates for energy form the basis of the biodegradation of these compounds. The main organisms for surfactant biodegradation, both in sewage and natural waters, are bacteria. Several Pseudomonas and Bacillus spp. have shown efficient degradation of anionic surfactants namely: sodium dodecyl sulphate (SDS), linear alkylbenzene sulphonate (LAS), sodium dodecylbenzenesulphonate (SDBS). Also, several microbial consortia constituting Alcaligenes spp., Citrobacter spp., etc. have shown efficacy in the degradation of surfactants. The biodegradation efficiency studies of these microbes/microbial consortia would be of immense help in formulating better solutions for the bioremediation of surfactants and help to reduce their potential environmental hazards.     

Species identity of insect cell lines

Summary Three mosquito cell cultures designated as Suitor's clone ofAedes aegypti, Culiseta inornata, andAedes vexans were shown to be moth by immunological, karyological, and isozyme analyses. The cells reacted with rabbit antimoth serum but not rabbit antimosquito serum. Chromosome analyses indicated Lepidopteran rather than Dipteran morphology, and three isozyme systems were confirmative. Any one of these assays would be sufficient to indicate that contamination had occurred and could be used as a periodic check for identity of cell cultures. Morphology and growth characteristics are also valid criteria to distinguish between these particular orders of insect cells. These studies were supported by Grant CA-04953-12 from the National Cancer Institute; General Research Support Grant FR-5582 from the National Institutes of Health; and Grant-in-Aid Contract M-43 from the State of New Jersey. Recipient of Research Career Award 5-K3-16,749 from the National Institutes of Health.