279 research outputs found

    Effect of Selecting Cereal Leaf Beetle (Coleoptera: Chrysomelidae) Males by Age and Feeding Behavior on Nondiapause Progeny

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    In a nondiapause culture of cereal leaf beetles, Oulema melanopus (Coleoptera: Chrysomelidae), females ovipositing within 20 days after emergence were considered nondiapause. However, sexually active males in the same generation could be nondiapause or prediapause. Changes in the nondiapause incidence were compared between progenies from\u3e 15 day old males that were feeding actively and photopositive (considered \u27nondiapause\u27 males) and progenies from younger males (nonselected males). Nondiapause females increased by 19% (n = 35 generations) and decreased 22% (n 31 generations) in the progenies of \u27nondiapause\u27 and nonselected males, respectively, suggesting that nondiapause males were selected in the former group, but prediapause males in the latter group substantially decreased nondiapause. In one generation, 14 progenies from individual pairs ranged from 21 to 100% nondiapause females, indicating that each sex in each parental pair was nondiapause, but nondiapause was incompletely expressed in most of the progenies. The percentage of \u27nondiapause\u27 males was not significantly different than, and was strongly correlated to the percentage of nondiapause females of the same generation, indicating that nondiapause was not sex-linked, and that selecting males by age and behavior decreased the probability of dilution of nondiapause by prediapause males

    Tillering Response of \u27Monon\u27 And \u27Newton\u27 Winter Wheats Infested With Biotype L Hessian Fly (Diptera: Cecidomyiidae) Larvae

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    Two wheat, Triticum aestivum, cultivars that differed in their ability to tiller were infested by ovipositing Hessian flies, Mayetiola destructor, under similar controlled conditions. Since a larva typically stunts and kills the stem where it feeds and develops, tiller development of fly infested-wheat seedlings is an important plant trait relative to grain yield. \u27Monon\u27 tillered more than \u27Newton at the 0 infestation level (control). \u27Monon\u27 had about the same number of tillers at 0, 1, 2, and 3 puparia (indicative of the number of feeding larvae) per plant; and \u27Newton\u27 had fewer tillers at 0 than 1, 2, or 3 puparia per stem. However, tillering of both cultivars was less at 4 or more puparia per stem, perhaps due to the depletion of plant nutrients. In general, for both cultivars there was a decrease in leaf length, number and wet weight as the number of puparia increased per tiller

    Electroantennogram Responses of the Armyworm (Lepidoptera: Noctuidae) and Cereal Leaf Beetle (Coleoptera: Chrysomelidae) to Volatile Chemicals of Seedling Oats

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    Armyworm, Pseudaletia unipuncta, eIectroantennogram (EAG) responses to 10 volatile chemicals of seedling oats and three of injured green plants were significantly different from each other while cereal leaf beetle, Oulema melallopus, EAG responses were not significantly different. The EAG responses of both species did not vary significantly with respect to sex, age, or between the antennae of the same specimen. (E)-2-hexenol, a compound extracted from injured green plants, yielded the highest peak response for the armyworm while more cereal leaf beetle antennae responded to this chemical than any other chemical. Armyworm antennallife averaged 38 + 20 min while those of the cereal leaf beetle averaged 6 + 14 min

    Storage and Behavior of Plant and Diet-Fed Adult Cereal Leaf Beetle, Oulema Melanopus (Coleoptera: Chrysomelidae)

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    The univoltine life cycle of the cereal leaf beetle Oulema melanopus (L.) in Michigan (Castro et al. 1965) is similar to that reported by Venturi (1942) in Europe. Adults emerge from pupal cells in the soil in mid-June to early July, feed voraciously for about three weeks, and enter aestivation sites. For the remainder of the summer and early autumn only a few adults can be found feeding on late-maturing native grasses. The beetles overwinter and usually emerge in late March to early April and resume feeding. Mating and oviposition occur, and larval development is usually completed by late June in southern Michigan. Techniques for rearing the cereal leaf beetle on greenhouse-grown small grain seedlings have been developed by Connin, et al. (1968). Maintaining these cultures requires collecting field adults, growing host material, and handling the cultures to insure that all stages will be available for study. In Michigan during July adults can be collected more economically and in greater numbers in the field than by rearing in the laboratory. A summary of collection techniques, laboratory feeding and storage conditions for large numbers of field-collected cereal leaf beetles is presented in this paper. In addition, the mortality during storage of newly emerged field collected beetles fed either barley seedlings or an artificial diet is compared

    The Conserved Core of Human Immunodeficiency Virus Type 1 Nef Is Essential for Association with Lck and for Enhanced Viral Replication in T-Lymphocytes

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    AbstractThe Nef protein of the primate lentiviruses, including human immunodeficiency virus type 1 (HIV-1) and simian immunodeficiency virus (SIV), is a myristylated protein associated with increased viral replication and enhanced pathogenicity. Both the potentiation of T-lymphocyte activation and the enhanced serine-phosphorylation of HIV-1 capsid by Nef correlate with increased viral replication. We report the functional interactions of the Nef proteins with Src kinases. The Nef proteins from HIV-1 and SIV bind to Lck as well as Hck, Lyn, and Fyn. The SH3 and SH2 domains of Lck are sufficient for coprecipitation with non-tyrosine-phosphorylated Nef proteins. The conserved core region of HIV-1 Nef is essential for the interaction with Lck and is also important for enhanced HIV-1 replication in T-lymphocytes. In addition, we show that SIV and HIV-1 Nef proteins are differentially tyrosine-phosphorylated. The kinase-active Lck tyrosine-phosphorylates SIVmac239 Nef but does not phosphorylate HIV-1 Nef. These data suggest that the association of Nef and Lck is central to the enhanced viral replication of HIV-1 and SIV in T-lymphocytes

    Storage and Behavior of Plant and Diet-Fed Adult Cereal Leaf Beetle, Oulema Melanopus (Coleoptera: Chrysomelidae)

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    The univoltine life cycle of the cereal leaf beetle Oulema melanopus (L.) in Michigan (Castro et al. 1965) is similar to that reported by Venturi (1942) in Europe. Adults emerge from pupal cells in the soil in mid-June to early July, feed voraciously for about three weeks, and enter aestivation sites. For the remainder of the summer and early autumn only a few adults can be found feeding on late-maturing native grasses. The beetles overwinter and usually emerge in late March to early April and resume feeding. Mating and oviposition occur, and larval development is usually completed by late June in southern Michigan. Techniques for rearing the cereal leaf beetle on greenhouse-grown small grain seedlings have been developed by Connin, et al. (1968). Maintaining these cultures requires collecting field adults, growing host material, and handling the cultures to insure that all stages will be available for study. In Michigan during July adults can be collected more economically and in greater numbers in the field than by rearing in the laboratory. A summary of collection techniques, laboratory feeding and storage conditions for large numbers of field-collected cereal leaf beetles is presented in this paper. In addition, the mortality during storage of newly emerged field collected beetles fed either barley seedlings or an artificial diet is compared

    Costs of Illness in the 1993 Waterborne Cryptosporidium Outbreak, Milwaukee, Wisconsin

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    To assess the total medical costs and productivity losses associated with the 1993 waterborne outbreak of cryptosporidiosis in Milwaukee, Wisconsin, including the average cost per person with mild, moderate, and severe illness, we conducted a retrospective cost-of-illness analysis using data from 11 hospitals in the greater Milwaukee area and epidemiologic data collected during the outbreak. The total cost of outbreak-associated illness was 96.2million:96.2 million: 31.7 million in medical costs and 64.6millioninproductivitylosses.Theaveragetotalcostsforpersonswithmild,moderate,andsevereillnesswere64.6 million in productivity losses. The average total costs for persons with mild, moderate, and severe illness were 116, 475,and475, and 7,808, respectively. The potentially high cost of waterborne disease outbreaks should be considered in economic decisions regarding the safety of public drinking water supplies

    V3 Loop Truncations in HIV-1 Envelope Impart Resistance to Coreceptor Inhibitors and Enhanced Sensitivity to Neutralizing Antibodies

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    The V1/V2 region and the V3 loop of the human immunodeficiency virus type I (HIV-1) envelope (Env) protein are targets for neutralizing antibodies and also play an important functional role, with the V3 loop largely determining whether a virus uses CCR5 (R5), CXCR4 (X4), or either coreceptor (R5X4) to infect cells. While the sequence of V3 is variable, its length is highly conserved. Structural studies indicate that V3 length may be important for interactions with the extracellular loops of the coreceptor. Consistent with this view, genetic truncation of the V3 loop is typically associated with loss of Env function. We removed approximately one-half of the V3 loop from three different HIV-1 strains, and found that only the Env protein from the R5X4 strain R3A retained some fusion activity. Loss of V1/V2 (ΔV1/V2) was well tolerated by this virus. Passaging of virus with the truncated V3 loop resulted in the derivation of a virus strain that replicated with wild-type kinetics. This virus, termed TA1, retained the V3 loop truncation and acquired several adaptive changes in gp120 and gp41. TA1 could use CCR5 but not CXCR4 to infect cells, and was extremely sensitive to neutralization by HIV-1 positive human sera, and by antibodies to the CD4 binding site and to CD4-induced epitopes in the bridging sheet region of gp120. In addition, TA1 was completely resistant to CCR5 inhibitors, and was more dependent upon the N-terminal domain of CCR5, a region of the receptor that is thought to contact the bridging sheet of gp120 and the base of the V3 loop, and whose conformation may not be greatly affected by CCR5 inhibitors. These studies suggest that the V3 loop protects HIV from neutralization by antibodies prevalent in infected humans, that CCR5 inhibitors likely act by disrupting interactions between the V3 loop and the coreceptor, and that altered use of CCR5 by HIV-1 associated with increased sensitivity to changes in the N-terminal domain can be linked to high levels of resistance to these antiviral compounds

    Reinspection of a Clinical Proteomics Tumor Analysis Consortium (CPTAC) Dataset with Cloud Computing Reveals Abundant Post-Translational Modifications and Protein Sequence Variants.

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    The Clinical Proteomic Tumor Analysis Consortium (CPTAC) has provided some of the most in-depth analyses of the phenotypes of human tumors ever constructed. Today, the majority of proteomic data analysis is still performed using software housed on desktop computers which limits the number of sequence variants and post-translational modifications that can be considered. The original CPTAC studies limited the search for PTMs to only samples that were chemically enriched for those modified peptides. Similarly, the only sequence variants considered were those with strong evidence at the exon or transcript level. In this multi-institutional collaborative reanalysis, we utilized unbiased protein databases containing millions of human sequence variants in conjunction with hundreds of common post-translational modifications. Using these tools, we identified tens of thousands of high-confidence PTMs and sequence variants. We identified 4132 phosphorylated peptides in nonenriched samples, 93% of which were confirmed in the samples which were chemically enriched for phosphopeptides. In addition, our results also cover 90% of the high-confidence variants reported by the original proteogenomics study, without the need for sample specific next-generation sequencing. Finally, we report fivefold more somatic and germline variants that have an independent evidence at the peptide level, including mutations in ERRB2 and BCAS1. In this reanalysis of CPTAC proteomic data with cloud computing, we present an openly available and searchable web resource of the highest-coverage proteomic profiling of human tumors described to date
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