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1.
Insects ; 13(12)2022 Dec 14.
Article in English | MEDLINE | ID: mdl-36555062

ABSTRACT

Pollinators are declining globally, potentially reducing both human food supply and plant diversity. To support pollinator populations, planting of nectar-rich plants with different flowering seasons is encouraged while promoting wind-pollinated plants, including grasses, is rarely recommended. However, many bees and other pollinators collect pollen from grasses which is used as a protein source. In addition to pollen, Hymenoptera may also collect honeydew from plants infested with aphids. In this study, insects consuming or collecting pollen from sweet sorghum, Sorghum bicolor, were recorded while pan traps and yellow sticky card surveys were placed in grain sorghum fields and in areas with Johnsongrass, Sorghum halepense to assess the Hymenoptera response to honeydew excreted by the sorghum aphid (SA), Melanaphis sorghi. Five genera of insects, including bees, hoverflies, and earwigs, were observed feeding on pollen in sweet sorghum, with differences observed by date, but not plant height or panicle length. Nearly 2000 Hymenoptera belonging to 29 families were collected from grain sorghum with 84% associated with aphid infestations. About 4 times as many Hymenoptera were collected in SA infested sorghum with significantly more ants, halictid bees, scelionid, sphecid, encyrtid, mymarid, diapriid and braconid wasps were found in infested sorghum plots. In Johnsongrass plots, 20 times more Hymenoptera were collected from infested plots. Together, the data suggest that sorghum is serving as a pollen food source for hoverflies, earwigs, and bees and sorghum susceptible to SA could provide energy from honeydew. Future research should examine whether planting strips of susceptible sorghum at crop field edges would benefit Hymenoptera and pollinators.

2.
Vaccine ; 25(16): 2974-83, 2007 Apr 20.
Article in English | MEDLINE | ID: mdl-17303293

ABSTRACT

Live attenuated measles virus (MV) vaccines have an impressive record of safety, efficacy and ability to induce life-long immunity against measles infection. Using reverse genetics technology, such negative-strand RNA viruses can now be rescued from cloned DNA. This technology allows the insertion of exogenous genes encoding foreign antigens into the MV genome in such a way that they can be expressed by the MV vaccine strain, without affecting virus structure, propagation and cell targeting. Recombinant viruses rescued from cloned cDNA induce immune responses against both measles virus and the cloned antigens. The tolerability of MV to gene(s) insertion makes it an attractive flexible vector system, especially if broad immune responses are required. The fact that measles replication strictly occurs in the cytoplasm of infected cells without DNA intermediate has important biosafety implications and adds to the attractiveness of MV as a vector. In this article we report the characteristics of reporter gene expression (GFP, LacZ and CAT) and the biochemical, biophysical and immunological properties of recombinant MV expressing heterologous antigens of simian immunogeficiency virus (SIV).


Subject(s)
Antigens, Viral/metabolism , Measles Vaccine/immunology , Measles virus/immunology , Measles/prevention & control , Vaccines, Attenuated/administration & dosage , Animals , Antigens, Viral/genetics , Cell Line , Chlorocebus aethiops , Genetic Vectors , Measles/virology , Measles Vaccine/genetics , Measles virus/genetics , Measles virus/growth & development , Measles virus/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Vaccines, Attenuated/genetics , Vaccines, Attenuated/immunology , Vero Cells
3.
Mol Cell Proteomics ; 4(11): 1725-40, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16085932

ABSTRACT

Using a combination of tandem affinity purification tagging and mass spectrometry, we characterized a novel, evolutionarily conserved protein phosphatase 4 (PP4)-containing complex (PP4cs, protein phosphatase 4, cisplatin-sensitive complex) that plays a critical role in the eukaryotic DNA damage response. PP4cs is comprised of the catalytic subunit PP4C; a known regulatory subunit, PP4R2; and a novel protein that we termed PP4R3. The Saccharomyces cerevisiae PP4R3 ortholog Psy2 was identified previously in a screen for sensitivity to the DNA-damaging agent and anticancer drug cisplatin. We demonstrated that deletion of any of the PP4cs complex orthologs in S. cerevisiae elicited cisplatin hypersensitivity. Furthermore human PP4R3 complemented the yeast psy2 deletion, and Drosophila melanogaster lacking functional PP4R3 (flfl) exhibited cisplatin hypersensitivity, suggesting a highly conserved role for PP4cs in DNA damage repair. Finally we found that PP4R3 may target PP4cs to the DNA damage repair machinery at least in part via an interaction with Rad53 (CHK2).


Subject(s)
Cisplatin/pharmacology , Conserved Sequence , Evolution, Molecular , Phosphoprotein Phosphatases/metabolism , Cell Line , DNA Damage , Drug Hypersensitivity , Humans , Models, Biological , Multiprotein Complexes/chemistry , Multiprotein Complexes/isolation & purification , Multiprotein Complexes/metabolism , Mutation/genetics , Phosphoprotein Phosphatases/chemistry , Phosphoprotein Phosphatases/genetics , Phosphoprotein Phosphatases/isolation & purification , Protein Binding , Saccharomyces cerevisiae/cytology , Saccharomyces cerevisiae/growth & development , Saccharomyces cerevisiae/metabolism , Saccharomyces cerevisiae Proteins/analysis , Saccharomyces cerevisiae Proteins/metabolism , Sequence Alignment , Two-Hybrid System Techniques
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