Assessment of Wild Mustard (Sinapis arvensis L.) Resistance to ALS-inhibiting Herbicides

There is an urgent need for rapid, accurate, and economical screening tests that can determine if weeds surviving a herbicide application are resistant. This chapter describes development and application of a simple root length bioassay technique for detection of wild mustard (Sinapis arvensis L.) resistance to ALS-inhibiting herbicides. This bioassay was performed in 2-oz WhirlPak® bags filled with 50 g of soil wetted to 100% moisture content at field capacity. Wild mustard seeds were pre-germinated in darkness in Petri dishes lined with moist filter paper for 2 days. Six seeds with well-developed radicles were planted in the non-treated soil and in soil with added herbicide, and plants were grown in a laboratory under fluorescent lights. After 4 days of growth, WhirlPak® bags were cut open, soil was washed away, intact plants were removed, and root length was measured with a ruler. The concentration of each herbicide in soil at which a significant root inhibition of susceptible biotype, but no root inhibition of a resistant biotype occurred was selected. Susceptibility/resistance of wild mustard populations was estimated by calculating the percentage of uninhibited roots of plants grown in the herbicide-treated soil as compared to the plants grown in the non-treated soil

Relationship of soil properties to pyroxasulfone bioactivity in a range of prairie soils

The relationship between pyroxasulfone bioactivity and soil properties has not been investigated in a wide range of soils typical of western Canada. In this study, 47 soils from Saskatchewan, Manitoba and Alberta, with varying organic matter content (1.5%–22.1%), pH (5.0–7.9), and clay content (6.8%–59.4%) were used to evaluate the effect of soil properties on pyroxasulfone bioactivity and its relevance to field application rates. Bioactivity was assessed by measuring the reduction of sugar beet shoot length after 7 days in response to 0, 92, 184, and 368 µg ai kg−1 pyroxasulfone concentration in soil. Multiple regression analysis showed that pyroxasulfone bioactivity was related to soil organic matter content, pH and clay content. Grouping the soils according to these properties allowed for a summarization of pyroxasulfone field application rates required to achieve bioactivity based on the magnitude of sugar beet shoot length inhibition (%). The estimated field application rates ranged from less than 120–480 g ai ha−1

Peptidyl arginine deiminase from Porphyromonas gingivalis abolishes anaphylatoxin C5a activity

Evasion of killing by the complement system, a crucial part of innate immunity, is a key evolutionary strategy of many human pathogens. A major etiological agent of chronic periodontitis, the Gram-negative bacterium Porphyromonas gingivalis produces a vast arsenal of virulence factors that compromise human defense mechanisms. One of these is peptidylarginine deiminase (PPAD), an enzyme unique to P. gingivalis among bacteria, which converts Arg residues in polypeptide chains into citrulline. Here, we report that PPAD citrullination of a critical C-terminal arginine of the anaphylatoxin C5a disabled the protein function. Treatment of C5a with PPAD in vitro resulted in decreased chemotaxis of human neutrophils and diminished calcium signaling in monocytic cell line U937 transfected with the C5a receptor (C5aR) and loaded with a fluorescent intracellular calcium probe: Fura 2-AM. Moreover, a low degree of citrullination of internal arginine residues by PPAD was also detected using mass spectrometry. Further, after treatment of C5 with outer membrane vesicles (OMVs) naturally shed by P. gingivalis we observed generation of C5a totally citrullinated at the C-terminal Arg74 residue (Arg74Cit). In stark contrast only native C5a was detected after treatment with PPAD-null OMVs. Our study suggests reduced antibacterial and proinflammatory capacity of citrullinated C5a, achieved via lower level of chemotactic potential of the modified molecule, and weaker cell activation. In the context of previous studies, which showed crosstalk between C5aR and toll-like receptors, as well as enhanced arthritis development in mice infected with PPAD expressing P. gingivalis, our findings support a crucial role of PPAD in the virulence of P. gingivalis