Non‐target site SDHI resistance is present as standing genetic variation in field populations of Zymoseptoria tritici

BACKGROUND A new generation of more active succinate dehydrogenase (Sdh) inhibitors (SDHIs) is currently widely used to control Septoria leaf blotch in northwest Europe. Detailed studies were conducted on Zymoseptoria tritici field isolates with reduced sensitivity to fluopyram and isofetamid; SDHIs which have only just or not been introduced for cereal disease control, respectively. RESULTS Strong cross‐resistance between fluopyram and isofetamid, but not with other SDHIs, was confirmed through sensitivity tests using laboratory mutants and field isolates with and without Sdh mutations. The sensitivity profiles of most field isolates resistant to fluopyram and isofetamid were very similar to a lab mutant carrying SdhC‐A84V, but no alterations were found in SdhB, C and D. Inhibition of mitochondrial Sdh enzyme activity and control efficacy in planta for those isolates was severely impaired by fluopyram and isofetamid, but not by bixafen. Isolates with similar phenotypes were not only detected in northwest Europe but also in New Zealand before the widely use of SDHIs. CONCLUSION This is the first report of SDHI‐specific non‐target site resistance in Z. tritici. Monitoring studies show that this resistance mechanism is present and can be selected from standing genetic variation in field populations. © 2017 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry

Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications

A synthetic strategy for the 2-phospha-1,3-butadiene derivatives [{(IPr)C(Ph)}P(cAAC$^{Me}$)] (3a) and [{(IPr)C(Ph)}P(cAAC$^{Cy}$)] (3b) (IPr = C{(NDipp)CH}$_{2}$, Dipp = 2,6-iPr$_{2}$C$_{6}$H$_{3}$; cAAC$^{Me}$ = C{(NDipp)CMe$_{2}$CH$_{2}$CMe$_{2}$}; cAAC$^{Cy}$ = C{(NDipp)CMe$_{2}$CH$_{2}$C(Cy)}, Cy = cyclohexyl) containing a C=C–P=C framework has been established. Compounds 3a and 3b have a remarkably small HOMO–LUMO energy gap (3a: 5.09; 3b: 5.05 eV) with a very high-lying HOMO (-4.95 eV for each). Consequently, 3a and 3b readily undergo one-electron oxidation with the mild oxidizing agent GaCl$_{3}$ to afford radical cations [{(IPr)C(Ph)}P(cAAC$^{R}$)]GaCl$_{4}$ (R = Me 4a, Cy 4b) as crystalline solids. The main UV-vis absorption band for 4a and 4b is red-shifted with respect to that of 3a and 3b, which is associated with the SOMO related transitions. The EPR spectra of compounds 4a and 4b each exhibit a doublet due to coupling of the unpaired electron with the $^{31}$P nucleus. Further oneelectron removal from the radical cations 4a and 4b is also feasible with GaCl$_{3}$, affording the dications [{(IPr)C(Ph)}P(cAAC$^{R}$)](GaCl$_{4}$)$_{2}$ (R = Me 5a, Cy 5b) as yellow crystals. The molecular structures of compounds 3–5 have been determined by X-ray diffraction and analyzed by DFT calculations

Terretonin N: A New Meroterpenoid from Nocardiopsis sp.

Hamed A, Abdel-Razek AS, Frese M, et al. Terretonin N: A New Meroterpenoid from Nocardiopsis sp. Molecules. 2018;23(2): 299.Terretonin N (1), a new highly oxygenated and unique tetracyclic 6-hydroxymeroterpenoid, was isolated together with seven known compounds from the ethyl acetate extract of a solid-state fermented culture of Nocardiopsis sp. Their structures were elucidated by spectroscopic analysis. The structure and absolute configuration of 1 were unambiguously determined by X-ray crystallography. The isolation and taxonomic characterization of Nocardiopsis sp. is reported. The antimicrobial activity and cytotoxicity of the strain extract and compound 1 were studied using different microorganisms and a cervix carcinoma cell line, respectively

X-ray photoemission electron microscopy for the study of semiconductor materials

Photoemission Electron Microscopy (PEEM) using X-rays is a novel combination of two established materials analysis techniques--PEEM using UV light, and Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy. This combination allows the study of elemental composition and bonding structure of the sample by NEXAFS spectroscopy with a high spatial resolution given by the microscope. A simple, two lens, 10 kV operation voltage PEEM has been used at the Stanford Synchrotron Radiation Laboratory and at the Advanced Light Source (ALS) in Berkeley to study various problems including materials of interest for the semiconductor industry. In the present paper the authors give a short overview over the method and the instrument which was used, and describe in detail a number of applications. These applications include the study of the different phases of titanium disilicide, various phases of boron nitride, and the analysis of small particles. A brief outlook is given on possible new fields of application of the PEEM technique, and the development of new PEEM instruments

Proposal for a unified nomenclature for target site mutations associated with resistance to fungicides

Evolved resistance to fungicides is a major problem limiting our ability to control agricultural, medical and veterinary pathogens and is frequently associated with substitutions in the amino acid sequence of the target protein. The convention for describing amino-acid substitutions is to cite the wild type amino acid, the codon number and the new amino acid, using the one letter amino acid code. It has frequently been observed that orthologous amino acid mutations have been selected in different species by fungicides from the same mode of action class, but the amino acids have different numbers. These differences in numbering arise from the different lengths of the proteins in each species. The purpose of the current paper is to propose a system for unifying the labelling of amino acids in fungicide target proteins. To do this we have produced alignments between fungicide target proteins of relevant species fitted to a well-studied “archetype” species. Orthologous amino acids in all species are then assigned numerical “labels” based on the position of the amino acid in the archetype protein

Crystalline anions based on classical N‐heterocyclic carbenes

Herein, the first stable anions K[SIPrBp] (4 a‐K) and K[IPrBp] (4 b‐K) (SIPrBp=BpC{N(Dipp)CH2}2, IPrBp=BpC{N(Dipp)CH}2; Bp=4‐PhC6H4; Dipp=2,6‐iPr2C6H3) derived from classical N‐heterocyclic carbenes (NHCs) (i.e. SIPr and IPr) have been isolated as violet crystalline solids. 4 a‐K and 4 b‐K are prepared by KC8 reduction of the neutral radicals [SIPrBp] (3 a) and [IPrBp] (3 b), respectively. The radicals 3 a and 3 b as well as [Me‐IPrBp] 3 c (Me‐IPrBp=BpC{N(Dipp)CMe}2) are accessible as crystalline solids on treatment of the respective 1,3‐imidazoli(ni)um bromides (SIPrBp)Br (2 a), (IPrBp)Br (2 b), and (Me-IPrBp)Br (2 c) with KC8. The cyclic voltammograms of 2 a-2 c exhibit two one‐electron reversible redox processes in -0.5 to -2.5 V region that correspond to the radicals 3 a-3 c and the anions (4 a-4 c)-. Computational calculations suggest a closed‐shell singlet ground state for (4 a-4 c)- with the singlet‐triplet energy gap of 17-24 kcal mol-1.Deutsche ForschungsgemeinschaftProjekt DEA

Kristalline Anionen auf Basis klassischer N‐heterocyclischer Carbene

Die ersten stabilen Anionen K[SIPrBp] (4 a-K) und K[IPrBp] (4 b-K) (SIPrBp=BpC{N(Dipp)CH2}2, IPrBp=BpC{N(Dipp)CH}2; Bp=4-PhC6H4; Dipp=2,6-iPr2C6H3), die von klassischen N-heterocyclischen Carbenen (NHCs) abgeleitet sind (d. h. SIPr und IPr), wurden als violette kristalline Feststoffe isoliert. 4 a-K und 4 b-K wurden durch die Reduktion der neutralen Radikale [SIPrBp] (3 a) bzw. [IPrBp] (3 b) mit KC8 hergestellt. Die Radikale 3 a und 3 b sowie [Me-IPrBp] (3 c) (Me-IPrBp=BpC{N(Dipp)CMe}2) liegen als kristalline Feststoffe vor, wenn die entsprechenden 1,3-Imidazoli(ni)umbromide (SIPrBp)Br (2 a), (IPrBp)Br (2 b) und (Me-IPrBp)Br (2 c) mit KC8 umgesetzt werden. Die Cyclovoltammogramme von 2 a-2 c zeigen zwei reversible Ein-Elektronen-Redoxprozesse im Bereich von -0.5 bis -2.5 V, die den Radikalen 3 a-3 c und den Anionen (4 a-4 c)- entsprechen. Quantenchemische Berechnungen deuten auf einen geschlossenschaligen Singulett-Grundzustand für (4 a-4 c)- mit einer Singulett-Triplett-Energielücke von 17-24 kcal mol-1 hin.Deutsche ForschungsgemeinschaftProjekt DEA

The diagnostic value of ultrasonography-derived edema of the temporal artery wall in giant cell arteritis: a second meta-analysis

<p>Abstract</p> <p>Background</p> <p>Ultrasonography of temporal arteries is not commonly used in the approach of patients with suspected giant cell arteritis (GCA) in clinical practice. A meta-analysis of primary studies available through April 2004 concluded that ultrasonography could indeed be helpful in diagnosing GCA. We specifically re-examined the diagnostic value of the ultrasonography-derived halo sign, a dark hypoechoic circumferential thickening around the artery lumen, indicating vasculitic wall edema, in GCA.</p> <p>Methods</p> <p>Original, prospective studies in patients with suspected GCA that examined ultrasonography findings of temporal arteries using the ACR 1990 classification criteria for GCA as reference standard, published through 2009, were identified. Only eight studies involving 575 patients, 204 of whom received the final diagnosis of GCA, fulfilled technical quality criteria for ultrasound. Weighted sensitivity and specificity estimates of the halo sign were assessed, their possible heterogeneity was investigated and pooled diagnostic odds ratio was determined.</p> <p>Results</p> <p>Unilateral halo sign achieved an overall sensitivity of 68% (95% CI, 0.61-0.74) and specificity of 91% (95% CI, 0.88-0.94) for GCA. The values of inconsistency coefficient (I²) of both sensitivity and specificity of the halo sign, showed significant heterogeneity concerning the results between studies. Pooled diagnostic odds ratio, expressing how much greater the odds of having GCA are for patients with halo sign than for those without, was 34 (95% CI, 8.21-138.23). Diagnostic odds ratio was further increased to 65 (95% CI, 17.86-236.82) when bilateral halo signs were present (sensitivity/specificity of 43% and 100%, respectively). In both cases, it was found that DOR was constant across studies.</p> <p>Conclusion</p> <p>Temporal artery edema demonstrated as halo sign should be always looked for in ultrasonography when GCA is suspected. Providing that currently accepted technical quality criteria are fulfilled, halo sign's sensitivity and specificity are comparable to those of autoantibodies used as diagnostic tests in rheumatology. Validation of revised GCA classification criteria which will include the halo sign may be warranted.</p