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Foliar anthracnose is one of the main diseases of onion (Allium cepa L.) under tropical and subtropical conditions. Thus far, only Colletotrichum gloeosporioides has been reported as the causal agent of this disease in Brazil. However, there are no extensive studies characterizing Colletotrichum isolates associated with onion anthracnose in the country. Here, 38 Colletotrichum isolates obtained from onion plants displaying foliar anthracnose across major Brazilian onion-producing regions were characterized using morphometric and molecular information. The Bayesian and Maximum Liklihood methods were used for an initial analysis of the β-tubulin gene (tub2) sequences of all isolates, resulting in the discrimination of nine haplotypes. Three haplotypes grouped with the reference species of the C. acutatum complex and six with the C. gloeosporioides complex. Sequences of either the glyceraldehyde-3-phosphate dehydrogenase (gapdh), actin (act), and calmodulin genes or the intergenic spacer (IGS) region between DNA lyase (apn2) gene and the mating-type mat1–2-1 locus were used to characterize a subset of isolates representing these nine distinct tub2 gene haplotypes. These analyses revealed five anthracnose-inducing Colletotrichum species, including three members of the C. acutatum species complex (C. nymphaeae, C. scovillei, and C. tamarilloi) and two of the C. gloeosporioides species complex (C. fructicola and C. theobromicola). Bioassays confirmed that all these Colletotrichum species are pathogenic to onion, inducing typical anthracnose symptoms on bulbs and leaves. Twenty-six out of 38 isolates were identified as C. theobromicola, indicating this fungus as the prevalent anthracnose pathogen under Brazilian conditions. This Colletotrichum species diversity will affect anthracnose management strategies, including chemical and cultural control as well as the identification and deployment of onion cultivars with species-specific and/or wide-spectrum tolerance/resistance. [ABSTRACT FROM AUTHOR]

2,2′-Bi[5-(2,5-dihydroxy-3,4,6-trichlorophenyl)thiazole] and 6-(2,5-dihydroxy-3,4,6-trichlorophenyl)-2-imino-3,4-dihydro-4H-1,4-thiazin-3-thione are synthesized from 2,5-dihydroxy-3,4,6,7-tetrachloro-2,3-dihydrobenzo[b]furan and dithiooxalyldiamide. The products are oxidized by FeCl3 to the corresponding trichloro-1,4-benzoquinonyl-substituted sulfur-containing heterocycles. N-Methylation of 2,2′-bithiazole by dimethyl sulfate gives 2,2′-bi[5-(2,5-dihydroxy-3,4,6-trichlorophenyl)-3-methylthiazolium] bismonomethyl sulfate. The last compound is readily transformed to 2,2′-bi[5-(2-hydroxy-5-oxido-3,4,6-trichlorophenyl)-3-methylthiazolium] bisbetaine. [ABSTRACT FROM AUTHOR]

In reaction with potassium butylxanthate and sodium tert-butyltrithionate, 2,5-dihydroxy-3,4,6,7-tetrachloro-2,3-dihydrobenzo[b]furan forms the products from nucleophilic substitution of a chlorine atom, i.e., O-butyl S-(2,5-dihydroxy-4,6,7-trichloro-2,3-dihydrobenzo[b]furan-3-yl) xanthate and S-tert-butyl S′-(2,5-dihydroxy-4,6,7-trichloro-2,3-dihydrobenzo[b]furan-3-yl) trithiocarbonate respectively. Recyclization of the xanthate in concentrated sulfuric acid gave 4-(2,5-dihydroxy-3,4,6-trichlorophenyl)-1,3-dithiol-2-one, which was oxidized by iron trichloride to the corresponding benzoquinone. Cyclization of the trithiocarbonate in the presence of trifluoroacetic and p-toluenesulfonic acid led to 7-hydroxy-5,6,8-trichloro-3a,8b-dithiolo[4,5-b]benzo[d]furan-2-thione. [ABSTRACT FROM AUTHOR]

Reaction of chloranil with excess pyridine gives the poorly stable 2,5-di(N-pyridinium)-3,6-dichloro-1,4-benzoquinone dichloride which is readily hydrolyzed to give the bisbetaine of 2,5-di(N-pyridinium)-1,4-benzoquinone-3,6-dioxide. Treatment with acid gives its mono- and bisprotonated derivatives as the perchlorate and dibromide and bromination gives the betaine 2-bromo-2,5-di(N-pyridinium)-5-cyclohexene-1,3,4-trione-6-oxide perbromide. The reaction of malonodinitrile with 2,5-di(N-pyridinium)-3,6-dichloro-1,4-benzoquinone dichloride in situ gives the poorly stable bisbetaine of 2,5-di(N-pyridinium)-7,7,8,8-tetracyanoquinodimethane-3,6-dioxide. [ABSTRACT FROM AUTHOR]

Fusarium oxysporum f. sp. lactucae (FOLac) is responsible for significant economic losses across major lettuce-producing regions around the world. Thus far, only FOLac race 1 isolates have been reported associated with Fusarium wilt outbreaks in Brazil. The most sustainable strategy for disease control is the pyramidization of race-specific resistance factors in lettuce cultivars. The loose-leafy cultivar 'Vanda' was found as one of the most promising sources of resistance to FOLac race 1. The genetic basis of this resistance was determined by analyzing the reaction to this pathogen of segregating populations derived from the cross 'Gisele' (susceptible) × 'Vanda' (pollen donor). A single molecular marker-genotyped F1 hybrid plant was selfed and individual plants of a segregating F2 population as well as 63 families F2:F3 were inoculated with a FOLac race 1 isolate by using the root-dipping method (3 × 106 conidia/ml). Our results confirmed the high levels of resistance of 'Vanda' even under very harsh experimental conditions. Overall, the reaction of the F1 plants and the segregating patterns of the F2 population (n = 82) and of the F2:F3 families (n = 838 plants) fit a single dominant gene/locus model. However, the phenotypic expression of resistance might suffer effects of additional genetic factor(s) (e.g., locus dosage, minor modifying genes, and incomplete penetrance). Notwithstanding, the high levels of FOLac race 1 resistance and its relatively simple genetic control makes 'Vanda' a major germplasm source for lettuce-breeding programs aiming to incorporate this trait in a wide array of elite lines from distinct varietal groups. [ABSTRACT FROM AUTHOR]

The article presents a case study which involves a 62-year-old female patient with hydropneumothorax and misplaced nasogastric tube. Topics discussed include the psychiatric ward admission of the patient due to akinetic mutism and malnutrition, the placement of the nasogastric tube in the patient for enteral nutrition and medication, and results of the physical and laboratory examinations performed such as chest X-ray and computed tomography (CT) scan.