The hymenolepiosis by Hymenolepis nana is a major public health problem in developing countries, and the commercial drugs against this parasitosis are not enough effective. The combination of antiparasitic and antioxidant agents has improved the treatment of some parasitoses. Thus, the development of new cestocidal and antioxidant agents to treat the hymenolepiosis cases is important. In the present study, four hydroxy- and four dihydroxy-chalcones were synthesized using the catalyst boron trifluoride diethyl etherate (BF3•OEt2). The antioxidant activity and antiparasitic against H. nana of chalcones were tested, as well as the toxicity by the brine shrimp lethality bioassay and the method of Lorke. The antioxidant activity was measured by three radical scavenging assays: 2,2’-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS), 2,2-diphenyl-1-picrylhydrazyl (DPPH), and ferric reducing antioxidant power (FRAP). The hydroxyl substitution pattern (number and position), mainly in ring B, was responsible for the chalcone antiparasitic activity. At least one meta or para hydroxyl group in ring B was essential for activity of the synthetic chalcones against H. nana; The time taken for the parasite to die by the 3b and 3e chalcones (20 mg/mL) treatment was up to six times lower than the control drug Praziquantel. On the other hand, chalcones with catechol structure in ring B (3g and 3h) showed the highest antioxidant values. The toxicity evaluations suggests that synthetic hydroxychalcones with cestocidal (3b and 3e) and antioxidant (3g and 3h) activities are safe compounds and potential in vivo agents to treat this parasitosis.

Background Isothiocyanates (ITCs) are natural products obtained from plants of the Brassicas family. They represent an environmentally friendly alternative for the control of phytopathogenic fungi. However, as it has been observed with synthetic fungicides, the possibility of inducing ITC-resistant strains is a major concern. It is, therefore, essential to understanding the molecular mechanisms of fungal resistance to ITCs. We analyzed a subtractive library containing 180 clones of an Alternaria alternata strain resistant to 2-propenyl ITC (2-pITC). After their sequencing, 141 expressed sequence tags (ESTs) were identified using the BlastX algorithm. The sequence assembly was carried out using CAP3 software; the functional annotation and metabolic pathways identification were performed using the Blast2GO program. Results The bioinformatics analysis revealed 124 reads with similarities to proteins involved in transcriptional control, defense and stress pathways, cell wall integrity maintenance, detoxification, organization and cytoskeleton destabilization; exocytosis, transport, DNA damage control, ribosome maintenance, and RNA processing. In addition, transcripts corresponding to enzymes as oxidoreductases, transferases, hydrolases, lyases, and ligases, were detected. Degradation pathways for styrene, aminobenzoate, and toluene were induced, as well as the biosynthesis of phenylpropanoid and several types of N-glycan. Conclusions The fungal response showed that natural compounds could induce tolerance/resistance mechanisms in organisms in the same manner as synthetic chemical products. The response of A. alternata to the toxicity of 2-pITC is a sophisticated phenomenon including the induction of signaling cascades targeting a broad set of cellular processes. Whole-transcriptome approaches are needed to elucidate completely the fungal response to 2-pITC.

Physicochemical characteristics of Ehretia tinifolia L. fruit are presented for the first time. The fruit of this plant is a small drupe of 8 mm diameter and weighs 0.2 g. Its pulp is slightly acidic (pH 5.8) with a high ratio of soluble solids (11 °Brix) to acidity (0.1%). The antioxidant activity of E. tinifolia fruits (DPPH, 303.8 mg EVC/100 g f.w.; ABTS, 84.1 mg EVC/100 g f.w.; DPPH, ABTS and EVC mean 1,1-diphenyl-2-picrylhydrazyl, 2,2'-azino-bis(3-ethylbenzothiazolin-6-sulfonate) diammonium salt, and equivalents of vitamin C, respectively) was similar or higher than reported for several tropical fruits (e.g. orange, guava, and prickly pear). Ehretia tinifolia fruit has a high content of ash (12.6 mg/100 g d.w.). The edible portion is an important source of selenium (0.1 mg/100 g d.w.) and total fatty acids were 834.8 mg/100g d.w.; the main fatty acids were palmitic (27.6%), linoleic (26.4%), linolenic (18.1%), and oleic (17.6%). The content of fatty acids of seeds was 5 137.5 mg/100 g d.w., with linoleic (54.3%), oleic (22.9%), and palmitic (12.7%) as main components.

Se presentan por vez primera características fisicoquímicas del fruto de Ehretia tinifolia L. Este fruto es una drupa pequeña de 8 mm de diámetro y 0.2 g, su pulpa es ligeramente ácida (pH 5.8) y la relación de sólidos solubles (11 °Brix) a acidez (0.1%) es alta. La actividad antioxidante de los frutos de E. tinifolia (DPPH, 303.8 mg EVC/100 g p.f.; ABTS, 84.1 mg EVC/100 g p.f.; EVC significa equivalentes de vitamina C) fue similar o mayor que lo registrado para varios frutos tropicales (e.g. naranja, guayaba o tuna). El fruto presenta un alto contenido de cenizas (12.6 mg/100 g p.s.). La porción comestible es una fuente importante de selenio (0.1 mg/100 g p.s.) y el total de ácidos grasos fue de 834.8 mg/100g p.s.; los principales ácidos grasos fueron palmítico (27.6%), linoleico (26.4%), linolénico (18.1%) y oléico (17.6%). El contenido de ácidos grasos de las semillas fue 5 137.5 mg/100 g p.s.; siendo los principales componentes el linoleico (54.3%), oleico (22.9%) y palmítico (12.7%).

Human gnathostomosis, a serious public health issue in Mexico, is endemic to Sinaloa. The disease is mainly caused by consumption of the raw meat of freshwater or estuarine fishes infected with the advanced third stage larvae (AL3) of Gnathostoma binucleatum. In the present study, we examined estuarine turtles with a sample consisting of 23 Trachemys scripta and 5 Kinosternon integrum from Sinaloa, Mexico for the presence of Gnathostoma larvae; such examination was made by the pressing method of skeletal muscles between 2 glass plates. The results showed that both turtles harbored G. binucleatum AL3; identification was achieved by morphology and also by PCR/sequencing of the ITS2 region of ribosomal DNA of the larvae. Infection prevalence was higher for K. integrum (80%) than for T. scripta (69.6%), but heavy infection (> 10 AL3/turtle) was observed in the larger sized individuals of T. scripta. Consumption of the raw meat of these turtles represents a risk to acquire the disease.

La gnathostomosis humana, un serio problema de salud pública en México, es endémica de Sinaloa. La enfermedad es principalmente ocasionada por el consumo de carne cruda de pescado de agua dulce o salobre infectado con larvas del tercer estadio avanzado (AL3) de Gnathostoma binucleatum. En la presente investigación, se examinaron tortugas estuarinas, 23 Trachemys scripta y 5 Kinosternon integrum, de Sinaloa, México para identificar la presencia de larvas de Gnathostoma; para ello se utilizó el método de compresión del tejido muscular entre 2 placas de vidrio. Los resultados mostraron que ambas especies de tortugas son hospederas de larvas AL3 de G. binucleatum; la identificación específica se basó en la morfología y composición molecular (por PCR/secuenciación de la región ribosomal ITS2) del DNA de las larvas. La prevalencia de la infección fue mayor en K. integrum (80%) que en T. scripta (69.6%), pero la intensidad fue más alta (> 10 AL3/tortuga) en las tortugas de mayor tamaño, T. scripta. El consumo de carne cruda de estas tortugas representa un riesgo para adquirir la enfermedad.