ABSTRACT
Background: Mild secretion defects are the most frequent and challenging blood platelet disorders to diagnose. Most δ-granule secretion tests lack validation, are not quantitative, or have unreliable response to weak platelet agonists. Objectives: To compare platelet serotonin secretion by HPLC-electrochemical detection technique (HPLC-ECD) with the reference isotopic test (3H-5-HT), evaluating its performance in clinical laboratories. Methods: The assay validation followed STARD-2015 recommendations. HPLC-ECD measured the nonsecreted serotonin remaining in platelet pellets after aggregation, comparing it with the reference 3H-5-HT assay. We studied subjects with inherited and aspirin-induced blood platelet disorders and assessed the HPLC-ECD operation for routine clinical diagnosis. Results: Calibration curves were linear (R2 = 0.997), with SD for residuals of 3.91% and analytical sensitivity of 5ng/mL. Intra- and interassay imprecision bias ranged between -8.5% and 2.1% and -9% and 3.1%, respectively. Serotonin recovery and stability were >95%, and the variability range of measurements was -5.5% to 4.6%. Statistical differences detected between tests were biologically irrelevant, with bias of 1.48% (SD, 8.43) and CI agreement of -18% to 15%. Both assays distinctly detected platelet secretion induced by 10 µM epinephrine and 4 µmM adenosine diphosphate. However, HPLC-ECD is quantitative and more sensitive to low serotonin content in blood platelets. Reference cutoffs for each agonist were determined in 87 subjects. Initially, the HPLC-ECD requires relatively expensive equipment and trained operators but has remarkably cheap running costs and a turn-around time of 24-36 hours. We have used this diagnostic tool routinely for >8 years. Conclusion: HPLC-ECD assay for platelet serotonin secretion is highly accurate, has advantages over the reference 3H-5-HT test, and is suitable as a clinical laboratory technique.
ABSTRACT
Tetra-ortho-fluoro-azobenzenes are a class of photoswitches useful for the construction of visible-light-controlled molecular systems. They can be used to achieve spatio-temporal control over the properties of a chosen bioactive molecule. However, the introduction of different substituents to the tetra-fluoro-azobenzene core can significantly affect the photochemical properties of the switch and compromise biocompatibility. Herein, we explored the effect of useful substituents, such as functionalization points, attachment handles, and water-solubilizing groups, on the photochemical properties of this photochromic system. In general, all the tested fluorinated azobenzenes exhibited favorable photochemical properties, such as high photostationary state distribution and long half-lives, both in organic solvents and in water. One of the azobenzene building blocks was functionalized with a trehalose group to enable the uptake of the photoswitch into mycobacteria. Following metabolic uptake and incorporation of the trehalose-based azobenzene in the mycobacterial cell wall, we demonstrated photoswitching of the azobenzene in the isolated total lipid extract.
Subject(s)
Photochemical Processes , Trehalose , Azo Compounds/chemistry , Water , BiologyABSTRACT
The spontaneous insertion of helical transmembrane (TM) polypeptides into lipid bilayers is driven by three sequential equilibria: solution-to-membrane interface (MI) partition, unstructured-to-helical folding, and MI-to-TM helix insertion. A bottleneck for understanding these three steps is the lack of experimental approaches to perturb membrane-bound hydrophobic polypeptides out of equilibrium rapidly and reversibly. Here, we report on a 24-residues-long hydrophobic α-helical polypeptide, covalently coupled to an azobenzene photoswitch (KCALP-azo), which displays a light-controllable TM/MI equilibrium in hydrated lipid bilayers. FTIR spectroscopy reveals that trans KCALP-azo folds as a TM α-helix (TM topology). After trans-to-cis photoisomerization of the azobenzene moiety with UV light (reversed with blue light), the helical structure of KCALP-azo is maintained, but its helix tilt increased from 32 ± 5° to 79 ± 8°, indication of a reversible TM-to-MI transition. Further analysis indicates that this transition is incomplete, with cis KCALP-azo existing in a â¼90% TM and â¼10% MI mixture.
ABSTRACT
Many studies have recently explored a new class of reversible photoswitching compounds named Donor-Acceptor Stenhouse Adducts (DASAs). Upon light irradiation, these systems evolve from a coloured open-chain to a colourless closed-ring form, while the thermal back-reaction occurs at room temperature. In order to fulfill the requirements for different applications, new molecules with specific properties need to be designed. For instance, shifting the activation wavelength towards the red part of the visible spectrum is of relevance to biological applications. By using accurate computational calculations, we have designed new DASAs and predicted some of their photophysical properties. Starting from well-studied donor and acceptor parts, we have shown that small chemical modifications can lead to substantial changes in both photophysical and photoswitching properties of the resulting DASAs. Furthermore, we have also analysed how these substitutions impact the electronic structure of the systems. Finally, some pertinent candidates have been successfully synthesized and their photoswitching properties have been characterized experimentally.
ABSTRACT
Donor-acceptor Stenhouse adducts (DASAs) are playing an outstanding role as innovative and versatile photoswitches. Until now, all the efforts have been spent on modifying the donor and acceptor moieties to modulate the absorption energy and improve the cyclization and reversion kinetics. However, there is a strong dependence on specific structural modifications and a lack of predictive behavior, mostly owing to the complex photoswitching mechanism. Here, by means of a combined experimental and theoretical study, the effect of chemical modification of the π-bridge linking the donor and acceptor moieties is systematically explored, revealing the significant impact on the absorption, photocyclization, and relative stability of the open form. In particular, a position along the π-bridge is found to be the most suited to redshift the absorption while preserving the cyclization. However, thermal back-reaction to the initial isomer is blocked. These effects are explained in terms of an increased acceptor capability offered by the π-bridge substituent that can be modulated. This strategy opens the path toward derivatives with infra-red absorption and a potential anchoring point for further functionalization.
ABSTRACT
Laboratories worldwide perform both hematological and coagulation testing on patients avoiding fasting time. In 2017, the Latin America Confederation of Clinical Biochemistry (COLABIOCLI) commissioned the Latin American Working Group for Preanalytical Phase (WG-PRE-LATAM) to study preanalytical variability and establish guidelines for preanalytical procedures to be applied by clinical laboratories and health care professionals. This study, on behalf of COLABIOCLI WG-PRE-LATAM, aims to evaluate the effect of the breakfast on routine hematology and coagulation laboratory testing. We studied 20 healthy volunteers who consumed a breakfast containing a standardized amount of carbohydrates, proteins, and lipids. We collected blood specimens for routine hematology and coagulation laboratory testing before breakfast and 1, 2, and 4 hours thereafter. Significant differences between samples were assessed by the Wilcoxon ranked-pairs test. Statistically significant differences ( p < 0.05) between basal and 4 hours after the breakfast were observed for red blood cells, hemoglobin, hematocrit, mean corpuscular volume, white blood cells, neutrophils, lymphocytes, monocytes, mean platelet volume, and activated partial thromboplastin time. In conclusion, the significant variations observed in several hematological parameters, and activated partial thromboplastin time due to breakfast feeding demonstrate that the fasting time needs to be carefully considered prior to performing routine hematological and coagulation testing to avoid interpretive mistakes of test results, and to guarantee patient safety. Therefore, COLABIOCLI WG-PRE-LATAM encourages laboratory quality managers to standardize the fasting requirements in their laboratory, i.e., 12 hours.
ABSTRACT
INTRODUCTION: In Andean countries, specifically in Ecuador, a food transition in the population has been observed because of economic growth. The Working Group for Preanalytical Phase in Latin America (WG-PRE-LATAM) of the Latin America Confederation of Clinical Biochemistry (COLABIOCLI) was established in 2017, and its main purpose is to study preanalytical variability and establish guidelines for preanalytical procedures in order to be implemented by clinical laboratories and healthcare professionals in Latin America. The aim of this study on behalf of COLABIOCLI WG-PRE-LATAM was to evaluate whether an Andean breakfast can interfere with routine biochemistry and immunochemistry laboratory tests. MATERIALS AND METHODS: We studied 20 healthy volunteers who consumed an Andean breakfast containing a standardized amount of carbohydrates, proteins and lipids. We collected blood specimens for laboratory tests before breakfast and 1, 2, and 4 hours thereafter. Significant differences between samples were assessed by the Wilcoxon ranked-pairs test. RESULTS: The Andean breakfast statistically (P ≤ 0.05), modified the results of the following tests: triglycerides, insulin, cortisol, thyroid stimulating hormone, free thyroxine, total protein, albumin, urea, creatinine, lactate dehydrogenase, alkaline phosphatase, amylase, lipase, total bilirubin, direct bilirubin, iron, calcium, phosphorus, magnesium, and uric acid. CONCLUSIONS: Andean breakfast can influence the routine biochemistry and immunochemistry laboratory tests and might expose patient safety to some risks. Therefore, the COLABIOCLI WG-PRE-LATAM calls attention and highlights that the fasting time needs to be carefully considered when performing blood testing in order to prevent spurious results and thus, reduce laboratory errors.
Subject(s)
Blood Chemical Analysis , Breakfast , Clinical Laboratory Techniques , Immunochemistry , Blood Specimen Collection , Fasting/blood , Humans , Latin AmericaABSTRACT
A diet rich in fruits and vegetables is known to decrease the risk of cardiovascular disease. However, the information regarding the antithrombotic activity (antiplatelet, anticoagulant, and fibrinolytic) of fruits and vegetables is scarce. The aim of this study was to assess the antithrombotic activity of extracts from fruits and vegetables widely consumed in central Chile. The study included samples of 19 fruits and 26 vegetables, representative of the local diet. The extracts prepared from each sample included an aqueous (juice or pressed solubles) and/or methanol-soluble fraction. The extracts were evaluated for antiplatelet, anticoagulant, and fibrinolytic activity in vitro at a final concentration of 1 mg/ml. The antiplatelet activity was assessed by platelet aggregation inhibition; anticoagulant activity was measured by the prothrombin time (PT), diluted prothrombin time (dPT), activated partial thromboplastin time (APTT), kaolin clotting time (KCT), and thrombin time. The fibrinolytic effect was determined with the euglobin clot lysis time and fibrin plate methods. Extracts of green beans and tomatoes inhibited platelet aggregation induced by ADP and arachidonic acid, in a concentration-dependent manner. The methanolic extracts of grapes prolonged the PT and dPT. Finally, extracts of raspberry prolonged the APTT and also presented fibrinolytic activity. In conclusion, from a screening that included a variety of fruits and vegetables, we found antiplatelet activity in green beans and tomatoes, anticoagulant activities in grapes and raspberries, whereas fibrinolytic activity was observed only in raspberries. Further investigations are necessary to advance in knowledge of the active compounds of these fruits and vegetables and their mechanisms of action.
Subject(s)
Anticoagulants/pharmacology , Blood Coagulation/drug effects , Fibrinolytic Agents/pharmacology , Fruit/chemistry , Plant Extracts/pharmacology , Platelet Aggregation Inhibitors/pharmacology , Vegetables/chemistry , Anticoagulants/isolation & purification , Blood Coagulation Tests , Blood Platelets/drug effects , Chile , Fibrinolytic Agents/isolation & purification , Humans , Plant Extracts/isolation & purification , Platelet Aggregation Inhibitors/isolation & purification , Thrombosis/prevention & controlABSTRACT
Light transmission platelet aggregation (PA), adapted to measure platelet secretion (PS), is the reference test for diagnosing platelet functional disorders (PFD). Problems with these assays include lack of standardisation, unknown reproducibility and lack of universally accepted diagnostic criteria. We addressed these issues in patients with inherited mucocutaneous bleeding (MCB). Normal and abnormal PA tests in 213 patients were reproducible in 93.3% and 90.4% of the cases, respectively. Mean intra-subject coefficient of variation for PA with strong agonists were <9% and mean intra-class correlation coefficient for weak agonists were >0.86 (P < 0.0001). Concomitant impaired PA with 10 micromol/l-adrenaline and 4 micromol/l-ADP was observed in 13.7% of the controls. This combination was not considered per se a criterion for PFD. PA with adrenaline > or = 42% or irreversible aggregation with 4 micromol/l ADP had 93% and 95% Negative Predictive Value for diagnosing PFD, respectively. PA defects were consistently associated with abnormal PS. In contrast, 14.3% of patients with MCB had isolated PS. Thus, standardized PA/PS assays are highly reproducible and concordant in normal and patient populations. Normal PA with adrenaline and low ADP concentration robustly predict a normal PA. Simultaneous PA/PS assays enable the diagnosis of isolated PS defects. This study confirmed that hereditary PA-PS defects are highly prevalent.
Subject(s)
Blood Platelet Disorders/diagnosis , Platelet Aggregation/physiology , Serotonin/metabolism , Adolescent , Adult , Blood Platelet Disorders/blood , Blood Platelets/metabolism , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Platelet Function Tests/methods , Prospective Studies , Reproducibility of Results , Young AdultABSTRACT
BACKGROUND: Patients with hereditary mucocutaneous bleeding are difficult to diagnose and many of them fulfill the category of bleeders of unknown cause (BUC). The pathogenic role of hyperfibrinolysis has received little attention, despite the successful use of antifibrinolytic drugs in treating many of these patients. Theoretically, decreased plasma procarboxypeptidase U (proCPU) levels or lower carboxypeptidase U (CPU) stability would result in higher fibrinolytic activity and bleeding tendency. METHODS: We analyzed plasma proCPU and the distribution of the Thr325Ile proCPU polymorphism in 193 patients with mucocutaneous bleeding of whom 116 were bleeders of unknown cause (BUC), and in 143 healthy, age and sex-matched controls. RESULTS: ProCPU concentration was higher in women than in men, increased with age, and was significantly correlated with clot lysis time, platelet count, APTT, and PT. However, proCPU levels were unexpectedly higher in patients than in controls (968+/-134 vs. 923+/-147 U/L, p=0.004). The allele distribution of the Thr325Ile proCPU polymorphism was similar in both groups, with a low percentage of homozygous Ile/Ile. CONCLUSIONS: Our results indicate that the proCPU system is not of major importance in the bleeding pathogenesis of these patients. The higher proCPU levels in the patients may even modestly counteract the bleeding tendency.
Subject(s)
Carboxypeptidase B2/blood , Carboxypeptidase B2/genetics , Hemorrhage/blood , Hemorrhage/physiopathology , Hemorrhagic Disorders/blood , Hemorrhagic Disorders/physiopathology , Adolescent , Adult , Alleles , Amino Acid Substitution , Child , Child, Preschool , Female , Gene Frequency , Genotype , Hemorrhage/genetics , Hemorrhagic Disorders/genetics , Humans , Isoleucine/chemistry , Isoleucine/genetics , Male , Middle Aged , Polymorphism, Genetic , Threonine/chemistry , Threonine/genetics , Young AdultABSTRACT
The larvae of scarab beetles, known as "white grubs" and belonging to the genera Phyllophaga and Anomala (Coleoptera: Scarabaeidae), are regarded as soil-dwelling pests in Mexico. During a survey conducted to find pathogenic bacteria with the potential to control scarab larvae, a native Serratia sp. (strain Mor4.1) was isolated from a dead third-instar Phyllophaga blanchardi larva collected from a cornfield in Tres Marías, Morelos, Mexico. Oral bioassays using healthy P. blanchardi larvae fed with the Mor4.1 isolate showed that this strain was able to cause an antifeeding effect and a significant loss of weight. Mortality was observed for P. blanchardi, P. trichodes, and P. obsoleta in a multidose experiment. The Mor4.1 isolate also caused 100% mortality 24 h after intracoelomic inoculation of the larvae of P. blanchardi, P. ravida, Anomala donovani and the lepidopteran insect Manduca sexta. Oral and injection bioassays were performed with concentrated culture broths of the Mor4.1 isolate to search for disease symptoms and mortality caused by extracellular proteins. The results have shown that Mor4.1 broths produce significant antifeeding effects and mortality. Mor4.1 broths treated with proteinase K lost the ability to cause disease symptoms and mortality, in both the oral and the injection bioassays, suggesting the involvement of toxic proteins in the disease. The Mor4.1 isolate was identified as a putative Serratia entomophila Mor4.1 strain based on numerical taxonomy and phylogenetic analyses done with the 16S rRNA gene sequence. The potential of S. entomophila Mor4.1 and its toxins to be used in an integrated pest management program is discussed.
Subject(s)
Coleoptera/growth & development , Coleoptera/microbiology , Pest Control, Biological , Plant Roots/parasitology , Serratia/classification , Serratia/pathogenicity , Animals , Bacterial Typing Techniques , Behavior, Animal , Feeding Behavior , Larva/microbiology , Mexico , Molecular Sequence Data , Phenotype , Sequence Analysis, DNA , Serratia/genetics , Serratia/isolation & purificationSubject(s)
Anti-Bacterial Agents , Bacterial Infections/drug therapy , Hospitalization , Hospitals, Pediatric , Hospitals, Teaching , Practice Patterns, Physicians' , Bacterial Infections/microbiology , Bolivia , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Prospective StudiesABSTRACT
Pregnant women with preeclampsia have increased serotonin levels, suggesting a possible role of this amine in abnormal pregnancy. With the hypothesis that an increase in serotonin would reduce volume expansion and cause fetal growth restriction, we evaluated the maternal and fetal effects of the administration of the serotonin precursor 5-hidroxytryptophan (5-HTP) to Sprague-Dawley rats. At pregnancy day 13 (n=19) or in random cycle nonpregnant rats (n=10), animals were assigned to a single injection of 5-HTP (100 mg/kg IP) or to a control group. Animals were studied at day 21, after overnight urinary collection. Additional pregnant rats received ketanserin (1 mg/kg), a 5-HT(2) receptor antagonist, 1 hour before 5-HTP injection. In pregnant rats, 5-HTP lowered plasma volume (control: 22+/-1.1; 5-HTP: 17+/-0.7 mL; P<0.001) and creatinine clearance, whereas serum creatinine and urinary protein excretion were increased; no changes were observed in nonpregnant rats. Systolic blood pressure did not change significantly. Urinary kallikrein activity and plasma aldosterone levels decreased only in pregnant animals. Fetal (control: 5.5+/-0.1; 5-HTP: 4.2+/-0.2 g; P<0.001) and placental weights were reduced. In nonpregnant and pregnant animals, 5-HTP caused profound renal morphological alterations and decreased kallikrein immunostaining. Preadministration of ketanserin abolished all of the changes associated with the use of 5-HTP. These data indicate that the administration of a serotonin precursor to pregnant rats limits plasma volume expansion and fetal growth via 5-HT(2) receptors, suggesting a possible role for serotonin in abnormal pregnancy. We postulate that an increased vascular resistance, both at the placental and renal levels, mediates these effects.
Subject(s)
5-Hydroxytryptophan/pharmacology , Fetal Weight/drug effects , Kallikreins/urine , Plasma Volume/drug effects , Pregnancy, Animal/metabolism , Aldosterone/blood , Animals , Blood Pressure/drug effects , Creatinine/blood , Disease Models, Animal , Female , Ketanserin/pharmacology , Pre-Eclampsia/metabolism , Pre-Eclampsia/physiopathology , Pregnancy , Random Allocation , Rats , Rats, Sprague-Dawley , Serotonin 5-HT2 Receptor AntagonistsABSTRACT
To properly characterize several isolates of Paecilomyces fumosoroseus, a fungal entomopathogen of whiteflies (Homoptera: Aleyrodidae) and other insect pests for biocontrol purposes, virulence towards Trialeurodes vaporariorum, and subtilisin-like (Pr1) and trypsin-like (Pr2) protease activity during propagule production were investigated in monospore cultures (MCs). The virulence of three MCs towards second instar whiteflies was measured and expressed as lethal median concentration (LC50). Number and widthlength ratio of propagules (blastospores, hyphal bodies, short hyphae, submerged conidia) and extracellular proteolytic activity was determined simultaneously in liquid medium. Total protease activity was assayed with azocasein, Pr1 and Pr2 activity was determined with the substrates N-Succinyl-Ala-Ala-Pro-Phe-p-nitroanilide and N-Benzoyl-Phe-Val-Arg-pnitroanilide, respectively. Natural variability in virulence, propagule production and cuticle-degrading proteases among isolates was observed. Bioassays showed a LC50 of 1.1 x 1,000, 2.5 x 10,000 and 7.6 x 10,000 conidia/ml for MCs EH-506/3, EH-503/3 and EH-520/3, respectively, EH-506/3 being the most virulent isolate. Isolate EH-503/3 produced the highest yield of propagules (7.7 x 10000000 propagules/ml), followed by EH-520/3 with 6.4 x 10000000 and EH-506/3 with 1.0 x 10000000 propagules/ml. Subtilisin-like (Pr1) and trypsin-like (Pr2) activity was present in the three MCs. Subtilisin-like (Pr1) activity was highest (745.7 UPr1/ml at 120 h) in the most virulent isolate, EH-506/3, pointing at Pr1 as a phenotypic marker of virulence for P. fumosoroseus. EH-506/3 appears to be a good candidate for whitefly biocontrol due to its high virulence, Pr1 concentration and rapid transition to blastospores in submerged liquid medium.
Subject(s)
Fungal Proteins/analysis , Hemiptera/microbiology , Paecilomyces/pathogenicity , Pest Control, Biological , Serine Endopeptidases/analysis , Animals , Chromogenic Compounds , Extracellular Fluid/enzymology , Oligopeptides/metabolism , Paecilomyces/enzymology , Paecilomyces/isolation & purification , Paecilomyces/physiology , Reproduction, Asexual , Substrate Specificity , VirulenceABSTRACT
BACKGROUND AND OBJECTIVES: Mucocutaneous bleeding (MCB) is the main expression of inherited disorders of primary hemostasis. However, the relative prevalence of these disorders, their clinical differential diagnosis, and the proportion of patients with MCB of unknown cause (BUC) after an initial comprehensive laboratory testing are unknown. DESIGN AND METHODS: We studied prospectively 280 consecutive patients with MCB and 299 matched controls, using strict inclusion and exclusion criteria. A single physician recorded the clinical data in a bleeding score and estimated the severity of bleeding in clinical categories. Laboratory criteria for the diagnosis of von Willebrand's disease (VWD) and platelet function defects were established from reference values derived from controls. RESULTS: Fifty patients (17.9%) had VWD (type 1VWD=45, type 2=5). Platelet function defects and mild clotting factor deficiencies were found in 65 (23.2%) and 11 (3.9%) patients, respectively. Thirteen (11.5%) patients had combined defects. The remaining 167(59.6%) patients had BUC, with prolonged bleeding time in 18.6% as their only abnormality. All these disorders, including BUC, were clinically undistinguishable. Moreover, no relationship was found between the severity of bleeding and VWF/platelet function variables. INTERPRETATION AND CONCLUSIONS: The diagnostic efficacy of a first laboratory testing in patients with hereditary MCB is 40.4%. Most patients have a disease(s) of high prevalence but unknown pathogenesis. Concurrent bleeding disorders in the same patient are frequent. Our results support the proposal that low plasma VWF levels, but also platelet function defects, should be considered risk factors rather than unequivocal causes of hemorrhages.
Subject(s)
Hemorrhage/etiology , Hemorrhagic Disorders/diagnosis , Mucous Membrane , Skin Diseases/etiology , Adolescent , Adult , Bleeding Time , Blood Platelet Disorders/blood , Blood Platelet Disorders/complications , Blood Platelet Disorders/diagnosis , Blood Platelet Disorders/epidemiology , Blood Platelets/drug effects , Blood Platelets/metabolism , Case Management , Case-Control Studies , Child , Child, Preschool , Coagulation Protein Disorders/blood , Coagulation Protein Disorders/complications , Coagulation Protein Disorders/diagnosis , Coagulation Protein Disorders/epidemiology , Epinephrine/pharmacology , Female , Hemoglobins/analysis , Hemorrhage/blood , Hemorrhagic Disorders/blood , Hemorrhagic Disorders/complications , Hemorrhagic Disorders/epidemiology , Hemorrhagic Disorders/genetics , Humans , Male , Medical History Taking , Middle Aged , Phenotype , Platelet Function Tests/instrumentation , Platelet Function Tests/methods , Predictive Value of Tests , Prevalence , Prospective Studies , Serotonin/metabolism , Severity of Illness Index , Signal Transduction , Spain/epidemiology , Surveys and Questionnaires , von Willebrand Diseases/blood , von Willebrand Diseases/classification , von Willebrand Diseases/complications , von Willebrand Diseases/diagnosis , von Willebrand Diseases/epidemiologyABSTRACT
Con el objetivo de caracterizar aislamientos para el control biológico demosquita blanca (Homoptera: Aleyrodidae), se estudiaron tres cultivosmonospóricos (CMs) de Paecilomyces fumosoroseus, hongo entomopatógenode la mosquita blanca (Homoptera: Aleyrodidae). Se determinó la virulencia enninfas de segundo estadio de la mosquita blanca expresada comoconcentración letal media (CL50). Se determinó la producción de propágulosfúngicos (blastosporas, cuerpos hifales, hifas cortas, conidios sumergidos)en medio líquido, se midió la relación de largo y ancho de los propágulos,y la actividad proteolítica (total; tipo subtilisina, Pr1 y tipo tripsina, Pr2)simultáneamente con la producción de propágulos. La proteasa total sedeterminó con azocaseina, y las actividades de Pr1 y Pr2 con N-Succinil-Ala-Ala-Pro-Phe-p-nitroanilida y N-Benzoil-Phe-Val-Arg-p-nitroanilida comosustratos específicos, respectivamente. Se observó variabilidad entre los tresCMs en cuanto a la virulencia, producción de propágulos y proteasas. Losbioensayos mostraron una CL50 de 1,1 x 103, 2,5 x 104 y 7,6 x 104 conidios/mlpara los CMs EH-506/3, EH-503/3 y EH-520/3, respectivamente.El CM donde se observó el mayor número de propágulos en las condicionesensayadas fue EH-503/3 (7,7 x 107), luego EH-520/3 con 6,4 x 107 y EH-506/3con 1,0 x 107 propágulos/ml. Las actividades enzimáticas de Pr1 y Pr2 sedemostraron en los tres CMs. La actividad tipo subtilisina (Pr1) fue mayor enel aislado más virulento (EH-506/3) con 745,7 UPr1/ml a las 120 h, y señala aPr1 como un marcador fenotípico de virulencia para P. fumosoroseus.EH-506/3 es un buen candidato para el control biológico de la mosquitablanca en México, por su alta virulencia, elevada concentración de Pr1 y surápida transición a blastosporas en el medio líquido ensayado(AU)
To properly characterize several isolates of Paecilomyces fumosoroseus,a fungal entomopathogen of whiteflies (Homoptera: Aleyrodidae) and otherinsect pests for biocontrol purposes, virulence towards Trialeurodesvaporariorum, and subtilisin-like (Pr1) and trypsin-like (Pr2) protease activityduring propagule production were investigated in monospore cultures (MCs).The virulence of three MCs towards second instar whiteflies was measuredand expressed as lethal median concentration (LC50). Number andwidthlength ratio of propagules (blastospores, hyphal bodies, short hyphae,submerged conidia) and extracellular proteolytic activity was determinedsimultaneously in liquid medium. Total protease activity was assayed withazocasein, Pr1 and Pr2 activity was determined with the substratesN-Succinyl-Ala-Ala-Pro-Phe-p-nitroanilide and N-Benzoyl-Phe-Val-Arg-pnitroanilide,respectively. Natural variability in virulence, propagule productionand cuticle-degrading proteases among isolates was observed. Bioassaysshowed a LC50 of 1.1 x 103, 2.5 x 104 and 7.6 x 104 conidia/ml for MCsEH-506/3, EH-503/3 and EH-520/3, respectively, EH-506/3 being the mostvirulent isolate. Isolate EH-503/3 produced the highest yield of propagules(7.7 x 107 propagules/ml), followed by EH-520/3 with 6.4 x 107 and EH-506/3with 1.0 x 107 propagules/ml. Subtilisin-like (Pr1) and trypsin-like (Pr2) activitywas present in the three MCs. Subtilisin-like (Pr1) activity was highest(745.7 UPr1/ml at 120 h) in the most virulent isolate, EH-506/3, pointing at Pr1as a phenotypic marker of virulence for P. fumosoroseus. EH-506/3 appears tobe a good candidate for whitefly biocontrol due to its high virulence,Pr1 concentration and rapid transition to blastospores in submerged liquidmedium(AU)
Subject(s)
Subtilisin/analysis , Trypsin/analysis , Paecilomyces/pathogenicity , Culicidae/pathogenicity , Pest Control, Biological , VirulenceABSTRACT
An in vitro micropropagation protocol is described for Galphimia glauca Cav. (Malpighighiaceae). Multiple shoots were formed in vitro from axillary bud explants inoculated on MS medium supplemented with indole-3-acetic acid (IAA) and kinetin (KN) combinations. A maximum of 20 shoots was obtained from a single bud in a 60-day culture period. In vitro-grown shoots were successfully rooted and transferred to field conditions (90 % survival). The sedative triterpenoid galphimine-B (1) content of micropropagated plants transferred to field conditions was similar to that of wild plants. Our results suggest that the in vitro propagation protocol described here will have positive effects on conservation of natural resources as well as on adequate techniques for multiplication of an important Mexican medicinal plant.
Subject(s)
Galphimia/chemistry , Galphimia/growth & development , Hypnotics and Sedatives/analysis , Triterpenes/analysis , Hypnotics and Sedatives/chemistry , Hypnotics and Sedatives/isolation & purification , Indoleacetic Acids/pharmacology , Kinetin/pharmacology , Molecular Structure , Pharmacognosy/methods , Plant Extracts/chemistry , Triterpenes/chemistry , Triterpenes/isolation & purificationABSTRACT
The hypoglycemic effect of methanol leaf extracts from Cecropia obtusifolia and C. peltata was evaluated in healthy mice. A significant decrease (p < 0.05) in plasma glucose levels was recorded 2 and 4 h after a single oral administration of methanol extracts (1 g/kg). This effect was correlated with the chlorogenic acid contents in both species; C. peltata, containing 19.84 +/- 1.64 mg of chlorogenic acid/g of dried leaves produced the highest decrease (D(alpha 2,60) = 20.18, p < 0.05) of plasma glucose levels (52.8%). The extracts of C. obtusifolia from Tabasco and Veracruz, showed similar hypoglycemic effects (33.3% and 35.7%, respectively) and chlorogenic acid contents (Tukey(0.05) = 1.8859) (13.3 +/- 3.2 mg/g and 13.1 +/- 1.6 mg/g, respectively). The hypoglycemic effect produced by different doses (0.1, 0.25, 0.50, 0.75 and 1 g/kg body wt, p.o.) of C. peltata showed a lineal relationship with chlorogenic acid content, reaching an ED(50) = 0.540 g/kg body wt for extract, and an ED(50) = 10.8 mg/kg body wt for chlorogenic acid. These results suggest that C. peltata is a better hypoglycemic agent than C. obtusifolia, and it could be considered for developing a phytomedicinal product to carry out clinical trials.
Subject(s)
Cecropia Plant/chemistry , Chlorogenic Acid/analogs & derivatives , Chlorogenic Acid/pharmacology , Hypoglycemic Agents/chemistry , Hypoglycemic Agents/pharmacology , Animals , Blood Glucose/drug effects , Chlorogenic Acid/analysis , Dose-Response Relationship, Drug , Male , Mice , Mice, Inbred BALB C , Molecular Structure , Phytotherapy , Plant Extracts/chemistry , Plant Leaves/chemistryABSTRACT
A methanol extract from the roots and aerial parts of Myrtillocactus geometrizans (Cactaceae) yielded peniocerol 1, macdougallin 2, and chichipegenin 3. The natural products 1, 2 their mixtures, MeOH and CH(2)Cl(2) extracts showed insecticidal and insect growth regulatory activity against fall armyworm [Spodoptera frugiperda J. E. Smith (Lepidoptera: Noctuidae)], an important insect pest of corn, and [Tenebrio molitor (Coleoptera)], a pest of stored grains in Mexico. The most active compounds were 1, 2, and a mixture (M(2)) of 1 and 2 (6:4). All these extracts, compounds and the mixture had insect growth regulating (IGR) activity between 5.0 and 50.0 ppm and insecticidal effects between 50 and 300 ppm in diets. The extracts were insecticidal to larvae, with lethal doses between 100 and 200 ppm. These compounds appear to have selective effects on the pre-emergence metabolism of Coleoptera, because in all treatments of the larvae of T. molitor, pupation were shortened and this process show precociousness in relation to controls. In contrast to S. frugiperda larvae, onset of pupation was noticeably delayed. Emergence in both cases was drastically diminished. In both pupae and in the few adults that were able to emerge, many deformations were observed. The results of these assays indicated that the compounds were more active than other known natural insect growth inhibitors such as gedunin and methanol extracts of Cedrela salvadorensis and Yucca periculosa. Peniocerol, macdougallin and chichipegenin, as well as mixtures of these substances, may be useful as natural insecticidal agents.
Subject(s)
Cactaceae/chemistry , Juvenile Hormones/pharmacology , Plant Extracts/pharmacology , Spodoptera/drug effects , Tenebrio/drug effects , Animals , Dose-Response Relationship, Drug , Insecticides/pharmacology , Larva , Limonins/pharmacology , Spodoptera/growth & development , Sterols/pharmacology , Tenebrio/growth & development , Toxicity TestsABSTRACT
Five pentasaccharide glycosides, murucins 1-5 (1-5), were isolated from the roots of the arboreal species Ipomoea murucoides, and their structures were elucidated by spectroscopic and chemical methods. Compounds 1-5 were evaluated for cytotoxicity against a small panel of cancer cell lines.