Larvicide potential of genus CrotonL. (Euphorbiaceae)inbiological control of Aedes aegyptiL. (Diptera: Culicidae)

The reemerging diseases caused by Aedes aegyptiare one of the main public health problems in the world. The control of mosquitoes using larvicidal compounds from products of plant origin is anexcellent alternative. This study aims to evaluate the larvicidal potential of fractions in hexane, chloroform, ethyl acetate and hydromethanol from the ethanolicleaf extract of two species of the genus CrotonL. (Euphorbiaceae) against larval forms of A. aegypti, as an alternative tool to control this vector. Dry leaves of Croton betaceusBaill. and Croton lundianus(Didr.) Müll.Arg. were used for biological tests. The compounds were extracted with ethanol (99.8%). The ethanolic extracts of the leaves were suspended in a methanol / water solution and were successively subjected to the liquid-liquid division process with solvents of different polarities: hexane, chloroform and ethyl acetate, giving rise to the four fractions. Larvicidal tests were performed with the ethanol extract and fractions resulting from the partition. In the study, the crude extract and the fractions showed larvicidal potential, being hexane fractionthe one with greatest activity.Mortality in C. betaceusfractions was up to 40%. Croton lundianuspresented mortality of up to 93.33% of the larvaesubmitted to the test. Data analysis showed larvicidal activity in the crude extract and fractions. The hexane fraction was more effective, especially in C. lundianus.

Repetitive element palindromic PCR (rep-PCR) as a genetic tool to study interspecific diversity in Euphorbiaceae family

Background The classification of diversity in germplasm collections is important for plant breeding. The repetitive element palindromic-polymerase chain reaction (rep-PCR) technique was used to investigate inter-specific diversity within 17 species from the Euphorbiaceae family using REP and BOX primers. Results The agglomerative cluster analysis was used to evaluate the scoring data. BOX and REP gave amplification with polymorphism of 98.84% and 100% respectively. REP marker demarcated between the subgenus peltatae. Both markers confirmed Jatropha tanjorensis as a natural hybrid between Jatropha gossypifolia and Jatropha curcas. Five random sequences from the rep-PCR gels were chosen, cloned and sequenced. The blast results demonstrated that the amplified products were from the mitochondrial genomes. Conclusion The rep-PCR molecular tool can be used to characterize diversity in plants as they are suitable for distinguishing eukaryotic genomes effectively.