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The inhibitory effect of Chrysomya rufifacies (Macquart) and Cochliomyia macellaria (Fabricius) larval excretions–secretions (ES) on Staphylococcus aureus was determined using a portable colorimetric method without the need for any dedicated spectral instrument. Polystyrene 96 well microplates were used and 100 μl of the bacterial inoculum (5 × 10⁵ CFU/ml) plus 100 μl of the dipteran exosecretions at different concentrations were added to each well. Subsequently, 50 μl of a 1% solution of the triphenyl tetrazolium chloride stain was added to each well to determine the bacterial viability. The color development in each well was measured with the ImageJ software S. aureus was exposed to different concentrations of the ES of both species individually. At a concentration of 800 ppm ES of C. rufifacies or Co. macellaria, bacterial growth was inhibited 97.45 ± 1.70% and 82.21 ± 1.88%, respectively. As expected, exposure to a lower concentration (i.e., 50 ppm) was less inhibitory (C. rufifacies ES, 77.65 ± 4.25% and Co. macellaria ES, 43.54 ± 4.63%). This study demonstrates for the first time the bactericidal activity of C. rufifacies and Co. macellaria ES against S. aureus. This finding is promising as it could result in the identification and synthesis of proteins capable of suppressing pathogen development in wounds. Additionally, the proposed method can simplify the use of expensive laboratory instruments for antimicrobial activity determination.

Applications of infective juveniles (IJ) of entomopathogenic nematodes (EPN) formulated in pellets are still limited. This is principally due to limited advances in the technology of formulation. We aimed to develop a new method of mechanical formulation through material flow and to analyse its effect on the survival time of encapsulated EPN by varying the granular materials, the components of the aqueous suspension, the age of the nematodes and by applying a surface coating (C) to the pellet. Three-day-old and two-month-old Steinernema glaseri IJ were encapsulated with different proportions of diatomaceous earth (DE) and attapulgite clay (AC). The aqueous suspension containing the nematodes was prepared with double distilled water (DDW), varying proportions of Opuntia ficus-indica mucilage (OM) or gelatin (GL), and a sunflower oil surface treatment. The pellets were stored at an average room temperature of 23 ± 6°C. The best results were obtained with the following proportions: 100DE:0AC and 50DE:50AC, using the OM suspension, three-day-old nematodes and a surface C, which resulted in an average of 14 days survival time. These results confirmed that the nematodes do not die during mechanical encapsulation and that the age of the IJ as well as the loss of moisture during storage at room temperature were the factors that decreased the survival of encapsulated EPN. It was concluded that it is necessary to use neonate IJ and to reduce the moisture transfer rate in the granular structure in order to delay the desiccation of the encapsulated nematodes.

To determine larvicidal activity of the essential oil, hydrolat and botanical extracts derived from leaves of Pseudocalymma alliaceum on mosquito larvae of Culex quinquefasciatus. Groups of twenty larvae were used in the larvicidal assays. The mortality, relative growth rate, the larval and pupal duration and viability was estimated. The essential oil was analyzed by solid phase microextraction using gas chromatography coupled to mass spectrometry. Essential oil at 800 ppm showed larvicidal activity at 24 h with lethal values of LC50 and LC90 of 267.33 and 493.63 ppm. The hydrolat at 20% and 10% on 2nd stage larvae showed 100% effectiveness after 24 h. The aqueous extract at 10% had a relative growth index of 0.58, while the ethanolic and methanolic extract obtained values of 0.76 and 0.70 and control reached 0.99. Larvae treated with 10% of methanol, ethanol and aqueous extract showed a reduction in larval duration of 5.00, 2.20 and 4.35 days; ethanol extract at 1% provoke decrease of 2.40 days in the development and exhibited an increment of 3.30 days when treated with 0.01%. Aqueous, ethanol and methanol extracts at 10% reduced in 6.15, 3.42 and 5.57 days pupal development. The main compounds were diallyl disulfide (50.05%), diallyl sulfide (11.77%) and trisulfide di-2-propenyl (10.37%). The study demonstrated for the first time, the larvicidal activity of the essential oil and hydrolat of Pseudocalymma alliaceum; aqueous, ethanol and methanol extracts inhibited the normal growth and development of mosquito larvae, prolonging and delaying larval and pupal duration.