About one hundred eggs, 200 µL of fermentation filtrate at varied concentrations (100%, 75%, 50%, 25%, 10%, and 5%), Czapek medium, and distilled water were poured into each 96-well plate well (He et al., 2020). The microliter plate was covered and put in a 28 °C incubator with constant humidity. An inverted microscope (ECLIPSE, Ti-S, Nikon) was used to observe the egg hatching at 2, 4, 6, and 8 days. Unhatched eggs were placed in distilled water to confirm A. tubingensis fermentation’s ovicidal or ovistatic properties [66]. In order to confirm the accuracy of the results, each treatment was carried out in triplicate. The cumulative hatching rate was determined by applying the following formula:
The hatching inhibition percentage was determined by using the following formula:
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.