Beauveria bassiana interacts with gut and hemocytes to manipulate Aedes aegypti immunity

Author:

Bitencourt Ricardo Oliveira Barbosa1,Corrêa Thaís Almeida1,Reis-Mallet Jacenir2,Santos Huarrison Azevedo1,Lowenberger Carl3,Moreira Haika Victória Sales1,Gôlo Patrícia Silva1,PinheiroBittencourt Vânia Rita Elias1,Angelo Isabele Costa1

Affiliation:

1. Veterinary Institute, Rural Federal University of Rio de Janeiro

2. Oswaldo Cruz Foundation, IOC-FIOCRUZ-RJ, RJ and FIOCRUZ-PI

3. Simon Fraser University

Abstract

Abstract Background: Mosquito-borne diseases affect millions of people. Chemical insecticides are currently employed against mosquitoes. However, many cases of insecticide resistance have been reported. Entomopathogenic fungi (EPF) have demonstrated potential as a bioinsecticide. Here, we assessed the invasion of the EPF Beauveria bassiana into Aedes aegyptilarvae and changes in the activity of phenoloxidase (PO) as a proxy for the general activation of the insect innate immune system. In addition, other cellular and humoral responses were evaluated. Methods: Larvae were exposed to blastospores or conidia of B. bassiana CG 206. After 24 and 48 hours, scanning electron microscopy (SEM) was conducted on the larvae. The hemolymph was collected to determine changes in total hemocyte concentration (THC), the dynamics of hemocytes, and to observe hemocyte-fungus interactions. In addition, the larvae were macerated to assess the activity of PO using L-DOPA conversion, and the expression of antimicrobial peptides (AMPs) was measured using quantitative Real-Time PCR. Results: Propagules invaded mosquitoes through the midgut, and blastopores were detected inside the hemocoel. Both propagules decreased the THC regardless of the time. By 24 h after exposure to conidia the percentage of granulocytes and oenocytoids increased while the prohemocytes decreased. By 48 h, the oenocytoid percentage increased significantly (P<0.05) in larvae exposed to blastospores; however, the other hemocyte types did not change significantly. Regardless of the time, SEM revealed hemocytes adhering to, and nodulating, blastospores. For the larvae exposed to conidia, these interactions were observed only at 48 h. Irrespective of the propagule, the PO activity increased only at 48 h. At 24 h, cathepsin B was upregulated by infection with conidia, whereas both propagules resulted in a downregulation of cecropin and defensin A. At 48 h, blastospores and conidia increased the expression of defensin A suggesting this may be an essential AMP against EPF. Conclusion: By 24 h, B. bassiana CG 206 occluded the midgut, reduced THC, did not stimulate PO activity, and downregulated AMP expression in larvae, all of which allowed the fungus to impair the larvae to facilitate infection. Our data reports a complex interplay between Ae. aegypti larvae and B. bassianaCG 206 demonstrating how this fungus can infect, affect, and kill Ae. aegypti larvae.

Publisher

Research Square Platform LLC

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